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Temporal dynamics of the bat wing transcriptome: Insight into gene-expression changes that enable protection against pathogen

Skin acts as a mechanical barrier between the body and its surrounding environment and plays an important role in resistance to pathogens. However, we still know little regarding skin responses to physiological changes, particularly with regard to responses against potential pathogens. We herein exe...

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Autores principales: Li, Aoqiang, Leng, Haixia, Li, Zhongle, Jin, Longru, Sun, Keping, Feng, Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815227/
https://www.ncbi.nlm.nih.gov/pubmed/36599840
http://dx.doi.org/10.1080/21505594.2022.2156185
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author Li, Aoqiang
Leng, Haixia
Li, Zhongle
Jin, Longru
Sun, Keping
Feng, Jiang
author_facet Li, Aoqiang
Leng, Haixia
Li, Zhongle
Jin, Longru
Sun, Keping
Feng, Jiang
author_sort Li, Aoqiang
collection PubMed
description Skin acts as a mechanical barrier between the body and its surrounding environment and plays an important role in resistance to pathogens. However, we still know little regarding skin responses to physiological changes, particularly with regard to responses against potential pathogens. We herein executed RNA-seq on the wing of the Rhinolophus ferrumequinum to assess gene-expression variations at four physiological stages: pre-hibernation, hibernation (early-hibernation and late-hibernation), and post-hibernation, as well as the gene-expression patterns of infected and uninfected bats with the Pseudogymnoascus destructans (Pd). Our results showed that a greater number of differentially expressed genes between the more disparate physiological stages. Functional enrichment analysis showed that the down-regulated response pathways in hibernating bats included phosphorus metabolism and immune response, indicating metabolic suppression and decreased whole immune function. We also found up-regulated genes in post-hibernating bats that included C-type lectin receptor signalling, Toll-like receptor signalling pathway, and cell adhesion, suggesting that the immune response and skin integrity of the wing were improved after bats emerged from their hibernation and that this facilitated clearing Pd from the integument. Additionally, we found that the genes involved in cytokine or chemokine activity were up-regulated in late-hibernation compared to early-hibernation and that FOSB regulation of immune cell activation was differentially expressed in bats infected with Pd during late-hibernation, implying that the host’s innate immune function was enhanced during late-hibernation so as to resist pathogenic infection. Our findings highlight the concept that maintenance of intrinsic immunity provides protection against pathogenic infections in highly resistant bats.
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spelling pubmed-98152272023-01-06 Temporal dynamics of the bat wing transcriptome: Insight into gene-expression changes that enable protection against pathogen Li, Aoqiang Leng, Haixia Li, Zhongle Jin, Longru Sun, Keping Feng, Jiang Virulence Research Article Skin acts as a mechanical barrier between the body and its surrounding environment and plays an important role in resistance to pathogens. However, we still know little regarding skin responses to physiological changes, particularly with regard to responses against potential pathogens. We herein executed RNA-seq on the wing of the Rhinolophus ferrumequinum to assess gene-expression variations at four physiological stages: pre-hibernation, hibernation (early-hibernation and late-hibernation), and post-hibernation, as well as the gene-expression patterns of infected and uninfected bats with the Pseudogymnoascus destructans (Pd). Our results showed that a greater number of differentially expressed genes between the more disparate physiological stages. Functional enrichment analysis showed that the down-regulated response pathways in hibernating bats included phosphorus metabolism and immune response, indicating metabolic suppression and decreased whole immune function. We also found up-regulated genes in post-hibernating bats that included C-type lectin receptor signalling, Toll-like receptor signalling pathway, and cell adhesion, suggesting that the immune response and skin integrity of the wing were improved after bats emerged from their hibernation and that this facilitated clearing Pd from the integument. Additionally, we found that the genes involved in cytokine or chemokine activity were up-regulated in late-hibernation compared to early-hibernation and that FOSB regulation of immune cell activation was differentially expressed in bats infected with Pd during late-hibernation, implying that the host’s innate immune function was enhanced during late-hibernation so as to resist pathogenic infection. Our findings highlight the concept that maintenance of intrinsic immunity provides protection against pathogenic infections in highly resistant bats. Taylor & Francis 2023-01-04 /pmc/articles/PMC9815227/ /pubmed/36599840 http://dx.doi.org/10.1080/21505594.2022.2156185 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Aoqiang
Leng, Haixia
Li, Zhongle
Jin, Longru
Sun, Keping
Feng, Jiang
Temporal dynamics of the bat wing transcriptome: Insight into gene-expression changes that enable protection against pathogen
title Temporal dynamics of the bat wing transcriptome: Insight into gene-expression changes that enable protection against pathogen
title_full Temporal dynamics of the bat wing transcriptome: Insight into gene-expression changes that enable protection against pathogen
title_fullStr Temporal dynamics of the bat wing transcriptome: Insight into gene-expression changes that enable protection against pathogen
title_full_unstemmed Temporal dynamics of the bat wing transcriptome: Insight into gene-expression changes that enable protection against pathogen
title_short Temporal dynamics of the bat wing transcriptome: Insight into gene-expression changes that enable protection against pathogen
title_sort temporal dynamics of the bat wing transcriptome: insight into gene-expression changes that enable protection against pathogen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815227/
https://www.ncbi.nlm.nih.gov/pubmed/36599840
http://dx.doi.org/10.1080/21505594.2022.2156185
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