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Replication of the Ordered, Nonredundant Library of Pseudomonas aeruginosa strain PA14 Transposon Insertion Mutants
Published on: May 4, 2018
Emergence of KPC-2-producing Pseudomonas aeruginosa sequence type 463 isolates in Hangzhou, China
Yan-yan Hu1, Dan-xia Gu1, Jia-chang Cai1
12nd Affiliated Hospital of Zhejiang University, Zhejiang University, Hangzhou, People's Republic of China.
Abstract:
Thirty-nine Klebsiella pneumoniae carbapenemase (KPC)-producing Pseudomonas aeruginosa isolates, all exhibiting high-level resistance to carbapenems and other β-lactam antibiotics, were isolated in Hangzhou, China. Molecular epidemiology analysis indicated the presence of two dominant clones, namely, clones A and B, both of which belong to sequence type 463 (ST463). A genetic environment analysis demonstrated that both clones harbor an ISKpn8 transposase, bla(KPC-2), and an ISKpn6-like transposase. These findings depict the features of clonal expansion and transmission of KPC-2-producing P. aeruginosa strains in Hangzhou, China.
Insights
Two dominant clones of carbapenem-resistant Klebsiella pneumoniae carbapenemase (KPC)-producing Pseudomonas aeruginosa were identified in Hangzhou, China. These strains, belonging to ST463, show clonal expansion and transmission, highlighting a public health concern.
Area of Science:
- Microbiology
- Genetics
- Infectious Diseases
Background:
- Klebsiella pneumoniae carbapenemase (KPC)-producing Pseudomonas aeruginosa poses a significant threat due to high-level resistance to carbapenems and beta-lactam antibiotics.
- The emergence and spread of antimicrobial resistance in P. aeruginosa are critical global health challenges.
Purpose of the Study:
- To investigate the molecular epidemiology and genetic characteristics of KPC-producing P. aeruginosa isolates from Hangzhou, China.
- To understand the clonal expansion and transmission patterns of these resistant strains.
Main Methods:
- Isolation and identification of P. aeruginosa strains.
- Antimicrobial susceptibility testing, focusing on carbapenem and beta-lactam resistance.
- Molecular epidemiology using techniques such as multilocus sequence typing (MLST) to determine sequence types (STs).
- Genetic environment analysis to identify mobile genetic elements associated with resistance genes.
Main Results:
- Thirty-nine KPC-producing P. aeruginosa isolates were identified, all exhibiting high-level resistance.
- Molecular epidemiology revealed two dominant clones, designated A and B, both belonging to sequence type 463 (ST463).
- Genetic analysis showed that both clones harbor an ISKpn8 transposase, the bla(KPC-2) gene, and an ISKpn6-like transposase.
Conclusions:
- The findings demonstrate clonal expansion and transmission of KPC-2-producing P. aeruginosa strains in Hangzhou, China.
- ST463 appears to be a significant clone associated with the spread of carbapenem resistance in this region.
- The presence of specific genetic elements like ISKpn8 and ISKpn6-like transposases likely facilitates the dissemination of the bla(KPC-2) gene.
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