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Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis

BACKGROUND: Infectious diseases have caused huge economic loss and food security issues in fish aquaculture. Current management and breeding strategies heavily rely on the knowledge of regulative mechanisms underlying disease resistance. Though the intestinal microbial community was linked with dise...

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Autores principales: Zhou, Qian, Zhu, Xue, Li, Yangzhen, Yang, Pengshuo, Wang, Shengpeng, Ning, Kang, Chen, Songlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503257/
https://www.ncbi.nlm.nih.gov/pubmed/36138436
http://dx.doi.org/10.1186/s40168-022-01346-4
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author Zhou, Qian
Zhu, Xue
Li, Yangzhen
Yang, Pengshuo
Wang, Shengpeng
Ning, Kang
Chen, Songlin
author_facet Zhou, Qian
Zhu, Xue
Li, Yangzhen
Yang, Pengshuo
Wang, Shengpeng
Ning, Kang
Chen, Songlin
author_sort Zhou, Qian
collection PubMed
description BACKGROUND: Infectious diseases have caused huge economic loss and food security issues in fish aquaculture. Current management and breeding strategies heavily rely on the knowledge of regulative mechanisms underlying disease resistance. Though the intestinal microbial community was linked with disease infection, there is little knowledge about the roles of intestinal microbes in fish disease resistance. Cynoglossus semilaevis is an economically important and widely cultivated flatfish species in China. However, it suffers from outbreaks of vibriosis, which results in huge mortalities and economic loss. RESULTS: Here, we used C. semilaevis as a research model to investigate the host-microbiome interactions in regulating vibriosis resistance. The resistance to vibriosis was reflected in intestinal microbiome on both taxonomic and functional levels. Such differences also influenced the host gene expressions in the resistant family. Moreover, the intestinal microbiome might control the host immunological homeostasis and inflammation to enhance vibriosis resistance through the microbe-intestine-immunity axis. For example, Phaeobacter regulated its hdhA gene and host cyp27a1 gene up-expressed in bile acid biosynthesis pathways, but regulated its trxA gene and host akt gene down-expressed in proinflammatory cytokines biosynthesis pathways, to reduce inflammation and resist disease infection in the resistant family. Furthermore, the combination of intestinal microbes and host genes as biomarkers could accurately differentiate resistant family from susceptible family. CONCLUSION: Our study uncovered the regulatory patterns of the microbe-intestine-immunity axis that may contribute to vibriosis resistance in C. semilaevis. These findings could facilitate the disease control and selective breeding of superior germplasm with high disease resistance in fish aquaculture. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01346-4.
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spelling pubmed-95032572022-09-24 Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis Zhou, Qian Zhu, Xue Li, Yangzhen Yang, Pengshuo Wang, Shengpeng Ning, Kang Chen, Songlin Microbiome Research BACKGROUND: Infectious diseases have caused huge economic loss and food security issues in fish aquaculture. Current management and breeding strategies heavily rely on the knowledge of regulative mechanisms underlying disease resistance. Though the intestinal microbial community was linked with disease infection, there is little knowledge about the roles of intestinal microbes in fish disease resistance. Cynoglossus semilaevis is an economically important and widely cultivated flatfish species in China. However, it suffers from outbreaks of vibriosis, which results in huge mortalities and economic loss. RESULTS: Here, we used C. semilaevis as a research model to investigate the host-microbiome interactions in regulating vibriosis resistance. The resistance to vibriosis was reflected in intestinal microbiome on both taxonomic and functional levels. Such differences also influenced the host gene expressions in the resistant family. Moreover, the intestinal microbiome might control the host immunological homeostasis and inflammation to enhance vibriosis resistance through the microbe-intestine-immunity axis. For example, Phaeobacter regulated its hdhA gene and host cyp27a1 gene up-expressed in bile acid biosynthesis pathways, but regulated its trxA gene and host akt gene down-expressed in proinflammatory cytokines biosynthesis pathways, to reduce inflammation and resist disease infection in the resistant family. Furthermore, the combination of intestinal microbes and host genes as biomarkers could accurately differentiate resistant family from susceptible family. CONCLUSION: Our study uncovered the regulatory patterns of the microbe-intestine-immunity axis that may contribute to vibriosis resistance in C. semilaevis. These findings could facilitate the disease control and selective breeding of superior germplasm with high disease resistance in fish aquaculture. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01346-4. BioMed Central 2022-09-23 /pmc/articles/PMC9503257/ /pubmed/36138436 http://dx.doi.org/10.1186/s40168-022-01346-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhou, Qian
Zhu, Xue
Li, Yangzhen
Yang, Pengshuo
Wang, Shengpeng
Ning, Kang
Chen, Songlin
Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis
title Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis
title_full Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis
title_fullStr Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis
title_full_unstemmed Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis
title_short Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis
title_sort intestinal microbiome-mediated resistance against vibriosis for cynoglossus semilaevis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503257/
https://www.ncbi.nlm.nih.gov/pubmed/36138436
http://dx.doi.org/10.1186/s40168-022-01346-4
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