Literature DB >> 17658704

Evaluation of a multiplex real-time RT-PCR for quantitative and differential detection of wild-type viruses and C-strain vaccine of Classical swine fever virus.

Jian-Jun Zhao1, Dan Cheng, Na Li, Yuan Sun, Zixue Shi, Qing-Hu Zhu, Changchun Tu, Guang-Zhi Tong, Hua-Ji Qiu.   

Abstract

Classical swine fever virus (CSFV) is the causative agent of classical swine fever (CSF), one of OIE listed diseases. Most of the currently available detection methods do not allow discrimination between wild-type CSF viruses and the vaccine strains. This study was designed to develop a multiplex real-time RT-PCR for the quantitative and differential detection of wild-type viruses and C-strain vaccine widely used in China. CSFV specific primers and two differently labeled TaqMan probes for the differentiation of wild-type viruses from C-strain vaccine were designed in the 5'-untranslated region of the viral genome of CSFV. The two TaqMan probes specifically hybridize wild-type viruses of different subgroups and C-strain vaccine, respectively, in the multiplex real-time RT-PCR, with no cross-reaction to a number of non-CSFV porcine viruses. The sensitivity of the assay for detecting wild-type and C-strain-type vaccine viruses was determined to be 41.8 and 81.5copies/microL viral RNA, respectively. Completely correct differentiation of wild-type viruses from C-strain vaccine was achieved when testing reference strains and characterized field isolates of CSFV in China. The multiplex real-time RT-PCR was able to detect the viral RNA in the whole blood samples of experimentally infected pigs as early as 2 days post-infection, 3 to 4 days prior to the onset of clinical signs in co-housed pigs. The agreements between the multiplex real-time RT-PCR and a multiplex RT-nested PCR for detection of wild-type and C-strain-type viruses were 96.9% and 100%, respectively, when detecting 106 different field samples. There is a positive correlation between the titers of C-strain vaccines titrated in rabbits and RNA copies quantitated by the multiplex real-time RT-PCR. The novel assay described here is rapid and sensitive, and is useful for differentiating field strains and C-strain of CSFV in China.

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Year:  2007        PMID: 17658704     DOI: 10.1016/j.vetmic.2007.04.046

Source DB:  PubMed          Journal:  Vet Microbiol        ISSN: 0378-1135            Impact factor:   3.293


  26 in total

1.  Generation and Efficacy Evaluation of a Recombinant Pseudorabies Virus Variant Expressing the E2 Protein of Classical Swine Fever Virus in Pigs.

Authors:  Yimin Wang; Jin Yuan; Xin Cong; Hua-Yang Qin; Chun-Hua Wang; Yongfeng Li; Su Li; Yuzi Luo; Yuan Sun; Hua-Ji Qiu
Journal:  Clin Vaccine Immunol       Date:  2015-08-26

2.  Thioredoxin 2 Is a Novel E2-Interacting Protein That Inhibits the Replication of Classical Swine Fever Virus.

Authors:  Su Li; Jinghan Wang; Wen-Rui He; Shuo Feng; Yongfeng Li; Xiao Wang; Yajin Liao; Hua-Yang Qin; Lian-Feng Li; Hong Dong; Yuan Sun; Yuzi Luo; Hua-Ji Qiu
Journal:  J Virol       Date:  2015-06-03       Impact factor: 5.103

3.  Co-expression of the C-terminal domain of Yersinia enterocolitica invasin enhances the efficacy of classical swine-fever-vectored vaccine based on human adenovirus.

Authors:  Helin Li; Pengbo Ning; Zhi Lin; Wulong Liang; Kai Kang; Lei He; Yanming Zhang
Journal:  J Biosci       Date:  2015-03       Impact factor: 1.826

4.  Genetic characterization of E2 gene of classical swine fever virus by restriction fragment length polymorphism and phylogenetic analysis.

Authors:  Ning Chen; Dejiang Li; Xuemei Yuan; Xiaoliang Li; Hongxia Hu; Binglin Zhu; Xiaoyuan Wan; Weihuan Fang
Journal:  Virus Genes       Date:  2010-03-09       Impact factor: 2.332

5.  A one-step real-time reverse transcription-polymerase chain reaction detection of classical swine fever virus using a minor groove binding probe.

Authors:  Guoyuan Wen; Jun Yang; Qingping Luo; Zhibin Hu; Nianhua Song; Rongrong Zhang; Hongling Wang; Diyun Ai; Ling Luo; Huabin Shao
Journal:  Vet Res Commun       Date:  2010-04-22       Impact factor: 2.459

6.  Poly(C)-binding protein 1, a novel N(pro)-interacting protein involved in classical swine fever virus growth.

Authors:  Dan Li; Su Li; Yuan Sun; Hong Dong; Yongfeng Li; Bibo Zhao; Dongwei Guo; Changjiang Weng; Hua-Ji Qiu
Journal:  J Virol       Date:  2012-12-05       Impact factor: 5.103

7.  Hemoglobin subunit beta interacts with the capsid protein and antagonizes the growth of classical swine fever virus.

Authors:  Dan Li; Hong Dong; Su Li; Muhammad Munir; Jianing Chen; Yuzi Luo; Yuan Sun; Lihong Liu; Hua-Ji Qiu
Journal:  J Virol       Date:  2013-03-13       Impact factor: 5.103

8.  Improved strategy for phylogenetic analysis of classical swine fever virus based on full-length E2 encoding sequences.

Authors:  Alexander Postel; Stefanie Schmeiser; Jennifer Bernau; Alexandra Meindl-Boehmer; Gediminas Pridotkas; Zuzana Dirbakova; Miroslav Mojzis; Paul Becher
Journal:  Vet Res       Date:  2012-06-07       Impact factor: 3.683

9.  Clustering of classical swine fever virus isolates by codon pair bias.

Authors:  Immanuel Leifer; Dirk Hoeper; Sandra Blome; Martin Beer; Nicolas Ruggli
Journal:  BMC Res Notes       Date:  2011-11-29

10.  Experimental infection of Bama miniature pigs with a highly virulent classical swine fever virus.

Authors:  Yuan Sun; Qian Jiang; Da-Yong Tian; Huan Lin; Hong Li; Qiu-Ying Han; Wen Han; Chang-De Si; Shou-Ping Hu; Zhuo Zhang; Lian-Dong Qu; Hua-Ji Qiu
Journal:  Virol J       Date:  2011-09-25       Impact factor: 4.099

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