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Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells

In our previous study, we demonstrated the propagation of mouse-passaged scrapie isolates with long incubation periods (L-type) derived from natural Japanese sheep scrapie cases in murine hypothalamic GT1-7 cells, along with disease-associated prion protein (PrP(Sc)) accumulation. We here analyzed t...

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Autores principales: Miyazawa, Kohtaro, Masujin, Kentaro, Okada, Hiroyuki, Ushiki-Kaku, Yuko, Matsuura, Yuichi, Yokoyama, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479544/
https://www.ncbi.nlm.nih.gov/pubmed/28636656
http://dx.doi.org/10.1371/journal.pone.0179317
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author Miyazawa, Kohtaro
Masujin, Kentaro
Okada, Hiroyuki
Ushiki-Kaku, Yuko
Matsuura, Yuichi
Yokoyama, Takashi
author_facet Miyazawa, Kohtaro
Masujin, Kentaro
Okada, Hiroyuki
Ushiki-Kaku, Yuko
Matsuura, Yuichi
Yokoyama, Takashi
author_sort Miyazawa, Kohtaro
collection PubMed
description In our previous study, we demonstrated the propagation of mouse-passaged scrapie isolates with long incubation periods (L-type) derived from natural Japanese sheep scrapie cases in murine hypothalamic GT1-7 cells, along with disease-associated prion protein (PrP(Sc)) accumulation. We here analyzed the susceptibility of GT1-7 cells to scrapie prions by exposure to infected mouse brains at different passages, following interspecies transmission. Wild-type mice challenged with a natural sheep scrapie case (Kanagawa) exhibited heterogeneity of transmitted scrapie prions in early passages, and this mixed population converged upon one with a short incubation period (S-type) following subsequent passages. However, when GT1-7 cells were challenged with these heterologous samples, L-type prions became dominant. This study demonstrated that the susceptibility of GT1-7 cells to L-type prions was at least 10(5) times higher than that to S-type prions and that L-type prion-specific biological characteristics remained unchanged after serial passages in GT1-7 cells. This suggests that a GT1-7 cell culture model would be more useful for the economical and stable amplification of L-type prions at the laboratory level. Furthermore, this cell culture model might be used to selectively propagate L-type scrapie prions from a mixed prion population.
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spelling pubmed-54795442017-07-05 Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells Miyazawa, Kohtaro Masujin, Kentaro Okada, Hiroyuki Ushiki-Kaku, Yuko Matsuura, Yuichi Yokoyama, Takashi PLoS One Research Article In our previous study, we demonstrated the propagation of mouse-passaged scrapie isolates with long incubation periods (L-type) derived from natural Japanese sheep scrapie cases in murine hypothalamic GT1-7 cells, along with disease-associated prion protein (PrP(Sc)) accumulation. We here analyzed the susceptibility of GT1-7 cells to scrapie prions by exposure to infected mouse brains at different passages, following interspecies transmission. Wild-type mice challenged with a natural sheep scrapie case (Kanagawa) exhibited heterogeneity of transmitted scrapie prions in early passages, and this mixed population converged upon one with a short incubation period (S-type) following subsequent passages. However, when GT1-7 cells were challenged with these heterologous samples, L-type prions became dominant. This study demonstrated that the susceptibility of GT1-7 cells to L-type prions was at least 10(5) times higher than that to S-type prions and that L-type prion-specific biological characteristics remained unchanged after serial passages in GT1-7 cells. This suggests that a GT1-7 cell culture model would be more useful for the economical and stable amplification of L-type prions at the laboratory level. Furthermore, this cell culture model might be used to selectively propagate L-type scrapie prions from a mixed prion population. Public Library of Science 2017-06-21 /pmc/articles/PMC5479544/ /pubmed/28636656 http://dx.doi.org/10.1371/journal.pone.0179317 Text en © 2017 Miyazawa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Miyazawa, Kohtaro
Masujin, Kentaro
Okada, Hiroyuki
Ushiki-Kaku, Yuko
Matsuura, Yuichi
Yokoyama, Takashi
Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells
title Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells
title_full Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells
title_fullStr Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells
title_full_unstemmed Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells
title_short Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells
title_sort selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using gt1-7 cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479544/
https://www.ncbi.nlm.nih.gov/pubmed/28636656
http://dx.doi.org/10.1371/journal.pone.0179317
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