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Mosquitoes in DENGUE MOSQUITOES the World? ARE MOST ACTIVE DURING BO the DAY AROUND a U S T YOUR YARD T SALTMARSH MOSQUITOES C ARE MOST a ACTIVE at DUSK
Mosquito awareness Did you know... Mosquito species there are 3500 vary in their species of biting behaviour mosquitoes in DENGUE MOSQUITOES the world? ARE MOST ACTIVE DURING BO THE DAY AROUND A U S T YOUR YARD T SALTMARSH MOSQUITOES C ARE MOST A ACTIVE AT DUSK AND DAWN F Council conducts 300 SPECIES IN AUSTRALIA mosquito control 40 SPECIES IN TOWNSVILLE World's COUNCIL CONDUCTS deadliest MOSQUITO CONTROL ON MOSQUITOES PUBLIC LAND, USING BOTH animals GROUND AND AERIAL TREATMENTS TO TARGET NUMBER OF PEOPLE MOSQUITO LARVAE. KILLED BY ANIMALS PER YEAR Mosquitoes wings beat 300-600 times per second Mosquitoes Mosquitoes can carry are attracted many diseases. to humans FROM THE ODOURS AND CARBON DIOXIDE WE EXPIRE FROM BREATHING Protect yourself OR SWEATING. townsville.qld.gov.au and your family Mosquitoes distance of travel 13 48 10 from mosquito bites from breeding point by using personal DENGUE MOSQUITO SALTMARSH MOSQUITO protection. 200M 50KM BREEDING PLACE Mosquito Mosquito Mosquito life cycle disease prevention A mosquito is an insect characterised by Protect yourself Did you know... Dengue. 1. Three body parts against disease-carrying Townsville City Do your weekly a. Head mosquitoes Council undertakes yard check. b. Thorax c. Abdomen reactive inspection ARE YOU MAKING DENGUE Mosquito borne How do of properties within MOSSIES WELCOME 2. A proboscis (for AROUND YOUR HOME? piercing and sucking) diseases found in mosquitoes the Townsville local TAKE RESPONSIBILITY TO 3. One pair of antennae Townsville include transmit government area PROTECT YOURSELF AND 4. One pair of wings YOUR FAMILY BY CHECKING Ross River virus diseases? based on customer YOUR YARD FOR ANYTHING 5. -
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 -
The Non-Human Reservoirs of Ross River Virus: a Systematic Review of the Evidence Eloise B
Stephenson et al. Parasites & Vectors (2018) 11:188 https://doi.org/10.1186/s13071-018-2733-8 REVIEW Open Access The non-human reservoirs of Ross River virus: a systematic review of the evidence Eloise B. Stephenson1*, Alison J. Peel1, Simon A. Reid2, Cassie C. Jansen3,4 and Hamish McCallum1 Abstract: Understanding the non-human reservoirs of zoonotic pathogens is critical for effective disease control, but identifying the relative contributions of the various reservoirs of multi-host pathogens is challenging. For Ross River virus (RRV), knowledge of the transmission dynamics, in particular the role of non-human species, is important. In Australia, RRV accounts for the highest number of human mosquito-borne virus infections. The long held dogma that marsupials are better reservoirs than placental mammals, which are better reservoirs than birds, deserves critical review. We present a review of 50 years of evidence on non-human reservoirs of RRV, which includes experimental infection studies, virus isolation studies and serosurveys. We find that whilst marsupials are competent reservoirs of RRV, there is potential for placental mammals and birds to contribute to transmission dynamics. However, the role of these animals as reservoirs of RRV remains unclear due to fragmented evidence and sampling bias. Future investigations of RRV reservoirs should focus on quantifying complex transmission dynamics across environments. Keywords: Amplifier, Experimental infection, Serology, Virus isolation, Host, Vector-borne disease, Arbovirus Background transmission dynamics among arboviruses has resulted in Vertebrate reservoir hosts multiple definitions for the key term “reservoir” [9]. Given Globally, most pathogens of medical and veterinary im- the diversity of virus-vector-vertebrate host interactions, portance can infect multiple host species [1]. -
