Development and application of an indirect ELISA for detection of antibodies against avian hepatitis E virus

► We develop an iELISA to detect reactive antibodies against avian HEV genotype 3. ► The iELISA method had an agreement rate of 97% with Western blot analysis. ► Seropositivity of avian HEV genotype 3 is not age dependent. ► Antibodies titers peak is detected in 20–29 weeks old chickens. An indirect...

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Veröffentlicht in:Journal of virological methods 2013-01, Vol.187 (1), p.32-36
Hauptverfasser: Zhao, Qin, Sun, Yani, Zhao, Jinan, Hu, Shoubin, Zhao, Feifei, Chen, Fuyong, Clavijo, Alfonso, Zhou, En-Min, Xiao, Yihong
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Sprache:eng
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Zusammenfassung:► We develop an iELISA to detect reactive antibodies against avian HEV genotype 3. ► The iELISA method had an agreement rate of 97% with Western blot analysis. ► Seropositivity of avian HEV genotype 3 is not age dependent. ► Antibodies titers peak is detected in 20–29 weeks old chickens. An indirect enzyme-linked immunosorbent assay (iELISA) that could detect immunoglobulin G antibodies against avian hepatitis E virus (HEV) was developed. This assay employs a truncated C-terminal 268-amino acid recombinant ORF2 protein from an avian HEV genotype 3 strain isolated in China (CaHEV) as the coating antigen. The antigen concentration and serum dilution were optimized using a checkerboard titration. A cut-off value of 0.368 at OD450nm was determined by testing 120 positive and 200 negative chicken sera for avian HEV antibodies using the two-graph receiver operating characteristic (TG-ROC) analysis. This iELISA has a sensitivity of 96.1% and a specificity of 95.8%. The overall agreement between the iELISA and a corresponding Western blot was 97%. The iELISA was used to evaluate the seroprevalence of avian HEV in poultry farms in the Shandong province. The avian HEV seropositive rate of 35.9% was determined by testing 1871 serum samples that were collected from 10 chicken flocks ranged from 10 to 60 weeks of age. The iELISA that was developed in this study can be used for detection of immunoglobulin G antibodies against avian HEV.
ISSN:0166-0934
1879-0984
DOI:10.1016/j.jviromet.2012.08.026