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Research Article

Cross-resistance to fluoroquinolones in multiple-antibiotic-resistant (Mar) Escherichia coli selected by tetracycline or chloramphenicol: decreased drug accumulation associated with membrane changes in addition to OmpF reduction.

S P Cohen, L M McMurry, D C Hooper, J S Wolfson, S B Levy
S P Cohen
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
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L M McMurry
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
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D C Hooper
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
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J S Wolfson
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
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S B Levy
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
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DOI: 10.1128/AAC.33.8.1318
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Article Information

DOI 
https://doi.org/10.1128/AAC.33.8.1318
PubMed 
2679373

Published By 
American Society for Microbiology Journals
History 
  • Published online August 1, 1989.

Author Information

  1. S P Cohen,
  2. L M McMurry,
  3. D C Hooper,
  4. J S Wolfson and
  5. S B Levy
  1. Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111.

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Cross-resistance to fluoroquinolones in multiple-antibiotic-resistant (Mar) Escherichia coli selected by tetracycline or chloramphenicol: decreased drug accumulation associated with membrane changes in addition to OmpF reduction.
S P Cohen, L M McMurry, D C Hooper, J S Wolfson, S B Levy
Antimicrobial Agents and Chemotherapy Aug 1989, 33 (8) 1318-1325; DOI: 10.1128/AAC.33.8.1318

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Cross-resistance to fluoroquinolones in multiple-antibiotic-resistant (Mar) Escherichia coli selected by tetracycline or chloramphenicol: decreased drug accumulation associated with membrane changes in addition to OmpF reduction.
S P Cohen, L M McMurry, D C Hooper, J S Wolfson, S B Levy
Antimicrobial Agents and Chemotherapy Aug 1989, 33 (8) 1318-1325; DOI: 10.1128/AAC.33.8.1318
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