Cargando…

Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis

ABSTRACT: Resistance and tolerance allow organisms to cope with potentially life-threatening pathogens. Recently introduced pathogens initially induce resistance responses, but natural selection favors the development of tolerance, allowing for a commensal relationship to evolve. Mycosis by Pseudogy...

Descripción completa

Detalles Bibliográficos
Autores principales: Lilley, Thomas M., Prokkola, Jenni M., Blomberg, Anna S., Paterson, Steve, Johnson, Joseph S., Turner, Gregory G., Bartonička, Tomáš, Bachorec, Erik, Reeder, DeeAnn M., Field, Kenneth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763535/
https://www.ncbi.nlm.nih.gov/pubmed/31506746
http://dx.doi.org/10.1007/s00442-019-04499-6
_version_ 1783454218692067328
author Lilley, Thomas M.
Prokkola, Jenni M.
Blomberg, Anna S.
Paterson, Steve
Johnson, Joseph S.
Turner, Gregory G.
Bartonička, Tomáš
Bachorec, Erik
Reeder, DeeAnn M.
Field, Kenneth A.
author_facet Lilley, Thomas M.
Prokkola, Jenni M.
Blomberg, Anna S.
Paterson, Steve
Johnson, Joseph S.
Turner, Gregory G.
Bartonička, Tomáš
Bachorec, Erik
Reeder, DeeAnn M.
Field, Kenneth A.
author_sort Lilley, Thomas M.
collection PubMed
description ABSTRACT: Resistance and tolerance allow organisms to cope with potentially life-threatening pathogens. Recently introduced pathogens initially induce resistance responses, but natural selection favors the development of tolerance, allowing for a commensal relationship to evolve. Mycosis by Pseudogymnoascus destructans, causing white-nose syndrome (WNS) in Nearctic hibernating bats, has resulted in population declines since 2006. The pathogen, which spread from Europe, has infected species of Palearctic Myotis for a longer period. We compared ecologically relevant responses to the fungal infection in the susceptible Nearctic M. lucifugus and less susceptible Palearctic M. myotis, to uncover factors contributing to survival differences in the two species. Samples were collected from euthermic bats during arousal from hibernation, a naturally occurring phenomenon, during which transcriptional responses are activated. We compared the whole-transcriptome responses in wild bats infected with P. destructans hibernating in their natural habitat. Our results show dramatically different local transcriptional responses to the pathogen between uninfected and infected samples from the two species. Whereas we found 1526 significantly upregulated or downregulated transcripts in infected M. lucifugus, only one transcript was downregulated in M. myotis. The upregulated response pathways in M. lucifugus include immune cell activation and migration, and inflammatory pathways, indicative of an unsuccessful attempt to resist the infection. In contrast, M. myotis appears to tolerate P. destructans infection by not activating a transcriptional response. These host-microbe interactions determine pathology, contributing to WNS susceptibility, or commensalism, promoting tolerance to fungal colonization during hibernation that favors survival. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00442-019-04499-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6763535
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-67635352019-10-07 Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis Lilley, Thomas M. Prokkola, Jenni M. Blomberg, Anna S. Paterson, Steve Johnson, Joseph S. Turner, Gregory G. Bartonička, Tomáš Bachorec, Erik Reeder, DeeAnn M. Field, Kenneth A. Oecologia Physiological Ecology–Original Research ABSTRACT: Resistance and tolerance allow organisms to cope with potentially life-threatening pathogens. Recently introduced pathogens initially induce resistance responses, but natural selection favors the development of tolerance, allowing for a commensal relationship to evolve. Mycosis by Pseudogymnoascus destructans, causing white-nose syndrome (WNS) in Nearctic hibernating bats, has resulted in population declines since 2006. The pathogen, which spread from Europe, has infected species of Palearctic Myotis for a longer period. We compared ecologically relevant responses to the fungal infection in the susceptible Nearctic M. lucifugus and less susceptible Palearctic M. myotis, to uncover factors contributing to survival differences in the two species. Samples were collected from euthermic bats during arousal from hibernation, a naturally occurring phenomenon, during which transcriptional responses are activated. We compared the whole-transcriptome responses in wild bats infected with P. destructans hibernating in their natural habitat. Our results show dramatically different local transcriptional responses to the pathogen between uninfected and infected samples from the two species. Whereas we found 1526 significantly upregulated or downregulated transcripts in infected M. lucifugus, only one transcript was downregulated in M. myotis. The upregulated response pathways in M. lucifugus include immune cell activation and migration, and inflammatory pathways, indicative of an unsuccessful attempt to resist the infection. In contrast, M. myotis appears to tolerate P. destructans infection by not activating a transcriptional response. These host-microbe interactions determine pathology, contributing to WNS susceptibility, or commensalism, promoting tolerance to fungal colonization during hibernation that favors survival. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00442-019-04499-6) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-09-10 2019 /pmc/articles/PMC6763535/ /pubmed/31506746 http://dx.doi.org/10.1007/s00442-019-04499-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Physiological Ecology–Original Research
Lilley, Thomas M.
Prokkola, Jenni M.
Blomberg, Anna S.
Paterson, Steve
Johnson, Joseph S.
Turner, Gregory G.
Bartonička, Tomáš
Bachorec, Erik
Reeder, DeeAnn M.
Field, Kenneth A.
Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis
title Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis
title_full Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis
title_fullStr Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis
title_full_unstemmed Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis
title_short Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis
title_sort resistance is futile: rna-sequencing reveals differing responses to bat fungal pathogen in nearctic myotis lucifugus and palearctic myotis myotis
topic Physiological Ecology–Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763535/
https://www.ncbi.nlm.nih.gov/pubmed/31506746
http://dx.doi.org/10.1007/s00442-019-04499-6
work_keys_str_mv AT lilleythomasm resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT prokkolajennim resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT blombergannas resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT patersonsteve resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT johnsonjosephs resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT turnergregoryg resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT bartonickatomas resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT bachorecerik resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT reederdeeannm resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis
AT fieldkennetha resistanceisfutilernasequencingrevealsdifferingresponsestobatfungalpathogeninnearcticmyotislucifugusandpalearcticmyotismyotis