Biological Control Strategies for Mosquito Vectors of Arboviruses
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Diversidade E Dinâmica De Microcrustáceos Em Áreas Úmidas Intermitentes
Universidade Federal do Rio Grande Instituto de Ciências Biológicas Pós-graduação em Biologia de Ambientes Aquáticos Continentais Diversidade e dinâmica de microcrustáceos em áreas úmidas intermitentes Maiby Glorize da Silva Bandeira Orientadora: Profa. Dra. Edélti F. Albertoni Coorientador: Prof. Dr. Luiz U. Hepp Rio Grande 2020 Universidade Federal do Rio Grande Instituto de Ciências Biológicas Pós-graduação em Biologia de Ambientes Aquáticos Continentais Diversidade e dinâmica de microcrustáceos em áreas úmidas intermitentes Aluna: Maiby Glorize da Silva Bandeira Orientadora: Profa. Dra. Edélti F. Albertoni Coorientador: Prof. Dr. Luiz U. Hepp Tese apresentada ao Programa de Pós- graduação em Biologia de Ambientes Aquáticos Continentais como requisito parcial para a obtenção do título de Doutora em Biologia de Ambientes Aquáticos Continentais. Rio Grande 2020 Dedico ao meu querido Andirobal (Monte Alegre-PA) Cujos moradores são a minha motivação diária Eles me mantém focada nos meus objetivos E me fazem ser mais persistente com os meus sonhos Que de certa forma são deles também. AGRADECIMENTOS Primeiramente a Deus que nunca desiste de mim. Segundo, à queridíssima profª. Edélti Albertoni que desde o meu primeiro email (no início de 2016), me aceitou e permitiu que eu realizasse mais um grande sonho na minha vida. Nunca terei palavras para expressar o carinho que ela, o prof. Cleber, a Manu e o Leandro tiveram comigo quando cheguei ao tenebroso frio do Sul. A Edélti não foi só uma orientadora, também foi mãe, amiga, conselheira e sempre nos acolheu com muito carinho, seja no laboratório ou no aconchego do seu lar. Sempre me apoiou nas minhas decisões, nas desilusões, nas conquistas, e soube me frear quando achou necessário. -
Philippine Species of Mesocyclops (Crustacea: Copepoda) As a Biological Control Agent of Aedes Aegypti (Linnaeus)
Philippine Species of Mesocyclops (Crustacea: Copepoda) as a Biological Control Agent of Aedes aegypti (Linnaeus) Cecilia Mejica Panogadia-Reyes*#, Estrella Irlandez Cruz** and Soledad Lopez Bautista*** *Department of Biology, Emilio Aguinaldo College, Ermita, Manila, MM, Philippines **Research Institute for Tropical Medicine, Alabang, Muntinlupa, MM, Philippines ***Department of Medical Technology, Emilio Aguinaldo College, Ermita, Manila, MM, Philippines Abstract The predatory capacity of two local populations of Mesocyclops aspericornis (Daday) and Mesocyclops ogunnus species were evaluated, for the first time in the Philippines, as a biological control agent for Aedes aegypti (L) mosquitoes. Under laboratory conditions, Mesocyclops attacked the mosquito first instar larvae by the tail, side and head. The mean of first instar larvae consumed by M. aspericornis and M. ogunnus were 23.96 and 15.00, respectively. An analysis of the variance showed that there was a highly significant difference between the mean number of first instar mosquito larvae consumed by M. aspericornis and by M. ogunnus, which indicated that the former is a more efficient predator of dengue mosquito larvae. The results of the small-scale field trials showed that the mean number of surviving larvae in experimental drums was 63.10 and in control drums was 202.95. The Student t-test of means indicated that there was a significant difference between the mean number of surviving larvae in the drums with and without M. aspericornis. The findings indicated that M. aspericornis females were good biological control agents, for they destroyed/consumed about two-thirds of the wild dengue mosquito larvae population. Keywords: Mesocyclops aspericornis, Mesocyclops ogunnus, biological control agent, Aedes aegypti, Aedes albopictus, Philippines. -
Data-Driven Identification of Potential Zika Virus Vectors Michelle V Evans1,2*, Tad a Dallas1,3, Barbara a Han4, Courtney C Murdock1,2,5,6,7,8, John M Drake1,2,8
