Molecular cloning and expression analysis of two type II crustin genes in the oriental river prawn, Macrobrachium nipponense

被引:16
|
作者
Dai, Xiaoling [1 ]
Huang, Xin [1 ]
Zhang, Zhuoxing [1 ]
Zhang, Ruidong [1 ]
Cao, Xueying [1 ]
Zhang, Chao [1 ]
Wang, Kaiqiang [1 ]
Ren, Qian [1 ,2 ,3 ]
机构
[1] Nanjing Normal Univ, Coll Marine Sci & Engn, Jiangsu Prov Engn Res Ctr Aquat Anim Breeding & G, Nanjing 210023, Peoples R China
[2] Shandong Normal Univ, Coll Life Sci, Shandong Prov Key Lab Anim Resistance Biol, Jinan 250014, Peoples R China
[3] Coinnovat Ctr Marine Bioind Technol Jiangsu Prov, Lianyungang 222005, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Gly-rich region; Crustins; Relish; Innate immunity; Macrobrachium nipponense; WHEY ACIDIC PROTEIN; CHINESE MITTEN CRAB; ANTIMICROBIAL PEPTIDES; RECOMBINANT EXPRESSION; LITOPENAEUS-VANNAMEI; ANTIBACTERIAL PEPTIDE; VIBRIO-ALGINOLYTICUS; INNATE IMMUNITY; HOST-DEFENSE; SHORE CRAB;
D O I
10.1016/j.fsi.2020.01.001
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Innate immunity is the primary defense of crustaceans against pathogens. Crustins, as antimicrobial peptides, are important to crustacean innate immunity. In this study, two kinds of Gly-rich crustin genes were cloned from Macrobrachium nipponense and were referred to as Mn-Gly-Cru1 and Mn-Gly-Cru2. These crustins belong to type II crustins with typical type II crustin structures. The full-length cDNA of Mn-Gly-Cru1 is 677 bp and contains a 576 bp open reading frame (ORF) encoding 191 amino acids. The full-length cDNA of Mn-Gly-Cru2 is 727 bp, with 573 bp ORF encoding 190 amino acids. The constructed phylogenetic tree indicated that Mn-Gly-Cru1 and Mn-Gly-Cru2 belong to the type IIa subfamily. RT-PCR analysis showed that Mn-Gly-Cru1 and Mn-Gly-Cru2 are widely distributed in various tissues. qRT-PCR results indicated that Mn-Gly-Cru1 is mainly expressed in the gills, whereas Mn-Gly-Cru2 is expressed at the highest level in hemocytes. The transcripts of Mn-Gly-Cru1 and Mn-Gly-Cru2 respond to bacterial or white spot syndrome virus (WSSV) stimuli. After injection of 48 h dsMnRelish, the expression of MnRelish, Mn-Gly-Cru1, and Mn-Gly-Cru2 were all inhibited. After WSSV, Vibrio parahaemolyticus, or Staphylococcus aureus challenge, MnRelish, Mn-Gly-Cru1, and Mn-Gly-Cru2 were all upregulated. However, the expression levels of MnRelish, Mn-Gly-Cru1, and Mn-Gly-Cru2 at 6 h bacteria or 36 h WSSV challenge were downregulated in Relish-silenced prawns when compared with the control (bacteria or WSSV challenge only, bacteria or WSSV challenge plus dsGFP injection). Results suggest that Mn-Gly-Cru1 and Mn-Gly-Cru2 play essential roles in M. nipponense innate immunity against bacteria or WSSV, and the expression levels of both genes are regulated by Relish transcriptional factor.
引用
收藏
页码:446 / 456
页数:11
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