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Preparation of Monoclonal Antibody Against σC Protein of Novel duck reovirus and Its Antigenic Epitope Identification |
HUA Jiong-Gang, YE Wei-Cheng, NI Zheng, CHEN Liu, ZHU Yin-Chu, YUN Tao*, ZHANG Cun* |
Institute of Animal Husbandry and Veterinary Sciences, Zhejiang Academy of Agriculture Sciences, Hangzhou 310021, China |
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Abstract Novel duck reovirus (NDRV) is a new pathogen discovered in recent years, which can cause diseases in multiple species of ducks and geese and huge economic losses to the duck industry in China. σC protein is one of the outer capsid proteins of NDRV, which is able to induce type-specific antibodies against the virus and functions in the identification and attachment of the virus to the target cell, probably via a receptor-mediated event. For the preparation of monoclonal antibody (McAb) against protein σC of NDRV and identification of antigen epitope, SP2/0 myeloma cells were fused with spleen from BALB/c mice (Mus musculus) immunized with purified recombinant σC expressed in Escherichia coli. Four hybidoma cell lines (A5-A1, A5-B6, A9-D4 and B9-6) stably secreting McAbs against σC of NDRV were identified by indirect ELISA. Western blot results showed that all 4 McAbs could recognize whole virus of NDRV and recombinant σ C protein from prokaryotic expression. Indirect immunofluorescence assay (IFA) indicated that 4 McAbs reacted positively with NDRV, but did not show cross reaction with Classical duck reovirus (CDRV) and Avian reovirus (ARV). The antigenic epitopes recognized by 4 McAbs were identified by synthetic overlapping peptide library and a series of truncated peptides, and the results showed that the core antigenic epitope of 177PILSGPADA185 was recognized by 3 McAbs (A5-A1, A5-B6, and B9-6). The antigenic epitopes recognized by A9-D4 might be spatial conformational epitopes. Conservative analysis showed that the antigenic epitope was highly conservative in the NDRV isolates from different regions and different hosts. The results suggested that 177PILSGPADA185 was a type-specific linear B-cell epitope of NDRV. This study could provide a basis for further research on the structure of σC protein and the establishment of NDRV clinical detection methods.
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Received: 23 April 2021
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Corresponding Authors:
*yt-t@163.com; zhangcun@aliyun.com
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[1] 陈海鹏, 云涛, 张存, 等. 2014. 新型番鸭呼肠孤病毒σC蛋白的原核表达及其抗原特性[J]. 浙江农业学报, 26(6): 1448-1452.
(Chen H P, Yun T, Zhang C, et al.2014. Prokaryotic expression of the recombinant σC protein of new Muscovy duck reovirus and preliminary study of the antigen characteristic[J]. Acta Agriculturae Zhejiangensis, 26(6): 1448-1452.)
[2] 陈少莺, 陈仕龙, 林锋强, 等. 2012. 新型鸭呼肠孤病毒的分离与鉴定[J]. 病毒学报, 28(3): 224-230.
(Chen S Y, Chen S L, Lin F Q, et al.2012. The isolation and identification of Novel duck reovirus[J]. Chinese Journal of Virology, 28(3): 224-230)
[3] 陈仕龙, 陈少莺, 程晓霞, 等. 2011. 3中禽类呼肠孤病毒血清学相关性及致细胞病变差异分析[J]. 畜牧兽医学报, 42(4): 533-537.
(Chen S L, Chen S Y, Cheng X X, et al.2011. The comparison of serologic relativity and CPE type of 3 Avian reovirus strains induced different diseases[J]. Acta veterinaria et Zootechnica Sinica, 42(4): 533-537.
[4] 丁明洋, 毕庄莉, 朱英奇, 等. 2015. 新型鸭呼肠孤病毒TH11株在BHK21细胞系中的增殖特性[J]. 中国兽医科学, 45(09): 918-922.
(Ding M Y, Bi Z L, Zhu Y Q, et al.2015. Proliferation characteristics of Novel duck reovirus strain TH11 in BHK-21 cells[J]. Chinese Veterinary Science, 45(9): 918-922.)
[5] 海蒂Z, 主编, 周宗安, 主译. 1991. 单克隆抗体技术手册[M]. 南京: 南京大学出版社, pp. 48-63.
(Heddy Z.1991. The Handbook of Monoclonal Antibody[M]. Nanjing University Press, Nanjing, China, pp. 48-63.)
[6] 黄瑜, 傅光华, 施少华, 等. 2009. 新致病型鸭呼肠孤病毒的分离鉴定[J].中国兽医杂志, 12(45): 29-31.
(Huang Y, Fu G H, Shi S H, et al.2009. Isolation and identification of a new pathogenic duck reovirus[J]. Chinese Journal of Veterinary Medicine, 12(45): 29-31.)
[7] 陆新浩, 刘鸿, 陈秋英, 等. 2011. 一种番鸭“新肝病”在浙江的流行特点分析[J]. 中国家禽, 33(15): 49-50.
(Lu X H, Liu H, Chen Q Y, et al.2011. Analysis on the epidemic characteristics of a new liver disease of Muscovy duck in Zhejiang[J]. China Poultry, 33(15): 49-50.)
[8] 吕殿红, 张毓金, 黄忠, 等. 2000. 番鸭新病—“花肝病”的病原研究[J]. 中国家禽, 22(7): 41-42.
