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Characterization of a murine model of non-lethal, symptomatic dengue virus infection

The mosquito-borne disease dengue is caused by four serologically- and genetically-related viruses, termed DENV-1 to DENV-4. Historical setbacks due to lack of human-like mouse models of dengue were partially remedied with characterization of lethal DENV-2 infection in immunocompromised AG129 mice (...

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Autores principales: Sarathy, Vanessa V., White, Mellodee, Li, Li, Kaiser, Jaclyn A., Campbell, Gerald A., Milligan, Gregg N., Bourne, Nigel, Barrett, Alan D. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861036/
https://www.ncbi.nlm.nih.gov/pubmed/29559699
http://dx.doi.org/10.1038/s41598-018-22618-w
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author Sarathy, Vanessa V.
White, Mellodee
Li, Li
Kaiser, Jaclyn A.
Campbell, Gerald A.
Milligan, Gregg N.
Bourne, Nigel
Barrett, Alan D. T.
author_facet Sarathy, Vanessa V.
White, Mellodee
Li, Li
Kaiser, Jaclyn A.
Campbell, Gerald A.
Milligan, Gregg N.
Bourne, Nigel
Barrett, Alan D. T.
author_sort Sarathy, Vanessa V.
collection PubMed
description The mosquito-borne disease dengue is caused by four serologically- and genetically-related viruses, termed DENV-1 to DENV-4. Historical setbacks due to lack of human-like mouse models of dengue were partially remedied with characterization of lethal DENV-2 infection in immunocompromised AG129 mice (deficient in IFN-α/β/γ receptors). Recently, our group established lethal AG129 mouse infection models of DENV-1, DENV-3, and DENV-4 using human isolates. Here we compare a non-lethal, disseminated model of DENV-3 infection using strain D83-144 to that of the lethal outcome following infection by strain C0360/94. Both strains belong to DENV-3 genotype II and differ by only 13 amino acids. Intraperitoneal inoculation of AG129 mice with strain D83-144 led to clinical signs of dengue infection, such as cytokine induction, thrombocytopenia, and systemic infection. However, C0360/94 infection led to features of severe human dengue, including coagulopathy and lethal outcome, whereas D83-144 infection does not. This study is the first to investigate a low passage, non-mouse lethal strain in AG129 mice and demonstrates that D83-144 infection induces milder features of human dengue than those induced by lethal C0360/94 infection. The results suggest that the AG129 mouse model has applications to investigate factors associated with mild or severe disease.
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spelling pubmed-58610362018-03-26 Characterization of a murine model of non-lethal, symptomatic dengue virus infection Sarathy, Vanessa V. White, Mellodee Li, Li Kaiser, Jaclyn A. Campbell, Gerald A. Milligan, Gregg N. Bourne, Nigel Barrett, Alan D. T. Sci Rep Article The mosquito-borne disease dengue is caused by four serologically- and genetically-related viruses, termed DENV-1 to DENV-4. Historical setbacks due to lack of human-like mouse models of dengue were partially remedied with characterization of lethal DENV-2 infection in immunocompromised AG129 mice (deficient in IFN-α/β/γ receptors). Recently, our group established lethal AG129 mouse infection models of DENV-1, DENV-3, and DENV-4 using human isolates. Here we compare a non-lethal, disseminated model of DENV-3 infection using strain D83-144 to that of the lethal outcome following infection by strain C0360/94. Both strains belong to DENV-3 genotype II and differ by only 13 amino acids. Intraperitoneal inoculation of AG129 mice with strain D83-144 led to clinical signs of dengue infection, such as cytokine induction, thrombocytopenia, and systemic infection. However, C0360/94 infection led to features of severe human dengue, including coagulopathy and lethal outcome, whereas D83-144 infection does not. This study is the first to investigate a low passage, non-mouse lethal strain in AG129 mice and demonstrates that D83-144 infection induces milder features of human dengue than those induced by lethal C0360/94 infection. The results suggest that the AG129 mouse model has applications to investigate factors associated with mild or severe disease. Nature Publishing Group UK 2018-03-20 /pmc/articles/PMC5861036/ /pubmed/29559699 http://dx.doi.org/10.1038/s41598-018-22618-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visithttp://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sarathy, Vanessa V.
White, Mellodee
Li, Li
Kaiser, Jaclyn A.
Campbell, Gerald A.
Milligan, Gregg N.
Bourne, Nigel
Barrett, Alan D. T.
Characterization of a murine model of non-lethal, symptomatic dengue virus infection
title Characterization of a murine model of non-lethal, symptomatic dengue virus infection
title_full Characterization of a murine model of non-lethal, symptomatic dengue virus infection
title_fullStr Characterization of a murine model of non-lethal, symptomatic dengue virus infection
title_full_unstemmed Characterization of a murine model of non-lethal, symptomatic dengue virus infection
title_short Characterization of a murine model of non-lethal, symptomatic dengue virus infection
title_sort characterization of a murine model of non-lethal, symptomatic dengue virus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861036/
https://www.ncbi.nlm.nih.gov/pubmed/29559699
http://dx.doi.org/10.1038/s41598-018-22618-w
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