4.6 Article

Chimeric Peptides Derived from Bovine Lactoferricin and Buforin II: Antifungal Activity against Reference Strains and Clinical Isolates of Candida spp.

Journal

ANTIBIOTICS-BASEL
Volume 11, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/antibiotics11111561

Keywords

Candida albicans; bovine lactoferricin; Buforin II; antimicrobial peptides; chimeras

Funding

  1. COLCIENCIAS [807-2018, 120380763646, 715-2018]

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Antimicrobial peptides are valuable resources for the discovery or design of potential antifungal candidates. Bovine lactoferricin and Buforin II are AMPs with great antimicrobial potential. Chimeras containing the minimal active motifs of these peptides were synthesized and evaluated for their antifungal activity against various strains of Candida. Some chimeras exhibited strong antifungal activity against specific strains.
Antimicrobial peptides (AMPs) are considered to be a valuable source for the identification and/or design of promising candidates for the development of antifungal treatments, since they have advantages such as lower tendency to induce resistance, ease of production, and high purity and safety. Bovine lactoferricin (LfcinB) and Buforin II (BFII) are AMPs to which great antimicrobial potential has been attributed. The minimum motives with antimicrobial activity derived from LfcinB and BFII are RRWQWR and RLLR, respectively. Nine chimeras containing the minimum motives of both peptides were synthesized and their antifungal activity against fluconazole (FLC)-sensitive and resistant C. albicans, C. glabrata, and C. auris strains was evaluated. The results showed that peptides C9: (RRWQWR)(2)K-Ahx-RLLRRRLLR and C6: KKWQWK-Ahx-RLLRRLLR exhibited the greatest antifungal activity against two strains of C. albicans, a FLC-sensitive reference strain and a FLC-resistant clinical isolate; no medically significant results were observed with the other chimeras evaluated (MIC similar to 200 mu g/mL). The chimera C6 was also active against sensitive and resistant strains of C. glabrata and C. auris. The combination of branched polyvalent chimeras together with FLC showed a synergistic effect against C. albicans. In addition to exhibiting antifungal activity against reference strains and clinical isolates of Candida spp., they also showed antibacterial activity against both Gram-positive and Gram-negative bacteria, suggesting that these chimeras exhibit a broad antimicrobial spectrum and can be considered to be promising molecules for therapeutic applications.

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