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A Susceptible Mouse Model for Zika Virus Infection
Zika virus (ZIKV) is a mosquito-borne pathogen which has recently spread beyond Africa and into Pacific and South American regions. Despite first being detected in 1947, very little information is known about the virus, and its spread has been associated with increases in Guillain-Barre syndrome and...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858159/ https://www.ncbi.nlm.nih.gov/pubmed/27149521 http://dx.doi.org/10.1371/journal.pntd.0004658 |
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author | Dowall, Stuart D. Graham, Victoria A. Rayner, Emma Atkinson, Barry Hall, Graham Watson, Robert J. Bosworth, Andrew Bonney, Laura C. Kitchen, Samantha Hewson, Roger |
author_facet | Dowall, Stuart D. Graham, Victoria A. Rayner, Emma Atkinson, Barry Hall, Graham Watson, Robert J. Bosworth, Andrew Bonney, Laura C. Kitchen, Samantha Hewson, Roger |
author_sort | Dowall, Stuart D. |
collection | PubMed |
description | Zika virus (ZIKV) is a mosquito-borne pathogen which has recently spread beyond Africa and into Pacific and South American regions. Despite first being detected in 1947, very little information is known about the virus, and its spread has been associated with increases in Guillain-Barre syndrome and microcephaly. There are currently no known vaccines or antivirals against ZIKV infection. Progress in assessing interventions will require the development of animal models to test efficacies; however, there are only limited reports on in vivo studies. The only susceptible murine models have involved intracerebral inoculations or juvenile animals, which do not replicate natural infection. Our report has studied the effect of ZIKV infection in type-I interferon receptor deficient (A129) mice and the parent strain (129Sv/Ev) after subcutaneous challenge in the lower leg to mimic a mosquito bite. A129 mice developed severe symptoms with widespread viral RNA detection in the blood, brain, spleen, liver and ovaries. Histological changes were also striking in these animals. 129Sv/Ev mice developed no clinical symptoms or histological changes, despite viral RNA being detectable in the blood, spleen and ovaries, albeit at lower levels than those seen in A129 mice. Our results identify A129 mice as being highly susceptible to ZIKV and thus A129 mice represent a suitable, and urgently required, small animal model for the testing of vaccines and antivirals. |
format | Online Article Text |
id | pubmed-4858159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48581592016-05-13 A Susceptible Mouse Model for Zika Virus Infection Dowall, Stuart D. Graham, Victoria A. Rayner, Emma Atkinson, Barry Hall, Graham Watson, Robert J. Bosworth, Andrew Bonney, Laura C. Kitchen, Samantha Hewson, Roger PLoS Negl Trop Dis Research Article Zika virus (ZIKV) is a mosquito-borne pathogen which has recently spread beyond Africa and into Pacific and South American regions. Despite first being detected in 1947, very little information is known about the virus, and its spread has been associated with increases in Guillain-Barre syndrome and microcephaly. There are currently no known vaccines or antivirals against ZIKV infection. Progress in assessing interventions will require the development of animal models to test efficacies; however, there are only limited reports on in vivo studies. The only susceptible murine models have involved intracerebral inoculations or juvenile animals, which do not replicate natural infection. Our report has studied the effect of ZIKV infection in type-I interferon receptor deficient (A129) mice and the parent strain (129Sv/Ev) after subcutaneous challenge in the lower leg to mimic a mosquito bite. A129 mice developed severe symptoms with widespread viral RNA detection in the blood, brain, spleen, liver and ovaries. Histological changes were also striking in these animals. 129Sv/Ev mice developed no clinical symptoms or histological changes, despite viral RNA being detectable in the blood, spleen and ovaries, albeit at lower levels than those seen in A129 mice. Our results identify A129 mice as being highly susceptible to ZIKV and thus A129 mice represent a suitable, and urgently required, small animal model for the testing of vaccines and antivirals. Public Library of Science 2016-05-05 /pmc/articles/PMC4858159/ /pubmed/27149521 http://dx.doi.org/10.1371/journal.pntd.0004658 Text en © 2016 Dowall et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Dowall, Stuart D. Graham, Victoria A. Rayner, Emma Atkinson, Barry Hall, Graham Watson, Robert J. Bosworth, Andrew Bonney, Laura C. Kitchen, Samantha Hewson, Roger A Susceptible Mouse Model for Zika Virus Infection |
title | A Susceptible Mouse Model for Zika Virus Infection |
title_full | A Susceptible Mouse Model for Zika Virus Infection |
title_fullStr | A Susceptible Mouse Model for Zika Virus Infection |
title_full_unstemmed | A Susceptible Mouse Model for Zika Virus Infection |
title_short | A Susceptible Mouse Model for Zika Virus Infection |
title_sort | susceptible mouse model for zika virus infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858159/ https://www.ncbi.nlm.nih.gov/pubmed/27149521 http://dx.doi.org/10.1371/journal.pntd.0004658 |
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