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Chikungunya virus infection in Cynomolgus macaques following Intradermal and aerosol exposure
BACKGROUND: Chikungunya virus (CHIKV) is transmitted via mosquito bite and potentially by aerosol, causing chikungunya fever and arthritic disease in humans. There are currently no licensed vaccines or antiviral therapeutics to protect against CHIKV infection in humans. Animal models recapitulating...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520379/ https://www.ncbi.nlm.nih.gov/pubmed/28728590 http://dx.doi.org/10.1186/s12985-017-0804-7 |
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author | Cirimotich, Chris M. Vela, Eric M. Garver, Jennifer Barnewall, Roy E. Miller, Brian D. Meister, Gabriel T. Rogers, James V. |
author_facet | Cirimotich, Chris M. Vela, Eric M. Garver, Jennifer Barnewall, Roy E. Miller, Brian D. Meister, Gabriel T. Rogers, James V. |
author_sort | Cirimotich, Chris M. |
collection | PubMed |
description | BACKGROUND: Chikungunya virus (CHIKV) is transmitted via mosquito bite and potentially by aerosol, causing chikungunya fever and arthritic disease in humans. There are currently no licensed vaccines or antiviral therapeutics to protect against CHIKV infection in humans. Animal models recapitulating human disease, especially for transmission by aerosol, are needed for licensure of such medical countermeasures. METHODS: Cynomolgus macaques (CMs) were challenged by intradermal (ID) inoculation or exposure to an aerosol containing CHIKV Ross strain at different target infectious doses (10(3)–10(7) plaque forming units (PFU)). The clinical and virologic courses of disease were monitored up to 14 days post-exposure. RESULTS: ID infection of CMs led to overt clinical disease, detectable viremia, and increased blood markers of liver damage. Animals challenged by aerosol exhibited viremia and increased liver damage biomarkers with minimal observed clinical disease. All animals survived CHIKV challenge. CONCLUSIONS: We have described CHIKV infection in CMs following ID inoculation and, for the first time, infection by aerosol. Based on limited reported cases in the published literature, the aerosol model recapitulates the virologic findings of human infection via this route. The results of this study provide additional evidence for the potential use of CMs as a model for evaluating medical countermeasures against CHIKV. |
format | Online Article Text |
id | pubmed-5520379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55203792017-07-21 Chikungunya virus infection in Cynomolgus macaques following Intradermal and aerosol exposure Cirimotich, Chris M. Vela, Eric M. Garver, Jennifer Barnewall, Roy E. Miller, Brian D. Meister, Gabriel T. Rogers, James V. Virol J Research BACKGROUND: Chikungunya virus (CHIKV) is transmitted via mosquito bite and potentially by aerosol, causing chikungunya fever and arthritic disease in humans. There are currently no licensed vaccines or antiviral therapeutics to protect against CHIKV infection in humans. Animal models recapitulating human disease, especially for transmission by aerosol, are needed for licensure of such medical countermeasures. METHODS: Cynomolgus macaques (CMs) were challenged by intradermal (ID) inoculation or exposure to an aerosol containing CHIKV Ross strain at different target infectious doses (10(3)–10(7) plaque forming units (PFU)). The clinical and virologic courses of disease were monitored up to 14 days post-exposure. RESULTS: ID infection of CMs led to overt clinical disease, detectable viremia, and increased blood markers of liver damage. Animals challenged by aerosol exhibited viremia and increased liver damage biomarkers with minimal observed clinical disease. All animals survived CHIKV challenge. CONCLUSIONS: We have described CHIKV infection in CMs following ID inoculation and, for the first time, infection by aerosol. Based on limited reported cases in the published literature, the aerosol model recapitulates the virologic findings of human infection via this route. The results of this study provide additional evidence for the potential use of CMs as a model for evaluating medical countermeasures against CHIKV. BioMed Central 2017-07-20 /pmc/articles/PMC5520379/ /pubmed/28728590 http://dx.doi.org/10.1186/s12985-017-0804-7 Text en © The Author(s). 2017 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 | Research Cirimotich, Chris M. Vela, Eric M. Garver, Jennifer Barnewall, Roy E. Miller, Brian D. Meister, Gabriel T. Rogers, James V. Chikungunya virus infection in Cynomolgus macaques following Intradermal and aerosol exposure |
title | Chikungunya virus infection in Cynomolgus macaques following Intradermal and aerosol exposure |
title_full | Chikungunya virus infection in Cynomolgus macaques following Intradermal and aerosol exposure |
title_fullStr | Chikungunya virus infection in Cynomolgus macaques following Intradermal and aerosol exposure |
title_full_unstemmed | Chikungunya virus infection in Cynomolgus macaques following Intradermal and aerosol exposure |
title_short | Chikungunya virus infection in Cynomolgus macaques following Intradermal and aerosol exposure |
title_sort | chikungunya virus infection in cynomolgus macaques following intradermal and aerosol exposure |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520379/ https://www.ncbi.nlm.nih.gov/pubmed/28728590 http://dx.doi.org/10.1186/s12985-017-0804-7 |
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