A New Orbivirus Isolated from Mosquitoes in North-Western Australia Shows Antigenic and Genetic Similarity to Corriparta Virus B
viruses Article A New Orbivirus Isolated from Mosquitoes in North-Western Australia Shows Antigenic and Genetic Similarity to Corriparta Virus but Does Not Replicate in Vertebrate Cells Jessica J. Harrison 1,†, David Warrilow 2,†, Breeanna J. McLean 1, Daniel Watterson 1, Caitlin A. O’Brien 1, Agathe M.G. Colmant 1, Cheryl A. Johansen 3, Ross T. Barnard 1, Sonja Hall-Mendelin 2, Steven S. Davis 4, Roy A. Hall 1 and Jody Hobson-Peters 1,* 1 Australian Infectious Diseases Research Centre, School of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia 4072, Australia; [email protected] (J.J.H.); [email protected] (B.J.M.); [email protected] (D.W.); [email protected] (C.A.O.B.); [email protected] (A.M.G.C.); [email protected] (R.T.B.); [email protected] (R.A.H.) 2 Public Health Virology Laboratory, Department of Health, Queensland Government, P.O. Box 594, Archerfield 4108, Australia; [email protected] (D.W.); [email protected] (S.H.-M.) 3 School of Pathology and Laboratory Medicine, The University of Western Australia, Nedlands 6009, Australia; [email protected] 4 Berrimah Veterinary Laboratory, Department of Primary Industries and Fisheries, Darwin 0828, Australia; [email protected] * Correspondence: [email protected]; Tel.: +61-7-3365-4648 † These authors contributed equally to the work. Academic Editor: Karyn Johnson Received: 19 February 2016; Accepted: 10 May 2016; Published: 20 May 2016 Abstract: The discovery and characterisation of new mosquito-borne viruses provides valuable information on the biodiversity of vector-borne viruses and important insights into their evolution. -
Sequencing of Historical Isolates, K-Mer Mining and High Serological Cross-Reactivity with Ross River Virus Argue Against the Presence of Getah Virus in Australia
pathogens Article Sequencing of Historical Isolates, K-mer Mining and High Serological Cross-Reactivity with Ross River Virus Argue against the Presence of Getah Virus in Australia 1, 1, 1 2 3 Daniel J. Rawle y , Wilson Nguyen y , Troy Dumenil , Rhys Parry , David Warrilow , Bing Tang 1, Thuy T. Le 1, Andrii Slonchak 2, Alexander A. Khromykh 2,4, Viviana P. Lutzky 1, Kexin Yan 1 and Andreas Suhrbier 1,4,* 1 Inflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia; [email protected] (D.J.R.); [email protected] (W.N.); [email protected] (T.D.); [email protected] (B.T.); [email protected] (T.T.L.); [email protected] (V.P.L.); [email protected] (K.Y.) 2 School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, QLD 4072, Australia; [email protected] (R.P.); [email protected] (A.S.); [email protected] (A.A.K.) 3 Public Health Virology Laboratory, Department of Health, Queensland Government, Brisbane, QLD 4108, Australia; [email protected] 4 GVN Center of Excellence, Australian Infectious Diseases Research Centre, Brisbane, QLD 4006 and 4072, Australia * Correspondence: [email protected] These authors equally contributed to this work. y Received: 14 September 2020; Accepted: 15 October 2020; Published: 16 October 2020 Abstract: Getah virus (GETV) is a mosquito-transmitted alphavirus primarily associated with disease in horses and pigs in Asia. GETV was also reported to have been isolated from mosquitoes in Australia in 1961; however, retrieval and sequencing of the original isolates (N544 and N554), illustrated that these viruses were virtually identical to the 1955 GETVMM2021 isolate from Malaysia. -
Novel RNA Viruses from the Transcriptome of Pheromone Glands in the Pink Bollworm Moth, Pectinophora Gossypiella
