R-Plasmid Transfer to and from Escherichia coli Strains Isolated from Human Fecal Samples

Abstract

Strains of Escherichia coli recently isolated from human feces were examined for the frequency with which they accept an R factor (R1) from a derepressed fi + strain of E. coli K-12 and transfer it to fecal and laboratory strains. Colicins produced by some of the isolates rapidly killed the other half of the mating pair; therefore, conjugation was conducted by a membrane filtration procedure whereby this effect was minimized. The majority of fecal E. coli isolates accepted the R factor at lower frequencies than K-12 F − , varying from 10 −2 per donor cell to undetectable levels. The frequencies with which certain fecal recipients received the R-plasmid were increased when its R + transconjugant was either cured of the R1-plasmid and remated with the fi + strain or backcrossed into the parental strain. The former suggests the loss of an incompatibility plasmid, and the latter suggests the modification of the R1-plasmid deoxyribonucleic acid (DNA). In general, the fecal R + E. coli transconjugants were less effective donors for K-12 F − and heterologous fecal strains than was the fi + K-12 strain, whereas the single strain of Citrobacter freundii examined was generally more competent. Passage of the R1-plasmid to strains of salmonellae reached mating frequencies of 10 −1 per donor cell when the recipient was a Salmonella typhi previously cured of its resident R-plasmid. However, two recently isolated strains of Salmonella accepted the R1-plasmid from E. coli K-12 R + or the R + E. coli transconjugants at frequencies of 5 × 10 −7 or less.