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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2017
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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. |
format | Online Article Text |
id | pubmed-5302833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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