Waters S M, Roskam E, Smith P E, Kenny D A, Popova M, Eugène M, Morgavi D P
School of Biological and Chemical Sciences and Ryan Institute, University of Galway, Galway, H91 TK33, Ireland.
School of Biological and Chemical Sciences and Ryan Institute, University of Galway, Galway, H91 TK33, Ireland; Animal and Bioscience Department, Teagasc Grange, Dunsany, Co. Meath, C15 PW93, Ireland.
J Dairy Sci. 2025 Jul;108(7):7591-7606. doi: 10.3168/jds.2024-25778. Epub 2025 Jan 29.
Ruminants play an important role in global food security and nutrition. The rumen microbial community provides ruminants with a unique ability to convert human indigestible plant matter into high quality edible protein. However, enteric CH produced in the rumen is both a potent GHG and a ME loss for ruminants. As the rumen microbiome constitutes 15% to 40% of the interanimal variation in enteric CH emissions, understanding the microbiological mechanisms underpinning ruminal methanogenesis and its interaction with the host animal is crucial for developing CH mitigation strategies. Variation in the relative abundance of different microbial species has been observed in cattle with contrasting residual CH emission and CH yield, with up to 20% of the variation in interanimal CH emissions attributable to the presence of a small number of microbial species. The demonstration of ruminotypes associated with high or low CH emissions suggests that interactions within complex microbial consortia and with their host are a major source of variation in CH emissions. Consequently, microbiome-assisted genomic approaches are being developed to select low CH-emitting cattle, with breeding values for enteric CH being included as part of national breeding programs. Generating rumen microbiome data for use in selection programs is expensive, therefore, identifying microbial biomarkers in milk or plasma to develop predictive models which include microbial predictors in equations based on animal-related data is required. A better understanding of the rumen microbiome has also aided the development and refinements of antimethanogenic feed additives. However, these strategies, which increase the amount of reducing equivalents in the rumen ecosystem, do not generally result in an enrichment of propionate or an improvement in animal performance. Current research aims to provide alternative sinks to reducing equivalents and to stimulate activity of commensal microbes or the supplementation of direct fed microbials to capture lost energy. Furthering our knowledge of the rumen microbiome and its interaction with the host will aid in the development of CH mitigation strategies for ruminant livestock.
反刍动物在全球粮食安全和营养方面发挥着重要作用。瘤胃微生物群落赋予反刍动物一种独特能力,即将人类无法消化的植物物质转化为高质量的可食用蛋白质。然而,瘤胃中产生的肠道甲烷既是一种强效温室气体,也是反刍动物的能量损失。由于瘤胃微生物群占动物间肠道甲烷排放差异的15%至40%,了解瘤胃甲烷生成的微生物学机制及其与宿主动物的相互作用对于制定甲烷减排策略至关重要。在具有不同残余甲烷排放和甲烷产量的牛中,已观察到不同微生物物种相对丰度的差异,动物间甲烷排放差异的高达20%可归因于少数微生物物种的存在。与高或低甲烷排放相关的瘤胃类型的证明表明,复杂微生物群落内部及其与宿主的相互作用是甲烷排放差异的主要来源。因此,正在开发微生物组辅助基因组方法来选择低甲烷排放的牛,肠道甲烷的育种值已被纳入国家育种计划。生成用于选择计划的瘤胃微生物组数据成本高昂,因此,需要在牛奶或血浆中识别微生物生物标志物,以开发预测模型,这些模型在基于动物相关数据的方程中纳入微生物预测因子。对瘤胃微生物组的更好理解也有助于抗甲烷生成饲料添加剂的开发和改进。然而,这些增加瘤胃生态系统中还原当量数量的策略通常不会导致丙酸的富集或动物生产性能的改善。当前的研究旨在为还原当量提供替代汇,并刺激共生微生物的活性或补充直接投喂的微生物以捕获损失的能量。加深我们对瘤胃微生物组及其与宿主相互作用的了解将有助于制定反刍家畜的甲烷减排策略。