Abstract
Detection of Arcanobacterium haemolyticum is based upon typical β-hemolysis and colony morphology, but it may go undetected if only conventional sheep blood agar media for detection of β-hemolytic streptococci are used. The influence of different culture media, atmospheres, and times of incubation for the recognition of colonies of 47 isolates of A. haemolyticum was studied. After 48 h of incubation, trypticase soy agar with 5% horse blood in 5% CO 2 was the best medium.
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