RESEARCH ARTICLE Data-driven identification of potential Zika virus vectors Michelle V Evans1,2*, Tad A Dallas1,3, Barbara A Han4, Courtney C Murdock1,2,5,6,7,8, John M Drake1,2,8 1Odum School of Ecology, University of Georgia, Athens, United States; 2Center for the Ecology of Infectious Diseases, University of Georgia, Athens, United States; 3Department of Environmental Science and Policy, University of California-Davis, Davis, United States; 4Cary Institute of Ecosystem Studies, Millbrook, United States; 5Department of Infectious Disease, University of Georgia, Athens, United States; 6Center for Tropical Emerging Global Diseases, University of Georgia, Athens, United States; 7Center for Vaccines and Immunology, University of Georgia, Athens, United States; 8River Basin Center, University of Georgia, Athens, United States Abstract Zika is an emerging virus whose rapid spread is of great public health concern. Knowledge about transmission remains incomplete, especially concerning potential transmission in geographic areas in which it has not yet been introduced. To identify unknown vectors of Zika, we developed a data-driven model linking vector species and the Zika virus via vector-virus trait combinations that confer a propensity toward associations in an ecological network connecting flaviviruses and their mosquito vectors. Our model predicts that thirty-five species may be able to transmit the virus, seven of which are found in the continental United States, including Culex quinquefasciatus and Cx. pipiens. We suggest that empirical studies prioritize these species to confirm predictions of vector competence, enabling the correct identification of populations at risk for transmission within the United States. *For correspondence: mvevans@ DOI: 10.7554/eLife.22053.001 uga.edu Competing interests: The authors declare that no competing interests exist. -
The Introduction of Toxorhynchites Brevipalpis Theobald Into the Purpose of This Brief Paper Is to Place on Record an Account Of
Vol. XIV, No. 2, March, 1951 237 The Introduction of Toxorhynchites brevipalpis Theobald into the Territory of Hawaii By DAVID D. BONNET MEDICAL ENTOMOLOGIST, DEPARTMENT OF HEALTH, HONOLULU and STEPHEN M. K. HU CHIEF, BUREAU OF MOSQUITO CONTROL, HONOLULU The purpose of this brief paper is to place on record an account of the introduction of the South African mosquito Toxorhynchites (= Megarhinus) * brevipalpis Theobald into the Territory of Hawaii. The importation of this insect and its establishment would, it is believed, aid in the control of the forest day mosquito, Aedes albopictus Skuse. Any type of container, whether it be a natural container such as a tree hole, bamboo stump, pineapple lily (Bilbergia sp.) or rock hole; or an artificial container such as a vine bowl, tin can, tub, auto tire or bottle, when filled with water, can serve as a breeding location for Aedes albopictus. This varied breeding habit complicates control as it neces sitates the treatment or elimination of a multitude of large and small water-holding containers. Adequate control has been obtained in the urban areas of Hawaii by premises-to-premises inspection, and house holder cooperation, following usual Aedes aegypti (L.) control pro cedures. There are, however, large areas outside the cities where such control measures are not feasible. These areas are principally mountain forest regions which contain a sufficient number of natural breeding situations to maintain a large mosquito population. This population of Aedes albopictus serves not only as a health menace and as a reservoir for reinvasion, but also discourages extensive use of many fine recreation areas. -
Spongeweed-Synthesized Silver Nanoparticles Are Highly Effective
Environ Sci Pollut Res (2016) 23:16671–16685 DOI 10.1007/s11356-016-6832-9 RESEARCH ARTICLE Eco-friendly drugs from the marine environment: spongeweed-synthesized silver nanoparticles are highly effective on Plasmodium falciparum and its vector Anopheles stephensi, with little non-target effects on predatory copepods Kadarkarai Murugan1,2 & Chellasamy Panneerselvam3 & Jayapal Subramaniam1 & Pari Madhiyazhagan1 & Jiang-Shiou Hwang4 & Lan Wang5 & Devakumar Dinesh1 & Udaiyan Suresh1 & Mathath Roni1 & Akon Higuchi6 & Marcello Nicoletti7 & Giovanni Benelli8,9 Received: 13 April 2016 /Accepted: 4 May 2016 /Published online: 16 May 2016 # Springer-Verlag Berlin Heidelberg 2016 Abstract Mosquitoes act as vectors of devastating pathogens (EDX), and X-ray diffraction (XRD). In mosquitocidal assays, and parasites, representing a key threat for millions of humans the 50 % lethal concentration (LC50)ofC. tomentosum extract and animals worldwide. The control of mosquito-borne dis- against Anopheles stephensi ranged from 255.1 (larva I) to eases is facing a number of crucial challenges, including the 487.1 ppm (pupa). LC50 of C. tomentosum-synthesized emergence of artemisinin and chloroquine resistance in AgNP ranged from 18.1 (larva I) to 40.7 ppm (pupa). In lab- Plasmodium parasites, as well as the presence of mosquito oratory, the predation efficiency of Mesocyclops aspericornis vectors resistant to synthetic and microbial pesticides. copepods against A. stephensi larvae was 81, 65, 17, and 9 % Therefore, eco-friendly tools are urgently required. Here, a (I, II, III, and IV instar, respectively). In AgNP contaminated synergic approach relying to nanotechnologies and biological environment, predation was not affected; 83, 66, 19, and 11 % control strategies is proposed. -
