[Analysis of ERG11 gene mutation in Candida albicans].

Ying-bin Wang, Hong Wang, Hui-yu Guo, Yong-zhong Zhao, Shen-qiu Luo
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Abstract

Objective: To study the relationship between fluconazole (FCZ)-resistance of Candida albicans and the mutation of ERG11 gene encoding FCZ-targeted enzyme.

Method: Three strains of FCZ-susceptible and 10 FCZ-resistent C. albicans were isolated from the urethra, vagina, oropharynx, respiratory tract, prostate secretion and blood samples. ERG11 gene was amplified by PCR using C.albicans genomic DNA extracts as the templates and the DNA sequences of the PCR products were determined and compared using BLAST and Clustal-W softwares.

Results: The comparison of ERG11 gene sequences identified mutations at 21 sites in 13 strains, including 17 same-sense and 4 missense mutations. Base substitutions at the sites of 348 bp and 383 bp resulting in D116E and K128T conversion may take place in both drug-resistant and drug-susceptible strains. The point mutation at the site of 1309 bp of FCZ-resistant strain may cause V437I change, and the base inversion at 1320 bp may give rise to A/C heterozygosity mutant of ERG11 gene, probably resulting in N440K conversion.

Conclusion: FCZ-resistance of C. albicans may be associated with point mutations of V437I and N440K in ERG11 gene, but not with the point mutations of D166E and K128T.

白色念珠菌ERG11基因突变分析
目的:探讨白色念珠菌氟康唑耐药与氟康唑靶向酶编码基因ERG11突变的关系。方法:从尿道、阴道、口咽、呼吸道、前列腺分泌物和血液中分离出3株fcz敏感白念珠菌和10株fcz耐药白念珠菌。以白色念珠菌基因组DNA提取物为模板,采用PCR扩增ERG11基因,用BLAST和Clustal-W软件对PCR产物的DNA序列进行测定和比较。结果:13株菌株的ERG11基因序列比较发现21个位点发生突变,其中同义突变17个,错义突变4个。耐药菌株和药敏菌株在348 bp和383 bp位点发生碱基替换,导致D116E和K128T转化。fcz抗性菌株1309 bp位点的点突变可能导致V437I改变,1320 bp位点的碱基倒置可能导致ERG11基因A/C杂合突变,可能导致N440K转化。结论:白色念珠菌耐药可能与ERG11基因V437I和N440K点突变有关,而与D166E和K128T点突变无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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