Entomology Publications Entomology 6-15-2021 Novel RNA Viruses from the Transcriptome of Pheromone Glands in the Pink Bollworm Moth, Pectinophora gossypiella Xiaoyi Dou Iowa State University Sijun Liu Iowa State University Victoria Soroker Institute of Plant Protection, ARO Ally Harari Institute of Plant Protection, ARO Russell Jurenka Iowa State University, [email protected] Follow this and additional works at: https://lib.dr.iastate.edu/ent_pubs Part of the Bioinformatics Commons, Entomology Commons, and the Genetics Commons The complete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ ent_pubs/596. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Entomology at Iowa State University Digital Repository. It has been accepted for inclusion in Entomology Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Novel RNA Viruses from the Transcriptome of Pheromone Glands in the Pink Bollworm Moth, Pectinophora gossypiella Abstract In this study, we analyzed the transcriptome obtained from the pheromone gland isolated from two Israeli populations of the pink bollworm Pectinophora gossypiella to identify viral sequences. The lab population and the field samples carried the same viral sequences. We discovered four novel viruses: two positive- sense single-stranded RNA viruses, Pectinophora gossypiella virus 1 (PecgV1, a virus of Iflaviridae) and Pectinophora gossypiella virus 4 (PecgV4, unclassified), and two negative-sense single-stranded RNA viruses, Pectinophora gossypiella virus 2 (PecgV2, a virus of Phasmaviridae) and Pectinophora gossypiella virus 3 (PecgV3, a virus of Phenuiviridae). -
Clinically Important Vector-Borne Diseases of Europe
Natalie Cleton, DVM Erasmus MC, Rotterdam Department of Viroscience [email protected] No potential conflicts of interest to disclose © by author ESCMID Online Lecture Library Erasmus Medical Centre Department of Viroscience Laboratory Diagnosis of Arboviruses © by author Natalie Cleton ESCMID Online LectureMarion Library Koopmans Chantal Reusken [email protected] Distribution Arboviruses with public health impact have a global and ever changing distribution © by author ESCMID Online Lecture Library Notifications of vector-borne diseases in the last 6 months on Healthmap.org Syndromes of arboviral diseases 1) Febrile syndrome: – Fever & Malaise – Headache & retro-orbital pain – Myalgia 2) Neurological syndrome: – Meningitis, encephalitis & myelitis – Convulsions & coma – Paralysis 3) Hemorrhagic syndrome: – Low platelet count, liver enlargement – Petechiae © by author – Spontaneous or persistent bleeding – Shock 4) Arthralgia,ESCMID Arthritis and Online Rash: Lecture Library – Exanthema or maculopapular rash – Polyarthralgia & polyarthritis Human arboviruses: 4 main virus families Family Genus Species examples Flaviviridae flavivirus Dengue 1-5 (DENV) West Nile virus (WNV) Yellow fever virus (YFV) Zika virus (ZIKV) Tick-borne encephalitis virus (TBEV) Togaviridae alphavirus Chikungunya virus (CHIKV) O’Nyong Nyong virus (ONNV) Mayaro virus (MAYV) Sindbis virus (SINV) Ross River virus (RRV) Barmah forest virus (BFV) Bunyaviridae nairo-, phlebo-©, orthobunyavirus by authorCrimean -Congo heamoragic fever (CCHFV) Sandfly fever virus -
Structural and Functional Characterization of the Severe Fever with Thrombocytopenia Syndrome Virus L Protein
bioRxiv preprint doi: https://doi.org/10.1101/2020.03.02.973065; this version posted March 3, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Structural and functional characterization of the Severe fever with thrombocytopenia syndrome virus L protein Dominik Vogel1#, Sigurdur Rafn Thorkelsson2#, Emmanuelle R. J. Quemin2, Kristina Meier1, Tomas Kouba3, Nadja Gogrefe1, Carola Busch1, Sophia Reindl1, Stephan Günther1,4, Stephen Cusack3, Kay Grünewald2, Maria Rosenthal1,* 1 Department of Virology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg, Hamburg, 20359, Germany 2 Centre for Structural Systems Biology, Heinrich-Pette-Institute, Leibniz Institute for Experimental Virology, University of Hamburg, Hamburg, Germany 3 European Molecular Biology Laboratory, 71 Avenue des Martyrs, CS 90181, 38042 Grenoble Cedex 9, France 4 German Center for Infection Research (DZIF), Partner site Hamburg – Lübeck – Borstel – Riems, Hamburg, 20359, Germany # These authors contributed equally to this work. * To whom correspondence should be addressed: Maria Rosenthal; Tel: +49 40 42818 942; Fax: +49 40 42818 931; Email: [email protected]. 