Research article

Transmissibility studies of vacuolar changes in the rostral colliculus of pigs

Timm Konold^1,2 , John Spiropoulos¹ , Melanie J Chaplin³ , Leigh Thorne³ , Yvonne I Spencer¹ , Gerald AH Wells¹ and Steve AC Hawkins¹

¹  Department of Pathology, Veterinary Laboratories Agency Weybridge, Woodham Lane, Addlestone, UK

²  Royal Veterinary College, Infection and Immunity Research Group, North Mymms, Hatfield, UK

³  Department of Molecular Pathogenesis and Genetics, Veterinary Laboratories Agency Weybridge, Woodham Lane, Addlestone, UK

author email corresponding author email

BMC Veterinary Research 2009, 5:35doi:10.1186/1746-6148-5-35

Published:	18 September 2009

Abstract

Background

Histopathological examinations of brains from healthy pigs have revealed localised vacuolar changes, predominantly in the rostral colliculus, that are similar to the neuropil vacuolation featured in the transmissible spongiform encephalopathies and have been described in pigs challenged parenterally with the agent causing bovine spongiform encephalopathy (BSE). Feedstuff containing BSE-contaminated meat and bone meal (MBM) may have been fed to pigs prior to the ban of mammalian MBM in feed of farmed livestock in the United Kingdom in 1996, but there is no evidence of the natural occurrence of a transmissible spongiform encephalopathy (TSE) in the domestic pig. Furthermore, experimental transmission of BSE to pigs by the oral route has been unsuccessful. A study was conducted to investigate whether the localised vacuolar changes in the porcine brain were associated with a transmissible aetiology and therefore biologically significant. Two groups of ten pigs were inoculated parenterally with vacuolated rostral colliculus from healthy pigs either born before 1996 or born after 1996. Controls included ten pigs similarly inoculated with rostral colliculus from New Zealand-derived pigs and nine pigs inoculated with a bovine BSE brain homogenate.

Results

None of the pigs inoculated with rostral colliculus developed a TSE-like neurological disease up to five years post inoculation when the study was terminated, and disease-associated prion protein, PrP^d, was not detected in the brains of these pigs. By contrast, eight of nine BSE-inoculated pigs developed neurological signs, two of which had detectable PrP^d by postmortem tests. No significant histopathological changes were detected to account for the clinical signs in the PrP^d-negative, BSE-inoculated pigs.

Conclusion

The findings in this study suggest that vacuolation in the porcine rostral colliculus is not caused by a transmissible agent and is probably a clinically insignificant change. The presence of neurological signs in pigs inoculated with BSE without detectable PrP^d raises the possibility that the BSE agent may produce a prion disease in pigs that remains undetected by the current postmortem tests.