PARITY AMONG THE RANDOMLY AMPLIFIED POLYMORPHIC DNA METHOD, MULTILOCUS ENZYME ELECTROPHORESIS, AND SOUTHERN BLOT HYBRIDIZATION WITH THE MODERATELY REPETITIVE DNA-PROBE CA3 FOR FINGERPRINTING CANDIDA-ALBICANS
C. Pujol et al., PARITY AMONG THE RANDOMLY AMPLIFIED POLYMORPHIC DNA METHOD, MULTILOCUS ENZYME ELECTROPHORESIS, AND SOUTHERN BLOT HYBRIDIZATION WITH THE MODERATELY REPETITIVE DNA-PROBE CA3 FOR FINGERPRINTING CANDIDA-ALBICANS, Journal of clinical microbiology, 35(9), 1997, pp. 2348-2358
Randomly amplified polymorphic DNA (RAPD) analysis, mutilocus enzyme e
lectrophoresis (MLEE), and Southern blot hybridization with moderately
repetitive DNA probes have emerged as effective fingerprinting method
s for the infectious fungus Candida albicans. The three methods Rave b
een compared for their capacities to identify identical or highly rela
ted isolates, to fluster weakly related isolates, to discriminate betw
een unrelated isolates, and to assess microevolution within a strain,
Bg computing similarity coefficients between 29 isolates from three ci
ties within the continental United States, strong concordance of the r
esults is demonstrated Fur RAPD analysis, MLEE, and Southern blot hybr
idization with the moderately repetitive probe Ca3, and weaker concord
ance of the results is demonstrated for these three fingerprinting met
hods and Southern blot hybridization with the moderately repetitive pr
obe CARE2. All methods were also demonstrated to be able to resolve mi
croevolution within a strain, with the Ca3 probe exhibiting the greate
st resolving power. The strong correlations demonstrated between polym
orphic markers assessed by the four independent fingerprinting methods
and the nonrandom association between loci demonstrated by RAPD analy
sis and. MLEE provide evidence for strong linkage disequilibrium and a
clonal population structure for C. albicans. In addition, a synapomor
phic allele, Pep-3A, was found to be present in all members of one of
the three clusters discriminated by RAPD analysis, MLEE, and Ca3 finge
rprinting, supporting the concordance of the clustering capacities of
the three methods, the robustness Of the clusters, and the clonal natu
re of the clusters.