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A Non-invasive, Biomarker Assay for Detecting Chronic Wasting Disease Pathology in White-tailed Deer

Robert D. Bradley, Emma K. Roberts, Asha E. Worsham, Megan N. Ashton, Emily A. Wright, Ned Saleh, View ORCID ProfileDaniel M. Hardy
doi: https://doi.org/10.1101/2022.07.20.500695
Robert D. Bradley
1Department of Biological Sciences, Texas Tech University, 2901 Main Street, Lubbock, TX 79409
2Natural Science Research Laboratory at the Museum of Texas Tech University, 3301 4th Street, Lubbock, TX 79415
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Emma K. Roberts
1Department of Biological Sciences, Texas Tech University, 2901 Main Street, Lubbock, TX 79409
3Climate Sciences Center, Texas Tech University, 2500 Broadway Ave, Lubbock, TX 79409
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Asha E. Worsham
4Department of Cell Biology & Biochemistry, Texas Tech University Health Sciences Center, 3601 4th St., Lubbock, TX 79430
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Megan N. Ashton
4Department of Cell Biology & Biochemistry, Texas Tech University Health Sciences Center, 3601 4th St., Lubbock, TX 79430
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Emily A. Wright
1Department of Biological Sciences, Texas Tech University, 2901 Main Street, Lubbock, TX 79409
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Ned Saleh
5Convergent Animal Health LLC, 118 Thoroughman Ave., Ferguson, MO 63135
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Daniel M. Hardy
4Department of Cell Biology & Biochemistry, Texas Tech University Health Sciences Center, 3601 4th St., Lubbock, TX 79430
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  • ORCID record for Daniel M. Hardy
  • For correspondence: daniel.hardy{at}ttuhsc.edu
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ABSTRACT

We describe a blood test that exploits differences in the abundance of diagnostic miRNA biomarkers associated with prion infections in cervids. Using sera from 93 pen-raised white-tailed deer euthanized after unintentional exposure to Chronic Wasting Disease (CWD), quantification of candidate reference and diagnostic miRNAs revealed sensitivity of the q-RT-PCR method to interference from sample degradation, requiring exclusion of 60 specimens that exhibited excessive hemolysis or yielded poor amplification of reference or diagnostic miRNAs. Subsequent quantification of three potentially diagnostic and two control miRNAs in the 33 remaining, minimally degraded sera established diagnostic criteria congruent (100% sensitivity, 92.3% specificity, 93.9% accuracy) with results from standard CWD diagnosis by microscopic detection of immunoreactivity in obex and/or medial retropharyngeal lymph nodes (conducted by the National Veterinary Services Laboratory, NVSL, Ames, IA). Overall, the miRNA assay proved to be at least as accurate and sensitive as other CWD testing alternatives to immunohistochemical diagnosis, albeit supported by data from relatively few animals owing to the challenge of acquiring usable specimens from animals euthanized in a mass depopulation. Nevertheless, for sera acquired antemortem, this biomarker-based test may represent a useful new resource for managing spread of CWD that offers the advantages of being rapid, sensitive, non-invasive, and amenable to high throughput scaling.

Competing Interest Statement

Ned Saleh is a named inventor of a US patent application: Apparatus and Method for High Throughput Compact Multiplexed micro-RNA Based Rapid Diagnostics with Monetizable Database, N. Saleh; R. Vierling Number: 22/63388262). All other authors declare no competing interests.

Footnotes

  • We have revised all sections of the manuscript for content and clarity.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-ND 4.0 International license.
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Posted August 23, 2022.
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A Non-invasive, Biomarker Assay for Detecting Chronic Wasting Disease Pathology in White-tailed Deer
Robert D. Bradley, Emma K. Roberts, Asha E. Worsham, Megan N. Ashton, Emily A. Wright, Ned Saleh, Daniel M. Hardy
bioRxiv 2022.07.20.500695; doi: https://doi.org/10.1101/2022.07.20.500695
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A Non-invasive, Biomarker Assay for Detecting Chronic Wasting Disease Pathology in White-tailed Deer
Robert D. Bradley, Emma K. Roberts, Asha E. Worsham, Megan N. Ashton, Emily A. Wright, Ned Saleh, Daniel M. Hardy
bioRxiv 2022.07.20.500695; doi: https://doi.org/10.1101/2022.07.20.500695

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