Podbielski A
Institute of Medical Microbiology, Klinikum RWTH, Technical University, Aachen, FRG.
Mol Gen Genet. 1993 Feb;237(1-2):287-300. doi: 10.1007/BF00282810.
The DNA of group A streptococci (GAS) encodes several important virulence factors such as the antiphagocytic M protein, the Ig-Fc-binding M-related proteins (FcrA-like and EnnX-like) and the complement factor-inactivating C5a peptidase. The corresponding genes emm, fcrA, ennX, and scpA, respectively, were assumed to be located close together in the GAS genome. Additionally, emm and scpA have been found to be under the positive, coordinate control of the virR locus, which led to the designation "vir regulon" for the corresponding genomic segment. In order to map the vir regulons of many GAS serotypes and to analyse any correlation between the organization of vir regulons and circumscribed heterogeneities within the emm, virR, and scpA genes, an approach using several distinct sets of polymerase chain reaction (PCR) experiments was chosen. By examination of the genomic DNA of 42 GAS isolates from 36 different M serotypes three patterns of vir regulon topography were found. The first, designated "large vir regulon" (LVR), consists of virR--fcrA(-like)--emm--ennX(-like)--scpA. The second, designated "small vir regulon" (SVR), contains virR--emm--scpA, and the last, designated "unusual vir regulon" (UVR), resembles SVR but contains additional heterogeneous sequences between emm and scpA. The patterns correlate with heterogeneities at the 3' ends of the virR and scpA genes, with the M classification system and the occurrence of specific non-coding intervening sequences within the vir regulons. The potential impact of these patterns on models to account for generation of vir regulons is discussed.
A群链球菌(GAS)的DNA编码几种重要的毒力因子,如抗吞噬的M蛋白、Ig-Fc结合M相关蛋白(FcrA样和EnnX样)以及补体因子失活C5a肽酶。相应的基因emm、fcrA、ennX和scpA分别被认为在GAS基因组中紧密相邻。此外,已发现emm和scpA受virR基因座的正向协同调控,这导致将相应的基因组片段命名为“vir调控子”。为了绘制多种GAS血清型的vir调控子图谱,并分析vir调控子的组织与emm、virR和scpA基因内特定异质性之间的任何相关性,我们选择了一种使用几组不同聚合酶链反应(PCR)实验的方法。通过检查来自36种不同M血清型的42株GAS分离株的基因组DNA,发现了三种vir调控子拓扑结构模式。第一种模式称为“大vir调控子”(LVR),由virR--fcrA(-样)--emm--ennX(-样)--scpA组成。第二种模式称为“小vir调控子”(SVR),包含virR--emm--scpA,最后一种模式称为“异常vir调控子”(UVR),与SVR相似,但在emm和scpA之间包含额外的异质序列。这些模式与virR和scpA基因3'端的异质性、M分类系统以及vir调控子内特定非编码间隔序列的出现相关。本文讨论了这些模式对解释vir调控子产生模型的潜在影响。