Evidence for an efflux pump mediating multiple antibiotic resistance in Salmonella enterica serovar Typhimurium
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Piddock, LJV
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Univ Birmingham, Div Infect & Immun, Antimicrobial Agents Res Grp, Birmingham B15 2TT, W Midlands, EnglandUniv Birmingham, Div Infect & Immun, Antimicrobial Agents Res Grp, Birmingham B15 2TT, W Midlands, England
Piddock, LJV
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White, DG
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机构:Univ Birmingham, Div Infect & Immun, Antimicrobial Agents Res Grp, Birmingham B15 2TT, W Midlands, England
White, DG
Gensberg, K
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机构:Univ Birmingham, Div Infect & Immun, Antimicrobial Agents Res Grp, Birmingham B15 2TT, W Midlands, England
Gensberg, K
Pumbwe, L
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机构:Univ Birmingham, Div Infect & Immun, Antimicrobial Agents Res Grp, Birmingham B15 2TT, W Midlands, England
Pumbwe, L
Griggs, DJ
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机构:Univ Birmingham, Div Infect & Immun, Antimicrobial Agents Res Grp, Birmingham B15 2TT, W Midlands, England
Griggs, DJ
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[1] Univ Birmingham, Div Infect & Immun, Antimicrobial Agents Res Grp, Birmingham B15 2TT, W Midlands, England
The mechanism of multiple antibiotic resistance in six isolates of Salmonella enterica serovar Typhimurium recovered from a patient treated with ciprofloxacin was studied to investigate the role of efflux in the resistance phenotype. Compared to the patient's pretherapy isolate (L3), five of six isolates accumulated less ciprofloxacin, three of six isolates accumulated less chloramphenicol, and all six accumulated less tetracycline. The accumulation of one or more antibiotics was increased by carbonyl cyanide m-chlorophenylhydrazone to concentrations similar to those accumulated by L3 for all isolates except one, in which accumulation of all three agents remained approximately half that of L3, All isolates had the published wild-type sequences of marO and marR, No increased expression of marA, tolC, or soxS was observed by Northern blotting; however, three isolates showed increased expression of acrB, which was confirmed by quantitative competitive reverse transcription-PCR. However, there were no mutations within acrR or the promoter region of acrAB in any of the isolates.
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Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, JapanTokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, Japan
Aono, R
Tsukagoshi, N
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Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, JapanTokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, Japan
Tsukagoshi, N
Yamamoto, M
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Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, JapanTokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, Japan
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Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, JapanTokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, Japan
Aono, R
Tsukagoshi, N
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Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, JapanTokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, Japan
Tsukagoshi, N
Yamamoto, M
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Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, JapanTokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, Japan