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Breed differences in the expression levels of gga-miR-222a in laying hens influenced H(2)S production by regulating methionine synthase genes in gut bacteria

BACKGROUND: The microbiota in the cecum of laying hens is crucial for host digestion, metabolism, and odor gas production. The results of recent studies have suggested that host microRNAs (miRNAs) can regulate gene expression of the gut microbiota. In the present study, the expression profiles of ho...

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Autores principales: Xing, Si-Cheng, Huang, Chun-Bo, Wu, Rui-Ting, Yang, Yi-Wen, Chen, Jing-Yuan, Mi, Jian-Dui, Wu, Yin-Bao, Wang, Yan, Liao, Xin-Di
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390279/
https://www.ncbi.nlm.nih.gov/pubmed/34433492
http://dx.doi.org/10.1186/s40168-021-01098-7
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author Xing, Si-Cheng
Huang, Chun-Bo
Wu, Rui-Ting
Yang, Yi-Wen
Chen, Jing-Yuan
Mi, Jian-Dui
Wu, Yin-Bao
Wang, Yan
Liao, Xin-Di
author_facet Xing, Si-Cheng
Huang, Chun-Bo
Wu, Rui-Ting
Yang, Yi-Wen
Chen, Jing-Yuan
Mi, Jian-Dui
Wu, Yin-Bao
Wang, Yan
Liao, Xin-Di
author_sort Xing, Si-Cheng
collection PubMed
description BACKGROUND: The microbiota in the cecum of laying hens is crucial for host digestion, metabolism, and odor gas production. The results of recent studies have suggested that host microRNAs (miRNAs) can regulate gene expression of the gut microbiota. In the present study, the expression profiles of host-derived miRNAs in the cecal content of two laying hen breeds; Hy-line Gray and Lohmann Pink, which have dissimilar H(2)S production, were characterized; and their effects on H(2)S production by regulating the expression of gut microbiota-associated genes were demonstrated. RESULTS: The differential expression of microbial serine O-acetyltransferase, methionine synthase, aspartate aminotransferase, methionine-gamma-lyase, and adenylylsulfate kinase between the two hen breeds resulted in lower H(2)S production in the Hy-line hens. The results also revealed the presence of miRNA exosomes in the cecal content of laying hens, and an analysis of potential miRNA-target relationships between 9 differentially expressed miRNAs and 9 differentially expressed microbial genes related to H(2)S production identified two methionine synthase genes, Odosp_3416 and BF9343_2953, that are targeted by gga-miR-222a. Interestingly, in vitro fermentation results showed that gga-miR-222a upregulates the expression of these genes, which increased methionine concentrations but decreased H(2)S production and soluble sulfide concentrations, indicating the potential of host-derived gga-miR-222a to reduce H(2)S emission in laying hens. CONCLUSION: The findings of the present study reveal both a physiological role by which miRNAs shape the cecal microbiota of laying hens and a strategy to use host miRNAs to manipulate the microbiome and actively express key microbial genes to reduce H(2)S emissions and breed environmentally friendly laying hens. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01098-7.
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spelling pubmed-83902792021-08-27 Breed differences in the expression levels of gga-miR-222a in laying hens influenced H(2)S production by regulating methionine synthase genes in gut bacteria Xing, Si-Cheng Huang, Chun-Bo Wu, Rui-Ting Yang, Yi-Wen Chen, Jing-Yuan Mi, Jian-Dui Wu, Yin-Bao Wang, Yan Liao, Xin-Di Microbiome Research BACKGROUND: The microbiota in the cecum of laying hens is crucial for host digestion, metabolism, and odor gas production. The results of recent studies have suggested that host microRNAs (miRNAs) can regulate gene expression of the gut microbiota. In the present study, the expression profiles of host-derived miRNAs in the cecal content of two laying hen breeds; Hy-line Gray and Lohmann Pink, which have dissimilar H(2)S production, were characterized; and their effects on H(2)S production by regulating the expression of gut microbiota-associated genes were demonstrated. RESULTS: The differential expression of microbial serine O-acetyltransferase, methionine synthase, aspartate aminotransferase, methionine-gamma-lyase, and adenylylsulfate kinase between the two hen breeds resulted in lower H(2)S production in the Hy-line hens. The results also revealed the presence of miRNA exosomes in the cecal content of laying hens, and an analysis of potential miRNA-target relationships between 9 differentially expressed miRNAs and 9 differentially expressed microbial genes related to H(2)S production identified two methionine synthase genes, Odosp_3416 and BF9343_2953, that are targeted by gga-miR-222a. Interestingly, in vitro fermentation results showed that gga-miR-222a upregulates the expression of these genes, which increased methionine concentrations but decreased H(2)S production and soluble sulfide concentrations, indicating the potential of host-derived gga-miR-222a to reduce H(2)S emission in laying hens. CONCLUSION: The findings of the present study reveal both a physiological role by which miRNAs shape the cecal microbiota of laying hens and a strategy to use host miRNAs to manipulate the microbiome and actively express key microbial genes to reduce H(2)S emissions and breed environmentally friendly laying hens. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01098-7. BioMed Central 2021-08-25 /pmc/articles/PMC8390279/ /pubmed/34433492 http://dx.doi.org/10.1186/s40168-021-01098-7 Text en © The Author(s) 2021 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
Xing, Si-Cheng
Huang, Chun-Bo
Wu, Rui-Ting
Yang, Yi-Wen
Chen, Jing-Yuan
Mi, Jian-Dui
Wu, Yin-Bao
Wang, Yan
Liao, Xin-Di
Breed differences in the expression levels of gga-miR-222a in laying hens influenced H(2)S production by regulating methionine synthase genes in gut bacteria
title Breed differences in the expression levels of gga-miR-222a in laying hens influenced H(2)S production by regulating methionine synthase genes in gut bacteria
title_full Breed differences in the expression levels of gga-miR-222a in laying hens influenced H(2)S production by regulating methionine synthase genes in gut bacteria
title_fullStr Breed differences in the expression levels of gga-miR-222a in laying hens influenced H(2)S production by regulating methionine synthase genes in gut bacteria
title_full_unstemmed Breed differences in the expression levels of gga-miR-222a in laying hens influenced H(2)S production by regulating methionine synthase genes in gut bacteria
title_short Breed differences in the expression levels of gga-miR-222a in laying hens influenced H(2)S production by regulating methionine synthase genes in gut bacteria
title_sort breed differences in the expression levels of gga-mir-222a in laying hens influenced h(2)s production by regulating methionine synthase genes in gut bacteria
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390279/
https://www.ncbi.nlm.nih.gov/pubmed/34433492
http://dx.doi.org/10.1186/s40168-021-01098-7
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