临床试验中多位点等位基因特异性PCR鉴定霍乱弧菌和副溶血性弧菌试剂盒的研制与性能研究

O. Chemisova, M. V. Poleeva, S. Vodopyanov, A. S. Vodopyanov, A. L. Trukhachev, R. V. Pisanov, V. D. Kruglikov, Alexey K. Noskov
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引用次数: 0

摘要

本研究的目的是开发、开展临床试验并评估“多位点等位基因特异性PCR鉴定霍乱弧菌和副溶血性弧菌试剂”(“Vibrio-screen FL”)的性能,用于指定医疗器械的国家注册。材料和方法。本文介绍了“Vibrio-screen FL”试剂盒的临床试验结果,该试剂盒是为优化鉴定和区分特别危险感染病原体的手段和方法而开发的。临床试验在俄罗斯联邦工商管理学院卫生和流行病学中心进行(许可证于2013年12月2日颁发)。ФС99 - 01 - 008342;根据2020年9月23日第20.ПМКИ-042/10.20号临床试验方案(2020年10月12日第01.AK-042/10.20号临床试验证书),卫生部于2013年5月16日第300n号批准)。为进行临床试验,以临床菌株弧菌等微生物为目标分析物。研究方法包括细菌学方法和多位点PCR。结果。“Vibrio-screen FL”试剂盒是临床实验室诊断专业使用的医疗器械。“Vibrio-screen FL”试剂盒在确定属弧菌时的分析灵敏度至少为106拷贝SecY基因;霍乱弧菌至少有106个hlyA基因副本;副溶血性弧菌至少有106个vppC基因拷贝。在确定分析特异性时,与其他微生物物种的DNA样品无非特异性反应。Vibrio-screen FL试剂盒是一种体外诊断医疗设备,符合预期用途要求,可采用多位点等位基因特异性聚合酶链反应与杂交荧光检测的方法,从培养的临床样品中分离出霍乱弧菌和副溶血性弧菌菌株。从08.02.2021收到注册证书№РЗН 2021/13360。根据roszdravnadzor2021年2月8日第1041号命令,顿河畔罗斯托夫鼠疫控制研究所的一种弧菌筛选FL试剂试剂盒获准在俄罗斯联邦境内分发。结论。“Vibrio-screen FL”试剂盒是一种高质量、有效、安全的体外诊断医疗器械,具有足够的诊断敏感性和特异性,可用于鉴定弧菌、霍乱弧菌和副溶血性弧菌核酸的特定片段,可用于临床实验室诊断和流行病学分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DEVELOPMENT AND STUDY OF THE PERFORMANCE OF THE REAGENT KIT FOR THE IDENTIFICATION OF VIBRIO CHOLERAE AND VIBRIO PARAHAEMOLYTICUS BY MULTILOCUS ALLELE-SPECIFIC PCR IN CLINICAL TRIALS
The aim of the study was to develop, conduct clinical trials and evaluate the performance of the "Reagent kit for identification of V. cholerae and V. parahaemolyticus by multilocus allele-specific PCR" ("Vibrio-screen FL") for the state registration of the specified medical device. Materials and methods. The results of clinical trials of the reagent kit "Vibrio-screen FL" that has been developed to optimize the means and methods of identification and differentiation of pathogens of particularly dangerous infections are presented in the article. Clinical trials were conducted at the Head Center of Hygiene and Epidemiology of the FMBA of Russia (license from 02.12.2013 No. ФС-99-01- 008342; permission of the Ministry of Health from 16.05.2013 No. 300n) in accordance with the program of clinical trials No. 20.ПМКИ-042/10.20 from 23.09.2020 (Clinical Trial Certificate No. 01.AK-042/10.20 dated 12.10.2020). To conduct clinical trials clinical strains of microorganisms Vibrio spp. and other microorganism species were used as target analytes. Research methods included bacteriological method and multilocus PCR . Results. The reagent kit "Vibrio-screen FL" is a medical device for professional use in clinical laboratory diagnostics. The analytical sensitivity of the reagent kit "Vibrio-screen FL" was at least 106 copies of the SecY gene when determining belonging to the genus Vibrio; to the species V. cholerae at least 106 copies of the hlyA gene; and to the species V. parahaemolyticus at least 106 copies of the vppC gene. When determining the analytical specificity, there were no non-specific reactions with DNA samples of other microorganism species. A medical device for in vitro diagnostics the reagent kit Vibrio-screen FL meets the requirements of the intended use, which allows it to be used for the differentiation of V. cholerae and V. parahaemolyticus strains isolated from a cultured clinical samples by the method of multilocus allele-specific polymerase chain reaction with hybridization-fluorescent detection. The registration certificate № РЗН 2021/13360 from 08.02.2021 was received. By order of Roszdravnadzordated 08.02.2021 No. 1041, a reagent kit Vibrio-screen FL by the Rostov-on-Don Plague Control Researsh Institute was admitted to distribution on the territory of the Russian Federation. Conclusions. The reagent kit "Vibrio-screen FL" is a high-quality, effective and safe medical device for in vitro diagnostics with sufficient diagnostic sensitivity and specificity to identify specific fragments of Vibrio spp., V. cholerae and V. parahaemolyticus nucleic acids, which allows it to be used in clinical laboratory diagnostics, for epidemiological analysis.
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