Efflux Pump Overexpression in Conjunction with Alternation of Outer Membrane Protein May Induce Acinetobacter baumannii Resistant to Imipenem

被引:29
作者
Luo, LiuLin [1 ,3 ]
Jiang, XiaoFei [4 ]
Wu, Qiong [2 ]
Wei, LiMing [5 ]
Li, JianHua [6 ]
Ying, ChunMei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Clin Lab, Renji Hosp, Sch Med, Shanghai 200127, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Clin Microbiol, Ruijin Hosp, Shanghai 200127, Peoples R China
[3] Tongji Univ Sch Med, Shanghai Pulm Hosp, Dept Clin Lab, Shanghai, Peoples R China
[4] Fudan Univ, Lab Ctr Med, Huashan Hosp, Shanghai Med Coll, Shanghai 200433, Peoples R China
[5] Fudan Univ, Inst Biomed Sci, Shanghai 200433, Peoples R China
[6] Fudan Univ, Key Lab Med Mol Virol, Shanghai 200433, Peoples R China
关键词
Acinetobacter baumannii; Efflux pump; Outer membrane protein; 2-dimensional electrophosis; Mass spectrometer; CARBAPENEM RESISTANCE; BETA-LACTAMASES; DECREASED SUSCEPTIBILITY; STRAIN; TIGECYCLINE; IDENTIFICATION; ADEABC; ANTIBIOTICS; TRANSPOSON; HOSPITALS;
D O I
10.1159/000323620
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background:To investigate the role of outer membrane proteins in Acinetobacter baumannii resistant to imipenem, 2 strains were procured from the same patient. Methods: The imipenem-resistant strain was obtained following a period of imipenem treatment in vivo. The multilocus sequence typing and repetitive extragenic palindromic PCR results indicated that the imipenem-resistant strain originated from the sensitive one. Results: Isoelectric focusing detected no carbapenemases, with neither OXA carbapenemases nor metallo-beta-lactamases found. Mass spectrophotometric analysis revealed that 3 outer membrane proteins were expressed differentially in the 2 strains: 2 downregulated proteins (OprD and CarO) and 1 upregulated the 34-kDa efflux pump protein in the resistant strain. A 32-fold decrease in the MIC for imipenem in the presence of Phe-Arg-beta-naphthylamide in the same strain indicated a possible involvement of the efflux pump mechanism in its resistance, which was consistent with the findings that the mRNA expression of the 34-kDa efflux pump gene was almost fivefold upregulated in the imipenem-resistant strain compared with that in the imipenem-sensitive strain. Such a significant difference, however, was not found in the expression of AdeB and AdeJ between the 2 strains, and AdeE was not detected. Conclusions: Our results suggested that downregulation of outer membrane proteins in conjunction with efflux pump overexpression might contribute to imipenem resistance induced in vivo in A. baumannii. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:77 / 84
页数:8
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