Center for Biologics Evaluation and Research, US Food and Drug Administration, 1401 Rockville Pike, HFM-470, Rockville, MD 20852, USA.
Mol Phylogenet Evol. 2012 Jan;62(1):515-28. doi: 10.1016/j.ympev.2011.11.002. Epub 2011 Nov 17.
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.
传统的支原体科物种分类主要基于表型标准,这些标准复杂、难以衡量,并且有可能受到分离株表型偏差的影响。适合支原体科表型特征描述的生化反应数量也非常有限,因此支原体科物种的最终鉴定策略基于比较血清学结果。然而,支原体科物种的血清学检测需要使用高性能免疫血清的性能面板,该面板包含针对该科每个已知物种的抗血清,这需要高水平的技术专业知识,并且只能由支原体参考实验室正确进行。此外,临床标本中存在未培养和苛刻的支原体科物种/分离株,这使得常规细菌学检测的应用变得复杂,甚至不可能。分析可用的遗传标记是对可培养物种和标准微生物学实验室中不可培养或苛刻的生物进行初步鉴定和系统发育分类的另一种方法。聚合酶β亚基基因(rpoB)和 16S-23S rRNA 基因间转录间隔区(ITS)的部分核苷酸序列已确定为所有已知的支原体科种的典型菌株和可用的非典型菌株。除了可用的 16S rRNA 基因数据外,ITS 和 rpoB 序列还用于推断这些物种之间的系统发育关系,并能够将支原体科分离株鉴定到种水平。ITS 和 rpoB 系统发育树与 16S rRNA 参考系统发育树的比较显示,支原体科物种的聚类模式相似,只有少数几个物种的 ITS 和 rpoB 比其相邻物种的差异更大。总体而言,我们的结果表明,ITS 和 rpoB 基因可以作为推断支原体科物种之间系统发育关系的有用互补遗传标记,并为选择适当的代谢和血清学测试以最终分类分离株提供有用的背景信息。总之,包括 ITS、rpoB 和 16S rRNA 基因在内的三靶序列分析被证明是一种可靠且有用的分类工具,可根据亲缘关系和序列相似性对支原体科内的物种进行区分。我们相信,这种方法也可能成为医学和兽医微生物学实验室中新型分离株常规分析和初步鉴定的有用工具。