| Literature DB >> 26005003 |
Yuzi Luo1, Lin Li1, Sophia Austermann-Busch2, Mei Dong3, Jingjing Xu1, Lina Shao1, Jianlin Lei1, Na Li3, Wen-Rui He1, Bibo Zhao1, Su Li1, Yongfeng Li1, Lihong Liu4, Paul Becher2, Yuan Sun5, Hua-Ji Qiu6.
Abstract
Classical swine fever (CSF), caused by classical swine fever virus (CSFV), is a devastating disease of swine worldwide. Although a mandatory vaccination with the modified live vaccine C-strain has been implemented in China for decades, CSF remains a serious threat to the swine industry. To facilitate the control and eradication of CSF in China, the E2-based marker vaccine rAdV-SFV-E2, an adenovirus-delivered, alphavirus replicon-vectored vaccine, has been developed. Accordingly, an accompanying discriminatory test that allows differentiating infected from vaccinated animals (DIVA) is required. Here, the enhanced expression of E(rns) protein of CSFV was achieved in the methyltropic yeast Pichia pastoris by codon-optimization of the E(rns) gene, and an indirect enzyme-linked immunosorbent assay (iELISA) based on the yeast-expressed E(rns) (yE(rns)) was developed and evaluated. The optimized iELISA was able to detect CSFV-specific antibodies in the serum samples from the CSFV-infected pigs as early as 6 days post-infection, and discriminate the CSFV-infected pigs from those vaccinated with rAdV-SFV-E2. The iELISA was evaluated using a panel of swine sera, and showed comparable sensitivity (94.6%) and specificity (97.1%), and the consistence rates with the virus neutralization test were 96.8% for CSFV-infected swine sera, 83.3% for C-strain-vaccinated swine sera, and 95.0% for field swine sera. In addition, the iELISA showed higher sensitivity (90.4%) compared with PrioCHECK CSFV E(rns) (59.6%). Taken together, the yE(rns)-based iELISA is specific and sensitive, representing a promising DIVA test for E2-based marker vaccines against CSF.Entities:
Keywords: Classical swine fever virus; Differentiation of infected from vaccinated animals (DIVA); E(rns) protein; Indirect enzyme-linked immunosorbent assay; Yeast expression
Mesh:
Substances:
Year: 2015 PMID: 26005003 DOI: 10.1016/j.jviromet.2015.05.006
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014