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Genomic variability of Mycoplasma hyopneumoniae within pig lung lobes
BACKGROUND: Genotypic variability in M. hyopneumoniae has been reported within and among herds. However, information regarding VNTR types within single lung lobes is lacking. The objective of his study was to analyse M. hyopneumoniae infections and their association with VNTR types and lung lesions...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842051/ https://www.ncbi.nlm.nih.gov/pubmed/33509284 http://dx.doi.org/10.1186/s40813-021-00195-1 |
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author | Tonni, Matteo Boniotti, M. Beatrice Gasparrini, Sara Guarneri, Flavia Formenti, Nicoletta Pieters, Maria Pasquali, Paolo Alborali, Giovanni L. |
author_facet | Tonni, Matteo Boniotti, M. Beatrice Gasparrini, Sara Guarneri, Flavia Formenti, Nicoletta Pieters, Maria Pasquali, Paolo Alborali, Giovanni L. |
author_sort | Tonni, Matteo |
collection | PubMed |
description | BACKGROUND: Genotypic variability in M. hyopneumoniae has been reported within and among herds. However, information regarding VNTR types within single lung lobes is lacking. The objective of his study was to analyse M. hyopneumoniae infections and their association with VNTR types and lung lesions at the lobe level. Lungs from 300 pigs from 10 farms experiencing an enzootic pneumonia outbreak were collected and scored. M. hyopneumoniae was detected by real-time PCR and genotyped by MLVA assay in all samples. RESULTS: The results showed genotypic variability within single pigs and among lung lobes. At the lobe level, infection with one VNTR type (SN infection) was dominant. Lobes with lesion scores > 0 were associated with positive results for real-time PCR. At the lobe level, no relationship was observed between infections with more than one genotype (MX infections) and the proportion of Mycoplasma-like lesions. Lesion-free lobes presented a higher proportion of MX infections than lobes scored > 0. M. hyopneumoniae was detected more frequently in the right lobe of the lung (p < 0.05), with a similar distribution within lobes for SN and MX infections. The anatomic conformation of swine lungs led to a higher prevalence of infections in the right lobe. However, this study showed that this condition did not affect the distribution of infections with multiple VNTR types. Nevertheless, careful consideration of sample selection should be practised for M. hyopneumoniae genotype analyses, including lung lobes with no visible lesions. CONCLUSION: The results did not show a significant association between the number of detected genotypes and the severity of the lesions at the lung lobe level, but revealed the unexpected detection of M. hyopneumoniae genotypes in lesion-free lobes. These results imply that a representative sampling of all lobes may lead to an accurate identification of the VNTR-type distribution. Further studies including factors that can affect pathogenetic evolution of this bacterium could shed light on the complexity of the relationship between genotypes and the lung lesions magnitude. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40813-021-00195-1. |
format | Online Article Text |
id | pubmed-7842051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78420512021-01-28 Genomic variability of Mycoplasma hyopneumoniae within pig lung lobes Tonni, Matteo Boniotti, M. Beatrice Gasparrini, Sara Guarneri, Flavia Formenti, Nicoletta Pieters, Maria Pasquali, Paolo Alborali, Giovanni L. Porcine Health Manag Research BACKGROUND: Genotypic variability in M. hyopneumoniae has been reported within and among herds. However, information regarding VNTR types within single lung lobes is lacking. The objective of his study was to analyse M. hyopneumoniae infections and their association with VNTR types and lung lesions at the lobe level. Lungs from 300 pigs from 10 farms experiencing an enzootic pneumonia outbreak were collected and scored. M. hyopneumoniae was detected by real-time PCR and genotyped by MLVA assay in all samples. RESULTS: The results showed genotypic variability within single pigs and among lung lobes. At the lobe level, infection with one VNTR type (SN infection) was dominant. Lobes with lesion scores > 0 were associated with positive results for real-time PCR. At the lobe level, no relationship was observed between infections with more than one genotype (MX infections) and the proportion of Mycoplasma-like lesions. Lesion-free lobes presented a higher proportion of MX infections than lobes scored > 0. M. hyopneumoniae was detected more frequently in the right lobe of the lung (p < 0.05), with a similar distribution within lobes for SN and MX infections. The anatomic conformation of swine lungs led to a higher prevalence of infections in the right lobe. However, this study showed that this condition did not affect the distribution of infections with multiple VNTR types. Nevertheless, careful consideration of sample selection should be practised for M. hyopneumoniae genotype analyses, including lung lobes with no visible lesions. CONCLUSION: The results did not show a significant association between the number of detected genotypes and the severity of the lesions at the lung lobe level, but revealed the unexpected detection of M. hyopneumoniae genotypes in lesion-free lobes. These results imply that a representative sampling of all lobes may lead to an accurate identification of the VNTR-type distribution. Further studies including factors that can affect pathogenetic evolution of this bacterium could shed light on the complexity of the relationship between genotypes and the lung lesions magnitude. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40813-021-00195-1. BioMed Central 2021-01-28 /pmc/articles/PMC7842051/ /pubmed/33509284 http://dx.doi.org/10.1186/s40813-021-00195-1 Text en © The Author(s) 2021 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/. 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 in a credit line to the data. |
spellingShingle | Research Tonni, Matteo Boniotti, M. Beatrice Gasparrini, Sara Guarneri, Flavia Formenti, Nicoletta Pieters, Maria Pasquali, Paolo Alborali, Giovanni L. Genomic variability of Mycoplasma hyopneumoniae within pig lung lobes |
title | Genomic variability of Mycoplasma hyopneumoniae within pig lung lobes |
title_full | Genomic variability of Mycoplasma hyopneumoniae within pig lung lobes |
title_fullStr | Genomic variability of Mycoplasma hyopneumoniae within pig lung lobes |
title_full_unstemmed | Genomic variability of Mycoplasma hyopneumoniae within pig lung lobes |
title_short | Genomic variability of Mycoplasma hyopneumoniae within pig lung lobes |
title_sort | genomic variability of mycoplasma hyopneumoniae within pig lung lobes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842051/ https://www.ncbi.nlm.nih.gov/pubmed/33509284 http://dx.doi.org/10.1186/s40813-021-00195-1 |
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