Sasa Miao, Xiaomei Xu, Tao Zeng, Yong Tian, Tiantian Gu, Li Chen, Jiayi Su, Lizhi Lu, Wenwu Xu
{"title":"基于16S rRNA基因测序和代谢组学的山马鸭产蛋微生物及代谢物研究","authors":"Sasa Miao, Xiaomei Xu, Tao Zeng, Yong Tian, Tiantian Gu, Li Chen, Jiayi Su, Lizhi Lu, Wenwu Xu","doi":"10.1016/j.psj.2025.105880","DOIUrl":null,"url":null,"abstract":"<div><div>Gut microbiota and metabolites play crucial roles in regulating poultry health, metabolism, and egg-laying performance. To elucidate the biological basis underlying differences in laying performance, this study employed 16S rRNA high-throughput sequencing and untargeted liquid chromatography-mass spectrometry (LC-MS/MS) to analyze the gut microbiota and serum metabolome of low-producing (LP) and high-producing (HP) Shanma ducks. The LP and HP groups exhibited significant differences in egg production performance, body size parameters, and slaughter traits. Firmicutes were the dominant phylum in the gut microbiota of both groups. However, Actinobacteria were significantly enriched in the HP group, while Campylobacter was more abundant in the LP group. Correlation analysis revealed a negative association between <em>Campylobacter</em> abundance and egg production, whereas <em>Corynebacterium</em> (belonging to Actinobacteria) showed a positive correlation. Non-targeted serum metabolomic analysis indicated that the differentially expressed metabolites were primarily enriched in nucleotide metabolism, choline metabolism, and glycerophospholipid metabolism pathways. Notably, <em>Campylobacter</em> abundance was negatively correlated with the levels of key metabolites involved in these pathways. Mantel analysis further confirmed a strong correlation between egg production and both gut microbiota composition and serum metabolomic profiles. Collectively, these findings provide new insights into the microbial and metabolic determinants of reproductive performance in ducks, offering a foundation for genetic selection and microbiota-targeted nutritional strategies to enhance laying efficiency in Shanma ducks.</div></div>","PeriodicalId":20459,"journal":{"name":"Poultry Science","volume":"104 12","pages":"Article 105880"},"PeriodicalIF":4.2000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exploration of microorganism and metabolites relation to the egg production of Shanma ducks based on 16S rRNA gene sequencing and metabolomics\",\"authors\":\"Sasa Miao, Xiaomei Xu, Tao Zeng, Yong Tian, Tiantian Gu, Li Chen, Jiayi Su, Lizhi Lu, Wenwu Xu\",\"doi\":\"10.1016/j.psj.2025.105880\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Gut microbiota and metabolites play crucial roles in regulating poultry health, metabolism, and egg-laying performance. To elucidate the biological basis underlying differences in laying performance, this study employed 16S rRNA high-throughput sequencing and untargeted liquid chromatography-mass spectrometry (LC-MS/MS) to analyze the gut microbiota and serum metabolome of low-producing (LP) and high-producing (HP) Shanma ducks. The LP and HP groups exhibited significant differences in egg production performance, body size parameters, and slaughter traits. Firmicutes were the dominant phylum in the gut microbiota of both groups. However, Actinobacteria were significantly enriched in the HP group, while Campylobacter was more abundant in the LP group. Correlation analysis revealed a negative association between <em>Campylobacter</em> abundance and egg production, whereas <em>Corynebacterium</em> (belonging to Actinobacteria) showed a positive correlation. Non-targeted serum metabolomic analysis indicated that the differentially expressed metabolites were primarily enriched in nucleotide metabolism, choline metabolism, and glycerophospholipid metabolism pathways. Notably, <em>Campylobacter</em> abundance was negatively correlated with the levels of key metabolites involved in these pathways. Mantel analysis further confirmed a strong correlation between egg production and both gut microbiota composition and serum metabolomic profiles. Collectively, these findings provide new insights into the microbial and metabolic determinants of reproductive performance in ducks, offering a foundation for genetic selection and microbiota-targeted nutritional strategies to enhance laying efficiency in Shanma ducks.</div></div>\",\"PeriodicalId\":20459,\"journal\":{\"name\":\"Poultry Science\",\"volume\":\"104 12\",\"pages\":\"Article 105880\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Poultry Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0032579125011216\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRICULTURE, DAIRY & ANIMAL SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poultry Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032579125011216","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
Exploration of microorganism and metabolites relation to the egg production of Shanma ducks based on 16S rRNA gene sequencing and metabolomics
Gut microbiota and metabolites play crucial roles in regulating poultry health, metabolism, and egg-laying performance. To elucidate the biological basis underlying differences in laying performance, this study employed 16S rRNA high-throughput sequencing and untargeted liquid chromatography-mass spectrometry (LC-MS/MS) to analyze the gut microbiota and serum metabolome of low-producing (LP) and high-producing (HP) Shanma ducks. The LP and HP groups exhibited significant differences in egg production performance, body size parameters, and slaughter traits. Firmicutes were the dominant phylum in the gut microbiota of both groups. However, Actinobacteria were significantly enriched in the HP group, while Campylobacter was more abundant in the LP group. Correlation analysis revealed a negative association between Campylobacter abundance and egg production, whereas Corynebacterium (belonging to Actinobacteria) showed a positive correlation. Non-targeted serum metabolomic analysis indicated that the differentially expressed metabolites were primarily enriched in nucleotide metabolism, choline metabolism, and glycerophospholipid metabolism pathways. Notably, Campylobacter abundance was negatively correlated with the levels of key metabolites involved in these pathways. Mantel analysis further confirmed a strong correlation between egg production and both gut microbiota composition and serum metabolomic profiles. Collectively, these findings provide new insights into the microbial and metabolic determinants of reproductive performance in ducks, offering a foundation for genetic selection and microbiota-targeted nutritional strategies to enhance laying efficiency in Shanma ducks.
期刊介绍:
First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers.
An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.