Menachery Vineet D, Gralinski Lisa E, Baric Ralph S, Ferris Martin T
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.
PLoS One. 2015 Jun 26;10(6):e0131451. doi: 10.1371/journal.pone.0131451. eCollection 2015.
Viral pathogenesis studies in mice have relied on markers of severe systemic disease, rather than clinically relevant measures, to evaluate respiratory virus infection; thus confounding connections to human disease. Here, whole-body plethysmography was used to directly measure changes in pulmonary function during two respiratory viral infections. This methodology closely tracked with traditional pathogenesis metrics, distinguished both virus- and dose-specific responses, and identified long-term respiratory changes following both SARS-CoV and Influenza A Virus infection. Together, the work highlights the utility of examining respiratory function following infection in order to fully understand viral pathogenesis.
小鼠的病毒发病机制研究一直依赖于严重全身性疾病的标志物,而非临床相关指标来评估呼吸道病毒感染;因此混淆了与人类疾病的联系。在此,采用全身体积描记法直接测量两种呼吸道病毒感染期间肺功能的变化。该方法与传统发病机制指标密切相关,区分了病毒特异性和剂量特异性反应,并确定了感染严重急性呼吸综合征冠状病毒(SARS-CoV)和甲型流感病毒后长期的呼吸变化。总之,这项研究突出了感染后检查呼吸功能对于全面理解病毒发病机制的作用。