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多种肠道细菌中tet(W)抗性基因侧翼序列的比较分析。

Comparative analysis of sequences flanking tet(W) resistance genes in multiple species of gut bacteria.

作者信息

Kazimierczak Katarzyna A, Flint Harry J, Scott Karen P

机构信息

Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen AB21 9SB, UK.

出版信息

Antimicrob Agents Chemother. 2006 Aug;50(8):2632-9. doi: 10.1128/AAC.01587-05.

Abstract

tet(W) is one of the most abundant tetracycline resistance genes found in bacteria from the mammalian gut and was first identified in the rumen anaerobe Butyrivibrio fibrisolvens 1.230, where it is highly mobile and its transfer is associated with the transposable chromosomal element TnB1230. In order to compare the genetic basis for tet(W) carriage in different bacteria, we studied sequences flanking tet(W) in representatives of seven bacterial genera originating in diverse gut environments. The sequences 657 bp upstream and 43 bp downstream of tet(W) were 96 to 100% similar in all strains examined. A common open reading frame (ORF) was identified downstream of tet(W) in five different bacteria, while another conserved ORF that flanked tet(W) in B. fibrisolvens 1.230 was also present upstream of tet(W) in a human colonic Roseburia isolate and in another rumen B. fibrisolvens isolate. In one species, Bifidobacterium longum (strain F8), a novel transposase was located within the conserved 657-bp region upstream of tet(W) and was flanked by imperfect direct repeats. Additional direct repeats 6 bp long were identified on each end of a chromosomal ORF interrupted by the insertion of the putative transposase and the tet(W) gene. This tet(W) gene was transferable at low frequencies between Bifidobacterium strains. A putative minielement carrying a copy of tet(W) was identified in B. fibrisolvens transconjugants that had acquired the tet(W) gene on TnB1230. Several different mechanisms, including mechanisms involving plasmids and conjugative transposons, appear to be involved in the horizontal transfer of tet(W) genes, but small core regions that may function as minielements are conserved.

摘要

tet(W)是在哺乳动物肠道细菌中发现的最常见的四环素抗性基因之一,最初是在瘤胃厌氧菌溶纤维丁酸弧菌1.230中鉴定出来的,在该菌中它具有高度的移动性,其转移与转座染色体元件TnB1230有关。为了比较不同细菌中携带tet(W)的遗传基础,我们研究了来自不同肠道环境的七个细菌属代表中tet(W)侧翼的序列。在所检测的所有菌株中,tet(W)上游657 bp和下游43 bp的序列相似度为96%至100%。在五种不同细菌中,tet(W)下游鉴定出一个共同的开放阅读框(ORF),而在溶纤维丁酸弧菌1.230中位于tet(W)侧翼的另一个保守ORF在人结肠罗氏菌分离株和另一种瘤胃溶纤维丁酸弧菌分离株中也位于tet(W)上游。在一个物种,即长双歧杆菌(菌株F8)中,一个新的转座酶位于tet(W)上游保守的657 bp区域内,两侧是不完美的直接重复序列。在被推定的转座酶和tet(W)基因插入中断的染色体ORF两端,鉴定出了额外的6 bp长的直接重复序列。这个tet(W)基因在双歧杆菌菌株之间能够以低频率转移。在通过TnB1230获得tet(W)基因的溶纤维丁酸弧菌接合子中,鉴定出一个携带tet(W)拷贝的推定微小元件。几种不同的机制,包括涉及质粒和接合转座子的机制,似乎都参与了tet(W)基因的水平转移,但可能作为微小元件起作用的小核心区域是保守的。

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