Your browser doesn't support javascript.
loading
Characterization of the Genetic Background of KPC-2-Producing Klebsiella pneumoniae with Insertion Elements Disrupting the ompK36 Porin Gene.
Wu, Lii-Tzu; Guo, Ming-Kai; Ke, Se-Chin; Lin, Yi-Pei; Pang, Yi-Chun; Nguyen, Hong-Thuy Vy; Chen, Chih-Ming.
Afiliação
  • Wu LT; The Institute of Medical Science and Department of Microbiology, China Medical University Hospital, Taichung, Taiwan.
  • Guo MK; The Institute of Medical Science and Department of Microbiology, China Medical University Hospital, Taichung, Taiwan.
  • Ke SC; Infection Control Office, Tungs' Taichung MetroHarbor Hospital, Taichung, Taiwan.
  • Lin YP; Department of Medical Technology, Jen-The Junior College of Medicine, Nursing and Management, Miaoli, Taiwan.
  • Pang YC; Department of Medical Research, Tungs' Taichung MetroHarbor Hospital, Taichung, Taiwan.
  • Nguyen HV; The Institute of Medical Science and Department of Microbiology, China Medical University Hospital, Taichung, Taiwan.
  • Chen CM; The Institute of Biomedical Sciences College of Medicine, China Medical University, Taichung, Taiwan.
Microb Drug Resist ; 26(9): 1050-1057, 2020 Sep.
Article em En | MEDLINE | ID: mdl-32283046
Carbapenemase-producing combined porin loss is one of the primary mechanisms for carbapenem resistance. Although mutations in ompK35 and ompK36 genes have often been identified in carbapenem-resistant Klebsiella pneumoniae, reports on the porin protein gene disruption by insertion sequence (IS) elements are varied. The ompK36 porin protein gene disruption by IS elements and OmpK36 production loss in six blaKPC-2-carrying K. pneumoniae isolates were detected in this study. IS903, ISEc68, and IS1 insertions were noted in the 3, 2, and 1 isolates, respectively. The six K. pneumoniae isolates showed five different pulsed-field gel electrophoresis patterns and belonged to four multilocus sequence typing types, ST4, ST11, ST15, and ST39. This study increases our understanding of the genetic background of KPC-2 carbapenemases in porin-defective clinical isolates and the contribution of OmpK36 production loss to carbapenem resistance.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Beta-Lactamases / Mutagênese Insercional / Porinas / Resistência beta-Lactâmica / Klebsiella pneumoniae Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Beta-Lactamases / Mutagênese Insercional / Porinas / Resistência beta-Lactâmica / Klebsiella pneumoniae Idioma: En Ano de publicação: 2020 Tipo de documento: Article