4.7 Article

Antigenic cross-reactivity among human, swine, rabbit and avian hepatitis E virus capsid proteins

期刊

VETERINARY MICROBIOLOGY
卷 265, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.vetmic.2022.109331

关键词

Hepatitis E virus; Capsid protein; Cross-reactivity; Antigenic relation; Common epitopes

资金

  1. National Natural Science Foundation of China [31972676]
  2. Key International Cooperative Research Project of National Natural Science Foundation of China [31720103919]

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This study analyzed the antigenic cross-reactivity among human, swine, rabbit, and avian hepatitis E virus (HEV) capsid proteins and found immunodominant epitopes in different species. These findings provide insights for the development of serological assays for diagnosing HEV infections in various animal species.
Hepatitis E virus (HEV), a zoonotic virus, infects many animal species, including humans. Capsid proteins of human, swine, rabbit and avian HEVs share 48 %-100 % amino acid identity. In the present study, antigenic cross-reactivity among human, swine, rabbit and avian HEV capsid proteins were analyzed in detail using indirect and blocking enzyme-linked immunosorbent assays (ELISAs). The C-terminal 268 amino acids of genotype 1 human, genotype 4 swine, genotype 3 rabbit and genotype B3 avian HEV capsid proteins served as coating antigens for ELISA. Hyperimmune rabbit antisera (against four HEV capsid proteins) and human, pig, rabbit and chicken clinical sera were as primary antibodies. Closely correlated and statistically indistinguishable results were obtained for detection of anti-HEV antibodies in human and pig sera using human, swine and rabbit HEV capsid proteins as coating antigens. Moderately correlated differences in detection of anti-HEV antibodies in rabbit sera were obtained using the three capsid proteins. Statistically significant differences with no correlations were obtained for anti-HEV antibodies detection in chicken sera between avian HEV capsid protein and human, swine and rabbit ones. Blocking ELISA results demonstrated that two common epitopes among the four species HEVs were immunodominant in avian HEV, but were non-immunodominant in human, swine and rabbit HEVs. Nevertheless, three epitopes common to human, swine and rabbit HEVs were all immunodominant epitopes for the three species HEVs. Collectively, these results demonstrate that anti-HEV antibodies in human and pig sera can be detected using human, swine and rabbit HEV capsid proteins. By contrast, for optimal detection of antiHEV antibodies in rabbit and chicken sera, the respective rabbit and avian HEV capsid proteins should be used. These results provide insights to guide future development of serological assays for diagnosing HEV infections in various animal species.

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