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Experimental infection of Foxes with European bat Lyssaviruses type-1 and 2
BACKGROUND: Since 1954, there have been in excess of 800 cases of rabies as a result of European Bat Lyssaviruses types 1 and 2 (EBLV-1, EBLV-2) infection, mainly in Serotine and Myotis bats respectively. These viruses have rarely been reported to infect humans and terrestrial mammals, as the only e...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694770/ https://www.ncbi.nlm.nih.gov/pubmed/19454020 http://dx.doi.org/10.1186/1746-6148-5-19 |
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author | Cliquet, Florence Picard-Meyer, Evelyne Barrat, Jacques Brookes, Sharon M Healy, Derek M Wasniewski, Marine Litaize, Estelle Biarnais, Mélanie Johnson, Linda Fooks, Anthony R |
author_facet | Cliquet, Florence Picard-Meyer, Evelyne Barrat, Jacques Brookes, Sharon M Healy, Derek M Wasniewski, Marine Litaize, Estelle Biarnais, Mélanie Johnson, Linda Fooks, Anthony R |
author_sort | Cliquet, Florence |
collection | PubMed |
description | BACKGROUND: Since 1954, there have been in excess of 800 cases of rabies as a result of European Bat Lyssaviruses types 1 and 2 (EBLV-1, EBLV-2) infection, mainly in Serotine and Myotis bats respectively. These viruses have rarely been reported to infect humans and terrestrial mammals, as the only exceptions are sheep in Denmark, a stone marten in Germany and a cat in France. The purpose of this study was to investigate the susceptibility of foxes to EBLVs using silver foxes (Vulpes vulpes) as a model. RESULTS: Our experimental studies have shown that the susceptibility of foxes to EBLVs is low by the intramuscular (IM) route, however, animals were sensitive to intracranial (IC) inoculation. Mortality was 100% for both EBLV-1 (~4.5 logs) and EBLV-2 (~3.0 logs) delivered by the IC route. Virus dissemination and inflammatory infiltrate in the brain were demonstrated but virus specific neutralising antibody (VNA) was limited (log(ED(50)) = 0.24–2.23 and 0.95–2.39 respectively for specific EBLV-1 and EBLV-2). Foxes were also susceptible, at a low level, to peripheral (IM) infection (~3.0 logs) with EBLV-1 but not EBLV-2. Three out of 21 (14.3%) foxes developed clinical signs between 14 and 24 days post-EBLV-1 infection. None of the animals given EBLV-2 developed clinical disease. CONCLUSION: These data suggest that the chance of a EBLV spill-over from bat to fox is low, but with a greater probability for EBLV-1 than for EBLV-2 and that foxes seem to be able to clear the virus before it reaches the brain and cause a lethal infection. |
format | Text |
id | pubmed-2694770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26947702009-06-11 Experimental infection of Foxes with European bat Lyssaviruses type-1 and 2 Cliquet, Florence Picard-Meyer, Evelyne Barrat, Jacques Brookes, Sharon M Healy, Derek M Wasniewski, Marine Litaize, Estelle Biarnais, Mélanie Johnson, Linda Fooks, Anthony R BMC Vet Res Research Article BACKGROUND: Since 1954, there have been in excess of 800 cases of rabies as a result of European Bat Lyssaviruses types 1 and 2 (EBLV-1, EBLV-2) infection, mainly in Serotine and Myotis bats respectively. These viruses have rarely been reported to infect humans and terrestrial mammals, as the only exceptions are sheep in Denmark, a stone marten in Germany and a cat in France. The purpose of this study was to investigate the susceptibility of foxes to EBLVs using silver foxes (Vulpes vulpes) as a model. RESULTS: Our experimental studies have shown that the susceptibility of foxes to EBLVs is low by the intramuscular (IM) route, however, animals were sensitive to intracranial (IC) inoculation. Mortality was 100% for both EBLV-1 (~4.5 logs) and EBLV-2 (~3.0 logs) delivered by the IC route. Virus dissemination and inflammatory infiltrate in the brain were demonstrated but virus specific neutralising antibody (VNA) was limited (log(ED(50)) = 0.24–2.23 and 0.95–2.39 respectively for specific EBLV-1 and EBLV-2). Foxes were also susceptible, at a low level, to peripheral (IM) infection (~3.0 logs) with EBLV-1 but not EBLV-2. Three out of 21 (14.3%) foxes developed clinical signs between 14 and 24 days post-EBLV-1 infection. None of the animals given EBLV-2 developed clinical disease. CONCLUSION: These data suggest that the chance of a EBLV spill-over from bat to fox is low, but with a greater probability for EBLV-1 than for EBLV-2 and that foxes seem to be able to clear the virus before it reaches the brain and cause a lethal infection. BioMed Central 2009-05-19 /pmc/articles/PMC2694770/ /pubmed/19454020 http://dx.doi.org/10.1186/1746-6148-5-19 Text en Copyright © 2009 Cliquet et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Cliquet, Florence Picard-Meyer, Evelyne Barrat, Jacques Brookes, Sharon M Healy, Derek M Wasniewski, Marine Litaize, Estelle Biarnais, Mélanie Johnson, Linda Fooks, Anthony R Experimental infection of Foxes with European bat Lyssaviruses type-1 and 2 |
title | Experimental infection of Foxes with European bat Lyssaviruses type-1 and 2 |
title_full | Experimental infection of Foxes with European bat Lyssaviruses type-1 and 2 |
title_fullStr | Experimental infection of Foxes with European bat Lyssaviruses type-1 and 2 |
title_full_unstemmed | Experimental infection of Foxes with European bat Lyssaviruses type-1 and 2 |
title_short | Experimental infection of Foxes with European bat Lyssaviruses type-1 and 2 |
title_sort | experimental infection of foxes with european bat lyssaviruses type-1 and 2 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694770/ https://www.ncbi.nlm.nih.gov/pubmed/19454020 http://dx.doi.org/10.1186/1746-6148-5-19 |
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