Comparison of immune cell populations in bronchoalveolar lavage cells and PBMC cytokine expressions in porcine reproductive and respiratory syndrome and porcine respiratory disease complex
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Porcine reproductive and respiratory syndrome (PRRS) is characterized by reproductive failure in sows and respiratory distress in all age pigs. Porcine respiratory disease complex (PRDC) is a disease caused by opportunistic bacterial infection secondary to a weakened immune system by a preceding respiratory infection. In this study, we tried to compare the immune responses in PRRS and PRDC groups to clearly characterize the disease severity. Eighty-five pigs were infected with various Korean field PRRS virus strains. Infected animals were classified into PRRS (n=32) and PRDC (n=53) groups based on lung le-sions such as interstitial pneumonia, suppurative pneumonia, and pleuropneumonia. The immune cell population of bronchoalveolar lavage cells (BALc) was evaluated on 14 and 28 days post infection (dpi) and PMBC cytokine expression was measured on 0, 3, 7, 14 dpi to investigate early inflammatory re-actions. Pulmonary lesion severity was negatively correlated with alveolar macrophage (AM) in both PRRS and PRDC groups on 14 and 28 dpi. AM in BALc was less populated in PRDC group on 28 dpi compared to PRRS group. AM in BALc was significantly less populated in PRDC group on 28 dpi compared to 14 dpi. In addition, cytotoxic T lymphocyte (CTL) in BALc was higher populated in PRDC group on 14 dpi and 28 dpi compared to PRRS group. In the case of PBMC cytokine TNF-, IFN-, IL-1, IFN-, FoxP3, and IL-2, the PRRS group showed higher expression than the PRDC group on 7 dpi, 14 dpi, 7 dpi, 14 dpi, 14 dpi, and 14 dpi, respectively. On the other hand, in the case of IFN-, IL-6, IL-8, IL-4, and IL-17, the PRDC group showed higher PBMC cytokine expression at 14 dpi, 7 dpi, 14 dpi, 3 dpi, and 3 dpi, respectively, than the PRRS group. Based on these results, our study could characterize differential immune responses in pigs with PRRS or PRDC.
Abstract
Porcine reproductive and respiratory syndrome (PRRS) is characterized by reproductive failure in sows and respiratory distress in all age pigs. Porcine respiratory disease complex (PRDC) is a disease caused by opportunistic bacterial infection secondary to a weakened immune system by a preceding respiratory infection. In this study, we tried to compare the immune responses in PRRS and PRDC groups to clearly characterize the disease severity. Eighty-five pigs were infected with various Korean field PRRS virus strains. Infected animals were classified into PRRS (n=32) and PRDC (n=53) groups based on lung le-sions such as interstitial pneumonia, suppurative pneumonia, and pleuropneumonia. The immune cell population of bronchoalveolar lavage cells (BALc) was evaluated on 14 and 28 days post infection (dpi) and PMBC cytokine expression was measured on 0, 3, 7, 14 dpi to investigate early inflammatory re-actions. Pulmonary lesion severity was negatively correlated with alveolar macrophage (AM) in both PRRS and PRDC groups on 14 and 28 dpi. AM in BALc was less populated in PRDC group on 28 dpi compared to PRRS group. AM in BALc was significantly less populated in PRDC group on 28 dpi compared to 14 dpi. In addition, cytotoxic T lymphocyte (CTL) in BALc was higher populated in PRDC group on 14 dpi and 28 dpi compared to PRRS group. In the case of PBMC cytokine TNF-, IFN-, IL-1, IFN-, FoxP3, and IL-2, the PRRS group showed higher expression than the PRDC group on 7 dpi, 14 dpi, 7 dpi, 14 dpi, 14 dpi, and 14 dpi, respectively. On the other hand, in the case of IFN-, IL-6, IL-8, IL-4, and IL-17, the PRDC group showed higher PBMC cytokine expression at 14 dpi, 7 dpi, 14 dpi, 3 dpi, and 3 dpi, respectively, than the PRRS group. Based on these results, our study could characterize differential immune responses in pigs with PRRS or PRDC.
