Placental Infection Associated with SARS-CoV-2 Wildtype Variant and Variants of Concern
Author:
Medel-Martinez Ana12ORCID, Paules Cristina1234ORCID, Peran María125, Calvo Pilar123, Ruiz-Martinez Sara1234, Ormazabal Cundin María6, Cebollada-Solanas Alberto6, Strunk Mark6, Schoorlemmer Jon267, Oros Daniel1234, Fabre Marta1245ORCID
Affiliation:
1. Instituto de Investigación Sanitario de Aragón (IIS Aragon), 50009 Zaragoza, Spain 2. Placental Pathophysiology & Fetal Programming Research Group, B46_20R & GIIS-028 del IISA, 50009 Zaragoza, Spain 3. Obstetrics Department, Hospital Clínico Universitario Lozano Blesa, 50009 Zaragoza, Spain 4. Red RICORS “Primary Care Interventions to Prevent Maternal and Child Chronic Diseases of Perinatal and Developmental Origin”, RD21/0012/0001, Instituto de Salud Carlos III, 28029 Madrid, Spain 5. Biochemistry Department, Hospital Clínico Universitario Lozano Blesa, 50009 Zaragoza, Spain 6. Instituto Aragonés de Ciencias de la Salud (IACS), Centro de Investigación Biomédica de Aragón (CIBA), 50009 Zaragoza, Spain 7. ARAID Foundation, 50009 Zaragoza, Spain
Abstract
The original SARS-CoV-2 lineages have been replaced by successive variants of concern (VOCs) over time. The aim of this study was to perform an assessment of the placental infection by SARS-CoV-2 according to the predominant variant at the moment of COVID-19 diagnosis. This was a prospective study of SARS-CoV-2-positive pregnant women between March 2020 and March 2022. The population was divided into pregnancies affected by COVID-19 disease during 2020 (Pre-VOC group) and pregnancies affected after December 2020 by SARS-CoV-2 variants of concern (VOC group). The presence of virus was assessed by RT-PCR, and the viral variant was determined by whole genome sequencing. A total of 104 placentas were examined, among which 54 cases belonged to the Pre-VOC group and 50 cases belonged to the VOC group. Sixteen positive placental RT-PCR tests for SARS-CoV-2 were reported. The NGS analysis confirmed the SARS-CoV-2 lineage in placenta tissue. All samples corresponded to the Pre-VOC group, whereas no placental presence of SARS-CoV-2 was detected in the VOC group (16, 29.6% vs. 0, 0.0% p = 0.000). Preterm birth (9, 16.7% vs. 2, 4%; p = 0.036) and hypertensive disorders of pregnancy (14, 25.9% vs. 3, 6%; p = 0.003) were more frequent in the Pre-VOC group than in the VOC group. Finally, the VOC group was composed of 23 unvaccinated and 27 vaccinated pregnant women; no differences were observed in the sub-analysis focused on vaccination status. In summary, SARS-CoV-2-positive placentas were observed only in pregnancies infected by SARS-CoV-2 wildtype. Thus, placental SARS-CoV-2 presence could be influenced by SARS-CoV-2 variants, infection timing, or vaccination status. According to our data, the current risk of SARS-CoV-2 placental infection after maternal COVID disease during pregnancy should be updated.
Funder
Government of Aragon FEDER Instituto de Salud Carlos III
Subject
Virology,Infectious Diseases
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