Cargando…
The use of oral fluids to monitor key pathogens in porcine respiratory disease complex
BACKGROUND: The usefulness of oral fluid (OF) sampling for surveillance of infections in pig populations is already accepted but its value as a tool to support investigations of porcine respiratory disease complex (PRDC) has been less well studied. This study set out to describe detection patterns o...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382517/ https://www.ncbi.nlm.nih.gov/pubmed/28405463 http://dx.doi.org/10.1186/s40813-017-0055-4 |
_version_ | 1782520116716503040 |
---|---|
author | Hernandez-Garcia, Juan Robben, Nardy Magnée, Damien Eley, Thomas Dennis, Ian Kayes, Sara M. Thomson, Jill R. Tucker, Alexander W. |
author_facet | Hernandez-Garcia, Juan Robben, Nardy Magnée, Damien Eley, Thomas Dennis, Ian Kayes, Sara M. Thomson, Jill R. Tucker, Alexander W. |
author_sort | Hernandez-Garcia, Juan |
collection | PubMed |
description | BACKGROUND: The usefulness of oral fluid (OF) sampling for surveillance of infections in pig populations is already accepted but its value as a tool to support investigations of porcine respiratory disease complex (PRDC) has been less well studied. This study set out to describe detection patterns of porcine reproductive and respiratory syndrome virus (PRRSV), porcine circovirus type 2 (PCV2), swine influenza virus type A (SIV) and Mycoplasma hyopneumoniae (M. hyo) among farms showing differing severity of PRDC. The study included six wean-to-finish pig batches from farms with historical occurrence of respiratory disease. OF samples were collected from six pens every two weeks from the 5(th) to the 21(st) week of age and tested by real time PCR for presence of PRRSV, SIV and M. hyo and by quantitative real time PCR for PCV2. Data was evaluated alongside clinical and post-mortem observations, mortality rate, slaughter pathology, histopathology, and immunohistochemistry testing data for PCV2 antigen where available. RESULTS: PRRSV and M. hyo were detectable in OF but with inconsistency between pens at the same sampling time and within pens over sequential sampling times. Detection of SIV in clinical and subclinical cases showed good consistency between pens at the same sampling time point with detection possible for periods of 2–4 weeks. Quantitative testing of OF for PCV2 indicated different patterns and levels of detection between farms unaffected or affected by porcine circovirus diseases (PCVD). There was good correlation of PCR results for multiple samples collected from the same pen but no associations were found between prevalence of positive test results and pen location in the building or sex of pigs. CONCLUSIONS: Detection patterns for PRRSV, SIV and M. hyo supported the effectiveness of OF testing as an additional tool for diagnostic investigation of PRDC but emphasised the importance of sampling from multiple pens and on multiple occasions. Preliminary evidence supported the measurement of PCV2 load in pooled OF as a tool for prediction of clinical or subclinical PCVD at farm level. |
format | Online Article Text |
id | pubmed-5382517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53825172017-04-12 The use of oral fluids to monitor key pathogens in porcine respiratory disease complex Hernandez-Garcia, Juan Robben, Nardy Magnée, Damien Eley, Thomas Dennis, Ian Kayes, Sara M. Thomson, Jill R. Tucker, Alexander W. Porcine Health Manag Research BACKGROUND: The usefulness of oral fluid (OF) sampling for surveillance of infections in pig populations is already accepted but its value as a tool to support investigations of porcine respiratory disease complex (PRDC) has been less well studied. This study set out to describe detection patterns of porcine reproductive and respiratory syndrome virus (PRRSV), porcine circovirus type 2 (PCV2), swine influenza virus type A (SIV) and Mycoplasma hyopneumoniae (M. hyo) among farms showing differing severity of PRDC. The study included six wean-to-finish pig batches from farms with historical occurrence of respiratory disease. OF samples were collected from six pens every two weeks from the 5(th) to the 21(st) week of age and tested by real time PCR for presence of PRRSV, SIV and M. hyo and by quantitative real time PCR for PCV2. Data was evaluated alongside clinical and post-mortem observations, mortality rate, slaughter pathology, histopathology, and immunohistochemistry testing data for PCV2 antigen where available. RESULTS: PRRSV and M. hyo were detectable in OF but with inconsistency between pens at the same sampling time and within pens over sequential sampling times. Detection of SIV in clinical and subclinical cases showed good consistency between pens at the same sampling time point with detection possible for periods of 2–4 weeks. Quantitative testing of OF for PCV2 indicated different patterns and levels of detection between farms unaffected or affected by porcine circovirus diseases (PCVD). There was good correlation of PCR results for multiple samples collected from the same pen but no associations were found between prevalence of positive test results and pen location in the building or sex of pigs. CONCLUSIONS: Detection patterns for PRRSV, SIV and M. hyo supported the effectiveness of OF testing as an additional tool for diagnostic investigation of PRDC but emphasised the importance of sampling from multiple pens and on multiple occasions. Preliminary evidence supported the measurement of PCV2 load in pooled OF as a tool for prediction of clinical or subclinical PCVD at farm level. BioMed Central 2017-04-05 /pmc/articles/PMC5382517/ /pubmed/28405463 http://dx.doi.org/10.1186/s40813-017-0055-4 Text en © The Author(s). 2017 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 Hernandez-Garcia, Juan Robben, Nardy Magnée, Damien Eley, Thomas Dennis, Ian Kayes, Sara M. Thomson, Jill R. Tucker, Alexander W. The use of oral fluids to monitor key pathogens in porcine respiratory disease complex |
title | The use of oral fluids to monitor key pathogens in porcine respiratory disease complex |
title_full | The use of oral fluids to monitor key pathogens in porcine respiratory disease complex |
title_fullStr | The use of oral fluids to monitor key pathogens in porcine respiratory disease complex |
title_full_unstemmed | The use of oral fluids to monitor key pathogens in porcine respiratory disease complex |
title_short | The use of oral fluids to monitor key pathogens in porcine respiratory disease complex |
title_sort | use of oral fluids to monitor key pathogens in porcine respiratory disease complex |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382517/ https://www.ncbi.nlm.nih.gov/pubmed/28405463 http://dx.doi.org/10.1186/s40813-017-0055-4 |
work_keys_str_mv | AT hernandezgarciajuan theuseoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT robbennardy theuseoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT magneedamien theuseoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT eleythomas theuseoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT dennisian theuseoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT kayessaram theuseoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT thomsonjillr theuseoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT tuckeralexanderw theuseoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT hernandezgarciajuan useoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT robbennardy useoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT magneedamien useoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT eleythomas useoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT dennisian useoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT kayessaram useoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT thomsonjillr useoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex AT tuckeralexanderw useoforalfluidstomonitorkeypathogensinporcinerespiratorydiseasecomplex |