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Characterization and Functional Evaluation of NK-lysin from Clownfish (Amphiprion ocellaris)

文献类型： 外文期刊

作者： Yu, Dapeng 1 ; Zhao, Haohang 1 ; Wen, Yiming 1 ; Li, Tao 3 ; Xia, Hongli 1 ; Wang, Zhiwen 1 ; Gan, Zhen 1 ; Xia, Liqun 1 ; Chen, Jianlin 1 ; Lu, Yishan 1 ;

作者机构： 1.Guangdong Ocean Univ, Shenzhen Inst, Shenzhen Publ Serv Platform Evaluat Marine Econ An, Guangdong Prov Engn Res Ctr Aquat Anim Hlth Assess, Shenzhen 518000, Peoples R China

2.Guangdong Ocean Univ, Coll Fisheries, Guangdong Prov Key Lab Pathogen Biol & Epidemiol A, Zhanjiang 524000, Peoples R China

3.Chinese Acad Fishery Sci, Shenzhen Base South China Sea Fisheries Res Inst, Shenzhen 518000, Peoples R China

关键词： Amphiprion ocellaris; NK-lysin; Pichia pastoris; antibacterial; antiviral

期刊名称：FISHES （ 影响因子：2.3； 五年影响因子：2.4 ）

ISSN：

年卷期： 2023 年 8 卷 11 期

页码：

收录情况： SCI

摘要： In previous studies, natural killer lysin (NK-lysin) emerged as a crucial antimicrobial peptide (AMP) discharged by NK cells and CTLs. The sequence of NK-lysin was cloned and discovered in some fishes, but its function remains unclear. In our study, we obtained a copy of NK-lysin from the spleen of the healthy clownfish (Amphiprion ocellaris; AoNK-lysin) through cloning and proceeded to investigate its potential functions and activities. The findings showed that the AoNK-lysin gene's open reading frame (ORF) had a length of 465 base pairs (bp) and encoded 154 amino acids (aa), which included a saposin B domain and six cysteine residues that are highly conserved, forming three intrachain disulfide bonds to carry out antimicrobial activity. The AoNK-lysin gene was widely present in different tissues, with the skin showing the highest expression, followed by the eye, intestine, and muscle. Additionally, the expression of AoNK-lysin was significantly upregulated in the immune organs (spleen, gill, intestine, and head kidney) of A. ocellaris after being challenged by Singapore group iridovirus (SGIV). Furthermore, a 399 base pair cDNA sequence that encodes the fully developed peptide of AoNK-lysin was successfully inserted into a secretion plasmid called pPIC9K. Subsequently, a significant amount of the recombinant AoNK-lysin protein was efficiently manufactured using the Pichia pastoris expression system. The antibacterial test demonstrated that the AoNK-lysin protein significantly suppressed the growth of various pathogens, particularly Streptococcus agalactiae, Streptococcus iniae, Salmonella typhi, Shigella sonnei, Pseudomonas aeruginosa, and Aeromonas caviae. The minimal inhibitory concentration (MIC) was found to be 7.81 mu g/mL. Further analysis of antiviral assays showed all the viral mRNA of SGIV to be significantly reduced after AoNK-lysin protein stimuli in FHM cells. Collectively, these discoveries indicate that AoNK-lysin exhibits features of both direct pathogen-killing abilities and inhibited virus replication.

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