• Kun Han, Robert V Blair, Naoki Iwanaga, Fengming Liu, Kasi E Russell-Lodrigue, Zhongnan Qin, Cecily C Midkiff, Nadia A Golden, Lara A Doyle-Meyers, Mohammad E Kabir, Kristin E Chandler, Kellie L Cutrera, Mi Ren, Christopher J Monjure, Gabrielle Lehmicke, Tracy Fischer, Brandon Beddingfield, Alanna G Wanek, Angela Birnbaum, Nicholas J Maness, Chad J Roy, Prasun K Datta, Jay Rappaport, Jay K Kolls, and Xuebin Qin.
• Tulane National Primate Research Center, Covington, Louisiana; and.
• Am. J. Respir. Cell Mol. Biol. 2021 Jan 1; 64 (1): 79-88.

AbstractPreclinical mouse models that recapitulate some characteristics of coronavirus disease (COVID-19) will facilitate focused study of pathogenesis and virus-host responses. Human agniotensin-converting enzyme 2 (hACE2) serves as an entry receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to infect people via binding to envelope spike proteins. Herein we report development and characterization of a rapidly deployable COVID-19 mouse model. C57BL/6J (B6) mice expressing hACE2 in the lung were transduced by oropharyngeal delivery of the recombinant human adenovirus type 5 that expresses hACE2 (Ad5-hACE2). Mice were infected with SARS-CoV-2 at Day 4 after transduction and developed interstitial pneumonia associated with perivascular inflammation, accompanied by significantly higher viral load in lungs at Days 3, 6, and 12 after infection compared with Ad5-empty control group. SARS-CoV-2 was detected in pneumocytes in alveolar septa. Transcriptomic analysis of lungs demonstrated that the infected Ad5-hACE mice had a significant increase in IFN-dependent chemokines Cxcl9 and Cxcl10, and genes associated with effector T-cell populations including Cd3 g, Cd8a, and Gzmb. Pathway analysis showed that several Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were enriched in the data set, including cytokine-cytokine receptor interaction, the chemokine signaling pathway, the NOD-like receptor signaling pathway, the measles pathway, and the IL-17 signaling pathway. This response is correlative to clinical response in lungs of patients with COVID-19. These results demonstrate that expression of hACE2 via adenovirus delivery system sensitized the mouse to SARS-CoV-2 infection and resulted in the development of a mild COVID-19 phenotype, highlighting the immune and inflammatory host responses to SARS-CoV-2 infection. This rapidly deployable COVID-19 mouse model is useful for preclinical and pathogenesis studies of COVID-19.

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