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首页> 外文期刊>Applied and Environmental Microbiology >Estimation of the Relative Abundance of DifferentBacteroides and Prevotella Ribotypes in Gut Samples by Restriction Enzyme Profiling of PCR-Amplified 16S rRNA Gene Sequences
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Estimation of the Relative Abundance of DifferentBacteroides and Prevotella Ribotypes in Gut Samples by Restriction Enzyme Profiling of PCR-Amplified 16S rRNA Gene Sequences

机译:通过PCR扩增的16S rRNA基因序列的限制性内切酶分析估算肠道样品中不同拟杆菌和核小球藻核型的相对丰度

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We describe an approach for determining the genetic composition ofBacteroides and Prevotellapopulations in gut contents based on selective amplification of 16S rRNA gene sequences (rDNA) followed by cleavage of the amplified material with restriction enzymes. The relative contributions of different ribotypes to total Bacteroides andPrevotella 16S rDNA are estimated after end labelling of one of the PCR primers, and the contribution ofBacteroides and Prevotellasequences to total eubacterial 16S rDNA is estimated by measuring the binding of oligonucleotide probes to amplified DNA.Bacteroides and Prevotella 16S rDNA accounted for between 12 and 62% of total eubacterial 16S rDNA in samples of ruminal contents from six sheep and a cow. Ribotypes 4, 5, 6, and 7, which include most cultivated rumen Prevotellastrains, together accounted for between 20 and 86% of the total amplified Bacteroides andPrevotella rDNA in these samples. The most abundantBacteroides or Prevotella ribotype in four animals, however, was ribotype 8, for which there is only one known cultured isolate, while ribotypes 1 and 2, which include many colonic Bacteroides spp., were the most abundant in two animals. This indicates that some abundantBacteroides and Prevotella groups in the rumen are underrepresented among cultured rumenPrevotella isolates. The approach described here provides a rapid, convenient, and widely applicable method for comparing the genotypic composition of bacterial populations in gut samples.
机译:我们描述了一种方法,用于根据选择性扩增16S rRNA基因序列(rDNA),然后用限制性内切酶切割扩增的物质,确定肠道内容中拟杆菌和拟杆菌的遗传组成。在PCR引物之一的末端标记后,估计了不同核糖型对总拟杆菌和Prevotella 16S rDNA的相对贡献,并且通过测量寡核苷酸探针与扩增DNA的结合来估算了拟杆菌和Prevotellas序列对总真细菌16S rDNA的贡献。在六只绵羊和一头牛的瘤胃内容物中,普氏杆菌16S rDNA占总真细菌16S rDNA的12%至62%。核糖类型4、5、6和7包括大多数培养的瘤胃Prevotellastrains,合起来占这些样品中总扩增的拟杆菌和Prevotella rDNA的20%至86%。然而,四只动物中最丰富的拟杆菌属或普雷沃特氏菌核糖型是8型核糖体,其中只有一种已知的培养分离株,而包括许多结肠杆菌属的核糖体1型和2型在两只动物中最丰富。这表明,在培养的瘤胃分离株中瘤胃中一些丰富的拟杆菌属和普氏杆菌组的代表性不足。此处描述的方法提供了一种快速,方便且广泛适用的方法,用于比较肠道样品中细菌种群的基因型组成。

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