Genomewide Identification of Genetic Determinants of Antimicrobial Drug Resistance in Pseudomonas aeruginosa

被引:95
作者
Doetsch, Andreas
Becker, Tanja
Pommerenke, Claudia
Magnowska, Zofia [2 ]
Jaensch, Lothar [2 ]
Haeussler, Susanne [1 ,3 ,4 ]
机构
[1] Helmholtz Ctr Infect Res, Young Investigator Res Grp, Chron Pseudomonas Infect Res Grp, D-38124 Braunschweig, Germany
[2] Helmholtz Ctr Infect Res, Prote Grp, D-38124 Braunschweig, Germany
[3] Hannover Med Sch, Ctr Expt & Clin Infect Res, TWINCORE, D-30625 Hannover, Germany
[4] Helmholtz Ctr Infect Res, D-30625 Hannover, Germany
关键词
MULTIPLE ANTIBIOTIC-RESISTANCE; CYSTIC-FIBROSIS PATIENTS; OUTER-MEMBRANE; ESCHERICHIA-COLI; PROTEIN-F; AMINOGLYCOSIDE ANTIBIOTICS; TETRACYCLINE RESISTANCE; BACTERIAL UPTAKE; MUTANT LIBRARY; EFFLUX OPERON;
D O I
10.1128/AAC.00035-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The emergence of antimicrobial drug resistance is of enormous public concern due to the increased risk of delayed treatment of infections, the increased length of hospital stays, the substantial increase in the cost of care, and the high risk of fatal outcomes. A prerequisite for the development of effective therapy alternatives is a detailed understanding of the diversity of bacterial mechanisms that underlie drug resistance, especially for problematic gram-negative bacteria such as Pseudomonas aeruginosa. This pathogen has impressive chromosomally encoded mechanisms of intrinsic resistance, as well as the potential to mutate, gaining resistance to current antibiotics. In this study we have screened the comprehensive nonredundant Harvard PA14 library for P. aeruginosa mutants that exhibited either increased or decreased resistance against 19 antibiotics commonly used in the clinic. This approach identified several genes whose inactivation sensitized the bacteria to a broad spectrum of different antimicrobials and uncovered novel genetic determinants of resistance to various classes of antibiotics. Knowledge of the enhancement of bacterial susceptibility to existing antibiotics and of novel resistance markers or modifiers of resistance expression may lay the foundation for effective therapy alternatives and will be the basis for the development of new strategies in the control of problematic multiresistant gram-negative bacteria.
引用
收藏
页码:2522 / 2531
页数:10
相关论文
共 49 条
[1]   n-hexane sensitivity of Escherichia coli due to low expression of imp/ostA encoding an 87 kDa minor protein associated with the outer membrane [J].
Abe, S ;
Okutsu, T ;
Nakajima, H ;
Kakuda, N ;
Ohtsu, W ;
Aono, R .
MICROBIOLOGY-SGM, 2003, 149 :1265-1273
[2]   Global gene expression as a function of the iron status of the bacterial cell:: Influence of differentially expressed genes in the virulence of the human pathogen Vibrio vulnificus [J].
Alice, Alejandro F. ;
Naka, Hiroaki ;
Crosa, Jorge H. .
INFECTION AND IMMUNITY, 2008, 76 (09) :4019-4037
[3]   Constitutive high expression of chromosomal β-lactamase in Pseudomonas aeruginosa caused by a new insertion sequence (IS1669) located in ampD [J].
Bagge, N ;
Ciofu, O ;
Hentzer, M ;
Campbell, JIA ;
Givskov, M ;
Hoiby, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (11) :3406-3411
[4]   Comparison of the Micronaut Merlin automated broth microtiter system with the standard agar dilution method for antimicrobial susceptibility testing of mucoid and nonmucoid Pseudomonas aeruginosa isolates from cystic fibrosis patients [J].
Balke, B ;
Hoy, L ;
Weissbrodt, H ;
Häussler, S .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2004, 23 (10) :765-771
[5]  
Barb AW, 2008, CURR PHARM BIOTECHNO, V9, P9
[6]   Role of AmpD, OprF and penicillin-binding proteins in β-lactam resistance in clinical isolates of Pseudomonas aeruginosa [J].
Bratu, Simona ;
Landman, David ;
Gupta, Jyoti ;
Quale, John .
JOURNAL OF MEDICAL MICROBIOLOGY, 2007, 56 (06) :809-814
[7]   Complex Ciprofloxacin Resistome Revealed by Screening a Pseudomonas aeruginosa Mutant Library for Altered Susceptibility [J].
Breidenstein, Elena B. M. ;
Khaira, Bhavjinder K. ;
Wiegand, Irith ;
Overhage, Joerg ;
Hancock, Robert E. W. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (12) :4486-4491
[8]   ROLES OF RIBOSOMAL-BINDING, MEMBRANE-POTENTIAL, AND ELECTRON-TRANSPORT IN BACTERIAL UPTAKE OF STREPTOMYCIN AND GENTAMICIN [J].
BRYAN, LE ;
KWAN, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1983, 23 (06) :835-845
[9]   PERSISTENCE OF PSEUDOMONAS-AERUGINOSA DURING CIPROFLOXACIN THERAPY OF A CYSTIC-FIBROSIS PATIENT - TRANSIENT RESISTANCE TO QUINOLONES AND PROTEIN-F-DEFICIENCY [J].
CHAMBERLAND, S ;
MALOUIN, F ;
RABIN, HR ;
SCHOLLAARDT, T ;
PARR, TR ;
BRYAN, LE .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 25 (06) :995-1010
[10]   Clinical significance and predictors of community-onset Pseudomonas aeruginosa bacteremia [J].
Cheong, Hae Suk ;
Kang, Cheol-In ;
Wi, Yu Mi ;
Kim, Eun Seok ;
Lee, Jin Seo ;
Ko, Kwan Soo ;
Chung, Doo Ryeon ;
Lee, Nam Yong ;
Song, Jae-Hoon ;
Peck, Kyong Ran .
AMERICAN JOURNAL OF MEDICINE, 2008, 121 (08) :709-714