Acclimation of replacement gilts to Mycoplasma hyopneumoniae: a case study of fogging with an aerosol inoculum
Ricardo Y. Nagae A B , David D. E. S. N. Barcellos A , Rafael R. Ulguim A , Taís R. Michaelsen B , João P. Zuffo B , Mariana S. Goslar B , Giovani R. Michelleto B , Jonatas Wolf B , Fernando P. Bortolozzo A and Karine L. Takeuti C *A Setor de Suínos, College of Veterinary Medicine – Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
B Seara Alimentos Ltda, Itajaí, Santa Catarina, Brazil.
C College of Veterinary Medicine – Universidade Feevale, Campo Bom, Brazil.
Animal Production Science 63(9) 869-877 https://doi.org/10.1071/AN22367
Submitted: 2 October 2022 Accepted: 15 April 2023 Published: 15 May 2023
© 2023 The Author(s) (or their employer(s)). Published by CSIRO Publishing
Abstract
Context: Mycoplasma hyopneumoniae causes enzootic pneumonia, predisposing pigs to infections with other respiratory pathogens. The main control measure is to reduce piglet exposure at lactation, which can be achieved by gilts’ acclimation prior to their entrance to the farms. One of the acclimation strategies is aerosol exposure with a positive inoculum by using a fogger. However, studies on its efficacy in gilts and their litters are lacking in the literature.
Aim: The aim of this case study was to assess the efficacy fogging with a positive inoculum of M. hyopneumoniae to expose negative gilts in an acclimation program. Moreover, the infection dynamics of M. hyopneumoniae were assessed in their piglets from lactation to slaughter.
Methods: The trial was performed in two phases. In Phase 1, a total of 34 and 107 gilts was selected from Farms A and B respectively, and then exposed to the inoculum through a fogger. In Phase 2, a subsample of 74 gilts from Farm B was followed to their first farrowing and 263 piglets born to those gilts were sampled from 15 to 170 days of age, and at slaughter, lung lesions were evaluated.
Key results: In Phase 1, the prevalence of positive gilts at 28 days post-exposure (dpe) was 100% and 98.1% in Farms A and B respectively. In Phase 2, 10.8% of gilts remained positive at 180 dpe and 0.8% of piglets were positive at 15 days of age (day) and 28.1% at 60 days, suggesting a possible vertical transmission.
Conclusion: The use of fogging with a lung homogenate positive for M. hyopneumoniae successfully acclimated negative gilts. However, it did not avoid the presence of positive gilts at farrowing and the detection of the bacterium in their progeny by polymerase chain reaction.
Implications: The exposure of gilts to M. hyopneumoniae at 150 days of age was successfully achieved by fogging. However, consideration should be given to exposing replacement gilts of a younger age in order to reduce the odds of detecting positive gilts at first farrowing.
Keywords: enzootic pneumonia, exposure, Friis, inoculum, longitudinal study, lung homogenate, PPLO, transmission.
References
Arsenakis I, Michiels A, Schagemann G, Gomez-Duran CO, Boyen F, Haesebrouck F, Maes DGD (2019) Effects of pre-farrowing sow vaccination against Mycoplasma hyopneumoniae on offspring colonisation and lung lesions. Veterinary Record 184, 222| Effects of pre-farrowing sow vaccination against Mycoplasma hyopneumoniae on offspring colonisation and lung lesions.Crossref | GoogleScholarGoogle Scholar |
Calsamiglia M, Pijoan C (2000) Colonisation state and colostral immunity to Mycoplasma hyopneumoniae of different parity sows. Veterinary Record 146, 530–532.
| Colonisation state and colostral immunity to Mycoplasma hyopneumoniae of different parity sows.Crossref | GoogleScholarGoogle Scholar |
Christensen G, Sorensen V, Mousing J (1999) Diseases of the respiratory system. In ‘Diseases of swine’. 1st edn. (Eds BE Straw, et al.) pp. 913–940. (Iowa State University Press: Ames, IA, USA)
Dewey CE, Straw BE (2006) Herd examination. In ‘Diseases of swine’. 9th edn. (Eds BE Straw, JJ Zimmerman, S D’Alliare) pp. 3–14. (Blackwell Publishing: Ames, IA, USA)
Dos Santos LF, Sreevatsan S, Torremorell M, Moreira MAS, Sibila M, Pieters M (2015) Genotype distribution of Mycoplasma hyopneumoniae in swine herds from different geographical regions. Veterinary Microbiology 175, 374–381.
| Genotype distribution of Mycoplasma hyopneumoniae in swine herds from different geographical regions.Crossref | GoogleScholarGoogle Scholar |
Dubosson CR, Conzelmann C, Miserez R, Boerlin P, Frey J, Zimmermann W, Häni H, Kuhnert P (2004) Development of two real-time PCR assays for the detection of Mycoplasma hyopneumoniae in clinical samples. Veterinary Microbiology 102, 55–65.
| Development of two real-time PCR assays for the detection of Mycoplasma hyopneumoniae in clinical samples.Crossref | GoogleScholarGoogle Scholar |
Fano E, Pijoan C, Dee S, Deen J (2007) Effect of Mycoplasma hyopneumoniae colonization at weaning on disease severity in growing pigs. The Canadian Journal of Veterinary Research 71, 195–200.
