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2016-29574 Reso
RESOLUTION NO. 2016 - 29574 A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. WHEREAS, Aedes aegypti mosquitos carrying the Zika virus, and persons infected with the Zika virus, have been identified within the City of Miami Beach (City); and WHEREAS, the Zika virus poses a serious health threat to the City's citizens and its visitors due to its link to microcephaly among infants born to infected pregnant women and potential neurological disorders in affected adults; and WHEREAS, methods to control and eradicate Zika-carrying mosquitos in the City include the spraying of pesticides, such as Naled, which also raise health concerns for the City's residents; and WHEREAS, one alternative to traditional mosquito control techniques is the use of genetically modified male mosquitos (0X513A) developed by Oxitec, Ltd. (a subsidiary of Intrexon Corp. (NYSE:XON)) that don't bite or transmit disease and which transmit a self- limiting gene to their offspring causing the offspring to die before becoming functioning adult mosquitos; and WHEREAS, Pinellas County, Florida has already requested the U.S. Department of Health and Human Services to utilize its "emergency use" authorization under Section 564 of the Food, Drug, and Cosmetic Act, as amended by the Pandemic and All-Hazards Preparedness Act of 2013, to allow Pinellas County to utilize OX513A mosquitos which have already been approved by the FDA for a pilot program in Monroe County, Florida; and WHEREAS, the use of genetically modified mosquitos to reduce Zika-carrying mosquitos has been used in Brazil, Grand Cayman Island, Panama, Columbia, and Malaysia and has resulted in reported reduction rates of 90% or higher, which is more effective than the traditional methods of spraying Naled and the larvicide Bti; and WHEREAS, on August 5, 2016, the FDA published a final environmental assessment and a finding of no significant impact relative to the use of genetically engineered mosquitos to control Zika-carrying mosquitos in a proposed field trial in Monroe County to be conducted in conjunction with the Florida Keys Mosquito Control District. NOW, THEREFORE, BE IT DULY RESOLVED BY THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, that the Mayor and City Commission hereby authorize the City Manager to send a letter to the U.S. Department of Health and Human Services to request permission from the U.S. Food & Drug Administration to explore the prospect of using genetically modified mosquitos to combat mosquitos carrying the Zika virus in the City of Miami Beach and urge Miami-Dade County to likewise request permission from the FDA to explore the prospect of using genetically modified mosquitos to combat mosquitos carrying the Zika virus in the County. PASSED AND ADOPTED this f day of September, 2016. ,it" ATTEST: Philip Le r `I. , Rafa-I E. Grp."-lado, Ci Clerk APPROVED AS TO ..'am w, �� FORM & LANGUAGE �4' .t\NI . & % (j & F R CU ION a ff N-••• .. k A C-47 1 -(2,1 411,.4 0. .. ,... ,,,,,,,,,,....„..„, . : ,,,,,„i` ,,, t City Attorney Dote lir I, �• INCORG 'ORATED I ' f: 8 - . Cn ,, ;' 40/_,., 1 7/ c— • !J + 0+ 6c : F:WTTO\TURN\RESOS GMO MOSQUITOS 2016-29574 RESO.doc City of Miami Beach, 1700 Convention Center Drive,Miami Beach,Florida 33139,www.miamibeachA.gov Office of the City Manager Tel:305-673-7010, Fax:305-673-7782 September 21, 2016 Secretary Sylvia Mathews Burwell U.S. Department of Health & Human Services 200 Independence Avenue, S.W. Washington, D.C. 20201 Re: Zika Virus in Miami Beach, Florida Dear Secretary Burwell, On September 14,2016,the City of Miami Beach Commission adopted a resolution authorizing me, as City Manager, to send this letter requesting permission from the Food and Drug Administration to explore the prospect of using genetically modified mosquitos to combat mosquitos carrying the Zika virus in the City of Miami Beach. A copy of the resolution is attached. The City Commission is making this request in the wake of the first identified, non- travel related cases of the Zika virus within our country's borders. As you are aware, the Zika virus poses a serious risk to our community, particularly to pregnant women and their unborn children. Despite relentless efforts by the City and Miami-Dade County to combat the spread of the virus, the recent discovery of another pool of mosquitoes that has tested positive for Zika reinforces the need for us to continue being as aggressive as we can be against Zika. With this in mind, we are specifically requesting that your office utilize its "emergency use" authorization pursuant to Section 564 of the Food, Drug and Cosmetic Act, as amended by the Pandemic and All-Hazards Preparedness Act of 2013 ("Section 564"). As Secretary of Health and Human Services,you may use the"emergency use"provisions of Section 564 to allow the City of Miami Beach to utilize the mosquitoes (OX 513A) that have been approved for the proposed pilot program in Monroe County, Florida. As you know, the FDA released its findings last month, which conclude that the proposed field trial in Monroe County would have no significant impact on the environment. Scientific studies also indicate that the use of the mosquitoes (0X513A) is more than 91 percent effective in eliminating the Aedes aegypti mosquito that carries the Zika virus. • We want to ensure that our City has every tool at its disposal to combat the spread of the Zika virus and, therefore, we request that our City Commission be authorized under Section 564 to utilize the mosquitoes (0X513A), without any undue delay, should the Commission deem it appropriate to employ this strategy. Pending your response to this request, the City will continue working closely with State of Florida and County officials to ensure that we are doing everything in our power to protect the health and well-being of our residents, businesses, and visitors against the spread of the Zika virus in our community. Thank you for your immediate attention and consideration to this request. Sincere , Jimmy . Mor I s CC: Mia i Beach City Commission, County Mayor, Carlos A. Gimenez Deputy Mayor, Alina T. Hudak vVe are comma"ed to proud ng exceoen'pjbhc serpce and safely to a'!who',.e wort and pay'r our,ibrart troplca, h,s'onC commun i' 9/19/2016 Coversheet New Business and Commission Requests-R9 W MIAMI BEACH COMMISSION MEMORANDUM TO: Honorable Mayor and Members of the City Commission FROM: Commissioner Rosen Gonzalez DATE: September 14,2016 SUBJECT: DISCUSS THE USE OF GENETICALLY MODIFIED MOSQUITOS (TECHNOLOGY) IN MIAMI BEACH. ANALYSIS Please place on September 14th Commission Meeting Agenda, a discussion item relating to OXITEC, LTD and their GMO mosquito technology. Studies show that releasing the GM mosquito into communities reduces the mosquito population by 90 percent. Given that Miami Beach is a series of barrier islands, this experiment would be a controlled environment and this company could easily measure its research. Legislative Tracking Commissioner Rosen Gonzalez ATTACHMENTS: Description D OXITEC. LTD o OXITEC. LTD 2 © Letter f/Elected Officials of Pinellas County to HHS Secretary • http://m iam ibeach.novusagenda.com/agendapublic/CoverSheet.aspx?Item ID=1456&M eeti nglD=235 1/1 fi U111 4fle CICLLU' U LCc1Uel UI PINELLAS4COUNTY August 26,2016 Secretary Sylvia Mathews Burwell U.S. Department of Health&Human Services 200 Independence Ave., S.W. Washington,D.C.20201 RE: Zika Virus in Pinellas County, Florida Dear Secretary Burwell: On behalf of many of the concerned, elected leaders in Pinellas County, Florida, we are writing you in the wake of the first identified, non-travel related case of the Zika virus within our county's borders. As representatives of the nearly one million residents of Pinellas County, we want to ensure that our county has every tool at its disposal to combat a potential spread of the virus. Specifically, we are requesting that your office utilize its"emergency use"authorization pursuant to Section 564 of the Food, Drug and Cosmetic Act, as amended by the Pandemic and All-Hazards Preparedness Act of 2013. ("Section 564"). As Secretary of Health and Human Services, you may use the "emergency use" provisions in Section 564 to allow Pinellas County to utilize the mosquitoes (0X5I3A) that have been approved for the proposed pilot program in Monroe County, Florida. As you know, the Food and Drug Administration ("FDA") released its findings earlier this month, which indicated the proposed field trial in Monroe County would have no significant impact on the environment. While the FDA's findings indicate there will be no significant environmental impact, there is evidence indicating the proposed field test could be up to 99%effective in eliminating the Aedes aegypti mosquito,which carries the Zika virus. Therefore, we request our County Commission be authorized to utilize this option, should they deem it necessary to combat the spread of the Zika virus in our community. We request our County Commission be authorized to do so under Section 564 without any undue delay. As you are aware,this virus poses a serious risk to our community,particularly to pregnant women and their unborn children. Our community cannot afford any delay in the utilization of every tool at our disposal. Thank you for your immediate attention to this matter. Sincerely, 0414.414941, P 24/4 ?P`. ..1611/141 (-1; Representative Chris Sprowls Congressman Dav' W.Jolly Senator Jack Latvala Senator Jeff Brandes Representative Larry Ahern c3(ea (948-*-74 tzt,. / Representative James Grant Representative Chris Latvala Representative Kathleen Peters Representative Darryl Rouson elko'La'°- Qkez..67r4" d ?"," itte,ak Commissioner Charlie Justice Commissioner Dave Eggers Commissioner Janet Long Commissioner John Morroni Commissioner Pat Gerard flaAay.. Woa�a � �e«Kvh`i- WeL�G Commissioner Karen Seel Commissioner Kenneth Welch 0 OXITEC FDA Publishes Final Finding of No Significant Impact and Environmental Assessment on Oxitec's Self-limiting Mosquito • Oxford, UK,5 August 2016-The US Food and Drug Administration's Center for Veterinary Medicine (FDA-CVM)today published a final finding of no significant Impact (FONSI) and final environmental assessment(EA)on