Reduction of virulence factor pyocyanin production in multidrug-resistant Pseudomonas aeruginosa

被引:18
作者
Fuse, Katsuhiro [1 ,2 ,3 ]
Fujimura, Shigeru [2 ]
Kikuchi, Toshiaki [1 ]
Gomi, Kazunori [1 ]
Iida, Yasuhiro [4 ]
Nukiwa, Toshihiro [1 ]
Watanabe, Akira [2 ]
机构
[1] Tohoku Univ, Dept Resp Med, Grad Sch Med, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Res Div Dev Antiinfect Agents, Inst Dev Aging & Canc, Aoba Ku, Sendai, Miyagi 9808575, Japan
[3] Tohoku Employees Pens Welf Hosp, Dept Pharm, Sendai, Miyagi, Japan
[4] Kanagawa Inst Technol, Dept Appl Chem, Fac Engn, Atsugi, Kanagawa, Japan
关键词
Multidrug-resistance; P; aeruginosa; Pyocyanin; MBL; METALLO-BETA-LACTAMASE; AIRWAY EPITHELIAL-CELLS; GRAM-NEGATIVE BACTERIA; GENE-EXPRESSION; NITRIC-OXIDE; OUTBREAK; INTEGRON; PCR; IDENTIFICATION; SECONDARY;
D O I
10.1007/s10156-012-0457-9
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Nosocomial infections caused by metallo-beta-lactamase (MBL)-producing multidrug-resistant (MDR) Pseudomonas aeruginosa have become a worldwide problem. Pyocyanin, a representative pigment produced by P. aeruginosa, is the major virulence factor of this organismThe aim of this study was to investigate the pyocyanin-producing ability of MBL-producing MDR P. aeruginosa. A total of 50 clinical isolates of P. aeruginosa, including 20 MDR strains, were collected at 18 general hospitals in Japan. The chromaticity and luminosity produced by pyocyanin in each isolate were measured. The quantity of pyocyanin and the expression of the phzM and phzS genes coding a pyocyanin synthesis enzyme were measured. MDR strains showed a bright yellow-green, while non-MDR strains tended to show a dark blue-green. The quantities of pyocyanin in MBL-producing strains and non-producing strains were 0.015 +/- A 0.002 and 0.41 +/- A 0.10 mu g, respectively. The expression of the phzM and phzS genes in the MDR strains was 11 and 14 %, respectively, of the expression in the non-MDR strains. When the MBL gene was transduced into P. aeruginosa and it acquired multidrug resistance, it was shown that the pyocyanin-producing ability decreased. The pathogenicity of MBL-producing MDR P. aeruginosa may be lower than that of non-MDR strains. These MBL-producing MDR strains may be less pathogenic than non-MDR strains. This may explain why MDR-P. aeruginosa is unlikely to cause infection but, rather, causes subclinical colonization only.
引用
收藏
页码:82 / 88
页数:7
相关论文
共 32 条
[1]  
[Anonymous], 2009, M100S19 CLIN LAB STA
[2]  
Arakawa Y, 2000, J CLIN MICROBIOL, V38, P40
[3]   ANTIBIOTIC ACTION OF PYOCYANIN [J].
BARON, SS ;
ROWE, JJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1981, 20 (06) :814-820
[4]  
Campbell J., 2011, CURR PROTOC CHEM BIO, V3
[5]   DIFFERENTIAL PRIMARY PLATING MEDIUM FOR ENHANCEMENT OF PIGMENT PRODUCTION BY PSEUDOMONAS-AERUGINOSA [J].
DALY, JA ;
BOSHARD, R ;
MATSEN, JM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1984, 19 (06) :742-743
[6]   Pseudomonas pyocyanine alters calcium signaling in human airway epithelial cells [J].
Denning, GM ;
Railsback, MA ;
Rasmussen, GT ;
Cox, CD ;
Britigan, BE .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1998, 274 (06) :L893-L900
[7]   Multi-drug resistant Pseudomonas aeruginosa outbreak in a burns unit -: an infection control study [J].
Douglas, MW ;
Mulholland, K ;
Denyer, V ;
Gottlieb, T .
BURNS, 2001, 27 (02) :131-135
[8]   IDENTIFICATION AND CHARACTERIZATION OF GENES FOR A 2ND ANTHRANILATE SYNTHASE IN PSEUDOMONAS-AERUGINOSA - INTERCHANGEABILITY OF THE 2 ANTHRANILATE SYNTHASES AND EVOLUTIONARY IMPLICATIONS [J].
ESSAR, DW ;
EBERLY, L ;
HADERO, A ;
CRAWFORD, IP .
JOURNAL OF BACTERIOLOGY, 1990, 172 (02) :884-900
[9]   EVALUATION OF 9-CHLORO-9-[4-(DIETHYLAMINO)PHENYL]-9,10-DIHYDRO-10-PHENYLACRIDINE HYDROCHLORIDE (C-390) IN BROTH AND AGAR MEDIA FOR IDENTIFICATION OF PSEUDOMONAS-AERUGINOSA [J].
FADER, RC ;
LATIMER, J ;
BANNISTER, E ;
LUCIA, H .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (09) :1901-1903
[10]   Regulation of gene expression by cell-to-cell communication: Acyl-homoserine lactone quorum sensing [J].
Fuqua, C ;
Parsek, MR ;
Greenberg, EP .
ANNUAL REVIEW OF GENETICS, 2001, 35 :439-468