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Detection and quantification of hepatopancreatic parvovirus in penaeid shrimp by real-time PCR assay
被引:6
作者:
Liu, Tianqi
[1
,2
]
Yang, Bing
[1
]
Song, Xiaoling
[1
]
Wang, Xiuhua
[1
]
Yuan, Yanyan
[1
,2
]
Liu, Li
[1
]
Huang, Jie
[1
]
机构:
[1] Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Maricultural Organism Dis Control & Mol Pathol La, Qingdao 266071, Shandong, Peoples R China
[2] Shanghai Ocean Univ, Coll Fisheries & Life Sci, Shanghai 201306, Peoples R China
关键词:
Hepatopancreatic parvovirus;
Real-time PCR;
TaqMan;
Detection;
COMPLETE NUCLEOTIDE-SEQUENCE;
POLYMERASE-CHAIN-REACTION;
HPV;
INFECTION;
MONODON;
VIRUS;
D O I:
10.1016/j.jip.2013.09.007
中图分类号:
Q95 [动物学];
学科分类号:
071002 ;
摘要:
As one of the major pathogens, hepatopancreatic parvovirus (HPV) can cause severe diseases in penaeid shrimp. We developed a TaqMan-based real-time PCR assay for the HPV detection in China. A pair of primers (HPVF and HPVR) and a TaqMan probe were designed according to the HPV genomic sequence of Chinese isolate (GenBank: GU371276). Our data showed that the primers and TaqMan probe were specific for HPV, and they exhibited no cross-reaction with infectious hypodermal and hematopoietic necrosis virus (IHHNV), white spot syndrome virus (WSSV) and specific pathogen free (SPF) shrimp DNA. The assay had a detection limit of four plasmid HPV DNA copies per reaction. Furthermore, HPV was detected in 16 of 21 Fenneropenaeus Chinensis, 3 of 52 Litopenaeus vannamei and 2 of 2 Marsupenaeus japonicus penaeid shrimp samples. In addition, HPV was also detected in crabs. Therefore, this assay could be successfully used as a sensitive and rapid molecular-based diagnostic method to screen HPV-free animals and survey the prevalence of HPV in cultured populations of penaeid shrimp in China. (C) 2013 Elsevier Inc. All rights reserved.
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页码:309 / 312
页数:4
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