肠道微生物组肠型通过宿主-微生物代谢串扰驱动奶山羊不同的泌乳性能。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Dangdang Wang, Qingyan Yin, Guangfu Tang, Li Sun, Junjian Yu, Yangchun Cao, Junhu Yao
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引用次数: 0

摘要

肠道微生物组在调节反刍动物的营养代谢和泌乳效率中起着关键作用,但其肠型的功能分层及其对奶山羊的影响仍未得到深入研究。在这里,我们在134只哺乳期奶山羊中发现了两种不同的肠道微生物肠道类型:TR-cluster (n = 43)富含Turicibacter, Romboutsia和Clostridium sensu stricto 1,而CO-cluster (n = 91)富含Christensenellaceae R-7和Oscillospiraceae UCG-005。tr组山羊的产奶量、脂肪校正产奶量和乳脂产量均较高,肠道中总挥发性脂肪酸(VFA)(包括乙酸、丙酸和丁酸)浓度升高,血清葡萄糖和总胆汁酸水平升高。尽管微生物多样性较低,但tr -簇在能量代谢、氨基酸代谢和脂质生物合成等代谢途径上功能丰富,而co -簇在膜转运和遗传信息处理方面功能丰富。共现网络分析揭示了不同的微生物相互作用模式和重点类群,tr -集群显示出更复杂的模块间连通性。此外,相关分析表明,tr簇富集的属,如Turicibacter和Romboutsia,与增强肠道发酵和改善泌乳性状呈正相关。总的来说,这些发现表明,肠道微生物肠型与奶山羊的肠道发酵和泌乳性状密切相关,为提高反刍动物生产力的微生物群靶向策略提供了新的见解。重要性:奶山羊对全球产奶量至关重要,但导致泌乳性能个体差异的肠道微生物驱动机制在很大程度上仍然未知。据我们所知,这是迄今为止最大的队列研究,全面表征了泌乳山羊的肠道微生物组肠型,并确定了它们对肠道发酵、宿主代谢和产奶量的影响。我们确定了两种不同的肠道类型,具有不同的微生物特征,功能能力和生态结构。值得注意的是,以Turicibacter, Romboutsia和Clostridium sensu stricto 1为主的肠道型与改善泌乳性能,提高VFA产量和有益的代谢特征有关。关键分类群和肠道特异性微生物相互作用的鉴定为反刍动物宿主-微生物组关系的研究提供了新的视角。我们的研究结果为精确的微生物组管理和有针对性的干预奠定了基础,以提高奶牛的健康和生产力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbiome enterotypes drive divergent lactation performance in dairy goats through host-microbe metabolic cross-talk.

The gut microbiome plays a pivotal role in modulating nutrient metabolism and lactation efficiency in ruminants, yet its functional stratification into enterotypes and implications for dairy goats remain unexplored. Here, we identified two distinct gut microbiome enterotypes in 134 lactating dairy goats: TR-cluster (n = 43) was enriched in Turicibacter, Romboutsia, and Clostridium sensu stricto 1, while CO-cluster (n = 91) exhibited higher abundance of Christensenellaceae R-7 and Oscillospiraceae UCG-005. Goats in the TR-cluster exhibited higher milk yield, fat-corrected milk yield, and milk fat yield, along with increased concentrations of total volatile fatty acids (VFA), including acetate, propionate, and butyrate in the gut, as well as elevated serum glucose and total bile acids levels. Despite lower microbial diversity, the TR-cluster was functionally enriched in metabolic pathways related to energy metabolism, amino acid metabolism, and lipid biosynthesis, whereas the CO-cluster showed enrichment in membrane transport and genetic information processing. Co-occurrence network analysis revealed distinct microbial interaction patterns and keystone taxa, with the TR-cluster displaying more complex inter-module connectivity. Moreover, correlation analyses demonstrated that TR-cluster-enriched genera, such as Turicibacter and Romboutsia, were positively associated with enhanced gut fermentation and improved lactation traits. Overall, these findings reveal that gut microbial enterotypes are strongly linked to gut fermentation and lactation traits in dairy goats, offering novel insights for microbiota-targeted strategies to improve ruminant productivity.

Importance: Dairy goats are critical for global milk production, yet the gut microbiome-driven mechanisms that underlie individual differences in lactation performance remain largely unknown. To our knowledge, this is the largest cohort study to date that comprehensively characterizes gut microbiome enterotypes in lactating dairy goats and establishes their impact on gut fermentation, host metabolism, and milk production. We identified two distinct enterotypes with different microbial signatures, functional capacities, and ecological structures. Notably, the enterotype dominated by Turicibacter, Romboutsia, and Clostridium sensu stricto 1 was associated with improved lactation performance, enhanced VFA production, and beneficial metabolic profiles. The identification of keystone taxa and enterotype-specific microbial interactions offers a new perspective on host-microbiome relationships in ruminants. Our findings lay the foundation for precision microbiome management and targeted interventions to enhance the health and productivity of dairy animals.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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