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Updated: May 18, 2026

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Assessing Transmissible Spongiform Encephalopathy Species Barriers with an In Vitro Prion Protein Conversion Assay
Published on: March 10, 2015
Prion search and cellular prion protein expression in stranded dolphins
Journal of Biological Regulators and Homeostatic Agents
|October 5, 2012
Summary
Researchers investigated prion disease (PD) in stranded dolphins along the Italian coast. While no definitive PrPSc was found, the study highlights concerns for prion biology and cetacean health.
Area of Science:
- Veterinary Neurology
- Marine Mammal Medicine
- Prion Disease Research
Background:
- A recent prion disease (PD) case in a bottlenose dolphin prompted an investigation into prion protein (PrPSc) presence in stranded cetaceans.
- The study examined brain and lymphoid tissues from striped, bottlenose, and Risso's dolphins stranded between 2007-2012.
Discussion:
- Microscopic encephalitis lesions were found in some dolphins, but no spongiform changes indicative of PD.
- Cellular prion protein (PrPC) was immunoreactive in the brain and lymphoid tissues of the examined dolphins.
- Immunohistochemistry and Western blot analyses did not detect PrPSc deposition, ruling out active prion disease in this cohort.
Key Insights:
- Despite negative PrPSc findings, the occurrence of PD in a wild dolphin remains a significant concern.
- The presence of PrPC in cetacean tissues warrants further investigation into prion biology.
- This study underscores the importance of monitoring marine mammals for emerging infectious diseases.
Outlook:
- Further research is needed to understand the potential for prion transmission within and between cetacean species.
- Continued surveillance of stranded marine mammals is crucial for early detection of diseases like PD.
- Findings contribute to cetacean conservation medicine and the broader understanding of prion diseases in wildlife.

