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TMPRSS2 and TMPRSS4 promote SARS-CoV-2 infection of human small intestinal enterocytes

机译:TMPRSS2和TMPRSS4促进人类小肠肠细胞的SARS-COV-2感染

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Gastrointestinal symptoms and fecal shedding of SARS-CoV-2 RNA are frequently observed in COVID-19. However, it is unclear whether SARS-CoV-2 replicates in the human intestine and contributes to possible fecal-oral transmission. Here, we report productive infection of SARS-CoV-2 in ACE2(+) mature enterocytes in human small intestinal enteroids. Expression of two mucosa-specific serine proteases, TMPRSS2 and TMPRSS4, facilitated SARS-CoV-2 spike fusogenic activity and promoted virus entry into host cells. We also demonstrate that viruses released into the intestinal lumen were inactivated by simulated human colonic fluid, and infectious virus was not recovered from the stool specimens of patients with COVID-19. Our results highlight the intestine as a potential site of SARS-CoV-2 replication, which may contribute to local and systemic illness and overall disease progression.
机译:在Covid-19中经常观察到SARS-COV-2 RNA的胃肠道症状和粪便脱落。 但是,目前尚不清楚SARS-COV-2是否在人类肠中复制并有助于可能的粪便传播。 在这里,我们报告了人类小肠肠toi中ACE2(+)成熟的肠细胞中SARS-COV-2的生产性感染。 TMPRSS2和TMPRSS4的两个粘膜特异性丝氨酸蛋白酶的表达促进了SARS-COV-2尖峰融合活性,并促进了病毒进入宿主细胞。 我们还证明,释放到肠腔中的病毒被模拟的人类结肠液灭活,并且没有从Covid-19患者的粪便标本中回收传染性病毒。 我们的结果突出了肠道作为SARS-COV-2复制的潜在部位,这可能导致局部和系统性疾病以及整体疾病的进展。

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