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A Public Health initiative on hepatitis E virus epidemiology, safety and control in Portugal – study protocol

BACKGROUND: The discovery of autochthonous hepatitis E in industrialized countries has changed the understanding of hepatitis E virus (HEV) infection in these regions, now known to be mainly due to zoonotic transmission of genotype 3. The foodborne route of transmission via consumption of contaminat...

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Autores principales: Mesquita, João R., Myrmel, Mette, Stene-Johansen, Kathrine, Øverbø, Joakim, Nascimento, Maria S. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715291/
https://www.ncbi.nlm.nih.gov/pubmed/26774897
http://dx.doi.org/10.1186/s12879-016-1341-5
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author Mesquita, João R.
Myrmel, Mette
Stene-Johansen, Kathrine
Øverbø, Joakim
Nascimento, Maria S. J.
author_facet Mesquita, João R.
Myrmel, Mette
Stene-Johansen, Kathrine
Øverbø, Joakim
Nascimento, Maria S. J.
author_sort Mesquita, João R.
collection PubMed
description BACKGROUND: The discovery of autochthonous hepatitis E in industrialized countries has changed the understanding of hepatitis E virus (HEV) infection in these regions, now known to be mainly due to zoonotic transmission of genotype 3. The foodborne route of transmission via consumption of contaminated meat from HEV infected pigs is well documented as well as the direct occupational exposure to animal reservoirs. Accumulating evidence also points to an emerging potential threat to blood safety after the identification of viremic blood donors and the documentation of HEV-contaminated blood or blood products. Moreover, the origin of several iatrogenic cases remains unclear and porcine-derived pharmaceutic products have been suspected as a cause. Severe morbidity following HEV infection in patients receiving immunosuppressive therapy and in those with severe immunodeficiency from other causes has been recently recognized as a serious consequence of this infection in industrialized countries. In Portugal no large-scale HEV seroprevalence study has been undertaken, no professional risk groups have been identified, and the risk of blood donation from HEV silent infected donors is unknown. The present paper describes seroepidemiological and molecular approaches to answer these questions. METHODS/DESIGN: To address these issues a study protocol was designed that will approach: i) the seroprevalence of HEV among the Portuguese general population; ii) HEV infection among butchers and slaughterhouse workers (occupational risk); iii) the silent HEV infection in Portuguese blood donors (HEV transfusion-associated risk); iv) the potential HEV contamination of porcine-derived pharmaceutical products. Commercial enzyme immunoassays and real-time/conventional RT-PCR assays will be used. DISCUSSION: This study is the first evaluation of the seroepidemiological status to HEV infection of the Portuguese population, the first to potentially identify professional risk groups, and to evaluate the safety of blood and blood products and porcine-derived pharmaceutics in Portugal. It will generate valuable data applicable for preventive and control measures against HEV infection (e.g., introduction of systematic screening of blood donors, control of blood products or porcine derived pharmaceutical products), thus helping to manage the burden of this viral disease.
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spelling pubmed-47152912016-01-17 A Public Health initiative on hepatitis E virus epidemiology, safety and control in Portugal – study protocol Mesquita, João R. Myrmel, Mette Stene-Johansen, Kathrine Øverbø, Joakim Nascimento, Maria S. J. BMC Infect Dis Study Protocol BACKGROUND: The discovery of autochthonous hepatitis E in industrialized countries has changed the understanding of hepatitis E virus (HEV) infection in these regions, now known to be mainly due to zoonotic transmission of genotype 3. The foodborne route of transmission via consumption of contaminated meat from HEV infected pigs is well documented as well as the direct occupational exposure to animal reservoirs. Accumulating evidence also points to an emerging potential threat to blood safety after the identification of viremic blood donors and the documentation of HEV-contaminated blood or blood products. Moreover, the origin of several iatrogenic cases remains unclear and porcine-derived pharmaceutic products have been suspected as a cause. Severe morbidity following HEV infection in patients receiving immunosuppressive therapy and in those with severe immunodeficiency from other causes has been recently recognized as a serious consequence of this infection in industrialized countries. In Portugal no large-scale HEV seroprevalence study has been undertaken, no professional risk groups have been identified, and the risk of blood donation from HEV silent infected donors is unknown. The present paper describes seroepidemiological and molecular approaches to answer these questions. METHODS/DESIGN: To address these issues a study protocol was designed that will approach: i) the seroprevalence of HEV among the Portuguese general population; ii) HEV infection among butchers and slaughterhouse workers (occupational risk); iii) the silent HEV infection in Portuguese blood donors (HEV transfusion-associated risk); iv) the potential HEV contamination of porcine-derived pharmaceutical products. Commercial enzyme immunoassays and real-time/conventional RT-PCR assays will be used. DISCUSSION: This study is the first evaluation of the seroepidemiological status to HEV infection of the Portuguese population, the first to potentially identify professional risk groups, and to evaluate the safety of blood and blood products and porcine-derived pharmaceutics in Portugal. It will generate valuable data applicable for preventive and control measures against HEV infection (e.g., introduction of systematic screening of blood donors, control of blood products or porcine derived pharmaceutical products), thus helping to manage the burden of this viral disease. BioMed Central 2016-01-16 /pmc/articles/PMC4715291/ /pubmed/26774897 http://dx.doi.org/10.1186/s12879-016-1341-5 Text en © Mesquita et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Mesquita, João R.
Myrmel, Mette
Stene-Johansen, Kathrine
Øverbø, Joakim
Nascimento, Maria S. J.
A Public Health initiative on hepatitis E virus epidemiology, safety and control in Portugal – study protocol
title A Public Health initiative on hepatitis E virus epidemiology, safety and control in Portugal – study protocol
title_full A Public Health initiative on hepatitis E virus epidemiology, safety and control in Portugal – study protocol
title_fullStr A Public Health initiative on hepatitis E virus epidemiology, safety and control in Portugal – study protocol
title_full_unstemmed A Public Health initiative on hepatitis E virus epidemiology, safety and control in Portugal – study protocol
title_short A Public Health initiative on hepatitis E virus epidemiology, safety and control in Portugal – study protocol
title_sort public health initiative on hepatitis e virus epidemiology, safety and control in portugal – study protocol
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715291/
https://www.ncbi.nlm.nih.gov/pubmed/26774897
http://dx.doi.org/10.1186/s12879-016-1341-5
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