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Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations

The entry of SARS-CoV-2 into host cells is dependent upon angiotensin-converting enzyme 2 (ACE2), which serves as a functional attachment receptor for the viral spike glycoprotein, and the serine protease TMPRSS2 which allows fusion of the viral and host cell membranes. We devised a quantitative mea...

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Autores principales: Ortiz-Fernández, Lourdes, Sawalha, Amr H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484169/
https://www.ncbi.nlm.nih.gov/pubmed/32759995
http://dx.doi.org/10.1038/s41435-020-0107-7
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author Ortiz-Fernández, Lourdes
Sawalha, Amr H
author_facet Ortiz-Fernández, Lourdes
Sawalha, Amr H
author_sort Ortiz-Fernández, Lourdes
collection PubMed
description The entry of SARS-CoV-2 into host cells is dependent upon angiotensin-converting enzyme 2 (ACE2), which serves as a functional attachment receptor for the viral spike glycoprotein, and the serine protease TMPRSS2 which allows fusion of the viral and host cell membranes. We devised a quantitative measure to estimate genetic determinants of ACE2 and TMPRSS2 expression and applied this measure to >2,500 individuals. Our data show significant variability in genetic determinants of ACE2 and TMPRSS2 expression among individuals and between populations, and indicate a genetic predisposition for lower expression levels of both key viral entry genes in African populations. These data suggest that host genetics related to viral entry mechanisms might influence inter-individual variability in disease susceptibility and severity of COVID-19.
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spelling pubmed-74841692021-02-06 Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations Ortiz-Fernández, Lourdes Sawalha, Amr H Genes Immun Article The entry of SARS-CoV-2 into host cells is dependent upon angiotensin-converting enzyme 2 (ACE2), which serves as a functional attachment receptor for the viral spike glycoprotein, and the serine protease TMPRSS2 which allows fusion of the viral and host cell membranes. We devised a quantitative measure to estimate genetic determinants of ACE2 and TMPRSS2 expression and applied this measure to >2,500 individuals. Our data show significant variability in genetic determinants of ACE2 and TMPRSS2 expression among individuals and between populations, and indicate a genetic predisposition for lower expression levels of both key viral entry genes in African populations. These data suggest that host genetics related to viral entry mechanisms might influence inter-individual variability in disease susceptibility and severity of COVID-19. 2020-08-06 2020-08 /pmc/articles/PMC7484169/ /pubmed/32759995 http://dx.doi.org/10.1038/s41435-020-0107-7 Text en http://creativecommons.org/licenses/by/4.0/ Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ortiz-Fernández, Lourdes
Sawalha, Amr H
Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations
title Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations
title_full Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations
title_fullStr Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations
title_full_unstemmed Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations
title_short Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations
title_sort genetic variability in the expression of the sars-cov-2 host cell entry factors across populations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484169/
https://www.ncbi.nlm.nih.gov/pubmed/32759995
http://dx.doi.org/10.1038/s41435-020-0107-7
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