Johnson Reed F, Hammoud Dima A, Perry Donna L, Solomon Jeffrey, Moore Ian N, Lackemeyer Matthew G, Bohannon Jordan K, Sayre Philip J, Minai Mahnaz, Papaneri Amy B, Hagen Katie R, Janosko Krisztina B, Jett Catherine, Cooper Kurt, Blaney Joseph E, Jahrling Peter B
Emerging Viral Pathogens Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD 21702, USA.
Center for Infectious Disease Imaging, Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA.
J Gen Virol. 2016 Aug;97(8):1942-1954. doi: 10.1099/jgv.0.000501. Epub 2016 May 9.
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.
我们之前证明,用牛痘病毒(CPXV)-布莱顿红(BR)对恒河猴(猕猴)进行小颗粒(0.5 - 3.0微米)气溶胶感染会导致暴发性呼吸道疾病,其特征为严重的肺实质病变,但只有有限的全身病毒传播以及有限的典型表皮痘样病变发展(约翰逊等人,2015年)。基于这些结果,并为了进一步将CPXV开发成改良的人类天花模型,我们评估了用CPXV - BR对恒河猴进行新型大颗粒气溶胶(7.0 - 9.0微米)暴露,并通过连续计算机断层扫描(CT)监测呼吸道疾病。正如预期的那样,大颗粒气溶胶暴露后,上呼吸道和大气道是病毒诱导病变的主要部位。恒河猴经大颗粒气溶胶CPXV暴露后出现严重的上呼吸道和大气道病变,全身传播有限。