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Effect of detergents on pathogenicity plasmids of escherichias

Krivoshein YuS1, Achkasova YuN, N I Bryzgunova

  • 1Crimean Medical Institute, Department of Microbiology, Simferopol, USSR.

Journal of Hygiene, Epidemiology, Microbiology, and Immunology
|January 1, 1988
PubMed

Insights

Cationic detergents like miramistin and catamine AB inhibit plasmid transfer in E. coli by disrupting cell structures, while anionic SDS eliminates specific plasmids. These findings impact understanding of bacterial conjugation and antibiotic resistance.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Biochemistry

Background:

  • Plasmids confer pathogenicity markers (Hly, Ent, Col, F, R) in E. coli.
  • Bacterial conjugation is a key mechanism for plasmid transfer and antimicrobial resistance dissemination.
  • Detergents can affect bacterial cell structures and functions.

Purpose of the Study:

  • To investigate the effects of cationic (miramistin, catamine AB) and anionic (SDS) detergents on plasmid elimination and transfer in E. coli.
  • To elucidate the mechanisms by which these detergents impact bacterial conjugation.

Main Methods:

  • Exposure of E. coli strains to subbacteriostatic concentrations of miramistin, catamine AB, and SDS.
  • Assessment of plasmid elimination and transfer frequencies via conjugation assays.
  • Microscopic examination of bacterial surface structures.

Main Results:

  • Cationic detergents miramistin and catamine AB suppressed plasmid transfer (Hly, Ent, F, R) without elimination, attributed to disruption of pili and surface structures.
  • Anionic SDS eliminated F and R plasmids but did not affect Hly, Ent, or Col plasmids.
  • Detergent action was concentration-dependent and affected donor, recipient, or conjugation medium.

Conclusions:

  • Cationic detergents interfere with bacterial conjugation by impairing surface structures essential for mating pair formation.
  • Anionic SDS exhibits plasmid-specific elimination activity, suggesting different mechanisms of action.
  • These findings offer insights into potential strategies for controlling plasmid-mediated gene transfer in bacteria.

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