<i>Listeria monocytogenes</i> Infection of Bat <i>Pipistrellus nathusii</i> Epithelial cells Depends on the Invasion Factors InlA and InlB
Olga Povolyaeva,
Yaroslava Chalenko,
Egor Kalinin,
Olga Kolbasova,
Elena Pivova,
Denis Kolbasov,
Sergey Yurkov,
Svetlana Ermolaeva
Affiliations
Olga Povolyaeva
Federal Research Center for Virology and Microbiology (FRCVM), 601125 Volginsky, Russia
Yaroslava Chalenko
Federal Research Center for Virology and Microbiology (FRCVM), Nizhny Novgorod Research Veterinary Institute Branch, Laboratory of Molecular Microbiology, 603022 Nizhny Novgorod, Russia
Egor Kalinin
Gamaleya Research Center of Epidemiology and Microbiology, Laboratory of Ecology of Pathogenic Bacteria, 123098 Moscow, Russia
Olga Kolbasova
Federal Research Center for Virology and Microbiology (FRCVM), 601125 Volginsky, Russia
Elena Pivova
Federal Research Center for Virology and Microbiology (FRCVM), 601125 Volginsky, Russia
Denis Kolbasov
Federal Research Center for Virology and Microbiology (FRCVM), 601125 Volginsky, Russia
Sergey Yurkov
Federal Research Center for Virology and Microbiology (FRCVM), 601125 Volginsky, Russia
Svetlana Ermolaeva
Federal Research Center for Virology and Microbiology (FRCVM), Nizhny Novgorod Research Veterinary Institute Branch, Laboratory of Molecular Microbiology, 603022 Nizhny Novgorod, Russia
L. monocytogenes is a widespread facultative intracellular pathogen. The range of natural hosts that supporting L. monocytogenes persistence in the environment has not been fully established yet. In this study, we were interested in the potential of L. monocytogenes to infect cells of bats, which are being increasingly recognized as a reservoir for microorganisms that are pathogenic to humans and domestic animals. A stable epithelial cell line was developed from the kidneys of Pipistrellus nathusii, a small bat widely distributed across Europe. The wild-type L. monocytogenes strain EGDe infected this cell line with an invasion efficiency of 0.0078 ± 0.0009%. Once it entered bat cells, L. monocytogenes doubled within about 70 min. When L. monocytogenes lacked either of the major invasion factors, InlA and InlB, invasion efficiency decreased by a factor of 10 and 25 respectively (p L. monocytogenes infection and that L. monocytogenes invasion of bat cells depends on the major invasion factors InlA and InlB. These results constitute the first report on in vitro studies of L. monocytogenes infection in bats.