Oxitec's self-limiting OX513A Aedes aegypti mosquito for an investigational trial in the Florida Keys. The finding concludes that a field trial of the Company's genetically engineered (GE) OX513A mosquitoes in Key Haven, Florida, will not result in a significant impact on the environment. The publication of the final FONSI and EA follows an FDA-led evaluation of potential Impacts on • health and the environment of the proposed trial.This culminated in the publication of a preliminary FONSI in March 2016, after which there was a period of public comment. These public comments were reviewed by the FDA-led team before the final documents were published today. Oxitec's Chief Executive Officer Hadyn Parry said, "We've been developing this approach for many years, and from these results we are convinced that our solution is both highly effective and has sound environmental credentials.We're delighted with the announcement today that the FDA, after their extensive review of our dossier and thousands of public comments for a trial in the Florida Keys, have published their final view that this will not have a significant impact on the environment. We are now looking forward to working with the community in the Florida Keys moving forward." The purpose of the proposed trial is to determine the efficacy of Oxitec's self-limiting mosquitoes for • the control of the local population of Aedes aegypti in Key Haven,Monroe County,Florida. Oxitec's self-limiting mosquitoes have been genetically engineered so that their offspring die before reaching adulthood. Male Oxitec mosquitoes, which do not bite or spread disease, are released to mate with wild female Aedes aegypti so that their offspring die, reducing the population. Efficacy trials in Brazil, Panama,and the Cayman Islands have tested this approach,and in each of these trials the population of Aedes aegypti was reduced by more than 90%— an exceptional level of control compared to conventional methods,such as insecticides. The FDA review team consisted of experts from the Center for Veterinary Medicine (CVM), the Centers for Disease Control and Prevention (CDC), and the Environmental Protection Agency (EPA). The FDA led an extensive review of evidence from trials in urban environments performed in Brazil ) and the Cayman Islands since 2009, and data from numerous safety studies, site inspections and independent experts. 1 For more information: Oxitec Florida Keys Project FAQ:http://www.oxitec.com/health/fiorida-keys-project/ Florida Keys Mosquito Control District:http://keysmosquito.org/latest-gm-information/ About Oxitec Oxitec is a pioneer in using genetic engineering to control Insect pests that spread disease and damage crops, and was founded in 2002 as a spinout from Oxford University (UK). Oxitec is a subsidiary of Intrexon Corporation (NYSE: XON), which engineers biology to help solve some of the world's biggest problems. Oxitec Contact: • Matthew Warren Press Officer Tel:+44(0) 1865 832 393 info @oxitec.com ØoxITEc Oxitec's Vector Control Solution A Paradigm Shift in Mosquito Control OXITEC TABLE OF CONTENTS EXECUTIVE SUMMARY 3 A GROWING GLOBAL THREAT FROM AN INVASIVE MOSQUITO SPECIES 3 AEDESAEGVPTI—PREFERENCE FOR HUMAN BLOOD;NUMEROUS CHALLENGES 4 FAST GROWING AND INCREASINGLY CHALLENGING VECTOR-BORNE DISEASES 4 o DENGUE VIRUS IS THE FASTEST GROWING VECTOR-BORNE DISEASE 5 o ZIKA VIRUS ONE OF THE MOST CHALLENGING THREATS TO HUMAN HEALTH 6 o CHIKUNGUNYA VIRUS AT THE CENTER OF NUMEROUS DIFFICULT DISORDERS 7 OXITEC'S MOSQUITO SOLUTION:THE'FRIENDLY MOSQUITO'TO HUMANS AND THE ECOSYSTEM 8 OXITEC'S PRECISE,REGULATED METHOD ONE OF SEVERAL VECTOR CONTROL APPROACHES ALTERING THE GENETICS OF AEDESAEGVPTI 10 SIGNIFICANT SCALABILITY;EXPANSION OF PRODUCTION CAPACITY UNDERWAY 13 OXITEC'S UNPARALLELED CONTROL OF THE AEDESAEGYPT/VECTOR 14 APPENDIX 1:FIELD DATA SUMMARIES FOR THE OX513AAEDESAEGYPT/SUPPRESSION PROJECTS 15 o EAST END,GRAND CAYMAN,CAYMAN ISLANDS 15 o ITABERABA NEIGHBOURHOOD,JUAZEIRO(BAHIA),BRAZIL 18 o NUEVO CHORRILLO,ARRAIJAN, PANAMA 20 APPENDIX 2:TABLES 23 APPENDIX 3:REFERENCES 23 APPENDIX 4:OXITEC PUBLICATIONS 27 ©2016 Intrexon Corporation.All rights reserved. 2 OXITEC Oxitec's Vector Control Solution: A Paradigm Shift in Mosquito Control Executive Summary Effective vector control, and more specifically mosquito control, is a complex and difficult problem as illustrated by the continuing prevalence and spread of mosquito-transmitted diseases globally. Through the responsible engineering of biology Oxitec has developed a paradigm shift in mosquito control leading to unparalleled levels in the suppression of Aedes aegypti, the main vector for several of the world's most damaging viruses including Zika, dengue, and chikungunya. Oxitec's revolutionary and environmentally friendly OX513A male mosquitoes are precisely engineered with a self-limiting gene that expresses a non-toxic and non-allergenic protein to prevent their offspring from surviving to adulthood. In five separate efficacy trials across three different countries, releases of Oxitec OX513A mosquitoes led to a greater than 90% reduction in the local Aedes aegypti populations. A Growing Global Threat from an Invasive Mosquito Species Difficult diseases attributable to arboviruses transmitted by the Aedes mosquito vector, principally Aedes aegypti, pose an increasing global threat to human health. Aedes aegypti is an invasive species, or a non-native species that causes ecological or economic harm in a new environment, in well over 100 countries. Its passage from West Africa to other continents occurred as a result of early trade between the Old and New Worlds. More recently, the rising trend of globalization coinciding with the halt of Aedes aegypti eradication programs roughly four decades ago has led to significant expansion of its territory. Today worldwide distribution of Aedes aegypti extends to all of the continents except Antarctica making it one of the most widespread species globally. It is estimated up to half of the world's population live alongside these dangerous mosquitoes.1 Globalization has benefitted their success in a number of ways including increasing urban populations as well as climate change expanding their potential habitats. Most relevant to the spread of disease, however, has been the development of modern transportation and means of travel and trade from one country to another.2 • r MP o V Figure 1. Global map of the predicted distribution of Ae.aegypti.The map depicts the probability of occurrence(from 0 blue to 1 red)at a spatial resolution of 5 km x 5 km.2 ©2016 Intrexon Corporation.All rights reserved. 3 OXITEC Aedes aegypti— Preference for Human Blood; Numerous Challenges The Aedes aegypti species is anthropophilic and its females' preference for biting humans to secure blood necessary to produce fertile eggs has led to breeding in and around our homes, office buildings, and schools. The domestication of these "container breeders" has made them extremely difficult to control. Among the many challenges associated with Aedes aegypti are: • Zika, dengue and chikungunya viruses are carried and transmitted to humans through female Aedes aegypti leading to widespread diseases with no cures." • Females are aggressive, repeat day-biters increasing the potential spread of diseases.' • Females can be born carrying viruses and therefore have an innate ability to transmit disease 3-s • Females lay 100 to 200 eggs per batch and can produce up to five batches during their two to four week lifetime.6 • Females will not lay an entire batch at one site, but rather spread eggs over two or more sites.' • Eggs can stay dormant for over six months and hatch at any time creating issues for conventional vector control approaches.8 • Larvae have been found in a host of artificial containers including discarded bottle caps, soda cans,cups and tires creating issues for conventional vector control approaches.' • Estimated annual costs of diseases Aedes aegypti transmits continue to rise. Excluding chikungunya and Zika, which the World Bank estimates will have an economic impact of $3.5 billion in Latin America in 2016,the estimated cost for dengue exceeded$39 billion in 2011.9,1° In addition, the repeated use of chemical insecticides is leading to rising resistance in Aedes aegypti worldwide creating operational challenges for mosquito control programs." Commonly used insecticides including organophosphates and pyrethroids are no longer effective in many areas. There has also been documented resistance in Aedes aegypti mosquitoes to the once widely-used DDT(dichlorodiphenyltrichloroethane),a powerful organochloride insecticide."Z This insecticide resistance is due to specific genetic traits which enable detoxification of insecticides allowing for the survival of wild mutant mosquitoes which 'naturally' have this genetic code. This genetic programming persists in the environment in subsequent generations of mosquitoes. Aside from this emerging resistance, many insecticides such as DDT have been banned due to poor environmental safety records. Fast Growing and Increasingly Challenging Vector-Borne Diseases Mosquitoes that transmit disease represent only a small fraction of the roughly 3500 mosquito species, yet they render this group of insects the deadliest animal family in the world.13 Over one million people die each year from the bite of a female mosquito. After its entry into the Americas from Africa, the invasive Aedes aegypti mosquito caused deadly yellow fever epidemics as far north as Philadelphia, Pennsylvania, and as far south as Buenos Aires, Argentina. Yellow fever is now mainly found in tropical and subtropical areas in South America and Africa with an estimated 200,000 cases each year causing 30,000 deaths.14 While a recent resurgence of yellow fever in Latin America and Africa has led to concerns and presents a potential serious health risk due to large population centers in these areas, this virus, for now, finds itself fourth on the list of dangerous arboviruses transmitted by Aedes aegypti.1546 Today, females of the Aedes aegypti species are the primary vector for three of the most damaging arboviruses to public health and economies of nations: ©2016 Intrexon Corporation.All rights reserved. 