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Histopathological lesions of Actinobacillus pleuropneumoniae serotype 8 in infected pigs
This study aimed to report, for the first time, histopathological lesions caused by an outbreak of acute Actinobacillus pleuropneumoniae serotype 8 infections in two farms in Cyprus. Lung tissue samples were collected from two different affected farms (a total of eight samples) for bacterial culture...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Urmia University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410112/ https://www.ncbi.nlm.nih.gov/pubmed/37564359 http://dx.doi.org/10.30466/vrf.2022.556971.3539 |
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author | Papatsiros, Vasileios Georgios Stylianaki, Ioanna Tsokana, Constantina Nikolaos Papakonstantinou, Georgios Christophorou, Marios Papaioannou, Nikolaos Athanasiou, Labrini Vasileios |
author_facet | Papatsiros, Vasileios Georgios Stylianaki, Ioanna Tsokana, Constantina Nikolaos Papakonstantinou, Georgios Christophorou, Marios Papaioannou, Nikolaos Athanasiou, Labrini Vasileios |
author_sort | Papatsiros, Vasileios Georgios |
collection | PubMed |
description | This study aimed to report, for the first time, histopathological lesions caused by an outbreak of acute Actinobacillus pleuropneumoniae serotype 8 infections in two farms in Cyprus. Lung tissue samples were collected from two different affected farms (a total of eight samples) for bacterial culture, multiplex polymerase chain reaction (PCR)-based serotyping and histopathological evaluation. Severe respiratory clinical signs, vomiting, anorexia, sudden deaths, a morbidity rate of around 25.00% and a mortality rate of over 60.00% in the fattening stage were reported. Macroscopic lesions included acute to subacute fibrotic, hemorrhagic and necrotizing pneumonia with occasionally encapsulated nodule-like abscesses and fibrous pleuritis. Histopathological evaluation revealed fibrous exudate between alveolar spaces and connective tissue, areas of necrosis mixed with alveolar macrophages, lymphocytes, plasma cells and necrotic leukocytes surrounding colonies of cocci. The bronchial and bronchiolar epithelia were degenerated and replaced by eosinophilic cell debris mixed with inflammatory cells. Several arteries and capillaries were clotted and/or infiltrated by inflammatory cells. In conclusion, these A. pleuropneumoniae serotype 8 cases were accompanied by acute illness, death and more pronounced bronchitis and bronchiolitis. |
format | Online Article Text |
id | pubmed-10410112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Urmia University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104101122023-08-10 Histopathological lesions of Actinobacillus pleuropneumoniae serotype 8 in infected pigs Papatsiros, Vasileios Georgios Stylianaki, Ioanna Tsokana, Constantina Nikolaos Papakonstantinou, Georgios Christophorou, Marios Papaioannou, Nikolaos Athanasiou, Labrini Vasileios Vet Res Forum Short Communication This study aimed to report, for the first time, histopathological lesions caused by an outbreak of acute Actinobacillus pleuropneumoniae serotype 8 infections in two farms in Cyprus. Lung tissue samples were collected from two different affected farms (a total of eight samples) for bacterial culture, multiplex polymerase chain reaction (PCR)-based serotyping and histopathological evaluation. Severe respiratory clinical signs, vomiting, anorexia, sudden deaths, a morbidity rate of around 25.00% and a mortality rate of over 60.00% in the fattening stage were reported. Macroscopic lesions included acute to subacute fibrotic, hemorrhagic and necrotizing pneumonia with occasionally encapsulated nodule-like abscesses and fibrous pleuritis. Histopathological evaluation revealed fibrous exudate between alveolar spaces and connective tissue, areas of necrosis mixed with alveolar macrophages, lymphocytes, plasma cells and necrotic leukocytes surrounding colonies of cocci. The bronchial and bronchiolar epithelia were degenerated and replaced by eosinophilic cell debris mixed with inflammatory cells. Several arteries and capillaries were clotted and/or infiltrated by inflammatory cells. In conclusion, these A. pleuropneumoniae serotype 8 cases were accompanied by acute illness, death and more pronounced bronchitis and bronchiolitis. Urmia University Press 2023 2023-07-15 /pmc/articles/PMC10410112/ /pubmed/37564359 http://dx.doi.org/10.30466/vrf.2022.556971.3539 Text en © 2023 Urmia University. All rights reserved https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.https://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Short Communication Papatsiros, Vasileios Georgios Stylianaki, Ioanna Tsokana, Constantina Nikolaos Papakonstantinou, Georgios Christophorou, Marios Papaioannou, Nikolaos Athanasiou, Labrini Vasileios Histopathological lesions of Actinobacillus pleuropneumoniae serotype 8 in infected pigs |
title | Histopathological lesions of Actinobacillus pleuropneumoniae serotype 8 in infected pigs |
title_full | Histopathological lesions of Actinobacillus pleuropneumoniae serotype 8 in infected pigs |
title_fullStr | Histopathological lesions of Actinobacillus pleuropneumoniae serotype 8 in infected pigs |
title_full_unstemmed | Histopathological lesions of Actinobacillus pleuropneumoniae serotype 8 in infected pigs |
title_short | Histopathological lesions of Actinobacillus pleuropneumoniae serotype 8 in infected pigs |
title_sort | histopathological lesions of actinobacillus pleuropneumoniae serotype 8 in infected pigs |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410112/ https://www.ncbi.nlm.nih.gov/pubmed/37564359 http://dx.doi.org/10.30466/vrf.2022.556971.3539 |
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