| Literature DB >> 18429444 |
Siwaporn Longyant1, Piengjan Poyoi, Parin Chaivisuthangkura, Thanawan Tejangkura, Weerawan Sithigorngul, Paisarn Sithigorngul, Sombat Rukpratanporn.
Abstract
The gene sequence encoding VP3 capsid protein of Taura syndrome virus (TSV) was cloned into pGEX-6P-1 expression vector and transformed into Escherichia coli BL21. After induction, recombinant GST-VP3 (rVP3) fusion protein was obtained and further purified by electro-elution before use in immunizing Swiss mice for production of monoclonal antibodies (MAb). One MAb specific to glutathione-S-transferase (GST) and 6 MAb specific to VP3 were selected using dot blotting and Western blotting. MAb specific to VP3 could be used to detect natural TSV infections in farmed whiteleg shrimp Penaeus vannamei by dot blotting and Western blotting, without cross reaction to shrimp tissues or other shrimp viruses, such as white spot syndrome virus (WSSV), yellow head virus (YHV), monodon baculovirus (MBV) and hepatopancreatic parvovirus (HPV). These MAb were also used together with those specific for WSSV to successfully detect TSV and WSSV in dual infections in farmed P. vannamei.Entities:
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Year: 2008 PMID: 18429444 DOI: 10.3354/dao01885
Source DB: PubMed Journal: Dis Aquat Organ ISSN: 0177-5103 Impact factor: 1.802