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Plant-Derived Decapeptide OSIP108 Interferes with Candida albicansBiofilm Formation without Affecting Cell Viability
- Source :
- Antimicrobial Agents and Chemotherapy; February 2014, Vol. 58 Issue: 5 p2647-2656, 10p
- Publication Year :
- 2014
-
Abstract
- ABSTRACTWe previously identified a decapeptide from the model plant Arabidopsis thaliana, OSIP108, which is induced upon fungal pathogen infection. In this study, we demonstrated that OSIP108 interferes with biofilm formation of the fungal pathogen Candida albicanswithout affecting the viability or growth of C. albicanscells. OSIP108 displayed no cytotoxicity against various human cell lines. Furthermore, OSIP108 enhanced the activity of the antifungal agents amphotericin B and caspofungin in vitroand in vivoin a Caenorhabditis elegans-C. albicansbiofilm infection model. These data point to the potential use of OSIP108 in combination therapy with conventional antifungal agents. In a first attempt to unravel its mode of action, we screened a library of 137 homozygous C. albicansmutants, affected in genes encoding cell wall proteins or transcription factors important for biofilm formation, for altered OSIP108 sensitivity. We identified 9 OSIP108-tolerant C. albicansmutants that were defective in either components important for cell wall integrity or the yeast-to-hypha transition. In line with these findings, we demonstrated that OSIP108 activates the C. albicanscell wall integrity pathway and that its antibiofilm activity can be blocked by compounds inhibiting the yeast-to-hypha transition. Furthermore, we found that OSIP108 is predominantly localized at the C. albicanscell surface. These data point to interference of OSIP108 with cell wall-related processes of C. albicans, resulting in impaired biofilm formation.
Details
- Language :
- English
- ISSN :
- 00664804 and 10986596
- Volume :
- 58
- Issue :
- 5
- Database :
- Supplemental Index
- Journal :
- Antimicrobial Agents and Chemotherapy
- Publication Type :
- Periodical
- Accession number :
- ejs32647080
- Full Text :
- https://doi.org/10.1128/AAC.01274-13