| Literature DB >> 32405028 |
Jie Zhou1,2, Cun Li3, Xiaojuan Liu3, Man Chun Chiu3, Xiaoyu Zhao3, Dong Wang3, Yuxuan Wei3, Andrew Lee3, Anna Jinxia Zhang4,3, Hin Chu4,3, Jian-Piao Cai3, Cyril Chik-Yan Yip3, Ivy Hau-Yee Chan5, Kenneth Kak-Yuen Wong5, Owen Tak-Yin Tsang6, Kwok-Hung Chan3, Jasper Fuk-Woo Chan4,3,7, Kelvin Kai-Wang To4,3,7, Honglin Chen4,3, Kwok Yung Yuen8,9,10.
Abstract
A novel coronavirus-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-emerged in humans in Wuhan, China, in December 2019 and has since disseminated globally1,2. As of April 16, 2020, the confirmed case count of coronavirus disease 2019 (COVID-19) had surpassed 2 million. Based on full-genome sequence analysis, SARS-CoV-2 shows high homology to SARS-related coronaviruses identified in horseshoe bats1,2. Here we show the establishment and characterization of expandable intestinal organoids derived from horseshoe bats of the Rhinolophus sinicus species that can recapitulate bat intestinal epithelium. These bat enteroids are fully susceptible to SARS-CoV-2 infection and sustain robust viral replication. Development of gastrointestinal symptoms in some patients with COVID-19 and detection of viral RNA in fecal specimens suggest that SARS-CoV-2 might cause enteric, in addition to respiratory, infection3,4. Here we demonstrate active replication of SARS-CoV-2 in human intestinal organoids and isolation of infectious virus from the stool specimen of a patient with diarrheal COVID-19. Collectively, we established the first expandable organoid culture system of bat intestinal epithelium and present evidence that SARS-CoV-2 can infect bat intestinal cells. The robust SARS-CoV-2 replication in human intestinal organoids suggests that the human intestinal tract might be a transmission route of SARS-CoV-2.Entities:
Mesh:
Year: 2020 PMID: 32405028 DOI: 10.1038/s41591-020-0912-6
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440