Department of Pathology and Laboratory Medicine, University of Texas Medical School at Houston, 6431 Fannin, Houston, TX 77030, USA.
Appl Environ Microbiol. 2011 Feb;77(4):1483-92. doi: 10.1128/AEM.01877-10. Epub 2010 Dec 17.
Borrelia burgdorferi, the causative agent of Lyme disease in North America, is an invasive pathogen that causes persistent multiorgan manifestations in humans and other mammals. Genetic studies of this bacterium are complicated by the presence of multiple plasmid replicons, many of which are readily lost during in vitro culture. The analysis of B. burgdorferi plasmid content by plasmid-specific PCR and agarose gel electrophoresis or other existing techniques is informative, but these techniques are cumbersome and challenging to perform in a high-throughput manner. In this study, a PCR-based Luminex assay was developed for determination of the plasmid content of the strain B. burgdorferi B31. This multiplex, high-throughput method allows simultaneous detection of the plasmid contents of many B. burgdorferi strains in a 96-well format. The procedure was used to evaluate the occurrence of plasmid loss in 44 low-passage B. burgdorferi B31 clones and in a library of over 4,000 signature-tagged mutagenesis (STM) transposon mutant clones. This analysis indicated that only 40% of the clones contained all plasmids, with (in order of decreasing frequency) lp5, lp56, lp28-1, lp25, cp9, lp28-4, lp28-2, and lp21 being the most commonly missing plasmids. These results further emphasize the need for careful plasmid analysis in Lyme disease Borrelia studies. Adaptations of this approach may also be useful in the evaluation of plasmid content and chromosomal gene variations in additional Lyme disease Borrelia strains and other organisms with variable genomes and in the correlation of these genetic differences with pathogenesis and other biological properties.
伯氏疏螺旋体(Borrelia burgdorferi)是北美的莱姆病病原体,是一种侵袭性病原体,可导致人类和其他哺乳动物的持续性多器官表现。该细菌的遗传研究受到多个质粒复制子的存在所复杂化,其中许多在体外培养过程中很容易丢失。通过质粒特异性 PCR 和琼脂糖凝胶电泳或其他现有技术对 B. burgdorferi 质粒含量进行分析是有益的,但这些技术繁琐,难以高通量进行。在这项研究中,开发了一种基于 PCR 的 Luminex 测定法,用于确定 B. burgdorferi B31 菌株的质粒含量。这种多重、高通量方法允许以 96 孔格式同时检测许多 B. burgdorferi 菌株的质粒含量。该程序用于评估 44 个低传代 B. burgdorferi B31 克隆和超过 4000 个特征标记诱变(STM)转座子突变克隆库中质粒丢失的发生情况。该分析表明,只有 40%的克隆含有所有质粒,(按频率降序排列)lp5、lp56、lp28-1、lp25、cp9、lp28-4、lp28-2 和 lp21 是最常见的缺失质粒。这些结果进一步强调了在莱姆病 Borrelia 研究中需要仔细进行质粒分析。这种方法的改编也可能有助于评估其他莱姆病 Borrelia 菌株和其他具有可变基因组的生物体中的质粒含量和染色体基因变异,并将这些遗传差异与发病机制和其他生物学特性相关联。