4 0 OXITEC 1. Dengue virus is the fastest growing vector-borne disease today. According to the Centers for Disease Control and Prevention (CDC), there are an estimated 400 million dengue infections each year in over 125 countries.17 Dengue fever is caused by any one of four wo°=` i,3 3!,b,�- r, ,r closely related dengue viruses (DENV) or ..1 e' .4 , serotypes: DEN 1, DEN 2, DEN-3 and DEN 4. DENV are single-stranded RNA viruses that 4 belong to the genus Flavivirus.'8 As many as ..�x � e ` 50% of dengue infected individuals are oeu � tic and have no clinical signs or r '. a �',, asymptomatic g symptoms of disease. The spectrum of illness can range from a mild non-specific febrile syndrome, to classic dengue fever 2004 ` , , �1 4.4944(DF), to the severe forms of the disease e 44 dengue hemorrhagic fever (DHF) and '' ; ha �. 3i 19 co..,"09Ft dengue shock syndrome(DSS). � . � "'' o9+a •° �w • ® 0941 �, oeFS p' In addition to these well-known q s I 1111 I °B" oars manifestations of dengue virus, there are a wide range of atypical multi-systemic '' manifestations including neurological Figure 2. The change in distribution of dengue serotypes between 1970 and 200418 disorders such as Guillain-Barre syndrome, meningoencephalitis, encephalitis, and encephalopathy, as well as presentations of gastrointestinal, lymphoreticular, cardiovascular, renal, and musculoskeletal conditions.20-23 Recovery from infection by one serotype of dengue provides lifelong immunity against it, yet cross-immunity to the other serotypes is partial and temporary. Subsequent infections by other Y Yp P serotypes increase the risk of developing severe dengue due to antibody-dependent enhancement,a known phenomenon in which neutralizing antiviral proteins facilitate virus entry into host cells, leading to increased infectivity and a more severe clinical infection.24 Before 1970 only nine countries experienced severe Figure 3.Laboratory-Confirmed DHF in the Americas dengue epidemics and they were largely confined to Prior to 1981 versus 1981-2003 Southeast Asia. This was likely due to the success of the Pan American Health Organization's Aedes aegypti Y ';`� -'4, "``,►-, eradication program that started in the 1950s which 40.4. t" '� protected the Americas from serious DENV epidemics. ,. Discontinuation of this eradication program in the Prior to 1 ti 1981- Ill 1981 • zoo3 + 1970s allowed the Americas to become re-infested t with Aedes aegypti mosquitoes, and large numbers of Nt. Source.WHOPAHOcDC " DHF cases began to appear in the Caribbean and Latin America in 1981 (Figure 3).25 Severe dengue is now endemic in more than 100 countries in regions of Africa,the Americas,the Eastern Mediterranean, South-East Asia and the Western Pacific. The number of DHF cases has climbed to roughly 500,000 annually resulting in an estimated 22,000 deaths. Severe dengue has become a leading cause of hospitalization and death among children in Asian and Latin American countries.26 ©2016 Intrexon Corporation.All rights reserved. 5 V, & 0XITEC 2. Zika virus has recently emerged as one of the most challenging threats to human health given its apparent links to microcephaly among infants born to infected women and neurological disorders such as Guillain-Barre syndrome (GBS).27-29 Since the beginning of 2015, Zika has spread rapidly through the Americas and active transmission of the virus is now present in over thirty countries and territories.3o,31 Figure 4.Countries and Territories in the Americas with Active Zika Virus Transmission" Like dengue, Zika (ZIKAV) is a single-stranded RNA virus that belongs to the genus Flavivirus.32 As '; many as 80% of Zika infected individuals are ' asymptomatic and have no clinical signs or symptoms of disease. The most common symptoms of Zika are fever, rash, joint pain, and i conjunctivitis, and the illness is usually mild lasting � � � up to a week. These minor reactions had - ' incorrectly given a false sense that Zika was of least concern with respect to the viral diseases spread by Aedes aegypti. In 2015 that perception drastically changed. a '. Just seven months after an initial epidemiological alert in May 2015 that public health authorities in Brazil were investigating a possible autochthonous transmission of the Zika virus,a second epidemiological alert was issued in December by the Pan American Health Organization/ World Health Organization (PAHO/WHO).33 This alert was issued given the increase of congenital anomalies such as microcephaly, GBS, and other neurological and autoimmune syndromes in areas where Zika virus was circulating and their possible relation to the virus. Within just one year of its first reported autochthonous transmission, Brazil is estimated to have between 400,000 to 1,300,000 cases of Zika and over 4,000 suspected cases of microcephaly.34'35 In addition to birth defects and neurological disorders, Zika has been associated with meningoencephalitis, a dangerous inflammation of the membranes that surround the brain, as well as acute myelitis.36'37 In February 2016, Zika became the first mosquito-borne disease to be declared a Public Health Emergency of International Concern (PHEIC) by the World Health Organization (WHO). They noted the cluster of microcephaly cases and other neurological disorders such as GBS reported 1 in Brazil, following a similar cluster in French Polynesia in 2014, and urged aggressive implementation of vector control measures to manage the Zika outbreak.38 .44t,s,t.i...4:?. — -. - 111 — - *. : - t4 - rtil" .'4i ' 7.016 a'` .�9."''s-iie. 174111 t*s. 007-2016 :::axl , 2015-2016 t.- —,�� a .. Figure 5.Global Spread of Zika Virus—Geographic zone-specific time ranges of known incidences are shown color-coded according to the year of the earliest reported case(locally-acquired cases or viral isolation)31 ©2016 Intrexon Corporation.All rights reserved. 6 "''' 0 OXITEC 3. Chikungunya virus results in numerous difficult disorders,from neurological to rheumatic and beyond. It swept into the Caribbean in 2013 and Central America thereafter.An epidemic soon followed with over 1,000,000 cases occurring within one year.39 Chikungunya has been identified in over 60 countries in Asia, Africa, Europe and the Americas. Within the United States,chikungunya virus disease became a nationally notifiable condition to CDC in 2015.40 Unlike dengue and Zika, chikungunya (CHIKV) is an 2015 RNA virus that belongs to the genus Alphavirus. Approximately 3% to 28% of chikungunya infected alla individuals are asymptomatic and have no clinical signs or symptoms of disease.41 It causes fever and severe joint pain, and other symptoms include muscle pain, headache, nausea, fatigue and rash which typically resolve in 7-10 days. The disease shares some clinical signs with dengue, and can be misdiagnosed in areas where dengue is common.42 2014 Chikungunya, like Zika and dengue, has resulted in a number of neurologic diseases such as Guillain-Barre syndrome, meningoencephalitis, myelitis, and cranial nerve palsies. Additionally CHIKV has been associated with rheumatic disorders including rheumatoid arthritis, spondyloarthritis, and undifferentiated - polyarthritis.43 Other serious complications that are • rare include myocarditis, ocular disease (uveitis, A � „"w retinitis), hepatitis, acute renal disease, and severe Figure 6.States in U.S.reporting travel-associated and bulbous lesions.' locally acnuirpri chikunpunva caspc in 7014 and 701S 4° Further, intrapartum transmission of CHIKV can result in complications for the baby, including neurologic disease, hemorrhagic symptoms,and myocardial disease.45 Observations also suggest possible maternal-fetal transmission of CHIKV during early pregnancy,yet risks appear to be very low 46 After maternal CHIKV infection,there are rare reports of spontaneous abortions.°' Chikungunya often causes large outbreaks with high attack rates, affecting one-third to three- quarters of the population in areas where the virus is circulating. Outbreaks of CHIKV disease have occurred in Africa, Asia, Europe, South America, islands in the Indian and Pacific Oceans, and islands in the Caribbean.41'47 Figure 7. May S`h May S`h—June 4th Puerto Rico Outbreak 1111141 g T*'i 1 t11 g Y�'i "r of CHIKV in 2014- �4 j { *► 1 NIP A* ; *� y� Geographic distribution y�i A s o'litt,11,4- � ��i 'A ,4�� �# of of laboratory-positive 1011.0,�ill�► �k *r��" '���� Chikungunya cases, May 5th-Aug 12`h 47 May 5`h—July 4`h May 5`h—Aug 12th * pia/ Ave- t s a►#_,�il�,. ©2016 Intrexon Corporation.All rights reserved. 7 0 0XITEC Dengue ,� � Chikungunya Yellow Fever Figure 8.Female Aedes aegypti is the primary vector for dengue,Zika,chikungunya and yellow fever In summary, Zika has generated a significant amount of warranted attention since its linkage with life-changing disorders in late 2015. Yet many years of research on dengue and chikungunya provide evidence these viruses also cause a number of devastating conditions without effective clinical preventions or treatments including neurological and rheumatic disorders. What is also evident is despite decades of research on arboviruses, we are still learning about their impact on the human system and they are all far from being fully understood. We also have yet to entirely comprehend the impact of co-infection of humans with multiple viruses, yet this is occurring.48 It is important to note that while we continue to learn more about these viruses and the many non-curable diseases associated with them,they continue to evolve. What is constant, however, among all of four of these devastating viruses — dengue, Zika, chikungunya and yellow fever—is their primary vector,the female Aedes aegypti(Figure 8). Oxitec's Mosquito Solution: the 'Friendly Mosquito' to Humans and the Ecosystem Oxitec has been focused on the control of Aedes aegypti for over a decade and has pioneered a biological method of vector control to suppress wild populations of this dangerous mosquito species. This novel approach utilizes male mosquitoes which don't bite or transmit disease and live less than a week. These '0X513A' males search for and mate with wild Aedes aegypti females.The offspring of these mating events inherit a self-limiting gene and die before becoming functional adults, thereby reducing the wild population. Importantly this approach leaves no environmental footprint. In addition to OX513A not pursuing humans because males do not bite, the power of this 4z= biological solution is evident in its species- specific targeting. Of the "3500 mosquito 0. species known to exist today, a select few spread disease.13 Aedes aegypti is one of the anthropophilic species transmitting arboviruses to humans. OX513A males control populations of this single dangerous species by mating with Aedes aegypti females. The remaining mosquito species, as well as beneficial insects like bees and butterflies, are not impacted by Oxitec's solution. This differs from other conventional approaches that do not discriminate which Figure 9.In Piracicaba,Brazil,96%of local residents in insects they kill, beneficial or non-beneficial, CECAP/Eldorado district support the Oxitec program causing significant effect on ecosystems. ©2016 Intrexon Corporation.All rights reserved. 