A Review of the Mosquito Species (Diptera: Culicidae) of Bangladesh Seth R
Irish et al. Parasites & Vectors (2016) 9:559 DOI 10.1186/s13071-016-1848-z RESEARCH Open Access A review of the mosquito species (Diptera: Culicidae) of Bangladesh Seth R. Irish1*, Hasan Mohammad Al-Amin2, Mohammad Shafiul Alam2 and Ralph E. Harbach3 Abstract Background: Diseases caused by mosquito-borne pathogens remain an important source of morbidity and mortality in Bangladesh. To better control the vectors that transmit the agents of disease, and hence the diseases they cause, and to appreciate the diversity of the family Culicidae, it is important to have an up-to-date list of the species present in the country. Original records were collected from a literature review to compile a list of the species recorded in Bangladesh. Results: Records for 123 species were collected, although some species had only a single record. This is an increase of ten species over the most recent complete list, compiled nearly 30 years ago. Collection records of three additional species are included here: Anopheles pseudowillmori, Armigeres malayi and Mimomyia luzonensis. Conclusions: While this work constitutes the most complete list of mosquito species collected in Bangladesh, further work is needed to refine this list and understand the distributions of those species within the country. Improved morphological and molecular methods of identification will allow the refinement of this list in years to come. Keywords: Species list, Mosquitoes, Bangladesh, Culicidae Background separation of Pakistan and India in 1947, Aslamkhan [11] Several diseases in Bangladesh are caused by mosquito- published checklists for mosquito species, indicating which borne pathogens. Malaria remains an important cause of were found in East Pakistan (Bangladesh). -
Aedes (Stegomyia ) Polynesiensis Marks
Aedes (Stegomyia) polynesiensis Marks Polynesian mosquito NZ Status: Not present –Unwanted Organisms © CINHP/G.MCCormaCk Vector and Pest Status Aedes polynesiensis is a veCtor of dengue, doG heartworm (Dirofilaria immitis) and filariasis (Wuchereria bancrofti) (Rosen, 1954; Lee et al., 1987). This speCies is also susceptible to infeCtion with Brugia pahangi and Brugia malayii (Trpis, 1981 in Lee et al., 1987). In the laboratory it has been shown to be Capable of transmitting Murray Valley enCephalitis (Rozeboom and MCLean, 1956 in Lee et al., 1987) Ross River virus (Gubler, 1981) and ChikunGunya (Richard, Paoaafaite and Cao-Lormeau, 2016a). The ability for Ae. polynesiensis to transmit Chikungunya is likely how the disease was able to spread rapidly thouGh areas where Ae. aegypti is sCarce or not present durinG an outbreak in FrenCh Polynesia in 2014-2015 (RiChard, Paoaafaite and Cao-Lormeau, 2016a). Aedes polynesiensis has also been found to be a veCtor for Zika virus, thouGh they had a low transmission rate (Calvez et al., 2018, Richard, Paoaafaite and Cao- Lormeau, 2016b) and while CompetenCe is poor they likely responsible for the spread of Zika virus where they are the predominate speCies (Richard, Paoaafaite and Cao-Lormeau, 2016b). Version 3: May 2019 Geographic Distribution Aedes polynesiensis is found only in the PaCific, in Fiji, Horne Islands, ElliCe Islands (Tuvalu), Tokelau Islands, Samoa, Northern and Southern Cook Islands, Marquesas Islands, SoCiety Islands, ManGarewa Islands, Alofi Island, Wallis and Futuna Island Austral Islands, Tuamotu ArChipelago and PitCairn Island (Lee et al., 1987). © 2006 M. Disbury SMS-NZB www.smsl.co.nz This map denotes only the Country or General areas where this speCies has been reCorded, not aCtual distribution Incursions and Interceptions Aedes polynesiensis has been interCepted on three ocCasions in New Zealand sinCe 2001. -
Male Mating Competitiveness of a Wolbachia-Introgressed Aedes Polynesiensis Strain Under Semi-Field Conditions" (2011)
