Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Appl Microbiol ; 107(4): 1298-307, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19486401

ABSTRACT

AIM: To investigate the nisin Z innocuity using normal human gingival fibroblast and epithelial cell cultures, and its synergistic effect with these gingival cells against Candida albicans adhesion and transition from blastospore to hyphal form. METHODS AND RESULTS: Cells were cultured to 80% confluence and infected with C. albicans in the absence or presence of various concentrations of nisin Z. Our results indicate that only high concentrations of nisin Z promoted gingival cell detachment and differentiation. Determination of the LD(50) showed that the fibroblasts were able to tolerate up to 80 microg ml(-1) for 24 h, dropping thereafter to 62 mug ml(-1) after 72 h of contact, compared to 160 microg ml(-1) after 24 h, and 80 microg ml(-1) after 72 h recorded by the gingival epithelial cells which displayed a greater resistance to nisin Z. The use of nisin Z even at low concentration (25 microg ml(-1)) at appropriate concentrations with gingival cells significantly reduced C. albicans adhesion to gingival monolayer cultures and inhibited the yeast's transition. CONCLUSION: These findings show that when used at non-toxic levels for human cells, nisin Z can be effective against C. albicans adhesion and transition and may synergistically interact with gingival cells for an efficient resistance against C. albicans. SIGNIFICANCE AND IMPACT OF THE STUDY: This study suggests the potential usefulness of nisin Z as an antifungal agent, when used in an appropriate range.


Subject(s)
Antifungal Agents/pharmacology , Candida albicans/drug effects , Gingiva/drug effects , Nisin/analogs & derivatives , Candida albicans/growth & development , Candida albicans/ultrastructure , Candidiasis, Oral/microbiology , Candidiasis, Oral/pathology , Cell Adhesion/drug effects , Cell Differentiation/drug effects , Cells, Cultured , Epithelial Cells/drug effects , Fibroblasts/drug effects , Gingiva/cytology , Gingiva/growth & development , Humans , Hyphae/growth & development , Lethal Dose 50 , Microbial Sensitivity Tests , Nisin/pharmacology
2.
J Appl Microbiol ; 105(5): 1630-9, 2008 Nov.
Article in English | MEDLINE | ID: mdl-19146497

ABSTRACT

AIMS: To investigate the efficacy of nisin Z, an antimicrobial peptide produced by certain strains of Lactococcus lactis against Candida albicans growth and transition. METHODS AND RESULTS: Candida albicans was cultured in the presence of various concentrations of nisin Z (1000, 500, and 100 microg ml(-1)) for different time points. Candida albicans growth was determined using the Alamar Blue assay. The yeast's transition from blastospore to hyphal form was assessed through optical microscope observations. The effect of nisin Z on C. albicans ultrastructure was followed by scanning and transmission electron microscopy. Our results show that nisin Z inhibited C. albicans growth beginning at 500 microg ml(-1). This inhibition was both time- and dose-dependent. Nisin Z was also active against C. albicans transition by significantly inhibiting the transformation of C. albicans from the blastospore to hyphal form. Treatments with nisin Z lead to ultrastructural disturbances of C. albicans. CONCLUSION: Our findings indicate that nisin Z significantly reduced C. albicans growth and transition. These effects may have occurred through ultrastructural modifications of this yeast. SIGNIFICANCE AND IMPACT OF THE STUDY: For the first time, effect of nisin Z on C. albicans was investigated. These results therefore suggest that nisin Z may have antifungal properties, and could be used as an antifungal molecule.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antifungal Agents/pharmacology , Candida albicans/drug effects , Nisin/analogs & derivatives , Candida albicans/growth & development , Candida albicans/ultrastructure , Cells, Cultured/drug effects , Colony Count, Microbial , Dose-Response Relationship, Drug , Hyphae/growth & development , Microscopy, Electron, Scanning Transmission , Nisin/pharmacology , Time Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...