Upon excision, conjugative transposon Tn916 forms a nonreplicating cir
cular intermediate (CI), which is essential both for transposition and
conjugal transfer. In this work we developed an assay to quantify the
circular forms of Tn916. By this method we defined a new measurable t
rait of Tn916-carrying strains: the ''CI copy number.'' CI dosage was
performed by nested PCR (with primers designed on Tn916 termini) in a
limiting dilution assay, where Poisson statistics were used to calcula
te the number of PCR amplification targets from the proportion of the
negative endpoints. The number of CI was normalized to the number of b
acterial chromosomes. This method enabled us to study the relationship
between CI copy number, presence of tetracycline (the resistance mark
er of Tn916) in the culture medium, and conjugation frequency. Three i
sogenic strains of Enterococcus faecalis OG1 with Tn916 inserted at di
fferent sites on the chromosome were investigated for CI content. CI c
opy number varied depending on the strain, ranging between 7.8 and 610
copies per 10(6) chromosomes. Growth in liquid media containing tetra
cycline provoked an important increase both in CI copy number and conj
ugation frequency. This effect was more marked in low-frequency donors
. While cell-cell contact during filter mating did not produce an incr
ease in CI copy number, Tn916 conjugation frequency was found to be de
pendent on CI copy number in donor cells. The dose-response curve show
ed a linear relationship with a slope of 0.74, for the entire range of
conjugation frequencies tested (from 5.1 x 10(-8) to 2.8 X 10(-6) tra
nsconjugants per donor). (C) 1995 Academic Press, Inc.