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A field-deployable diagnostic assay for the visual detection of misfolded prions

Diagnostic tools for the detection of protein-misfolding diseases (i.e., proteopathies) are limited. Gold nanoparticles (AuNPs) facilitate sensitive diagnostic techniques via visual color change for the identification of a variety of targets. In parallel, recently developed quaking-induced conversio...

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Autores principales: Christenson, Peter R., Li, Manci, Rowden, Gage, Schwabenlander, Marc D., Wolf, Tiffany M., Oh, Sang-Hyun, Larsen, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293997/
https://www.ncbi.nlm.nih.gov/pubmed/35851406
http://dx.doi.org/10.1038/s41598-022-16323-y
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author Christenson, Peter R.
Li, Manci
Rowden, Gage
Schwabenlander, Marc D.
Wolf, Tiffany M.
Oh, Sang-Hyun
Larsen, Peter A.
author_facet Christenson, Peter R.
Li, Manci
Rowden, Gage
Schwabenlander, Marc D.
Wolf, Tiffany M.
Oh, Sang-Hyun
Larsen, Peter A.
author_sort Christenson, Peter R.
collection PubMed
description Diagnostic tools for the detection of protein-misfolding diseases (i.e., proteopathies) are limited. Gold nanoparticles (AuNPs) facilitate sensitive diagnostic techniques via visual color change for the identification of a variety of targets. In parallel, recently developed quaking-induced conversion (QuIC) assays leverage protein-amplification and fluorescent signaling for the accurate detection of misfolded proteins. Here, we combine AuNP and QuIC technologies for the visual detection of amplified misfolded prion proteins from tissues of wild white-tailed deer infected with chronic wasting disease (CWD), a prion disease of cervids. Our newly developed assay, MN-QuIC, enables both naked-eye and light-absorbance measurements for detection of misfolded prions. MN-QuIC leverages basic laboratory equipment that is cost-effective and portable, thus facilitating real-time prion diagnostics across a variety of settings. In addition to laboratory-based tests, we deployed to a rural field-station in southeastern Minnesota and tested for CWD on site. We successfully demonstrated that MN-QuIC is functional in a non-traditional laboratory setting by performing a blinded analysis in the field and correctly identifying all CWD positive and CWD not-detected deer at the field site in 24 h, thus documenting the portability of the assay. White-tailed deer tissues used to validate MN-QuIC included medial retropharyngeal lymph nodes, parotid lymph nodes, and palatine tonsils. Importantly, all of the white-tailed deer (n = 63) were independently tested using ELISA, IHC, and/or RT-QuIC technologies and results secured with MN-QuIC were 95.7% and 100% consistent with these tests for positive and non-detected animals, respectively. We hypothesize that electrostatic forces help govern the AuNP/prion interactions and conclude that MN-QuIC has great potential for sensitive, field-deployable diagnostics for CWD, with future potential diagnostic applications for a variety of proteopathies.
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spelling pubmed-92939972022-07-20 A field-deployable diagnostic assay for the visual detection of misfolded prions Christenson, Peter R. Li, Manci Rowden, Gage Schwabenlander, Marc D. Wolf, Tiffany M. Oh, Sang-Hyun Larsen, Peter A. Sci Rep Article Diagnostic tools for the detection of protein-misfolding diseases (i.e., proteopathies) are limited. Gold nanoparticles (AuNPs) facilitate sensitive diagnostic techniques via visual color change for the identification of a variety of targets. In parallel, recently developed quaking-induced conversion (QuIC) assays leverage protein-amplification and fluorescent signaling for the accurate detection of misfolded proteins. Here, we combine AuNP and QuIC technologies for the visual detection of amplified misfolded prion proteins from tissues of wild white-tailed deer infected with chronic wasting disease (CWD), a prion disease of cervids. Our newly developed assay, MN-QuIC, enables both naked-eye and light-absorbance measurements for detection of misfolded prions. MN-QuIC leverages basic laboratory equipment that is cost-effective and portable, thus facilitating real-time prion diagnostics across a variety of settings. In addition to laboratory-based tests, we deployed to a rural field-station in southeastern Minnesota and tested for CWD on site. We successfully demonstrated that MN-QuIC is functional in a non-traditional laboratory setting by performing a blinded analysis in the field and correctly identifying all CWD positive and CWD not-detected deer at the field site in 24 h, thus documenting the portability of the assay. White-tailed deer tissues used to validate MN-QuIC included medial retropharyngeal lymph nodes, parotid lymph nodes, and palatine tonsils. Importantly, all of the white-tailed deer (n = 63) were independently tested using ELISA, IHC, and/or RT-QuIC technologies and results secured with MN-QuIC were 95.7% and 100% consistent with these tests for positive and non-detected animals, respectively. We hypothesize that electrostatic forces help govern the AuNP/prion interactions and conclude that MN-QuIC has great potential for sensitive, field-deployable diagnostics for CWD, with future potential diagnostic applications for a variety of proteopathies. Nature Publishing Group UK 2022-07-18 /pmc/articles/PMC9293997/ /pubmed/35851406 http://dx.doi.org/10.1038/s41598-022-16323-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Christenson, Peter R.
Li, Manci
Rowden, Gage
Schwabenlander, Marc D.
Wolf, Tiffany M.
Oh, Sang-Hyun
Larsen, Peter A.
A field-deployable diagnostic assay for the visual detection of misfolded prions
title A field-deployable diagnostic assay for the visual detection of misfolded prions
title_full A field-deployable diagnostic assay for the visual detection of misfolded prions
title_fullStr A field-deployable diagnostic assay for the visual detection of misfolded prions
title_full_unstemmed A field-deployable diagnostic assay for the visual detection of misfolded prions
title_short A field-deployable diagnostic assay for the visual detection of misfolded prions
title_sort field-deployable diagnostic assay for the visual detection of misfolded prions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293997/
https://www.ncbi.nlm.nih.gov/pubmed/35851406
http://dx.doi.org/10.1038/s41598-022-16323-y
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