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New insights into the classification and integration specificity of Streptococcus integrative conjugative elements through extensive genome exploration.

机译:通过广泛的基因组探索,对链球菌整合结合元件的分类和整合特异性的新见解。

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摘要

Recent genome analyses suggest that integrative and conjugative elements (ICEs) are widespread in bacterial genomes and therefore play an essential role in horizontal transfer. However, only a few of these elements are precisely characterized and correctly delineated within sequenced bacterial genomes. Even though previous analysis showed the presence of ICEs in some species of Streptococci, the global prevalence and diversity of ICEs was not analyzed in this genus. In this study, we searched for ICEs in the completely sequenced genomes of 124 strains belonging to 27 streptococcal species. These exhaustive analyses revealed 105 putative ICEs and 26 slightly decayed elements whose limits were assessed and whose insertion site was identified. These ICEs were grouped in seven distinct unrelated or distantly related families, according to their conjugation modules. Integration of these streptococcal ICEs is catalyzed either by a site-specific tyrosine integrase, a low-specificity tyrosine integrase, a site-specific single serine integrase, a triplet of site-specific serine integrases or a DDE transposase. Analysis of their integration site led to the detection of 18 target-genes for streptococcal ICE insertion including eight that had not been identified previously (ftsK, guaA, lysS, mutT, rpmG, rpsI, traG, and ebfC). It also suggests that all specificities have evolved to minimize the impact of the insertion on the host. This overall analysis of streptococcal ICEs emphasizes their prevalence and diversity and demonstrates that exchanges or acquisitions of conjugation and recombination modules are frequent.
机译:最近的基因组分析表明,整合和结合元件(ICEs)在细菌基因组中很普遍,因此在水平转移中起着至关重要的作用。然而,在测序的细菌基因组中,这些元素中只有少数是精确表征和正确描绘的。即使以前的分析表明某些种类的链球菌中都存在ICE,但该属并未分析ICE的全球流行性和多样性。在这项研究中,我们在属于27个链球菌物种的124个菌株的完全测序基因组中搜索ICE。这些详尽的分析揭示了105个推定的ICE和26个轻度衰变的元素,它们的极限值得到了评估,并确定了插入位置。根据其共轭模块,这些ICE分为七个不同的不相关或遥远相关的族。这些链球菌ICE的整合可通过位点特异性酪氨酸整合酶,低特异性酪氨酸整合酶,位点特异性单丝氨酸整合酶,位点特异性丝氨酸整合三联体或DDE转座酶来催化。对它们整合位点的分析导致检测到18个链球菌ICE插入的靶基因,其中包括8个以前未发现的靶基因(ftsK,guaA,lysS,mutT,rpmG,rpsI,traG和ebfC)。它还表明,所有特异性都在发展,以尽量减少插入对宿主的影响。对链球菌ICE的整体分析强调了它们的普遍性和多样性,并证明了交换和获得缀合和重组模块非常频繁。

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