Investigation of optimal procedures for storage and use of plasma samples suitable for gene doping tests

Gene doping, which is prohibited in horseracing and equestrian sports, can be performed by introducing exogenous genes, known as transgenes, into the bodies of postnatal animals. To detect exogenous genes, a method utilizing quantitative polymerase chain reaction (qPCR) with a hydrolysis probe was d...

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Bibliographic Details
Published inJournal of Equine Science Vol. 34; no. 2; pp. 21 - 27
Main Authors TOZAKI, Teruaki, OHNUMA, Aoi, KIKUCHI, Mio, ISHIGE, Taichiro, KAKOI, Hironaga, HIROTA, Kei-ichi, TAKAHASHI, Yuji, NAGATA, Shun-ichi
Format Journal Article
LanguageEnglish
Published Japan Japanese Society of Equine Science 01.06.2023
Japan Science and Technology Agency
The Japanese Society of Equine Science
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Summary:Gene doping, which is prohibited in horseracing and equestrian sports, can be performed by introducing exogenous genes, known as transgenes, into the bodies of postnatal animals. To detect exogenous genes, a method utilizing quantitative polymerase chain reaction (qPCR) with a hydrolysis probe was developed to test whole blood and plasma samples, thereby protecting the fairness of competition and the rights of stakeholders in horseracing and equestrian sports. Therefore, we aimed to develop sample storage methods suitable for A and B samples in gene doping tests using blood. For sample A, sufficient qPCR detection was demonstrated after refrigeration for 1 to 2 weeks post collection. For sample B, the following procedures were confirmed to be suitable for storage: 1) centrifugation after sample receipt, 2) frozen storage, 3) natural thawing at room temperature, and 4) centrifugation without mixing blood cell components. Our results indicated that long-term cryopreservation yielded good plasma components from frozen blood samples even though it destroyed blood cells, indicating its applicability to the gene doping test using sample B, which can be stored for later use. Sample storage procedures are as important as detection methods in doping tests. Therefore, the series of procedures that we evaluated in this study will contribute to the efficient performance of gene doping tests through qPCR using blood samples.
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ISSN:1340-3516
1347-7501
DOI:10.1294/jes.34.21