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[Dynamics of drug resistance in Proteus mirabilis cultures 1970-1985]

Insights

Antimicrobial resistance in Proteus mirabilis strains showed dynamic changes between 1970-1985. While resistance to ampicillin increased, chloramphenicol resistance decreased, with many strains remaining susceptible to other drugs.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Pharmacology

Background:

  • Proteus mirabilis is a significant opportunistic pathogen.
  • Understanding antimicrobial resistance patterns is crucial for effective treatment.
  • Longitudinal studies are needed to track evolving resistance trends.

Purpose of the Study:

  • To investigate the dynamics of antimicrobial resistance in clinical Proteus mirabilis strains over a 15-year period (1970-1985).
  • To identify trends in resistance to 18 different chemotherapeutic drugs.
  • To characterize patterns of multidrug resistance in Proteus mirabilis.

Main Methods:

  • Retrospective analysis of antimicrobial susceptibility testing data.
  • Inclusion of 669 clinical isolates of Proteus mirabilis.
  • Monitoring resistance profiles over specified intervals between 1970 and 1985.

Main Results:

  • Increased resistance to ampicillin and carbenicillin was observed.
  • Resistance to cephalosporins remained stable.
  • A transient increase in aminoglycoside resistance was followed by a decrease.
  • Decreased chloramphenicol resistance and increased sensitivity were noted.
  • High levels of resistance to tetracycline, doxycycline, rifampicin, novobiocin, furazolidone, and furagin persisted.
  • No increase in strains resistant to 5-7 drugs; most frequent resistance was to 2-4 drugs.
  • Proteus strains were categorized into 69 distinct resistance variants.

Conclusions:

  • Proteus mirabilis exhibits dynamic antimicrobial resistance patterns.
  • Specific antibiotics like ampicillin and carbenicillin show increasing resistance.
  • A significant proportion of strains maintained stable resistance to certain drug classes.
  • The study identified key resistance profiles and variants within Proteus mirabilis populations.

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