Volokhov Dmitriy V, George Joseph, Liu Sue X, Ikonomi Pranvera, Anderson Christine, Chizhikov Vladimir
Center of Biologics Evaluation and Research, Office of Vaccines Research and Review, Division of Viral Products, Laboratory of Methods Development, US Food and Drug Administration, Rockville, MD 20852, USA.
Appl Microbiol Biotechnol. 2006 Aug;71(5):680-98. doi: 10.1007/s00253-005-0280-7. Epub 2006 Feb 10.
We have completed sequencing the 16S-23S rRNA intergenic transcribed spacer (ITS) region of most known Mycoplasma , Acholeplasma , Ureaplasma , Mesoplasma , and Spiroplasma species. Analysis of the sequence data revealed a significant interspecies variability and low intraspecies polymorphism of the ITS region among Mollicutes . This finding enabled the application of a combined polymerase chain reaction-microarray technology for identifying Mollicutes species. The microarray included individual species-specific oligonucleotide probes for characterizing human Mollicutes species and other species known to be common cell line contaminants. Evaluation of the microarray was conducted using multiple, previously characterized, Mollicutes species. The microarray analysis of the samples used demonstrated a highly specific assay, which is capable of rapid and accurate discrimination among Mollicutes species.
我们已完成对大多数已知支原体、无胆甾原体、脲原体、中支原体和螺原体物种的16S - 23S rRNA基因间隔转录区(ITS)的测序。序列数据分析显示,柔膜菌纲各物种间ITS区域存在显著差异,而种内多态性较低。这一发现使得聚合酶链反应 - 微阵列技术得以应用于柔膜菌纲物种的鉴定。该微阵列包含用于鉴定人类柔膜菌纲物种及其他已知常见细胞系污染物物种的单个物种特异性寡核苷酸探针。使用多个先前已鉴定的柔膜菌纲物种对该微阵列进行了评估。对所使用样本的微阵列分析显示该检测具有高度特异性,能够快速准确地区分柔膜菌纲各物种。