“…A small amount of sterile salt solution was injected into the edge of the lesion and, after waiting for several minutes, material was then aspirated and placed in blood broth. Twenty-two strains were isolated and studied, according to the following standard methods: sugar fermentation with one per cent lactose, mannite, salicin, trehalose, and sorbital, final pH in dextrose broth, the reduction of methylene blue, the hydrolysis of sodium hippurate, hemolysis on blood agar plates (4); the type of colony, on surface plates of neopeptone agar (5); the erythrogenic toxin production, the serological classification,2 and the fibrinolysin production. Toxin-antitoxin neutralization tests were carried out when the presence of toxin was found.…”