摘要
目的 表达P[9]轮状病毒(rotaviruses,RV)GST-VP8*蛋白,研究其与组织血型抗原(histo-blood group antigen,HBGA)受体的结合方式。了解广东省汕尾市人群P[9]RV特异性抗体水平,并分析其与HBGA受体的相关性。方法 构建pGEX-4T-1- VP8*重组质粒,利用原核表达系统表达纯化VP8*蛋白,目的蛋白经Western bolt确定其特异性,采用酶联免疫吸附试验检测GST-VP8*蛋白与唾液HBGA受体结合方式。利用VP8*蛋白检测广东省汕尾市人群P[9]RV抗体,并检测该人群HBGA受体表型,分析P[9]RV抗体与HBGA的相关性。结果 成功表达了P[9]RV VP8*蛋白,并发现其与A型分泌型HBGA受体特异结合,不结合B、O型分泌型及非分泌型HBGA受体。A型、Le b+/Le y+和分泌型HBGA个体配对的血清中P[9]RV特异性IgG阳性率明显较高。结论 P[9]RV识别A型分泌型HBGA受体,这将有助于理解RV的流行病学,为RV进一步防控提供试验依据。
We express the GST-VP8* proteins of P[9] rotavirus and explore its binding pattern with HBGA receptor. We detect P[9] rotavirus antibody in Shanwei area of Guangdong, and analyze the association of positive antibody rate with HBGA receptor. The recombinant plasmid pGEX-4T-1- VP8* was conducted and expressed. The binding pattern of P[9] RV GST-VP8* proteins and HBGA receptor were identified by enzyme-linked immunosorbent assay(ELISA). The HBGA phenotypes of the individuals in Shanwei of Guangdong were determined in Saliva samples. P[9] RV IgG antibodies in sera was measured by ELISA using P[9]VP8* proteins as capture antigens to analysis the correlation between P[9] RV IgG and HBGA. In this study,[9] RV VP8* proteins were successfully expressed. P[9] RV VP8* proteins bind to type A secretor, but not to B、O secretor or all nonsecretor. The correlation between positive rate of P[9] specific IgG in serum and host Lewis and secretor phenotypes has been found among 206 studied serum samples, which would help further understanding of rotavirus epidemiology and provides a scientific basis to prevent and control rotavirus.
作者
侯玉珍
龙艳
郭伦爱
陈俊锐
张绪富
戴迎春
HOU Yu-zhen;LONG Yan;GUO Lun-ai;CHEN Jun-rui;ZHANG Xu-fu;DAI Ying-chun(Department of Epidemiology,School of Public Health, Southern Medical University,Guangzhou 510515,China;School of Traditional Chinese Medicine, Southern Medical University,Guangzhou, Guangdong 510515,China)
出处
《中国人兽共患病学报》
CAS
CSCD
北大核心
2019年第8期688-693,共6页
Chinese Journal of Zoonoses
基金
国家自然科学基金面上项目(No.31771007,No.81773975和No.81473402)
广州市科技计划项目产学研协同创新重大专项民生科技研究专题(No.201604020111)联合资助~~