EDITORIAL article

Front. Vet. Sci.

Sec. Animal Nutrition and Metabolism

Volume 12 - 2025 | doi: 10.3389/fvets.2025.1610490

This article is part of the Research TopicCrosslinking of feed nutrients, microbiome and production in ruminantsView all 17 articles

Editorial: Crosslinking of feed nutrients, microbiome and production in ruminants

Provisionally accepted
  • 1College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, Hubei Province, China
  • 2Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, Beijing, China
  • 3Department of Animal Science and Technology, College of Animal Science, Zhejiang University, Hangzhou, Zhejiang Province, China
  • 4Department of Immunobiology, School of Medicine, Yale University, New Haven, Connecticut, United States
  • 5Department of Animal Nutrition and Feed Science, College of Animal Science and Technology, Faculty of Animal Science, Nanjing Agricultural University, Nanjing, Liaoning Province, China

The final, formatted version of the article will be published soon.

In ruminants, the rumen serves as the primary organ responsible for converting plant-based feed into nutrients and energy. Research indicated that microbial derivatives, dietary composition, and host metabolism collectively affect rumen metabolite concentrations and microbial community structure, shaping the mechanisms of host-microbiota interactions (1). Ruminants rely on symbiotic relationships with complex rumen microbial communities, which specialize in degrading recalcitrant plant polymers such as cellulose and hemicellulose, converting them into digestible compounds. These microbes are critical for the productivity and health of ruminants, directly contributing to volatile fatty acid (VFA) production and microbial protein biosynthesis, which are essential for milk efficiency (2). Additionally, bacterial communities influence growth performance as well as milk yield and composition in dairy cattle (3). Conversely, rumen microbiota structure is modulated by host species, dietary energy levels, and environmental factor (4). This topic primarily explores nutritional interventions to regulate growth performance, rumen fermentation, and microbial composition in ruminants.Diet and feed additives are potent modulators of rumen microbiota, serving as substrates for microbial metabolism and thereby altering rumen environments and species composition. Early dietary interventions may help establish rumen microbial communities, leading to long-term changes in community structure and function, ultimately affecting host phenotypes (5). For instance, Liu et al. found that supplementing 0.3% moringa polysaccharides in milk replacer for early-weaned goat kids increased average daily gain (ADG), feed intake, serum immunoglobulins (IgA and IgM), rumen muscle thickness, rumen wall thickness, and rumen pH, while also enriching Actinobacteria and Butyrivibrio species in the rumen. Zhang et al. reported that adding 1,500 mg/kg guanidinoacetic acid to the diet elevated ruminal ammonia nitrogen concentration and total reducing sugar flow into the small intestine, improving creatine levels, glucose utilization, and ADG in lambs. Hou et al. demonstrated that 5% residual black wolfberry fruit supplementation enhanced growth performance in Duolang sheep, optimized rumen fermentation parameters without negatively affecting microbial structure, and improved economic returns. Luo et al. found that nisin and monensin supplementation in fattening Hu sheep reduced ruminal acetate concentration and altered fermentation patterns but did not affect growth performance or health.Studies suggested that fermented feed products can enhance antioxidant and immune capacity, improve rumen fermentation, and modulate microbial communities in ruminants (6). Cheng et al. reported that 15% fermented rice husk feed improved growth performance, nutrient digestibility, and ruminal propionate, butyrate, and valerate concentrations in Hu sheep, while enriching fiber-degrading bacteria (e.g., Ruminococcus) and suppressing inefficient taxa (e.g., Rikenellaceae RC9). Thus, fermented rice husk represents a promising alternative to conventional roughage. Zhang et al. observed that fermented soybean meal did not affect milk yield in lactating cows but increased serum prolactin levels and altered rumen microbiota, potentially benefiting long-term health and productivity. Liu et al. demonstrated that dietary fermented jujube powder (FJP) enhanced ADG and feed efficiency by promoting nutrient degradation and VFA production via microbial enzyme activity. Additionally, elevated serum total antioxidant capacity and reduced malondialdehyde levels