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Virally-vectored vaccine candidates against white-nose syndrome induce anti-fungal immune response in little brown bats (Myotis lucifugus)

White-nose syndrome (WNS) caused by the fungus, Pseudogymnoascus destructans ( Pd ) has killed millions of North American hibernating bats. Currently, methods to prevent the disease are limited. We conducted two trials to assess potential WNS vaccine candidates in wild-caught Myotis lucifugus . In a...

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Bibliographic Details
Published in:Scientific reports 2019-05, Vol.9 (1), p.6788-6788, Article 6788
Main Authors: Rocke, Tonie E., Kingstad-Bakke, Brock, Wüthrich, Marcel, Stading, Ben, Abbott, Rachel C., Isidoro-Ayza, Marcos, Dobson, Hannah E., dos Santos Dias, Lucas, Galles, Kevin, Lankton, Julia S., Falendysz, Elizabeth A., Lorch, Jeffrey M., Fites, J. Scott, Lopera-Madrid, Jaime, White, J. Paul, Klein, Bruce, Osorio, Jorge E.
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Language:English
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Summary:White-nose syndrome (WNS) caused by the fungus, Pseudogymnoascus destructans ( Pd ) has killed millions of North American hibernating bats. Currently, methods to prevent the disease are limited. We conducted two trials to assess potential WNS vaccine candidates in wild-caught Myotis lucifugus . In a pilot study, we immunized bats with one of four vaccine treatments or phosphate-buffered saline (PBS) as a control and challenged them with Pd upon transfer into hibernation chambers. Bats in one vaccine-treated group, that received raccoon poxviruses (RCN) expressing Pd calnexin (CAL) and serine protease (SP), developed WNS at a lower rate (1/10) than other treatments combined (14/23), although samples sizes were small. The results of a second similar trial provided additional support for this observation. Bats vaccinated orally or by injection with RCN-CAL and RCN-SP survived Pd challenge at a significantly higher rate (P = 0.01) than controls. Using RT-PCR and flow cytometry, combined with fluorescent in situ hybridization, we determined that expression of IFN-γ transcripts and the number of CD4 + T-helper cells transcribing this gene were elevated (P 
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-019-43210-w