Frontiers in Cellular and Infection Microbiology (Jul 2021)

SARS-CoV-2 Infects Endothelial Cells In Vivo and In Vitro

  • Fengming Liu,
  • Fengming Liu,
  • Kun Han,
  • Robert Blair,
  • Kornelia Kenst,
  • Zhongnan Qin,
  • Berin Upcin,
  • Philipp Wörsdörfer,
  • Cecily C. Midkiff,
  • Joseph Mudd,
  • Elizaveta Belyaeva,
  • Nicholas S. Milligan,
  • Tyler D. Rorison,
  • Nicole Wagner,
  • Jochen Bodem,
  • Lars Dölken,
  • Bertal H. Aktas,
  • Richard S. Vander Heide,
  • Xiao-Ming Yin,
  • Jay K. Kolls,
  • Chad J. Roy,
  • Chad J. Roy,
  • Jay Rappaport,
  • Jay Rappaport,
  • Süleyman Ergün,
  • Xuebin Qin,
  • Xuebin Qin

DOI
https://doi.org/10.3389/fcimb.2021.701278
Journal volume & issue
Vol. 11

Abstract

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SARS-CoV-2 infection can cause fatal inflammatory lung pathology, including thrombosis and increased pulmonary vascular permeability leading to edema and hemorrhage. In addition to the lung, cytokine storm-induced inflammatory cascade also affects other organs. SARS-CoV-2 infection-related vascular inflammation is characterized by endotheliopathy in the lung and other organs. Whether SARS-CoV-2 causes endotheliopathy by directly infecting endothelial cells is not known and is the focus of the present study. We observed 1) the co-localization of SARS-CoV-2 with the endothelial cell marker CD31 in the lungs of SARS-CoV-2-infected mice expressing hACE2 in the lung by intranasal delivery of adenovirus 5-hACE2 (Ad5-hACE2 mice) and non-human primates at both the protein and RNA levels, and 2) SARS-CoV-2 proteins in endothelial cells by immunogold labeling and electron microscopic analysis. We also detected the co-localization of SARS-CoV-2 with CD31 in autopsied lung tissue obtained from patients who died from severe COVID-19. Comparative analysis of RNA sequencing data of the lungs of infected Ad5-hACE2 and Ad5-empty (control) mice revealed upregulated KRAS signaling pathway, a well-known pathway for cellular activation and dysfunction. Further, we showed that SARS-CoV-2 directly infects mature mouse aortic endothelial cells (AoECs) that were activated by performing an aortic sprouting assay prior to exposure to SARS-CoV-2. This was demonstrated by co-localization of SARS-CoV-2 and CD34 by immunostaining and detection of viral particles in electron microscopic studies. Moreover, the activated AoECs became positive for ACE-2 but not quiescent AoECs. Together, our results indicate that in addition to pneumocytes, SARS-CoV-2 also directly infects mature vascular endothelial cells in vivo and ex vivo, which may contribute to cardiovascular complications in SARS-CoV-2 infection, including multipleorgan failure.

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