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本文引用的文献

1
The presence of insertion elements IS861 and IS1548 in group B streptococci.B族链球菌中插入元件IS861和IS1548的存在。
Folia Microbiol (Praha). 2003;48(1):105-10. doi: 10.1007/BF02931285.
2
Genome sequence of Streptococcus agalactiae, a pathogen causing invasive neonatal disease.无乳链球菌的基因组序列,一种导致新生儿侵袭性疾病的病原体。
Mol Microbiol. 2002 Sep;45(6):1499-513. doi: 10.1046/j.1365-2958.2002.03126.x.
3
Complete genome sequence and comparative genomic analysis of an emerging human pathogen, serotype V Streptococcus agalactiae.一种新出现的人类病原体——血清型V组无乳链球菌的全基因组序列及比较基因组分析
Proc Natl Acad Sci U S A. 2002 Sep 17;99(19):12391-6. doi: 10.1073/pnas.182380799. Epub 2002 Aug 28.
4
Chromosomal analysis of group B streptococcal clinical strains; bac gene-positive strains are genetically homogenous.B族链球菌临床菌株的染色体分析;bac基因阳性菌株在遗传上是同质的。
FEMS Microbiol Lett. 2002 Feb 19;208(1):93-8. doi: 10.1111/j.1574-6968.2002.tb11066.x.
5
Molecular profiles of group B streptococcal surface protein antigen genes: relationship to molecular serotypes.B族链球菌表面蛋白抗原基因的分子特征:与分子血清型的关系。
J Clin Microbiol. 2002 Feb;40(2):620-6. doi: 10.1128/JCM.40.2.620-626.2002.
6
Mutually exclusive distribution of IS1548 and GBSi1, an active group II intron identified in human isolates of group B streptococci.IS1548与GBSi1(在B族链球菌的人类分离株中鉴定出的一种活性II组内含子)的互斥分布。
J Bacteriol. 2001 Apr;183(8):2560-9. doi: 10.1128/JB.183.8.2560-2569.2001.
7
Analysis of restriction fragment length polymorphisms of the insertion sequence IS1381 in group B Streptococci.B族链球菌中插入序列IS1381的限制性片段长度多态性分析
J Infect Dis. 2000 Jan;181(1):364-8. doi: 10.1086/315205.
8
Identification of a novel insertion sequence element in Streptococcus agalactiae. bspeller@imib.rwth-aachen.de.无乳链球菌中一种新型插入序列元件的鉴定。bspeller@imib.rwth-aachen.de。
Gene. 2000 Jan 4;241(1):51-6. doi: 10.1016/s0378-1119(99)00469-2.
9
Serotypes VI and VIII predominate among group B streptococci isolated from pregnant Japanese women.从日本孕妇中分离出的B族链球菌中,血清型VI和VIII占主导地位。
J Infect Dis. 1999 Apr;179(4):1030-3. doi: 10.1086/314666.
10
Insertion sequences.插入序列
Microbiol Mol Biol Rev. 1998 Sep;62(3):725-74. doi: 10.1128/MMBR.62.3.725-774.1998.

基于ISSa4的无乳链球菌菌株分化及ISSa4插入多个靶位点的鉴定

ISSa4-based differentiation of Streptococcus agalactiae strains and identification of multiple target sites for ISSa4 insertions.

作者信息

Dmitriev Alexander, Shen Adong, Shen Xuzhuang, Yang Yonghong

机构信息

Institute of Experimental Medicine, Academy of Medical Sciences, Saint Petersburg 197376, Russia.

出版信息

J Bacteriol. 2004 Feb;186(4):1106-9. doi: 10.1128/JB.186.4.1106-1109.2004.

DOI:10.1128/JB.186.4.1106-1109.2004
PMID:14762005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC344221/
Abstract

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.

摘要

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。