目的 运用融合PCR和同源重组技术敲除白色假丝酵母菌FLO8基因，并初步分析敲除菌株药物敏感性(药敏)情况。方法 运用融合PCR将FLO8基因的上下游片段与筛选标记融合在一起构成同源敲除组件，再用高效醋酸锂转染法将敲除组件转染入白色假丝酵母菌SN152，在营养缺陷板上进行筛选，通过2次同源重组敲除FLO8的2条等位基因。采用点板法比较FLO8未敲除株与敲除株药敏情况。结果 成功构建白色假丝酵母菌SN152 FLO8双等位基因缺失株，且耐药性FLO8-/->FLO8＋/->SN152。结论 融合PCR结合同源重组技术能高效、快速构建白色假丝酵母菌FLO8基因缺失株，白色假丝酵母菌FLO8基因与药敏相关，且FLO8拷贝数越少耐药性越强。

Objective To knock out the FLO8 gene in Candida albicans using fusion PCR combined with homologous recombination and analyze drug sensitivity in FLO8 gene knockout strains preliminarily. Methods Upstream and downstream flanking sequences of FLO8 gene were fused with selection markers by fusion PCR to construct homologous knockout fragments, which were then transfected into Candida albicans SN152 by high efficient lithium acetate transfection method. Positive strains were screened on nutritional defect medium and two alleles in FLO8 gene were knocked out by performing the homologous recombination twice. Drug sensitivity was compared between strains with and without FLO8 gene by spot assay. Results The Candida albicans SN152 FLO8-/- double allelic deletion strains were successfully constructed. Drug resistance in FLO8-/- was greater than that in FLO8＋/-, which was greater than that in SN152. Conclusion Fusion PCR combined with homologous recombination can rapidly and efficiently construct Candida albicans FLO8 gene deletion strains. Candida albicans FLO8 gene is associated with drug sensitivity and drug resistance increases with the decrease in copy number.