8 OXITEC Understanding the potential hazards associated with approaches to mosquito control that change the biology of the insect and persist through subsequent generations, Oxitec intently focused on a self-limiting solution that does not carry that risk. Neither the Oxitec mosquitoes nor their progeny persist over time in the environment.49 Another design aspect imperative to Oxitec was engineering a built-in biological marker identifiable in the , ecosystem enabling superior monitoring. 004 f' The ability to monitor the deployment and impact of a treatment is important for the implementation of successful vector control programs. Therefore Oxitec's mosquitoes are engineered with a fluorescent color marker, providing a means of both visual and molecular tracking for mosquitoes in the rearing facility and in the field. Through this Figure 10.Brazil press describe Oxitec solution as system it is possible to collect larvae from The Friendly Mosquito' the area of release and determine the proportion of Oxitec mosquitoes versus wild pest mosquitoes as a measure of population suppression. This built-in marker allows superior traceability,offering a precise, efficient and cost-effective monitoring tool for adaptive management programs,as well as quality control and safety assurance processes. Efficacy trials of Oxitec's technology all resulted in Aedes °.4 Treated Area with OX513A aegypti population suppression Control area below the threshold designated in o.3 a peer-reviewed model for dengue I epidemic disease transmission."'" 0.2 Despite their widespread use insecticides have not achieved this o level of vector suppression. 0.1 'I Additionally OX513A can control and repress those populations of 0 ♦ A• Aedes aegypti that carry oti Os, o'y, o1� olti o'ti o�� o'er o�' 01 o�'' Al' e1" \A% $� eery e1' eery e1' (A� tai insecticide resistance genes,which 4,a° Pt° . ' ,�° �° ,�° �F° °° ee / Ja �Ja 4,4 yet p o., ec. , <te are leading to a rising tide of Trial in collaboration with University of Sao Paulo and Moscomed ineffectiveness of conventional Figure 11.Oxitec's OX513A results in Mandacaru,Brazil suppressed insecticides. Aedes aegypti by>90%and sustained control through rainy season Furthermore with >150 million Oxitec mosquitoes released to date through use in field suppression programs, no off-target effects have been observed, no evolution of resistance to the self-limiting gene has been seen, and there has never been any assortative mating detected. The solution has been successfully applied alongside other interventions such as insecticide applications and is compatible with all other interventions. OX513A has been approved by Brazil's National Biosafety Technical Commission (CTNBio)for releases throughout the country,53 received a preliminary finding of no significant impact from the U.S. Food and Drug Administration,54 and also has been issued a positive recommendation for planned operational deployments by the World Health Organization.55 ©2016 lntrexon Corporation.All rights reserved. 9 OXITEC Oxitec's Precise, Regulated Method One of Several Vector Control Approaches Altering the Genetics of Aedes aegypti There are several vector control methods that genetically alter the biology of mosquitoes, yet Oxitec's is the only one currently regulated as a recombinant organism. With this distinction comes a high level of science-based stringent regulatory overview for Oxitec along with a level of community inquiry through non-governmental organizations. These are welcome as safety is of the upmost importance to Oxitec. p P With the protection of people in mind, regulatory review of any method to control Aedes aegypti that changes the genetics of these mosquitoes at the molecular level should be considered. Approaches that do not trigger the narrow regulatory definition of a genetically engineered (GE) organism frequently fall outside of regulatory examination to ensure they are safe and thoroughly evaluated before use in the field. Oxitec's Precise,Self-limiting Approach to Control Aedes aegypti: Oxitec's self-limiting approach holds significant advantages over other vector control methods that genetically alter the biology of mosquitoes. Modification to the genome of Oxitec's engineered strain has been thoroughly characterized and is genomically stable. Evaluation over 150 generations has shown the self-limiting gene is inherited in a Mendelian fashion with no change in performance. Furthermore, Oxitec strains have shown strong performance profiles in the assessment of mating fitness against a wild-type comparator strain.56'57 This is consistent with the field results demonstrating OX513A males can compete for mates well enough to significantly suppress target field populations of Aedes aegypti.495052 Moreover, after releases are stopped and mosquitoes die, this self-limiting vector control solution does not persist in the environment.49 For an additional level of safety, Oxitec has engineered a biological fluorescent color marker enabling robust monitoring capabilities and measures of responsiveness built into the system. As previously mentioned, understanding the potential hazards with approaches to mosquito control that change the biology of the insect that may persist in the gene pool through subsequent generations,Oxitec intently focused on a self-limiting solution that did not carry that risk. Other Approaches to Mosquito Control That Cause Genetic Changes in Aedes aegypti: Other approaches to Aedes aegypti population control lead to genetic changes at the molecular level that in some cases are random or not well defined. Despite not being regulated as GE organisms, several of these methods could lead to mutagenesis in Aedes aegypti that may sustain in wild populations with unknown consequences. 1. Chemical Insecticides — The repeated use of chemical insecticides is leading to rising resistance worldwide creating operational challenges for mosquito control programs." Commonly used insecticides including organophosphates (i.e., temephos, malathion, fenitrothion) and pyrethroids (i.e., permethrin, bifenthrin, deltamethrin) are no longer effective for Aedes aegypti in many areas.58-60 Additionally there has also been documented Aedes aegypti resistance to the once widely-used DDT.12 ©2016 Intrexon Corporation.All rights reserved. 10 010XITEC This resistance to chemical insecticides is due to particular genetic traits that allow for mutant mosquitoes to survive. While the underlying molecular mechanisms, including the identification of enzymes involved in insecticide detoxification, have been studied, they are not completely understood.60 Molecular screening for common insecticide target-site mutations in Aedes aegypti have shown a high frequency mutation of 'knock down resistance' in the sodium channel, as well as significant elevated activities of cytochrome P450 monooxygenases, glutathione S-transferases and carboxylesterases at both larval and adult stages.68-6° In addition to insecticide resistance hampering conventional control and eradication efforts, these genetic modifications that arise from insecticide resistance persist in the gene pools of subsequent generations of Aedes aegypti mosquitoes. 2. Radiation-based Sterile Insect Technique (SIT)—Regardless of the source of radiation, X-ray or gamma, this form of SIT mosquito control may result in genetic instability of the insect through random and difficult to categorize genomic changes. This damage to, and inexact mutation of, DNA may have unpredictable effects that persist in the environment. The basis of radiation sterilization is the induction of random dominant lethal mutations that render males sterile. Studies on radiation impacting the biology of mosquitoes have described a marked species difference in radiation sensitivity, measurable negative effects on insect performance in the laboratory, as well as a need to radio-sterilize males as adults in order to minimize the fitness cost of the radiation.61-63 Utilization of less than fully sterile insects may lead to the release of males bearing unknown genetic changes, including mutations conferring insecticide resistance, which can remain in the gene pool and continue propagating in subsequent generations.64'65 3. Wolbachia - Another vector control approach that impacts the biology of Aedes aegypti is the artificial insertion of Wolbachia into the mosquito.66 Wolbachia is an intracellular bacterium that is associated with reproductive alterations of its hosts including parthenogenesis,cytoplasmic incompatibility,and feminization of genetically male hosts.67 While there are numerous strains of Wolbachia that are naturally present in a number of insects including mosquitoes(collectively all strains infect up to 40%of insect species), none occur naturally in Aedes aegypti.1'68 Various studies on insects and mosquitoes with Wolbachia, either artificially-inserted or naturally-occurring, have shown: • Aedes albopictus mosquitoes can naturally be superinfected with two Wolbachia strains (wAlbA,wAlbB),yet are still able to transmit chikungunya and dengue virus;69•70 • Aedes aegypti artificially modified with the wMel strain of Wolbachia show a reduction in dengue virus replication but virus is still found in the saliva of these engineered mosquitoes which therefore have the capacity,even if reduced,to transmit disease;71 • Wolbachia significantly enhances West Nile virus infection in the Culex tarsalis mosquito;72 • Wolbachia enhances malaria parasite infection in Anopheles gambiae and Culex pipiens mosquitoes;73-75 ©2016 Intrexon Corporation.All rights reserved. 