How Do Deer Respiratory Epithelial Cells Weather The Initial Storm of SARS-CoV-2?
Davila, K. M. S.; Nelli, R. K.; Phadke, K. S.; Ruden, R. M.; Sang, Y.; Bellaire, B. H.; Gimenez-Lirola, L. G.; Miller, L. C.
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The potential infectivity of SARS-CoV-2 in animals raises a public health and economic concern, particularly the high susceptibility of white-tailed deer (WTD) to SARS-CoV-2. The disparity in the disease outcome between humans and WTD is very intriguing, as the latter are often asymptomatic, subclinical carriers of SARS-CoV-2. To date, no studies have evaluated the innate immune factors responsible for the contrasting SARS-CoV-2-associated disease outcomes in these mammalian species. A comparative transcriptomic analysis in primary respiratory epithelial cells of human (HRECs) and WTD (Deer-RECs) infected with SARS-CoV-2 was assessed throughout 48 hours post inoculation (hpi). Both HRECs and Deer-RECs were susceptible to SARS-COV-2, with significantly (P < 0.001) lower virus replication in Deer-RECs. The number of differentially expressed genes (DEG) gradually increased in Deer-RECs but decreased in HRECs throughout the infection. The ingenuity pathway analysis of DEGs further identified that genes commonly altered during SARS-CoV-2 infection mainly belong to cytokine and chemokine response pathways mediated via IL-17 and NF-{kappa}B signaling pathways. Inhibition of the NF-{kappa}B signaling in the Deer-RECs pathway was predicted as early as 6 hpi. The findings from this study could explain the lack of clinical signs reported in WTD in response to SARS-CoV-2 infection as opposed to the severe clinical outcomes reported in humans. HIGHLIGHTSO_LIWhite-tailed deer primary respiratory epithelial cells are susceptible to SARS- CoV-2 without causing hyper cytokine gene expression. C_LIO_LIDownregulation of IL-17 and NF-{kappa}B signaling pathways after SARS-CoV-2 infection could be key to the regulated cytokine response in deer cells. C_LIO_LIDeer innate immune system could play a critical role in early antiviral and tissue repair response following SARS-CoV-2 infection. C_LI
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