Uptake of minocycline and tetracycline by tetracycline-susceptible and -resistant bacteria

Antimicrob Agents Chemother. 1973 Jun;3(6):662-4. doi: 10.1128/AAC.3.6.662.

Abstract

Minocycline (7-dimethylamino-6-demethyl-6-deoxytetracycline) is a new semisynthetic tetracycline with potent activity against tetracycline-susceptible bacterial pathogens and unique activity against tetracycline-resistant staphylococci. Studies to determine the basis for this unique activity showed that, whereas tetracycline-resistant staphylococci took up less (3)H-tetracycline than the susceptible cells, both the tetracycline-resistant and -susceptible cells accumulated equivalent amounts of (14)C-minocycline. In contrast, tetracycline-resistant Escherichia coli cells were relatively resistant to minocycline and accumulated less of both drugs than did the susceptible organisms. It is proposed that minocycline is effective against tetracycline-resistant staphylococci because of its ability to penetrate the cells sufficiently to reach inhibiting concentrations at sensitive reaction sites.

Publication types

  • Comparative Study

MeSH terms

  • Drug Resistance, Microbial*
  • Escherichia coli / drug effects*
  • Escherichia coli / metabolism
  • Minocycline / metabolism
  • Staphylococcus / drug effects*
  • Staphylococcus / metabolism
  • Tetracycline / metabolism*

Substances

  • Tetracycline
  • Minocycline