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

1 Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA 2 Microbial Genetics Group, School of Biological Sciences, University of Sussex, Falmer, Brighton BN1 9QG, UK 3 Laboratories of Microbial Pathogenesis, Medical Research Service, VA Medical Center...

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Published in:Microbiology (Society for General Microbiology) 1998-03, Vol.144 (3), p.621-627
Main Authors: Veal, Wendy L, Yellen, Ansley, Balthazar, Jacqueline T, Pan, Wubin, Spratt, Brian G, Shafer, William M
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description 1 Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA 2 Microbial Genetics Group, School of Biological Sciences, University of Sussex, Falmer, Brighton BN1 9QG, UK 3 Laboratories of Microbial Pathogenesis, Medical Research Service, VA Medical Center (Atlanta), Decatur, GA 30033, USA ABSTRACT 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. Author for correspondence: William M. Shafer. Tel: +1 404 728 7688. Fax: + 1 404 329 2210. e-mail: wshafer@emory.edu Keywords: gonococci, efflux pump, antibiotic hypersusceptibility Present address: TerraGen Diversity Inc., University of British Columbia, Vancouver, Canada V6T 123. Present address: Wellcome Trust Centre for the Epidemiology of Infectious Diseases, Department of Zoology, Oxford University, South Parks Road, Oxford OX1 3PS, UK.
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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. Author for correspondence: William M. Shafer. Tel: +1 404 728 7688. Fax: + 1 404 329 2210. e-mail: wshafer@emory.edu Keywords: gonococci, efflux pump, antibiotic hypersusceptibility Present address: TerraGen Diversity Inc., University of British Columbia, Vancouver, Canada V6T 123. 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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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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. Author for correspondence: William M. Shafer. Tel: +1 404 728 7688. Fax: + 1 404 329 2210. e-mail: wshafer@emory.edu Keywords: gonococci, efflux pump, antibiotic hypersusceptibility Present address: TerraGen Diversity Inc., University of British Columbia, Vancouver, Canada V6T 123. Present address: Wellcome Trust Centre for the Epidemiology of Infectious Diseases, Department of Zoology, Oxford University, South Parks Road, Oxford OX1 3PS, UK.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>9534233</pmid><doi>10.1099/00221287-144-3-621</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1350-0872
ispartof Microbiology (Society for General Microbiology), 1998-03, Vol.144 (3), p.621-627
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source Alma/SFX Local Collection
subjects Amino Acid Sequence
Bacterial Outer Membrane Proteins - genetics
Bacterial Proteins
Bacteriology
Base Sequence
Biological and medical sciences
Carrier Proteins - genetics
Drug Resistance, Microbial
Drug Resistance, Multiple - genetics
Ferredoxin-NADP Reductase
Fundamental and applied biological sciences. Psychology
Gene Amplification
Gene Deletion
Genetics
Humans
Lipoproteins - genetics
Membrane Proteins - genetics
Membrane Transport Proteins
Microbiology
Molecular Sequence Data
Neisseria gonorrhoeae
Neisseria gonorrhoeae - drug effects
Neisseria gonorrhoeae - genetics
Neisseria gonorrhoeae - metabolism
Operon
Repressor Proteins - genetics
Sequence Analysis, DNA
Species Specificity
Suppression, Genetic
Transformation, Bacterial
title Loss-of-function mutations in the mtr efflux system of Neisseria gonorrhoeae
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