MOLECULAR SUBTYPES AND ANTIFUNGAL SUSCEPTIBILITIES OF SERIAL CRYPTOCOCCUS-NEOFORMANS ISOLATES IN HUMAN-IMMUNODEFICIENCY-VIRUS - ASSOCIATED CRYPTOCOCCOSIS
Me. Brandt et al., MOLECULAR SUBTYPES AND ANTIFUNGAL SUSCEPTIBILITIES OF SERIAL CRYPTOCOCCUS-NEOFORMANS ISOLATES IN HUMAN-IMMUNODEFICIENCY-VIRUS - ASSOCIATED CRYPTOCOCCOSIS, The Journal of infectious diseases, 174(4), 1996, pp. 812-820
Serial isolates of Cryptococcus neofonnans from 33 human immunodeficie
ncy virus-infected patients with cryptococcosis were analyzed to deter
mine whether persistence might result from reinfection with a new cryp
tococcal strain or acquisition of antifungal resistance, Isolates were
subtyped by multilocus enzyme electrophoresis (MEE), electrophoretic
karyotyping (EK), random-amplified polymorphic DNA (RAPD), and the CNR
E-1 DNA probe, MICs of amphotericin B, fluconazole, and 5-fluorocytosi
ne were determined, No changes in MEE or RAPD subtypes were detected i
n serial isolates from any patient, Isolates from 8 patients (24%) sho
wed alterations in EK only (mobility change in two or more bands) but
not with any other subtyping method, MICs did not change significantly
in isolates from 30 patients, In 1 case, the fluconazole MIC increase
d stepwise over 18 months, suggesting development of resistance, These
overall invariant subtyping and MIC results confirm previous studies
suggesting that persistent cryptococcal infection is due to relapse ra
ther than reinfection or antifungal drug resistance.