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通过对PCR扩增的16S rRNA基因序列进行限制性酶切图谱分析,估算肠道样本中不同拟杆菌和普雷沃氏菌核糖型的相对丰度。

Estimation of the relative abundance of different Bacteroides and Prevotella ribotypes in gut samples by restriction enzyme profiling of PCR-amplified 16S rRNA gene sequences.

作者信息

Wood J, Scott K P, Avgustin G, Newbold C J, Flint H J

机构信息

Rowett Research Institute, Bucksburn, Aberdeen AB21 9SB, United Kingdom.

出版信息

Appl Environ Microbiol. 1998 Oct;64(10):3683-9. doi: 10.1128/AEM.64.10.3683-3689.1998.

Abstract

We describe an approach for determining the genetic composition of Bacteroides and Prevotella populations 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 and Prevotella 16S rDNA are estimated after end labelling of one of the PCR primers, and the contribution of Bacteroides and Prevotella sequences 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 Prevotella strains, together accounted for between 20 and 86% of the total amplified Bacteroides and Prevotella rDNA in these samples. The most abundant Bacteroides 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 abundant Bacteroides and Prevotella groups in the rumen are underrepresented among cultured rumen Prevotella isolates. The approach described here provides a rapid, convenient, and widely applicable method for comparing the genotypic composition of bacterial populations in gut samples.

摘要

我们描述了一种基于16S rRNA基因序列(rDNA)的选择性扩增,随后用限制性内切酶切割扩增产物来确定肠道内容物中拟杆菌属和普雷沃菌属菌群基因组成的方法。在对其中一个PCR引物进行末端标记后,估计不同核糖体型对总拟杆菌属和普雷沃菌属16S rDNA的相对贡献,并通过测量寡核苷酸探针与扩增DNA的结合来估计拟杆菌属和普雷沃菌属序列对总真细菌16S rDNA的贡献。在六只绵羊和一头奶牛的瘤胃内容物样本中,拟杆菌属和普雷沃菌属16S rDNA占总真细菌16S rDNA的12%至62%。核糖体型4、5、6和7包括了大多数已培养的瘤胃普雷沃菌菌株,在这些样本中,它们总共占扩增的拟杆菌属和普雷沃菌属rDNA总量的20%至86%。然而,在四只动物中最丰富的拟杆菌属或普雷沃菌属核糖体型是核糖体型8,已知只有一个培养分离株属于该型,而包括许多结肠拟杆菌属物种的核糖体型1和2在两只动物中最为丰富。这表明瘤胃中一些丰富的拟杆菌属和普雷沃菌属菌群在已培养的瘤胃普雷沃菌分离株中代表性不足。本文所述方法为比较肠道样本中细菌菌群的基因型组成提供了一种快速、便捷且广泛适用的方法。

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