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The Characterization of OXA-232 Carbapenemase-Producing ST437 Klebsiella pneumoniae in China.
Weng, Xingbei; Shi, Qiucheng; Wang, Sheng; Shi, Yubo; Sun, Dinghe; Yu, Yunsong.
Afiliação
  • Weng X; Department of Laboratory Medicine, Ningbo Hospital, Zhejiang University School of Medicine, Ningbo, China.
  • Shi Q; Department of Laboratory Medicine, Ningbo First Hospital, Ningbo, China.
  • Wang S; Department of Infectious Diseases, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • Shi Y; Key Laboratory of Microbial Technology and Bioinformatics of Zhejiang Province, Hangzhou, China.
  • Sun D; Department of Laboratory Medicine, Ningbo Hospital, Zhejiang University School of Medicine, Ningbo, China.
  • Yu Y; Department of Laboratory Medicine, Ningbo First Hospital, Ningbo, China.
Can J Infect Dis Med Microbiol ; 2020: 5626503, 2020.
Article em En | MEDLINE | ID: mdl-32724486
ABSTRACT
Carbapenem-resistant Klebsiella pneumoniae (CRKP) was epidemic around the world and become a global threat to public health. The most important carbapenem-resistant mechanism is producing carbapenemases, especially Klebsiella pneumoniae carbapenemase (KPC), which is prevalent in the international clonal complex CC11. The high-risk multidrug-resistant CC11 is widespread worldwide, and KPC-producing and (New Delhi metallo) NDM-producing strains had been reported in this clonal complex before; moreover, cases with the CC11 strain faced more severe forms of drug resistance and treatment challenges than other clonal complexes. In this study, we identified an OXA-232-producing ST437 Klebsiella pneumoniae isolate in China, which belonged to CC11. The isolate was resistant to ß-lactams, aminoglycosides, and fluoroquinolones but susceptible to fosfomycin, tigecycline, and colistin. The bla OXA-232 gene was located on a 6141 bp ColKP3-type nonconjugative plasmid, and the plasmid was transformed by chemical transformation successfully. This is the first report of OXA-232-producing ST437 K. pneumoniae in China, a new clone of high-risk multidrug-resistant CC11.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article