从不同临床标本分离的白色念珠菌的抗真菌耐药性和毒力决定因素的优势

Houdaii H. El-Houssaini, W. Elkhatib, Omnia M. Elnabawy, H. Nasser
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引用次数: 1

摘要

由于其毒力决定因素,白色念珠菌仍然是医院获得性真菌感染的最常见原因。对抗真菌治疗的耐药性急剧增加,由于其潜在的毒性,减少了少数可用的治疗选择。然而,白色念珠菌毒力决定因素与耐药谱之间的关系需要进一步研究。从不同临床标本中分离出25株白色念珠菌。对不同抗真菌药物进行抗菌谱分析,验证其最低抑菌浓度(mic)。毒力决定因素包括细胞外水解酶、生物膜形成和细胞表面疏水性(CSH)。分析了实验分离株的毒力决定因素与耐药谱之间的相关性,以及它们与临床标本来源的潜在关联。所有分离株均对两性霉素B、制霉菌素和米卡芬净敏感,对氯曲霉唑、氟康唑和伏立康唑100%耐药。分别在52%、68%和100%的分离株中检测到磷脂酶、蛋白酶和溶血素的细胞外水解活性,而在24%和20%的分离株中分别显示出CSH和生物膜的产生。CSH分别与两性霉素B和氟康唑mic呈显著正相关(p < 0.05)和负相关(p < 0.05)。临床分离株来源对部分耐药和毒力模式有显著影响(p < 0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antifungal resistance and predominance of virulence determinants among Candida albicans isolated from various clinical specimens
Candida albicans remains the most common cause of hospital-acquired fungal infections due to its virulence determinants. Resistance to antifungal therapy has increased dramatically, narrowing the few available therapeutic options due to their potential toxicity. However, the association between C. albicans virulence determinants and resistance profiles needs further investigation. C. albicans (n= 25) isolated from various clinical samples were identified. Antibiogram analysis of the tested isolates against different antifungal agents was performed and their minimum inhibitory concentrations (MICs) were verified. Virulence determinants including extracellular hydrolytic enzymes, biofilm formation, and cell surface hydrophobicity (CSH) were investigated. Correlations between virulence determinants and resistance profiles of the experimented isolates, in addition to their potential association with the source of clinical specimens, were analyzed. All isolates were amphotericin B, nystatin and micafungin sensitive, while 100% were clotrimazole, fluconazole and voriconazole resistant. Extracellular hydrolytic activities were detected in 52, 68 and 100% of the tested isolates for phospholipase, protease, and hemolysin, respectively, while CSH and biofilm production was shown in 24 and 20% of isolates, respectively. CSH had significant (p < 0.05) positive as well as negative associations with amphotericin B and fluconazole MICs, respectively. Source of clinical isolates showed significant (p < 0.05) influence on some resistance and virulence patterns.
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