| Literature DB >> 24642357 |
Kairong Wang1, Jiexi Yan1, Wen Dang1, Junqiu Xie1, Bo Yan1, Wenjin Yan1, Mengyang Sun1, Bangzhi Zhang1, Mingxia Ma1, Yanyan Zhao1, Fengjing Jia1, Ranran Zhu1, Wei Chen1, Rui Wang2.
Abstract
With the increasing emergence of resistant fungi, the discovery and development of novel antifungal therapeutics were urgently needed. Compared with conventional antibiotics, the limited propensity of AMPs to induce resistance in pathogens has attracted great interest. In the present study, the antifungal activity and its mechanism-of-action of polybia-MPI, a cationic peptide from the venom of Social wasp Polybia Paulista was investigated. We demonstrated that polybia-MPI could potently inhibit the growth of Candida albicans (C. albicans) and Candida glabrata (C. glabrata). The 50% inhibitory concentrations (IC50) of Polybia-MPI against cancer cells were much higher than the MICs against the tested C. albicans and C. glabrata cells, indicating that polybia-MPI had high selectivity between the fungal and mammalian cells. Our results also indicated that membrane disturbance mechanism was involved in the antifungal activity. Furthermore, polybia-MPI could inhibit the bio film forming of C. glabrata, which was frequently associated with clinically significant biofilm. These results suggest that polybia-MPI has great advantages in the development of antifungal agents.Entities:
Keywords: Antifungal activity; Antimicrobial peptide; Biofilm formation; Polybia-MPI
Mesh:
Substances:
Year: 2014 PMID: 24642357 DOI: 10.1016/j.peptides.2014.03.005
Source DB: PubMed Journal: Peptides ISSN: 0196-9781 Impact factor: 3.750