11 0 OXITEC • Temperature impacts Wolbachia-malaria interaction in Anopheles mosquitoes suggesting impact of transfection might vary across diverse environments;76 • rated enhancement rather than suppression Wolbachia infections have demonstrated pp ression of pathogens in insects such as crop pests;77 and • Horizontal gene transfer(HGT) between Wolbachia and their insect hosts has led to the acquisition of evolutionary innovation as research suggests the transfer of genes to host has functional significance.78 • HGT is the process whereby Wolbachia's genes are transferred to their hosts impacting the biology of the infected insects. Studies have found transfers ranging from nearly the entire Wolbachia genome (>1 megabase)to short insertions (<500 base pairs) into the genomes of various insect and nematode species.79 82 Despite the fact that through HGT Wolbachia could effectively introduce over 1,000 new genes, this vector control method avoids the rigorous regulatory examination for recombinant genetic engineering (which typically introduces only a few genes) because this approach does not fall within the narrow definition of 'genetically engineered' from a regulatory perspective. 4. Wolbachia and Insecticide Resistant Mosquitoes- In order to boost invasiveness, it has been proposed to release host mosquitoes infected with Wolbachia that also carry insecticide resistance genes for better survival in urban areas. Increasing tolerance in mosquito populations by using those with genetic traits that are biologically resistant to insecticides would make them more difficult to control and compound the already prevalent insecticide resistance problem, jeopardizing future vector control efforts.83 5. Radiation-based SIT and Wolbachia — Wolbachia insertion into Aedes aegypti is currently being investigated in combination with radiation-induced sterility. Irradiation to sterilize any female mosquitoes would allow for lower sex-sorting stringency, but also expose Wolbachia strains and mosquitoes simultaneously to mutagenic radiation with unknown consequences.84 6. RNA interference (RNAi) — Some groups have been investigating genetically engineered gene-silencing in mosquitoes to induce sterility by using RNAi. However this technique, which also alters the biology of a mosquito, has only been tested in proof of concept studies in the laboratory, and field efficacy has not been evaluated.85 Demonstrating potent biological effect to effectively reduce Aedes populations with reliable, repeatable male selection and sterility will be vital ahead of broader release of the RNAi treated mosquitoes into the environment. 7. Gene Drive—Another potential genetic engineering strategy for population replacement of disease-carrying mosquitoes that alters the biology of the insect is called gene drive. This approach relies on driving a gene of interest into a wild population to reduce pathogen replication. These gene drive systems are designed to establish themselves in the environment permanently, raising concerns regarding irreversible changes to vector and disease dynamics.86 ©2016 Intrexon Corporation.All rights reserved. 12 ,....„,,, 0 OXITEC In summary,for over ten years Oxitec has been focused on the control of Aedes aegypti populations through the responsible engineering of biology. The self-limiting aspect of Oxitec's approach is unique to itself, while all of the other methods referenced here may persist in the environment potentially leading to undesirable consequences. From the perspective of the Oxitec Chemical Gene Drives, public's safety, it is imperative Approach Insecticides Wolbachia that all approaches resulting in undefined genetic changes, Q e ill 0 specially those that may persist Q in subsequent generations of these dangerous disease- 1 1 1 transmitting Aedes aegypti ilZ S 00* * *0* mosquitoes, go through rigorous 0*I** **1** safety checks like those in place ,W * *** for solutions defined as4 'genetically engineered'. At the 1 moment, the scrutiny given to GE * *** **1 products focuses more on how the * 0 product was made, rather than Does Not Persist Persists in Persists in the inherent qualities of the in Environment Environment Environment products themselves. Figure 12.Self-limiting approach of Oxitec that does not persist in the environment compared to other approaches with genetic alterations that may remain in the ecosystem. Significant Scalability; Expansion of Production Capacity Underway The power and scalability of biological solutions that utilize mosquitoes can be relatively easy to see from a production point of view. Oxitec's biological engineered approach is embedded from the outset within each egg from its OX513A strain. Given a female mosquito can yield approximately 250 male mosquitoes within five weeks, by month five almost four billion OX513A male mosquito eggs can be bred from that single female and her offspring. To give perspective on yield from egg production to final product here is a brief overview of a factory with capacity of four million eggs per week. Approximately three and a half million are hatched for egg colony and production with the remainder stored for backup. Eggs can be stored for up to 6 weeks. Two million larvae are reared every week for the Release Generation colony producing around 571,000 male pupae. After taking into account pupae and adult mortality during emergence and releases, approximately 543,000 adult OX513A male mosquitoes are available for release per week. (Figure 13).$' Egg Production Mass rearing—Male production Available for (4 million) field release ,\ (543,000 male r OX513A) u Sex sortAdult .:u,.� Larvae P}.ipae � Release \Iv/ males '1 le t t l h easot'e rat on .__ .. Figure 13.Small scale factory production schematic for OX513A ©2016 Intrexon Corporation.All rights reserved. 13 OXITEC Total Released Total Production Capacity 58.3 n ao N 3,273 m — 41.6 2 ti X m - 473 O w Zn o 2 O v iUy 18.2 18.9 6 218 283 o Q 3.3 5 7 3.9 § 3 5 I I 10 12 39 2010 2011 2012 2013 2014 2015 2016 YTD 2010 2011 2012 2013 2014 2015 2016 2017 Figure 14.Total OX513A releases from 2010 through 2016 and estimated total OX513A production capacity from 2010 through 2017. For 2016 and 2017 estimates include existing and planned production facilities. To date over 150 million Oxitec mosquitoes have been released through use in field suppression programs across Brazil, Panama, Malaysia, and the Cayman Islands (Figure 14). The solution has been successfully applied alongside other interventions such as insecticide applications. OX513A is compatible with all other conventional approaches. The production capacity for Oxitec's pioneering solution has been steadily increasing since the first releases in 2010. In preparation of increasing demand for its proprietary vector control solution, Oxitec is initiating a new mosquito production facility in Piracicaba that will have capacity to protect over 300,000 people.With its existing and planned production facilities, total production capacity is expected to grow significantly in 2016 and 2017(Figure 14). Oxitec's Unparalleled Control of the Aedes aegypti Vector Using a biological approach in which self-limiting genetic programming is installed from the outset in the offspring of these damaging Aedes aegypti is paramount to effectively reach and reduce their populations. To date, suppression programs with ,, „ � Oxitec mosquitoes have delivered 4.ps tt' 99°o superior results to any other known -96uo ga ar�, intervention for Aedes aegypti. - Oxitec's species-specific biological approach has been used to _92 successfully decrease wild populations of Aedes aegypti in five efficacy trials across Brazil, Cayman 42,44 53 Figure 15. Suppression results of Aedes aegypti from five separate outdoor Islands and Panama. Following efficacy trials using OX513A the release of sufficient numbers of OX513A to target suppression, the local Aedes aegypti populations were reduced by >90% (Figure 15)within four months in one trial,six months in three trials,and nine months in the remaining trial. Appendix 1 ('Field Data Summaries')has details on three of these trials. Through the responsible engineering of biology, Oxitec has developed a new paradigm of self- limiting, species-specific vector control resulting in dramatic reductions of dangerous Aedes aegypti mosquitoes, without persistence or harm to the ecosystem, representing a major scientific and environmental advance. ©2016 Intrexon Corporation.All rights reserved. 14 rx: OXITEC Appendix 1 Field Data Summaries for the OX513A Aedes aegypti Suppression Projects: 1. East End, Grand Cayman, Cayman Islands (Page 15) 2. Itaberaba neighbourhood, Juazeiro (Bahia), Brazil (Page 18) 3. Nuevo Chorrillo, Arraijan, Panama (Page 20) 1. East End, Grand Cayman, Cayman Islands From May 2010 to October 2010 a demonstration of OX513A Ae. aegypti took place in East End, on the Southeast coast of Grand Cayman, one of the three islands that form the Cayman Islands. The area covered was 16 hectacres with 291 residents. The suppression of wild Ae. aegypti achieved equaled 96%. 4 r ; y -- • r � P t 4* < ♦f" Figure 1.Aerial photograph of East End showing the areas A(treated with OX513A), 8(buffer zone), C(untreated control).Lat:19.297,Long:-81.109. Location and project East End is a sparsely populated residential area that has a tropical climate with distinct seasonality of Ae. aegypti. Populations are lower during the dry season (November to April; 30°C) and increase markedly during the rainy season (May to October; 26°C). This was a challenging coastal environment with a high population of the vector and where no other control methods had been used. ©2016 Intrexon Corporation.All rights reserved. 