Literature DB >> 31694975

Establishment of a Highly Sensitive Assay for Detection of Hepatitis E Virus-Specific Immunoglobulins.

Gérard Krause1,2,3, Claudia Sievers4, Katrin Bohm4, Julia Strömpl4, Andi Krumbholz5, Roland Zell6.   

Abstract

Hepatitis E, a liver disease caused by infection with the hepatitis E virus (HEV), is a worldwide emerging disease. The diagnosis is based on the detection of viral RNA and of HEV-specific immunoglobulins (Ig). For the latter, various assays are commercially available but still lack harmonization. In this study, a Luminex-based multiplex serological assay was established that measures the presence of total IgG, IgA, and IgM antibodies, targeting a short peptide derived from the viral E2 protein. For the validation, 160 serum samples with a known HEV serostatus were used to determine the assay cutoff and accuracy. Thereby, HEV IgG- and RNA-positive sera were identified with a sensitivity of 100% and a specificity of 98% (95% confidence interval [CI], 94% to 100%). Application of the assay by retesting 514 serum samples previously characterized with different HEV-IgG or total antibody tests revealed a high level of agreement between the assays (Cohen's kappa, 0.58 to 0.99). The established method is highly sensitive and specific and can be easily implemented in a multiplex format to facilitate rapid differential diagnostics with a few microliters of sample input.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  E2 antigen; S hepatitis E virus; anti-HEV immunoglobulins; antibody prevalence; multiplex assay

Mesh:

Substances:

Year:  2020        PMID: 31694975      PMCID: PMC6989076          DOI: 10.1128/JCM.01029-19

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  43 in total

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10.  Hepatitis E virus (HEV): molecular cloning and sequencing of the full-length viral genome.

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