Productive Infection of Mouse Mammary Glands and Human Mammary Epithelial Cells by Zika Virus
Mathieu Hubert,
Aurélie Chiche,
Vincent Legros,
Patricia Jeannin,
Thomas Montange,
Antoine Gessain,
Pierre-Emmanuel Ceccaldi,
Aurore Vidy
Affiliations
Mathieu Hubert
Unité Épidémiologie et Physiopathologie des Virus Oncogènes, UMR Centre National de la Recherche Scientifique 3569, Département Virologie, Institut Pasteur, 75015 Paris, France
Aurélie Chiche
Groupe à 5 ans Plasticité cellulaire et Modélisation des Maladies, Département Biologie du Développement et cellules souches, Institut Pasteur, 75015 Paris, France
Vincent Legros
Unité Épidémiologie et Physiopathologie des Virus Oncogènes, UMR Centre National de la Recherche Scientifique 3569, Département Virologie, Institut Pasteur, 75015 Paris, France
Patricia Jeannin
Unité Épidémiologie et Physiopathologie des Virus Oncogènes, UMR Centre National de la Recherche Scientifique 3569, Département Virologie, Institut Pasteur, 75015 Paris, France
Thomas Montange
Unité Épidémiologie et Physiopathologie des Virus Oncogènes, UMR Centre National de la Recherche Scientifique 3569, Département Virologie, Institut Pasteur, 75015 Paris, France
Antoine Gessain
Unité Épidémiologie et Physiopathologie des Virus Oncogènes, UMR Centre National de la Recherche Scientifique 3569, Département Virologie, Institut Pasteur, 75015 Paris, France
Pierre-Emmanuel Ceccaldi
Unité Épidémiologie et Physiopathologie des Virus Oncogènes, UMR Centre National de la Recherche Scientifique 3569, Département Virologie, Institut Pasteur, 75015 Paris, France
Aurore Vidy
Unité Épidémiologie et Physiopathologie des Virus Oncogènes, UMR Centre National de la Recherche Scientifique 3569, Département Virologie, Institut Pasteur, 75015 Paris, France
Zika virus (ZIKV) belongs to the large category of arboviruses. Surprisingly, several human-to-human transmissions of ZIKV have been notified, either following sexual intercourse or from the mother to fetus during pregnancy. Importantly, high viral loads have been detected in the human breast milk of infected mothers, and the existence of breastfeeding as a new mode of mother-to-child transmission of ZIKV was recently hypothesized. However, the maternal origin of infectious particles in breast milk is currently unknown. Here, we show that ZIKV disseminates to the mammary glands of infected mice after both systemic and local exposure with differential kinetics. Ex vivo, we demonstrate that primary human mammary epithelial cells were sensitive and permissive to ZIKV infection in this study. Moreover, by using in vitro models, we prove that mammary luminal- and myoepithelial-phenotype cell lines are both able to produce important virus progeny after ZIKV exposure. Our data suggest that the dissemination of ZIKV to the mammary glands and subsequent infection of the mammary epithelium could be one mechanism of viral excretion in human breast milk.