Heterogeneity in antifungal susceptibility of clones of Candida albicans isolated on single and sequential visits from a HIV-infected southern Chinese cohort
Yh. Samaranayake et al., Heterogeneity in antifungal susceptibility of clones of Candida albicans isolated on single and sequential visits from a HIV-infected southern Chinese cohort, J ORAL PATH, 30(6), 2001, pp. 336-346
The increased frequency and severity of candidal infections in human immuno
deficiency virus (HIV)-infected individuals has prompted the wide use of an
tifungals, such as amphotericin B, ketoconazole, and fluconazole, resulting
in the emergence of drug-resistant strains of Candida albicans. To study t
his phenomenon in an ethnic Chinese cohort, we isolated multiple colonies o
f Candida from the oral cavities of 16 HIV-infected patients on single and
subsequent sequential visits over a period of 12 months. Ten of the 16 pati
ents had sporadic episodes of oropharyngeal candidiasis (Group A), while th
e remainder were asymptomatic with respect to this condition (Group B). Ora
l rinses were collected and immediately processed in the laboratory for the
isolation of C. albicans in a standard manner. A total of 433 C. albicans
isolates were tested for their susceptibility to amphotericin B, ketoconazo
le and fluconazole by an agar diffusion method using the commercially avail
able E-test. All tested isolates demonstrated variable susceptibility to am
photericin B, ketoconazole and fluconazole. The minimum inhibitory concentr
ation (MLC) of the isolates for amphotericin B, ketoconazole and fluconazol
e ranged from <0.002-1.5 <mu>g/ml, <0.002-4.0 <mu>g/ml and <0.016-32 <mu>g/
ml, respectively. Sequential isolates of a few patients demonstrated variab
le susceptibility to all the antifungals, and no discernible MIC pattern em
erged either in group A or B over time. Interestingly, significant variatio
n in antifungal susceptibility was also noted in isolates obtained from the
same patient on a single visit. Sequential yeast isolates in 9 of 16 patie
nts (56%) demonstrated significant differences in MIC within and between vi
sits for both amphotericin B and ketoconazole, while a lower percentage - 4
4% (7/16) - exhibited this trait for fluconazole. Our study demonstrates th
e diversity in antifungal susceptibility in either commensal or "infective"
oral strains of C. albicans in HIV disease, and shows the need for vigilan
ce for the emergence of resistant strains, and for frequent antifungal susc
eptibility studies.