Hepatitis E virus neutralization by porcine serum antibodies

Author:

Gremmel Nele1ORCID,Keuling Oliver2,Eiden Martin3,Groschup Martin H.3ORCID,Johne Reimar4,Becher Paul1ORCID,Baechlein Christine1ORCID

Affiliation:

1. Department of Infectious Diseases, Institute of Virology, University of Veterinary Medicine , Hannover, Germany

2. Institute for Terrestrial and Aquatic Wildlife Research, University of Veterinary Medicine , Hannover, Germany

3. Institute of Novel and Emerging Infectious Diseases, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health , Greifswald, Insel Riems, Germany

4. Department of Biological Safety, German Federal Institute for Risk Assessment , Berlin, Germany

Abstract

ABSTRACT The consumption of raw or undercooked meat products poses a serious risk for human hepatitis E virus (HEV) infections. In many high-income countries, domestic pigs and wild boars represent the main animal reservoirs for HEV and are usually identified by reverse transcription-PCR and antibody enzyme-linked immunosorbent assay (ELISA). In order to characterize the humoral immune response in more detail, a cell culture-based serum neutralization assay using a culture-adapted HEV strain was established here. Measurement of neutralizing antibodies was only possible after removing the viral quasi-envelope by detergent treatment. Serum samples of 343 wild boars from Northern Germany were first analyzed for anti-HEV IgG using an in-house ELISA, resulting in 19% positive samples. Subsequently, a subset of 41 representative samples was tested with the neutralization assay, and the results correlated well with those obtained by ELISA. Not only the human HEV strain 47832c but also two porcine HEV strains were shown to be neutralized by porcine serum antibodies. Neutralizing activity was also found in samples containing both HEV-specific antibodies and HEV RNA. Testing of serum samples derived from two experimentally infected domestic pigs showed a steep increase in neutralizing activity at 24 or 51 days post infection, dependent on the used infectious dose. The developed assay can be useful for characterization of the humoral immune response after HEV infection and for assessing the efficiency of HEV vaccine candidates.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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