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California Encephalitis Orthobunyaviruses in Northern Europe
California encephalitis orthobunyaviruses in northern Europe NIINA PUTKURI Department of Virology Faculty of Medicine, University of Helsinki Doctoral Program in Biomedicine Doctoral School in Health Sciences Academic Dissertation To be presented for public examination with the permission of the Faculty of Medicine, University of Helsinki, in lecture hall 13 at the Main Building, Fabianinkatu 33, Helsinki, 23rd September 2016 at 12 noon. Helsinki 2016 Supervisors Professor Olli Vapalahti Department of Virology and Veterinary Biosciences, Faculty of Medicine and Veterinary Medicine, University of Helsinki and Department of Virology and Immunology, Hospital District of Helsinki and Uusimaa, Helsinki, Finland Professor Antti Vaheri Department of Virology, Faculty of Medicine, University of Helsinki, Helsinki, Finland Reviewers Docent Heli Harvala Simmonds Unit for Laboratory surveillance of vaccine preventable diseases, Public Health Agency of Sweden, Solna, Sweden and European Programme for Public Health Microbiology Training (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden Docent Pamela Österlund Viral Infections Unit, National Institute for Health and Welfare, Helsinki, Finland Offical Opponent Professor Jonas Schmidt-Chanasit Bernhard Nocht Institute for Tropical Medicine WHO Collaborating Centre for Arbovirus and Haemorrhagic Fever Reference and Research National Reference Centre for Tropical Infectious Disease Hamburg, Germany ISBN 978-951-51-2399-2 (PRINT) ISBN 978-951-51-2400-5 (PDF, available -
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. -
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. -
MOSQUITOES of the SOUTHEASTERN UNITED STATES
L f ^-l R A R > ^l^ ■'■mx^ • DEC2 2 59SO , A Handbook of tnV MOSQUITOES of the SOUTHEASTERN UNITED STATES W. V. King G. H. Bradley Carroll N. Smith and W. C. MeDuffle Agriculture Handbook No. 173 Agricultural Research Service UNITED STATES DEPARTMENT OF AGRICULTURE \ I PRECAUTIONS WITH INSECTICIDES All insecticides are potentially hazardous to fish or other aqpiatic organisms, wildlife, domestic ani- mals, and man. The dosages needed for mosquito control are generally lower than for most other insect control, but caution should be exercised in their application. Do not apply amounts in excess of the dosage recommended for each specific use. In applying even small amounts of oil-insecticide sprays to water, consider that wind and wave action may shift the film with consequent damage to aquatic life at another location. Heavy applications of insec- ticides to ground areas such as in pretreatment situa- tions, may cause harm to fish and wildlife in streams, ponds, and lakes during runoff due to heavy rains. Avoid contamination of pastures and livestock with insecticides in order to prevent residues in meat and milk. Operators should avoid repeated or prolonged contact of insecticides with the skin. Insecticide con- centrates may be particularly hazardous. Wash off any insecticide spilled on the skin using soap and water. If any is spilled on clothing, change imme- diately. Store insecticides in a safe place out of reach of children or animals. Dispose of empty insecticide containers. Always read and observe instructions and precautions given on the label of the product. UNITED STATES DEPARTMENT OF AGRICULTURE Agriculture Handbook No. -
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. -
Mosquitoes of Western Uganda
HHS Public Access Author manuscript Author ManuscriptAuthor Manuscript Author J Med Entomol Manuscript Author . Author Manuscript Author manuscript; available in PMC 2019 May 26. Published in final edited form as: J Med Entomol. 2012 November ; 49(6): 1289–1306. doi:10.1603/me12111. Mosquitoes of Western Uganda J.-P. Mutebi1, M. B. Crabtree1, R. J. Kent Crockett1, A. M. Powers1, J. J. Lutwama2, and B. R. Miller1 1Centers for Disease Control and Prevention (CDC), 3150 Rampart Road, Fort Collins, Colorado 80521. 