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.03.02.973065; this version posted March 3, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. ABSTRACT The Bunyavirales order contains several emerging viruses with high epidemic potential, including Severe fever with thrombocytopenia syndrome virus (SFTSV). -
A Look Into Bunyavirales Genomes: Functions of Non-Structural (NS) Proteins
viruses Review A Look into Bunyavirales Genomes: Functions of Non-Structural (NS) Proteins Shanna S. Leventhal, Drew Wilson, Heinz Feldmann and David W. Hawman * Laboratory of Virology, Rocky Mountain Laboratories, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA; [email protected] (S.S.L.); [email protected] (D.W.); [email protected] (H.F.) * Correspondence: [email protected]; Tel.: +1-406-802-6120 Abstract: In 2016, the Bunyavirales order was established by the International Committee on Taxon- omy of Viruses (ICTV) to incorporate the increasing number of related viruses across 13 viral families. While diverse, four of the families (Peribunyaviridae, Nairoviridae, Hantaviridae, and Phenuiviridae) contain known human pathogens and share a similar tri-segmented, negative-sense RNA genomic organization. In addition to the nucleoprotein and envelope glycoproteins encoded by the small and medium segments, respectively, many of the viruses in these families also encode for non-structural (NS) NSs and NSm proteins. The NSs of Phenuiviridae is the most extensively studied as a host interferon antagonist, functioning through a variety of mechanisms seen throughout the other three families. In addition, functions impacting cellular apoptosis, chromatin organization, and transcrip- tional activities, to name a few, are possessed by NSs across the families. Peribunyaviridae, Nairoviridae, and Phenuiviridae also encode an NSm, although less extensively studied than NSs, that has roles in antagonizing immune responses, promoting viral assembly and infectivity, and even maintenance of infection in host mosquito vectors. Overall, the similar and divergent roles of NS proteins of these Citation: Leventhal, S.S.; Wilson, D.; human pathogenic Bunyavirales are of particular interest in understanding disease progression, viral Feldmann, H.; Hawman, D.W. -
Mosquito-Borne Viruses, Insect-Specific
FULL PAPER Virology Mosquito-borne viruses, insect-specific flaviviruses (family Flaviviridae, genus Flavivirus), Banna virus (family Reoviridae, genus Seadornavirus), Bogor virus (unassigned member of family Permutotetraviridae), and alphamesoniviruses 2 and 3 (family Mesoniviridae, genus Alphamesonivirus) isolated from Indonesian mosquitoes SUPRIYONO1), Ryusei KUWATA1,2), Shun TORII1), Hiroshi SHIMODA1), Keita ISHIJIMA3), Kenzo YONEMITSU1), Shohei MINAMI1), Yudai KURODA3), Kango TATEMOTO3), Ngo Thuy Bao TRAN1), Ai TAKANO1), Tsutomu OMATSU4), Tetsuya MIZUTANI4), Kentaro ITOKAWA5), Haruhiko ISAWA6), Kyoko SAWABE6), Tomohiko TAKASAKI7), Dewi Maria YULIANI8), Dimas ABIYOGA9), Upik Kesumawati HADI10), Agus SETIYONO10), Eiichi HONDO11), Srihadi AGUNGPRIYONO10) and Ken MAEDA1,3)* 1)Laboratory of Veterinary Microbiology, Joint Faculty of Veterinary Medicine, Yamaguchi University, 1677-1 Yoshida, Yamaguchi 753-8515, Japan 2)Faculty of Veterinary Medicine, Okayama University of Science, 1-3 Ikoino-oka, Imabari, Ehime 794-8555, Japan 3)Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan 4)Research and Education Center for Prevention of Global Infectious Diseases of Animals, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu, Tokyo 183-8508, Japan 5)Pathogen Genomics Center, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan 6)Department of Medical Entomology, National Institute of Infectious Diseases, 1-23-1 -
