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Seroprevalence and Incidence of hepatitis E in Blood Donors in Upper Austria

BACKGROUND: In recent years various studies showed, that hepatitis E virus (HEV) is a growing public health problem in many developed countries. Therefore, HEV infections might bear a transmission risk by blood transfusions. The clinical relevance still requires further investigations. The aim of th...

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Autores principales: Fischer, Carina, Hofmann, Martina, Danzer, Martin, Hofer, Katja, Kaar, Jennifer, Gabriel, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4353625/
https://www.ncbi.nlm.nih.gov/pubmed/25751574
http://dx.doi.org/10.1371/journal.pone.0119576
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author Fischer, Carina
Hofmann, Martina
Danzer, Martin
Hofer, Katja
Kaar, Jennifer
Gabriel, Christian
author_facet Fischer, Carina
Hofmann, Martina
Danzer, Martin
Hofer, Katja
Kaar, Jennifer
Gabriel, Christian
author_sort Fischer, Carina
collection PubMed
description BACKGROUND: In recent years various studies showed, that hepatitis E virus (HEV) is a growing public health problem in many developed countries. Therefore, HEV infections might bear a transmission risk by blood transfusions. The clinical relevance still requires further investigations. The aim of this study was to provide an overview of acute HEV infections in Upper Austrian blood donors as well as a risk estimation of this transfusion-related infection. METHODS AND FINDINGS: A total of 58,915 blood donors were tested for HEV RNA using a commercial HEV RT-PCR Kit. 7 of these donors (0.01%) were PCR-positive with normal laboratory parameters in absence of clinical signs of hepatitis. Viral load determined by quantitative real-time PCR showed a HEV nucleic acid concentration of 2,217 293,635 IU/ml. At follow-up testing (2–11 weeks after donation) all blood donors had negative HEV RNA results. Additionally, genotyping was performed by amplification and sequencing of the ORF1 or ORF2 region of the HEV genome. All HEV RNA positive donor samples revealed a genotype 3 isolate. For the antibody screening, anti-HEV IgM and IgG were detected by ELISA. Follow up serological testing revealed that no donor was seropositive for HEV IgM or IgG antibodies at time of donation. Moreover, we verified the prevalence of anti-HEV IgG in 1,203 of the HEV RNA negative tested blood donors. Overall 13.55% showed positive results for anti-HEV IgG. CONCLUSIONS: In the presented study, we investigated HEV infections in blood donations of Upper Austria over 1 year. We concluded that 1 out of 8,416 blood donations is HEV RNA positive. Seroprevalence of anti HEV IgG results in an age-related increase of 13.55%. Therefore, based on this data, we recommend HEV-PCR screening to prevent transmission of hepatitis E virus by transfusion.
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spelling pubmed-43536252015-03-17 Seroprevalence and Incidence of hepatitis E in Blood Donors in Upper Austria Fischer, Carina Hofmann, Martina Danzer, Martin Hofer, Katja Kaar, Jennifer Gabriel, Christian PLoS One Research Article BACKGROUND: In recent years various studies showed, that hepatitis E virus (HEV) is a growing public health problem in many developed countries. Therefore, HEV infections might bear a transmission risk by blood transfusions. The clinical relevance still requires further investigations. The aim of this study was to provide an overview of acute HEV infections in Upper Austrian blood donors as well as a risk estimation of this transfusion-related infection. METHODS AND FINDINGS: A total of 58,915 blood donors were tested for HEV RNA using a commercial HEV RT-PCR Kit. 7 of these donors (0.01%) were PCR-positive with normal laboratory parameters in absence of clinical signs of hepatitis. Viral load determined by quantitative real-time PCR showed a HEV nucleic acid concentration of 2,217 293,635 IU/ml. At follow-up testing (2–11 weeks after donation) all blood donors had negative HEV RNA results. Additionally, genotyping was performed by amplification and sequencing of the ORF1 or ORF2 region of the HEV genome. All HEV RNA positive donor samples revealed a genotype 3 isolate. For the antibody screening, anti-HEV IgM and IgG were detected by ELISA. Follow up serological testing revealed that no donor was seropositive for HEV IgM or IgG antibodies at time of donation. Moreover, we verified the prevalence of anti-HEV IgG in 1,203 of the HEV RNA negative tested blood donors. Overall 13.55% showed positive results for anti-HEV IgG. CONCLUSIONS: In the presented study, we investigated HEV infections in blood donations of Upper Austria over 1 year. We concluded that 1 out of 8,416 blood donations is HEV RNA positive. Seroprevalence of anti HEV IgG results in an age-related increase of 13.55%. Therefore, based on this data, we recommend HEV-PCR screening to prevent transmission of hepatitis E virus by transfusion. Public Library of Science 2015-03-09 /pmc/articles/PMC4353625/ /pubmed/25751574 http://dx.doi.org/10.1371/journal.pone.0119576 Text en © 2015 Fischer et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fischer, Carina
Hofmann, Martina
Danzer, Martin
Hofer, Katja
Kaar, Jennifer
Gabriel, Christian
Seroprevalence and Incidence of hepatitis E in Blood Donors in Upper Austria
title Seroprevalence and Incidence of hepatitis E in Blood Donors in Upper Austria
title_full Seroprevalence and Incidence of hepatitis E in Blood Donors in Upper Austria
title_fullStr Seroprevalence and Incidence of hepatitis E in Blood Donors in Upper Austria
title_full_unstemmed Seroprevalence and Incidence of hepatitis E in Blood Donors in Upper Austria
title_short Seroprevalence and Incidence of hepatitis E in Blood Donors in Upper Austria
title_sort seroprevalence and incidence of hepatitis e in blood donors in upper austria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4353625/
https://www.ncbi.nlm.nih.gov/pubmed/25751574
http://dx.doi.org/10.1371/journal.pone.0119576
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