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Ticks harbor and excrete chronic wasting disease prions
Chronic wasting disease (CWD) is a fatal neurodegenerative disease caused by infectious prions (PrP(CWD)) affecting cervids. Circulating PrP(CWD) in blood may pose a risk for indirect transmission by way of hematophagous ectoparasites acting as mechanical vectors. Cervids can carry high tick infesta...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185559/ https://www.ncbi.nlm.nih.gov/pubmed/37188858 http://dx.doi.org/10.1038/s41598-023-34308-3 |
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author | Inzalaco, H. N. Bravo-Risi, F. Morales, R. Walsh, D. P. Storm, D. J. Pedersen, J. A. Turner, W. C. Lichtenberg, S. S. |
author_facet | Inzalaco, H. N. Bravo-Risi, F. Morales, R. Walsh, D. P. Storm, D. J. Pedersen, J. A. Turner, W. C. Lichtenberg, S. S. |
author_sort | Inzalaco, H. N. |
collection | PubMed |
description | Chronic wasting disease (CWD) is a fatal neurodegenerative disease caused by infectious prions (PrP(CWD)) affecting cervids. Circulating PrP(CWD) in blood may pose a risk for indirect transmission by way of hematophagous ectoparasites acting as mechanical vectors. Cervids can carry high tick infestations and exhibit allogrooming, a common tick defense strategy between conspecifics. Ingestion of ticks during allogrooming may expose naïve animals to CWD, if ticks harbor PrP(CWD). This study investigates whether ticks can harbor transmission-relevant quantities of PrP(CWD) by combining experimental tick feeding trials and evaluation of ticks from free-ranging white-tailed deer (Odocoileus virginianus). Using the real-time quaking-induced conversion (RT-QuIC) assay, we show that black-legged ticks (Ixodes scapularis) fed PrP(CWD)-spiked blood using artificial membranes ingest and excrete PrP(CWD). Combining results of RT-QuIC and protein misfolding cyclic amplification, we detected seeding activity from 6 of 15 (40%) pooled tick samples collected from wild CWD-infected white-tailed deer. Seeding activities in ticks were analogous to 10–1000 ng of CWD-positive retropharyngeal lymph node collected from deer upon which they were feeding. Estimates revealed a median infectious dose range of 0.3–42.4 per tick, suggesting that ticks can take up transmission-relevant amounts of PrP(CWD) and may pose a CWD risk to cervids. |
format | Online Article Text |
id | pubmed-10185559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101855592023-05-17 Ticks harbor and excrete chronic wasting disease prions Inzalaco, H. N. Bravo-Risi, F. Morales, R. Walsh, D. P. Storm, D. J. Pedersen, J. A. Turner, W. C. Lichtenberg, S. S. Sci Rep Article Chronic wasting disease (CWD) is a fatal neurodegenerative disease caused by infectious prions (PrP(CWD)) affecting cervids. Circulating PrP(CWD) in blood may pose a risk for indirect transmission by way of hematophagous ectoparasites acting as mechanical vectors. Cervids can carry high tick infestations and exhibit allogrooming, a common tick defense strategy between conspecifics. Ingestion of ticks during allogrooming may expose naïve animals to CWD, if ticks harbor PrP(CWD). This study investigates whether ticks can harbor transmission-relevant quantities of PrP(CWD) by combining experimental tick feeding trials and evaluation of ticks from free-ranging white-tailed deer (Odocoileus virginianus). Using the real-time quaking-induced conversion (RT-QuIC) assay, we show that black-legged ticks (Ixodes scapularis) fed PrP(CWD)-spiked blood using artificial membranes ingest and excrete PrP(CWD). Combining results of RT-QuIC and protein misfolding cyclic amplification, we detected seeding activity from 6 of 15 (40%) pooled tick samples collected from wild CWD-infected white-tailed deer. Seeding activities in ticks were analogous to 10–1000 ng of CWD-positive retropharyngeal lymph node collected from deer upon which they were feeding. Estimates revealed a median infectious dose range of 0.3–42.4 per tick, suggesting that ticks can take up transmission-relevant amounts of PrP(CWD) and may pose a CWD risk to cervids. Nature Publishing Group UK 2023-05-15 /pmc/articles/PMC10185559/ /pubmed/37188858 http://dx.doi.org/10.1038/s41598-023-34308-3 Text en © The Author(s) 2023 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 Inzalaco, H. N. Bravo-Risi, F. Morales, R. Walsh, D. P. Storm, D. J. Pedersen, J. A. Turner, W. C. Lichtenberg, S. S. Ticks harbor and excrete chronic wasting disease prions |
title | Ticks harbor and excrete chronic wasting disease prions |
title_full | Ticks harbor and excrete chronic wasting disease prions |
title_fullStr | Ticks harbor and excrete chronic wasting disease prions |
title_full_unstemmed | Ticks harbor and excrete chronic wasting disease prions |
title_short | Ticks harbor and excrete chronic wasting disease prions |
title_sort | ticks harbor and excrete chronic wasting disease prions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185559/ https://www.ncbi.nlm.nih.gov/pubmed/37188858 http://dx.doi.org/10.1038/s41598-023-34308-3 |
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