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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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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. |
format | Online Article Text |
id | pubmed-5069946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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