Oropouche virus infects human trophoblasts and placenta explants

Christina J. Megli (), Rebecca K. Zack, Jackson J. McGaughey, Ryan M. Hoehl, Taylor Snisky, Amy L. Hartman and Cynthia M. McMillen ()
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Christina J. Megli: Gynecology and Reproductive Sciences
Rebecca K. Zack: Gynecology and Reproductive Sciences
Jackson J. McGaughey: Center for Vaccine Research
Ryan M. Hoehl: Center for Vaccine Research
Taylor Snisky: Magee-Womens Research Institute
Amy L. Hartman: Center for Vaccine Research
Cynthia M. McMillen: Center for Vaccine Research

Nature Communications, 2025, vol. 16, issue 1, 1-10

Abstract: Abstract Clinical and epidemiologic evidence from the 2023–24 outbreak of Oropouche virus (OROV) has demonstrated increased severity in clinical disease and adverse pregnancy outcomes including miscarriage, stillbirth, and neonatal demise. Serological evidence suggests vertical transmission of OROV may be responsible. OROV has not been studied in the context of pregnancy and has an unknown ability to infect the relevant tissues of the maternal-fetal interface; therefore, the mechanisms of vertical transmission are unknown. We use human cytotrophoblast and syncytiotrophoblast stem cell cultures, polarized trophoblast stem cell organoids, and placenta explants to demonstrate that OROV (BeAn19991) infects and replicates in human tissues of the maternal-fetal interface including cytotrophoblasts and the microbial-resistant cell, syncytiotrophoblast. Viral replication is robust within the first 24 hour post infection and infection may be dependent on gestational age. These data indicate tissues at the maternal-fetal interface are susceptible to OROV infection and may facilitate vertical transmission, leading to adverse pregnancy outcomes.

Date: 2025
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DOI: 10.1038/s41467-025-61138-w

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