Loss-of-function mutations in the mtr efflux system of Neisseria gonorrhoeae

被引:33
作者
Veal, WL
Yellen, A
Balthazar, JT
Pan, WB
Spratt, BG
Shafer, WM [1 ]
机构
[1] Emory Univ, Sch Med, Dept Immunol & Microbiol, Atlanta, GA 30322 USA
[2] Univ Sussex, Sch Biol Sci, Microbial Genet Grp, Brighton BN1 9QG, E Sussex, England
[3] Vet Affairs Med Ctr, Med Res Serv, Labs Microbial Pathogenesis, Decatur, GA 30033 USA
来源
MICROBIOLOGY-SGM | 1998年 / 144卷
基金
英国惠康基金;
关键词
gonococci; efflux pump; antibiotic hypersusceptibility;
D O I
10.1099/00221287-144-3-621
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Resistance of Neisseria gonorrhoeae to antimicrobial hydrophobic agents (HAs) has been ascribed to the mtr (multiple transferable resistance) operon. This operon is composed of the mtrR gene, which encodes a transcriptional repressor (MtrR), and a three-gene complex (mtrCDE), which encodes cell envelope proteins (MtrC-MtrD-MtrE) that form an energy-dependent efflux pump. HA-hypersusceptible strains are often isolated from patients, but the genetic basis for such hypersusceptibility was heretofore unknown. The genetic basis of HA hypersusceptibility in laboratory-derived strains BR54 and BR87 was studied to learn if this trait could be linked to mutations in the mtr operon, Mutations in the mtrR gene of these strains that could be phenotypically suppressed by mutations in their mtrC or mtrD genes were identified. Thus, small deletions (4-10 bp) in the mtrC or mtrD genes of strains BR87 and BR54 that would result in the production of truncated efflux pump proteins that serve as a membrane fusion protein (MtrC) or transporter of HAs (MtrD) were found to be responsible for their HA-hypersusceptible property.
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页码:621 / 627
页数:7
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