Applied Research Associates, Inc, Panama City, FL, USA.
J Appl Microbiol. 2012 Oct;113(4):767-78. doi: 10.1111/j.1365-2672.2012.05402.x. Epub 2012 Aug 21.
The aim of this study was to demonstrate a prototype tool for measuring infectivity of an aerosolized human pathogen - influenza A/PR/8/34 (H1N1) virus - using a small-animal model in the Controlled Aerosol Test System (CATS).
Intranasal inoculation of nonadapted H1N1 virus into C57BL, BALB/c and CD-1 mice caused infection in all three species. Respiratory exposure of CD-1 mice to the aerosolized virus at graduated doses was accomplished in a modified rodent exposure apparatus. Weight change was recorded for 7 days postexposure, and viral populations in lung tissue homogenates were measured post mortem by DNA amplification (qRT-PCR), direct fluorescence and microscopic evaluation of cytopathic effect. Plots of weight change and of PCR cycle threshold vs delivered dose were linear to threshold doses of ~40 TCID(50) and ~12 TCID(50) , respectively.
MID(50) for inspired H1N1 aerosols in CD-1 mice is between 12 and 40 TCID(50) ; proportionality to dose of weight loss and viral populations makes the CD-1 mouse a useful model for measuring infectivity by inhalation.
In the CATS, this mouse-virus model provides the first quantitative method to evaluate the ability of respiratory protective technologies to attenuate the infectivity of an inspired pathogenic aerosol.
本研究旨在使用小动物模型(受控气溶胶测试系统(CATS))证明一种用于测量雾化人类病原体——甲型流感病毒/PR/8/34(H1N1)病毒——感染力的原型工具。
非适应 H1N1 病毒的鼻腔接种导致所有三种物种的感染。在改良的啮齿动物暴露装置中,以递增剂量对 CD-1 小鼠进行雾化病毒的呼吸道暴露。暴露后 7 天记录体重变化,并用 DNA 扩增(qRT-PCR)、直接荧光和细胞病变效应的显微镜评估来测量肺组织匀浆中的病毒群。体重变化和 PCR 循环阈值与递送剂量的关系图呈线性关系,到阈值剂量分别为40TCID(50)和12TCID(50)。
CD-1 小鼠吸入 H1N1 气溶胶的 MID(50)值在 12 和 40TCID(50)之间;体重减轻和病毒数量与剂量成正比,使 CD-1 小鼠成为测量吸入感染性的有用模型。
在 CATS 中,这种小鼠-病毒模型提供了第一个定量方法来评估呼吸保护技术减弱吸入致病性气溶胶感染性的能力。