Screening high-efficiency promoter to construct trans-vp28 vp28 gene Anabaena sp. PCC7120 against white spot syndrome virus of Litopenaeus vannamei

被引:1
|
作者
Chen, Xin-Yu [1 ]
Yu, Dian-Jiang [2 ]
Jia, Rui [1 ,3 ]
机构
[1] Shanghai Ocean Univ, Coll Marine Sci & Ecol Environm, Shanghai 201306, Peoples R China
[2] Xiamen Univ, Coll Life Sci, Xiamen 361104, Peoples R China
[3] Marine Biomed Sci & Technol Innovat Platform Lin G, Shanghai 201306, Peoples R China
关键词
White spot syndrome virus (WSSV); Promoter modifications; vp28; Anabaena sp. PCC7120; Enzyme activities; Litopenaeus vannamei; PENAEUS-MONODON; SUPEROXIDE-DISMUTASE; SYNTHETIC BIOLOGY; EXPRESSION; CYANOBACTERIUM; SHRIMP; ANTIOXIDANT; HEPATOPANCREAS; INFECTION; ENZYMES;
D O I
10.1016/j.fsi.2024.109912
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
This study aimed to select high-quality promoters to construct trans-vp28 gene Anabaena sp. PCC7120 and feed Litopenaeus vannamei to assess the effect of L.vannamei against white spot syndrome virus (WSSV). Transgenic algae were created using five plasmids containing PrbcL, Pcpc560, Ptrc, Ptac, and PpsbA. According to the gene expression efficiency and the growth index of transgenic algae, Pcpc560 was determined to be the most efficient promoter. Shrimps were continuously fed trans-vp28 gene Anabaena sp. PCC7120 for one week and then challenged with WSSV. After the challenge, the transgenic algae group (vp28-7120 group) was continuously immunized [continuous immunization for 0 days (vp28-7120-0d); continuous immunization for 2 days (vp28-7120-2d); continuous immunization for 4 days (vp28-7120-4d)]. After seven days, the daily survival rate of each experimental group was continuously tracked. Following the viral challenge, the hepatopancreas samples were assayed for their levels of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), thioredoxin peroxidase (TPX), acid phosphatase (ACP), and alkaline phosphatase (AKP) at varying time intervals. In comparison to the positive control group (challenge and no vaccination) and the wild-type group (challenge, fed wild-type Anabaena sp. PCC7120), the vp28-7120 group (challenge, fed trans-vp28 gene Anabaena sp. PCC7120) exhibited a remarkable increase in survival rates, reaching 50 % (vp28-7120-0d), 76.67 % (vp28-7120-2d), and 80 % (vp28-7120-4d). Furthermore, the vp28-7120 group consistently displayed significantly higher activities of SOD, CAT, GSH-Px, ACP, and AKP, while exhibiting notably lower TPX activity, when compared to the control group. These results indicate that the Pcpc560 promoter effectively elevated the expression level of the exogenous vp28 gene and spurred the growth of the trans-vp28 gene Anabaena sp. PCC7120. Consequently, trans-vp28 gene Anabaena sp. PCC7120 significantly bolstered the immunity of L.vannamei. Therefore, utilizing the Pcpc560 promoter to develop trans-vp28 gene Anabaena sp. PCC7120 based oral vaccine is highly beneficial for industrial-scale cultivation, advancing its commercialization prospects.
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页数:7
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