University of Kentucky UKnowledge Entomology Faculty Publications Entomology 8-2-2011 Male mating competitiveness of a Wolbachia- introgressed Aedes polynesiensis strain under semi- field conditions Eric W. Chambers University of Kentucky Limb Hapairai Institut Louis Malardé, French Polynesia Bethany A. Peel University of Kentucky, [email protected] Hervé Bossin Institut Louis Malardé, French Polynesia Stephen L. Dobson University of Kentucky, [email protected] Right click to open a feedback form in a new tab to let us know how this document benefits oy u. Follow this and additional works at: https://uknowledge.uky.edu/entomology_facpub Part of the Entomology Commons Repository Citation Chambers, Eric W.; Hapairai, Limb; Peel, Bethany A.; Bossin, Hervé; and Dobson, Stephen L., "Male mating competitiveness of a Wolbachia-introgressed Aedes polynesiensis strain under semi-field conditions" (2011). Entomology Faculty Publications. 28. https://uknowledge.uky.edu/entomology_facpub/28 This Article is brought to you for free and open access by the Entomology at UKnowledge. It has been accepted for inclusion in Entomology Faculty Publications by an authorized administrator of UKnowledge. For more information, please contact [email protected]. Male mating competitiveness of a Wolbachia-introgressed Aedes polynesiensis strain under semi-field conditions Notes/Citation Information Published in PLoS Neglected Tropical Diseases, v. 5, no. 8, e1271. © 2011 Chambers et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Digital Object Identifier (DOI) http://dx.doi.org/10.1371/journal.pntd.0001271 This article is available at UKnowledge: https://uknowledge.uky.edu/entomology_facpub/28 Male Mating Competitiveness of a Wolbachia-Introgressed Aedes polynesiensis Strain under Semi-Field Conditions Eric W. -
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 4—An Update April 2013 Prepared by: Pam L. Fuller, Amy J. Benson, and Matthew J. Cannister U.S. Geological Survey Southeast Ecological Science Center Gainesville, Florida Prepared for: U.S. Fish and Wildlife Service Southeast Region Atlanta, Georgia Cover Photos: Silver Carp, Hypophthalmichthys molitrix – Auburn University Giant Applesnail, Pomacea maculata – David Knott Straightedge Crayfish, Procambarus hayi – U.S. Forest Service i Table of Contents Table of Contents ...................................................................................................................................... ii List of Figures ............................................................................................................................................ v List of Tables ............................................................................................................................................ vi INTRODUCTION ............................................................................................................................................. 1 Overview of Region 4 Introductions Since 2000 ....................................................................................... 1 Format of Species Accounts ...................................................................................................................... 2 Explanation of Maps ................................................................................................................................ -
Survivorship in Aedes Polynesiensis with Artificial Wolbachia Infection Types
Reactive Oxygen Species Production and Brugia pahangi Survivorship in Aedes polynesiensis with Artificial Wolbachia Infection Types Elizabeth S. Andrews1, Philip R. Crain1, Yuqing Fu1,2, Daniel K. Howe3, Stephen L. Dobson1* 1 Department of Entomology, College of Agriculture, University of Kentucky, Lexington, Kentucky, United States of America, 2 Tropical Research and Education Center, University of Florida, Homestead, Florida, United States of America, 3 Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, Kentucky, United States of America Abstract Heterologous transinfection with the endosymbiotic bacterium Wolbachia has been shown previously to induce pathogen interference phenotypes in mosquito hosts. Here we examine an artificially infected strain of Aedes polynesiensis, the primary vector of Wuchereria bancrofti, which is the causative agent of Lymphatic filariasis (LF) throughout much of the South Pacific. Embryonic microinjection was used to transfer the wAlbB infection from Aedes albopictus into an aposymbiotic strain of Ae. polynesiensis. The resulting strain (designated ‘‘MTB’’) experiences a stable artificial infection with high maternal inheritance. Reciprocal crosses of MTB with naturally infected wild-type Ae. polynesiensis demonstrate strong bidirectional incompatibility. Levels of reactive oxygen species (ROS) in the MTB strain differ significantly relative to that of the wild-type, indicating an impaired ability to regulate oxidative stress. Following a challenge with Brugia pahangi, the number of filarial worms achieving the infective stage is significantly reduced in MTB as compared to the naturally infected and aposymbiotic strains. Survivorship of MTB differed significantly from that of the wild-type, with an interactive effect between survivorship and blood feeding. The results demonstrate a direct correlation between decreased ROS levels and decreased survival of adult female Aedes polynesiensis. -
