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Chikungunya virus transmission between Aedes albopictus and laboratory mice

BACKGROUND: Chikungunya virus (CHIKV) is a mosquito-borne alphavirus associated with epidemics of acute and chronic arthritic disease in humans. Aedes albopictus has emerged as an important new natural vector for CHIKV transmission; however, mouse models for studying transmission have not been devel...

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Autores principales: Hugo, Leon E., Prow, Natalie A., Tang, Bing, Devine, Greg, Suhrbier, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069946/
https://www.ncbi.nlm.nih.gov/pubmed/27760560
http://dx.doi.org/10.1186/s13071-016-1838-1
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author Hugo, Leon E.
Prow, Natalie A.
Tang, Bing
Devine, Greg
Suhrbier, Andreas
author_facet Hugo, Leon E.
Prow, Natalie A.
Tang, Bing
Devine, Greg
Suhrbier, Andreas
author_sort Hugo, Leon E.
collection PubMed
description BACKGROUND: Chikungunya virus (CHIKV) is a mosquito-borne alphavirus associated with epidemics of acute and chronic arthritic disease in humans. Aedes albopictus has emerged as an important new natural vector for CHIKV transmission; however, mouse models for studying transmission have not been developed. METHODS: Aedes albopictus mosquitoes were infected with CHIKV via membrane feeding and by using infected adult wild-type C57BL/6 mice. Paraffin sections of infected mosquitoes were analysed by immunofluorescent antibody staining using an anti-CHIKV antibody. CHIKV-infected mosquitoes were used to infect adult C57BL/6 and interferon response factor 3 and 7 deficient (IRF3/7(-/-)) mice. RESULTS: Feeding mosquitoes on blood meals with CHIKV titres > 5 log(10)CCID(50)/ml, either by membrane feeding or feeding on infected mice, resulted in  ≥ 50 % of mosquitoes becoming infected. However, CHIKV titres in blood meals  ≥ 7 log(10)CCID(50)/ml were required before salivary glands showed significant levels of immunofluorescent staining with an anti-CHIKV antibody. Mosquitoes fed on blood meals of 7.5 (but not 5.9) log(10)CCID(50)/ml were able efficiently to transmit virus to adult C57BL/6 and IRF3/7(-/-) mice, with the latter mice showing overt signs of arthritis post-infection. CONCLUSIONS: The results provide a simple in vivo model for studying transmission of CHIKV from mosquitoes to mammals and also argue against a resistance barrier to CHIKV infection in adult mice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1838-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-50699462016-10-24 Chikungunya virus transmission between Aedes albopictus and laboratory mice Hugo, Leon E. Prow, Natalie A. Tang, Bing Devine, Greg Suhrbier, Andreas Parasit Vectors Short Report BACKGROUND: Chikungunya virus (CHIKV) is a mosquito-borne alphavirus associated with epidemics of acute and chronic arthritic disease in humans. Aedes albopictus has emerged as an important new natural vector for CHIKV transmission; however, mouse models for studying transmission have not been developed. METHODS: Aedes albopictus mosquitoes were infected with CHIKV via membrane feeding and by using infected adult wild-type C57BL/6 mice. Paraffin sections of infected mosquitoes were analysed by immunofluorescent antibody staining using an anti-CHIKV antibody. CHIKV-infected mosquitoes were used to infect adult C57BL/6 and interferon response factor 3 and 7 deficient (IRF3/7(-/-)) mice. RESULTS: Feeding mosquitoes on blood meals with CHIKV titres > 5 log(10)CCID(50)/ml, either by membrane feeding or feeding on infected mice, resulted in  ≥ 50 % of mosquitoes becoming infected. However, CHIKV titres in blood meals  ≥ 7 log(10)CCID(50)/ml were required before salivary glands showed significant levels of immunofluorescent staining with an anti-CHIKV antibody. Mosquitoes fed on blood meals of 7.5 (but not 5.9) log(10)CCID(50)/ml were able efficiently to transmit virus to adult C57BL/6 and IRF3/7(-/-) mice, with the latter mice showing overt signs of arthritis post-infection. CONCLUSIONS: The results provide a simple in vivo model for studying transmission of CHIKV from mosquitoes to mammals and also argue against a resistance barrier to CHIKV infection in adult mice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1838-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-19 /pmc/articles/PMC5069946/ /pubmed/27760560 http://dx.doi.org/10.1186/s13071-016-1838-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Hugo, Leon E.
Prow, Natalie A.
Tang, Bing
Devine, Greg
Suhrbier, Andreas
Chikungunya virus transmission between Aedes albopictus and laboratory mice
title Chikungunya virus transmission between Aedes albopictus and laboratory mice
title_full Chikungunya virus transmission between Aedes albopictus and laboratory mice
title_fullStr Chikungunya virus transmission between Aedes albopictus and laboratory mice
title_full_unstemmed Chikungunya virus transmission between Aedes albopictus and laboratory mice
title_short Chikungunya virus transmission between Aedes albopictus and laboratory mice
title_sort chikungunya virus transmission between aedes albopictus and laboratory mice
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069946/
https://www.ncbi.nlm.nih.gov/pubmed/27760560
http://dx.doi.org/10.1186/s13071-016-1838-1
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