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一种新型 T4SS 介导的 DNA 转移,由苏云金芽孢杆菌以色列亚种的接合质粒 pXO16 所利用。

A novel T4SS-mediated DNA transfer used by pXO16, a conjugative plasmid from Bacillus thuringiensis serovar israelensis.

机构信息

Laboratory of Food and Environmental Microbiology, Earth and Life Institute, Université catholique de Louvain, Louvain-la-Neuve, B-1348, Belgium.

出版信息

Environ Microbiol. 2018 Apr;20(4):1550-1561. doi: 10.1111/1462-2920.14084. Epub 2018 Apr 6.

Abstract

The entomopathogenic Bacillus thuringiensis serovar israelensis displays peculiar conjugative transfer capabilities, accounted for by the large conjugative plasmid pXO16 (350 kb). The efficient and fast conjugative transfers are accompanied by a macroscopic aggregation of bacterial partners. Moreover, pXO16 has proven capable of effective mobilization and the retro-transfer of both mobilizable and 'non-mobilizable' plasmids. In this work, the aggregation phenomenon is shown to promote pXO16 transfer while not being mandatory for transfer. Transfer of pXO16 to B. thuringiensis recipient strains that do not display aggregation is observed as well, hence enlarging the previously defined host range. The use of variant calling analysis of transconjugants allowed for observation of up to 791 kb chromosomal regions mobilization. Previous analysis of pXO16 did not reveal any Type IV Secretion System (T4SS) homologs, which suggested the presence of an unusual conjugative system. A FtsK/SpOIIIE ATPase gene proved here to be necessary for conjugative transfer. Additionally, the analysis of natural restriction-modification systems in both conjugative partners gave credit to a ssDNA transfer mechanism. A 'transfer israelensis plasmid' (tip) region containing this ATPase gene was shown to code for other potential T4SS proteins, illustrating a conjugative system distantly related to the other known Gram-positive T4SSs.

摘要

苏云金芽胞杆菌以色列亚种表现出特殊的共轭转移能力,这归因于大型共轭质粒 pXO16(350 kb)。有效的快速共轭转移伴随着细菌伴侣的宏观聚集。此外,pXO16 已被证明能够有效地动员和反向转移可动员和“不可动员”的质粒。在这项工作中,聚集现象被证明可以促进 pXO16 的转移,而转移不是必需的。即使在不显示聚集的苏云金芽胞杆菌受体菌株中也观察到了 pXO16 的转移,从而扩大了先前定义的宿主范围。转导子的变体调用分析的使用允许观察到多达 791 kb 的染色体区域动员。先前对 pXO16 的分析并未揭示任何类型 IV 分泌系统 (T4SS) 同源物,这表明存在一种不寻常的共轭系统。在这里证明,FtsK/SpOIIIE ATP 酶基因对于共轭转移是必需的。此外,对共轭体中天然限制修饰系统的分析证实了 ssDNA 转移机制的存在。一个包含该 ATP 酶基因的“转移以色列质粒”(tip)区域被证明编码其他潜在的 T4SS 蛋白,说明了与其他已知革兰氏阳性 T4SS 远相关的共轭系统。

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