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Pathogenic variability among Pasteurella multocida type A isolates from Brazilian pig farms
BACKGROUND: Pasteurella multocida type A (PmA) is considered a secondary agent of pneumonia in pigs. The role of PmA as a primary pathogen was investigated by challenging pigs with eight field strains isolated from pneumonia and serositis in six Brazilian states. Eight groups of eight pigs each were...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103967/ https://www.ncbi.nlm.nih.gov/pubmed/30134904 http://dx.doi.org/10.1186/s12917-018-1565-2 |
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author | Oliveira Filho, João Xavier de Morés, Marcos Antônio Zanella Rebellato, Raquel Kich, Jalusa Deon Cantão, Maurício Egidio Klein, Catia Silene Guedes, Roberto Maurício Carvalho Coldebella, Arlei Barcellos, David Emílio Santos Neves de Morés, Nelson |
author_facet | Oliveira Filho, João Xavier de Morés, Marcos Antônio Zanella Rebellato, Raquel Kich, Jalusa Deon Cantão, Maurício Egidio Klein, Catia Silene Guedes, Roberto Maurício Carvalho Coldebella, Arlei Barcellos, David Emílio Santos Neves de Morés, Nelson |
author_sort | Oliveira Filho, João Xavier de |
collection | PubMed |
description | BACKGROUND: Pasteurella multocida type A (PmA) is considered a secondary agent of pneumonia in pigs. The role of PmA as a primary pathogen was investigated by challenging pigs with eight field strains isolated from pneumonia and serositis in six Brazilian states. Eight groups of eight pigs each were intranasally inoculated with different strains of PmA (1.5 mL/nostril of 10e7 CFU/mL). The control group (n = 12) received sterile PBS. The pigs were euthanized by electrocution and necropsied by 5 dpi. Macroscopic lesions were recorded, and swabs and fragments of thoracic and abdominal organs were analyzed by bacteriological and pathological assays. The PmA strains were analyzed for four virulence genes (toxA: toxin; pfhA: adhesion; tbpA and hgbB: iron acquisition) by PCR and sequencing and submitted to multilocus sequence typing (MLST). RESULTS: The eight PmA strains were classified as follows: five as highly pathogenic (HP) for causing necrotic bronchopneumonia and diffuse fibrinous pleuritis and pericarditis; one as low pathogenic for causing only focal bronchopneumonia; and two as nonpathogenic because they did not cause injury to any pig. PCR for the gene pfhA was positive for all five HP isolates. Sequencing demonstrated that the pfhA region of the HP strains comprised four genes: tpsB1, pfhA1, tpsB2 and pfhA2. The low and nonpathogenic strains did not contain the genes tpsB2 and pfhA2. A deletion of four bases was observed in the pfhA gene in the low pathogenic strain, and an insertion of 37 kb of phage DNA was observed in the nonpathogenic strains. MLST clustered the HP isolates in one group and the low and nonpathogenic isolates in another. Only the nonpathogenic isolates matched sequence type 10; the other isolates did not match any type available in the MLST database. CONCLUSIONS: The hypothesis that some PmA strains are primary pathogens and cause disease in pigs without any co-factor was confirmed. The pfhA region, comprising the genes tpsB1, tpsB2, pfhA1 and pfhA2, is related to the pathogenicity of PmA. The HP strains can cause necrotic bronchopneumonia, fibrinous pleuritis and pericarditis in pigs and can be identified by PCR amplification of the gene pfhA2. |
format | Online Article Text |
id | pubmed-6103967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61039672018-08-30 Pathogenic variability among Pasteurella multocida type A isolates from Brazilian pig farms Oliveira Filho, João Xavier de Morés, Marcos Antônio Zanella Rebellato, Raquel Kich, Jalusa Deon Cantão, Maurício Egidio Klein, Catia Silene Guedes, Roberto Maurício Carvalho Coldebella, Arlei Barcellos, David Emílio Santos Neves de Morés, Nelson BMC Vet Res Research Article BACKGROUND: Pasteurella multocida type A (PmA) is considered a secondary agent of pneumonia in pigs. The role of PmA as a primary pathogen was investigated by challenging pigs with eight field strains isolated from pneumonia and serositis in six Brazilian states. Eight groups of eight pigs each were intranasally inoculated with different strains of PmA (1.5 mL/nostril of 10e7 CFU/mL). The control group (n = 12) received sterile PBS. The pigs were euthanized by electrocution and necropsied by 5 dpi. Macroscopic lesions were recorded, and swabs and fragments of thoracic and abdominal organs were analyzed by bacteriological and pathological assays. The PmA strains were analyzed for four virulence genes (toxA: toxin; pfhA: adhesion; tbpA and hgbB: iron acquisition) by PCR and sequencing and submitted to multilocus sequence typing (MLST). RESULTS: The eight PmA strains were classified as follows: five as highly pathogenic (HP) for causing necrotic bronchopneumonia and diffuse fibrinous pleuritis and pericarditis; one as low pathogenic for causing only focal bronchopneumonia; and two as nonpathogenic because they did not cause injury to any pig. PCR for the gene pfhA was positive for all five HP isolates. Sequencing demonstrated that the pfhA region of the HP strains comprised four genes: tpsB1, pfhA1, tpsB2 and pfhA2. The low and nonpathogenic strains did not contain the genes tpsB2 and pfhA2. A deletion of four bases was observed in the pfhA gene in the low pathogenic strain, and an insertion of 37 kb of phage DNA was observed in the nonpathogenic strains. MLST clustered the HP isolates in one group and the low and nonpathogenic isolates in another. Only the nonpathogenic isolates matched sequence type 10; the other isolates did not match any type available in the MLST database. CONCLUSIONS: The hypothesis that some PmA strains are primary pathogens and cause disease in pigs without any co-factor was confirmed. The pfhA region, comprising the genes tpsB1, tpsB2, pfhA1 and pfhA2, is related to the pathogenicity of PmA. The HP strains can cause necrotic bronchopneumonia, fibrinous pleuritis and pericarditis in pigs and can be identified by PCR amplification of the gene pfhA2. BioMed Central 2018-08-22 /pmc/articles/PMC6103967/ /pubmed/30134904 http://dx.doi.org/10.1186/s12917-018-1565-2 Text en © The Author(s). 2018 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 | Research Article Oliveira Filho, João Xavier de Morés, Marcos Antônio Zanella Rebellato, Raquel Kich, Jalusa Deon Cantão, Maurício Egidio Klein, Catia Silene Guedes, Roberto Maurício Carvalho Coldebella, Arlei Barcellos, David Emílio Santos Neves de Morés, Nelson Pathogenic variability among Pasteurella multocida type A isolates from Brazilian pig farms |
title | Pathogenic variability among Pasteurella multocida type A isolates from Brazilian pig farms |
title_full | Pathogenic variability among Pasteurella multocida type A isolates from Brazilian pig farms |
title_fullStr | Pathogenic variability among Pasteurella multocida type A isolates from Brazilian pig farms |
title_full_unstemmed | Pathogenic variability among Pasteurella multocida type A isolates from Brazilian pig farms |
title_short | Pathogenic variability among Pasteurella multocida type A isolates from Brazilian pig farms |
title_sort | pathogenic variability among pasteurella multocida type a isolates from brazilian pig farms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103967/ https://www.ncbi.nlm.nih.gov/pubmed/30134904 http://dx.doi.org/10.1186/s12917-018-1565-2 |
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