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  • COVID-19 and vertical transmission: assessing the expression of ACE2 / TMPRSS2 in the human fetus and placenta to assess the risk of SARS-CoV-2 infection

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    Jones522239_Accepted.pdf (487.8Kb)
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    Version of Record (VoR)
    Author(s)
    Beesley, Max A
    Davidson, Joseph R
    Panariello, Francesco
    Shibuya, Soichi
    Scaglioni, Dominic
    Jones, Brendan C
    Maksym, Katarzyna
    Ogunbiyi, Olumide
    Sebire, Neil J
    Cacchiarelli, Davide
    David, Anna L
    De Coppi, Paolo
    Gerli, Mattia FM
    Griffith University Author(s)
    Jones, Blake
    Year published
    2021
    Metadata
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    Abstract
    BACKGROUND: While pregnant women have been identified as a potentially at-risk group concerning COVID-19 infection, little is known regarding the susceptibility of the fetus to infection. Co-expression of ACE2 and TMPRSS2 has been identified as a pre-requisite for infection, and expression across different tissues is known to vary between children and adults. However, the expression of these proteins in the fetus is unknown. METHODS: We performed a retrospective analysis of a single cell data repository. The data were then validated at both gene and protein level by performing RT-qPCR and two-colour immunohistochemistry on ...
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    BACKGROUND: While pregnant women have been identified as a potentially at-risk group concerning COVID-19 infection, little is known regarding the susceptibility of the fetus to infection. Co-expression of ACE2 and TMPRSS2 has been identified as a pre-requisite for infection, and expression across different tissues is known to vary between children and adults. However, the expression of these proteins in the fetus is unknown. METHODS: We performed a retrospective analysis of a single cell data repository. The data were then validated at both gene and protein level by performing RT-qPCR and two-colour immunohistochemistry on a library of second-trimester human fetal tissues. FINDINGS: TMPRSS2 is present at both gene and protein level in the predominantly epithelial fetal tissues analysed. ACE2 is present at significant levels, only in the fetal intestine and kidney and is not expressed in the fetal lung. The placenta also does not co-express the two proteins across the second trimester or at term. INTERPRETATION: This dataset indicates that the lungs are unlikely to be a viable route of SARS-CoV2 fetal infection. The fetal kidney, despite presenting both the proteins required for the infection, is anatomically protected from the exposure to the virus. However, the GI tract is likely to be susceptible to infection due to its high co-expression of both proteins, as well as its exposure to potentially infected amniotic fluid.
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    Journal Title
    BJOG: An International Journal of Obstetrics & Gynaecology
    DOI
    https://doi.org/10.1111/1471-0528.16974
    Copyright Statement
    © 2021 by the authors.BJOG: An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd.This is an open access article under the terms of the Creative Commons Attribution License, which permits use,distribution and reproduction in any medium, provided the original work is properly cited.
    Subject
    Clinical sciences
    Paediatrics
    ACE2
    COVID-19
    Fetal Infection
    SARS-CoV2
    TMPRSS2
    vertical transmission
    Publication URI
    http://hdl.handle.net/10072/410296
    Collection
    • Journal articles

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