Abstract
Objective To develop an antibody-array system for multiple detection of antibodies against Japanese B encephalitis virus (JEV),Tick-borne encephalitis virus (TBV),Dengue virus ( DENV ),West Nile virus (WNV),Western equine encephalitis virus (WEEV) and East Equine encephalitis virus (EEEV).Methods Recombined antigens were spotted on array as capture antigens.Specific antibodies were detected by using a sandwich ELISA format.Rabbit antiserum was employed to select and confirm the specificity of antigens and to optimize the conditions of the assay.The detection efficiency of the system was validated by 40 clinical suspected serum samples and compared with the relative ELISA assays.Results Eleven recombined antigens were selected as diagnostic antigens with high specificity.Better detection could be achieved when scale of antigen concentrations were within 0.125-0.900 mg/ml and the serum dilutions were 1:100-1:1000.When detecting the 26 clinical suspected TBE serum samples,20 were IgG positive (76.9%),and 17 were IgM positive (65.3%) which was 96.1% and 84.6% consistent with the relevant ELLSA tests,the 8 clinical suspected JEV serum samples,4 were IgG positive (50.0%),and 5 were IgM positive (62.0%),which was 86.3% and 90.1% consistent with the relevant ELLSA tests.As for the 22 DEN serum samples,13 were IgG positive (60%) and 15 were IgM positive (68%) which was 85% and 93% consistent with ELISA.The specificity of the assay was 100% and the sensitivity was higher than the relative ELISAs.Conclusion The developed antibody-array is highly specific and reliable,which could be used for the detection of antibodies against the 6 arboviruses. Key words: Arboviruses; Antibody-array; Detection
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