Center for Animal Nutrition and Welfare, Clinical Department for Farm Animals and Food System Science, University of Veterinary Medicine Vienna, Vienna, Austria.
Christian Doppler Laboratory for Innovative Gut Health Concepts of Livestock, Vienna, Austria.
Microbiol Spectr. 2024 Oct 3;12(10):e0094424. doi: 10.1128/spectrum.00944-24. Epub 2024 Aug 20.
This study explores the dynamics of immune gene expression, ruminal metabolome, and gut microbiota in cows due to the duration of high-grain feeding, shedding light on host response and microbial dynamics in parallel. Cows consumed forage for a week, then gradually transitioned to a high-grain diet, which they consumed for 4 weeks. Immune response was evaluated in ruminal papillae by expression of genes related to the nuclear factor-kappaB (NFkB) pathway and correlated with the microbiota. Rumen metabolome was evaluated with high-performance liquid chromatography coupled with mass spectrometry and anion-exchange chromatography. Rumen and fecal microbiota were evaluated with 16S rRNA gene amplicon sequencing. In the rumen, expression of inflammation-associated genes increased with the duration on high grain, indicating activation of pro-inflammatory cascades; microbial diversity decreased with a high-grain diet but stabilized after week 3 on high grain. Changes in microbial relative abundance and metabolite enrichment were observed throughout the 4 weeks on high grain, with increments in propionogenic taxa (i.e., ). Metabolite enrichment analysis showed that at the start of high-grain feeding, simple carbohydrates were enriched; then, these were substituted by their fermentation products. There were correlations between certain ruminal bacterial taxa (i.e., UCG-005) and expression of genes of the NFkB pathway, suggesting the influence of these taxa on host immune response. In feces, microbial diversity and several members initially declined but recovered by weeks 3 and 4. Overall, despite the stabilization of microbial diversity, changes in microbial relative abundance and proinflammatory genes were observed throughout high-grain feeding, suggesting that cows need more than 4 weeks to fully adjust once consuming a high-grain diet.IMPORTANCEDespite the stepwise diet transition typically assumed to serve for animal adaptation, expression of signaling receptors, mediators, and downstream targets of nuclear factor-kappaB pathway were found throughout the 4 weeks on high grain, which correlated with changes in the rumen microbial profile. In addition, although microbial diversity recovered in the feces and stabilized in the rumen in week 3 on high grain, we observed changes in microbial relative abundance throughout the 4 weeks on high grain, suggesting that cows need more than 4 weeks to adjust once consuming this diet. Findings are particularly important to consider when planning experiments involving dietary changes.
本研究探讨了奶牛因高谷物喂养时间而导致的免疫基因表达、瘤胃代谢组和肠道微生物群的动态变化,揭示了宿主反应和微生物动态变化是平行的。奶牛先采食饲草一周,然后逐渐过渡到高谷物日粮,持续 4 周。通过核因子-κB(NFkB)途径相关基因的表达来评估瘤胃乳头的免疫反应,并与微生物群相关联。通过高效液相色谱与质谱联用和阴离子交换色谱评估瘤胃代谢组。通过 16S rRNA 基因扩增子测序评估瘤胃和粪便微生物群。在瘤胃中,与炎症相关的基因表达随着高谷物喂养时间的增加而增加,表明促炎级联反应的激活;高谷物日粮使微生物多样性降低,但在第 3 周后趋于稳定。在高谷物喂养的 4 周内,观察到微生物相对丰度和代谢物富集的变化,丙酸产生菌(即 )增加。代谢物富集分析表明,在高谷物喂养的初始阶段,简单碳水化合物被富集;然后,它们被发酵产物取代。某些瘤胃细菌分类群(即 UCG-005)与 NFkB 途径基因的表达之间存在相关性,这表明这些分类群对宿主免疫反应的影响。在粪便中,微生物多样性和几个 成员最初下降,但在第 3 和第 4 周恢复。总体而言,尽管微生物多样性趋于稳定,但在高谷物喂养期间仍观察到微生物相对丰度和促炎基因的变化,这表明奶牛在开始高谷物日粮后需要 4 周以上的时间才能完全适应。
重要的是,尽管通常假设逐步的饮食过渡有助于动物适应,但在高谷物喂养的 4 周内都发现了 NFkB 途径的信号受体、介质和下游靶基因的表达,这与瘤胃微生物群谱的变化相关。此外,尽管在高谷物喂养的第 3 周,粪便中的微生物多样性恢复且在瘤胃中趋于稳定,但在高谷物喂养的 4 周内,我们观察到微生物相对丰度的变化,这表明奶牛在开始这种饮食后需要 4 周以上的时间才能适应。这些发现对于在涉及饮食变化的实验中非常重要,应考虑这些发现。