In 10 of 34 adult cats infected with Sporothrix schenckii, demonstrable lesions healed spontaneously in 31 to 88 days after inoculation of the organism. None of 5 untreated cats developed additional visible lesions during the period of observation, nor were they positive for S. schenckii by culture at necropsy. Five animals were treated with Solu-Medrol R to determine if the apparent clinical cure was also accompanied by a mycological cure. Lesions reappeared at, or near, the site of the original lesions in 3 of the 5 treated cats from 4 to 6 months after the initial lesions healed. Fungi were cultured both from the regional lymph node and from exudate of the skin lesions. Thus, it appears that viable S. schenckii may be sequestered in tissues for at least 6 months without showing clinical evidence of their presence. Moreover, apparently "healed" lesions may be reactivated and progress to typical demonstrable skin lesions following immuno-suppression.Previous work in our laboratory [1,2] has demonstrated that the domestic cat can be used as an experimental host to study various aspects of sporotrichosis. As part of a larger study to test the effects of various drugs on skin lesions produced by Sporothrix schenckii, 34 cats were infected with S. schenckii and all showed demonstrable lesions. In 10 of these animals, lesions healed spontaneously without medication. In an effort to determine if this apparent clinical cure was also a mycological one, 5 cats were given a course of methyl-predisolone sodium succinate (Solu-Medrol R) to suppress immune responses. This report documents the response observed in these animals following administration of the drug.
MATERIAL AND METHODS
FungusThe organism used in this study was the Fossler strain ATCC 14804 originally isolated from a typical lymphatic lesion on the arm of an adult male in 1960. Yeast phase cells were used for inoculation and were grown for 10-14 days on modified Kelley's media agar slants at 37 °C [13]. They were harvested by washing them from the agar slants with sterile buffered saline. This buffer was also used to wash the cells twice and to suspend them at the desired concentration.
Experimental animalsAdult domestic cats of either sex and of varied background were immunized against feline distemper and pneumonitis before use in this experiment. All animals were maintained in individual cages in the same room and were examined regularly