Département de biologie, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Département de biologie, Université de Sherbrooke, Sherbrooke, Quebec, Canada
J Bacteriol. 2019 Apr 24;201(10). doi: 10.1128/JB.00731-18. Print 2019 May 15.
Conjugative plasmids of incompatibility group C (IncC), formerly known as A/C, disseminate antibiotic resistance genes globally in diverse pathogenic species of genomic island 1 (SGI1) can be mobilized by IncC plasmids and was recently shown to reshape the conjugative type IV secretion system (T4SS) encoded by these plasmids to evade entry exclusion. Entry exclusion blocks DNA translocation between cells containing identical or highly similar plasmids. Here, we report that the protein encoded by the entry exclusion gene of IncC plasmids () mediates entry exclusion in recipient cells through recognition of the IncC-encoded TraG protein in donor cells. Phylogenetic analyses based on EexC and TraG homologs predicted the existence of at least three different exclusion groups among IncC-related conjugative plasmids. Mating assays using Eex proteins encoded by representative IncC and IncA (former A/C) and related untyped plasmids confirmed these predictions and showed that the IncC and IncA plasmids belong to the C exclusion group, thereby explaining their apparent incompatibility despite their compatible replicons. Representatives of the two other exclusion groups (D and E) are untyped conjugative plasmids found in sp. Finally, we determined through domain swapping that the carboxyl terminus of the EexC and EexE proteins controls the specificity of these exclusion groups. Together, these results unravel the role of entry exclusion in the apparent incompatibility between IncA and IncC plasmids while shedding light on the importance of the TraG subunit substitution used by SGI1 to evade entry exclusion. IncA and IncC conjugative plasmids drive antibiotic resistance dissemination among several pathogenic species of due to the diversity of drug resistance genes that they carry and their ability to mobilize antibiotic resistance-conferring genomic islands such as SGI1 of While historically grouped as "IncA/C," IncA and IncC replicons were recently confirmed to be compatible and to abolish each other's entry into the cell in which they reside during conjugative transfer. The significance of our study is in identifying an entry exclusion system that is shared by IncA and IncC plasmids. It impedes DNA transfer to recipient cells bearing a plasmid of either incompatibility group. The entry exclusion protein of this system is unrelated to any other known entry exclusion proteins.
不相容群 C(IncC)的结合质粒,以前称为 A/C,在基因组岛 1(SGI1)的不同致病性物种中全球传播抗生素耐药基因,可由 IncC 质粒动员,最近表明可重塑这些质粒编码的共轭型 IV 型分泌系统(T4SS),以逃避进入排斥。进入排斥阻止了含有相同或高度相似质粒的细胞之间的 DNA 易位。在这里,我们报告 IncC 质粒的进入排斥基因()编码的蛋白通过识别供体细胞中 IncC 编码的 TraG 蛋白在受体细胞中介导进入排斥。基于 EexC 和 TraG 同源物的系统发育分析预测了 IncC 相关结合质粒中至少存在三个不同的排斥组。使用代表 IncC 和 IncA(前 A/C)和相关未分型质粒的 Eex 蛋白进行的交配试验证实了这些预测,并表明 IncC 和 IncA 质粒属于 C 排斥组,从而解释了它们的明显不兼容性,尽管它们具有兼容的复制子。另外两个排斥组(D 和 E)的代表是未分型的结合质粒,发现于 属。最后,我们通过结构域交换确定了 EexC 和 EexE 蛋白的羧基末端控制这些排斥组的特异性。总之,这些结果揭示了进入排斥在 IncA 和 IncC 质粒之间的明显不兼容性中的作用,同时阐明了 SGI1 用于逃避进入排斥的 TraG 亚基替换的重要性。IncA 和 IncC 结合质粒由于它们携带的多种耐药基因以及它们能够动员抗生素耐药性赋予的基因组岛(如 属的 SGI1),导致几种致病性物种的抗生素耐药性传播。虽然历史上被归类为“IncA/C”,但 IncA 和 IncC 复制子最近被证实是兼容的,并在共轭转移过程中消除了彼此在其所在细胞中的进入。我们研究的意义在于鉴定一个由 IncA 和 IncC 质粒共享的进入排斥系统。它阻止了携带任一不相容组质粒的受体细胞中的 DNA 转移。该系统的进入排斥蛋白与任何其他已知的进入排斥蛋白无关。