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Subclinical bovine spongiform encephalopathy infection in transgenic mice expressing porcine prion protein

The Journal of Neuroscience : the official Journal of the Society for Neuroscience publica este artículo de investigación

26 de mayo de 2004

The bovine-porcine species barrier to bovine spongiform encephalopathy (BSE) infection was explored by generating transgenic mouse lines expressing the porcine prion protein (PrP) gene. All of the porcine transgenic (poTg) mice showed clinical signs of BSE after intracerebral inoculation with a high-titer BSE inoculum. The protease-resistant PrP (PrP(res)) was detected in 14% (3 of 22) of the BSE-infected poTg mice by immunohistochemical or immunoblot analysis. Despite being able to infect 42% (5 of 12) of control mice, a low-dose BSE inoculum failed to penetrate the species barrier in our poTg mouse model. The findings of these infectivity studies suggest that there is a strong species barrier between cows and pigs. However, after second-passage infection of poTg mice using brain homogenates of BSE-inoculated mice scoring negative for the incoming prion protein as inoculum, it was possible to detect the presence of the infectious agent. Thus, porcine-adapted BSE inocula were efficient at infecting poTg mice, giving rise to an incubation period substantially reduced from 300 to 177 d after inoculation and to the presence of PrP(res) in 100% (21 of 21) of the mice. We were therefore able to conclude that initial exposure to the bovine prion may lead to subclinical infection such that brain homogenates from poTg mice classified as uninfected on the basis of the absence of PrP(res) are infectious when used to reinoculate poTg mice. Collectively, our findings suggest that these poTg mice could be used as a sensitive bioassay model for prion detection in pigs




Castilla J., Gutierrez-Adan A., Brun A., Doyle D., Pintado B., Ramirez MA., Salguero FJ., Parra B., Segundo FD., Sanchez-Vizcaino JM., Rogers M. y Torres JM.




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Subclinical bovine spongiform encephalopathy infection in transgenic mice expressing porcine prion protein

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Subclinical bovine spongiform encephalopathy infection in transgenic mice expressing porcine prion protein



Participantes:

Universidad ComplutenseDepartamento de Sanidad Animal. Facultad de Veterinaria. Universidad Complutense (UCM).

Universidad ComplutenseServicio de Inmunología Viral y Medicina Preventiva (SUAT). Centro de Vigilancia Sanitaria Veterinaria (VISAVET). Universidad Complutense (UCM).

Instituto Nacional de Investigación y Tecnología Agraria y AlimentariaCentro de Investigación en Sanidad Animal (CISA). Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA).

Instituto Nacional de Investigación y Tecnología Agraria y AlimentariaDepartamento de Reproducción Animal y Conservación de Recursos Zoogenéticos. Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA).

University College DublinUCD Conway Institute of Biomolecular & Biomedical Research. University College Dublin (UCD).

University College DublinDepartment of Zoology. University College Dublin (UCD).







FACTOR YEAR Q
7.907 2004

NLMID: 8102140

PMID: 15163699

ISSN: 0270-6474



TÍTULO: Subclinical bovine spongiform encephalopathy infection in transgenic mice expressing porcine prion protein


REVISTA: J Neurosci


NUMERACIÓN: 24(21):5063-9


AÑO: 2004


EDITORIAL: Society for Neuroscience


AUTORES: Castilla J., Gutierrez-Adan A., Brun A., Doyle D., Pintado B., Ramirez MA., Salguero FJ., Parra B., Segundo FD., Sanchez-Vizcaino JM., Rogers M. and Torres JM.


José Manuel Sánchez-Vizcaíno Rodríguez

DOI: https://doi.org/10.1523/JNEUROSCI.5400-03.2004


CITA ESTA PUBLICACIÓN:

Castilla J., Gutierrez-Adan A., Brun A., Doyle D., Pintado B., Ramirez MA., Salguero FJ., Parra B., Segundo FD., Sanchez-Vizcaino JM., Rogers M. y Torres JM. Subclinical bovine spongiform encephalopathy infection in transgenic mice expressing porcine prion protein. The Journal of Neuroscience : the official Journal of the Society for Neuroscience. 24(21):5063-9. 2004. (A). ISSN: 0270-6474. DOI: 10.1523/JNEUROSCI.5400-03.2004


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