참고문헌 (32)
- Albina, E, "Epidemiology of porcine reproductive and respiratory syndrome (PRRS): An overview", Vet. Microbiol, 55(1), pp.309~316 (1997)
- Bacha Jr W. J., "Color atlas of veterinary histology", pp.3~10 (2012), John Wiley & Sons, Inc
- Choi C., "Expression of Inflammatory Cytokines in Pigs Experimentally Infected with Mycoplasma hyopneumoniae", J. Comp. Pathol, 134(1), pp.40~46 (2006)
- Choi Y. K., "Retrospective analysis of etiologic agents associated with respiratory diseases in pigs", The Canadian veterinary journal, 44(9), pp.735~ (2003)
- Darwich L., "Immunology of porcine circovirus type 2 (PCV2)", Virus Res, 164(1-2), pp.61~67 (2012)
- Darwich L., "Genetic and immunobiological diversities of porcine reproductive and respiratory syndrome genotype I strains", Vet. Microbiol, 150(1), pp.49~62 (2011)
- Garcia-Morante B., "Assessment of Mycoplasma hyopneumoniae-induced pneumonia using different lung lesion scoring systems: a comparative review", J. Comp. Pathol, 154(2-3), pp.125~134 (2016)
- Gómez-Laguna, J., "Acute phase response in porcine reproductive and respiratory syndrome virus infection", Comp. Immunol. Microbiol. Infect. Dis, 33(6), pp.e51~e58 (2010)
- Gómez-Laguna J., "Cytokine Expression by Macrophages in the Lung of Pigs Infected with the Porcine Reproductive and Respiratory Syndrome Virus", J. Comp. Pathol, 142(1), pp.51~60 (2010)
- Halbur P. G., "Comparison of the pathogenicity of two US porcine reproductive and respiratory syndrome virus isolates with that of the Lelystad virus", Vet. Pathol, 32(6), pp.648~660 (1995)
- Han K., "Comparison of the virulence of European and North American genotypes of porcine reproductive and respiratory syndrome virus in experimentally infected pigs", The Veterinary Journal, 195(3), pp.313~318 (2013)
- Hansen M. S., "An Investigation of the Pathology and Pathogens Associated with Porcine Respiratory Disease Complex in Denmark", J. Comp. Pathol, 143(2), pp.120~131 (2010)
- Jensen, H. E., "Necropsy: a handbook and atlas", pp.83~103 (2011), Samfundslitteratur
- Kang H., "Geographic distribution and molecular analysis of porcine reproductive and respiratory syndrome viruses circulating in swine farms in the Republic of Korea between 2013 and 2016", BMC Vet. Res, 14(1), pp.160~ (2018)
- Lee, S.-M., "Porcine reproductive and respiratory syndrome virus field isolates differ in in vitro interferon phenotypes", Vet. Immunol. Immunopathol, 102(3), pp.217~231 (2004)
- Loving C. L., "Innate and adaptive immunity against Porcine Reproductive and Respiratory Syndrome Virus", Vet. Immunol. Immunopathol, 167(1), pp.1~14 (2015)
- Loving C. L., "Differential type I interferon activation and susceptibility of dendritic cell populations to porcine arterivirus", Immunology, 120(2), pp.217~229 (2007)
- Lunney J. K., "Porcine reproductive and respiratory syndrome virus(PRRSV) : pathogenesis and interaction with the immune system", Annual review of animal biosciences, 4, pp.129~154 (2016)
- Mateu E., "The challenge of PRRS immunology", The Veterinary Journal, 177(3), pp.345~351 (2008)
- Opriessnig T., "Polymicrobial respiratory disease in pigs", Anim. Health Res. Rev, 12(2), pp.133~148 (2011)
- Palzer A., "Associations between pathogens in healthy pigs and pigs with pneumonia", Vet. Rec, 162(9), pp.267~271 (2008)
- Shi M., "Phylogeny-based evolutionary, demographical, and geographical dissection of North American type 2 porcine reproductive and respiratory syndrome viruses", J. Virol, 84(17), pp.8700~8711 (2010)
- Summerfield, A., "The porcine dendritic cell family", Dev. Comp. Immunol, 33(3), pp.299~309 (2009)
- Sun, Y., "Interplay between interferon-mediated innate immunity and porcine reproductive and respiratory syndrome virus", Viruses, 4(4), pp.424~446 (2012)
- Thacker, E. L., "Immunology of the Porcine Respiratory Disease Complex", Vet. Clin. North Am. Food Anim. Pract, 17(3), pp.551~565 (2001)
- Thanawongnuwech, R., "Increased Production of Proinflammatory Cytokines following Infection with Porcine Reproductive and Respiratory Syndrome Virus and Mycoplasma hyopneumoniae", Clin. Vaccine Immunol, 11(5), pp.901~908 (2004)
- Van Gucht, S., "The combination of PRRS virus and bacterial endotoxin as a model for multifactorial respiratory disease in pigs", Vet. Immunol. Immunopathol, 102(3), pp.165~178 (2004)
- Van Gucht, S., "Interaction between porcine reproductive-respiratory syndrome virus and bacterial endotoxin in the lungs of pigs: potentiation of cytokine production and respiratory disease", J. Clin. Microbiol, 41(3), pp.960~966 (2003)
- Winer, J., "Development and validation of real-time quantitative reverse transcriptase–polymerase chain reaction for monitoring gene expression in cardiac myocytes in vitro", Anal. Biochem, 270(1), pp.41~49 (1999)
- Yoon, K.-J., "Characterization of the humoral immune response to porcine reproductive and respiratory syndrome (PRRS) virus infection", J. Vet. Diagn. Invest, 7(3), pp.305~312 (1995)
- Zachary, J. F., "Pathologic Basis of Veterinary Disease", pp.329~ (2012), Elsevier Mosby
- Zimmerman, J. J., "Diseases of Swine", pp.685~708 (2019), John Wiley & Sons, Inc
