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Comparative evaluation of rumen metagenome community using qPCR and MG-RAST

机译:使用qPCR和MG-RAST比较瘤胃基因组学群落

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摘要

Microbial profiling of metagenome communities have been studied extensively using MG-RAST and other related metagenome annotation databases. Although, database based taxonomic profiling provides snapshots of the metagenome architecture, their reliability needs to be validated through more accurate methods. Here, we performed qPCR based absolute quantitation of selected rumen microbes in the liquid and solid fraction of the rumen fluid of river buffalo adapted to varying proportion of concentrate to green or dry roughages and compared with the MG-RAST based annotation of the metagenomes sequences of 16S r-DNA amplicons and high throughput shotgun sequencing. Animals were adapted to roughage-to-concentrate ratio in the proportion of 50:50, 75:25 and 100:00, respectively for six weeks. At the end of each treatment, rumen fluid was collected at 3h post feeding. qPCR revealed that the relative abundance of Prevotella bryantii was higher, followed by the two cellulolytic bacteria Fibrobacter succinogens and Ruminococcus flavefaciens that accounted up to 1.33% and 0.78% of the total rumen bacteria, respectively. While, Selenomonas ruminantium and archaea Methanomicrobiales were lower in microbial population in the rumen of buffalo. There was no statistically significant difference between the enumerations shown by qPCR and analysis of the shotgun sequencing data by MG-RAST except for Prevotella. These results indicate the variations in abundance of different microbial species in buffalo rumen under varied feeding regimes as well as in different fractions of rumen liquor, i.e. solid and the liquid. The results also present the reliability of shotgun sequencing to describe metagenome and analysis/annotation by MG-RAST.
机译:使用MG-RAST和其他相关的元基因组注释数据库对元基因组群落的微生物特征进行了广泛的研究。尽管基于数据库的分类分析提供了元基因组架构的快照,但仍需要通过更准确的方法来验证其可靠性。在这里,我们进行了基于qPCR的绝对定量分析,对水牛河瘤胃液中液体和固体部分中的瘤胃微生物进行了绝对定量,以适应​​浓缩物相对于绿色或干燥粗饲料的变化比例,并与基于MG-RAST的代谢组基因组序列注释进行了比较16S r-DNA扩增子和高通量shot弹枪测序。使动物分别以50:50、75:25和100:00的比例适应粗饲料与浓缩物的比例,持续六周。每次治疗结束时,在喂食后3小时收集瘤胃液。 qPCR结果表明,布鲁氏丙酸杆菌的相对丰度较高,其次是两种纤维素分解细菌琥珀酸纤维杆菌和黄褐球菌,分别占瘤胃细菌总数的1.33%和0.78%。而在水牛的瘤胃中,微生物中的Selenomonas ruminantium和古细菌Methanomicrobiales较低。通过qPCR进行的计数与通过MG-RAST进行的gun弹枪测序数据分析之间的统计上无统计学差异(除普雷沃氏菌外)。这些结果表明,在不同的饲喂方式下,水牛瘤胃中不同微生物种类的丰度变化以及瘤胃液(即固体和液体)的不同馏分。结果还显示了shot弹枪测序描述MG-RAST的元基因组和分析/注释的可靠性。

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