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.
引用
收藏
页码:309 / 312
页数:4
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