An Expeditious Neutralization Assay for Porcine Reproductive and Respiratory Syndrome Virus Based on a Recombinant Virus Expressing Green Fluorescent Protein

被引:1
作者
Wang, Juan [1 ]
Yan, Jiecong [1 ]
Wang, Shuaiyong [1 ]
Chen, Ronglin [1 ]
Xing, Yanru [1 ]
Liu, Qingyan [1 ]
Gao, Shuolei [1 ]
Zhu, Yuxiang [1 ]
Li, Jiannan [1 ]
Zhou, Yanjun [1 ]
Shan, Tongling [1 ]
Tong, Wu [1 ]
Zheng, Hao [1 ]
Kong, Ning [1 ]
Jiang, Yifeng [1 ]
Liu, Changlong [1 ]
Tong, Guangzhi [1 ,2 ]
Yu, Hai [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, Shanghai Vet Res Inst, Shanghai 200241, Peoples R China
[2] Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou 225009, Peoples R China
关键词
PRRSV; infectious clones; reporter virus; enhanced GFP; neutralizing antibodies; neutralization assay; PASSIVE TRANSFER; PRRSV; IMMUNITY; ANTIBODIES; PIGS; PROTECTION; EFFICACY; STRAIN; DIFFER;
D O I
10.3390/cimb46020066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Due to the extensive genetic and antigenic variation in Porcine Reproductive and Respiratory Syndrome Virus (PRRSV), as well as its rapid mutability and evolution, PRRS prevention and control can be challenging. An expeditious and sensitive neutralization assay for PRRSV is presented to monitor neutralizing antibodies (NAbs) in serum during vaccine research. Here, a PRRSV expressing eGFP was successfully rescued with reverse genetics based on the infectious clone HuN4-F112-eGFP which we constructed. The fluorescent protein expressions of the reporter viruses remained stable for at least five passages. Based on this reporter virus, the neutralization assay can be easily used to evaluate the level of NAbs by counting cells with green fluorescence. Compared with the classical CPE assay, the newly developed assay increases sensitivity by one- to four-fold at the early antibody response stage, thus saving 2 days of assay waiting time. By using this assay to unveil the dynamics of neutralizing antibodies against PRRSV, priming immunity through either a single virulent challenge or only vaccination could produce limited NAbs, but re-infection with PRRSV would induce a faster and stronger NAb response. Overall, the novel HuN4-F112-eGFP-based neutralization assay holds the potential to provide a highly efficient platform for evaluating the next generation of PRRS vaccines.
引用
收藏
页码:1047 / 1063
页数:17
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