Wetzels Stefanie U, Mann Evelyne, Metzler-Zebeli Barbara U, Pourazad Poulad, Qumar Muhammad, Klevenhusen Fenja, Pinior Beate, Wagner Martin, Zebeli Qendrim, Schmitz-Esser Stephan
Department for Farm Animals and Veterinary Public Health, Institute of Animal Nutrition and Functional Plant Compounds, University of Veterinary Medicine ViennaVienna, Austria; Department of Farm Animal and Public Health in Veterinary Medicine, Institute for Milk Hygiene, Milk Technology and Food Science, University of Veterinary Medicine ViennaVienna, Austria; Department for Farm Animals and Veterinary Public Health, Research Cluster Animal Gut Health, University of Veterinary Medicine ViennaVienna, Austria.
Department of Farm Animal and Public Health in Veterinary Medicine, Institute for Milk Hygiene, Milk Technology and Food Science, University of Veterinary Medicine ViennaVienna, Austria; Department for Farm Animals and Veterinary Public Health, Research Cluster Animal Gut Health, University of Veterinary Medicine ViennaVienna, Austria.
Front Microbiol. 2016 Mar 4;7:274. doi: 10.3389/fmicb.2016.00274. eCollection 2016.
The impact of a long-term subacute rumen acidosis (SARA) on the bovine epimural bacterial microbiome (BEBM) and its consequences for rumen health is poorly understood. This study aimed to investigate shifts in the BEBM during a long-term transient SARA model consisting of two concentrate-diet-induced SARA challenges separated by a 1-week challenge break. Eight cows were fed forage and varying concentrate amounts throughout the experiment. In total, 32 rumen papilla biopsies were taken for DNA isolation (4 sampling time points per cow: at the baseline before concentrate was fed, after the first SARA challenge, after the challenge break, and after the second SARA challenge). Ruminal pH was continuously monitored. The microbiome was determined using Illumina MiSeq sequencing of the 16S rRNA gene (V345 region). In total 1,215,618 sequences were obtained and clustered into 6833 operational taxonomic units (OTUs). Campylobacter and Kingella were the most abundant OTUs (16.5 and 7.1%). According to ruminal pH dynamics, the second challenge was more severe than the first challenge. Species diversity estimates and evenness increased during the challenge break compared to all other sampling time points (P < 0.05). During both SARA challenges, Kingella- and Azoarcus-OTUs decreased (0.5 and 0.4 fold-change) and a dominant Ruminobacter-OTU increased during the challenge break (18.9 fold-change; P < 0.05). qPCR confirmed SARA-related shifts. During the challenge break noticeably more OTUs increased compared to other sampling time points. Our results show that the BEBM re-establishes the baseline conditions slower after a SARA challenge than ruminal pH. Key phylotypes that were reduced during both challenges may help to establish a bacterial fingerprint to facilitate understanding effects of SARA conditions on the BEBM and their consequences for the ruminant host.
长期亚急性瘤胃酸中毒(SARA)对牛瘤胃壁细菌微生物群(BEBM)的影响及其对瘤胃健康的后果目前了解甚少。本研究旨在调查在长期短暂SARA模型中BEBM的变化,该模型由两次精料日粮诱导的SARA挑战组成,中间间隔1周的挑战间歇期。在整个实验过程中,给8头奶牛饲喂草料和不同量的精料。总共采集了32份瘤胃乳头活检样本用于DNA提取(每头奶牛4个采样时间点:饲喂精料前的基线期、第一次SARA挑战后、挑战间歇期后以及第二次SARA挑战后)。持续监测瘤胃液pH值。使用Illumina MiSeq对16S rRNA基因(V345区域)进行测序来确定微生物群。总共获得了1,215,618条序列,并聚类为6833个操作分类单元(OTU)。弯曲杆菌属和金氏菌属是最丰富的OTU(分别占16.5%和7.1%)。根据瘤胃液pH动态变化,第二次挑战比第一次挑战更严重。与所有其他采样时间点相比,挑战间歇期的物种多样性估计值和均匀度增加(P<0.05)。在两次SARA挑战期间,金氏菌属和固氮弧菌属OTU减少(变化倍数分别为0.5和0.4),而在挑战间歇期一个占主导的瘤胃杆菌属OTU增加(变化倍数为18.9;P<0.05)。定量PCR证实了与SARA相关的变化。与其他采样时间点相比,在挑战间歇期明显有更多的OTU增加。我们的结果表明,SARA挑战后BEBM恢复到基线条件的速度比瘤胃液pH值慢。在两次挑战期间减少的关键系统发育型可能有助于建立细菌指纹,以促进理解SARA条件对BEBM的影响及其对反刍动物宿主的后果。