Jin Di, Zhao Shengguo, Zheng Nan, Bu Dengpan, Beckers Yves, Denman Stuart E, McSweeney Christopher S, Wang Jiaqi
State Key Laboratory of Animal Nutrition, Institute of Animal Science, Chinese Academy of Agricultural SciencesBeijing, China; Precision Livestock and Nutrition Unit, Gembloux Agro-Bio Tech, University of LiègeGembloux, Belgium; Laboratory of Quality and Safety Risk Assessment for Dairy Products of Ministry of Agriculture (Beijing), Institute of Animal Science, Chinese Academy of Agricultural SciencesBeijing, China.
State Key Laboratory of Animal Nutrition, Institute of Animal Science, Chinese Academy of Agricultural SciencesBeijing, China; Laboratory of Quality and Safety Risk Assessment for Dairy Products of Ministry of Agriculture (Beijing), Institute of Animal Science, Chinese Academy of Agricultural SciencesBeijing, China.
Front Microbiol. 2017 Mar 7;8:385. doi: 10.3389/fmicb.2017.00385. eCollection 2017.
Ureolytic bacteria are key organisms in the rumen producing urease enzymes to catalyze the breakdown of urea to ammonia for the synthesis of microbial protein. However, little is known about the diversity and distribution of rumen ureolytic microorganisms. The urease gene () has been the target gene of choice for analysis of the urea-degrading microorganisms in various environments. In this study, we investigated the predominant genes of the ureolytic bacteria in the rumen of dairy cows using high-throughput sequencing. Six dairy cows with rumen fistulas were assigned to a two-period cross-over trial. A control group ( = 3) were fed a total mixed ration without urea and the treatment group ( = 3) were fed rations plus 180 g urea per cow per day at three separate times. Rumen bacterial samples from liquid and solid digesta and rumen wall fractions were collected for gene amplification and sequencing using Miseq. The wall-adherent bacteria (WAB) had a distinct ureolytic bacterial profile compared to the solid-adherent bacteria (SAB) and liquid-associated bacteria (LAB) but more than 55% of the sequences did not affiliate with any known taxonomically assigned urease genes. Diversity analysis of the genes showed that the Shannon and Chao1 indices for the rumen WAB was lower than those observed for the SAB and LAB ( < 0.01). The most abundant genes were affiliated with Methylococcaceae, Clostridiaceae, Paenibacillaceae, Helicobacteraceae, and Methylophilaceae families. Compared with the rumen LAB and SAB, relative abundance of the OTUs affiliated with and genera were significantly higher ( < 0.05) in the WAB. Supplementation with urea did not alter the composition of the detected ureolytic bacteria. This study has identified significant populations of ureolytic WAB representing genera that have not been recognized or studied previously in the rumen. The taxonomic classification of rumen genes in the dairy cow indicates that the majority of ureolytic bacteria are yet to be identified. This survey has expanded our knowledge of gene information relating to the rumen ureolytic microbial community, and provides a basis for obtaining regulatory targets of ureolytic bacteria to moderate urea hydrolysis in the rumen.
尿素分解菌是瘤胃中的关键微生物,它们产生脲酶来催化尿素分解为氨,用于合成微生物蛋白。然而,关于瘤胃尿素分解微生物的多样性和分布却知之甚少。脲酶基因()一直是分析各种环境中尿素降解微生物的首选目标基因。在本研究中,我们使用高通量测序技术研究了奶牛瘤胃中尿素分解菌的主要基因。六头装有瘤胃瘘管的奶牛被分配到一个两阶段交叉试验中。对照组( = 3)饲喂不含尿素的全混合日粮,治疗组( = 3)在三个不同时间每天每头奶牛额外饲喂180克尿素。从液体和固体消化物以及瘤胃壁部分采集瘤胃细菌样本,使用Miseq进行基因扩增和测序。与固体附着菌(SAB)和液体相关菌(LAB)相比,壁附着菌(WAB)具有独特的尿素分解细菌谱,但超过55%的序列与任何已知分类学指定的脲酶基因不相关。对基因的多样性分析表明,瘤胃WAB的香农指数和Chao1指数低于SAB和LAB( < 0.01)。最丰富的基因与甲基球菌科、梭菌科、芽孢杆菌科、螺杆菌科和嗜甲基菌科有关。与瘤胃LAB和SAB相比,WAB中与属和属相关的OTU相对丰度显著更高( < 0.05)。添加尿素并未改变检测到的尿素分解菌的组成。本研究确定了大量未被识别或研究过的瘤胃尿素分解WAB代表属。奶牛瘤胃基因的分类表明,大多数尿素分解菌尚未被鉴定。这项调查扩展了我们对瘤胃尿素分解微生物群落相关基因信息的了解,并为获得尿素分解菌的调控靶点以调节瘤胃中的尿素水解提供了依据。