Cough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditions

Abstract Background The association of cough with Mycoplasma hyopneumoniae (MHP) DNA detection in specimens was evaluated under conditions in which the MHP status of inoculated and contact-infected pen mates was closely monitored for 59 days post-inoculation (DPI). Methods Seven-week-old pigs (n = 3...

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Main Authors: Ana Paula S. Poeta Silva, Gabriel Y. Storino, Franco S. Matias Ferreyra, Min Zhang, Eduardo Fano, Dale Polson, Chong Wang, Rachel J. Derscheid, Jeffrey J. Zimmerman, Maria J. Clavijo, Bailey L. Arruda
Format: Article
Language:English
Published: BMC 2022-01-01
Series:Porcine Health Management
Subjects:
Online Access:https://doi.org/10.1186/s40813-022-00249-y
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author Ana Paula S. Poeta Silva
Gabriel Y. Storino
Franco S. Matias Ferreyra
Min Zhang
Eduardo Fano
Dale Polson
Chong Wang
Rachel J. Derscheid
Jeffrey J. Zimmerman
Maria J. Clavijo
Bailey L. Arruda
author_facet Ana Paula S. Poeta Silva
Gabriel Y. Storino
Franco S. Matias Ferreyra
Min Zhang
Eduardo Fano
Dale Polson
Chong Wang
Rachel J. Derscheid
Jeffrey J. Zimmerman
Maria J. Clavijo
Bailey L. Arruda
author_sort Ana Paula S. Poeta Silva
collection DOAJ
description Abstract Background The association of cough with Mycoplasma hyopneumoniae (MHP) DNA detection in specimens was evaluated under conditions in which the MHP status of inoculated and contact-infected pen mates was closely monitored for 59 days post-inoculation (DPI). Methods Seven-week-old pigs (n = 39) were allocated to five rooms (with one pen). Rooms contained 9 pigs each, with 1, 3, 6, or 9 MHP-inoculated pigs, respectively, except Room 5 (three sham-inoculated pigs). Cough data (2 × week) and specimens, tracheal swabs (2 × week), oral fluids (daily), drinker wipes (~ 1 × week), and air samples (3 × week) were collected. At 59 DPI, pigs were euthanized, and lung and trachea were evaluated for gross and microscopic lesions. Predictive cough value to MHP DNA detection in drinker and oral fluid samples were estimated using mixed logistic regression. Results Following inoculation, MHP DNA was first detected in tracheal swabs from inoculated pigs (DPI 3), then oral fluids (DPI 8), air samples (DPI 10), and drinker wipes (21 DPI). MHP DNA was detected in oral fluids in 17 of 59 (Room 1) to 43 of 59 (Room 3) samples, drinker wipes in 4 of 8 (Rooms 2 and 3) to 5 of 8 (Rooms 1 and 4) samples, and air samples in 5 of 26 (Room 2) or 3 of 26 (Room 4) samples. Logistic regression showed that the frequency of coughing pigs in a pen was associated with the probability of MHP DNA detection in oral fluids (P < 0.01) and nearly associated with drinker wipes (P = 0.08). Pathology data revealed an association between the period when infection was first detected and the severity of gross lung lesions. Conclusions Dry, non-productive coughs suggest the presence of MHP, but laboratory testing and MHP DNA detection is required for confirmation. Based on the data from this study, oral fluids and drinker wipes may provide a convenient alternative for MHP DNA detection at the pen level when cough is present. This information may help practitioners in specimen selection for MHP surveillance.
