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Gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (PWD) in pigs

BACKGROUND: Post-weaning diarrhoea (PWD) is a multifactorial condition and the most well documented infectious cause is enterotoxigenic Escherichia coli. The objective of the study was to investigate possible associations between pathological manifestations and pathogens in pigs with and without PWD...

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Autores principales: Blirup-Plum, Sophie Amalie, Jensen, Henrik Elvang, Nielsen, Søren Saxmose, Pankoke, Karen, Hansen, Mette Sif, Pedersen, Ken Steen, Eriksen, Esben Østergaard, Nielsen, Jens Peter, Olsen, John Elmerdahl, Kudirkiene, Egle, Larsen, Lars Erik, Goecke, Nicole Bakkegård, Barington, Kristiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316552/
https://www.ncbi.nlm.nih.gov/pubmed/37400879
http://dx.doi.org/10.1186/s13028-023-00693-y
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author Blirup-Plum, Sophie Amalie
Jensen, Henrik Elvang
Nielsen, Søren Saxmose
Pankoke, Karen
Hansen, Mette Sif
Pedersen, Ken Steen
Eriksen, Esben Østergaard
Nielsen, Jens Peter
Olsen, John Elmerdahl
Kudirkiene, Egle
Larsen, Lars Erik
Goecke, Nicole Bakkegård
Barington, Kristiane
author_facet Blirup-Plum, Sophie Amalie
Jensen, Henrik Elvang
Nielsen, Søren Saxmose
Pankoke, Karen
Hansen, Mette Sif
Pedersen, Ken Steen
Eriksen, Esben Østergaard
Nielsen, Jens Peter
Olsen, John Elmerdahl
Kudirkiene, Egle
Larsen, Lars Erik
Goecke, Nicole Bakkegård
Barington, Kristiane
author_sort Blirup-Plum, Sophie Amalie
collection PubMed
description BACKGROUND: Post-weaning diarrhoea (PWD) is a multifactorial condition and the most well documented infectious cause is enterotoxigenic Escherichia coli. The objective of the study was to investigate possible associations between pathological manifestations and pathogens in pigs with and without PWD. The study was conducted as a case–control study and included a total of 173 pigs from 9 different commercial intensive indoor production herds in eastern Denmark. RESULTS: Based on clinical examination, a total of 89 piglets with PWD (cases) and 84 piglets without PWD (controls) were included. Most of the pigs (n = 105/173) presented gastric lesions, which were more frequently observed in the control group. The odds of gastric ulcers were lower among pigs with PWD compared to pigs without PWD with an odds ratio (OR) of 0.2 (0.0; 0.7). Abnormal content in the colon was associated with PWD, with an OR of 6.5 (3.2; 14.3). No apparent association was found between lesions and the various pathogens or a combination of these. The odds of neutrophilic granulocyte infiltration were lower in the jejunum among pigs with PWD (OR 0.3 [0.1; 0.6]) compared to pigs without PWD. The association between neutrophilic granulocyte infiltration in jejunum and PWD differed between the herds (P = 0.03). Furthermore, the associations between PWD and hyperleukocytosis (P = 0.04) or infiltration of eosinophilic granulocytes (P = 0.04) in ileum were also herd dependent. Histopathology revealed several lesions not relatable to PWD. CONCLUSION: The association between lesions and specific pathogens or PWD is more complex than anticipated. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13028-023-00693-y.
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spelling pubmed-103165522023-07-04 Gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (PWD) in pigs Blirup-Plum, Sophie Amalie Jensen, Henrik Elvang Nielsen, Søren Saxmose Pankoke, Karen Hansen, Mette Sif Pedersen, Ken Steen Eriksen, Esben Østergaard Nielsen, Jens Peter Olsen, John Elmerdahl Kudirkiene, Egle Larsen, Lars Erik Goecke, Nicole Bakkegård Barington, Kristiane Acta Vet Scand Research BACKGROUND: Post-weaning diarrhoea (PWD) is a multifactorial condition and the most well documented infectious cause is enterotoxigenic Escherichia coli. The objective of the study was to investigate possible associations between pathological manifestations and pathogens in pigs with and without PWD. The study was conducted as a case–control study and included a total of 173 pigs from 9 different commercial intensive indoor production herds in eastern Denmark. RESULTS: Based on clinical examination, a total of 89 piglets with PWD (cases) and 84 piglets without PWD (controls) were included. Most of the pigs (n = 105/173) presented gastric lesions, which were more frequently observed in the control group. The odds of gastric ulcers were lower among pigs with PWD compared to pigs without PWD with an odds ratio (OR) of 0.2 (0.0; 0.7). Abnormal content in the colon was associated with PWD, with an OR of 6.5 (3.2; 14.3). No apparent association was found between lesions and the various pathogens or a combination of these. The odds of neutrophilic granulocyte infiltration were lower in the jejunum among pigs with PWD (OR 0.3 [0.1; 0.6]) compared to pigs without PWD. The association between neutrophilic granulocyte infiltration in jejunum and PWD differed between the herds (P = 0.03). Furthermore, the associations between PWD and hyperleukocytosis (P = 0.04) or infiltration of eosinophilic granulocytes (P = 0.04) in ileum were also herd dependent. Histopathology revealed several lesions not relatable to PWD. CONCLUSION: The association between lesions and specific pathogens or PWD is more complex than anticipated. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13028-023-00693-y. BioMed Central 2023-07-03 /pmc/articles/PMC10316552/ /pubmed/37400879 http://dx.doi.org/10.1186/s13028-023-00693-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Blirup-Plum, Sophie Amalie
Jensen, Henrik Elvang
Nielsen, Søren Saxmose
Pankoke, Karen
Hansen, Mette Sif
Pedersen, Ken Steen
Eriksen, Esben Østergaard
Nielsen, Jens Peter
Olsen, John Elmerdahl
Kudirkiene, Egle
Larsen, Lars Erik
Goecke, Nicole Bakkegård
Barington, Kristiane
Gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (PWD) in pigs
title Gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (PWD) in pigs
title_full Gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (PWD) in pigs
title_fullStr Gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (PWD) in pigs
title_full_unstemmed Gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (PWD) in pigs
title_short Gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (PWD) in pigs
title_sort gastro-intestinal lesions are not relatable to diarrhoea or specific pathogens in post-weaning diarrhoea (pwd) in pigs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316552/
https://www.ncbi.nlm.nih.gov/pubmed/37400879
http://dx.doi.org/10.1186/s13028-023-00693-y
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