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Loss of R factors promoted by bacteriophage M13 and the M13 carrier state

Insights

Bacteriophage M13 infection can eliminate R factors from Escherichia coli, converting R(+) cells to R(-). Genetic factors influence elimination efficiency, and some cells become M13 carriers maintaining the R factor intracellularly.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • R factors (resistance plasmids) confer antibiotic resistance to bacteria.
  • Bacteriophage M13 infection is known to eliminate certain plasmids like F' factors.
  • The effect of M13 on R factor elimination in Escherichia coli was not fully understood.

Purpose of the Study:

  • To investigate the elimination of derepressed R factors (fi(+) or fi(-)) in Escherichia coli by bacteriophage M13 infection.
  • To explore factors influencing the efficiency of R factor elimination.
  • To characterize the M13 carrier state in R(+) cells.

Main Methods:

  • Infection of various Hfr strains of Escherichia coli carrying derepressed R factors with bacteriophage M13.
  • Assessment of R factor loss and conversion to the R(-) state.
  • Identification and characterization of M13 carrier strains among unconverted R(+) cells.

Main Results:

  • M13 infection successfully eliminated R factors in a significant proportion of infected Escherichia coli cells, resulting in R(-) conversion.
  • Variability in elimination efficiency was observed, suggesting the involvement of host genetic factors independent of the R factor.
  • A fraction of infected, unconverted R(+) cells became M13 carrier strains, maintaining the R factor intracellularly.

Conclusions:

  • Bacteriophage M13 infection is an effective method for eliminating R factors in Escherichia coli.
  • Host genetics play a role in modulating the efficiency of R factor elimination by M13.
  • An intracellular carrier state for M13 and R factors can be established and maintained within single bacterial cells.

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