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Integrated multi-omics of the gastrointestinal microbiome and ruminant host reveals metabolic adaptation underlying early life development

生物 微生物群 脂肪酸代谢 瘤胃 代谢组学 新陈代谢 脂肪酸 寄主(生物学) 代谢途径 微生物代谢 代谢组 组学 细菌 生物化学 生物信息学 遗传学 发酵
作者
Xiaoting Yan,Huazhe Si,Yuhang Zhu,Songze Li,Han Yu,Hanlu Liu,Rui Du,Phillip B. Pope,Qiang Qiu,Zhipeng Li
出处
期刊:Microbiome [Springer Nature]
卷期号:10 (1) 被引量:10
标识
DOI:10.1186/s40168-022-01396-8
摘要

Abstract Background The gastrointestinal tract (GIT) microbiome of ruminants and its metabolic repercussions vastly influence host metabolism and growth. However, a complete understanding of the bidirectional interactions that occur across the host-microbiome axis remains elusive, particularly during the critical development stages at early life. Here, we present an integrative multi-omics approach that simultaneously resolved the taxonomic and functional attributes of microbiota from five GIT regions as well as the metabolic features of the liver, muscle, urine, and serum in sika deer ( Cervus nippon ) across three key early life stages. Results Within the host, analysis of metabolites over time in serum, urine, and muscle ( longissimus lumborum ) showed that changes in the fatty acid profile were concurrent with gains in body weight. Additional host transcriptomic and metabolomic analysis revealed that fatty acid β -oxidation and metabolism of tryptophan and branched chain amino acids play important roles in regulating hepatic metabolism. Across the varying regions of the GIT, we demonstrated that a complex and variable community of bacteria, viruses, and archaea colonized the GIT soon after birth, whereas microbial succession was driven by the cooperative networks of hub populations. Furthermore, GIT volatile fatty acid concentrations were marked by increased microbial metabolic pathway abundances linked to mannose (rumen) and amino acids (colon) metabolism. Significant functional shifts were also revealed across varying GIT tissues, which were dominated by host fatty acid metabolism associated with reactive oxygen species in the rumen epithelium, and the intensive immune response in both small and large intestine. Finally, we reveal a possible contributing role of necroptosis and apoptosis in enhancing ileum and colon epithelium development, respectively. Conclusions Our findings provide a comprehensive view for the involved mechanisms in the context of GIT microbiome and ruminant metabolic growth at early life.

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