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10.15252/msb.202110232

http://scihub22266oqcxt.onion/10.15252/msb.202110232
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suck abstract from ncbi


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pmid33904651      Mol+Syst+Biol 2021 ; 17 (4): e10232
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  • Single-cell analyses reveal SARS-CoV-2 interference with intrinsic immune response in the human gut #MMPMID33904651
  • Triana S; Metz-Zumaran C; Ramirez C; Kee C; Doldan P; Shahraz M; Schraivogel D; Gschwind AR; Sharma AK; Steinmetz LM; Herrmann C; Alexandrov T; Boulant S; Stanifer ML
  • Mol Syst Biol 2021[Apr]; 17 (4): e10232 PMID33904651show ga
  • Exacerbated pro-inflammatory immune response contributes to COVID-19 pathology. However, despite the mounting evidence about SARS-CoV-2 infecting the human gut, little is known about the antiviral programs triggered in this organ. To address this gap, we performed single-cell transcriptomics of SARS-CoV-2-infected intestinal organoids. We identified a subpopulation of enterocytes as the prime target of SARS-CoV-2 and, interestingly, found the lack of positive correlation between susceptibility to infection and the expression of ACE2. Infected cells activated strong pro-inflammatory programs and produced interferon, while expression of interferon-stimulated genes was limited to bystander cells due to SARS-CoV-2 suppressing the autocrine action of interferon. These findings reveal that SARS-CoV-2 curtails the immune response and highlights the gut as a pro-inflammatory reservoir that should be considered to fully understand SARS-CoV-2 pathogenesis.
  • |*Single-Cell Analysis[MESH]
  • |COVID-19/virology[MESH]
  • |Gastrointestinal Microbiome[MESH]
  • |Humans[MESH]
  • |In Situ Hybridization, Fluorescence[MESH]
  • |Intestines/*immunology[MESH]
  • |Organoids/metabolism[MESH]
  • |SARS-CoV-2/*physiology[MESH]


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