期刊
ZOOLOGICAL RESEARCH
卷 43, 期 6, 页码 1041-1062出版社
SCIENCE PRESS
DOI: 10.24272/j.issn.2095-8137.2022.443
关键词
SARS-CoV-2; Rhesus macaque; Animal model; Single-nucleus RNA sequencing; Antiviral immune defects; Multiple organs
类别
资金
- National Basic Research Program of China [2020YFA0804000, 2020YFC0842000, 2020YFA0112200, 2021YFC2301703]
- Strategic Priority Research Program of the Chinese Academy of Sciences [XDB32010100]
- Special Associate Research Program of the Chinese Academy of Sciences [E1290601]
- National Natural Science Foundation of China [32122037, 81891001, 32192411, 32100512, U1902215]
- Collaborative Research Fund of the Chinese Institute for Brain Research, Beijing [2020-NKX-PT-03]
- CAS Project for Young Scientists in Basic Research [YSBR-013]
- China Association for Science and Technology [2020QNRC001]
- National Resource Center for NonHuman Primates
This study analyzed single-nucleus transcriptomes from multiple organs of SARS-CoV-2-infected rhesus macaques, revealing that the liver had the most significant global transcriptional alterations. Lung epithelial cells, especially AT2 and ciliated cells, showed significant impairment, while fibroblasts exhibited signs of fibrosis. The kidney dataset indicated a tropism of tubule cells to SARS-CoV-2 infection, leading to membranous nephropathy. Pathological changes were also observed in astrocytes and oligodendrocytes in the cerebral cortex. Overall, this study broadened our understanding of disease features and immune defects caused by SARS-CoV-2 infection.
Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes diverse clinical manifestations and tissue injuries in multiple organs. However, cellular and molecular understanding of SARS-CoV-2 infection-associated pathology and immune defense features in different organs remains incomplete. Here, we profiled approximately 77 000 single-nucleus transcriptomes of the lung, liver, kidney, and cerebral cortex in rhesus macaques (Macaca mulatta) infected with SARS-CoV-2 and healthy controls. Integrated analysis of the multi-organ dataset suggested that the liver harbored the strongest global transcriptional alterations. We observed prominent impairment in lung epithelial cells, especially in AT2 and ciliated cells, and evident signs of fibrosis in fibroblasts. These lung injury characteristics are similar to those reported in patients with coronavirus disease 2019 (COVID-19). Furthermore, we found suppressed MHC class I/II molecular activity in the lung, inflammatory response in the liver, and activation of the kynurenine pathway, which induced the development of an immunosuppressive microenvironment. Analysis of the kidney dataset highlighted tropism of tubule cells to SARS-CoV-2, and we found membranous nephropathy (an autoimmune disease) caused by podocyte dysregulation. In addition, we identified the pathological states of astrocytes and oligodendrocytes in the cerebral cortex, providing molecular insights into COVID-19-related neurological implications. Overall, our multi-organ single-nucleus transcriptomic survey of SARS-CoV-2-infected rhesus macaques broadens our understanding of disease features and antiviral immune defects caused by SARS-CoV-2 infection, which may facilitate the development of therapeutic interventions for COVID-19.
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