Taxonomy of the Order Bunyavirales: Second Update 2018
HHS Public Access Author manuscript Author ManuscriptAuthor Manuscript Author Arch Virol Manuscript Author . Author manuscript; Manuscript Author available in PMC 2020 March 01. Published in final edited form as: Arch Virol. 2019 March ; 164(3): 927–941. doi:10.1007/s00705-018-04127-3. TAXONOMY OF THE ORDER BUNYAVIRALES: SECOND UPDATE 2018 A full list of authors and affiliations appears at the end of the article. Abstract In October 2018, the order Bunyavirales was amended by inclusion of the family Arenaviridae, abolishment of three families, creation of three new families, 19 new genera, and 14 new species, and renaming of three genera and 22 species. This article presents the updated taxonomy of the order Bunyavirales as now accepted by the International Committee on Taxonomy of Viruses (ICTV). Keywords Arenaviridae; arenavirid; arenavirus; bunyavirad; Bunyavirales; bunyavirid; Bunyaviridae; bunyavirus; emaravirus; Feraviridae; feravirid, feravirus; fimovirid; Fimoviridae; fimovirus; goukovirus; hantavirid; Hantaviridae; hantavirus; hartmanivirus; herbevirus; ICTV; International Committee on Taxonomy of Viruses; jonvirid; Jonviridae; jonvirus; mammarenavirus; nairovirid; Nairoviridae; nairovirus; orthobunyavirus; orthoferavirus; orthohantavirus; orthojonvirus; orthonairovirus; orthophasmavirus; orthotospovirus; peribunyavirid; Peribunyaviridae; peribunyavirus; phasmavirid; phasivirus; Phasmaviridae; phasmavirus; phenuivirid; Phenuiviridae; phenuivirus; phlebovirus; reptarenavirus; tenuivirus; tospovirid; Tospoviridae; tospovirus; virus classification; virus nomenclature; virus taxonomy INTRODUCTION The virus order Bunyavirales was established in 2017 to accommodate related viruses with segmented, linear, single-stranded, negative-sense or ambisense RNA genomes classified into 9 families [2]. Here we present the changes that were proposed via an official ICTV taxonomic proposal (TaxoProp 2017.012M.A.v1.Bunyavirales_rev) at http:// www.ictvonline.org/ in 2017 and were accepted by the ICTV Executive Committee (EC) in [email protected]. -
Risk Groups: Viruses (C) 1988, American Biological Safety Association
Rev.: 1.0 Risk Groups: Viruses (c) 1988, American Biological Safety Association BL RG RG RG RG RG LCDC-96 Belgium-97 ID Name Viral group Comments BMBL-93 CDC NIH rDNA-97 EU-96 Australia-95 HP AP (Canada) Annex VIII Flaviviridae/ Flavivirus (Grp 2 Absettarov, TBE 4 4 4 implied 3 3 4 + B Arbovirus) Acute haemorrhagic taxonomy 2, Enterovirus 3 conjunctivitis virus Picornaviridae 2 + different 70 (AHC) Adenovirus 4 Adenoviridae 2 2 (incl animal) 2 2 + (human,all types) 5 Aino X-Arboviruses 6 Akabane X-Arboviruses 7 Alastrim Poxviridae Restricted 4 4, Foot-and- 8 Aphthovirus Picornaviridae 2 mouth disease + viruses 9 Araguari X-Arboviruses (feces of children 10 Astroviridae Astroviridae 2 2 + + and lambs) Avian leukosis virus 11 Viral vector/Animal retrovirus 1 3 (wild strain) + (ALV) 3, (Rous 12 Avian sarcoma virus Viral vector/Animal retrovirus 1 sarcoma virus, + RSV wild strain) 13 Baculovirus Viral vector/Animal virus 1 + Togaviridae/ Alphavirus (Grp 14 Barmah Forest 2 A Arbovirus) 15 Batama X-Arboviruses 16 Batken X-Arboviruses Togaviridae/ Alphavirus (Grp 17 Bebaru virus 2 2 2 2 + A Arbovirus) 18 Bhanja X-Arboviruses 19 Bimbo X-Arboviruses Blood-borne hepatitis 20 viruses not yet Unclassified viruses 2 implied 2 implied 3 (**)D 3 + identified 21 Bluetongue X-Arboviruses 22 Bobaya X-Arboviruses 23 Bobia X-Arboviruses Bovine 24 immunodeficiency Viral vector/Animal retrovirus 3 (wild strain) + virus (BIV) 3, Bovine Bovine leukemia 25 Viral vector/Animal retrovirus 1 lymphosarcoma + virus (BLV) virus wild strain Bovine papilloma Papovavirus/