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KMID : 0545120140240070905
Journal of Microbiology and Biotechnology
2014 Volume.24 No. 7 p.905 ~ p.913
Novel Anticandidal Activity of a Recombinant Lampetra japonica RGD3 Protein
Caiping Wu

Li Lu
Yuanyuan Zheng
Xin Liu
Rong Xiao
Jihong Wang
Qingwei Li
Abstract
Lj-RGD3, an RGD (Arg-Gly-Asp) toxin protein from the salivary gland of Lampetra japonica, exhibits antifungal activity against Candida albicans. Lj-RGD3 has three RGD motifs and shows homology to histidine-rich glycoprotein. We synthesised two mutant derivatives of Lj-RGD3: Lj-26, which lacks all three RGD motifs and contains no His residues; and Lj-112, which lacks only the three RGD motifs. We investigated the effects of the wild-type and mutated toxins on a gram-positive bacterium (Escherichia coli), a gram-negative bacterium (Staphylococcus aureus), and a fungus (C. albicans). rLj-RGD3 and its mutants exhibited antifungal but not antibacterial activity, as measured by a radial diffusion assay. The C. albicans inhibition zone induced by rLj-112 was larger than that induced by the other proteins, and its inhibitory effect on C. albicans was dose-dependent. In viable-count assays, the rLj-112 MIC was 7.7 ¥ìM, whereas the MIC of the positive control (ketoconazole) was 15 ¥ìM. Time-kill kinetics demonstrated that rLj-112 effectively killed C. albicans at 1¡¿ and 2¡¿ MIC within 12 and 6 h, respectively. Electron microscopy analysis showed that rLj-RGD3 and rLj-112 induced C. albicans lysis. Our results demonstrate a novel anticandidal activity for rLj-RGD3 and its mutant derivatives.
KEYWORD
Lampetra japonica, rLj-RGD3, AMPs, anticandidal
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