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抗真菌药物对白色念珠菌分离株菌液活力的影响。

Effects of antifungal agents in sap activity of Candida albicans isolates.

机构信息

Instituto de Patologia Tropical e Saúde Pública da, Universidade Federal de Goiás, Av. Delenda Resende de Melo S/N, Goiânia, Goiás, Brazil.

出版信息

Mycopathologia. 2010 Feb;169(2):91-8. doi: 10.1007/s11046-009-9232-6. Epub 2009 Aug 15.

Abstract

Some antifungal agents have shown to exert effects on expression of virulent factors of Candida as the production of secretory aspartyl proteinase (Sap). In this study, we sought to determine and to compare the influence of fluconazole and voriconazole in proteinase activity of this microorganism. Thirty-one isolates obtained from oral mucosa of human immunodeficiency virus positive (HIV) patients were used in this study. The minimal inhibitory concentrations (MIC) of fluconazole and voriconazole were determined using the broth microdilution method with RPMI 1640 medium and with yeast carbon base-bovine serum albumin (YCB-BSA) medium. The Sap activity following by digestion of BSA as substrate was determined for four Candida albicans strains arbitrarily chosen according to susceptibility (susceptible or resistant) to fluconazole or voriconazole. Besides, the SAP1 to SAP7 genes were screened by PCR for the same isolates that were determined by the Sap activity. In vitro susceptibility testing using the two media presented similar MIC values. Increased Sap activity was observed in resistant isolates on presence of drugs, but the Sap activity by susceptible isolates to azoles showed different behavior on the presence of drug. We detected the presence of SAP1 to SAP7 genes from all susceptible or resistant C. albicans isolates. The present study provides important data about the proteinase activity and the presence of genes of SAP family in fluconazole and voriconazole susceptible or resistant C. albicans isolates.

摘要

一些抗真菌药物已被证明对念珠菌毒力因子的表达有影响,如分泌天冬氨酸蛋白酶(Sap)的产生。在这项研究中,我们试图确定并比较氟康唑和伏立康唑对这种微生物蛋白酶活性的影响。从人类免疫缺陷病毒阳性(HIV)患者的口腔黏膜中获得了 31 株分离株用于本研究。使用 RPMI 1640 培养基和酵母碳基础-牛血清白蛋白(YCB-BSA)培养基进行微量肉汤稀释法测定氟康唑和伏立康唑的最小抑菌浓度(MIC)。根据对氟康唑或伏立康唑的敏感性(敏感或耐药)任意选择 4 株白色念珠菌菌株,测定作为底物的 BSA 消化后的 Sap 活性。此外,还通过 PCR 筛选了相同分离株的 SAP1 至 SAP7 基因,这些分离株通过 Sap 活性来确定。两种培养基的体外药敏试验显示出相似的 MIC 值。在存在药物的情况下,耐药分离株的 Sap 活性增加,但对唑类药物敏感的分离株的 Sap 活性在存在药物时表现出不同的行为。我们从所有敏感或耐药的 C. albicans 分离株中检测到 SAP1 至 SAP7 基因的存在。本研究提供了关于氟康唑和伏立康唑敏感或耐药 C. albicans 分离株的蛋白酶活性和 SAP 家族基因存在的重要数据。

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