Acquisition of resistance to carbapenems in multidrug-resistant clinical strains of Acinetobacter baumannii:: Natural Insertional inactivation of a gene encoding a member of a novel family of β-barrel outer membrane proteins

被引:203
作者
Mussi, MA
Limansky, AS
Viale, AM
机构
[1] Univ Nacl Rosario, Inst Mol & Cellular Biol, CONICET, IBR, RA-2000 Rosario, Santa Fe, Argentina
[2] Univ Nacl Rosario, Dept Microbiol, Fac Ciencias Bioquim & Farmaceut, RA-2000 Rosario, Santa Fe, Argentina
关键词
D O I
10.1128/AAC.49.4.1432-1440.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The outer membrane proteins responsible for the influx of carbapenem P-lactam antibiotics in the nonfermentative gram-negative pathogen Acinetobacter baumannii are still poorly characterized. Resistance to both imipenem and meropenem in multidrug-resistant clinical strains of A. baumannii is associated with the loss of a heat-modifiable 29-kDa outer membrane protein, designated CarO. The chromosomal locus containing the carO gene was cloned and characterized from different clinical isolates. Only one carO copy, present in a single transcriptional unit, was found in the A. baumannii genome. The carO gene encodes a polypeptide of 247 amino acid residues with a typical N-terminal signal sequence and a predicted transmembrane P-barrel topology. Its absence from different carbapenem-resistant clinical isolates of A. baumannii resulted from the disruption of carO by distinct insertion elements. The overall data thus support the notion that CarO participates in the influx of carbapenem antibiotics in A. baumannii. Moreover, database searches identified the presence of carO homologs only in species of the genera Acinetobacter, Moraxella, and Psychrobacter, disclosing the existence of a novel family of outer membrane proteins restricted to the family Moraxellaceae of the class gamma-Proteobacteria.
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页码:1432 / 1440
页数:9
相关论文
共 37 条
[1]   Identification and characterization of outer membrane proteins G1a and G1b of Moraxella catarrhalis [J].
Adlowitz, DG ;
Hiltke, T ;
Lesse, AJ ;
Murphy, TF .
VACCINE, 2004, 22 (20) :2533-2540
[2]   Characterization of OXA-25, OXA-26, and OXA-27, molecular class D β-lactamases associated with carbapenem resistance in clinical isolates of Acinetobacter baumannii [J].
Afzal-Shah, M ;
Woodford, N ;
Livermore, DM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (02) :583-588
[3]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[4]  
AMYES SGB, 1996, ACINETOBACTER MICROB, P185
[5]   A Hidden Markov Model method, capable of predicting and discriminating β-barrel outer membrane proteins -: art. no. 29 [J].
Bagos, PG ;
Liakopoulos, TD ;
Spyropoulos, IC ;
Hamodrakas, SJ .
BMC BIOINFORMATICS, 2004, 5 (1)
[6]   Acinetobacter spp, as nosocomial pathogens: Microbiological, clinical, and epidemiological features [J].
BergogneBerezin, E ;
Towner, KJ .
CLINICAL MICROBIOLOGY REVIEWS, 1996, 9 (02) :148-+
[7]   Characterization of a nosocomial outbreak caused by a multiresistant Acinetobacter baumannii strain with a carbapenem-hydrolyzing enzyme:: High-level carbapenem resistance in A. baumannii is not due solely to the presence of β-lactamases [J].
Bou, G ;
Cerveró, G ;
Domínguez, MA ;
Quereda, C ;
Martínez-Beltrán, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (09) :3299-3305
[8]   Imipenem resistance among Acinetobacter baumannii: Association with reduced expression of a 33-36 kDa outer membrane protein [J].
Clark, RB .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1996, 38 (02) :245-251
[9]  
DIONISI HM, 1995, BIOTECHNIQUES, V19, P348
[10]   Relationship between β-lactamase production, outer membrane protein and penicillin-binding protein profiles on the activity of carbapenems against clinical isolates of Acinetobacter baumannii [J].
Fernández-Cuenca, F ;
Martínez-Martínez, L ;
Conejo, MC ;
Ayala, JA ;
Perea, EJ ;
Pascual, A .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (03) :565-574