(Lv D H, Zhang Y J, Huang Z, et al.2000. Research on the mosaic liver disease in Muscovy duck[J]. China Poultry, 22(7): 41-42.)
[9] 王光锋, 王永坤, 王建业, 等. 2003. 一株鹅源呼肠孤病毒的分离与鉴定[J]. 中国家禽, 25(15): 8-10.
(Wang G F, Wang Y K, Wang J Y, et al.2003. The isolation and identification of a goose-origin reovirus[J]. China Poultry, 25(15): 8-10.)
[10] 吴宝成, 陈家祥, 姚金水. 2001. 番鸭呼肠孤病毒的分离与鉴定[J]. 福建农业大学学报, 30(2): 227-230.
(Wu B C, Chen J X, Yao J S, et al.2001. Isolation and identification of Muscovy duck reovirus[J]. Journal of Fujian Agricultural University, 30(2): 227-230)
[11] 席娜, 赵国辉, 孙恩成, 等. 2014. 蓝舌病病毒8型VP2蛋白单克隆抗体的制备及其抗原表位鉴定[J]. 中国预防兽医学报, 36(4): 318-322.
(Xi N, Zhao G H, Sun E C, et al.2017. Proparation of the monoclonal antibodies against VP2 protein of Bluetongue virus serotype 8 and the VP2 B-cell epitope identification[J]. Chinese Journal of Preventive Veterinary Medicine, 36(4): 318-322.)
[12] 云涛, 张存, 华炯钢, 等. 2016. 鸭呼肠孤病毒基因Ⅰ型与Ⅱ型鉴别诊断RT-PCR方法的建立与应用[J]. 农业生物技术学报, 24(12): 1964-1972.
(Yun T, Zhang C, Hua J G, et al.2016. Establishment of differential diagnostic method with RT-PCR for duck reovirus genotypeⅠandⅡ[J]. Journal of Agricultural Biotechnology, 24(12): 1964-1972).
[13] Calvo P G, Fox G C, Parrado X L H, et al.2005. Structure of the carboxy-terminal receptor-binding domain of Avian reovirus fibre sigma C[J]. Journal of Molecular Biology, 354(1): 137-149.
[14] Li N, Hong T, Wang Y, et al.2016. The pathogenicity of Novel duck reovirus in Cherry Valley ducks[J]. Veterinary microbiology, 192: 181-185.
[15] Liu H J, Giambrone J J.1997. Amplification, cloning and sequencing of the σC-encoded gene of Avian reovirus[J]. Journal of Virological Methods, 63(1-2): 203-208.
[16] Liu H J, Lee L H, Hsu H W, et al.2003. Molecular evolution of Avian reovirus: Evidence for genetic diversity and reassortment of the S-class genome segments and multiple cocirculating lineages[J]. Virology, 314(1): 336-349.
[17] Liu Q, Zhang G, Huang Y, et al.2011. Isolation and characterization of a reovirus causing spleen necrosis in Pekin ducklings[J]. Veterinary microbiology, 148(2-4): 200-206.
[18] Ma G, Wang D, Shi J, et al.2012. Complete genomic sequence of a reovirus isolate from Pekin ducklings in China[J]. Journal of Virology, 86(23): 13137.
[19] Martínez-Costas J, Grande A, Varela R, et al.1997. Protein architecture of Avian reovirus S1133 and identification of the cell attachment protein[J]. Journal of Virology, 71(1): 59-64.
[20] Shapouri M R S, Marième Kane, Letarte M, et al.1995, Cloning, sequencing and expression of the S1 gene of Avian reovirus[J]. Journal of General Virology, 76(6): 1515-1520.
[21] Shih W L, Hsu H W, Liao M H, et al.2004. Avian reovirus sigmaC protein induces apoptosis in cultured cells[J]. Virology, 321(1): 65-74.
[22] Wang D, Shi J J, Yuan Y, et al.2013. Complete sequence of a reovirus associated with necrotic focus formation in the liver and spleen of Muscovy ducklings[J]. Veterinary Microbiology, 166(1-2): 109-122.
[23] Yun T, Chen H P, Hua J G, et al.2015. Molecular characterization of the σC-encoding gene from novel duck reovirus[J]. Journal of Animal & Plant Sciences, 25(3 Suppl. 1): 33-41.
[24] Yun T, Chen H P, Yu B, et al.2015. Development and application of an indirect ELISA for the detection of antibodies to novel duck reovirus[J]. Journal Virological Methods, 220: 55-59.
[25] Yun T, Ye W C, Ni Z, et al.2012. Complete genomic sequence of goose-origin reovirus from China[J]. Journal of Virology, 86(23): 10257.
[26] Yun T, Yu B, Ni Z, et al.2014. Genomic characteristics of a novel reovirus from Muscovy duckling in China[J]. Veterinary Microbiology, 168(1-2): 261-271.
[27] Yun T, Yu B, Ye W C, et al.2013. Isolation and genomic characterization of a classical Muscovy duck reovirus isolated in Zhejiang, China[J]. Infection, Genetics and Evolution, 20: 444-453.
[28] Zheng X, Wang D, Ning K, et al.2016. A duck reovirus variant with a unique deletion in the sigma C gene exhibiting high pathogenicity in Pekin ducklings[J]. Virus Research, 215: 37-41. |
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