Garza-Moreno L, Segalés J, Pieters M, Romagosa A, Sibila M (2018) Acclimation strategies in gilts to control Mycoplasma hyopneumoniae infection. Veterinary Microbiology 219, 23–29.
| Acclimation strategies in gilts to control Mycoplasma hyopneumoniae infection.Crossref | GoogleScholarGoogle Scholar |
Gourgues SF, Fano E, Sebarté AA, Grasa EL, Caravaca IH, Vázquez FAG, Vega VR, Garcia-Morante B (2020) Assessment of nebulization technology for gilt exposure to Mycoplasma hyopneumoniae as an acclimation strategy. Journal of Swine Health and Production 28, 294–301.
Li X, Qiao M, Sun M, Tian K (2018) A duplex real-time PCR assay for the simultaneous detection of porcine circovirus 2 and circovirus 3. Virologica Sinica 33, 181–186.
| A duplex real-time PCR assay for the simultaneous detection of porcine circovirus 2 and circovirus 3.Crossref | GoogleScholarGoogle Scholar |
Madec F, Kobisch M (1982) Bilan lesionnel des poumons de porcs charcutiers à l’abattoir. Journées Recherche Porcine 14, 405–412.
Maes D, Sibila M, Kuhnert P, Segalés J, Haesebrouck F, Pieters M (2018) Update on Mycoplasma hyopneumoniae infections in pigs: knowledge gaps for improved disease control. Transboundary and Emerging Diseases 65, 110–124.
| Update on Mycoplasma hyopneumoniae infections in pigs: knowledge gaps for improved disease control.Crossref | GoogleScholarGoogle Scholar |
Meyns T, Maes D, Dewulf J, Vicca J, Haesebrouck F, Kruif Ad (2004) Quantification of the spread of Mycoplasma hyopneumoniae in nursery pigs using transmission experiments. Preventive Veterinary Medicine 66, 265–275.
| Quantification of the spread of Mycoplasma hyopneumoniae in nursery pigs using transmission experiments.Crossref | GoogleScholarGoogle Scholar |
Michiels A, Vranckx K, Piepers S, Del Pozo Sacristán R, Arsenakis I, Boyen F, Haesebrouck F, Maes D (2017) Impact of diversity of Mycoplasma hyopneumoniae strains on lung lesions in slaughter pigs. Veterinary Research 48, 2
| Impact of diversity of Mycoplasma hyopneumoniae strains on lung lesions in slaughter pigs.Crossref | GoogleScholarGoogle Scholar |
Nathues H, Fournie G, Wieland B, Pfeiffer DU, Stärk KDC (2016) Modelling the within-herd transmission of Mycoplasma hyopneumoniae in closed pig herds. Porcine Health Management 2, 10
| Modelling the within-herd transmission of Mycoplasma hyopneumoniae in closed pig herds.Crossref | GoogleScholarGoogle Scholar |
Nickel M, Toohill E, Lehman J (2018) Use of a hurricane fogger for Mycoplasma hyopneumoniae inoculation in nursery age gilts. In ‘Proceedings of 49th annual meeting of the American association of swine veterinarians’. pp. 97–98. (San Diego, CA, USA)
Pantoja LG, Pettit K, Dos Santos LF, Tubbs R, Pieters M (2016) Mycoplasma hyopneumoniae genetic variability within a swine operation. Journal of Veterinary Diagnostic Investigation 28, 175–179.
| Mycoplasma hyopneumoniae genetic variability within a swine operation.Crossref | GoogleScholarGoogle Scholar |
Pieters M, Fano E (2016) Mycoplasma hyopneumoniae in gilts. Veterinary Record 178, 122–123.
| Mycoplasma hyopneumoniae in gilts.Crossref | GoogleScholarGoogle Scholar |
Pieters M, Maes D (2019) Mycoplasmosis. In ‘Diseases of swine’, 11th edn. (Eds JJ Zimmermann, LA Karriker, A Ramirez, KJ Schwartz, GW Stevenson, J Zhang) pp. 863–883. (Wiley-Blackwell: Ames, IA, USA)
Pieters M, Pijoan C, Fano E, Dee S (2009) An assessment of the duration of Mycoplasma hyopneumoniae infection in an experimentally infected population of pigs. Veterinary Microbiology 134, 261–266.
| An assessment of the duration of Mycoplasma hyopneumoniae infection in an experimentally infected population of pigs.Crossref | GoogleScholarGoogle Scholar |
Pieters M, Cline GS, Payne BJ, Prado C, Ertl JR, Rendahl AK (2014) Intra-farm risk factors for Mycoplasma hyopneumoniae colonization at weaning age. Veterinary Microbiology 172, 575–580.
| Intra-farm risk factors for Mycoplasma hyopneumoniae colonization at weaning age.Crossref | GoogleScholarGoogle Scholar |
Robbins RC, Betlach AM, Mondragon-Evans MR, Pieters M (2019) Development of a herd-specific lung homogenate for exposure to Mycoplasma hyopneumoniae under field conditions. Journal of Swine Health and Production 27, 221–227.
