AUTHOR=Liang Quanhui , Jiang Xiaoyuan , Hu Lingfei , Yin Zhe , Gao Bo , Zhao Yuee , Yang Wenhui , Yang Huiying , Tong Yigang , Li Weixuan , Jiang Lingxiao , Zhou Dongsheng 

TITLE=Sequencing and Genomic Diversity Analysis of IncHI5 Plasmids

JOURNAL=Frontiers in Microbiology

VOLUME=9

YEAR=2019

URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2018.03318

DOI=10.3389/fmicb.2018.03318

ISSN=1664-302X

ABSTRACT=<p>IncHI plasmids could be divided into five different subgroups IncHI1–5. In this study, the complete nucleotide sequences of seven <italic>bla</italic><sub>IMP</sub>- or <italic>bla</italic><sub>VIM</sub>-carrying IncHI5 plasmids from <italic>Klebsiella pneumoniae</italic>, <italic>K. quasipneumoniae</italic>, and <italic>K. variicola</italic> were determined and compared in detail with all the other four available sequenced IncHI5 plasmids. These plasmids carried conserved IncHI5 backbones composed of <italic>repHI5B</italic> and a <italic>repFIB</italic>-like gene (replication), <italic>parABC</italic> (partition), and <italic>tra1</italic> (conjugal transfer). Integration of a number of accessory modules, through horizontal gene transfer, at various sites of IncHI5 backbones resulted in various deletions of surrounding backbone regions and thus considerable diversification of IncHI5 backbones. Among the accessory modules were three kinds of resistance accessory modules, namely Tn<italic>10</italic> and two antibiotic resistance islands designated ARI-A and ARI-B. These two islands, inserted at two different fixed sites (one island was at one site and the other was at a different site) of IncHI5 backbones, were derived from the prototype Tn<italic>3</italic>-family transposons Tn<italic>1696</italic> and Tn<italic>6535</italic>, respectively, and could be further discriminated as various intact transposons and transposon-like structures. The ARI-A or ARI-B islands from different IncHI5 plasmids carried distinct profiles of antimicrobial resistance markers and associated mobile elements, and complex events of transposition and homologous recombination accounted for assembly of these islands. The carbapenemase genes <italic>bla</italic><sub>IMP-4</sub>, <italic>bla</italic><sub>IMP-38</sub> and <italic>bla</italic><sub>VIM-1</sub> were identified within various class 1 integrons from ARI-A or ARI-B of the seven plasmids sequenced in this study. Data presented here would provide a deeper insight into diversification and evolution history of IncHI5 plasmids.</p>