Development of a TaqMan-based real-time PCR assay for the specific detection of porcine circovirus 3

被引:48
作者
Wang, Jianchang [1 ]
Zhang, Yongning [3 ]
Wang, Jinfeng [1 ]
Liu, Libing [1 ]
Pang, Xiaoyu [2 ]
Yuan, Wanzhe [2 ]
机构
[1] Hebei Entry Exit Inspect & Quarantine Bur, Ctr Inspect & Quarantine, Shijiazhuang 050051, Hebei, Peoples R China
[2] Agr Univ Hebei, Coll Vet Med, 38 Lingyusi St, Baoding 071001, Hebei, Peoples R China
[3] Chinese Acad Inspect & Quarantine, Inst Anim Quarantine, Beijing 100176, Peoples R China
关键词
Porcine circovirus 3; Cap gene; TaqMan probe; Real-time PCR; DISEASE; CHINA; PIGS;
D O I
10.1016/j.jviromet.2017.07.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Porcine circovirus 3 (PCV3) is a novel circovirus that was associated with porcine dermatitis and nephropathy syndrome, reproductive failure, and multisystemic inflammation. The objective of this study was to develop a rapid, simple, specific and sensitive TaqMan-based real-time PCR assay for PCV3 detection. Specific primers and probe were designed for the cap gene of PCV3 within the conserved region of viral genome. The assay was highly specific for PCV3, without cross-reactions with other non-targeted pig viruses. The detection limit of this assay was 102 copies. The assay had an efficiency of 95.7%, a regression squared value (R-2) of 0.994 and showed a linear range of 10(2)-10(7) copies PCV3 DNA per reaction. The assay was also very reproducible, with the infra- and inter-assay coefficient of variation less than 2.0%. For the 112 archived clinical samples collected from 2014 to March 2017, the PCV3 positive ratio was 12.5% (14/112) with the real-time PCR. The presence of the PCV3 dated back to at least 2014 in China and samples collected in 2017 had the highest PCV3 positive ratio (46.7%, 7/15). The real-time PCR assay could be used for detection of PCV3 in epidemiological and pathogenesis studies.
引用
收藏
页码:177 / 180
页数:4
相关论文
共 18 条
[1]   Isolation of porcine circovirus-like viruses from pigs with a wasting disease in the USA and Europe [J].
Allan, GM ;
McNeilly, F ;
Kennedy, S ;
Daft, B ;
Clarke, EG ;
Ellis, JA ;
Haines, DM ;
Meehan, BM ;
Adair, BM .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 1998, 10 (01) :3-10
[2]   Quantitation of porcine circovirus type 2 isolated from serum/plasma and tissue samples of healthy pigs and pigs with postweaning multisystemic wasting syndrome using a TaqMan-based real-time PCR [J].
Brunborg, IM ;
Moldal, T ;
Jonassen, CM .
JOURNAL OF VIROLOGICAL METHODS, 2004, 122 (02) :171-178
[3]   Identification and genetic characterization of porcine circovirus type 3 in China [J].
Ku, X. ;
Chen, F. ;
Li, P. ;
Wang, Y. ;
Yu, X. ;
Fan, S. ;
Qian, P. ;
Wu, M. ;
He, Q. .
TRANSBOUNDARY AND EMERGING DISEASES, 2017, 64 (03) :703-708
[4]   Differentiation of PCV1 and PCV2 by a multiplex real-time PCR assay [J].
Li, J. ;
Shi, J-l. ;
Wu, X-y. ;
Cong, X-y. ;
Xu, S-j. ;
Yuan, X-y. ;
Wu, J-q. ;
Sun, W-b. ;
Du, Y-j. ;
Peng, Z. ;
Wang, J-b. ;
Huang, B-h. .
VETERINARY RECORD, 2013, 173 (14) :346-+
[5]   Prevalence and genetic variation of porcine circovirus type 2 in Hebei, China from 2004 to 2014 [J].
Li, Limin ;
Yuan, Wanzhe ;
Guo, Haiyong ;
Ma, Zengjun ;
Song, Qinye ;
Wang, Xiaobo ;
Li, Hongyuan .
GENE, 2016, 586 (02) :222-227
[6]   Real-time PCR in virology [J].
Mackay, IM ;
Arden, KE ;
Nitsche, A .
NUCLEIC ACIDS RESEARCH, 2002, 30 (06) :1292-1305
[7]   Molecular biology of Porcine circovirus:: analyses of gene expression and viral replication [J].
Mankertz, A ;
Çaliskan, R ;
Hattermann, K ;
Hillenbrand, B ;
Kurzendoerfer, P ;
Mueller, B ;
Schmitt, C ;
Steinfeldt, T ;
Finsterbusch, T .
VETERINARY MICROBIOLOGY, 2004, 98 (02) :81-88
[8]   Porcine circovirus type 2-associated disease: Update on current terminology, clinical manifestations, pathogenesis, diagnosis, and intervention strategies [J].
Opriessnig, Tanja ;
Meng, Xiang-Jin ;
Halbur, Patrick G. .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2007, 19 (06) :591-615
[9]  
Palinski R, 2017, J VIROL, V91, DOI [10.1128/JVI.01879-16, 10.1128/jvi.01879-16]
[10]  
Shen H., 2017, TRANSBOUND EMERG DIS