15 OXITEC The primary objective of the project was to make sustained releases of OX513A males at a level sufficient to suppress the local Ae. aegypti population. The population suppression was demonstrated through a comparative assessment of a single area treated with OX513A and an untreated control area (Figure 1). Results achieved Throughout the study changes in release rate Preparation I Suppression preceded corresponding changes in the A 08 Release Rate and Mating Fraction percentage of progeny obtained from ovitraps 14W that carried the fluorescent marker (Figure 2A). o 0.6 1200 This value is indicative of the proportion of local SAales/person/,reek filowo o 0.4 f —Mating fraction females mating OX513A males (mating - 600 E fraction), a factor that ultimately guides the 02 400 rate of population suppression. Behavioural and Ih III I - 200 mating competitiveness studies were B 0 conducted during preparation phase from _2.5 Relative EntomologicaiIndex which the release rate necessary to achieve e 2 suppression could be established. OX513A a1.5 —Relative ovitrap index numbers sufficient to target suppression of the 1 —Relative num6eregas/trap local Ae. aegypti population began early July. g0.5 Substantial suppression of the local population 7 o followed within four months. c Weather Data 200 =Rainfall 4O A number of different metrics were used to E 150 —Temperature 35 assess local Ae. aegypti populations, before and Imo ' after suppression, allowing the percentage 5° 1 1 1 I 1 25 E suppression to be ascertained. Ovitrap surveys ° ''� , t.. .►.......I.. ...1_I..I..... 20 PP P Y tic ; were the principal monitoring tool deployed in v9 1 'J P ‘4`� o� both treated and untreated sites. Any change in the local population of the OX513A-treated area Figure 2.(A)Number of OX513A males was quantified relative to the untreated area. released per person per week and estimated This was done by dividing the values for the mating fraction during the study. (B)Relative treated area by those of the untreated area to number of eggs per trap and ovitrap index. give relative mean number of eggs caught per (C)Average daily temperature and weekly trap and relative ovitrap index(Figure 2B). ru infnll rhrrinn tha ctrrrhr Adult population sampling in areas receiving treatment provided a ratio of recaptured OX513A to local Ae. aegypti males, allowing the population density of adult local Ae. aegypti to be estimated. Pupae per person were calculated according to the method described in Focks et al. with site- specific parameters for the temperature and human population density in the treated area.51 For all metrics, a substantial suppression of local Ae. aegypti population was observed following treatment with OX513A males, including a 96% reduction in the number of mosquito eggs recovered from ovitraps(Appendix 1). Commentary A primary consideration for public health agencies is maintaining the vector population below the level required for sustained disease transmission. Disease transmission thresholds are dynamic and dependent upon multiple factors.These factors vary spatially and temporally making predictions for ©2016 Intrexon Corporation.All rights reserved. 16 OXITEC specific localities difficult. However, using the temperature dependent model proposed by Focks et al., a generic prediction for dengue transmission thresholds that are related to initial serotype prevalence (also termed herd immunity)is possible.5' Despite the potential negative effects imposed by migration (as outlined below), during this demonstration study the local Ae. aegypti population was reduced to below the transmission threshold predicted for when two-thirds of the population possesses immunity(seroprevalence rate of 67%), thereby demonstrating the potential for this technology to have a positive impact upon dengue transmission rates(Figure 3). The treated area was not isolated with 7.0 regard to the Ae. aegypti populations 6.0 - as it was adjacent to the untreated in 0 area (area B) where populations of Ae. aegypti remained high. The relatively Q. 4.0 - small size of the treatment site meant w3 0 it was subject to migration of local Ae. aegypti, which can typically disperse 0 2.0 - 67% about 100 metres in its lifetime (5-10 o. 1.0 -_ _ _ _ _ 33.2, days),from neighbouring area. 0.0 — — — , - ©g Releases of OX513A were stopped in Before After October 2010, but monitoring continued for a further 9 months. Figure 3. Suppression of Ae. aegypti population in During this time the Ae. aegypti pupae per person relative to predicted dengue population remained suppressed transmission thresholds at three initial seroprevalence relative to the untreated control site. rates of 0 (0.42 pupae per person), 33 (0.61), and 67% This was despite the fact that the site (1.27). was relatively small, and susceptible to migration as discussed above. Related publication Harris et al. (2012) Successful suppression of a field mosquito population by sustained release of engineered male mosquitoes. Nature Biotechnology 30(9).52 ©2016 Intrexon Corporation.All rights reserved. 17 OXITEC 2. Itaberaba neighbourhood, Juazeiro (Bahia), Brazil From May 2011 to October 2012 Moscamed and the University of Sao Paulo conducted a project to suppress local Ae aegypti using the strain OX513A in Itaberaba, a neighbourhood in the southeast of the city of Juazeiro, Bahia. The area covered was 5.5 hectacres with 900 residents. The suppression of wild Ae. aegypti achieved equaled 93%. • i . t or- r x •, Figure 4. Aerial photograph of Itaberaba showing the areas A (treated with OX513A), 8 (buffer zone), C (untreated control).Lat:-9.450,Long:-40.482. Location and project Itaberaba is a densely populated urban setting with a semi-arid climate and limited seasonality of Ae. aegypti. Populations of the mosquito are present all year round although lower during the dry season (May to October; 25°C) and higher during the rainy season (November to April; 28°C). The site was identified by the local vector control agency as a disease hotspot with a consistently high vector population.The primary objective of the project was to achieve substantial suppression of the local Ae. aegypti population in this challenging area. The population suppression was demonstrated through a comparative assessment of a single area treated with OX513A and an untreated control area (Figure 4). Results achieved Throughout the study changes in release rate preceded corresponding changes in the percentage of progeny obtained from ovitraps that carried the fluorescent marker (Figure 5A). This value is indicative of the proportion of local females mating OX513A males (mating fraction), a factor that ultimately guides the rate of population suppression. An extended preparation phase of releases below the threshold needed to achieve suppression enabled extensive behavioural and mating competitiveness studies, building detailed knowledge of the release numbers required for suppression. The high and relatively stable year round Ae. aegypti population provided an ideal setting for these studies. OX513A numbers sufficient to target suppression of the local Ae. aegypti population began ©2016 Intrexon Corporation.All rights reserved. 18 0 OXITEC in early 2012. Substantial suppression followed within six months (Figure 5). The local population was then maintained at very low levels despite the treated area being relatively small and susceptible to migration of Ae. aegypti from Preparation Suppression adjacent untreated areas where the Ae. A Release Rate and Mating Fraction 1200 aegypti population remained high. 1O 1000 0.8 - 1♦Maies/person/week u A number of different metrics were used to p —Mating fraction assess local Ae. aegypti populations, before soo and after suppression, allowing the 3 °.d 400 percentage suppression to be ascertained. °_2 •�� �I���1� d 200 Ovitrap surveys were the principal monitoring 0A """...-.111111"" ) !�t_I�11..0 tool deployed in both treated and untreated B to - Relative Entomological Index sites. Any change in the local population of Si - Relative ovitrap index the OX513A-treated area was quantified I a —Relative numbereggs/trap relative to the untreated area. This was done 4 by dividing the values for the treated area by 2 - those of the untreated area to give relative = mean number of eggs caught per trap and C Weather Data relative ovitrap index(Figure 5B). E 100 m MI nfall (j E 80 • 35 Adult population sampling in areas receiving —Temperature treatment provided a ratio of recaptured Y 20_ 44441441 25 E OX513A to local Ae. aegypti males, allowing 3 ° .--_.. `..., .>I ,, 1.__. . 20 atiti �,;. �a`.t iry .Y't ti~ the population density of adult local Ae. F ,J ,¢ o0 Fa aegypti to be estimated. Pupae per person Figure 5.(A)Number of OX513A males were calculated according to the method released per person per week and estimated • described in Focks et al. with site specific mating fraction during the study. (B)Relative parameters for the temperature and human population density in the treated area.sl For number of eggs per trap and ovitrap index. (C) all metrics, a substantial suppression of local Average daily temperature and weekly rainfall Ae. aegypti population was observed during the study. following treatment with OX513A males, including a 93% reduction in the number of mosquito eggs recovered from ovitraps (Appendix 1). Commentary A primary consideration for public health agencies is maintaining the vector population below the level required for sustained disease transmission. Disease transmission thresholds are dynamic and dependent upon multiple factors.These factors vary spatially and temporally making predictions for specific localities difficult. However, using the temperature dependent model proposed by Focks et al., a generic prediction for dengue transmission thresholds that are related to initial serotype prevalence(also termed herd immunity)is possible.51 Despite the potential negative effects imposed by migration (as outlined below), during this demonstration study the local Ae. aegypti population was reduced to below the transmission threshold predicted for when there is no previous immunity in the population (seroprevalence rate of 0%) (Figure 6). This demonstrates the strong potential for this technology to reduce dengue transmission rates,even in areas where the human population is totally susceptible to the disease. ©2016 Intrexon Corporation.All rights reserved. 