首页 | 本学科首页   官方微博 | 高级检索  
     


Adhesive Properties and Hydrolytic Enzymes of Oral Candida albicans Strains
Authors:Emira Noumi  Mejdi Snoussi  Hajer Hentati  Kacem Mahdouani  Lucas del Castillo  Eulogio Valentin  Rafael Sentandreu  Amina Bakhrouf
Affiliation:1.Laboratoire d’Analyse, Traitement et Valorisation des Polluants de l’Environnement et des Produits,Département de Microbiologie, Faculté de Pharmacie,Monastir,Tunisie;2.Departamento de Microbiologia y Ecología, Facultad de Farmacia,Universidad de Valencia,Burjassot, Valencia,Spain;3.Laboratoire de Microbiologie,H?pital Ebn El Jazzar de Kairouan,Kairouan,Tunisie;4.Departamento de Microbiologia y Ecología, Facultad de Farmacia,Universidad de Valencia,Burjassot, Valencia,Spain;5.Service de Médecine et Chirurgie Buccales,Clinique Odontologique de Monastir,Monastir,Tunisie
Abstract:Several virulence factors in Candida albicans strains such as production of hydrolytic enzymes and biofilm formation on surfaces and cells can contribute to their pathogenicity. For this, control of this opportunistic yeast is one of the factors reducing the nosocomial infection. The aim of this study was to investigate biofilm formation on polystyrene and polymethylmethacrylate and the production of hydrolytic enzymes in Candida albicans strains isolated from the oral cavity of patients suffering from denture stomatitis. All strains were identified by macroscopic, microscopic analysis and the ID 32 C system. Our results showed that 50% of the total strains produced phospholipase. Furthermore, protease activity was detected in seven (35%) strains. All Candida albicans strains were beta haemolytic. All C. albicans strains adhered to polystyrene 96-well microtiter plate at different degrees, and the metabolic activity of C. albicans biofilm formed on polymethylmethacrylate did not differ between tested strains. The atomic force micrographs demonstrated that biofilm of Candida albicans strains was organized in small colonies with budding cells.
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号