2007
DOI: 10.1128/aac.00924-06
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Efficacy of the De Novo-Derived Antimicrobial Peptide WLBU2 against Oral Bacteria

Abstract: The efficacy of a novel synthetic antimicrobial peptide (WLBU2) was evaluated against three oral microorganisms (grown planktonically): Streptococcus gordonii, Fusobacterium nucleatum, and Porphyromonas gingivalis. WLBU2 killed all three species, with F. nucleatum being the most susceptible. WLBU2 also reduced the bacterial burden of S. gordonii and F. nucleatum biofilms.

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Cited by 12 publications
(12 citation statements)
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“…Although the number of P. gingivalis and P. inter- media cells in physiological saline spontaneously decreased, LFcin B at a relatively high concentration (0.4 mg/ml) further reduced the numbers of these bacteria. These results obtained with LFcin B seem to be in accord with those obtained in previous studies with other antimicrobial peptides, in which their activities against P. gingivalis and P. intermedia were weak or were not seen at all (8,29,32). P. gingivalis and P. intermedia colonize and grow as biofilms within subgingival plaque (14,27).…”
Section: Vol 53 2009supporting
confidence: 81%
“…Although the number of P. gingivalis and P. inter- media cells in physiological saline spontaneously decreased, LFcin B at a relatively high concentration (0.4 mg/ml) further reduced the numbers of these bacteria. These results obtained with LFcin B seem to be in accord with those obtained in previous studies with other antimicrobial peptides, in which their activities against P. gingivalis and P. intermedia were weak or were not seen at all (8,29,32). P. gingivalis and P. intermedia colonize and grow as biofilms within subgingival plaque (14,27).…”
Section: Vol 53 2009supporting
confidence: 81%
“…These are distinct from those in nature, with simpler but rationally engineered composition, obtained by varying the amino acid content and sequence and overall peptide length to achieve enhanced activity and very low cytotoxic properties [57]. For example, Mietzner and co-workers [58][59][60][61] have developed a series of de novo peptides based on structure-function properties observed in natural AMPs. They engineered the peptide composition to achieve enhanced potency, selectivity and stability.…”
Section: Antimicrobial Peptidesmentioning
confidence: 99%
“…These sequences incorporate characteristics common to natural AMPs with changes designed to increase stability and function within a range of biological media. Deslouches and coworkers have designed de novo AMPs that display improved activity over a broad range of conditions including physiologic NaCl, in the presence of divalent cations, and in serum [161163]. These peptides have also shown good selectivity for Pseudomonas aeruginosa over mammalian cells within a co-culture system [157] and excellent activity against both gram positive and gram negative multidrug resistant organisms [164].…”
Section: Antimicrobial Peptides (Amps) – Promising Therapeutics Fomentioning
confidence: 99%