Fourteen Staphvlococcus epidermidis strains were biotyped according to the scheme of Baird-Parker and tested for their sensitivities to S. epidermidis typing phages. Tetracycline-susceptible strains were tested for the capacity to be transduced to resistance. Five strains, all of biotype 1, were lysed by one or more phages. Five of eight biotype 1 strains were transduced to tetracycline resistance with rates of 10-8 to 10-'. Three strains of other biotypes were not transduced, nor was PS 73, an unusual coagulase-negative strain. The transducing phage 4367 was isolated from the lysogenic tetracycline-resistant donor strain. The phage morphologically resembles serological group B S. aureus phages. Restriction and modification were indicated from the efficiency of plating on phage-sensitive strains.In many instances, antibiotic resistance may be transferred between strains of Staphylococcus aureus by transduction. A recent study with S. epidermidis demonstrated that in this staphylococcal species: as well as between species, antibiotic resistance may be transduced by S. epidermidis phages, (16). In this study, we report the transduction of tetracycline resistance by an S. epidermidis phage induced from a naturally lysogenic, tetracycline-resistant donor to biochemically related S. epidermidis strains. The strains were grouped into biotypes according to the classification of Baird-Parker (3) and were phage-typed with S. epidermidis phages. Morphology of the transducing phage and plating efficiencies on some phage-sensitive hosts were also studied. School. An S. epidermidis phage, )367, was isolated from strain 367, a naturally lysogenic, tetracyclineresistant strain, by cross-spotting supernatant fluids of broth cultures on various bacterial lawns. Bacteriophages for phage-typing and their propagating strains were obtained from J. Verhoef, Laboratorium voor Microbiologie der Rijksuniversiteit, Utrecht, Holland.Four preparations of 4)367, each propagated in a different phage-sensitive strain, were also included in typing.Media and biochemical tests. Cultures were maintained on Brain Heart Infusion Agar (Difco) slants. For phage propagations and assays, the base layer was Trypticase Soy Agar (TSA; BBL), and the overlay was 0.7%1c (w/v) agar in nutrient broth plus 0.004%1, (w/v) calcium chloride. Trypticase Soy Broth (TSB) was used throughout. except that overnight cultures of strain 367 for ultraviolet (UV) induction of the transducing phage were grown in Brain Heart Infusion broth. Overnight cultures of recipients for transduction were grown on tryptone agar (Oxoid) slants.Standard tests for the differentiation of staphylococci (10) were used for catalase and for anaerobic glucose fermentation. Free coagulase was determined in Difco coagulase plasma; tests were read at 2 hr and after overnight incubation at 37 C. Pigment production was tested on Staphylococcus 110 Agar (Difco).Biochemical tests for grouping S. epidermidis were modified from the methods described by Baird-Parker (2). Fermentation of mannitol, lactose,...