首页> 外文期刊>Antimicrobial agents and chemotherapy. >Facultative sterol uptake in an ergosterol-deficient clinical isolate of candida glabrata harboring a missense mutation in ERG11 and exhibiting cross-resistance to azoles and amphotericin B
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Facultative sterol uptake in an ergosterol-deficient clinical isolate of candida glabrata harboring a missense mutation in ERG11 and exhibiting cross-resistance to azoles and amphotericin B

机译:在ERG11中发生错义突变并表现出对唑类和两性霉素B交叉耐药性的光滑念珠菌缺乏麦角固醇的临床分离株中兼性固醇摄取

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We identified a clinical isolate of Candida glabrata (CG156) exhibiting flocculent growth and cross-resistance to fluconazole (FLC), voriconazole (VRC), and amphotericin B (AMB), with MICs of 256, 256, and 32 μg ml -1, respectively. Sterol analysis using gas chromatography-mass spectrometry (GC-MS) revealed that CG156 was a sterol 14α-demethylase (Erg11p) mutant, wherein 14&;-methylated intermediates (lanosterol was 80% of the total) were the only detectable sterols. ERG11 sequencing indicated that CG156 harbored a single-amino-acid substitution (G315D) which nullified the function of native Erg11p. In heterologous expression studies using a doxycycline-regulatable Saccharomyces cerevisiae erg11 strain, wild-type C. glabrata Erg11p fully complemented the function of S. cerevisiae sterol 14α-demethylase, restoring growth and ergosterol synthesis in recombinant yeast; mutated CG156 Erg11p did not. CG156 was culturable using sterol-free, glucose-containing yeast minimal medium ( glcYM). However, when grown on sterol-supplemented glcYM (with ergosta 7,22-dienol, ergosterol, cholestanol, cholesterol, Δ 7-cholestenol, or desmosterol), CG156 cultures exhibited shorter lag phases, reached higher cell densities, and showed alterations in cellular sterol composition. Unlike comparator isolates (harboring wild-type ERG11) that became less sensitive to FLC and VRC when cultured on sterol-supplemented glcYM, facultative sterol uptake by CG156 did not affect its azole-resistant phenotype. Conversely, CG156 grown using glcYM with ergosterol (or with ergosta 7,22-dienol) showed increased sensitivity to AMB; CG156 grown using glcYM with cholesterol (or with cholestanol) became more resistant (MICs of 2 and 64 μg AMB ml -1, respectively). Our results provide insights into the consequences of sterol uptake and metabolism on growth and antifungal resistance in C. glabrata.
机译:我们确定了临床分离的光滑念珠菌(CG156),其对絮凝剂的生长和对氟康唑(FLC),伏立康唑(VRC)和两性霉素B(AMB)的交叉耐药性,MIC均大于256,大于256和32μgml- 1,分别。使用气相色谱-质谱(GC-MS)进行的甾醇分析显示CG156是固醇14α-脱甲基酶(Erg11p)突变体,其中14&-甲基化的中间体(羊毛甾醇占总数的80%以上)是唯一可检测到的固醇。 ERG11测序表明CG156带有一个单氨基酸取代(G315D),这使天然Erg11p的功能无效。在使用强力霉素调节的酿酒酵母erg11菌株进行的异源表达研究中,野生型光滑小球藻Erg11p完全补充了酿酒酵母固醇14α-脱甲基酶的功能,恢复了重组酵母中的生长和麦角固醇的合成。突变的CG156 Erg11p没有。可以使用无固醇,含葡萄糖的酵母基本培养基(glcYM)培养CG156。但是,当在添加了固醇的glcYM(含有麦角甾醇7,22-二烯醇,麦角固醇,胆固醇,胆固醇,Δ7-胆固醇或去氢甾醇)上生长时,CG156培养物显示出较短的迟滞期,达到较高的细胞密度,并显示出细胞变化固醇成分。与在固醇补充的glcYM上培养时对FLC和VRC较不敏感的比较株(携带野生型ERG11)不同,CG156吸收兼性固醇不会影响其耐唑性表型。相反,使用glcYM和麦角固醇(或麦角甾醇7,22-二烯醇)生长的CG156对AMB的敏感性增加;使用glcYM与胆固醇(或胆固醇)一起生长的CG156更具抗性(MIC分别为2和> 64μgAMB ml -1)。我们的结果提供了洞察C. glabrata中固醇摄取和代谢对生长和抗真菌抗性的影响的见解。

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