19 OXITEC 1.4 - The treated area was not isolated with 67% regard to the Ae. aegypti populations as 1.2 it was a suburb within a larger city where c 9, 1.0 - populations of Ae. aegypti remained c. 0.8 - high. The relatively small size of the 33% treatment site meant it was subject to 0.6 - — — w 0% migration of local Ae. Aegypti, which can • 0'4 - typically disperse about 100 metres in its 0.2 - lifetime,from neighbouring areas. 0.0 The results of this study show an Before After excellent degree of control and suggest that, even in small areas with a high Figure 6. Suppression of Ae. aegypti population in degree of migration, sustained releases pupae per person relative to predicted dengue of OX513A can offer outstanding transmission thresholds at three initial reductions in the local Ae. aegypti seroprevalence rates of 0(0.42 pupae per person), 33 population. This indicates that Oxitec's (0.61), and 67%(1.27). technology can be used to combat Ae. aegypti hotspots as well as for wide area control strategies in which the impact of migration is reduced. Related Publication Carvalho et al. (2015) Suppression of a Field Population of Aedes aegypti in Brazil by Sustained Release of Transgenic Male Mosquitoes. PLoS Negl Trop Dis 9(7):e0003864.5° 3. Nuevo Chorrillo, Arraijan, Panama From April 2014 to October 2014 the Gorgas Institute conducted a project to suppress local Ae. aegypti using the strain OX513A in Nuevo Chorrillo,a neighbourhood west of Panama City. The area covered was 10 hectacres with 900 residents. The suppression of wild Ae. aegypti achieved equaled 93%. N Untreated areal _/ Untreated area 1 Figure 7.Aerial photograph of neighbourhoods in Arraijan,showing the OX513A treated site and . Treated / both untreated control sites. area • Lat:8.952355;Long:-79.699245. ©2016 Intrexon Corporation.All rights reserved. 20 ; 0 OXITEC Location and project The neighbourhood of Nuevo Chorrillo has a moderate human population density, a tropical maritime climate, and marked seasonality of Ae. aegypti. Populations of this mosquito are present all year round although are lower during the dry season (December to April; 26°C) and higher during the wet season (May to November; 26°C). Vector surveillance over several years confirmed a predominating Ae. aegypti population with an increasing presence of Ae. albopictus. The primary objective of the project was to assess whether releases of OX513A prevented the annual surge in local Ae. aegypti that accompanies the increased rainfall of the wet season. Performance was measured by comparing the abundance of Ae. aegypti relative to two nearby untreated sites (Figure 7). This study was the first OX513A suppression trial to be completed in an area where both Ae. aegypti and Ae. albopictus co-exist. Results achieved The first fluorescent larvae were observed just Intervention one week after releases began, demonstrating A Release Rate and Mating Fraction 300. the inherent mating compatibility of OX513A 1A 250 males with females of the local strain. Over the o.g sou course of the treatment period, the majority of 0.6 150 progeny collected from ovitraps carried the 04 1507, fluorescent marker. This reflected the 0.2 g taiesipersnniweek o proportion of local females successfully mated Mating fraction OA - by OX513A males(also termed mating fraction), e a factor that ultimately guides the rate of 2 Relative Entomological Index —Avg larval Index vs U3 population control(Figure 8A). Avg larval ndex vs U2 1 '- —Avg larvae/trap vs US Several different metrics were used to assess g -411141/4 --Avg vs U2 mosquito abundance both before and after — \ { suppression, allowing the levels of Ae. aegypti o control to be determined.To accommodate the C ao Weather Data 35 presence of Ae. albopictus, all eggs collected 30 : olweekiy rainfall c were hatched and reared to the late-larval a 20 —Temperature stage so that species identification of every „ 251- individual could be completed. Egg trap 0 _..1 I(I 1111 ( (� ((�_�L)((�i� (ovitrap) data are therefore presented as larvae v`~ ��° limo- .1 ,,7 41,7 (as opposed to eggs) to accurately reflect the life-stage assessed. Figure 8.(A)Numbers of OX513A males released per person per week and estimated mating Weekly ovitrap surveys were the principal fractions(proportions of local female Ae. aegypti monitoring tool deployed in both treated and untreated sites. Any changes over time in the mated by OX513A males). (B)Relative numbers local populations were quantified by dividing of eggs per trap and relative ovitrap indexes. U1: the number of Ae. aegypti caught in the untreated area 1;U2:untreated area 2. (C)Mean treated area by those caught in the untreated daily temperatures and weekly rainfall. areas. This produced relative mean numbers of larvae caught per trap and relative ovitrap indexes (Figure 8B). Surveillance of adult populations, using commercially available BG Sentinel® traps (Biogents,Germany) in the treated site and untreated area 1, provided a ratio of recaptured OX513A males to local Ae. aegypti males.These data were used to estimate the population densities of local Ae. aegypti adults and corresponding pupae per person values according to the method described by ©2016 Intrexon Corporation.All rights reserved. 21 .,.. OXITEC Focks et al., with site-specific parameters for the temperature and human population density in the treated area.51 For all metrics, a substantial suppression of the local Ae. aegypti population was observed following treatment with OX513A males,including a 93%reduction in the number of larvae per trap(Appendix 1). Substantial control of the local Ae. aegypti population had been achieved within six months after releases began;the population was then maintained at this low-level in the treated area despite the intense pest pressures in both untreated areas as the wet season progressed. Commentary A primary consideration for public health agencies is maintaining vector populations below the levels required for sustained disease transmission. Disease transmission thresholds are dynamic and dependent upon multiple factors.These factors vary spatially and temporally making predictions for specific localities difficult. However, using the temperature dependent model proposed by Focks et al., generic predictions for dengue transmission thresholds that are related to initial serotype prevalence (also termed herd immunity) are possible.51 Mark-release-racapture statistics and known numbers of OX513A males released at the treated site were used to estimate local population sizes. Despite the potential negative effects imposed by migration (as outlined below), in the treated area the local Ae. aegypti population was maintained below the transmission threshold predicted for a population without prior immunity(seroprevalence rate of 0%) (Figure 9). In contrast,the untreated areas showed significantly increased infestation during the wet season to the point that there was a risk of a dengue epidemic even with 33% serotype prevalence. This demonstrates the potential for this technology to hold vector populations below the dengue transmission threshold, even in areas where the human population is fully susceptible to the disease. The treated site was within a wider 4 suburb where populations of Ae. - 66% aegypti remained high and was o 3 therefore subject to migration of a mosquitoes from these adjacent areas. `m 2 a. a) — — - 33 These results demonstrate the ability °!° a 1 — — - Q°%° of Oxitec technology to efficiently a contain Ae. aegypti even in difficult areas, mitigating against dengue outbreaks before the disease has Before After established. •Untreated 1 •Treated Figure 9. Suppression of Ae. aegypti population in pupae per person relative to predicted dengue transmission thresholds at three initial seroprevalence rates of 0(1.05 pupae per person),33(1.55), and 67%(3.41). Related publication Gorman et al. (2016). Short-term suppression of Aedes aegypti using genetic control does not facilitate Aedes albopictus. Pest Management Science, DOI: 10.1002/ps.4151.49 ©2016 Intrexon Corporation.All rights reserved. 22 k OXITEC Appendix 2: Tables x a 0 o f0 t\/1 E. x ,a Lam+ = ZT °1 ON a v -v -251 ( o - ° _c ° n os o a, -a ar -o v o; > Y 0 Y > Y cu Q Q T, co ro ; m m f9 �0 3 is 0. b �' v > v v a o o a W v CC .r O v OG ... J J 1.East End,Grand Cayman,Cayman Islands Before suppression 7.91 1.70 30.2% 1.36 1047 6.72 After suppression 1.10 0.07 5.4% 0.23 61 1.09 Reduction 86% 96% 82% 83% 84% 84% 2.Itaberaba neighbourhood,Juazeiro(Bahia),Brazil Before suppression 20.5 2.85 36.7% 1.61 418 0.7 After suppression 1.71 0.21 6.3% 0.35 20 0.04 Reduction 92% 93% 83% 78% 95% 95% 3.Nuevo Chorrillo,Arraijan,Panama Larvae per trap Larval index a--1 N a i N O O O O > > > 2 19 (9 ro CO 71, Tu cc cc Before suppression 0.93 1.41 0.90 1.34 After suppression 0.08 0.07 0.19 0.16 Reduction 93% 84% Summary of observed reductions in abundance of Ae.aegypti.Relative values were calculated by dividing those for the treated area by those of the relevant untreated area.Larval reductions are presented as mean values across both untreated areas.T=treated;U1=untreated 1;U2=untreated 2. Appendix 3: References 1. World Health Organization. Mosquito control:can it stop Zika at source?.Accessed March 12,2016. http://www.who.int/emergencies/zika-virus/articles/mosquito-control/en/. 2. Kraemer MU,Sinka ME,Duda KA, Mylne ACl,Shearer FM,et al. (2015)The global distribution of the arbovirus vectors Aedes aegypti and Ae.albopictus.Elife 4,e08347. 3. Joshi V,Mourya DT,and Sharma RC.(2002)Persistence of dengue-3 virus through transovarial transmission passage in successive generations of Aedes aegypti mosquitoes.Am J Trop Med Hyg 67, 158-161. 4. Khin MM,and Than KA.(1983)Transovarial transmission of dengue 2 virus by Aedes aegypti in nature.Am J Trop Med Hyg 32,590-594. 5. Lee HL,and Rohani A.(2005)Transovarial Transmission of Dengue Virus in Aedes aegypti and Aedes albopictus in Relation to Dengue Outbreak in an Urban Area in Malaysia. WHO Dengue Bulletin 29, 106-111. 6. Charles Darwin Foundation. Galapagos Species Checklist:Aedes aegypti.Accessed March 14,2016. http://www.darwinfoundation.orddatazone/checklists/11720/. ©2016 Intrexon Corporation.All rights reserved. 