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肺炎链球菌中新插入序列IS1381的鉴定与特征分析

Identification and characterization of IS1381, a new insertion sequence in Streptococcus pneumoniae.

作者信息

Sánchez-Beato A R, García E, López R, García J L

机构信息

Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

出版信息

J Bacteriol. 1997 Apr;179(7):2459-63. doi: 10.1128/jb.179.7.2459-2463.1997.

Abstract

A new insertion sequence (IS1381) was identified in the genome of Streptococcus pneumoniae R6 as an 846-bp segment containing 20-bp terminal inverted repeats and flanked by 7-bp direct repeats. The three sequenced copies of this element have two overlapping open reading frame (ORF) genes named orfA and orfB. However, significant variations between individual copies were found, suggesting that inactivating mutations have occurred in an original single ORF. Accordingly, the consensus IS1381 element derived from the comparison of the three available copies should contain a single ORF sufficient to encode a basic protein of 267 amino acids which exhibited high similarity to the putative transposases of ISL2 from Lactobacillus helveticus and of IS702 from the cyanobacterium Calothrix sp. strain PCC 7601. A minimum of five to seven copies were detected by hybridization experiments in the R6 genome. In remarkable contrast with the two previously reported pneumococcal insertion sequences, several copies of IS1381 have been detected in all of the clinical isolates tested so far. Interestingly, Streptococcus oralis NCTC 11427 (type strain), a close relative of pneumococcus, does not contain this element, but its occurrence in the type strain of Streptococcus mitis (NCTC 12261) suggests that this species has exchanged DNA with S. pneumoniae directly or through an intermediate species.

摘要

在肺炎链球菌R6基因组中鉴定出一个新的插入序列(IS1381),它是一个846bp的片段,包含20bp的末端反向重复序列,两侧为7bp的正向重复序列。该元件的三个测序拷贝有两个重叠的开放阅读框(ORF)基因,分别命名为orfA和orfB。然而,发现各个拷贝之间存在显著差异,这表明在一个原始的单一ORF中发生了失活突变。因此,通过比较三个可用拷贝得出的共有IS1381元件应包含一个单一的ORF,足以编码一个267个氨基酸的碱性蛋白,该蛋白与瑞士乳杆菌的ISL2和蓝细菌Calothrix sp.菌株PCC 7601的IS702的推定转座酶具有高度相似性。通过杂交实验在R6基因组中检测到至少五到七个拷贝。与之前报道的两个肺炎球菌插入序列形成显著对比的是,在迄今为止测试的所有临床分离株中都检测到了多个IS1381拷贝。有趣的是,肺炎链球菌的近亲口腔链球菌NCTC 11427(模式菌株)不包含该元件,但它在缓症链球菌模式菌株(NCTC 12261)中的存在表明该物种已直接或通过中间物种与肺炎链球菌交换了DNA。

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