Comparison of DNA Enzyme Immunoassay and Line Probe Assays (Inno-LiPA HCV I and II) for Hepatitis C Virus Genotyping

Author:

Le Pogam S.1,Dubois F.12,Christen R.3,Raby C.1,Cavicchini A.4,Goudeau A.1

Affiliation:

1. Département de Microbiologie Médicale et Moléculaire, CNRS EP 117-CHU Bretonneau, 37044 Tours Cedex,1

2. Institut Régional pour la Santé, 37521 La Riche Cedex,2 and

3. Observatoire Océanologique-Station Zoologique, CNRS and UniversitéPierre et Marie Curie, 06230 Villefranche-sur-Mer Cedex,3 France, and

4. Diagnostics Division, SORIN Biomedica, 13040 Saluggia (VC), Italy4

Abstract

ABSTRACT Two methods for genotyping hepatitis C virus (DNA enzyme immunoassay [DEIA] and line probe assay [Inno-LiPA HCV I and II]) were compared on 120 samples and of these 87% were assigned to the same subtype by both assays. There were 15 subtyping discrepancies which involved 5% of type 1 isolates and 90% of type 2 isolates. Amplified products from the core and 5′ untranslated regions (UTR) were sequenced to resolve conflicts. Type 1 discordant samples had a guanosine at position −99 in the 5′ UTR, a characteristic of genotype 1b, and a core region typical of subtype 1a. The eight isolates classified as 2a/2c by LiPA and as subtype 2c by DEIA belonged to type 2.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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