Title Convergence of MCR-8.2 and Chromosome-Mediated Resistance to Colistin and Tigecycline in an NDM-5-Producing ST656 Klebsiella pneumoniae Isolate From a Lung Transplant Patient in China
Authors Zhao, Jiankang
Li, Ziyao
Zhang, Yulin
Liu, Xinmeng
Lu, Binghuai
Cao, Bin
Affiliation China Japan Friendship Hosp, Lab Clin Microbiol & Infect Dis, Dept Pulm & Crit Care Med,Natl Clin Res Ctr Resp, Natl Ctr Resp Med,Ctr Resp Med, Beijing, Peoples R China
Chinese Acad Med Sci & Peking Union Med Coll, Inst Resp Med, Beijing, Peoples R China
Peking Univ, Tsinghua Univ, Joint Ctr Life Sci, Beijing, Peoples R China
Capital Med Univ, Dept Resp Med, Beijing, Peoples R China
Keywords ESCHERICHIA-COLI
BETA-LACTAMASE
MECHANISMS
SUSCEPTIBILITY
PLASMIDS
RAMA
Issue Date 11-Jul-2022
Publisher FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY
Abstract We characterized the first NDM- 5 and MCR- 8.2 co- harboring ST656 Klebsiella pneumoniae clinical isolate, combining with chromosomal gene-mediated resistance to colistin and tigecycline. The K. pneumoniae KP32558 was isolated from the bronchoalveolar lavage fluid from a lung transplant patient. Complete genome sequences were obtained through Illumina HiSeq sequencing and nanopore sequencing. The acquired resistance genes and mutations in chromosome-encoded genes associated with colistin and tigecycline resistance were analyzed. Comparative genomic analysis was conducted between mcr-8.2-carrying plasmids. The K. pneumoniae KP32558 was identified as a pan-drug resistant bacteria, belonging to ST656, and harbored plasmid-encoded blaNDM- 5 and mcr-8.2 genes. The blaNDM- 5 gene was located on an IncX3 type plasmid. The mcr-8.2 gene was located on a conjugative plasmid pKP32558-2-mcr8, which had a common ancestor with another two mcr-8.2carrying plasmids pMCR8_020135 and pMCR8_095845. The MIC of KP32558 for colistin was 256 mg/L. The mcr-8.2 gene and mutations in the two- component system, pmrA and crrB, and the regulator mgrB, had a synergistic effect on the highlevel colistin resistance. The truncation in the acrR gene, related to tigecycline resistance, was also identified. K. pneumoniae has evolved a variety of complex resistance mechanisms to the last-resort antimicrobials, close surveillance is urgently needed to monitor the prevalence of this clone.
URI http://hdl.handle.net/20.500.11897/658530
ISSN 2235-2988
DOI 10.3389/fcimb.2022.922031
Indexed SCI(E)
Appears in Collections: 生命科学学院

Files in This Work
There are no files associated with this item.

Web of Science®


0

Checked on Last Week

Scopus®



Checked on Current Time

百度学术™


0

Checked on Current Time

Google Scholar™





License: See PKU IR operational policies.