A TaqMan real-time PCR assay for quantifying white spot syndrome virus (WSSV) infections in wild broodstock and hatchery-reared postlarvae of fleshy shrimp, Fenneropenaeus chinensis

被引:48
作者
Jang, In-Kwon [2 ]
Meng, Xian-Hong [1 ,2 ]
Seo, Hyung-Chul [2 ]
Cho, Yeong-Rok [2 ]
Kim, Bong-Rae [2 ]
Ayyaru, Gopalakannan [2 ]
Kim, Jong-Sheek [2 ]
机构
[1] CAFS, Yellow Sea Fisheries Res Inst, Qingdao 266071, Peoples R China
[2] Natl Fisheries Res & Dev Inst, W Sea Mariculture Res Ctr, Taean 357945, Chungnam, South Korea
关键词
TaqMan real-time PCR; White spot syndronie virus (WSSV); Fenneropenaeus chinensis; Wild broodstock; Hatchery; SYNDROME BACULOVIRUS WSBV; PENAEUS-MONODON; CAPTURED BROODERS; QUANTIFICATION; DISEASES;
D O I
10.1016/j.aquaculture.2008.10.038
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
In the present study, a highly sensitive and specific TaqMan real-time PCR was developed to quantify white spot syndrome virus (WSSV) infections in wild broodstock and hatchery-reared postlarvae of fleshy shrimp, Fenneropenaeus chinensis. A total of 159 individuals Of Wild F chinensis brooders from 3 locations were captured and 210 postlarvae (PL1-8) were obtained from seven commercial hatcheries in 2007 in South Korea. The WSSV infections in 3 broodstocks showed a wide range, from 0 to 2.28 x 10(6) (with a mean of 1.50 x 10(4)) copies ng(-1) of DNA. Out of 159 brooders assayed, 39 (24.5%) were negative and 120 (75.5%) were positive: 153 (96.2%) showed less than 100 copies (mean 10.2 copies). 111 (69.8%) showed less than 10 copies and only 6 individuals (3.8%) showed high infections with a range of 2.36 x 10(2) to 2.28 x 10(6) copies ng(-1) of DNA. In 210 postlarvae, a range of 2.6 to 713.6 (with, mean of 220) copies g(-1) of DNA was observed. The mean WSSV copy number in the postlarvae was 7.9 x 10(5), which was equivalent to 8.5 x 10(5) copies mg(-1) of postlarvae weight. A total of 87.1% of postlarvae were WSSV positive and except for two hatcheries (H-4 and H-7) the postlarvae of all the other five hatcheries were positive. Even postlarvae from the same hatchery, especially of hatcheries H-4 and H-5, showed a wide range of WSSV infection resulting in higher infections than other hatcheries. There were 34.3% of the postlarvae assayed in the present study that showed very low infection, with less than 10 copies ng(-1) of DNA. Based on our results, it is recommended to pre-screen broodstock or larvae for selective breeding, stocking in production systems or stock enhancement. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:40 / 45
页数:6
相关论文
共 34 条
[1]  
Briggs M., 2004, RAP PUBL, P92
[2]   Sampling and evaluation of white spot syndrome virus in commercially important Atlantic penaeid shrimp stocks [J].
Chapman, RW ;
Browdy, CL ;
Savin, S ;
Prior, S ;
Wenner, E .
DISEASES OF AQUATIC ORGANISMS, 2004, 59 (03) :179-185
[3]  
Chen SN, 1995, SWIMMING THROUGH TROUBLED WATER, P29
[4]   Pathogenicity of a baculovirus infection causing white spot syndrome in cultured penaeid shrimp in Taiwan [J].
Chou, HY ;
Huang, CY ;
Wang, CH ;
Chiang, HC ;
Lo, CF .
DISEASES OF AQUATIC ORGANISMS, 1995, 23 (03) :165-173
[5]  
Deng Deng, 2005, Journal of Fisheries of China, V29, P74
[6]  
Deng JY, 1983, ACTA OCEANOL SIN, V5, P107
[7]   Detection and quantification of infectious hypodermal and hematopoietic necrosis virus and white spot virus in shrimp using real-time quantitative PCR and SYBR green chemistry [J].
Dhar, AK ;
Roux, MM ;
Klimpel, KR .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (08) :2835-2845
[8]  
DHAR AK, 2001, AQUACULTURE, V237, P59
[9]   Quantitative real time PCR for the measurement of white spot syndrome virus in shrimp [J].
Durand, SV ;
Lightner, DV .
JOURNAL OF FISH DISEASES, 2002, 25 (07) :381-389
[10]   Qualitative and quantitative studies on the relative virus load of tails and heads of shrimp acutely infected with WSSV [J].
Durand, SV ;
Redman, RM ;
Mohney, LL ;
Tang-Nelson, K ;
Bonami, JR ;
Lightner, DV .
AQUACULTURE, 2003, 216 (1-4) :9-18