在泌乳奶牛发生以谷物为基础的亚急性瘤胃酸中毒(SARA)期间,酵母菌发酵产生的后益生菌可稳定瘤胃液体消化液中的微生物群。

IF 6.3 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Junfei Guo, Zhengxiao Zhang, Le Luo Guan, Ilkyu Yoon, Jan C Plaizier, Ehsan Khafipour
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引用次数: 0

摘要

背景:亚急性瘤胃酸中毒(SARA)是高产奶牛的一种常见代谢紊乱,与瘤胃和肠道微生物群失调以及宿主炎症有关。本研究评估了两种来自酿酒酵母发酵产物(SCFP)的益生元对反复接受谷物型 SARA 挑战的泌乳奶牛瘤胃液体相关微生物群的影响。从产前 4 周到产后 12 周,总共 32 头瘤胃插管奶牛被随机分配到 4 个处理组。处理组包括对照组日粮或添加益生元的日粮(SCFPa,14 克/天 Original XPC;SCFPb-1X,19 克/天 NutriTek;SCFPb-2X,38 克/天 NutriTek,Diamond V,美国爱荷华州锡达拉皮兹)。在产后第 5 周(SARA1)和第 8 周(SARA2)进行谷物 SARA 挑战,用含有 50% 磨碎大麦和 50% 磨碎小麦的颗粒饲料取代 20% DM 的基础混合饲料 (TMR)。对瘤胃液体样本的总 DNA 进行 V3-V4 16S rRNA 基因扩增片段测序。比较了不同处理和 SARA 阶段的瘤胃微生物群特征:结果:两种 SARA 挑战都降低了瘤胃液体微生物群的多样性和丰富度,改变了整体组成(β-多样性)及其预测功能,包括碳水化合物和氨基酸代谢途径。SARA 挑战还减少了微生物共现网络中不同类群之间显著关联的数量、中心类群的数量及其组成。补充 SCFP 后益生菌,尤其是 SCFPb-2X,可增强瘤胃微生物群的稳健性。补充了 SCFP 的奶牛在面临 SARA 挑战时,群落成员的相对丰度波动较小。补充 SCFP 能促进乳酸利用菌和纤维分解菌(包括反刍球菌科和 Lachnospiraceae 成员)的数量,还能在非 SARA 和 SARA 阶段增加中枢类群的数量。补充 SCFPb-2X 可防止瘤胃液消化物中与醋酸盐浓度、α 和 β 多样性指标呈正相关的中心分类群的丰度波动:结论:诱导 SARA 挑战降低了泌乳奶牛瘤胃液微生物群的丰富度和多样性,并引起了瘤胃液微生物群中主要细菌系统的波动。补充 SCFP 后益生菌可减轻 SARA 对瘤胃液微生物群的不利影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Postbiotics from Saccharomyces cerevisiae fermentation stabilize microbiota in rumen liquid digesta during grain-based subacute ruminal acidosis (SARA) in lactating dairy cows.

Background: Subacute ruminal acidosis (SARA) is a common metabolic disorder of high yielding dairy cows, and it is associated with dysbiosis of the rumen and gut microbiome and host inflammation. This study evaluated the impact of two postbiotics from Saccharomyces cerevisiae fermentation products (SCFP) on rumen liquid associated microbiota of lactating dairy cows subjected to repeated grain-based SARA challenges. A total of 32 rumen cannulated cows were randomly assigned to 4 treatments from 4 weeks before until 12 weeks after parturition. Treatment groups included a Control diet or diets supplemented with postbiotics (SCFPa, 14 g/d Original XPC; SCFPb-1X, 19 g/d NutriTek; SCFPb-2X, 38 g/d NutriTek, Diamond V, Cedar Rapids, IA, USA). Grain-based SARA challenges were conducted during week 5 (SARA1) and week 8 (SARA2) after parturition by replacing 20% DM of the base total mixed ration (TMR) with pellets containing 50% ground barley and 50% ground wheat. Total DNA from rumen liquid samples was subjected to V3-V4 16S rRNA gene amplicon sequencing. Characteristics of rumen microbiota were compared among treatments and SARA stages.

Results: Both SARA challenges reduced the diversity and richness of rumen liquid microbiota, altered the overall composition (β-diversity), and its predicted functionality including carbohydrates and amino acids metabolic pathways. The SARA challenges also reduced the number of significant associations among different taxa, number of hub taxa and their composition in the microbial co-occurrence networks. Supplementation with SCFP postbiotics, in particular SCFPb-2X, enhanced the robustness of the rumen microbiota. The SCFP supplemented cows had less fluctuation in relative abundances of community members when exposed to SARA challenges. The SCFP supplementation promoted the populations of lactate utilizing and fibrolytic bacteria, including members of Ruminococcaceae and Lachnospiraceae, and also increased the numbers of hub taxa during non-SARA and SARA stages. Supplementation with SCFPb-2X prevented the fluctuations in the abundances of hub taxa that were positively correlated with the acetate concentration, and α- and β-diversity metrics in rumen liquid digesta.

Conclusions: Induction of SARA challenges reduced microbiota richness and diversity and caused fluctuations in major bacterial phyla in rumen liquid microbiota in lactating dairy cows. Supplementation of SCFP postbiotics could attenuate adverse effects of SARA on rumen liquid microbiota.

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