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首页> 外文期刊>Mycoses: Diagnosis, therapy and prophylaxis of fungal diseases >The antifungal properties of chicken egg cystatin against Candida yeast isolates showing different levels of azole resistance
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The antifungal properties of chicken egg cystatin against Candida yeast isolates showing different levels of azole resistance

机译:鸡半胱氨酸蛋白酶抑制剂对念珠菌分离株具有不同水平的唑抗性

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摘要

The increasing incidence of fungal infections together with the emergence of strains resistant to currently available antifungal drugs calls for the development of new classes of antimycotics. Naturally occurring antifungal proteins and peptides are of interest because of low toxicity, immunornodulatory potential and mechanisms of action distinct from those of currently available drugs. In this study, the potent antifungal activity of cystatin, affinity-purified from chicken egg white (CEWC), against the most frequent human fungal pathogens of the genus Candida was identified and characterised. CEWC inhibited the growth of azole-sensitive Candida albicans isolates with minimal inhibitory concentration (MIC) values ranging from 0.8 to 3.3 mumol l~(-1), a potency comparable with those of fluconazole and histatin 5, the antimicrobial peptide of the human saliva. Similarly to histatin 5, CEWC activity was not compromised in azole-resistant isolates overproducing the multidrug efflux transporters Cdr1p and Cdr2p and did not antagonise fluconazole or amphotericin B. CEWC had candidacidal activity, as revealed by the time-kill assay, and, similarly to histatin 5, completely inhibited the growth at supra-MIC concentrations. This was in contrast to the fungistatic effect and trailing growth observed with fluconazole. CEWC inhibited the growth of Candida parapsilosis and Candida tropicalis at similar concentrations, whereas Candida glabrata was more resistant to CEWC.
机译:真菌感染的发生率增加,以及对目前可用的抗真菌药物产生抗药性的菌株的出现,要求开发新型的抗真菌药。天然存在的抗真菌蛋白和肽由于其低毒性,免疫调节潜力和不同于目前可用药物的作用机理而受到关注。在这项研究中,鉴定并鉴定了从鸡蛋白(CEWC)中亲和纯化的胱抑素对念珠菌最常见的人类真菌病原体的有效抗真菌活性。 CEWC抑制了对唑敏感的白色念珠菌分离株的生长,最小抑菌浓度(MIC)值范围为0.8至3.3μmoll〜(-1),其效力与人类唾液中的抗菌肽fluconazole和histatin 5相当。 。与组蛋白5相似,CEWC活性在过量产生多药外排转运蛋白Cdr1p和Cdr2p的抗唑类菌株中没有受到损害,并且没有拮抗氟康唑或两性霉素B的活性。组蛋白5在超MIC浓度下完全抑制生长。这与氟康唑观察到的抑菌作用和拖尾生长相反。 CEWC以相似的浓度抑制了副念珠菌和热带念珠菌的生长,而光滑念珠菌对CEWC的抵抗力更高。

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