Placental Expression of ACE2 and TMPRSS2 in Maternal Severe Acute Respiratory Syndrome Coronavirus 2 Infection: Are Placental Defenses Mediated by Fetal Sex?

Author:

Shook Lydia L12,Bordt Evan A3,Meinsohn Marie-Charlotte4,Pepin David4,De Guzman Rose M12,Brigida Sara12,Yockey Laura J15,James Kaitlyn E1,Sullivan Mackenzie W1,Bebell Lisa M6,Roberts Drucilla J7,Kaimal Anjali J1,Li Jonathan Z8,Schust Danny9,Gray Kathryn J10,Edlow Andrea G12ORCID

Affiliation:

1. Department of Obstetrics and Gynecology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

2. Vincent Center for Reproductive Biology, Massachusetts General Hospital, Boston, Massachusetts, USA

3. Department of Pediatrics, Lurie Center for Autism, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

4. Pediatric Surgical Research Laboratories, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

5. Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

6. Division of Infectious Diseases, Massachusetts General Hospital, MGH Center for Global Health, and Harvard Medical School, Boston, Massachusetts, USA

7. Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

8. Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts, USA

9. Department of Obstetrics, Gynecology, and Women’s Health, University of Missouri, Columbia, Missouri, USA

10. Department of Obstetrics and Gynecology, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA

Abstract

Abstract Background Expression of angiotensin-converting enzyme 2 (ACE2) and type II transmembrane serine protease (TMPRSS2), host molecules required for viral entry, may underlie sex differences in vulnerability to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. We investigated whether placental ACE2 and TMPRSS2 expression vary by fetal sex in the presence of maternal SARS-CoV-2 infection. Methods Placental ACE2 and TMPRSS2 expression was quantified by quantitative reverse transcription polymerase chain reaction (RT-PCR) and by Western blot in 68 pregnant women (38 SARS-CoV-2 positive, 30 SARS-CoV-2 negative) delivering at Mass General Brigham from April to June 2020. The impact of fetal sex and maternal SARS-CoV-2 exposure on ACE2 and TMPRSS2 was analyzed by 2-way analysis of variance (ANOVA). Results Maternal SARS-CoV-2 infection impacted placental TMPRSS2 expression in a sexually dimorphic fashion (2-way ANOVA interaction, P = .002). We observed no impact of fetal sex or maternal SARS-CoV-2 status on ACE2. TMPRSS2 expression was significantly correlated with ACE2 expression in males (Spearman ρ = 0.54, P = .02) but not females (ρ = 0.23, P = .34) exposed to maternal SARS-CoV-2. Conclusions Sex differences in placental TMPRSS2 but not ACE2 were observed in the setting of maternal SARS-CoV-2 infection, which may have implications for offspring vulnerability to placental infection.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institute on Mental Health

National Heart, Lung, and Blood Institute

Claflin Award from the Massachusetts General Hospital Executive Committee on Research

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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