-
Cytochalasans act as inhibitors of biofilm formation of staphylococcus aureus
- Back
Metadata
Document Title
Cytochalasans act as inhibitors of biofilm formation of staphylococcus aureus
Author
Yuyama K.T., Wendt L., Surup F., Kretz R., Chepkirui C., Wittstein K., Boonlarppradab C., Wongkanoun S., Luangsa-Ard J., Stadler M., Abraham W.-R.
Name from Authors Collection
Scopus Author ID
57189995748
Affiliations
Department Chemical Microbiology, Helmholtz Centre for Infection Research (HZI), Inhoffenstra?e 7, Braunschweig, 38124, Germany; Department Microbial Drugs, Helmholtz Centre for Infection Research (HZI), Inhoffenstra?e 7, Braunschweig, 38124, Germany; National Centre for Genetic Engineering and Biotechnology (BIOTEC), NSTDA, 113 Thailand Science Park, Phahonyothin Road, Klong Nueng, Klong LuangPathum Thani 12120, Thailand
Type
Article
Source Title
Biomolecules
ISSN
2218273X
Year
2018
Volume
8
Issue
4
Open Access
All Open Access, Gold, Green
Publisher
MDPI AG
DOI
10.3390/biom8040129
Format
Abstract
During the course of our ongoing work to discover new inhibitors of biofilm formation of Staphylococcus aureus from fungal sources, we observed biofilm inhibition by cytochalasans isolated from cultures of the ascomycete Hypoxylon fragiforme for the first time. Two new compounds were purified by a bioassay-guided fractionation procedure; their structures were elucidated subsequently by nuclear magnetic resonance (NMR) spectroscopy and high-resolution mass spectrometry (HR-MS). This unexpected finding prompted us to test further cytochalasans from other fungi and from commercial sources for comparison. Out of 21 cytochalasans, 13 showed significant inhibition of Staphylococcus aureus biofilm formation at subtoxic levels. These findings indicate the potential of cytochalasans as biofilm inhibitors for the first time, also because the minimum inhibitory concentrations (MIC) are independent of the anti-biofilm activities. However, cytochalasans are known to be inhibitors of actin, making some of them very toxic for eukaryotic cells. Since the chemical structures of the tested compounds were rather diverse, the inclusion of additional derivatives, as well as the evaluation of their selectivity against mammalian cells vs. the bacterium, will be necessary as next step in order to develop structure-activity relationships and identify the optimal candidates for development of an anti-biofilm agent. © 2018, MDPI AG. All rights reserved.
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
Funding Sponsor
Horizon 2020 Framework Programme
License
CC BY
Rights
Author
Publication Source
Scopus