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Immunological findings of West Caucasian bat virus in an accidental host - ASM

Mary Wilson

Well-known member
23 January 2025

https://doi.org/10.1128/jvi.01914-24

Martina Castellan, Gianpiero Zamperin, Greta Foiani, Maira Zorzan, Maria Francesca Priore, Petra Drzewnioková, EricaMelchiotti, Marta Vascellari, Isabella Monne, Sergio Crovella, StefaniaLeopardi, Paola De Benedictis

ABSTRACT

The Lyssavirus genus includes seventeen viral species able to cause rabies, an acute and almost invariably fatal encephalomyelitis of mammals. Rabies virus (RABV), which represents the type species of the genus, is a multi-host pathogen that over the years has undergone multiple events of host-switching, thus occupying several geographical and ecological niches. In contrast, non-RABV lyssaviruses are mainly confined within a single natural host with rare spillover events. In this scenario, unveiling the mechanisms underlying the host immune response against a virus is crucial to understand the dynamics of infection and to predict the probability of colonization/adaptation to a new target species. Presently, the host response to lyssaviruses has only been partially explored, with the majority of data extrapolated from RABV infection. West Caucasian bat virus (WCBV), a divergent lyssavirus, has recently been associated with a spillover event to a domestic cat, raising concern about the risks to public health due to the circulation of the virus in its natural host. Through this study we have investigated the immune response determined by the WCBV versus two widely known lyssaviruses. We selected the Syrian hamster as representative of an accidental host, and chose the intramuscular route in order to mimic the natural infection. In hamsters, WCBV was highly pathogenic, determining 100% lethality and mild encephalitis. In comparison with Duvenhage virus (DUVV) and RABV, we found that WCBV displayed an intermediate ability to promote cellular antiviral response, produce pro-inflammatory cytokines, and recruit and activate lymphocytes in the hamsters’ central nervous system.​

https://journals.asm.org/doi/10.1128/jvi.01914-24
 
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