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The Panel wishes to thank managers and members of the Gelatine Manufacturers of Europe (GME) for providing data and information, and to the EFSA staff member Jose Angel Gomez Ruiz for extracting and interpreting the data from the EFSA's food consumption database.

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BSE risk posed by ruminant collagen and gelatine derived from bones

Publicado en:Efsa Journal. 22 (7): e8883- - 2024-07-01 22(7), DOI: 10.2903/j.efsa.2024.8883

Autores: Koutsoumanis, K; Allende, A; Bolton, D; Bover-Cid, S; Chemaly, M; De Cesare, A; Herman, L; Hilbert, F; Lindqvist, R; Nauta, M; Nonno, R; Peixe, L; Ru, GSP; Simmons, M; Skandamis, P; Suffredini, E; Adkin, A; Andreoletti, O; Griffin, J; Lanfranchi, B; Ortiz-Pelaez, A; Ordonez, AA

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Resumen

The European Commission requested an estimation of the BSE risk (C-, L- and H-BSE) from gelatine and collagen derived from ovine, caprine or bovine bones, and produced in accordance with Regulation (EC) No 853/2004, or Regulation (EC) No 1069/2009 and its implementing Regulation (EU) No 142/2011. A quantitative risk assessment was developed to estimate the BSE infectivity, measured in cattle oral infectious dose 50 (CoID50), in a small size batch of gelatine including one BSE-infected bovine or ovine animal at the clinical stage. The model was built on a scenario where all ruminant bones could be used for the production of gelatine and high-infectivity tissues remained attached to the skull (brain) and vertebral column (spinal cord). The risk and exposure pathways defined for humans and animals, respectively, were identified. Exposure routes other than oral via food and feed were considered and discussed but not assessed quantitatively. Other aspects were also considered as integrating evidence, like the epidemiological situation of the disease, the species barrier, the susceptibility of species to BSE and the assumption of an exponential dose-response relationship to determine the probability of BSE infection in ruminants. Exposure to infectivity in humans cannot be directly translated to risk of disease because the transmission barrier has not yet been quantified, although it is considered to be substantial, i.e. much greater amounts of infectivity would be needed to successfully infect a human and greater in the oral than in the parenteral route of exposure. The probability that no new case of BSE in the cattle or small ruminant population would be generated through oral exposure to gelatine made of ruminant bones is 99%-100% (almost certain) This conclusion is based on the current state of knowledge, the epidemiological situation of the disease and the current practices, and is also valid for collagen.

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