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Antiadhesion and Antibiofilm Activities of High Molecular Weight Coffee Components against Streptococcus mutans

Authors :
Adele Papetti
Anna Maria Schito
Monica Stauder
Gabriella Gazzani
Maria Daglia
Carla Pruzzo
Dora Mascherpa
Stauder, M.
Papetti, Adele
Mascherpa, D.
Schito, A. M.
Gazzani, Gabriella
Pruzzo, C.
Daglia, Maria
Publication Year :
2010
Publisher :
American Chemical Society:1155 Sixteenth Street Northwest:Washington, DC 20036:(800)227-5558, EMAIL: service@acs.org, INTERNET: http://www.pubs.acs.org, Fax: (614)447-3671, 2010.

Abstract

In previous studies we demonstrated that green and roasted coffee contains low molecular weight (LMW) compounds capable of inhibiting the ability of Streptococcus mutans, the major causative agent of human dental caries, to adhere to hydroxyapatite (HA) beads. This study addressed the ability of the whole high molecular weight coffee fraction (cHMW) and of its melanoidin and non-melanoidin components (GFC1-5), applied at concentrations that occur in coffee beverages, to (i) inhibit S. mutans growth; (ii) affect S. mutans sucrose-dependent adhesion to and detachment from saliva-coated HA beads (sHA); and (iii) inhibit biofilm development on microtiter plates. The results indicated that only cHMW is endowed with antimicrobial activity. The cHMW fraction and each of the five GFC components inhibited S. mutans adhesion, the strongest effect being exerted by cHMW (91%) and GFC1 (88%). S. mutans detachment from sHA was four times greater (∼20%) with cHMW and the GFC1 and GFC4 melanoidins than with controls. Finally, biofilm production by S. mutans was completely abolished by cHMW and was reduced by 20% by the melanoidin components GFC2 and GFC4 and by the non-melanoidin component GFC5 compared with controls. Altogether these findings show that coffee beverage contains both LMW compounds and HMW melanoidin and non-melanoidin components with a strong ability to interfere in vitro with the S. mutans traits relevant for cariogenesis.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....61fac70b2c8b38c8ba9be205f953f69d