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Hardy, D. M.

Publications and source records attributed to Hardy, D. M..

2 recordsLinked to original sources

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

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.

molecular biology↗

Degraded RNA from human anterior cruciate ligaments yields valid gene expression profiles

BackgroundCorrelating gene expression patterns with biomechanical properties of connective tissues provides insight into molecular processes underlying development and maintenance of the tissues physical characteristics. Cadaveric tissues such as human knees are widely considered suitable for biomechanical studies, but their usefulness for gene expression experiments is potentially limited by unavoidable, nuclease-mediated degradation of RNA. MethodsWe quantified mRNAs encoding 84 extracellular matrix components and five housekeeping proteins in intact and partially degraded RNA from human anterior cruciate ligaments (ACLs), and compared relative amounts of the individual mRNAs by regression analysis. ResultsHuman ACL RNA degraded in vitro by limited ribonuclease digestion (N=6) resembled degraded RNA isolated from cadaveric tissue. PCR threshold cycle (Ct) values from degraded RNAs ranged variably higher than values obtained from their corresponding non-degraded RNAs, reflecting both the expected loss of target templates in the degraded preparations as well as differences in the extent of degradation. Relative Ct values obtained for mRNA targets in degraded preparations correlated strongly with the corresponding target levels in non-degraded RNA, both for each ACL as well as for pooled results from all six ACLs. Nuclease-mediated degradation produced similar, strongly correlated losses of housekeeping and non-housekeeping gene mRNAs. Expression profiling of RNA degraded in situ yielded comparable results, confirming that in vitro digestion suitably mimicked degradation by endogenous ribonucleases in frozen and thawed ACL. ConclusionPCR-based expression analyses can yield valid mRNA profiles from partially degraded RNA preparations such as those obtained from cadaveric knees and other skeletal motion segments used in biomechanical studies. Legitimate comparisons between variably degraded tissues can be made by normalizing quantitative data to an appropriate housekeeping transcript.

molecular biology↗