Genetic and Functional Characterization of Congenital HCMV Clinical Strains in Ex Vivo First Trimester Placental Model
Deborah Andouard,
Valentin Tilloy,
Elodie Ribot,
Melissa Mayeras,
Daniel Diaz-Gonzalez,
Chahrazed El Hamel,
Fabienne Piras-Douce,
Nathalie Mantel,
Sophie Alain
Affiliations
Deborah Andouard
Bacteriology-Virology-Hygien Department, National Reference Center for Herpesviruses, Centre Hospitalier Universitaire de Limoges, 87000 Limoges, France
Valentin Tilloy
Bacteriology-Virology-Hygien Department, National Reference Center for Herpesviruses, Centre Hospitalier Universitaire de Limoges, 87000 Limoges, France
Elodie Ribot
Bacteriology-Virology-Hygien Department, National Reference Center for Herpesviruses, Centre Hospitalier Universitaire de Limoges, 87000 Limoges, France
Melissa Mayeras
Bacteriology-Virology-Hygien Department, National Reference Center for Herpesviruses, Centre Hospitalier Universitaire de Limoges, 87000 Limoges, France
Daniel Diaz-Gonzalez
RESINFIT—Antimicrobials: Molecular Supports of Resistances and Therapeutic Innovations, UMR Inserm 1092, University of Limoges, 87000 Limoges, France
Chahrazed El Hamel
Pediatric Department, Mother and Child Biobank (CB-HME), Hôpital de la Mère et de l’enfant, CHU Limoges, 87000 Limoges, France
Fabienne Piras-Douce
Sanofi Vaccines R&D, 69280 Marcy-l’étoile, France
Nathalie Mantel
Sanofi Vaccines R&D, 69280 Marcy-l’étoile, France
Sophie Alain
Bacteriology-Virology-Hygien Department, National Reference Center for Herpesviruses, Centre Hospitalier Universitaire de Limoges, 87000 Limoges, France
Human cytomegalovirus (HCMV) is the leading cause of congenital viral infection, leading to a variety of symptoms in the unborn child that range from asymptomatic to death in utero. Our objective was to better understand the mechanisms of placental infection by HCMV clinical strains, particularly during the first trimester of pregnancy. We thus characterized and compared the replication kinetics of various HCMV clinical strains and laboratory strains by measuring viral loads in an ex vivo model of first trimester villi and decidua, and used NGS and PCA analysis to analyze the genes involved in cell tropism and virulence factors. We observed that first trimester villi and decidua are similarly permissive to laboratory and symptomatic strains, and that asymptomatic strains poorly replicate in decidua tissue. PCA analysis allowed us to segregate our clinical strains based on their clinical characteristics, suggesting a link between gene mutations and symptoms. All these results bring forth elements that can help better understand the mechanisms that induce the appearance of symptoms or in the congenitally infected newborn.