首页> 美国卫生研究院文献>Journal of Animal Science >PSXIV-23 Characterization of microbial communities associated with the rumen lining digesta and rumen fluid from beef cattle consuming a high energy diet using 16S rRNA gene amplicon sequencing
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PSXIV-23 Characterization of microbial communities associated with the rumen lining digesta and rumen fluid from beef cattle consuming a high energy diet using 16S rRNA gene amplicon sequencing

机译:PSXIV-23使用16S rRNA基因扩增子测序从牛肉衬里Digesta和瘤胃流体相关的微生物衬里馏分和瘤胃液相关的微生物组合的表征

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摘要

The true etiology of liver abscesses is not well known. Therefore, the objective of this study was to characterize the microbial communities in the rumen lining, digesta, and rumen fluid from beef cattle consuming a high energy diet, using 16S rRNA gene amplicon sequencing. Twelve crossbred feedlot steers (450 ±10 kg; ~ 3.0 years of age) fitted with ruminal fistulas, consuming a high energy finishing diet (1.43 NEg, Mcal/kg DM) for 21 d were utilized in this experiment. Microbial DNA from three regions within the rumen [rumen lining (ventral/lateral), digesta (geometric center of the rumen), and rumen fluid] was extracted and the V4 region of the 16S rRNA gene was amplified and sequenced. Across all sample regions, bacterial sequences were classified into 34 phyla, 76 classes, 143 orders, and 254 families. Bacteroidetes and Firmicutes were the predominant phyla present across all samples. The relative abundance of Bacteroidetes detected in rumen fluid was lesser (P < 0.05) when compared to bacteria sampled from the rumen lining and digesta. In contrast, the relative abundance of Firmicutes were greater (P < 0.05) in rumen fluid and the rumen lining when compared to digesta samples. There are very few publications describing the complex community of the rumen microbiome. To our knowledge this is the first publication categorizing microbial populations in three distinct locations within the rumen using next generation sequencing in feedlot cattle.
机译:肝脏脓肿的真实病因并不众所周知。因此,本研究的目的是使用16S rRNA基因扩增子测序来表征瘤胃衬里,Digesta和瘤胃牛的瘤胃流体中的微生物群。在本实验中使用了12次杂交饲料带(450±10kg;〜3〜3〜3〜3〜3.0岁)。在本实验中使用了21d的高能完成饮食(1.43NEG,MCAL / KG DM)。提取来自瘤胃内的三个区域的微生物DNA [瘤胃衬里(腹侧/侧面),腔内(瘤胃的几何中心)和瘤胃流体],并扩增16S rRNA基因的V4区并测序。在所有样本区域,细菌序列分为34个耕作,76级,143个订单和254个家庭。菌兵和迫切性是所有样品中存在的主要phyla。与从瘤胃衬里和Digesta取样的细菌相比,在瘤胃液中检测到的细菌的相对丰度较小(P <0.05)。相比之下,与Digesta样品相比,瘤胃液中的相对丰度更大(P <0.05)和瘤胃衬里。很少有描述瘤胃微生物组的复杂社区的出版物。据我们所知,这是第一次在瘤胃内使用下一代测序在瘤胃中的三个不同位置进行分类的出版物。

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