SpALF4: A newly identified anti-lipopolysaccharide factor from the mud crab Scylla paramamosain with broad spectrum antimicrobial activity

被引:33
|
作者
Zhu, Lei [1 ,2 ]
Lan, Jiang-Feng [3 ]
Huang, Yan-Qing [1 ,2 ]
Zhang, Chao [4 ]
Zhou, Jun-Fang [1 ,2 ]
Fang, Wen-Hong [1 ,2 ]
Yao, Xiao-Juan [1 ,2 ]
Wang, Hao [1 ,2 ]
Li, Xin-Cang [1 ,2 ]
机构
[1] Chinese Acad Fishery Sci, East China Sea Fisheries Res Inst, Shanghai 200090, Peoples R China
[2] Minist Agr, Key Lab East China Sea & Ocean Fishery Resources, Shanghai 200090, Peoples R China
[3] Shandong Univ, Sch Life Sci, Jinan 250100, Shandong, Peoples R China
[4] Henan Normal Univ, Coll Fisheries, Xinxiang 453007, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
SpALF4; Expression pattern; Binding activity; Antimicrobial activity; BLACK TIGER SHRIMP; ANTI-LPS FACTOR; MOLECULAR-CLONING; PENAEUS-MONODON; GENOMIC ORGANIZATION; PORTUNUS-TRITUBERCULATUS; FACTOR ALF; IN-VIVO; PEPTIDES; ISOFORM;
D O I
10.1016/j.fsi.2013.10.023
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Anti-lipopolysaccharide factors (ALFs) are antimicrobial peptides with binding and neutralizing activities to lipopolysaccharide (LPS) in crustaceans. This study identified and characterized a novel ALF homolog (SpALF4) from the mud crab Scylla paramamosain. The complete cDNA of SpALF4 had 756 bp with a 381 bp open reading frame encoding a protein with 126 aa. The deduced protein contained a signal peptide and a LPS-binding domain. SpALF4 shared the highest identity with PtALF5 at amino acid level but exhibited low similarity with most of other crustacean ALFs. Furthermore, different from the previously identified three SpALF homologs and most of other ALFs, SpALF4 had a low isoelectric point (pI) for the mature peptide and the LPS-binding domain with the values of 6.93 and 6.74, respectively. These results indicate that SpALF4 may be a unique ALF homolog with special biological function in the mud crab. Similar to the spatial structure of ALFPm3, SpALF4 contains three alpha-helices packed against a four-strand beta-sheet, and an amphipathic loop formed by a disulphide bond between two conserved cysteine residues in LPS-binding domain. SpALF4, mainly distributed in hemocytes, could be upregulated by Vibrio harveyi, Staphylococcus aureus, or white spot syndrome virus. Recombinant SpALF4 could inhibit the growth of Gram-negative bacteria (V harveyi, Vibrio anguillarum, Vibrio alginolyticus, Aeromonas hydrophila, Pseudomonas putida), Gram-positive bacteria (S. aureus and Bacillus megaterium), and a fungus Candida albicans to varying degrees. Further study showed that it could also bind to all the aforementioned microorganisms excepts. aureus. These results demonstrate that SpALF4 is a unique ALF homolog with potent antimicrobial activity against bacteria and fungi. This characteristic suggests SpALF4 plays an essential function in immune defense against pathogen invasion in mud crab. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:172 / 180
页数:9
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