Differential production of proinflammatory cytokines in the pig lung during different respiratory virus infections: correlations with pathogenicity

Res Vet Sci. 1999 Aug;67(1):47-52. doi: 10.1053/rvsc.1998.0277.

Abstract

The acute stages of infection with swine influenza virus (SIV), porcine respiratory coronavirus (PRCV) and porcine reproductive-respiratory syndrome virus (PRRSV) were shown to differ in terms of clinical and lung inflammatory effects and proinflammatory cytokine profiles in bronchoalveolar lavage (BAL) fluids. Caesarian-derived colostrum-deprived pigs were inoculated intratracheally with one of the three viruses. SIV infection was followed within 1 day post inoculation (d PI) by characteristic respiratory and general signs, and excessive lung epithelial desquamation and neutrophil infiltration (38 to 56 per cent of BAL cells at 1 d PI vs 0 to 1 per cent in controls). High concentrations of bioactive interferon-alpha (IFN -alpha), tumour necrosis factor-alpha (TNF -alpha) and interleukin-1 (IL -1) coincided with peak symptoms and neutrophil infiltration. PRCV infection was asymptomatic and produced a mild bronchointerstitial pneumonitis and neutrophil infiltration (13 to 22 per cent of BAL cells at 4 d PI). IFN -alpha titres parallelled those found during SIV infection, TNF -alpha was negligible and IL -1 undetectable. PRRSV infection induced anorexia and lethargy between 3 and 5 d PI. There was marked infiltration with mononuclear cells in alveolar septa and BAL fluids between 7 and 10 d PI, while neutrophils remained at less than 11 per cent of BAL cells at any time. IL -1 was produced from three throughout 10 d PI, while IFN -alpha production was minimal and TNF -alpha undetectable. These data strongly suggest that proinflammatory cytokines can be important mediators of viral respiratory disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bronchoalveolar Lavage Fluid
  • Coronavirus / pathogenicity
  • Coronavirus / physiology
  • Coronavirus Infections / metabolism
  • Coronavirus Infections / veterinary*
  • Coronavirus Infections / virology
  • Cytokines / biosynthesis*
  • Influenza A virus / pathogenicity
  • Influenza A virus / physiology
  • Lung / metabolism
  • Lung / virology*
  • Orthomyxoviridae Infections / metabolism
  • Orthomyxoviridae Infections / veterinary*
  • Orthomyxoviridae Infections / virology
  • Porcine Reproductive and Respiratory Syndrome / metabolism*
  • Porcine respiratory and reproductive syndrome virus / pathogenicity
  • Porcine respiratory and reproductive syndrome virus / physiology
  • Swine
  • Swine Diseases / metabolism*
  • Swine Diseases / virology*
  • Virus Replication

Substances

  • Cytokines