Kinetics of immune responses in deer mice experimentally infected with sin nombre virus
Author
dc.contributor.author
Schountz, Tony
Author
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Acuña Retamar, Mariana
Author
dc.contributor.author
Feinstein, Shira
Author
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Prescott, Joseph
Author
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Torres Pérez, Fernando
Author
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Podell, Brendan
Author
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Peters, Staci
Author
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Ye, Chunyan
Author
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Black, William C.
Author
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Hjelle, Brian
Admission date
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2019-03-11T13:19:40Z
Available date
dc.date.available
2019-03-11T13:19:40Z
Publication date
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2012
Cita de ítem
dc.identifier.citation
Journal of Virology, Volumen 86, Issue 18, 2018, Pages 10015-10027
Identifier
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0022538X
Identifier
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10985514
Identifier
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10.1128/JVI.06875-11
Identifier
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https://repositorio.uchile.cl/handle/2250/165701
Abstract
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Deer mice are the principal reservoir hosts of Sin Nombre virus, the etiologic agent of most hantavirus cardiopulmonary syndrome cases in North America. Infection of deer mice results in persistence without conspicuous pathology, and most, if not all, infected mice remain infected for life, with periods of viral shedding. The kinetics of viral load, histopathology, virus distribution, and immune gene expression in deer mice were examined. Viral antigen was detected as early as 5 days postinfection and peaked on day 15 in the lungs, hearts, kidneys, and livers. Viral RNA levels varied substantially but peaked on day 15 in the lungs and heart, and antinucleocapsid IgG antibodies appeared in some animals on day 10, but a strong neutralizing antibody response failed to develop during the 20-day experiment. No clinical signs of disease were observed in any of the infected deer mice. Most genes were repressed on day 2, suggesting a typical early downregulation of gene expression often observ