is an encapsulated fungal organism that can cause disease in apparently im-munocompetent, as well as immunocompromised, hosts. Since 1930, successive subculture has been used to preserve C. neoformans
isolates in our Fungus Collection. In the 1970s, some of these Fungus Collection samples were selected to be subjected to a different methods of maintenance that of lyophilized. Our objective was to analyze C. neoformans
isolates in order to make a comparative evaluation between these two methods of preservation. The overall aim of this study was to qualify the preservation technique used in our mycology laboratory since the technique used might affect the survival, stability and purity of the primary isolates in culture.
The samples were analyzed using classical mycology methods and using the randomly amplified polymorphic DNA technique.In the analysis of phenotypes and genotypes, the typical characteristics of C. neoformans
were found to differ in relation to the different methods of preservation employed.
The aim of this study was to demonstrate the importance of selecting the appropriate method of preservation for fungus collections. This selection can affect the survival and purity of the cultures, and preserve the stability of their physiological, biochemical, and genetic characteristics.