首页> 外文期刊>Molecular phylogenetics and evolution >RNA polymerase beta subunit (rpoB) gene and the 16S-23S rRNA intergenic transcribed spacer region (ITS) as complementary molecular markers in addition to the 16S rRNA gene for phylogenetic analysis and identification of the species of the family Mycoplasmataceae
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RNA polymerase beta subunit (rpoB) gene and the 16S-23S rRNA intergenic transcribed spacer region (ITS) as complementary molecular markers in addition to the 16S rRNA gene for phylogenetic analysis and identification of the species of the family Mycoplasmataceae

机译:除了16S rRNA基因外,RNA聚合酶β亚基(rpoB)基因和16S-23S rRNA基因间转录间隔区(ITS)作为互补分子标记,可用于系统分析和鉴定支原体科的物种

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Conventional classification of the species in the family Mycoplasmataceae is mainly based on phenotypic criteria, which are complicated, can be difficult to measure, and have the potential to be hampered by phenotypic deviations among the isolates. The number of biochemical reactions suitable for phenotypic characterization of the Mycoplasmataceae is also very limited and therefore the strategy for the final identification of the Mycoplasmataceae species is based on comparative serological results. However, serological testing of the Mycoplasmataceae species requires a performance panel of hyperimmune sera which contains anti-serum to each known species of the family, a high level of technical expertise, and can only be properly performed by mycoplasma-reference laboratories. In addition, the existence of uncultivated and fastidious Mycoplasmataceae species/isolates in clinical materials significantly complicates, or even makes impossible, the application of conventional bacteriological tests. The analysis of available genetic markers is an additional approach for the primary identification and phylogenetic classification of cultivable species and uncultivable or fastidious organisms in standard microbiological laboratories. The partial nucleotide sequences of the RNA polymerase β-subunit gene (rpoB) and the 16S-23S rRNA intergenic transcribed spacer (ITS) were determined for all known type strains and the available non-type strains of the Mycoplasmataceae species. In addition to the available 16S rRNA gene data, the ITS and rpoB sequences were used to infer phylogenetic relationships among these species and to enable identification of the Mycoplasmataceae isolates to the species level. The comparison of the ITS and rpoB phylogenetic trees with the 16S rRNA reference phylogenetic tree revealed a similar clustering patterns for the Mycoplasmataceae species, with minor discrepancies for a few species that demonstrated higher divergence of their ITS and rpoB in comparison to their neighbor species. Overall, our results demonstrated that the ITS and rpoB gene could be useful complementary phylogenetic markers to infer phylogenetic relationships among the Mycoplasmataceae species and provide useful background information for the choice of appropriate metabolic and serological tests for the final classification of isolates. In summary, three-target sequence analysis, which includes the ITS, rpoB, and 16S rRNA genes, was demonstrated to be a reliable and useful taxonomic tool for the species differentiation within the family Mycoplasmataceae based on their phylogenetic relatedness and pairwise sequence similarities. We believe that this approach might also become a valuable tool for routine analysis and primary identification of new isolates in medical and veterinary microbiological laboratories.
机译:支原体科中物种的常规分类主要基于表型标准,该标准复杂,难以测量,并且可能受到分离株之间表型差异的阻碍。适用于支原体科表型表征的生化反应的数目也非常有限,因此,最终鉴定支原体科物种的策略是基于比较血清学结果。但是,支原体科物种的血清学测试需要一种超免疫血清的性能检测组,该组包含针对该家族每个已知物种的抗血清,高水平的技术专长,并且只能由支原体参考实验室正确进行。另外,临床材料中未培养的和挑剔的支原体物种/分离物的存在显着使常规细菌学检测的应用复杂化,甚至使之不可能。对可用遗传标记的分析是在标准微生物实验室中对可培养物种和不可培养或难养生物进行初步鉴定和系统发育分类的另一种方法。确定了所有已知类型菌株和支原体物种可用的非类型菌株的RNA聚合酶β亚基基因(rpoB)和16S-23S rRNA基因间转录间隔区(ITS)的部分核苷酸序列。除了可获得的16S rRNA基因数据外,还使用ITS和rpoB序列来推断这些物种之间的系统发育关系,并能够鉴定到支原体中的支原体。 ITS和rpoB系统发育树与16S rRNA参考系统树的比较显示,支原体物种具有相似的聚类模式,少数物种的差异较小,这表明其ITS和rpoB与其邻域物种相比具有更高的发散度。总体而言,我们的研究结果表明,ITS和rpoB基因可能是有用的互补系统发生标记,可以推断支原体物种之间的系统发生关系,并为选择合适的代谢和血清学测试菌株的最终分类提供有用的背景信息。综上所述,三目标序列分析(包括ITS,rpoB和16S rRNA基因)被证明是可靠的和有用的分类学工具,用于基于支原体的系统发育相关性和成对的序列相似性来区分支原体。我们认为,这种方法也可能会成为医学和兽医微生物实验室中常规分析和新鉴定新菌株的有价值的工具。

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