An analysis of the benefit of using HEV genotype 3 antigens in detecting anti-HEV IgG in a European population.

<h4>Background</h4>The benefit of using serological assays based on HEV genotype 3 in industrialised settings is unclear. We compared the performance of serological kits based on antigens from different HEV genotypes.<h4>Methods</h4>Taking 20 serum samples from patients in so...

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Autores principales: Annatina Schnegg, Philippe Bürgisser, Cyril André, Alain Kenfak-Foguena, Giorgia Canellini, Darius Moradpour, Florence Abravanel, Jacques Izopet, Matthias Cavassini, Katharine E A Darling
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spelling oai:doaj.org-article:1b1d81a8c78147b5ba703475c6b22b512021-11-18T07:46:37ZAn analysis of the benefit of using HEV genotype 3 antigens in detecting anti-HEV IgG in a European population.1932-620310.1371/journal.pone.0062980https://doaj.org/article/1b1d81a8c78147b5ba703475c6b22b512013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23667554/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>The benefit of using serological assays based on HEV genotype 3 in industrialised settings is unclear. We compared the performance of serological kits based on antigens from different HEV genotypes.<h4>Methods</h4>Taking 20 serum samples from patients in southwest France with acute HEV infection (positive PCR for HEV genotype 3) and 550 anonymised samples from blood donors in southwest Switzerland, we tested for anti-HEV IgG using three enzyme immunoassays (EIAs) (MP Diagnostics, Dia.Pro and Fortress) based on genotype 1 and 2 antigens, and one immunodot assay (Mikrogen Diagnostik recomLine HEV IgG/IgM) based on genotype 1 and 3 antigens.<h4>Results</h4>All acute HEV samples and 124/550 blood donor samples were positive with ≥1 assay. Of PCR-confirmed patient samples, 45%, 65%, 95% and 55% were positive with MP Diagnostics, Dia.Pro, Fortress and recomLine, respectively. Of blood donor samples positive with ≥1 assay, 120/124 (97%), were positive with Fortress, 19/124 (15%) were positive with all EIAs and 51/124 (41%) were positive with recomLine. Of 11/20 patient samples positive with recomLine, stronger reactivity for HEV genotype 3 was observed in 1/11(9%), and equal reactivity for both genotypes in 5/11 (45.5%).<h4>Conclusions</h4>Although recomLine contains HEV genotype 3, it has lower sensitivity than Fortress in acute HEV infection and fails to identify infection as being due to this genotype in approximately 45% of patients. In our single blood donor population, we observe wide variations in measured seroprevalence, from 4.2% to 21.8%, depending on the assay used.Annatina SchneggPhilippe BürgisserCyril AndréAlain Kenfak-FoguenaGiorgia CanelliniDarius MoradpourFlorence AbravanelJacques IzopetMatthias CavassiniKatharine E A DarlingPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 5, p e62980 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Annatina Schnegg
Philippe Bürgisser
Cyril André
Alain Kenfak-Foguena
Giorgia Canellini
Darius Moradpour
Florence Abravanel
Jacques Izopet
Matthias Cavassini
Katharine E A Darling
An analysis of the benefit of using HEV genotype 3 antigens in detecting anti-HEV IgG in a European population.
description <h4>Background</h4>The benefit of using serological assays based on HEV genotype 3 in industrialised settings is unclear. We compared the performance of serological kits based on antigens from different HEV genotypes.<h4>Methods</h4>Taking 20 serum samples from patients in southwest France with acute HEV infection (positive PCR for HEV genotype 3) and 550 anonymised samples from blood donors in southwest Switzerland, we tested for anti-HEV IgG using three enzyme immunoassays (EIAs) (MP Diagnostics, Dia.Pro and Fortress) based on genotype 1 and 2 antigens, and one immunodot assay (Mikrogen Diagnostik recomLine HEV IgG/IgM) based on genotype 1 and 3 antigens.<h4>Results</h4>All acute HEV samples and 124/550 blood donor samples were positive with ≥1 assay. Of PCR-confirmed patient samples, 45%, 65%, 95% and 55% were positive with MP Diagnostics, Dia.Pro, Fortress and recomLine, respectively. Of blood donor samples positive with ≥1 assay, 120/124 (97%), were positive with Fortress, 19/124 (15%) were positive with all EIAs and 51/124 (41%) were positive with recomLine. Of 11/20 patient samples positive with recomLine, stronger reactivity for HEV genotype 3 was observed in 1/11(9%), and equal reactivity for both genotypes in 5/11 (45.5%).<h4>Conclusions</h4>Although recomLine contains HEV genotype 3, it has lower sensitivity than Fortress in acute HEV infection and fails to identify infection as being due to this genotype in approximately 45% of patients. In our single blood donor population, we observe wide variations in measured seroprevalence, from 4.2% to 21.8%, depending on the assay used.
format article
author Annatina Schnegg
Philippe Bürgisser
Cyril André
Alain Kenfak-Foguena
Giorgia Canellini
Darius Moradpour
Florence Abravanel
Jacques Izopet
Matthias Cavassini
Katharine E A Darling
author_facet Annatina Schnegg
Philippe Bürgisser
Cyril André
Alain Kenfak-Foguena
Giorgia Canellini
Darius Moradpour
Florence Abravanel
Jacques Izopet
Matthias Cavassini
Katharine E A Darling
author_sort Annatina Schnegg
title An analysis of the benefit of using HEV genotype 3 antigens in detecting anti-HEV IgG in a European population.
title_short An analysis of the benefit of using HEV genotype 3 antigens in detecting anti-HEV IgG in a European population.
title_full An analysis of the benefit of using HEV genotype 3 antigens in detecting anti-HEV IgG in a European population.
title_fullStr An analysis of the benefit of using HEV genotype 3 antigens in detecting anti-HEV IgG in a European population.
title_full_unstemmed An analysis of the benefit of using HEV genotype 3 antigens in detecting anti-HEV IgG in a European population.
title_sort analysis of the benefit of using hev genotype 3 antigens in detecting anti-hev igg in a european population.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/1b1d81a8c78147b5ba703475c6b22b51
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