| Literature DB >> 27166137 |
Reed F Johnson1, Dima A Hammoud2, Donna L Perry3, Jeffrey Solomon4, Ian N Moore5, Matthew G Lackemeyer3, Jordan K Bohannon3, Philip J Sayre3, Mahnaz Minai5, Amy B Papaneri1, Katie R Hagen3, Krisztina B Janosko3, Catherine Jett3, Kurt Cooper3, Joseph E Blaney6, Peter B Jahrling1,3.
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.Entities:
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Year: 2016 PMID: 27166137 PMCID: PMC5764124 DOI: 10.1099/jgv.0.000501
Source DB: PubMed Journal: J Gen Virol ISSN: 0022-1317 Impact factor: 3.891