2Department of Arbovirology, Uganda Virus Research Institute (UVRI), P.O. Box 49, Entebbe, Uganda. Abstract The mosquito fauna in many areas of western Uganda has never been studied and is currently unknown. One area, Bwamba County, has been previously studied and documented but the species lists have not been updated for more than 40 years. This paucity of data makes it difficult to determine which arthropod-borne viruses pose a risk to human or animal populations. Using CO2 baited-light traps, from 2008 through 2010, 67,731 mosquitoes were captured at five locations in western Uganda including Mweya, Sempaya, Maramagambo, Bwindi (BINP), and Kibale (KNP). Overall, 88 mosquito species, 7 subspecies and 7 species groups in 10 genera were collected. The largest number of species was collected at Sempaya (65 species), followed by Maramagambo (45), Mweya (34), BINP (33), and KNP (22). However, species diversity was highest in BINP (Simpson’s Diversity Index 1-D = 0.85), followed by KNP (0.80), Maramagambo (0.79), Sempaya (0.67), and Mweya (0.56). Only six species (Aedes (Aedimorphus) cumminsii (Theobald), Aedes (Neomelaniconion) circumluteolus (Theobald), Culex (Culex) antennatus (Becker), Culex (Culex) decens group, Culex (Lutzia) tigripes De Grandpre and De Charmoy, and Culex (Oculeomyia) annulioris Theobald), were collected from all 5 sites suggesting large differences in species composition among sites. -
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. -
Productivity of Natural and Artificial Containers for Aedes Polynesiensis and Aedes Aegypti in Four American Samoan Villages
Medical and Veterinary Entomology (2007) 21, 22–29 Productivity of natural and artificial containers for Aedes polynesiensis and Aedes aegypti in four American Samoan villages T . R . B U R K O T 1,2 , T. HANDZEL 1 , M . A . SCHMAEDICK 3 , J . T U F A 4 , J . M . ROBERTS 1 a n d P . M . G R A V E S 5 1 Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, U.S.A. , 2 Division of Vector-Borne Infectious Diseases, Centers for Disease Control , Fort Collins, Colorado, U.S.A. , 3 Division of Community and Natural Resources, American Samoa Community College, Pago Pago, American Samoa , 4 Department of Health, American Samoa Government, Pago Pago, American Samoa and 5 EpiVec, Atlanta, Georgia, U.S.A. Abstract . Six mosquito species were identified in a survey of containers associated with 347 households in four villages in American Samoa. Aedes polynesiensis Marks (Diptera: Culicidae) and Aedes aegypti (L) were the most abundant species, represent- ing 57% and 29% of the mosquitoes identified. Culex quinquefasciatus (Say), Culex annulirostris (Skuse) , Aedes oceanicus (Belkin) and Toxorhynchites amboinensis (Doleschall) were also found. Aedes aegypti and Ae. polynesiensis showed distinct dif- ferences in their use of containers, preferring large and small containers, respectively. By contrast with previous studies, Ae. polynesiensis utilized domestic and natural con- tainers with equal frequency, whereas Ae. aegypti continued to be found predominantly in domestic containers. Only 15% of containers holding immature mosquitoes included pupae and fewer than 10 Aedes spp. pupae were found in most containers with pupae. -
Probable Contribution of Culex Quinquefasciatus Mosquitoes to The
Lutomiah et al. Parasites Vectors (2021) 14:138 https://doi.org/10.1186/s13071-021-04632-6 Parasites & Vectors RESEARCH Open Access Probable contribution of Culex quinquefasciatus mosquitoes to the circulation of chikungunya virus during an outbreak in Mombasa County, Kenya, 2017–2018 Joel Lutomiah1*, Francis Mulwa1, James Mutisya1, Edith Koskei1, Solomon Langat2, Albert Nyunja1, Hellen Koka1, Samson Konongoi1, Edith Chepkorir1, Victor Ofula1, Samuel Owaka1, Fredrick Eyase2,3 and Rosemary Sang1 Abstract Background: Chikungunya virus is an alphavirus, primarily transmitted by Aedes aegypti and Ae. albopictus. In late 2017–2018, an outbreak of chikungunya occurred in Mombasa county, Kenya, and investigations were conducted to establish associated entomological risk factors. Methods: Homes were stratifed and water-flled containers inspected for immature Ae. aegypti, and larval indices were calculated. Adult mosquitoes were collected in the same homesteads using BG-Sentinel and CDC light traps and screened for chikungunya virus. Experiments were also conducted to determine the ability of Culex quinquefasciatus to transmit chikungunya virus. Results: One hundred thirty-one houses and 1637 containers were inspected; 48 and 128 of them, respectively, were positive for immature Ae. aegypti, with the house index (36.60), container index (7.82) and Breteau index (97.71) recorded. Jerry cans (n 1232; 72.26%) and clay pots (n 2; 0.12%) were the most and least inspected containers, respectively, while drums,= the second most commonly sampled= (n 249; 15.21%), were highly positive (65.63%) and productive (60%). Tires and jerry cans demonstrated the highest and= lowest breeding preference ratios, 11.36 and 0.2, respectively. Over 6900 adult mosquitoes were collected and identifed into 15 species comprising Cx. -
