Department of Infectious Diseases, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310016, China.
Key Laboratory of Microbial Technology and Bioinformatics of Zhejiang Province, Hangzhou, Zhejiang 310016, China.
J Antimicrob Chemother. 2021 Apr 13;76(5):1130-1134. doi: 10.1093/jac/dkab005.
To characterize a blaOXA-58- and blaNDM-1-containing MDR plasmid from a rare Acinetobacter baumannii lineage and compare it with related plasmids to explore the distribution and evolution of a new plasmid group.
A. baumannii DETAB-P2 was isolated from a rectal swab of an intensive care patient. Antibiotic susceptibility was determined using broth microdilution. DETAB-P2 was mated with A. baumannii ATCC 17978 and putative transconjugants were characterized by S1/PFGE and Southern hybridization. WGS was performed on the Illumina and Oxford Nanopore platforms. MLST was performed with the Pasteur and Oxford schemes. Antibiotic resistance genes were identified with ABRicate. Plasmid sequence annotation was performed manually. Complete plasmids in GenBank with the same rep gene were used for comparative analyses.
A. baumannii DETAB-P2 was ST138 by the Pasteur scheme and a novel Oxford type, ST2209. It transferred blaOXA-58 and blaNDM-1 to ATCC 17978 in the 100 072 bp plasmid pDETAB2 that also carried bleMBL, sul2, aacC2d, tet(39), msr(E)-mph(E) and putative mercury resistance and RND efflux system determinants. pDETAB2 represents a new plasmid type, GR34, and contained 16 pdif sites and several novel dif modules. Only a 10 kbp core sequence is shared amongst pDETAB2 and 18 further GR34 plasmids in GenBank, with diverse accessory regions comprised of various dif modules.
GR34 plasmids are found in several Acinetobacter species from diverse environments. They display considerable variation in accessory content owing to the presence of pdif sites and an array of dif modules, some of which contain antibiotic resistance genes.
从罕见的鲍曼不动杆菌谱系中鉴定出一种携带 blaOXA-58 和 blaNDM-1 的 MDR 质粒,并将其与相关质粒进行比较,以探索新质粒组的分布和进化。
从一名重症监护患者的直肠拭子中分离出鲍曼不动杆菌 DETAB-P2。使用肉汤微量稀释法测定抗生素敏感性。DETAB-P2 与鲍曼不动杆菌 ATCC 17978 进行交配,并用 S1/PFGE 和 Southern 杂交法对假定的转导体进行特征分析。使用 Illumina 和 Oxford Nanopore 平台进行 WGS。采用巴斯德和牛津方案进行 MLST。使用 ABRicate 识别抗生素抗性基因。使用 GenBank 中具有相同 rep 基因的完整质粒进行比较分析。
鲍曼不动杆菌 DETAB-P2 经巴斯德方案鉴定为 ST138,经牛津方案鉴定为新型 ST2209。它将 blaOXA-58 和 blaNDM-1 转移到 ATCC 17978 中,位于 100072bp 的质粒 pDETAB2 中,该质粒还携带 bleMBL、sul2、aacC2d、tet(39)、msr(E)-mph(E)和推定的汞抗性和 RND 外排系统决定子。pDETAB2 代表一种新的质粒类型,GR34,包含 16 个 pdif 位点和几个新的 dif 模块。在 GenBank 中,pDETAB2 与 18 个进一步的 GR34 质粒仅共享 10kbp 的核心序列,而其不同的辅助区域则由各种 dif 模块组成。
GR34 质粒存在于来自不同环境的几种不动杆菌属物种中。由于存在 pdif 位点和一系列 dif 模块,它们的辅助区内容存在很大差异,其中一些模块包含抗生素抗性基因。