Lipoteichoic acid from Staphylococcus aureus exacerbates respiratory disease in porcine respiratory coronavirus-infected pigs
- PMID: 20409735
- PMCID: PMC2932768
- DOI: 10.1016/j.tvjl.2010.03.001
Lipoteichoic acid from Staphylococcus aureus exacerbates respiratory disease in porcine respiratory coronavirus-infected pigs
Abstract
The objective of this study was to assess if lipoteichoic acid (LTA), produced by Staphylococcus aureus, exacerbates respiratory disease in porcine respiratory coronavirus (PRCV)-infected pigs, as has previously been shown with lipopolysaccharide. Piglets were inoculated with PRCV and 24h later with S. aureus LTA. Clinical signs, lung virus titres, inflammatory cells and cytokines in bronchoalveolar lavage fluid (BALF) were compared with those of animals in PRCV- and LTA-inoculated control groups. All PRCV-LTA-inoculated pigs except one developed severe respiratory disease, whereas clinical signs in the control groups were minimal or absent. Virus titres and grossly visible pulmonary lesions were similar in the PRCV-LTA- and PRCV-inoculated groups and were not detected in the LTA group. Neutrophil percentages in BALF were higher in the PRCV-LTA than in the PRCV group. There was no significant difference in interferon (IFN)-γ, interleukin (IL)-1, IL-6, IL-12/IL-23 and tumour necrosis factor (TNF)-α concentrations in BALF between the PRCV-LTA and PRCV groups, but levels of IL-6, IL-12/IL-23 and IFN-γ were higher in the PRCV-LTA-inoculated than in the LTA-inoculated controls. The findings suggest that the experimentally-induced respiratory disease was not mediated by cytokine over-production, but rather reflected the concerted action of particular cytokine interactions and/or as yet unidentified mediators. This is the first in vivo study to report the synergistic interaction between a virus and LTA in enhancing the severity of respiratory disease in the pig. Given that Gram-positive bacteria, capable of producing LTA, are commonly found in pig accommodation, the role of this compound in the development of the porcine respiratory disease complex requires further investigation.
Copyright © 2010 Elsevier Ltd. All rights reserved.
Figures
Similar articles
-
A potential role for tumour necrosis factor-alpha in synergy between porcine respiratory coronavirus and bacterial lipopolysaccharide in the induction of respiratory disease in pigs.J Med Microbiol. 2000 Jul;49(7):613-620. doi: 10.1099/0022-1317-49-7-613. J Med Microbiol. 2000. PMID: 10882086
-
Altered pathogenesis of porcine respiratory coronavirus in pigs due to immunosuppressive effects of dexamethasone: implications for corticosteroid use in treatment of severe acute respiratory syndrome coronavirus.J Virol. 2007 Dec;81(24):13681-93. doi: 10.1128/JVI.01702-07. Epub 2007 Oct 17. J Virol. 2007. PMID: 17942563 Free PMC article.
-
Coinfection of pigs with porcine respiratory coronavirus and Bordetella bronchiseptica.Vet Microbiol. 2008 Apr 1;128(1-2):36-47. doi: 10.1016/j.vetmic.2007.09.025. Epub 2007 Oct 12. Vet Microbiol. 2008. PMID: 18022332 Free PMC article.
-
Proinflammatory cytokines and viral respiratory disease in pigs.Vet Res. 2000 Mar-Apr;31(2):187-213. doi: 10.1051/vetres:2000113. Vet Res. 2000. PMID: 10779199 Review.
-
In vivo studies on cytokine involvement during acute viral respiratory disease of swine: troublesome but rewarding.Vet Immunol Immunopathol. 2002 Sep 10;87(3-4):161-8. doi: 10.1016/s0165-2427(02)00047-8. Vet Immunol Immunopathol. 2002. PMID: 12072230 Free PMC article. Review.
Cited by
-
Staphylococcus aureus colonization and non-influenza respiratory viruses: Interactions and synergism mechanisms.Virulence. 2018;9(1):1354-1363. doi: 10.1080/21505594.2018.1504561. Virulence. 2018. PMID: 30058450 Free PMC article. Review.
-
Prior infection of pigs with a recent human H3N2 influenza virus confers minimal cross-protection against a European swine H3N2 virus.Influenza Other Respir Viruses. 2013 Nov;7(6):1260-8. doi: 10.1111/irv.12105. Epub 2013 Mar 29. Influenza Other Respir Viruses. 2013. PMID: 23551882 Free PMC article.
-
Comparative Pathogenesis of Bovine and Porcine Respiratory Coronaviruses in the Animal Host Species and SARS-CoV-2 in Humans.J Clin Microbiol. 2020 Jul 23;58(8):e01355-20. doi: 10.1128/JCM.01355-20. Print 2020 Jul 23. J Clin Microbiol. 2020. PMID: 32522830 Free PMC article. Review.
-
Intestinal microbiota and chronic constipation.Springerplus. 2016 Jul 19;5(1):1130. doi: 10.1186/s40064-016-2821-1. eCollection 2016. Springerplus. 2016. PMID: 27478747 Free PMC article. Review.
-
Effect of LPS and LTA stimulation on the expression of TLR-pathway genes in PBMCs of Akkaraman lambs in vivo.Trop Anim Health Prod. 2021 Jan 3;53(1):65. doi: 10.1007/s11250-020-02491-4. Trop Anim Health Prod. 2021. PMID: 33392825 Free PMC article.
References
-
- Atanasova K., Van Gucht S., Barbé F., Lefebvre D., Chiers K., Van Reeth K. Lung cell tropism and inflammatory cytokine-profile of porcine respiratory coronavirus infection. Open Veterinary Science Journal. 2008;2:117–126.
-
- Bastos K., Marinho C., Barboza R., Russo M., Alvarez J., D’Imperio Lima M. What kind of message does IL-12/IL-23 bring to macrophages and dendritic cells? Microbes and Infection. 2004;6:630–636. - PubMed
-
- Brockmeier S., Halbur P., Thacker E. Porcine respiratory disease complex. In: Brogden K., Guthmiller J., editors. Polymicrobial Diseases. American Society for Microbiology; Washington, DC: 2002. pp. 231–258.
-
- Christensen G., Sorensen V., Mousing J. Diseases of the respiratory system. In: Straw B., D’Allaire S., Mengeling W., Taylor D., editors. Diseases of Swine. Iowa State University Press; Ames, Iowa, USA: 1999. pp. 913–940.
-
- Crook B., Robertson J., Glass S., Botheroyd E., Lacey J., Topping M. Airborne dust, ammonia, microorganisms, and antigens in pig confinement houses and the respiratory health of exposed farm workers. American Industrial Hygiene Association Journal. 1991;52:271–279. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