Copepoda: Crustacea) in the Neotropics Silva, WM.* Departamento Ciências Do Ambiente, Campus Pantanal, Universidade Federal De Mato Grosso Do Sul – UFMS, Av
Diversity and distribution of the free-living freshwater Cyclopoida (Copepoda: Crustacea) in the Neotropics Silva, WM.* Departamento Ciências do Ambiente, Campus Pantanal, Universidade Federal de Mato Grosso do Sul – UFMS, Av. Rio Branco, 1270, CEP 79304-020, Corumbá, MS, Brazil *e-mail: [email protected] Received March 26, 2008 – Accepted March 26, 2008 – Distributed November 30, 2008 (With 1 figure) Abstract Cyclopoida species from the Neotropics are listed and their distributions are commented. The results showed 148 spe- cies in the Neotropics, where 83 species were recorded in the northern region (above upon Equator) and 110 species in the southern region (below the Equator). Species richness and endemism are related more to the number of specialists than to environmental complexity. New researcher should be made on to the Copepod taxonomy and the and new skills utilized to solve the main questions on the true distributions and Cyclopoida diversity patterns in the Neotropics. Keywords: Cyclopoida diversity, Copepoda, Neotropics, Americas, latitudinal distribution. Diversidade e distribuição dos Cyclopoida (Copepoda:Crustacea) de vida livre de água doce nos Neotrópicos Resumo Foram listadas as espécies de Cyclopoida dos Neotrópicos e sua distribuição comentada. Os resultados mostram um número de 148 espécies, sendo que 83 espécies registradas na Região Norte (acima da linha do Equador) e 110 na Região Sul (abaixo da linha do Equador). A riqueza de espécies e o endemismo estiveram relacionados mais com o número de especialistas do que com a complexidade ambiental. Novos especialistas devem ser formados em taxo- nomia de Copepoda e utilizar novas ferramentas para resolver as questões sobre a real distribuição e os padrões de diversidade dos Copepoda Cyclopoida nos Neotrópicos. -
1020 1630 Chambers.Pdf
Advances in Wolbachia-based biological control of mosquitoes: lessons learned from the South Pacific Eric W. Chambers Department of Biology Valdosta State University, Valdosta GA Outline of Presentation • What’s the problem? - Review of lymphatic filariasis • Aedes polynesiensis – A unique mosquito • Wolbachia based control of Aedes polynesiensis • Future research Lymphatic filariasis (LF) • Global Distribution-endemic in 83 countries – 120 million infected – 1 billion at risk Lymphatic filariasis in the Pacific Northern Marianas Guam Marshall Islands Federated States of Micronesia Palau Nauru Kiribati Kiribati Kiribati Papua New Guinea (Phoenix) (Line Tuvalu Islands) Periodic Tokelau Solomon Is Cook Wallis & Islands Futuna Samoa Fiji Am Vanuatu Samoa Subperiodic New Niue Caledonia Tonga French Polynesia Pitcairn Australia New Zealand Lymphatic filariasis vectors in the Pacific Vector Countries Where Found Aedes cooki Niue Aedes fijiensis Fiji Aedes horrensces Fiji Aedes kochi Papua New Guinea Aedes marshallensis Kiribati Aedes oceanicus Tonga Aedes polynesiensis Am Samoa, Samoa, Cook Islands, Tokelau, Tuvalu, French Polynesia, Wallis and Futuna, Fiji Aedes pseudoscutellaris Fiji Aedes rotumae Rotuma Island in Fiji Aedes samoanus Samoa Aedes tabu Tonga Aedes tutuilae Samoa Aedes upolenis Samoa Ochlerotatus vigilax New Caledonia, Fiji An punctulatus complex Papua New Guinea, Solomon Islands, Vanuatu Culex annulirostris Irian Jaya Culex quinquefasciatus Kiribati, Pelau, Fed States Micronesia, PNG, Fiji, etc Mansonia uniformis Papua New Guinea Aedes polynesiensis (Marks) Courtesy Renee Chambers • Found only on the islands of the South Pacific • Day-biting mosquito • Exophilic • Major vector of lymphatic filariasis (LF) French Polynesia Is MDA enough in the South Pacific? • Treatment with DEC since 1955 • Antigen prevalence of 4.6% • Mosquito infection rate of 1.4% Society islands – Marquesas = 12.3% Tahiti = 11.5% Australes-Tuamotu Gambier = 12.3% Slide credit: Herve Bossin What makes transmission of LF by Aedes polynesiensis in the South Pacific unique? 1.