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组蛋白5和人乳铁蛋白可抑制氟康唑耐药白念珠菌临床分离株的生物膜形成。

Histatin 5 and human lactoferrin inhibit biofilm formation of a fluconazole resistant Candida albicans clinical isolate.

作者信息

Curvelo José A R, Moraes Daniel C DE, Anjos Camila A Dos, Portela Maristela B, Soares Rosangela M A

机构信息

Instituto de Microbiologia Paulo de Goés, Universidade Federal do Rio de Janeiro, Avenida Carlos Chagas Filho, 373, 21941-590 Rio de Janeiro, RJ, Brazil.

Faculdade de Odontologia, Universidade Federal Fluminense, Rua Mario Santos Braga, 28, 24020-140 Niterói, RJ, Brazil.

出版信息

An Acad Bras Cienc. 2019;91(1):e20180045. doi: 10.1590/0001-3765201920180045. Epub 2019 Apr 8.

Abstract

Candida albicans is the most important fungal pathogen that causes infections in humans. Biofilms are hard-to-treat structures due to their high antifungal resistance. Saliva is a fluid that contains antimicrobial substances acting as the first-line of defense against pathogens, and its immune components may be potential tools for the discovery of new treatments against candidiasis. To evaluate the activity of histatin 5 and human lactoferrin against biofilm formation. A fluconazole-resistant Candida albicans clinical isolate was used as the model microorganism. Morphogenesis was evaluated by differential counting. Biofilm quantification was performed by XTT reduction assay. Thickness and topography of biofilms were assessed through confocal laser scanning microscopy (CLSM). Histatin 5 inhibited yeast-to-hyphae transition in a dose-dependent manner, while the effect of human lactoferrin on this process was inversely proportional to its concentration. Both compounds were able to significantly inhibit biofilm metabolic activity. Histatin 5 reduced biofilm thickness. Histatin 5 and human lactoferrin exhibited in vitro cytotoxicity against a fluconazole-resistant Candida albicans biofilm, which points to the potential application of these compounds in the treatment of biofilms formed by this fungus, especially in resistant infections.

摘要

白色念珠菌是引起人类感染的最重要的真菌病原体。生物膜由于其高度的抗真菌耐药性而难以治疗。唾液是一种含有抗菌物质的液体,作为抵御病原体的第一道防线,其免疫成分可能是发现抗念珠菌病新疗法的潜在工具。为了评估组蛋白5和人乳铁蛋白对生物膜形成的活性。使用耐氟康唑的白色念珠菌临床分离株作为模型微生物。通过差异计数评估形态发生。通过XTT还原试验进行生物膜定量。通过共聚焦激光扫描显微镜(CLSM)评估生物膜的厚度和形貌。组蛋白5以剂量依赖的方式抑制酵母向菌丝的转变,而人乳铁蛋白对这一过程的影响与其浓度成反比。两种化合物都能够显著抑制生物膜的代谢活性。组蛋白5降低了生物膜厚度。组蛋白5和人乳铁蛋白对耐氟康唑的白色念珠菌生物膜表现出体外细胞毒性,这表明这些化合物在治疗由这种真菌形成的生物膜方面具有潜在应用,尤其是在耐药感染中。

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