Identification of clinical and environmental isolates of Cryptococcus neoformans by AP-PCR fingerpri

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Objective To detect Cryptococcus neoformans strains isolated from clinic and environment, observe the relationship between PCR fingerprinting patts and serotypes, and find the typing standard about Cryptococcus neoformans by AP-PCR fingerprinting.Methods Three primers, including CN1 (GTG)5, CN2 (GACA)4 and CN3 (GATA)4, were used to distinguish variations among strains of C. neoformans. Of the three primers, the distinguishable fingerprinting bands for serotype of C. neoformans and other Cryptococcus species were yielded by primer CN2. With this primer, 48 clinical and environmental isolates of C. neoformans were investigated by AP-PCR.Results Of 38 serotype A strains, 34 strains produced complete identical fingerprinting patts. Other 4 strains had different fingerprinting patts. Two strains of serotype B and C yield indistinguishable fingerprinting patts. Three strains of serotype D and other Cryptococcus had different fingerprinting patts.Conclusions The strains of serotype A had similar and stable fingerprinting patts. Some strains of serotype B and C had indistinguishable fingerprinting patts. Same serotype strains from different sources may produce different AP-PCR fingerprinting patts. The AP-PCR fingerprinting is a rapid, simple and available method for identification of Cryptococcus neoformans.
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