Institute of Microbiology and Infection, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK.
Department of Infectious Diseases, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, 310016, PR China.
Microb Genom. 2022 Jun;8(6). doi: 10.1099/mgen.0.000840.
Carbapenem and other antibiotic resistance genes (ARGs) can be found in plasmids in , but many plasmid types in this genus have not been well-characterized. Here we describe the distribution, diversity and evolutionary capacity of group 13 (GR13) plasmids that are found in species from diverse environments. Our investigation was prompted by the discovery of two GR13 plasmids in isolated in an intensive care unit (ICU). The plasmids harbour distinct accessory genes: pDETAB5 contains and genes that confer resistance to four further antibiotic classes, while pDETAB13 carries putative alcohol tolerance determinants. Both plasmids contain multiple modules, which are flanked by p sites recognized by XerC/XerD tyrosine recombinases. The ARG-containing modules in pDETAB5 are almost identical to those found in pDETAB2, a GR34 plasmid from an unrelated isolated in the same ICU a month prior. Examination of a further 41 complete, publicly available plasmid sequences revealed that the GR13 pangenome consists of just four core but 1186 accessory genes, 123 in the shell and 1063 in the cloud, reflecting substantial capacity for diversification. The GR13 core genome includes genes for replication and partitioning, and for a putative tyrosine recombinase. Accessory segments encode proteins with diverse putative functions, including for metabolism, antibiotic/heavy metal/alcohol tolerance, restriction-modification, an anti-phage system and multiple toxin–antitoxin systems. The movement of modules and actions of insertion sequences play an important role in generating diversity in GR13 plasmids. Discrete GR13 plasmid lineages are internationally disseminated and found in multiple species, which suggests they are important platforms for the accumulation, horizontal transmission and persistence of accessory genes in this genus.
碳青霉烯类和其他抗生素耐药基因(ARGs)可存在于质粒中,但该属的许多质粒类型尚未得到很好的描述。在这里,我们描述了在来自不同环境的 物种中发现的 组 13(GR13)质粒的分布、多样性和进化能力。我们的调查是由在重症监护病房(ICU)中分离出的两种 GR13 质粒的发现所引发的。这些质粒携带独特的辅助基因:pDETAB5 含有 和赋予对另外四种抗生素类别的耐药性的基因,而 pDETAB13 携带假定的酒精耐受决定因素。两个质粒都含有多个 模块,这些模块被 XerC/XerD 酪氨酸重组酶识别的 p 位点所包围。pDETAB5 中含 ARG 的 模块几乎与一个月前在同一 ICU 中分离的来自无关 的 GR34 质粒 pDETAB2 中发现的那些相同。对另外 41 个完整的、公开可用的质粒序列的检查表明,GR13 泛基因组仅由四个核心基因组成,但有 1186 个辅助基因,其中 123 个在外壳中,1063 个在云中,反映出多样化的巨大能力。GR13 核心基因组包括复制和分区以及假定的酪氨酸重组酶的基因。辅助片段编码具有多种假定功能的蛋白质,包括代谢、抗生素/重金属/酒精耐受、限制修饰、抗噬菌体系统和多个毒素-抗毒素系统。 模块的移动和插入序列的作用在 GR13 质粒的多样性产生中起着重要作用。离散的 GR13 质粒谱系在国际上传播,并在多种 物种中发现,这表明它们是该属中辅助基因积累、水平传播和持续存在的重要平台。