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Host immunity to repeated rabies virus infection in big brown bats

Bats are natural reservoirs for the majority of lyssaviruses globally, and are unique among mammals in having exceptional sociality and longevity. Given these facets, and the recognized status of bats as reservoirs for rabies viruses (RABVs) in the Americas, individual bats may experience repeated e...

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Autores principales: Turmelle, A. S., Jackson, F. R., Green, D., McCracken, G. F., Rupprecht, C. E.
Formato: Texto
Lenguaje:English
Publicado: Society for General Microbiology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052523/
https://www.ncbi.nlm.nih.gov/pubmed/20519458
http://dx.doi.org/10.1099/vir.0.020073-0
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author Turmelle, A. S.
Jackson, F. R.
Green, D.
McCracken, G. F.
Rupprecht, C. E.
author_facet Turmelle, A. S.
Jackson, F. R.
Green, D.
McCracken, G. F.
Rupprecht, C. E.
author_sort Turmelle, A. S.
collection PubMed
description Bats are natural reservoirs for the majority of lyssaviruses globally, and are unique among mammals in having exceptional sociality and longevity. Given these facets, and the recognized status of bats as reservoirs for rabies viruses (RABVs) in the Americas, individual bats may experience repeated exposure to RABV during their lifetime. Nevertheless, little information exists with regard to within-host infection dynamics and the role of immunological memory that may result from abortive RABV infection in bats. In this study, a cohort of big brown bats (Eptesicus fuscus) was infected intramuscularly in the left and right masseter muscles with varying doses [10(−0.1)–10(4.9) median mouse intracerebral lethal doses (MICLD(50))] of an E. fuscus RABV variant isolated from a naturally infected big brown bat. Surviving bats were infected a second time at 175 days post-(primary) infection with a dose (10(3.9)–10(4.9) MICLD(50)) of the same RABV variant. Surviving bats were infected a third time at either 175 or 305 days post-(secondary) infection with a dose (10(4.9) MICLD(50)) of the same RABV variant. When correcting for dose, similar mortality was observed following primary and secondary infection, but reduced mortality was observed following the third and last RABV challenge, despite infection with a high viral dose. Inducible RABV-neutralizing antibody titres post-infection were ephemeral among infected individuals, and dropped below levels of detection in several bats between subsequent infections. These results suggest that long-term repeated infection of bats may confer significant immunological memory and reduced susceptibility to RABV infection.
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spelling pubmed-30525232011-09-01 Host immunity to repeated rabies virus infection in big brown bats Turmelle, A. S. Jackson, F. R. Green, D. McCracken, G. F. Rupprecht, C. E. J Gen Virol Animal Bats are natural reservoirs for the majority of lyssaviruses globally, and are unique among mammals in having exceptional sociality and longevity. Given these facets, and the recognized status of bats as reservoirs for rabies viruses (RABVs) in the Americas, individual bats may experience repeated exposure to RABV during their lifetime. Nevertheless, little information exists with regard to within-host infection dynamics and the role of immunological memory that may result from abortive RABV infection in bats. In this study, a cohort of big brown bats (Eptesicus fuscus) was infected intramuscularly in the left and right masseter muscles with varying doses [10(−0.1)–10(4.9) median mouse intracerebral lethal doses (MICLD(50))] of an E. fuscus RABV variant isolated from a naturally infected big brown bat. Surviving bats were infected a second time at 175 days post-(primary) infection with a dose (10(3.9)–10(4.9) MICLD(50)) of the same RABV variant. Surviving bats were infected a third time at either 175 or 305 days post-(secondary) infection with a dose (10(4.9) MICLD(50)) of the same RABV variant. When correcting for dose, similar mortality was observed following primary and secondary infection, but reduced mortality was observed following the third and last RABV challenge, despite infection with a high viral dose. Inducible RABV-neutralizing antibody titres post-infection were ephemeral among infected individuals, and dropped below levels of detection in several bats between subsequent infections. These results suggest that long-term repeated infection of bats may confer significant immunological memory and reduced susceptibility to RABV infection. Society for General Microbiology 2010-09 /pmc/articles/PMC3052523/ /pubmed/20519458 http://dx.doi.org/10.1099/vir.0.020073-0 Text en Copyright © 2010, SGM
spellingShingle Animal
Turmelle, A. S.
Jackson, F. R.
Green, D.
McCracken, G. F.
Rupprecht, C. E.
Host immunity to repeated rabies virus infection in big brown bats
title Host immunity to repeated rabies virus infection in big brown bats
title_full Host immunity to repeated rabies virus infection in big brown bats
title_fullStr Host immunity to repeated rabies virus infection in big brown bats
title_full_unstemmed Host immunity to repeated rabies virus infection in big brown bats
title_short Host immunity to repeated rabies virus infection in big brown bats
title_sort host immunity to repeated rabies virus infection in big brown bats
topic Animal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052523/
https://www.ncbi.nlm.nih.gov/pubmed/20519458
http://dx.doi.org/10.1099/vir.0.020073-0
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