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Differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (Myotis myotis)

The acute phase response (APR) is an evolutionarily well-conserved part of the innate immune defense against pathogens. However, recent studies in bats yielded surprisingly diverse results compared to previous APR studies on both vertebrate and invertebrate species. This is especially interesting du...

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Autores principales: Seltmann, Anne, Troxell, Sara A., Schad, Julia, Fritze, Marcus, Bailey, Liam D., Voigt, Christian C., Czirják, Gábor Á.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464231/
https://www.ncbi.nlm.nih.gov/pubmed/36088405
http://dx.doi.org/10.1038/s41598-022-18240-6
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author Seltmann, Anne
Troxell, Sara A.
Schad, Julia
Fritze, Marcus
Bailey, Liam D.
Voigt, Christian C.
Czirják, Gábor Á.
author_facet Seltmann, Anne
Troxell, Sara A.
Schad, Julia
Fritze, Marcus
Bailey, Liam D.
Voigt, Christian C.
Czirják, Gábor Á.
author_sort Seltmann, Anne
collection PubMed
description The acute phase response (APR) is an evolutionarily well-conserved part of the innate immune defense against pathogens. However, recent studies in bats yielded surprisingly diverse results compared to previous APR studies on both vertebrate and invertebrate species. This is especially interesting due to the known role of bats as reservoirs for viruses and other intracellular pathogens, while being susceptible to extracellular microorganisms such as some bacteria and fungi. To better understand these discrepancies and the reservoir-competence of bats, we mimicked bacterial, viral and fungal infections in greater mouse-eared bats (Myotis myotis) and quantified different aspects of the APR over a two-day period. Individuals reacted most strongly to a viral (PolyI:C) and a bacterial (LPS) antigen, reflected by an increase of haptoglobin levels (LPS) and an increase of the neutrophil-to-lymphocyte-ratio (PolyI:C and LPS). We did not detect fever, leukocytosis, body mass loss, or a change in the overall functioning of the innate immunity upon challenge with any antigen. We add evidence that bats respond selectively with APR to specific pathogens and that the activation of different parts of the immune system is species-specific.
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spelling pubmed-94642312022-09-12 Differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (Myotis myotis) Seltmann, Anne Troxell, Sara A. Schad, Julia Fritze, Marcus Bailey, Liam D. Voigt, Christian C. Czirják, Gábor Á. Sci Rep Article The acute phase response (APR) is an evolutionarily well-conserved part of the innate immune defense against pathogens. However, recent studies in bats yielded surprisingly diverse results compared to previous APR studies on both vertebrate and invertebrate species. This is especially interesting due to the known role of bats as reservoirs for viruses and other intracellular pathogens, while being susceptible to extracellular microorganisms such as some bacteria and fungi. To better understand these discrepancies and the reservoir-competence of bats, we mimicked bacterial, viral and fungal infections in greater mouse-eared bats (Myotis myotis) and quantified different aspects of the APR over a two-day period. Individuals reacted most strongly to a viral (PolyI:C) and a bacterial (LPS) antigen, reflected by an increase of haptoglobin levels (LPS) and an increase of the neutrophil-to-lymphocyte-ratio (PolyI:C and LPS). We did not detect fever, leukocytosis, body mass loss, or a change in the overall functioning of the innate immunity upon challenge with any antigen. We add evidence that bats respond selectively with APR to specific pathogens and that the activation of different parts of the immune system is species-specific. Nature Publishing Group UK 2022-09-10 /pmc/articles/PMC9464231/ /pubmed/36088405 http://dx.doi.org/10.1038/s41598-022-18240-6 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Seltmann, Anne
Troxell, Sara A.
Schad, Julia
Fritze, Marcus
Bailey, Liam D.
Voigt, Christian C.
Czirják, Gábor Á.
Differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (Myotis myotis)
title Differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (Myotis myotis)
title_full Differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (Myotis myotis)
title_fullStr Differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (Myotis myotis)
title_full_unstemmed Differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (Myotis myotis)
title_short Differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (Myotis myotis)
title_sort differences in acute phase response to bacterial, fungal and viral antigens in greater mouse-eared bats (myotis myotis)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464231/
https://www.ncbi.nlm.nih.gov/pubmed/36088405
http://dx.doi.org/10.1038/s41598-022-18240-6
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