Antifungal susceptibility testing of dermatophytes: Establishing a medium for inducing conidial growth and evaluation of susceptibility of clinical isolates
Cj. Jessup et al., Antifungal susceptibility testing of dermatophytes: Establishing a medium for inducing conidial growth and evaluation of susceptibility of clinical isolates, J CLIN MICR, 38(1), 2000, pp. 341-344
A standardized reference method for dermatophyte in vitro susceptibility te
sting is lacking, In a previous study, Norris et al, (H. A. Norris, B. E. E
lewski, and M. A. Ghannoum, J. Am. Acad, Dermatol, 40(6, part 2):S9-S13) es
tablished the optimal medium and other growth variables. However, the earli
er study did not address two issues: (i) selection of an optimal medium for
conidial formation by dermatophytes and (ii) validation of the method with
a large number of dermatophytes, The present study addresses these two poi
nts. To select which agar medium best supported conidial growth, representa
tive isolates of dermatophytes were grown on different agars, Preliminary e
xperiments showed that only oatmeal cereal agar supported the production of
conidia by Trichophyton rubrum, We tested the abilities of 251 T. rubrum i
solates to form conidia using three different cereal agars and potato dextr
ose agar, Overall, oatmeal cereal and rice agar media were comparable in th
eir abilities to support T. rubrum conidial growth. Next, we used the oatme
al cereal agar for conidial formation along with the optimal conditions for
dermatophyte susceptibility testing proposed by Norris ct al, and determin
ed the antifungal susceptibilities of 217 dermatophytes to fluconazole, gri
seofulvin, itraconazole, and terbinafine, Relative to the other agents test
ed, terbinafine possessed the highest antifungal activity against all of th
e dermatophytes. The mean +/- standard error of the mean. MICs of fluconazo
le, itraconazole, terbinafine, and griseofulvin were 2.07 +/- 0.29, 0.13 +/
- 0.01, 0.002 +/- 0.0003, and 0.71 +/- 0.05 mu g/ml, respectively. This stu
dy is the first step in the identification of optimal conditions that could
be used for the standardization of the antifungal susceptibility testing m
ethod for dermatophytes. Inter- and intralaboratory agreement as well as cl
inical correlations need to be established.