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
[11]   Major viral diseases of the black tiger prawn (Penaeus monodon) in Thailand [J].
Flegel, TW .
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 1997, 13 (04) :433-442
[12]  
Han Hyon-Sob, 2006, Journal of Fisheries Science and Technology, V9, P75
[13]  
HEO MS, 2000, FISH PATHOL, V13, P7
[14]   Detection of WSSV in cultured shrimps, captured brooders, shrimp postlarvae and water samples in Bangladesh by PCR using different primers [J].
Hossain, MS ;
Otta, SK ;
Chakraborty, A ;
Kumar, HS ;
Karunasagar, I ;
Karunasagar, I .
AQUACULTURE, 2004, 237 (1-4) :59-71
[15]   Studies on effective PCR screening strategies for white spot syndrome virus (WSSV) detection in Penaeus monodon brooders [J].
Hsu, HC ;
Lo, CF ;
Lin, SC ;
Liu, KF ;
Peng, SE ;
Chang, YS ;
Chen, LL ;
Liu, WJ ;
Kou, GH .
DISEASES OF AQUATIC ORGANISMS, 1999, 39 (01) :13-19
[16]  
Jang I.K., 2007, J AQUACULTURE, V20, P278
[17]  
Kim B.A., 1973, Bulletin Fish Res Dev Agency, VNo. 11, P7
[18]  
KIM CK, 1997, J FISH PATHOL, V10, P87
[19]   TaqMan real-time PCR for detection of hepatopancreatic parvovirus from Australia [J].
La Fauce, Kathy A. ;
Layton, Ramon ;
Owens, Leigh .
JOURNAL OF VIROLOGICAL METHODS, 2007, 140 (1-2) :10-16
[20]  
Lightner D. V., 1996, A handbook of shrimp pathology and diagnostic procedures for diseases of cultured penaeid shrimp