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. 2011 Nov 17:4:501.
doi: 10.1186/1756-0500-4-501.

Studies of the transmissibility of the agent of bovine spongiform encephalopathy to the domestic chicken

Affiliations

Studies of the transmissibility of the agent of bovine spongiform encephalopathy to the domestic chicken

Jo Moore et al. BMC Res Notes. .

Abstract

Background: Transmission of the prion disease bovine spongiform encephalopathy (BSE) occurred accidentally to cattle and several other mammalian species via feed supplemented with meat and bone meal contaminated with infected bovine tissue. Prior to United Kingdom controls in 1996 on the feeding of mammalian meat and bone meal to farmed animals, the domestic chicken was potentially exposed to feed contaminated with the causal agent of BSE. Although confirmed prion diseases are unrecorded in avian species a study was undertaken to transmit BSE to the domestic chicken by parenteral and oral inoculations. Transmissibility was assessed by clinical monitoring, histopathological examinations, detection of a putative disease form of an avian prion protein (PrP) in recipient tissues and by mouse bioassay of tissues. Occurrence of a progressive neurological syndrome in the primary transmission study was investigated by sub-passage experiments.

Results: No clinical, pathological or bioassay evidence of transmission of BSE to the chicken was obtained in the primary or sub-passage experiments. Survival data showed no significant differences between control and treatment groups. Neurological signs observed, not previously described in the domestic chicken, were not associated with significant pathology. The diagnostic techniques applied failed to detect a disease associated form of PrP.

Conclusion: Important from a risk assessment perspective, the present study has established that the domestic chicken does not develop a prion disease after large parenteral exposures to the BSE agent or after oral exposures equivalent to previous exposures via commercial diets. Future investigations into the potential susceptibility of avian species to mammalian prion diseases require species-specific immunochemical techniques and more refined experimental models.

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Figures

Figure 1
Figure 1
Kaplan-Meier survival data for primary exposure study. Survival data is shown for chickens challenged with BSE parenterally (orange), orally (blue) and the saline-challenged control group (black).
Figure 2
Figure 2
Kaplan-Meier survival data for sub-passage study. Survival data is shown for chickens challenged intracranially with inoculum made from parenterally (orange), orally (blue) BSE-challenged chickens exhibiting the neurological syndrome, from clinically normal saline-challenged control chickens (black) of the primary exposure study and a separate intracranially saline-challenged control group (grey).

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