» Articles » PMID: 17578924

Amyloidogenic Potential of Foie Gras

Overview
Specialty Science
Date 2007 Jun 21
PMID 17578924
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

The human cerebral and systemic amyloidoses and prion-associated spongiform encephalopathies are acquired or inherited protein folding disorders in which normally soluble proteins or peptides are converted into fibrillar aggregates. This is a nucleation-dependent process that can be initiated or accelerated by fibril seeds formed from homologous or heterologous amyloidogenic precursors that serve as an amyloid enhancing factor (AEF) and has pathogenic significance in that disease may be transmitted by oral ingestion or parenteral administration of these conformationally altered components. Except for infected brain tissue, specific dietary sources of AEF have not been identified. Here we report that commercially available duck- or goose-derived foie gras contains birefringent congophilic fibrillar material composed of serum amyloid A-related protein that acted as a potent AEF in a transgenic murine model of secondary (amyloid A protein) amyloidosis. When such mice were injected with or fed amyloid extracted from foie gras, the animals developed extensive systemic pathological deposits. These experimental data provide evidence that an amyloid-containing food product hastened the development of amyloid protein A amyloidosis in a susceptible population. On this basis, we posit that this and perhaps other forms of amyloidosis may be transmissible, akin to the infectious nature of prion-related illnesses.

Citing Articles

The Promising Role of Selenium and Yeast in the Fight Against Protein Amyloidosis.

Kieliszek M, Sapazhenkava K Biol Trace Elem Res. 2024; 203(3):1251-1268.

PMID: 38829477 PMC: 11872778. DOI: 10.1007/s12011-024-04245-x.


Deactivation of the Unfolded Protein Response Aggravated Renal AA Amyloidosis in HSF1 Deficiency Mice.

Liu W, Xia S, Yao F, Huo J, Qian J, Liu X Mol Cell Biol. 2024; 44(5):165-177.

PMID: 38758542 PMC: 11123510. DOI: 10.1080/10985549.2024.2347937.


The first report of polymorphisms of the prion protein gene () in Pekin ducks ().

Jeong M, Wang Z, Zou W, Kim Y, Jeong B Front Vet Sci. 2023; 10:1273050.

PMID: 38026621 PMC: 10664711. DOI: 10.3389/fvets.2023.1273050.


Health concerns about possible long-term effects of legally marketed milk and dairy from animals with intramammary infections.

Schadt I Front Public Health. 2023; 11:1200924.

PMID: 37701910 PMC: 10494540. DOI: 10.3389/fpubh.2023.1200924.


Food protein-derived amyloids do not accelerate amyloid β aggregation.

Rahman M, Sanches Pires R, Herneke A, Gowda V, Langton M, Biverstal H Sci Rep. 2023; 13(1):985.

PMID: 36720893 PMC: 9889329. DOI: 10.1038/s41598-023-28147-5.


References
1.
Murphy C, Eulitz M, Hrncic R, Sletten K, Westermark P, Williams T . Chemical typing of amyloid protein contained in formalin-fixed paraffin-embedded biopsy specimens. Am J Clin Pathol. 2001; 116(1):135-42. DOI: 10.1309/TWBM-8L4E-VK22-FRH5. View

2.
Korenaga T, Fu X, Xing Y, Matsusita T, Kuramoto K, Syumiya S . Tissue distribution, biochemical properties, and transmission of mouse type A AApoAII amyloid fibrils. Am J Pathol. 2004; 164(5):1597-606. PMC: 2222805. DOI: 10.1016/S0002-9440(10)63718-2. View

3.
Guo J, Aldrich C, Mason W, Pugh J . Characterization of serum amyloid A protein mRNA expression and secondary amyloidosis in the domestic duck. Proc Natl Acad Sci U S A. 1996; 93(25):14548-53. PMC: 26170. DOI: 10.1073/pnas.93.25.14548. View

4.
Korenaga T, Yan J, Sawashita J, Matsushita T, Naiki H, Hosokawa M . Transmission of amyloidosis in offspring of mice with AApoAII amyloidosis. Am J Pathol. 2006; 168(3):898-906. PMC: 1606535. DOI: 10.2353/ajpath.2006.050350. View

5.
McAdam K, Raynes J, Alpers M, Westermark G, Westermark P . Amyloidosis: a global problem common in Papua New Guinea. P N G Med J. 1996; 39(4):284-96. View