Does the human placenta express the canonical cell entry mediators for SARS-CoV-2?

Author:

Pique-Regi Roger123ORCID,Romero Roberto12456ORCID,Tarca Adi L137ORCID,Luca Francesca23ORCID,Xu Yi13,Alazizi Adnan2,Leng Yaozhu13,Hsu Chaur-Dong138,Gomez-Lopez Nardhy139ORCID

Affiliation:

1. Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services, Detroit, United States

2. Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, United States

3. Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, United States

4. Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, United States

5. Department of Epidemiology and Biostatistics, Michigan State University, East Lansing, United States

6. Detroit Medical Center, Detroit, United States

7. Department of Computer Science, Wayne State University College of Engineering, Detroit, United States

8. Department of Physiology, Wayne State University School of Medicine, Detroit, United States

9. Department of Biochemistry, Microbiology and Immunology, Wayne State University School of Medicine, Detroit, United States

Abstract

The pandemic of coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has affected more than 10 million people, including pregnant women. To date, no consistent evidence for the vertical transmission of SARS-CoV-2 exists. The novel coronavirus canonically utilizes the angiotensin-converting enzyme 2 (ACE2) receptor and the serine protease TMPRSS2 for cell entry. Herein, building upon our previous single-cell study (Pique-Regi et al., 2019), another study, and new single-cell/nuclei RNA-sequencing data, we investigated the expression of ACE2 and TMPRSS2 throughout pregnancy in the placenta as well as in third-trimester chorioamniotic membranes. We report that co-transcription of ACE2 and TMPRSS2 is negligible in the placenta, thus not a likely path of vertical transmission for SARS-CoV-2. By contrast, receptors for Zika virus and cytomegalovirus, which cause congenital infections, are highly expressed by placental cell types. These data show that the placenta minimally expresses the canonical cell-entry mediators for SARS-CoV-2.

Funder

National Institutes of Health

Wayne State University

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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