Transmissible drug-resistance (R) factor was transduced in the system of
SalmonellaE group with phage epsilon, and its transduction rate was 10
-8.
The transduction rate of R factor with epsilon phage that had existed as prophage in R
+host cell and was induced by UV irradiation increased about 10
2 times than that of ordinary transduction.
The R factor carrying TC resistance marker was consistently segregated by transduction with epsilon phage.
The R
+transductant was not lysogeniged by transducing epsilon phage, indicating non-lysogenic conversion and non-immunity toward the transducing epsilon phage.
The R factor of transductant was non-transmissible by conjugation and not eliminated by acriflavine treatment. But the R factor of transductant was transduced again by epsilon phage that had existed as prophage in R
+transductant or that was newly infected to R
+transductant.
The R factor of R
+transductant of
S. chittagongwas transmissible by conjugation at 10
6times lower frequency than that of R factor that was transferred by conjugation, and was eliminated by acriflavine treatment in low frequency.
In transduction of R factor R
+ transductant with the same epsilon phage that had transduced high frequency transductant (HFT) was obtained and its transduction rate was 10
-2.
The transmission of R factor to R
+transductant was higher than that to R
-or R
+cell to which R factor was transmitted by conjugation.
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