Ueki Hiroshi, Kiso Maki, Furusawa Yuri, Iida Shun, Yamayoshi Seiya, Nakajima Noriko, Imai Masaki, Suzuki Tadaki, Kawaoka Yoshihiro
Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan.
Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo 162-8655, Japan.
Viruses. 2024 Mar 29;16(4):537. doi: 10.3390/v16040537.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) often causes severe viral pneumonia. Although many studies using mouse models have examined the pathogenicity of SARS-CoV-2, COVID-19 pathogenesis remains poorly understood. In vivo imaging analysis using two-photon excitation microscopy (TPEM) is useful for elucidating the pathology of COVID-19, providing pathological insights that are not available from conventional histological analysis. However, there is no reporter SARS-CoV-2 that demonstrates pathogenicity in C57BL/6 mice and emits sufficient light intensity for two-photon in vivo imaging. Here, we generated a mouse-adapted strain of SARS-CoV-2 (named MASCV2-p25) and demonstrated its efficient replication in the lungs of C57BL/6 mice, causing fatal pneumonia. Histopathologic analysis revealed the severe inflammation and infiltration of immune cells in the lungs of MASCV2-p25-infected C57BL/6 mice, not unlike that observed in COVID-19 patients with severe pneumonia. Subsequently, we generated a mouse-adapted reporter SARS-CoV-2 (named MASCV-Venus-p9) by inserting the fluorescent protein-encoding gene Venus into MASCV2-p25 and sequential lung-to-lung passages in C57BL/6 mice. C57BL/6 mice infected with MASCV2-Venus-p9 exhibited severe pneumonia. In addition, the TPEM of the lungs of the infected C57BL/6J mice showed that the infected cells emitted sufficient levels of fluorescence for easy observation. These findings suggest that MASCV2-Venus-p9 will be useful for two-photon in vivo imaging studies of the pathogenesis of severe COVID-19 pneumonia.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)常引发严重病毒性肺炎。尽管许多使用小鼠模型的研究已检测了SARS-CoV-2的致病性,但新冠病毒疾病(COVID-19)的发病机制仍知之甚少。利用双光子激发显微镜(TPEM)进行的体内成像分析有助于阐明COVID-19的病理情况,提供传统组织学分析无法获得的病理见解。然而,尚无在C57BL/6小鼠中表现出致病性且能发出足够光强度用于双光子体内成像的报告基因SARS-CoV-2。在此,我们构建了一种适应小鼠的SARS-CoV-2毒株(命名为MASCV2-p25),并证明其能在C57BL/6小鼠的肺部高效复制,引发致命性肺炎。组织病理学分析显示,感染MASCV2-p25的C57BL/6小鼠肺部有严重炎症和免疫细胞浸润,这与重症COVID-19患者中观察到的情况并无不同。随后,我们通过将编码荧光蛋白的基因Venus插入MASCV2-p25并在C57BL/6小鼠中进行肺对肺连续传代,构建了一种适应小鼠的报告基因SARS-CoV-2(命名为MASCV-Venus-p9)。感染MASCV2-Venus-p9的C57BL/6小鼠表现出严重肺炎。此外,对感染的C57BL/6J小鼠肺部进行的TPEM显示,被感染细胞发出的荧光水平足以便于观察。这些发现表明,MASCV2-Venus-p9将有助于对重症COVID-19肺炎发病机制进行双光子体内成像研究。