Transcriptomic characterization of the functional and morphological development of the rumen wall in weaned lambs fed a diet containing yeast co-cultures of Saccharomyces cerevisiae and Kluyveromyces marxianus.

IF 2.9 2区 农林科学 Q1 VETERINARY SCIENCES Frontiers in Veterinary Science Pub Date : 2025-01-22 eCollection Date: 2025-01-01 DOI:10.3389/fvets.2025.1510689
Zixuan Xu, Lan Yang, Hui Chen, Pengxiang Bai, Xiao Li, Dacheng Liu
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Abstract

Introduction: In lambs, the function of the rumen is incompletely developed at weaning, and the inclusion of yeast cultures in the diet can profoundly influence the morphological and functional development of the rumen.

Methods: In this study, the effects of Saccharomyces cerevisiae and Kluyveromyces marxianus (NM) yeast co-cultures on ruminal histomorphology were assessed, and corresponding transcriptomic changes within the rumen epithelium were identified. In total, 24 lambs were grouped into four groups of six lambs including a control (C) group fed a basal diet, and N, M, and NM groups in which lambs were fed the basal diet, respectively, supplemented with Saccharomyces cerevisiae yeast cultures (30 g/d per head), Kluyveromyces marxianus yeast cultures (30 g/d per head), and co-cultures of both yeasts (30 g/d per head), the experiment lasted for 42 d.

Results: In morphological analyses, lambs from the NM group presented with significant increases in papilla length, papilla width, and epithelial thickness in the rumen relative to lambs in the C group (p < 0.05). Transcriptomic analyses revealed 202 genes that were differentially expressed between samples from the C and NM groups, with the largest proportion of these genes being associated with the oxidative phosphorylation pathway. In a weighted gene coexpression network analysis, a positive correlation was observed between the MEgreen and MEpurple modules and rumen morphology. Of these modules, the MEgreen module was found to be more closely linked to fatty acid metabolism and oxidative phosphorylation, whereas the MEpurple module was linked to oxidative phosphorylation and fatty acid degradation. Ultimately, these results suggest that dietary supplementation with NM has driven the degradation of fatty acids, the induction of oxidative phosphorylation, the acceleration of lipid metabolism, the production of ATP to sustain ruminal growth, and the maintenance of intracellular NADH/NAD+ homeostasis on weaned lambs and is superior to single yeast fermentation.

Discussion: These results thus offer a theoretical foundation for further studies examining the mechanisms through which NM cultures can influence ruminal development in lambs.

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饲喂酵母与酿酒酵母共培养的断奶羔羊瘤胃壁功能和形态发育的转录组学特征
摘要:羔羊在断奶时瘤胃功能发育不完全,饲粮中添加酵母培养物会对瘤胃形态和功能发育产生深远影响。方法:研究了酿酒酵母和马氏克鲁维酵母(NM)共培养物对瘤胃组织形态学的影响,并鉴定了瘤胃上皮内相应的转录组变化。将24只羔羊分为4组,每组6只,其中对照组饲喂基础饲粮,N、M、NM组分别饲喂基础饲粮,在基础饲粮中添加酿酒酵母培养物(30 g/d /头)、马氏克卢维酵母培养物(30 g/d /头)和两种酵母的共培养物(30 g/d /头),试验期42 d。形态学分析显示,与C组相比,NM组羔羊瘤胃乳头长度、宽度和上皮厚度均显著增加(p < 0.05)。转录组学分析显示,C组和NM组样品之间存在202个基因差异表达,其中大部分基因与氧化磷酸化途径相关。在加权基因共表达网络分析中,MEgreen和MEpurple模块与瘤胃形态呈正相关。在这些模块中,MEgreen模块被发现与脂肪酸代谢和氧化磷酸化联系更紧密,而MEpurple模块与氧化磷酸化和脂肪酸降解联系更紧密。综上所述,饲粮中添加NM可促进断奶羔羊脂肪酸降解,诱导氧化磷酸化,加速脂质代谢,产生ATP以维持瘤胃生长,维持细胞内NADH/NAD+稳态,且优于单一酵母发酵。讨论:因此,这些结果为进一步研究NM培养物影响羔羊瘤胃发育的机制提供了理论基础。
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来源期刊
Frontiers in Veterinary Science
Frontiers in Veterinary Science Veterinary-General Veterinary
CiteScore
4.80
自引率
9.40%
发文量
1870
审稿时长
14 weeks
期刊介绍: Frontiers in Veterinary Science is a global, peer-reviewed, Open Access journal that bridges animal and human health, brings a comparative approach to medical and surgical challenges, and advances innovative biotechnology and therapy. Veterinary research today is interdisciplinary, collaborative, and socially relevant, transforming how we understand and investigate animal health and disease. Fundamental research in emerging infectious diseases, predictive genomics, stem cell therapy, and translational modelling is grounded within the integrative social context of public and environmental health, wildlife conservation, novel biomarkers, societal well-being, and cutting-edge clinical practice and specialization. Frontiers in Veterinary Science brings a 21st-century approach—networked, collaborative, and Open Access—to communicate this progress and innovation to both the specialist and to the wider audience of readers in the field. Frontiers in Veterinary Science publishes articles on outstanding discoveries across a wide spectrum of translational, foundational, and clinical research. The journal''s mission is to bring all relevant veterinary sciences together on a single platform with the goal of improving animal and human health.
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