Two nanobody-based immunoassays to differentiate antibodies against genotype 1 and 2 porcine reproductive and respiratory syndrome virus

Xu Chen1, Yueting Chang1, Lu Zhang1, Xinyu Zhao1, Zhihan Li1, Zhijie Zhang1, Pinpin Ji1, Qingyuan Liu1, Jiakai Zhao1, Jiahong Zhu1, Baoyuan Liu1, Xinjie Wang2, Yani Sun1(), Qin Zhao1()()

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Animal Disease ›› 2024, Vol. 4 ›› Issue (1) : 9. DOI: 10.1186/s44149-024-00114-1

Two nanobody-based immunoassays to differentiate antibodies against genotype 1 and 2 porcine reproductive and respiratory syndrome virus

  • Xu Chen1, Yueting Chang1, Lu Zhang1, Xinyu Zhao1, Zhihan Li1, Zhijie Zhang1, Pinpin Ji1, Qingyuan Liu1, Jiakai Zhao1, Jiahong Zhu1, Baoyuan Liu1, Xinjie Wang2, Yani Sun1(), Qin Zhao1()()
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Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) infection causes significant economic loss to the global pig industry. Genotype 1 and 2 PRRSV (PRRSV-1 and -2) infections have been reported in China, Europe and America. For accurate prevention, nanobodies were first used as diagnostic reagents for PRRSV typing. In this study three nanobodies targeting both PRRSV-1 and -2, two targeting PRRSV-1 and three targeting PRRSV-2, were screened and produced. To develop two competitive ELISAs (cELISAs), the g1-2-PRRSV-Nb3-HRP nanobody was chosen for the g1-2-cELISA, to detect common antibodies against PRRSV-1 and -2, and the g1-PRRSV-Nb136-HRP nanobody was chosen for the g1-cELISA, to detect anti-PRRSV-1 antibodies. The two cELISAs were developed using PRRSV-1-N protein as coating antigen, and the amounts for both were 100 ng/well. The optimized dilution of testing pig sera was 1:20, the optimized reaction times were 30 min, and the colorimetric reaction times were 15 min. Then, the cut-off values of the g1-2-cELISA and g1-cELISA were 26.6% and 35.6%, respectively. Both of them have high sensitivity, strong specificity, good repeatability, and stability. In addition, for the 1534 clinical pig sera, an agreement rate of 99.02% (Kappa values=0.97) was determined between the g1-2-cELISA and the commercial IDEXX ELISA kit. For the g1-cELSIA, it can specifically detect anti-PRRSV-1 antibodies in the clinical pig sera. Importantly, combining two nanobody-based cELISAs can differentially detect antibodies against PRRSV-1 and -2.

Keywords

PRRSV / Competitive ELISA / Nanobody / Antigen epitope

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Xu Chen, Yueting Chang, Lu Zhang, Xinyu Zhao, Zhihan Li, Zhijie Zhang, Pinpin Ji, Qingyuan Liu, Jiakai Zhao, Jiahong Zhu, Baoyuan Liu, Xinjie Wang, Yani Sun, Qin Zhao. Two nanobody-based immunoassays to differentiate antibodies against genotype 1 and 2 porcine reproductive and respiratory syndrome virus. Animal Disease, 2024, 4(1): 9 https://doi.org/10.1186/s44149-024-00114-1

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Funding
Natural Science Foundation for Young Scientists of Shanxi Province(2022JC-12); Key Technologies Research and Development Program of Guangzhou Municipality(2023YFD1800304); Innovative Research Group Project of the National Natural Science Foundation of China(32273041)
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