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dc.contributor.authorZhang, Tian
dc.contributor.authorWang, Zhejun
dc.contributor.authorHancock, Robert E. W.
dc.contributor.authorHaapasalo, Markus
dc.contributor.authorde la Fuente Nunez, Cesar
dc.date.accessioned2017-04-10T15:24:25Z
dc.date.available2017-04-10T15:24:25Z
dc.date.issued2016-11
dc.date.submitted2016-08
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/108007
dc.description.abstractAlmost all dental diseases are caused by biofilms that consist of multispecies communities. DJK-5, which is a short D-enantiomeric, protease-resistant peptide with broad-spectrum anti-biofilm activity, was tested for its effect on oral multispecies biofilms. Peptide DJK-5 at 10 μg/mL effectively prevented the growth of these microbes in culture media in a time-dependent manner. In addition to the prevention of growth, peptide DJK-5 completely killed both Streptococcus mutans and Enterococcus faecalis suspended from biofilms after 30 minutes of incubation in liquid culture media. DJK-5 also led to the effective killing of microbes in plaque biofilm. The proportion of bacterial cells killed by 10 μg/mL of DJK-5 was similar after 1 and 3 days, both exceeding 85%. DJK-5 was able to significantly prevent biofilm formation over 3 days (P = 0.000). After 72 hours of exposure, DJK-5 significantly reduced and almost completely prevented plaque biofilm production by more than 90% of biovolume compared to untreated controls (P = 0.000). The proportion of dead biofilm bacteria at the 10 μg/mL DJK-5 concentration was similar for 1- and 3-day-old biofilms, whereby >86% of the bacteria were killed. DJK-5 was also able to kill >79% and >85% of bacteria, respectively, after one-time and three brief treatments of 3-day-old biofilms. The combination of DJK-5 and chlorhexidine showed the best bacterial killing among all treatments, with ~83% and >88% of bacterial cells killed after 1 and 3 minutes, respectively. No significant difference was found in the percentage of biofilm killing amongst three donor plaque samples after DJK-5 treatment. In particular, DJK-5 showed strong performance in inhibiting biofilm development and eradicating pre-formed oral biofilms compared to L-enantiomeric peptide 1018. DJK-5 was very effective against oral biofilms when used alone or combined with chlorhexidine, and may be a promising agent for use in oral anti-biofilm strategies in the future.en_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (R31AI098701)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0166997en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourcePLoSen_US
dc.titleTreatment of Oral Biofilms by a D-Enantiomeric Peptideen_US
dc.typeArticleen_US
dc.identifier.citationZhang, Tian; Wang, Zhejun; Hancock, Robert E. W.; de la Fuente-Núñez, César; Haapasalo, Markus. “Treatment of Oral Biofilms by a D-Enantiomeric Peptide.” Edited by Surajit Bhattacharjya. PLOS ONE 11, no. 11 (November 23, 2016): e0166997.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.contributor.mitauthorde la Fuente Nunez, Cesar
dc.relation.journalPLOS ONEen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsZhang, Tian; Wang, Zhejun; Hancock, Robert E. W.; de la Fuente-Núñez, César; Haapasalo, Markusen_US
dspace.embargo.termsNen_US
mit.licensePUBLISHER_CCen_US


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