{"title":"甲型病毒复制子颗粒表达抗原接种猪后对猪瘟病毒(CSFV)特异性IgA、IgG和IgM抗体反应的评价","authors":"M. M. Hossain, Raymond Rr Rowl","doi":"10.4172/2379-1764.1000213","DOIUrl":null,"url":null,"abstract":"Classical swine fever virus (CSFV) E2 glycoprotein was expressed in an alphavirus based replicon particles (RP) expression system. A fluorescent microsphere immunoassay (FMIA) has been developed for the detection of CSFV E2-specific antibody in swine vaccinated with alphavirus RP. CSFV full length E2 (aa 1-376) was fragmented into several pieces and recombinant proteins were expressed in Escherichia coli. Purified proteins were conjugated to microsphere beads, the target antigens were assembled into a single multiplex, and tested against sera vaccinated with alphavirus-expressed antigens. The results reported as mean fluorescence intensity (MFI) obtained from the median value for at least 100 microspheres and the MFI values converted to positive per sample (S/P) ratio. Of the eight recombinant E2 proteins evaluated in this study, the highest MFI values were obtained for E2 (aa 1-181). CSFV E2 glycoprotein was expressed in alphavirus based replicon expression system. The results show that vaccinated animals had CSFV-specific IgA, IgG and IgM in serum and oral fluids. The MFI values for the negative serum sample showed 20-70-fold reduction compared to positive serum sample. Antibody response to CSFV antigens were IgG>IgM>IgA. The results demonstrated that the simultaneous detection of IgG, IgM and IgA antibodies could provide an improved diagnostic tool.","PeriodicalId":7277,"journal":{"name":"Advanced techniques in biology & medicine","volume":"10 1","pages":"1-6"},"PeriodicalIF":0.0000,"publicationDate":"2017-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Evaluation of Classical Swine Fever Virus (CSFV)-Specific IgA, IgG, and IgM Antibody response in Swine Vaccinated with Alphavirus Replicon Particles-Expressed Antigens\",\"authors\":\"M. M. Hossain, Raymond Rr Rowl\",\"doi\":\"10.4172/2379-1764.1000213\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Classical swine fever virus (CSFV) E2 glycoprotein was expressed in an alphavirus based replicon particles (RP) expression system. A fluorescent microsphere immunoassay (FMIA) has been developed for the detection of CSFV E2-specific antibody in swine vaccinated with alphavirus RP. CSFV full length E2 (aa 1-376) was fragmented into several pieces and recombinant proteins were expressed in Escherichia coli. Purified proteins were conjugated to microsphere beads, the target antigens were assembled into a single multiplex, and tested against sera vaccinated with alphavirus-expressed antigens. The results reported as mean fluorescence intensity (MFI) obtained from the median value for at least 100 microspheres and the MFI values converted to positive per sample (S/P) ratio. Of the eight recombinant E2 proteins evaluated in this study, the highest MFI values were obtained for E2 (aa 1-181). CSFV E2 glycoprotein was expressed in alphavirus based replicon expression system. The results show that vaccinated animals had CSFV-specific IgA, IgG and IgM in serum and oral fluids. The MFI values for the negative serum sample showed 20-70-fold reduction compared to positive serum sample. Antibody response to CSFV antigens were IgG>IgM>IgA. The results demonstrated that the simultaneous detection of IgG, IgM and IgA antibodies could provide an improved diagnostic tool.\",\"PeriodicalId\":7277,\"journal\":{\"name\":\"Advanced techniques in biology & medicine\",\"volume\":\"10 1\",\"pages\":\"1-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced techniques in biology & medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2379-1764.1000213\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced techniques in biology & medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2379-1764.1000213","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Evaluation of Classical Swine Fever Virus (CSFV)-Specific IgA, IgG, and IgM Antibody response in Swine Vaccinated with Alphavirus Replicon Particles-Expressed Antigens
Classical swine fever virus (CSFV) E2 glycoprotein was expressed in an alphavirus based replicon particles (RP) expression system. A fluorescent microsphere immunoassay (FMIA) has been developed for the detection of CSFV E2-specific antibody in swine vaccinated with alphavirus RP. CSFV full length E2 (aa 1-376) was fragmented into several pieces and recombinant proteins were expressed in Escherichia coli. Purified proteins were conjugated to microsphere beads, the target antigens were assembled into a single multiplex, and tested against sera vaccinated with alphavirus-expressed antigens. The results reported as mean fluorescence intensity (MFI) obtained from the median value for at least 100 microspheres and the MFI values converted to positive per sample (S/P) ratio. Of the eight recombinant E2 proteins evaluated in this study, the highest MFI values were obtained for E2 (aa 1-181). CSFV E2 glycoprotein was expressed in alphavirus based replicon expression system. The results show that vaccinated animals had CSFV-specific IgA, IgG and IgM in serum and oral fluids. The MFI values for the negative serum sample showed 20-70-fold reduction compared to positive serum sample. Antibody response to CSFV antigens were IgG>IgM>IgA. The results demonstrated that the simultaneous detection of IgG, IgM and IgA antibodies could provide an improved diagnostic tool.