McAuliffe Laura, Churchward Colin P, Lawes Joanna R, Loria Guido, Ayling Roger D, Nicholas Robin Aj
Mycoplasma Group, Department of Statutory and Exotic Bacteria, Veterinary Laboratories Agency (Weybridge), Surrey, KT15 3NB, UK.
BMC Microbiol. 2008 Nov 7;8:193. doi: 10.1186/1471-2180-8-193.
Mycoplasma agalactiae is the main cause of contagious agalactia, a serious disease of sheep and goats, which has major clinical and economic impacts. Previous studies of M. agalactiae have shown it to be unusually homogeneous and there are currently no available epidemiological techniques which enable a high degree of strain differentiation.
We have developed variable number tandem repeat (VNTR) analysis using the sequenced genome of the M. agalactiae type strain PG2. The PG2 genome was found to be replete with tandem repeat sequences and 4 were chosen for further analysis. VNTR 5 was located within the hypothetical protein MAG6170 a predicted lipoprotein. VNTR 14 was intergenic between the hypothetical protein MAG3350 and the hypothetical protein MAG3340. VNTR 17 was intergenic between the hypothetical protein MAG4060 and the hypothetical protein MAG4070 and VNTR 19 spanned the 5' end of the pseudogene for a lipoprotein MAG4310 and the 3' end of the hypothetical lipoprotein MAG4320. We have investigated the genetic diversity of 88 M. agalactiae isolates of wide geographic origin using VNTR analysis and compared it with pulsed field gel electrophoresis (PFGE) and random amplified polymorphic DNA (RAPD) analysis. Simpson's index of diversity was calculated to be 0.324 for PFGE and 0.574 for VNTR analysis. VNTR analysis revealed unexpected diversity within M. agalactiae with 9 different VNTR types discovered. Some correlation was found between geographical origin and the VNTR type of the isolates.
VNTR analysis represents a useful, rapid first-line test for use in molecular epidemiological analysis of M. agalactiae for outbreak tracing and control.
无乳支原体是绵羊和山羊的一种严重疾病——传染性无乳症的主要病因,该病具有重大临床和经济影响。先前对无乳支原体的研究表明其异常单一,目前尚无能够实现高度菌株分化的流行病学技术。
我们利用无乳支原体模式菌株PG2的测序基因组开发了可变数目串联重复序列(VNTR)分析方法。发现PG2基因组富含串联重复序列,并选择了4个进行进一步分析。VNTR 5位于假定蛋白MAG6170(一种预测的脂蛋白)内。VNTR 14位于假定蛋白MAG3350和假定蛋白MAG3340之间的基因间隔区。VNTR 17位于假定蛋白MAG4060和假定蛋白MAG4070之间的基因间隔区,VNTR 19跨越脂蛋白MAG4310假基因的5'端和假定脂蛋白MAG4320的3'端。我们利用VNTR分析研究了88株来自广泛地理区域的无乳支原体分离株的遗传多样性,并将其与脉冲场凝胶电泳(PFGE)和随机扩增多态性DNA(RAPD)分析进行了比较。PFGE的辛普森多样性指数计算为0.324,VNTR分析为0.574。VNTR分析揭示了无乳支原体内部意外的多样性,发现了9种不同的VNTR类型。在分离株的地理来源和VNTR类型之间发现了一些相关性。
VNTR分析是一种用于无乳支原体分子流行病学分析以进行疫情追踪和控制的有用、快速的一线检测方法。