Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Aug 6;383(6):590-592.
doi: 10.1056/NEJMc2011400. Epub 2020 May 13.

Multiorgan and Renal Tropism of SARS-CoV-2

Affiliations

Multiorgan and Renal Tropism of SARS-CoV-2

Victor G Puelles et al. N Engl J Med. .
No abstract available

PubMed Disclaimer

Figures

Figure 1
Figure 1. Multiorgan SARS-CoV-2 Tropism and Spatially Resolved Affinity for Kidney Cells.
Panel A shows detection of SARS-CoV-2 in the organs in association with the number of coexisting conditions in each patient. The red arrow highlights the viral load in the kidneys (one of the most common targets of SARS-CoV-2). Viremia as such did not correlate with the detected multiorgan tropism. NA denotes not available. Panel B shows the SARS-CoV-2 viral load in key organs, with a broad organotropism of the virus. The red arrow highlights the viral load in the kidneys, and the red rectangles indicate the median values in all organs. Each gray dot represents data from one patient. Panel C shows renal tropism detected with the use of in situ hybridization (spatially resolved viral RNA detection) and indirect immunofluorescence (spatially resolved viral protein detection) with confocal microscopy. In situ hybridization showed SARS-CoV-2 RNA detected in the lung and renal parenchyma (boxed areas show examples in each organ). Immunofluorescence of the lung specimen showed cells with SARS-CoV-2 protein (boxed areas), and immunofluorescence of the kidney specimen showed SARS-CoV-2 protein in areas of the glomerular epithelial (orange arrow), endothelial (white arrows), and tubular (white outline) cells. Scale bars represent 50 μm in the in situ hybridization images and 10 μm in the immunofluorescence images. PCR denotes polymerase chain reaction.

Comment in

  • Uncovering SARS-CoV-2 kidney tropism.
    Musah S. Musah S. Nat Rev Mol Cell Biol. 2021 Aug;22(8):509. doi: 10.1038/s41580-021-00370-w. Epub 2021 Apr 15. Nat Rev Mol Cell Biol. 2021. PMID: 33859371 Free PMC article.

References

    1. Coronavirus disease 2019 (COVID-2019): situation report — 51. Geneva: World Health Organization, 2020. (https://www.who.int/docs/default-source/coronaviruse/situation-reports/2...).
    1. Zou L, Ruan F, Huang M, et al. SARS-CoV-2 viral load in upper respiratory specimens of infected patients. N Engl J Med 2020;382:1177-1179. - PMC - PubMed
    1. Sungnak W, Huang N, Bécavin C, et al. SARS-CoV-2 entry factors are highly expressed in nasal epithelial cells together with innate immune genes. Nat Med 2020. April 23 (Epub ahead of print). - PMC - PubMed
    1. Su H, Yang M, Wan C, et al. Renal histopathological analysis of 26 postmortem findings of patients with COVID-19 in China. Kidney Int 2020. April 9 (Epub ahead of print). - PMC - PubMed
    1. Pei G, Zhang Z, Peng J, et al. Renal involvement and early prognosis in patients with COVID-19 pneumonia. J Am Soc Nephrol 2020. April 28 (Epub ahead of print). - PMC - PubMed

Publication types

MeSH terms