23 a . ;, OXITEC 7. Foster WA,and Walker EE.(2002)Mosquitoes(Culicidae).in Medical and Veterinary Entomology (Mullen,G.,and Durden,L.eds.),Academic Press,San Diego,CA.pp 597. 8. Centers for Disease Control and Prevention. Dengue and the Aedes aegypti Mosquito.Accessed March 12,2016.http://www.cdc.gov/dengue/resources/30Jan2012/aegyptifactsheet.pdf. 9. Lewis JT,and Magalhaes L.(2016)World Bank Calculates Zika's Economic Cost in Latin America. The Wall Street Journal.Accessed February 18,2016.http://www.wsi.com/articles/world-bank-calculates- zikas-economic-cost-in-latin-america-1455811201?mod=fox australian. 10. Selck FW,Adalja AA,and Boddie CR.(2014)An estimate of the global health care and lost productivity costs of dengue.Vector Borne Zoonotic Dis 14,824-826. 11. 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Appendix 4: Oxitec Publications Description of the OX513A strain and production • Phuc HK,Andreasen MH,Burton R,Vass C,Epton MJ,Pape G, Fu G,Condon KC,Scaife S,Donnelly CA, Coleman PG,White-Cooper H,Alphey L.(2007)Late-acting dominant lethal genetic systems and mosquito control.BMC Biology 5:11. • Carvalho DO,Wilke ABB,Nimmo DD,Naish N, McKemey AR,Gray P, Marrelli MT,Virginio JF,Alphey L, Capurro ML.(2014) Mass production of genetically modified Aedes aegypti for field releases in Brazil.JoVE 83:e3579. Studies on OX513A phenotype • Lee HL,et al. No evidence for successful interspecific cross-mating of transgenic Aedes aegypti(L.)and wild type Aedes albopictus Skuse.(2009)Trop Biomed.26(3):312-319. • Nazni WA,et al.Susceptibility status of RIDL Aedes aegypti(L.)against conventional insecticides.(2009) Dengue Bulletin 33:124-129 • Kongmee M,Nimmo D,Labbe G,Beech C,Grieco J,Alphey L,Achee N.(2010)Irritant and repellent behavioral responses of Aedes aegypti male populations developed for RIDL®disease control strategies.J Med Entomol 47(6):1092-1098. • Bargielowski I,Nimmo D,Alphey L,Koella JC.(2011)Comparison of Life History Characteristics of the Genetically Modified OX513A Line and a Wild Type Strain of Aedes aegypti.PLoS ONE 6:e20699. • Massonnet-Bruneel B,Corre-Catelin N, Lacroix R,Lees RS,Phuc HK, Nimmo D,Alphey L,Reiter P.(2012) Fitness of transgenic mosquito Aedes aegypti males carrying a dominant lethal genetic system.PLoS One 8: e62711. • Oreenaiza MN,Wesley D,Wong HM,Teoh GN,Khairul A,Nor Azlina AH,Winskill P,Azahari AH, Muhammad ZS,Lacroix R,Scaife S, McKemey AR,Beech C,Alphey L,Nimmo DD,Nazni WA,Lee HL.(2012) Oral ingestion of transgenic RIDL Ae.aegypti larvae has no negative effect on two predator Toxorhynchites species.PLoS One 8:e58805. • Curtis Z,Matzen K,Neira Oviedo M,Nimmo D,Gray P,Winskill P,Locatelli MAF,Jardim WF,Warner S, Alphey L,Beech C.(2015)Assessment of the impact of potential tetracycline exposure on the phenotype of Aedes aegypti OX513A:implications for field use.PLOS Neglected Tropical Diseases 9(8): e0003999.PLOS Neglected Tropical Diseases 9(8):e0003999. • Patil PB,et al.Mating competitiveness and life-table comparisons between transgenic and Indian wild- type Aedes aegypti.(2015)L. Pest Management Science 71:957-965. ©2016 Intrexon Corporation.All rights reserved. 27 OXITEC Studies on OX513A field releases • Harris AF,McKemey AR,Nimmo D,Curtis Z,Black I,Morgan SA,Neira Oviedo M,Lacroix R, Naish N, Morrison N,Amandine C,Stevenson J,Scaife S, Dafa'alla T,Fu G,Phillips C,Miles A, Raduan N,Kelly N, Beech C,Donnelly CA, Petrie WD,Alphey,L.(2012)Successful suppression of a field mosquito population by sustained release of engineered male mosquitoes.Nature Biotech 30:828-830 • Lee HL,Vasan S,Nazni WA,Iswarti I,Norhaida H,Selvi 5,Alphey L,Shahnaz M.(2013)Mating compatibility and competitiveness of transgenic and wild type Aedes aegypti(L.)under contained semi-field conditions.Transgenic Research 22:47-57.doi: 10.1007/s11248-012-9625- • Neira M,Lacroix R,Caceres L, Kaiser PE,Young J,Pineda L,Black I,Sosa N,Nimmo D,Alphey L,McKemey A.(2014)Estimation of Aedes aegypti(Diptera:Culicidae)population size and adult male survival in an urban area in Panama.Mem Inst Oswaldo Cruz 109(7):879-86. • Winskill P,Harris AF,Morgan SA,Stevenson 1,Raduan N,Alphey L,McKemey AR,Donnelly CA.(2014) Genetic control of Aedes aegypti:data-driven modelling to assess the effect of releasing different life stages and the potential for long-term suppression.Parasit Vectors 13;7:68.doi:10.1186/1756-3305-7-68. • Winskill P,Carvalho DO,Capurro ML,Alphey L,Donnelly CA,McKemey AR.(2015)Dispersal of engineered male Aedes aegypti mosquitoes.PLOS NTD 9(11):e0004156. • Carvalho DO, McKemey AR,Garziera L,Lacroix R,Donnelly CA,Alphey L,Malavasi A,Capurro ML.(2015) Suppression of a field population of Aedes aegypti in Brazil by sustained release of transgenic male mosquitoes.PLOS NTD 9(7):e0003864 • Gorman K,Young J,Pineda L, Marquez R,Sosa N, Bernal D,Torres R,Soto Y,Lacroix R,Naish N,Kaiser P, Tepedino K,Philips G,Kosmann C,Caceres L.(2016)Short-term suppression of Aedes aegypti using genetic control does not facilitate Aedes albopictus. Pest Management Science 72(3):618-628. • Morris,E.J.(2011).A semi-quantitative approach to GMO risk-benefit analysis.Transgenic Research 20(5), 1055-1071. ©2016 Intrexon Corporation.All rights reserved. 28 MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Honorable Mayor Carlos A. Gimenez Stephen P. Clark Center 111 N.W. 1st Street Miami, FL 33128 Dear Honorable Mayor Gimenez, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Raf el E. Gr nado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive, Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Deputy Mayor Alina T. Hudak Stephen P. Clark Center 111 N.W. 1st Street 29th Floor Miami, FL 33128 Dear Deputy Mayor Hudak, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, 7-31 Rafael E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel:305-673-7411 September 27, 2016 Commissioner Barbara J. Jordan Stephen P. Clark Center 111 N.W. 1st Street, Suite 220 Miami, FL 33128 Dear Commissioner Jordan, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Rafael E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Jaes StephenChairman P.e Clark n Mon Center time 111 N.W. 1st Street, Suite 220 Miami, FL 33128 Dear Chairman Monestime, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Raf el E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Commissioner Audrey Edmonson Stephen P. Clark Center 111 N.W. 1st Street, Suite 220 Miami, FL 33128 Dear Commissioner Edmonson, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Raf el E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamilpeachfl.gov Office of the City Clerk Tel:305-673-7411 September 27, 2016 Commissioner Sally A. Heyman Stephen P. Clark Center 111 N.W. 1st Street, Suite 220 Miami, FL 33128 Dear Commissioner Heyman, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, R ael E. ranado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach,Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Commissioner Bruno A. Barreiro Stephen P. Clark Center 111 N.W. 1st Street, Suite 220 Miami, FL 33128 Dear Commissioner Barreiro, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Rafa I E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach,Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Commissioner Rebeca Sosa Stephen P. Clark Center 111 N.W. 1st Street, Suite 220 Miami, FL 33128 Dear Commissioner Sosa, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Raf el E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Commissioner Xavier L. Suarez Stephen P. Clark Center 111 N.W. 1st Street, Suite 220 Miami, FL 33128 Dear Commissioner Suarez, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Raf el E. ranado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Commissioner Daniella Levine Cava Stephen P. Clark Center 111 N.W. 1st Street, Suite 220 Miami, FL 33128 Dear Commissioner Cava, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Rafael . Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Commissioner Dennis C. Moss Stephen P. Clark Center 111 N.W. 1st Street, Suite 320 Miami, FL 33128 Dear Commissioner Moss, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, XII Rafael E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Commissioner Javier D. Souto Stephen P. Clark Center 111 N.W. 1st Street, Suite 320 Miami, FL 33128 Dear Commissioner Souto, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Rafael E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Commissioner Juan C. Zapata Stephen P. Clark Center 111 N.W. 1st Street, Suite 320 Miami, FL 33128 Dear Commissioner Zapata, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully,, / Rafael E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive,Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-741 1 September 27, 2016 Commissioner Jose "Pepe" Diaz Stephen P. Clark Center 111 N.W. 1st Street, Suite 320 Miami, FL 33128 Dear Commissioner Diaz, Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Rafael E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez MIAMI BEACH City of Miami Beach, 1700 Convention Center Drive, Miami Beach, Florida 33139,www.miamibeachfl.gov Office of the City Clerk Tel: 305-673-7411 September 27, 2016 Vice-Chair Esteban Bovo, Jr. Stephen P. Clark Center 111 N.W. 1st Street, Suite 320 Miami, FL 33128 Dear Vice-Chair Bovo, Jr., Attached please find a copy of City of Miami Beach Resolution No. 2016-29574: A RESOLUTION OF THE MAYOR AND CITY COMMISSION OF THE CITY OF MIAMI BEACH, FLORIDA, AUTHORIZING THE CITY MANAGER TO SEND A LETTER TO THE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES TO REQUEST PERMISSION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN THE CITY OF MIAMI BEACH AND URGING MIAMI-DADE COUNTY (COUNTY) TO LIKEWISE REQUEST PERMISSION FROM THE FDA TO EXPLORE THE PROSPECT OF USING GENETICALLY MODIFIED MOSQUITOS TO COMBAT MOSQUITOS CARRYING THE ZIKA VIRUS IN COUNTY. This Resolution was unanimously passed and adopted by the Mayor and City Commission of the City of Miami Beach on September 14, 2016. The letter to the U.S. Department of Health and Human Services from Jimmy Morales, City Manager, is attached hereto. If you need additional information, please do not hesitate to call. Respectfully, Rafael E. Granado City Clerk c: Commissioner Kristen Rosen Gonzalez