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抗鹅星状病毒Cap蛋白单克隆抗体的制备及鉴定
引用本文:孙佳卉,刘志艺,黄聪,李传峰,刘光清,陈宗艳. 抗鹅星状病毒Cap蛋白单克隆抗体的制备及鉴定[J]. 中国动物传染病学报, 2021, 0(1): 58-63
作者姓名:孙佳卉  刘志艺  黄聪  李传峰  刘光清  陈宗艳
作者单位:中国农业科学院上海兽医研究所
基金项目:上海市自然科学基金(19ZR146880);国家自然科学基金-新疆联合基金(U1703177);上海市科委科技创新(13391901602)。
摘    要:自2016年以来,鹅星状病毒(GoAstV)已成为当前危害鹅养殖业生产的重要病原体之一,雏鹅均易感,主要引起9~19日龄雏鹅死亡,以雏鹅腿关节肿胀及肾脏尿酸盐沉积导致肾炎为主要病征.建立相应的病原学与血清学检测方法对于防控该病至关重要.为建立基于病毒Cap蛋白的诊断技术,本研究构建了鹅星状病毒去核定位信号肽的Cap基因...

关 键 词:鹅星状病毒  Cap蛋白  原核表达  单克隆抗体

Preparation and Identification of Monoclonal Antibodies against Cap Protein for Goose Astrovirus
SUN Jiahui,LIU Zhiyi,HUANG Cong,LI Chuanfeng,LIU Guangqing,CHEN Zongyan. Preparation and Identification of Monoclonal Antibodies against Cap Protein for Goose Astrovirus[J]. Chinese Journal of Animal Infectious Diseases, 2021, 0(1): 58-63
Authors:SUN Jiahui  LIU Zhiyi  HUANG Cong  LI Chuanfeng  LIU Guangqing  CHEN Zongyan
Affiliation:(Shanghai Veterinary Research Institute,CAAS,Shanghai 200241,China)
Abstract:Goose astrovirus(GoAstV)has been one of the infectious agents for goslings since 2016.Goose astrovirus mainly infection causes illness,growth retardation and even deaths and characterized by uric acid salt deposits and gout in legs.The development of appropriate etiological and serological detection methods is essential to prevent and control the spread of the disease.In this study,the prokaryotic expression plasmid pET-30a-Cap containing Cap gene was constructed and transformed into BL21(DE3)for expression of the recombinant protein with IPTG induction.The expressed protein was examined in SDS-PAGE and Western blot.The results showed that the recombinant protein was mainly released into the culture supernatant and had a molecular mass of about 28 kDa as demonstrated in SDS-PAGE.The recombinant protein was then purified using His purification column.The purified protein was used to immunize BALB/cmice for preparation of monoclonal antibodies(mAbs).The immunized mice showed high ELISA titer(>51200)post-immunization and their spleen cells were fused with myeloma cells to get hybridomas.The hybridoma cells were cloned 3 times and 5 mAbs specific to Cap protein were obtained for further characterization.The isotyping of these mAbs revealed that 1A5G10,5B7G8 and 9C3E11 had the heavy chain type IgG1 and 1C11B11 and 9A12B12 had the heavy chain type IgG2b.All these MAbs had light chain typeκ.MAbs 5B7G8 reacted with GoAstV in Western blot and mAbs 1C11B11 and 9A12B12 reacted with GoAstV in both Western blot and immunofluorescence assay.The availability of these mAbs laid solid foundation for further development of diagnostic methods of GoAstV.
Keywords:Goose astrovirus  capsid protein  prokaryotic expression  monoclonal antibody
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