Maehara Kiyoshi, Hirokawa Atsushi, Watanabe Hinata, Otani Norihiro, Wan Jiawei, Shirai Takanaga, Takemasa Tohru, Watanabe Koichi, Nishi Takeki, Sato Ken, Shimmura Suzuka, Nguyen Kieu D M, Takahashi Yoichiro, Sugasawa Takehito
Doctoral Program in Medical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8572, Japan.
College of Medicine, School of Medicine and Health Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8572, Japan.
Int J Mol Sci. 2025 Jun 26;26(13):6129. doi: 10.3390/ijms26136129.
In recent years, as gene therapy technology has rapidly developed, there has been growing concern that it could be misused by athletes as a means of doping. However, current testing methods for gene doping have a range of limitations and require further improvement. Furthermore, significant progress has been made in the fields of blood storage, next-generation sequencing (NGS), and LabDroid (experimental robots). Against this background, this study was implemented to develop a test method for gene doping using dried blood spot (DBS), NGS, and the LabDroid "Maholo". As a first step, recombinant adeno-associated virus containing the human erythropoietin gene (h) was injected into mice to establish a gene doping model. Subsequently, DBS was created using whole blood. Maholo was used to extract DNA from the DBS and to create DNA libraries for NGS. NGS in combination with bioinformatic analysis clearly identified DNA fragments that provided definitive evidence of gene doping in the mouse model, which were absent in the control mouse. To the best of our knowledge, this is the first attempt to use a biological model of h gene doping in conjunction with Maholo, NGS, and DBS. This method should facilitate the further development of gene doping tests.
近年来,随着基因治疗技术的迅速发展,人们越来越担心它可能被运动员滥用作兴奋剂手段。然而,目前基因兴奋剂的检测方法存在一系列局限性,需要进一步改进。此外,在血液储存、下一代测序(NGS)和LabDroid(实验机器人)领域也取得了重大进展。在此背景下,本研究旨在开发一种利用干血斑(DBS)、NGS和LabDroid“Maholo”进行基因兴奋剂检测的方法。第一步,将含有人类促红细胞生成素基因(h)的重组腺相关病毒注射到小鼠体内,建立基因兴奋剂模型。随后,用全血制作干血斑。利用Maholo从干血斑中提取DNA,并为NGS创建DNA文库。NGS结合生物信息学分析清楚地鉴定出了能在小鼠模型中提供基因兴奋剂确凿证据的DNA片段,而对照小鼠中则没有这些片段。据我们所知,这是首次尝试将h基因兴奋剂的生物学模型与Maholo、NGS和DBS结合使用。该方法应有助于基因兴奋剂检测的进一步发展。