Classification of Mosquitoes in Tribe Aedini 925
FORUM Classification of Mosquitoes in Tribe Aedini (Diptera: Culicidae): Paraphylyphobia, and Classification Versus Cladistic Analysis HARRY M. SAVAGE Centers for Disease Control and Prevention, P.O. Box 2087, Fort Collins, CO 80522 J. Med. Entomol. 42(6): 923Ð927 (2005) Downloaded from https://academic.oup.com/jme/article/42/6/923/886357 by guest on 29 September 2021 ABSTRACT Many mosquito species are important vectors of human and animal diseases, and others are important nuisance species. To facilitate communication and information exchange among pro- fessional groups interested in vector-borne diseases, it is essential that a stable nomenclature be maintained. For the Culicidae, easily identiÞable genera based on morphology are an asset. Major changes in generic concept, the elevation of 32 subgenera within Aedes to generic status, and changes in hundreds of species names proposed in a recent article demand consideration by all parties interested in mosquito-borne diseases. The entire approach to Aedini systematics of these authors was ßawed by an inordinate fear of paraphyletic taxa or Paraphylyphobia, and their inability to distinguish between classiÞcation and cladistic analysis. Taxonomists should refrain from making taxonomic changes based on preliminary data, and they should be very selective in assigning generic names to only the most important and well-deÞned groups of species. KEY WORDS Aedini classiÞcation, Aedes, Ochlerotatus, paraphylyphobia, mosquito classiÞcation MANY MOSQUITO SPECIES IN the tribe Aedini, a cosmo- In this communication, I brießy review taxonomic politan group represented by 11 genera and Ϸ1,239 categories in a zoological classiÞcation, the Interna- species, are important vectors of human and animal tional Code of Zoological Nomenclature (the Code), diseases, and many others are of considerable eco- the development of generic concept within the Cu- nomic importance as nuisance or pest species. -
Polynesian Mosquito American Samoa Community College Pests and Diseases of American Samoa Community & Natural Resources Number 7 Cooperative Research & Extension 2005
Polynesian Mosquito American Samoa Community College Pests and Diseases of American Samoa Community & Natural Resources Number 7 Cooperative Research & Extension 2005 Introduction. The Polynesian mosquito, Aedes polynesiensis, is an important vector of dengue and filariasis and is found in abundance on all the Samoan Islands. It is a native of the South Pacific, occur- ring also in portions of the Cook Islands, Fiji, French Polynesia, Pitcairn, Tuvalu, and Wallis and Futuna. This mosquito is primarily a daytime feeder, with peak biting times in the early morning and late afternoon. It can also carry heartworm of dogs. Eggs Larva Adult female Life cycle. Females deposit their tiny, brown, elongate-oval eggs individually just above the water line in natural or artificial contain- ers, including discarded tires, buckets, metal drums, coconut shells, fallen leaves, tin cans, cups, tree holes, and crab holes. The eggs hatch when rain falls, raising the water level and submerging the eggs. The larvae develop in the stagnant water, feeding on decay- ing organic matter and associated microorganisms. After about 7 days the full grown larvae turn into pupae. Like the larvae, the pu- pae can swim, but they do not feed. The pupal stage lasts 2-3 days, after which the adult mosquito emerges. Both male and female adults feed on nectar and other plant fluids to obtain energy. Females must Pupa feed on blood in order to form eggs, but males do not feed on blood. Hosts for the females include humans, pigs, dogs, horses, birds, Filariasis transmission. Filariasis is caused by tiny worms. A mos- and other animals.