indicated improved oxidative defense, underscoring FJP's potential as a functional feed additive.Yeast culture (YC), a feed additive rich in yeast cell wall components (e.g., mannan oligosaccharides, and β-glucans) and fermentation metabolites (e.g., organic acids, B vitamins, and enzymes), stabilizes rumen pH and promotes fiber-degrading bacteria, enhancing feed efficiency (7). Li et al. found that 10 g/d YC supplementation in dairy goats increased milk yield and ruminal acetate, butyrate, and VFA concentrations while reducing NH₃-N levels, suggesting improved microbial protein synthesis. Zhang et al. reported that Saccharomyces cerevisiae-fermented sorghum distillers' grains reduced weight loss in early-lactation goats and improved milk quality, likely via bile acid and caffeine metabolism pathways linked to energy and immune regulation.Milk, a vital nutrient source for humans, contains lactose, triglycerides, proteins, minerals, and vitamins. β-casein, a major milk protein, exists in two primary genotypes (A1 and A2), differing at position 67 (histidine in A1, proline in A2). A2 milk (from A2A2 genotype cows) is considered more digestible and health-promoting. Zhao et al. identified unique rumen microbial and metabolic profiles (e.g., arachidonic acid, adrenic acid, glycocholic acid, taurine, and g_Acetobacter) in A2A2 cows, correlating with higher milk fat content. Arachidonic acid, a key biomarker, may enhance milk fat synthesis by activating lipogenic genes. Amino acids (AAs), the building blocks of proteins, are central to protein nutrition. Reducing dietary protein levels while supplementing limiting AAs (e.g., lysine and methionine) can meet ruminant requirements. Wang et al. showed that a 3 : 1 ratio of rumen-protected Lys and Met in Holstein bulls improved nitrogen efficiency and stabilized rumen microbiota without compromising intake or digestibility, offering a strategy for stress-resistant feeding. L-carnosine, a dipeptide with antioxidant and anti-inflammatory properties, was shown by Meng et al. to enhance growth performance in fattening lambs by modulating gut microbiota and serum metabolites, promoting protein synthesis and energy metabolism.Alfalfa hay, a widely used forage in livestock production due to its high palatability, low fiber content, and high protein content (17%-22%), exhibits nutrient variability depending on cultivar, storage method, and harvest stage, which may influence dairy cow performance and rumen microbiota. La et al. observed that while alfalfa hay from different sources (Spanish SAH vs. American AAH) significantly altered rumen microbial composition and function in dairy cows, these changes did not affect production performance, nutrient digestibility, or blood biochemical parameters. This suggested SAH as a viable alternative to mitigate market supply fluctuations while maintaining productivity.As demand for high-quality dairy and beef rises, Holstein cattle-a globally dominant dairy breed-have been extensively studied, whereas indigenous breeds like Chinese Sanhe cattle (dualpurpose for milk and meat) remain under-researched. Liu et al. compared rumen microbiota between multiparous Sanhe and Holstein cows, finding similar species composition but abundance variations by parity and breed. Rumen ecology strongly correlated with metabolic patterns, yet breed remained the decisive factor for productivity. Crossbreeding, a strategy to enhance growth and feed efficiency, introduces superior traits into local breeds. Zhang et al. demonstrated that crossbreeding altered rumen microbiota and metabolites, significantly improving growth. ♂Poll Dorset × ♀Hu crosses enhanced fiber fermentation and energy supply, while ♂Southdown × ♀Hu crosses optimized amino acid metabolism for protein synthesis, providing insights for breeding and nutrition strategies.In summary, ruminant digestion relies on intricate host-microbe symbiosis, where feed nutrients shape microbial activity, influencing nutrient absorption and production outcomes. Future research should focus on precision microbiota modulation, functional feed development, and sustainable farming to enhance productivity, product quality, and environmental stewardship. These advances will revolutionize ruminant production systems.

Keywords: Ruminants, Feed nutrients, Rumen microbiome, Rumen fermentation, interactions

Received: 12 Apr 2025; Accepted: 02 Jun 2025.

Copyright: © 2025 Xu, Du, Xu, Hu, Zhao, Li, Song and Shen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Qingbiao Xu, College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, 430070, Hubei Province, China

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