Roos LR, Fano E, Homwong N, Payne B, Pieters M (2016) A model to investigate the optimal seeder-to-naïve ratio for successful natural Mycoplasma hyopneumoniae gilt exposure prior to entering the breeding herd. Veterinary Microbiology 184, 51–58.
| A model to investigate the optimal seeder-to-naïve ratio for successful natural Mycoplasma hyopneumoniae gilt exposure prior to entering the breeding herd.Crossref | GoogleScholarGoogle Scholar |
Sibila M, Nofrarías M, López-Soria S, Segalés J, Riera P, Llopart D, Calsamiglia M (2007) Exploratory field study on Mycoplasma hyopneumoniae infection in suckling pigs. Veterinary Microbiology 121, 352–356.
| Exploratory field study on Mycoplasma hyopneumoniae infection in suckling pigs.Crossref | GoogleScholarGoogle Scholar |
Sørensen V, Ahrens P, Barfod K, Feenstra AA, Feld NC, Friis NF, Bille-Hansen V, Jensen NE, Pedersen MW (1997) Mycoplasma hyopneumoniae infection in pigs: duration of the disease and evaluation of four diagnostic assays. Veterinary Microbiology 54, 23–34.
| Mycoplasma hyopneumoniae infection in pigs: duration of the disease and evaluation of four diagnostic assays.Crossref | GoogleScholarGoogle Scholar |
Sosa C, Blois A, Ibáñez F, Tamiozzo P (2019) Genetic diversity of Mycoplasma hyopneumoniae in Mendoza province. Revista Argentina de Microbiología 51, 229–233.
| Genetic diversity of Mycoplasma hyopneumoniae in Mendoza province.Crossref | GoogleScholarGoogle Scholar |
Sponheim A, Alvarez J, Fano E, Schmaling E, Dee S, Hanson D, Wetzell T, Pieters M (2020) Comparison of the sensitivity of laryngeal swabs and deep tracheal catheters for detection of Mycoplasma hyopneumoniae in experimentally and naturally infected pigs early and late after infection. Veterinary Microbiology 241, 108500
| Comparison of the sensitivity of laryngeal swabs and deep tracheal catheters for detection of Mycoplasma hyopneumoniae in experimentally and naturally infected pigs early and late after infection.Crossref | GoogleScholarGoogle Scholar |
Takeuti KL, de Barcellos DESN, de Lara AC, Kunrath CF, Pieters M (2017a) Detection of Mycoplasma hyopneumoniae in naturally infected gilts over time. Veterinary Microbiology 203, 215–220.
| Detection of Mycoplasma hyopneumoniae in naturally infected gilts over time.Crossref | GoogleScholarGoogle Scholar |
Takeuti KL, de Barcellos DESN, de Andrade CP, de Almeida LL, Pieters M (2017b) Infection dynamics and genetic variability of Mycoplasma hyopneumoniae in self-replacement gilts. Veterinary Microbiology 208, 18–24.
| Infection dynamics and genetic variability of Mycoplasma hyopneumoniae in self-replacement gilts.Crossref | GoogleScholarGoogle Scholar |
Takeuti KL, Michaelsen TR, Sabedot C, Nagae RY, Forner RAN, Mazzarollo A, de Barcellos DESN, Pieters M (2022) Mycoplasma hyopneumoniae detection by PCR in naturally infected finishing pigs. Journal of Microbiological Methods 197, 106475
| Mycoplasma hyopneumoniae detection by PCR in naturally infected finishing pigs.Crossref | GoogleScholarGoogle Scholar |
Tobias TJ, Bouma A, Klinkenberg D, Daemen AJJM, Stegeman JA, Wagenaar JA, Duim B (2012) Detection of Actinobacillus pleuropneumoniae in pigs by real-time quantitative PCR for the apxIVA gene. The Veterinary Journal 193, 557–560.
| Detection of Actinobacillus pleuropneumoniae in pigs by real-time quantitative PCR for the apxIVA gene.Crossref | GoogleScholarGoogle Scholar |
Villarreal I, Maes D, Meyns T, Gebruers F, Calus D, Pasmans F, Haesebrouck F (2009) Infection with a low virulent Mycoplasma hyopneumoniae isolate does not protect piglets against subsequent infection with a highly virulent M. hyopneumoniae isolate. Vaccine 27, 1875–1879.
| Infection with a low virulent Mycoplasma hyopneumoniae isolate does not protect piglets against subsequent infection with a highly virulent M. hyopneumoniae isolate.Crossref | GoogleScholarGoogle Scholar |
Zhang J, Harmon KM (2014) RNA extraction from swine samples and detection of Influenza A virus in swine by real-time RT-PCR. Methods in Molecular Biology 1161, 277–293.
| RNA extraction from swine samples and detection of Influenza A virus in swine by real-time RT-PCR.Crossref | GoogleScholarGoogle Scholar |