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Quantitative real time PCR for the measurement of white spot syndrome virus in shrimp
Author(s) -
Durand S V,
Lightner D V
Publication year - 2002
Publication title -
journal of fish diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.819
H-Index - 85
eISSN - 1365-2761
pISSN - 0140-7775
DOI - 10.1046/j.1365-2761.2002.00367.x
Subject(s) - white spot syndrome , shrimp , biology , hepatopancreas , penaeus monodon , virus , virology , hemolymph , polymerase chain reaction , gill , real time polymerase chain reaction , penaeus , gene , fishery , fish <actinopterygii> , genetics , ecology
Quantitative real time PCR, recently developed in molecular biology, is applied in this paper to quantify the white spot syndrome virus (WSSV) in infected shrimp tissue. The WSSV content in moribund shrimp of all species tested ( Penaeus stylirostris, P. monodon, P. vannamei ) ranged from 2.0 × 10 4 to 9.0 × 10 10 WSSV copies μg –1 of total DNA ( n =26). In whole moribund post‐larvae, 4.3 × 10 9 WSSV copies μg –1 of DNA were detected which is equivalent to 5.7 × 10 10 WSSV copies g –1 of post‐larvae. The comparison of WSSV content between different tissues showed that muscle and hepatopancreas tissues contained 10 times less virus than gills, pleopods and haemolymph. With inocula of known virus content, bioassays by immersion challenge showed that a minimum of five logs of WSSV copies was necessary to establish disease in the challenged shrimp. In contrast, five logs of WSSV copies injected into shrimp muscle produced a LT‐50 of 52 h. This real time polymerase chain reaction (PCR) technique is sensitive (four copies), specific (negative with DNA from shrimp baculoviruses and parvoviruses), dynamic (seven logs) and easy to perform (96 tests in <4 h).