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Autoclave treatment fails to completely inactivate DLB alpha-synuclein seeding activity

Synucleinopathies are characterized by the deposition of alpha-synuclein (α-syn) aggregates in brain tissue. Pathological α-syn aggregates propagate in a prion-like manner and display prion-like biochemical properties. Using RT-QuIC, we measured α-syn seeding activity from brains of Dementia with Le...

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Autores principales: Han, Jung-Youn, Park, Kyung-Je, Park, Hoo-Chang, Lee, Yu-Ran, Moore, Roger A., Sohn, Hyun-Joo, Choi, Young Pyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009011/
https://www.ncbi.nlm.nih.gov/pubmed/36923008
http://dx.doi.org/10.1016/j.bbrep.2023.101446
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author Han, Jung-Youn
Park, Kyung-Je
Park, Hoo-Chang
Lee, Yu-Ran
Moore, Roger A.
Sohn, Hyun-Joo
Choi, Young Pyo
author_facet Han, Jung-Youn
Park, Kyung-Je
Park, Hoo-Chang
Lee, Yu-Ran
Moore, Roger A.
Sohn, Hyun-Joo
Choi, Young Pyo
author_sort Han, Jung-Youn
collection PubMed
description Synucleinopathies are characterized by the deposition of alpha-synuclein (α-syn) aggregates in brain tissue. Pathological α-syn aggregates propagate in a prion-like manner and display prion-like biochemical properties. Using RT-QuIC, we measured α-syn seeding activity from brains of Dementia with Lewy body (DLB) patients post autoclave. Here, we show that autoclaving at 121 °C removes one to two log(10) of α-syn seeding activity but the remaining 50% seeding dose (SD(50)) is more than 107/mg tissue. DLB brain samples autoclaved at 132 °C still revealed an SD(50) of approximately 106/mg tissue. Our data suggest that DLB α-syn seeds are incompletely inactivated by standard autoclave, thus highlighting the need for evaluating laboratory procedures that fully inactivate them.
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spelling pubmed-100090112023-03-14 Autoclave treatment fails to completely inactivate DLB alpha-synuclein seeding activity Han, Jung-Youn Park, Kyung-Je Park, Hoo-Chang Lee, Yu-Ran Moore, Roger A. Sohn, Hyun-Joo Choi, Young Pyo Biochem Biophys Rep Short Communication Synucleinopathies are characterized by the deposition of alpha-synuclein (α-syn) aggregates in brain tissue. Pathological α-syn aggregates propagate in a prion-like manner and display prion-like biochemical properties. Using RT-QuIC, we measured α-syn seeding activity from brains of Dementia with Lewy body (DLB) patients post autoclave. Here, we show that autoclaving at 121 °C removes one to two log(10) of α-syn seeding activity but the remaining 50% seeding dose (SD(50)) is more than 107/mg tissue. DLB brain samples autoclaved at 132 °C still revealed an SD(50) of approximately 106/mg tissue. Our data suggest that DLB α-syn seeds are incompletely inactivated by standard autoclave, thus highlighting the need for evaluating laboratory procedures that fully inactivate them. Elsevier 2023-03-03 /pmc/articles/PMC10009011/ /pubmed/36923008 http://dx.doi.org/10.1016/j.bbrep.2023.101446 Text en © 2023 Korea Brain Research Institute, Animal and Plant Quarantine Agency https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short Communication
Han, Jung-Youn
Park, Kyung-Je
Park, Hoo-Chang
Lee, Yu-Ran
Moore, Roger A.
Sohn, Hyun-Joo
Choi, Young Pyo
Autoclave treatment fails to completely inactivate DLB alpha-synuclein seeding activity
title Autoclave treatment fails to completely inactivate DLB alpha-synuclein seeding activity
title_full Autoclave treatment fails to completely inactivate DLB alpha-synuclein seeding activity
title_fullStr Autoclave treatment fails to completely inactivate DLB alpha-synuclein seeding activity
title_full_unstemmed Autoclave treatment fails to completely inactivate DLB alpha-synuclein seeding activity
title_short Autoclave treatment fails to completely inactivate DLB alpha-synuclein seeding activity
title_sort autoclave treatment fails to completely inactivate dlb alpha-synuclein seeding activity
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009011/
https://www.ncbi.nlm.nih.gov/pubmed/36923008
http://dx.doi.org/10.1016/j.bbrep.2023.101446
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