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Immune response of hibernating European bats to a fungal challenge
Immunological responses of hibernating mammals are suppressed at low body temperatures, a possible explanation for the devastating effect of the white-nose syndrome on hibernating North American bats. However, European bats seem to cope well with the fungal causative agent of the disease. To better...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826279/ https://www.ncbi.nlm.nih.gov/pubmed/31649120 http://dx.doi.org/10.1242/bio.046078 |
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author | Fritze, Marcus Costantini, David Fickel, Jörns Wehner, Dana Czirják, Gábor Á. Voigt, Christian C. |
author_facet | Fritze, Marcus Costantini, David Fickel, Jörns Wehner, Dana Czirják, Gábor Á. Voigt, Christian C. |
author_sort | Fritze, Marcus |
collection | PubMed |
description | Immunological responses of hibernating mammals are suppressed at low body temperatures, a possible explanation for the devastating effect of the white-nose syndrome on hibernating North American bats. However, European bats seem to cope well with the fungal causative agent of the disease. To better understand the immune response of hibernating bats, especially against fungal pathogens, we challenged European greater mouse-eared bats (Myotis myotis) by inoculating the fungal antigen zymosan. We monitored torpor patterns, immune gene expressions, different aspects of the acute phase response and plasma oxidative status markers, and compared them with sham-injected control animals at 30 min, 48 h and 96 h after inoculation. Torpor patterns, body temperatures, body masses, white blood cell counts, expression of immune genes, reactive oxygen metabolites and non-enzymatic antioxidant capacity did not differ between groups during the experiment. However, zymosan injected bats had significantly higher levels of haptoglobin than the control animals. Our results indicate that hibernating greater mouse-eared bats mount an inflammatory response to a fungal challenge, with only mild to negligible consequences for the energy budget of hibernation. Our study gives a first hint that hibernating European bats may have evolved a hibernation-adjusted immune response in order to balance the trade-off between competent pathogen elimination and a prudent energy-saving regime. |
format | Online Article Text |
id | pubmed-6826279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68262792019-11-04 Immune response of hibernating European bats to a fungal challenge Fritze, Marcus Costantini, David Fickel, Jörns Wehner, Dana Czirják, Gábor Á. Voigt, Christian C. Biol Open Research Article Immunological responses of hibernating mammals are suppressed at low body temperatures, a possible explanation for the devastating effect of the white-nose syndrome on hibernating North American bats. However, European bats seem to cope well with the fungal causative agent of the disease. To better understand the immune response of hibernating bats, especially against fungal pathogens, we challenged European greater mouse-eared bats (Myotis myotis) by inoculating the fungal antigen zymosan. We monitored torpor patterns, immune gene expressions, different aspects of the acute phase response and plasma oxidative status markers, and compared them with sham-injected control animals at 30 min, 48 h and 96 h after inoculation. Torpor patterns, body temperatures, body masses, white blood cell counts, expression of immune genes, reactive oxygen metabolites and non-enzymatic antioxidant capacity did not differ between groups during the experiment. However, zymosan injected bats had significantly higher levels of haptoglobin than the control animals. Our results indicate that hibernating greater mouse-eared bats mount an inflammatory response to a fungal challenge, with only mild to negligible consequences for the energy budget of hibernation. Our study gives a first hint that hibernating European bats may have evolved a hibernation-adjusted immune response in order to balance the trade-off between competent pathogen elimination and a prudent energy-saving regime. The Company of Biologists Ltd 2019-10-24 /pmc/articles/PMC6826279/ /pubmed/31649120 http://dx.doi.org/10.1242/bio.046078 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Fritze, Marcus Costantini, David Fickel, Jörns Wehner, Dana Czirják, Gábor Á. Voigt, Christian C. Immune response of hibernating European bats to a fungal challenge |
title | Immune response of hibernating European bats to a fungal challenge |
title_full | Immune response of hibernating European bats to a fungal challenge |
title_fullStr | Immune response of hibernating European bats to a fungal challenge |
title_full_unstemmed | Immune response of hibernating European bats to a fungal challenge |
title_short | Immune response of hibernating European bats to a fungal challenge |
title_sort | immune response of hibernating european bats to a fungal challenge |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826279/ https://www.ncbi.nlm.nih.gov/pubmed/31649120 http://dx.doi.org/10.1242/bio.046078 |
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