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Modeling Powassan virus infection in Peromyscus leucopus, a natural host

The tick-borne flavivirus, Powassan virus (POWV) causes life-threatening encephalitis in humans in North America and Europe. POWV is transmitted by ixodid tick vectors that feed on small to medium-sized mammals, such as Peromyscus leucopus mice, which may serve as either reservoir, bridge or amplifi...

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Autores principales: Mlera, Luwanika, Meade-White, Kimberly, Saturday, Greg, Scott, Dana, Bloom, Marshall E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302833/
https://www.ncbi.nlm.nih.gov/pubmed/28141800
http://dx.doi.org/10.1371/journal.pntd.0005346
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author Mlera, Luwanika
Meade-White, Kimberly
Saturday, Greg
Scott, Dana
Bloom, Marshall E.
author_facet Mlera, Luwanika
Meade-White, Kimberly
Saturday, Greg
Scott, Dana
Bloom, Marshall E.
author_sort Mlera, Luwanika
collection PubMed
description The tick-borne flavivirus, Powassan virus (POWV) causes life-threatening encephalitis in humans in North America and Europe. POWV is transmitted by ixodid tick vectors that feed on small to medium-sized mammals, such as Peromyscus leucopus mice, which may serve as either reservoir, bridge or amplification hosts. Intraperitoneal and intracranial inoculation of 4-week old Peromyscus leucopus mice with 10(3) PFU of POWV did not result in overt clinical signs of disease. However, following intracranial inoculation, infected mice seroconverted to POWV and histopathological examinations revealed that the mice uniformly developed mild lymphocytic perivascular cuffing and microgliosis in the brain and spinal cord from 5 to 15 days post infection (dpi), suggesting an early inflammatory response. In contrast, intracranial inoculation of 4-week old C57BL/6 and BALB/c mice was lethal by 5 dpi. Intraperitoneal inoculation was lethal in BALB/c mice, but 40% (2/5) of C57BL/6 mice survived. We concluded that Peromyscus leucopus mice infected i.c. with a lethal dose of POWV support a limited infection, restricted to the central nervous system and mount an antibody response to the virus. However, they fail to develop clinical signs of disease and are able to control the infection. These results suggest the involvement of restriction factors, and the mechanism by which Peromyscus leucopus mice restrict POWV infection remains under study.
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spelling pubmed-53028332017-03-03 Modeling Powassan virus infection in Peromyscus leucopus, a natural host Mlera, Luwanika Meade-White, Kimberly Saturday, Greg Scott, Dana Bloom, Marshall E. PLoS Negl Trop Dis Research Article The tick-borne flavivirus, Powassan virus (POWV) causes life-threatening encephalitis in humans in North America and Europe. POWV is transmitted by ixodid tick vectors that feed on small to medium-sized mammals, such as Peromyscus leucopus mice, which may serve as either reservoir, bridge or amplification hosts. Intraperitoneal and intracranial inoculation of 4-week old Peromyscus leucopus mice with 10(3) PFU of POWV did not result in overt clinical signs of disease. However, following intracranial inoculation, infected mice seroconverted to POWV and histopathological examinations revealed that the mice uniformly developed mild lymphocytic perivascular cuffing and microgliosis in the brain and spinal cord from 5 to 15 days post infection (dpi), suggesting an early inflammatory response. In contrast, intracranial inoculation of 4-week old C57BL/6 and BALB/c mice was lethal by 5 dpi. Intraperitoneal inoculation was lethal in BALB/c mice, but 40% (2/5) of C57BL/6 mice survived. We concluded that Peromyscus leucopus mice infected i.c. with a lethal dose of POWV support a limited infection, restricted to the central nervous system and mount an antibody response to the virus. However, they fail to develop clinical signs of disease and are able to control the infection. These results suggest the involvement of restriction factors, and the mechanism by which Peromyscus leucopus mice restrict POWV infection remains under study. Public Library of Science 2017-01-31 /pmc/articles/PMC5302833/ /pubmed/28141800 http://dx.doi.org/10.1371/journal.pntd.0005346 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Mlera, Luwanika
Meade-White, Kimberly
Saturday, Greg
Scott, Dana
Bloom, Marshall E.
Modeling Powassan virus infection in Peromyscus leucopus, a natural host
title Modeling Powassan virus infection in Peromyscus leucopus, a natural host
title_full Modeling Powassan virus infection in Peromyscus leucopus, a natural host
title_fullStr Modeling Powassan virus infection in Peromyscus leucopus, a natural host
title_full_unstemmed Modeling Powassan virus infection in Peromyscus leucopus, a natural host
title_short Modeling Powassan virus infection in Peromyscus leucopus, a natural host
title_sort modeling powassan virus infection in peromyscus leucopus, a natural host
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302833/
https://www.ncbi.nlm.nih.gov/pubmed/28141800
http://dx.doi.org/10.1371/journal.pntd.0005346
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