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Repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis E virus infection within and between pig farms
Humans can become infected with hepatitis E virus (HEV) by consumption of undercooked pork. To reduce the burden of HEV in humans, mitigation on pig farms is needed. HEV is found on most pig farms globally, yet within-farm seroprevalence estimates vary considerably. Understanding of the underlying v...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264715/ https://www.ncbi.nlm.nih.gov/pubmed/35799280 http://dx.doi.org/10.1186/s13567-022-01068-3 |
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author | Meester, Marina Bouwknegt, Martijn Hakze-van der Honing, Renate Vernooij, Hans Houben, Manon van Oort, Sophie van der Poel, Wim H. M. Stegeman, Arjan Tobias, Tijs |
author_facet | Meester, Marina Bouwknegt, Martijn Hakze-van der Honing, Renate Vernooij, Hans Houben, Manon van Oort, Sophie van der Poel, Wim H. M. Stegeman, Arjan Tobias, Tijs |
author_sort | Meester, Marina |
collection | PubMed |
description | Humans can become infected with hepatitis E virus (HEV) by consumption of undercooked pork. To reduce the burden of HEV in humans, mitigation on pig farms is needed. HEV is found on most pig farms globally, yet within-farm seroprevalence estimates vary considerably. Understanding of the underlying variation in infection dynamics within and between farms currently lacks. Therefore, we investigated HEV infection dynamics by sampling 1711 batches of slaughter pigs from 208 Dutch farms over an 8-month period. Four farm types, conventional, organic, and two types with strict focus on biosecurity, were included. Sera were tested individually with an anti-HEV antibody ELISA and pooled per batch with PCR. All farms delivered seropositive pigs to slaughter, yet batches (resembling farm compartments) had varying results. By combining PCR and ELISA results, infection moment and extent per batch could be classified as low transmission, early, intermediate or late. Cluster analysis of batch infection moments per farm resulted in four clusters with distinct infection patterns. Cluster 1 farms delivered almost exclusively PCR negative, ELISA positive batches to slaughter (PCR(−)ELISA(+)), indicating relatively early age of HEV infection. Cluster 2 and 3 farms delivered 0.3 and 0.7 of batches with intermediate infection moment (PCR(+)ELISA(+)) respectively and only few batches with early infection. Cluster 4 farms delivered low transmission (PCR(−)ELISA(−)) and late infection (PCR(+)ELISA(−)) batches, demonstrating that those farms can prevent or delay HEV transmission to farm compartments. Farm type partly coincided with cluster assignment, indicating that biosecurity and management are related to age of HEV infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-022-01068-3. |
format | Online Article Text |
id | pubmed-9264715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92647152022-07-09 Repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis E virus infection within and between pig farms Meester, Marina Bouwknegt, Martijn Hakze-van der Honing, Renate Vernooij, Hans Houben, Manon van Oort, Sophie van der Poel, Wim H. M. Stegeman, Arjan Tobias, Tijs Vet Res Research Article Humans can become infected with hepatitis E virus (HEV) by consumption of undercooked pork. To reduce the burden of HEV in humans, mitigation on pig farms is needed. HEV is found on most pig farms globally, yet within-farm seroprevalence estimates vary considerably. Understanding of the underlying variation in infection dynamics within and between farms currently lacks. Therefore, we investigated HEV infection dynamics by sampling 1711 batches of slaughter pigs from 208 Dutch farms over an 8-month period. Four farm types, conventional, organic, and two types with strict focus on biosecurity, were included. Sera were tested individually with an anti-HEV antibody ELISA and pooled per batch with PCR. All farms delivered seropositive pigs to slaughter, yet batches (resembling farm compartments) had varying results. By combining PCR and ELISA results, infection moment and extent per batch could be classified as low transmission, early, intermediate or late. Cluster analysis of batch infection moments per farm resulted in four clusters with distinct infection patterns. Cluster 1 farms delivered almost exclusively PCR negative, ELISA positive batches to slaughter (PCR(−)ELISA(+)), indicating relatively early age of HEV infection. Cluster 2 and 3 farms delivered 0.3 and 0.7 of batches with intermediate infection moment (PCR(+)ELISA(+)) respectively and only few batches with early infection. Cluster 4 farms delivered low transmission (PCR(−)ELISA(−)) and late infection (PCR(+)ELISA(−)) batches, demonstrating that those farms can prevent or delay HEV transmission to farm compartments. Farm type partly coincided with cluster assignment, indicating that biosecurity and management are related to age of HEV infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-022-01068-3. BioMed Central 2022-07-07 2022 /pmc/articles/PMC9264715/ /pubmed/35799280 http://dx.doi.org/10.1186/s13567-022-01068-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Meester, Marina Bouwknegt, Martijn Hakze-van der Honing, Renate Vernooij, Hans Houben, Manon van Oort, Sophie van der Poel, Wim H. M. Stegeman, Arjan Tobias, Tijs Repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis E virus infection within and between pig farms |
title | Repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis E virus infection within and between pig farms |
title_full | Repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis E virus infection within and between pig farms |
title_fullStr | Repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis E virus infection within and between pig farms |
title_full_unstemmed | Repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis E virus infection within and between pig farms |
title_short | Repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis E virus infection within and between pig farms |
title_sort | repeated cross-sectional sampling of pigs at slaughter indicates varying age of hepatitis e virus infection within and between pig farms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264715/ https://www.ncbi.nlm.nih.gov/pubmed/35799280 http://dx.doi.org/10.1186/s13567-022-01068-3 |
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