The expression and purification of WSSV134 from white spot syndrome virus and its inhibitory effect on caspase activity from Penaeus monodon

被引:6
作者
Bowornsakulwong, Thanunthon [1 ]
Charoensapsri, Walaiporn [2 ,3 ]
Rattanarojpong, Triwit [1 ]
Khunrae, Pongsak [1 ]
机构
[1] King Mongkuts Univ Technol Thonburi, Fac Sci, Dept Microbiol, Bangkok 10140, Thailand
[2] Mahidol Univ, Ctr Excellence Shrimp Mol Biol & Biotechnol Cent, Fac Sci, Bangkok 10400, Thailand
[3] Natl Sci & Technol Dev Agcy, Natl Ctr Genet Engn & Biotechnol BIOTEC, Pathum Thani 12120, Thailand
关键词
WSSV134; Apoptosis; White spot syndrome virus; Caspase; ANTI-APOPTOSIS PROTEIN; SHRIMP; CLONING; GENE; P35; MORTALITY; INFECTION; CLEAVAGE; VANNAMEI;
D O I
10.1016/j.pep.2016.10.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
WSSV134 or VP36A protein of white spot syndrome virus was previously reported to be able to reduce apoptosis in Sf-9 cells transfected with caspase of Penaeus monodon (PmCasp). The protein was therefore believed to have a role in supporting the survival of WSSV inside the host cells during infection. However, the anti-apoptosis activity of WSSV134 involved in the inhibition of PmCasp is still unclear. In this study, we produced a recombinant WSSV134 (rWSSV134) and tested for its ability to inhibit PmCasp in vitro. The results from a caspase inhibition assay revealed that rWSSV134 could inhibit PmCasp in a dose dependent manner. Since WSSV134 was predicted to contain three potential caspase binding sites, corresponding to the D54, D104 and D259, we then employed site-directed mutagenesis to investigate the involvement of these sites in PmCasp inhibition. D54A and D259A mutants could still inhibit PmCasp while D104A mutant lacks this activity. Our results confirmed that the WSSV134 is an inhibitor for PmCasp and that residue D104 is important for PmCasp inhibition. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:123 / 128
页数:6
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