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Exposure of rhesus monkeys to cowpox virus Brighton Red by large-particle aerosol droplets results in an upper respiratory tract disease.


ABSTRACT: We previously demonstrated that small-particle (0.5-3.0?µm) aerosol infection of rhesus monkeys (Macaca mulatta) with cowpox virus (CPXV)-Brighton Red (BR) results in fulminant respiratory tract disease characterized by severe lung parenchymal pathology but only limited systemic virus dissemination and limited classic epidermal pox-like lesion development (Johnson et al., 2015). Based on these results, and to further develop CPXV as an improved model of human smallpox, we evaluated a novel large-particle aerosol (7.0-9.0?µm) exposure of rhesus monkeys to CPXV-BR and monitored for respiratory tract disease by serial computed tomography (CT). As expected, the upper respiratory tract and large airways were the major sites of virus-induced pathology following large-particle aerosol exposure. Large-particle aerosol CPXV exposure of rhesus macaques resulted in severe upper airway and large airway pathology with limited systemic dissemination.

SUBMITTER: Johnson RF 

PROVIDER: S-EPMC5764124 | biostudies-literature | 2016 Aug

REPOSITORIES: biostudies-literature

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Exposure of rhesus monkeys to cowpox virus Brighton Red by large-particle aerosol droplets results in an upper respiratory tract disease.

Johnson Reed F RF   Hammoud Dima A DA   Perry Donna L DL   Solomon Jeffrey J   Moore Ian N IN   Lackemeyer Matthew G MG   Bohannon Jordan K JK   Sayre Philip J PJ   Minai Mahnaz M   Papaneri Amy B AB   Hagen Katie R KR   Janosko Krisztina B KB   Jett Catherine C   Cooper Kurt K   Blaney Joseph E JE   Jahrling Peter B PB  

The Journal of general virology 20160509 8


We previously demonstrated that small-particle (0.5-3.0 µm) aerosol infection of rhesus monkeys (Macaca mulatta) with cowpox virus (CPXV)-Brighton Red (BR) results in fulminant respiratory tract disease characterized by severe lung parenchymal pathology but only limited systemic virus dissemination and limited classic epidermal pox-like lesion development (Johnson et al., 2015). Based on these results, and to further develop CPXV as an improved model of human smallpox, we evaluated a novel large  ...[more]

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