Published online by Cambridge University Press: 14 April 2009
By the use of appropriate strains of Escherichia coli, Shigella flexneri and Salmonella typhimurium with and without an R factor, R100, the mechanism of ‘curing’ of R factor by acridine dyes was examined. This R factor was shown to confer increased sensitivity to acriflavine upon the host cells. E. coli strain W-3630, once infected with R100, has never been observed to segregate R− cells. When mixtures of R+ and R− cells of this strain were grown in acriflavine broth, the proportion of R− cells increased and was also correlated with the proportion in the initial inoculum. Other bacterial strains carrying R100 segregate R~ cells spontaneously. Growth tests starting with varying proportion of R+ and R− cells of these strains in acriflavine broth also gave a marked correlation between the initial and final proportions of R− cells, and indicated that the main cause of ‘curing’ the R factor was the selective enrichment of R− segregants present in the initial inocula or arising spontaneously during growth of the R+ culture. These results suggest that the mechanisms underlying the ‘curing’ of F and R factors are different. Tests with several acridine dyes gave results similar to those with acriflavine.