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Development of a World Health Organization International Reference Panel for different genotypes of hepatitis E virus for nucleic acid amplification testing.

Authors :
Baylis, Sally A.
Hanschmann, Kay-Martin O.
Matsubayashi, Keiji
Sakata, Hidekatsu
Roque-Afonso, Anne-Marie
Kaiser, Marco
Corman, Victor M.
Kamili, Saleem
Aggarwal, Rakesh
Trehanpati, Nirupma
Gärtner, Thomas
Thomson, Emma C.
Davis, Christopher A.
da Silva Filipe, Ana
Abdelrahman, Tamer T.
Blümel, Johannes
Terao, Eriko
Source :
Journal of Clinical Virology. Oct2019, Vol. 119, p60-67. 8p.
Publication Year :
2019

Abstract

• Hepatitis E virus (HEV) is the most common cause of acute hepatitis worldwide. • Nucleic acid testing (NAT) is important for the confirmation of acute hepatitis E infection • A World Health Organization International Reference Panel (IRP) for HEV genotypes NAT has been established. • The IRP contains all four major genotypes of HEV that infect humans, including clinically important sub-genotypes. • The IRP is an important resource for HEV NAT assay validation. Globally, hepatitis E virus (HEV) is a major cause of acute viral hepatitis. Epidemiology and clinical presentation of hepatitis E vary greatly by location and are affected by the HEV genotype. Nucleic acid amplification technique (NAT)-based assays are important for the detection of acute HEV infection as well for monitoring chronic cases of hepatitis E. The aim of the study was to evaluate a panel of samples containing different genotypes of HEV for use in nucleic NAT-based assays. The panel of samples comprises eleven different members including HEV genotype 1a (2 strains), 1e, 2a, 3b, 3c, 3e, 3f, 4c, 4g as well as a human isolate related to rabbit HEV. Each laboratory assayed the panel members directly against the 1st World Health Organization (WHO) International Standard (IS) for HEV RNA (6329/10) which is based upon a genotype 3 a strain. The samples for evaluation were distributed to 24 laboratories from 14 different countries and assayed on three separate days. Of these, 23 participating laboratories returned a total of 32 sets of data; 17 from quantitative assays and 15 from qualitative assays. The assays used consisted of a mixture of in-house developed and commercially available assays. The results showed that all samples were detected consistently by the majority of participants, although in some cases, some samples were detected less efficiently. Based on the results of the collaborative study the panel (code number 8578/13) was established as the "1st International Reference Panel (IRP) for all HEV genotypes for NAT-based assays" by the WHO Expert Committee on Biological Standardization. This IRP will be important for assay validation and ensuring adequate detection of different genotypes and clinically important sub-genotypes of HEV. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13866532
Volume :
119
Database :
Academic Search Index
Journal :
Journal of Clinical Virology
Publication Type :
Academic Journal
Accession number :
138547831
Full Text :
https://doi.org/10.1016/j.jcv.2019.05.006