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spelling doaj.art-7df73f3b7ee04399a6ef6f6bc3b850382022-12-21T16:35:06ZengBMCPorcine Health Management2055-56602022-01-018111310.1186/s40813-022-00249-yCough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditionsAna Paula S. Poeta Silva0Gabriel Y. Storino1Franco S. Matias Ferreyra2Min Zhang3Eduardo Fano4Dale Polson5Chong Wang6Rachel J. Derscheid7Jeffrey J. Zimmerman8Maria J. Clavijo9Bailey L. Arruda10Department of Veterinary Diagnostic and Production Animal Medicine, Iowa State UniversitySchool of Agricultural and Veterinarian Sciences, São Paulo State University (Unesp)Department of Veterinary Diagnostic and Production Animal Medicine, Iowa State UniversityDepartment of Statistics, College of Liberal Arts and Sciences, Iowa State UniversityBoehringer Ingelheim Animal Health US Inc.Boehringer Ingelheim Animal Health US Inc.Department of Veterinary Diagnostic and Production Animal Medicine, Iowa State UniversityDepartment of Veterinary Diagnostic and Production Animal Medicine, Iowa State UniversityDepartment of Veterinary Diagnostic and Production Animal Medicine, Iowa State UniversityDepartment of Veterinary Diagnostic and Production Animal Medicine, Iowa State UniversityDepartment of Veterinary Diagnostic and Production Animal Medicine, Iowa State UniversityAbstract Background The association of cough with Mycoplasma hyopneumoniae (MHP) DNA detection in specimens was evaluated under conditions in which the MHP status of inoculated and contact-infected pen mates was closely monitored for 59 days post-inoculation (DPI). Methods Seven-week-old pigs (n = 39) were allocated to five rooms (with one pen). Rooms contained 9 pigs each, with 1, 3, 6, or 9 MHP-inoculated pigs, respectively, except Room 5 (three sham-inoculated pigs). Cough data (2 × week) and specimens, tracheal swabs (2 × week), oral fluids (daily), drinker wipes (~ 1 × week), and air samples (3 × week) were collected. At 59 DPI, pigs were euthanized, and lung and trachea were evaluated for gross and microscopic lesions. Predictive cough value to MHP DNA detection in drinker and oral fluid samples were estimated using mixed logistic regression. Results Following inoculation, MHP DNA was first detected in tracheal swabs from inoculated pigs (DPI 3), then oral fluids (DPI 8), air samples (DPI 10), and drinker wipes (21 DPI). MHP DNA was detected in oral fluids in 17 of 59 (Room 1) to 43 of 59 (Room 3) samples, drinker wipes in 4 of 8 (Rooms 2 and 3) to 5 of 8 (Rooms 1 and 4) samples, and air samples in 5 of 26 (Room 2) or 3 of 26 (Room 4) samples. Logistic regression showed that the frequency of coughing pigs in a pen was associated with the probability of MHP DNA detection in oral fluids (P < 0.01) and nearly associated with drinker wipes (P = 0.08). Pathology data revealed an association between the period when infection was first detected and the severity of gross lung lesions. Conclusions Dry, non-productive coughs suggest the presence of MHP, but laboratory testing and MHP DNA detection is required for confirmation. Based on the data from this study, oral fluids and drinker wipes may provide a convenient alternative for MHP DNA detection at the pen level when cough is present. This information may help practitioners in specimen selection for MHP surveillance.https://doi.org/10.1186/s40813-022-00249-yMycoplasma hyopneumoniaeEnzootic pneumoniaTracheal swabsOral fluidsWater samplesAir samples
spellingShingle Ana Paula S. Poeta Silva
Gabriel Y. Storino
Franco S. Matias Ferreyra
Min Zhang
Eduardo Fano
Dale Polson
Chong Wang
Rachel J. Derscheid
Jeffrey J. Zimmerman
Maria J. Clavijo
Bailey L. Arruda
Cough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditions
Porcine Health Management
Mycoplasma hyopneumoniae
Enzootic pneumonia
Tracheal swabs
Oral fluids
Water samples
Air samples
title Cough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditions
title_full Cough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditions
title_fullStr Cough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditions
title_full_unstemmed Cough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditions
title_short Cough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditions
title_sort cough associated with the detection of mycoplasma hyopneumoniae dna in clinical and environmental specimens under controlled conditions
topic Mycoplasma hyopneumoniae
Enzootic pneumonia
Tracheal swabs
Oral fluids
Water samples
Air samples
url https://doi.org/10.1186/s40813-022-00249-y
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