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无乳支原体的锁相突变体:确定高频Vpma抗原变异的分子开关

Phase-locked mutants of Mycoplasma agalactiae: defining the molecular switch of high-frequency Vpma antigenic variation.

作者信息

Chopra-Dewasthaly Rohini, Citti Christine, Glew Michelle D, Zimmermann Martina, Rosengarten Renate, Jechlinger Wolfgang

机构信息

Institute of Bacteriology, Mycology and Hygiene, Department of Pathobiology, University of Veterinary Medicine Vienna, Veterinärplatz 1, A-1210 Vienna, Austria.

出版信息

Mol Microbiol. 2008 Mar;67(6):1196-210. doi: 10.1111/j.1365-2958.2007.06103.x. Epub 2008 Jan 30.

Abstract

Mycoplasma agalactiae, an important pathogen of small ruminants, exhibits antigenic diversity by switching the expression of multiple surface lipoproteins called Vpmas (Variable proteins of M. agalactiae). Although phase variation has been shown to play important roles in many host-pathogen interactions, the biological significance and the mechanism of Vpma oscillations remain largely unclear. Here, we demonstrate that all six Vpma proteins are expressed in the type strain PG2 and all undergo phase variation at an unusually high frequency. Furthermore, targeted gene disruption of the xer1 gene encoding a putative site-specific recombinase adjacent to the vpma locus was accomplished via homologous recombination using a replicon-based vector. Inactivation of xer1 abolished further Vpma switching and the 'phase-locked' mutants (PLMs) continued to steadily express only a single Vpma product. Complementation of the wild-type xer1 gene in PLMs restored Vpma phase variation thereby proving that Xer1 is essential for vpma inversions. The study is not only instrumental in enhancing our ability to understand the role of Vpmas in M. agalactiae infections but also provides useful molecular approaches to study potential disease factors in other 'difficult-to-manipulate' mycoplasmas.

摘要

无乳支原体是小型反刍动物的一种重要病原体,它通过切换多种称为Vpmas(无乳支原体可变蛋白)的表面脂蛋白的表达来展现抗原多样性。尽管相变已被证明在许多宿主 - 病原体相互作用中发挥重要作用,但Vpma振荡的生物学意义和机制仍 largely不清楚。在这里,我们证明所有六种Vpma蛋白都在模式菌株PG2中表达,并且都以异常高的频率经历相变。此外,通过使用基于复制子的载体进行同源重组,完成了对编码与vpma基因座相邻的假定位点特异性重组酶的xer1基因的靶向基因破坏。xer1的失活消除了进一步的Vpma切换,并且“锁相”突变体(PLMs)继续稳定地仅表达单一的Vpma产物。在PLMs中野生型xer1基因的互补恢复了Vpma相变,从而证明Xer1对于vpma倒位是必不可少的。该研究不仅有助于提高我们理解Vpmas在无乳支原体感染中的作用的能力,而且还提供了有用的分子方法来研究其他“难以操作”的支原体中的潜在疾病因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0356/2268961/bfc479ec9113/mmi0067-1196-f1.jpg

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