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Functional characterization of two defensins, HlDFS1 and HlDFS2, from the hard tick Haemaphysalis longicornis

Authors :
Ta Sun
Wen Pan
Yanhui Song
Jingpin Zhang
Jingwen Wang
Jianfeng Dai
Source :
Parasites & Vectors, Vol 10, Iss 1, Pp 1-8 (2017)
Publication Year :
2017
Publisher :
BMC, 2017.

Abstract

Abstract Background Ticks are second to mosquitoes as vectors of human arthropod-borne diseases. Ticks rely heavily on antimicrobial peptides (AMPs) to defend against microbes and defensins are major components of innate immunity in ticks. Results Two novel defensin genes, named HlDFS1 and HlDFS2, were identified from a cDNA library of the hard tick Haemaphysalis longicornis collected in southeast China. The peptides encoded by both genes shares typical features of type-2 arthropod defensin superfamily. The expressions of both genes increased in ticks during blood-feeding. The synthetic minimum functional peptides HlDFS1 and HlDFS2 showed broad spectrum antimicrobial activity against various Gram-positive and Gram-negative bacteria. Moreover, HlDFS1 and HlDFS2 exhibit bactericidal activity to some drug resistant bacteria. HlDFS1, but not HlDFS2, showed inhibitory activity against fungus Candida albicans. HlDFS1 and HlDFS2 had no significant hemolysis effect on human erythrocytes at low concentrations and did not impair mammalian cell survival. Finally, HlDFS1 and HlDFS2 significantly protected mice against lethal infection by Staphylococcus aureus and Micrococcus luteus. Conclusions HlDFS1 and HlDFS2 are two novel functional defensins from the hard tick Haemaphysalis longicornis. They showed bactericidal activity against various Gram-positive and Gram-negative bacteria and significantly protect mice against lethal bacterial infection. Thus, HlDFS1 and HlDFS2 can be introduced to the medical field as new drug candidates with antibacterial activity.

Details

Language :
English
ISSN :
17563305
Volume :
10
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Parasites & Vectors
Publication Type :
Academic Journal
Accession number :
edsdoj.34cc2f365bde4f148b0aa284a2c56ad1
Document Type :
article
Full Text :
https://doi.org/10.1186/s13071-017-2397-9