Dmitriev Alexander, Shen Adong, Shen Xuzhuang, Yang Yonghong
Institute of Experimental Medicine, Academy of Medical Sciences, Saint Petersburg 197376, Russia.
J Bacteriol. 2004 Feb;186(4):1106-9. doi: 10.1128/JB.186.4.1106-1109.2004.
A collection of 113 epidemiologically unrelated Streptococcus agalactiae strains were studied (group B streptococcus; GBS): they belonged to different serotypes and were isolated from pregnant women in China and Russia. The insertion sequence ISSa4 was found in 21 of 113 strains (18,6%). All of the strains with ISSa4 belonged to serotypes II and II/c and were characterized by the presence of IS1381 and IS861 as well as the absence of IS1548 and GBSi1. All of the strains with ISSa4 possessed both bca and bac virulence genes coding for alpha and beta antigens, respectively. Among 21 ISSa4-positive strains, 13 different HindIII patterns (D1 to D13) hybridizing with an ISSa4 probe were found. One of them (D13) contained a single HindIII hybridization fragment 6.5 kb in size that was found to be specific for all ISSa4-positive GBS strains. Multiple target sites for insertions of ISSa4 were identified and included a putative pathogenicity island, "housekeeping" genes, and intergenic regions, as well as the genes for hypothetical proteins. No significant similarity was observed in the sequences of the target genes for ISSa4 insertions, in the relative location of the target genes on the chromosome, or the biological functions of the encoded proteins. The possible significance of ISSa4-based differentiation of the strains and the presence of possible "hot spots" for insertions of ISSa4 in GBS genome are discussed.
对113株流行病学上不相关的无乳链球菌菌株(B组链球菌;GBS)进行了研究:它们属于不同血清型,从中国和俄罗斯的孕妇中分离得到。在113株菌株中有21株(18.6%)发现了插入序列ISSa4。所有携带ISSa4的菌株均属于血清型II和II/c,其特征是存在IS1381和IS861,同时不存在IS1548和GBSi1。所有携带ISSa4的菌株都同时拥有分别编码α和β抗原的bca和bac毒力基因。在21株ISSa4阳性菌株中,发现了与ISSa4探针杂交的13种不同的HindIII酶切图谱(D1至D13)。其中一种(D13)包含一个大小为6.5 kb的单一HindIII杂交片段,该片段被发现对所有ISSa4阳性GBS菌株具有特异性。确定了ISSa4插入的多个靶位点,包括一个假定的致病岛、“管家”基因、基因间区域以及假定蛋白的基因。在ISSa4插入的靶基因序列、靶基因在染色体上的相对位置或编码蛋白的生物学功能方面未观察到明显相似性。讨论了基于ISSa4对菌株进行分化的可能意义以及GBS基因组中ISSa4插入可能的“热点”的存在情况。