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首页> 外文期刊>Journal of Clinical Microbiology >Novel Molecular Method for Identification of Streptococcus pneumoniae Applicable to Clinical Microbiology and 16S rRNA Sequence-Based Microbiome Studies
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Novel Molecular Method for Identification of Streptococcus pneumoniae Applicable to Clinical Microbiology and 16S rRNA Sequence-Based Microbiome Studies

机译:鉴定肺炎链球菌的新型分子方法,适用于临床微生物学和基于16S rRNA序列的微生物组研究

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摘要

The close phylogenetic relationship of the important pathogen Streptococcus pneumoniae and several species of commensal streptococci, particularly Streptococcus mitis and Streptococcus pseudopneumoniae, and the recently demonstrated sharing of genes and phenotypic traits previously considered specific for S. pneumoniae hamper the exact identification of S. pneumoniae. Based on sequence analysis of 16S rRNA genes of a collection of 634 streptococcal strains, identified by multilocus sequence analysis, we detected a cytosine at position 203 present in all 440 strains of S. pneumoniae but replaced by an adenosine residue in all strains representing other species of mitis group streptococci. The S. pneumoniae-specific sequence signature could be demonstrated by sequence analysis or indirectly by restriction endonuclease digestion of a PCR amplicon covering the site. The S. pneumoniae-specific signature offers an inexpensive means for validation of the identity of clinical isolates and should be used as an integrated marker in the annotation procedure employed in 16S rRNA-based molecular studies of complex human microbiotas. This may avoid frequent misidentifications such as those we demonstrate to have occurred in previous reports and in reference sequence databases.
机译:重要的病原体肺炎链球菌与几种共生的链球菌,尤其是链球菌和假性链球菌有密切的系统发育关系,而且最近证明的以前认为对肺炎链球菌特异的基因和表型性状的共享妨碍了肺炎链球菌的准确鉴定。基于多基因座序列分析确定的634株链球菌菌株的16S rRNA基因的序列分析,我们在所有440株肺炎链球菌菌株中的203位检测到了胞嘧啶,但在代表其他物种的所有菌株中被腺苷残基取代组的链球菌。肺炎链球菌特异性序列标记可通过序列分析或通过限制性核酸内切酶消化覆盖该位点的PCR扩增子间接证明。肺炎链球菌特异的签名为验证临床分离株的身份提供了一种廉价的手段,并应在复杂的人类微生物群的基于16S rRNA的分子研究中所采用的注释程序中用作整合标记。这可以避免频繁的错误识别,例如我们在先前的报告和参考序列数据库中证明的错误识别。

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