Type 1, 2, and 1/2-Hybrid IncC Plasmids From China

A collection of 11 IncC plasmids from China were fully sequenced herein and compared with reference plasmids pR148 and pR55. These 13 plasmids could be assigned into three different subgroups: type 1, type 2, and type 1/2 hybrid. Type 1/2-hybrid plasmids most likely emerged from homologous recombina...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in microbiology Vol. 10; p. 2508
Main Authors Cheng, Qiaoxiang, Jiang, Xiaoyuan, Xu, Yanan, Hu, Lingfei, Luo, Wenbo, Yin, Zhe, Gao, Huixia, Yang, Wenhui, Yang, Huiying, Zhao, Yuee, Zhao, Xiaodong, Zhou, Dongsheng, Dai, Erhei
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 15.11.2019
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:A collection of 11 IncC plasmids from China were fully sequenced herein and compared with reference plasmids pR148 and pR55. These 13 plasmids could be assigned into three different subgroups: type 1, type 2, and type 1/2 hybrid. Type 1/2-hybrid plasmids most likely emerged from homologous recombination between type 1 and type 2 plasmids. Different IncC plasmids had evolved to acquire quite different profiles of accessory modules and thus different collections of resistance genes. The accessory resistance modules included not only the bla CMY -carrying region, the ARI-A island, and the ARI-B island, but also various additional kinds of resistance islands such as the bla CTX–M -carrying regions and the MDR regions. Insertion of accessory modules was sometimes accompanied by deletion, inversion, and translocation of surrounding backbone regions. pR148 and pR55 were confirmed to have the most complete backbones for type 1 and type 2, respectively. This was the first report of a bla IMP– 8 -carrying IncC plasmid, and that of three novel mobile elements: a Tn 1696 -derived unit transposon Tn 6395 , a class 2 integron In2-76, and an insertion sequence IS Ecl10 .
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
These authors have contributed equally to this work
Reviewed by: Christopher John Harmer, The University of Sydney, Australia; Ibrahim Bitar, Charles University, Czechia
Edited by: Costas C. Papagiannitsis, University of Thessaly, Greece
This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2019.02508