We have reevaluated the antibiotic susceptibilities of group A beta-hemolytic streptococci in view of recent reports of a high prevalence of erythromycin resistance in Japan and of an increase in penicillin treatment failures in the United States. A total of 474 isolates recovered during a 2-to 3-month period in 1980 were tested. All were susceptible by microtiter broth dilution to a penicillin concentration of c0.03 ,ug/ml (minimal inhibitory concentration), and 473 were killed by c0.06 ug/ml (minimal bactericidal concentration). Erythromycin minimal inhibitory concentrations showed a bimodal distribution: 95% were -0.06,tg/ ml, and 5% were 21 ,ug/ml. Of the minimal bactericidal concentrations, 21% were 21 ,ug/ml and 3% were :16 ug/ml. Group A beta-hemolytic streptococci remain susceptible to the inhibitory and bactericidal actions of penicillin, thus providing no in vitro explanation for the bacteriological relapses reported in some clinical studies. Unlike the Japanese experience, only 5% of our isolates were resistant to erythromycin (minimal inhibitory concentration, 21 ug/ml); however, 22% were tolerant (ratio of minimal inhibitory/bactericidal concentrations, 232).Although in vitro resistance to penicillin has not been described for group A beta-hemolytic Streptococcus, a trend of increasing resistance to erythromycin has been reported (2-4, 9). Recently some clinicians have noted an increased incidence of treatment failure as compared with data relating to treatment results derived 2 decades ago (6,7,(10)(11)(12)14). In view of these findings, we have evaluated antibiotic susceptibilities of group A beta-hemolytic Streptococcus strains recently isolated from patients in Oklahoma.MATERIALS AND METHODS Group A beta-hemolytic Streptococcus isolates. Throat cultures submitted to the microbiology laboratories of Oklahoma Children's Memorial Hospital and the Oklahoma State Department of Health yielded 474 group A beta-hemolytic Streptococcus (S. pyogenes) isolates. Isolates originated, geographically, from a statewide region. Serogroup identification was based on the fluorescent-antibody technique, and hemolysis was determined by macroscopic examination of primary streak plate cultures containing 4 to 5% defibrinated sheep blood. Inocula were stabbed to facilitate detection of oxygen-labile hemolysin. Plates were incubated at 35 to 370C in an atmosphere containing 6% C02 and were examined at 24 and 48 h.Group A beta-hemolytic Streptococcus colonies were transferred to blood agar plates and maintained in pure culture at room temperature until susceptibility tests were performed. Susceptibility testing. Growth from 18-to 24-h cultures on sheep blood agar plates was adjusted to a density of approximately 10' colony-forming units per ml in Mueller-Hinton broth. A 1:10 dilution was then made in 5 ml of broth for micro-broth dilution testing, or a 1:20 dilution was made before agar dilution testing. Agar dilution tests were performed on antibiotic-supplemented Mueller-Hinton agar containing 5% sheep blood. Inoculati...