Development of an Integrated System for Molecular-Genetic Identification of Yersinia pestis Strains

Q3 Medicine
K. A. Nikiforov, E. G. Oglodin, M. A. Makashova, A. N. Balykova, D. V. Utkin, L. M. Kukleva, G. A. Eroshenko, V. Kutyrev
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引用次数: 0

Abstract

The paper describes a developed comprehensive system for molecular-genetic identification of Yersinia pestis strains according to their appurtenance to certain subspecies, biovars, phylo-geographic populations, using realtime PCR (RT-PCR), allele-specific RT-PCR, and multiplex PCR with hybridization fluorescent registration of results on a solid substrate. Application of this system makes it possible to establish the appurtenance of Y. pestis strains to the following phylogenetic branches: 0.ANT1, 0.ANT2, 0.ANT3, 0.ANT5, 3.ANT, 4.ANT of antique biovar of the main subspecies; 2.MED0, 2.MED1, 2.MED2, 2.MED3, 2.MED4 of medieval biovar of the main subspecies; 1.IN1, 1.IN2, 1.IN3 of intermedium biovar of the main subspecies; 1.ORI1, 1.ORI2, 1.ORI3 of oriental biovar of the main subspecies; 0.PE3 (angolica subspecies), 0.PE7 (tibetica subspecies) and 0.PE10 (qinghaica subspecies). The first stage of the studies within the frames of the developed system is indication of plague agent using registered diagnostic drugs. The second stage is the determination of belonging to individual subspecies through RT-PCR or by the method of multiplex PCR system with hybridization-fluorescent registration of results on a solid substrate, which also allows for establishing to which biovars of the main subspecies and the main phylogenetic lines of the ancient biovar the strains belong. The third stage is the identification of strain appurtenance to phylogenetic branches by the AS-RT-PCR method. The designed complex system for molecular-genetic identification of Y. pestis strains can be applied at the regional and federal levels of the laboratory network of the Russian Federation for diagnostics of infectious diseases. Its use will considerably facilitate and increase the efficiency of intraspecific differentiation of Y. pestis strains within the framework of the epidemiological investigation of outbreaks or importation of strains of plague pathogen into the territory of the Russian Federation or during the certification of strains in collection activities.
鼠疫耶尔森菌分子遗传鉴定集成系统的建立
本文介绍了一种根据特定亚种、生物变种、门地理种群的隶属关系,利用实时聚合酶链式反应(RT-PCR)、等位基因特异性聚合酶链式反应和多重聚合酶链式反应在固体基质上杂交荧光登记结果,开发的鼠疫耶尔森菌分子遗传鉴定综合系统。该系统的应用使鼠疫杆菌菌株可以建立以下系统发育分支的附属物:主要亚种古老生物型的0.ANT1、0.ANT2、0.ANT3、0.ANT5、3.ANT、4.ANT;主要亚种中世纪生物型的2.MED0、2.MED1、2.MED2、2.MED3、2.MED4;主要亚种中间生物型的1.IN1,1.IN2,1.IN3;主要亚种东方生物型的1.ORI1、1.ORI2、1.ORI3;0.PE3(安哥拉亚种)、0.PE7(西藏亚种)和0.PE10(青海亚种)。在已开发的系统框架内进行的第一阶段研究是使用注册诊断药物指示鼠疫病原体。第二阶段是通过RT-PCR或多重PCR系统的方法确定属于单个亚种,并在固体基质上对结果进行杂交荧光登记,这也允许确定菌株属于主要亚种的哪些生物变种和古代生物变种的主要系统发育系。第三阶段是利用AS-RTP聚合酶链式反应方法鉴定属于系统发育分支的菌株。设计的鼠疫杆菌菌株分子遗传鉴定复杂系统可应用于俄罗斯联邦传染病诊断实验室网络的地区和联邦层面。在对俄罗斯联邦境内鼠疫病原体爆发或输入菌株进行流行病学调查的框架内,或在采集活动中对菌株进行认证期间,它的使用将大大促进和提高鼠疫杆菌菌株的种内分化效率。
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来源期刊
Problemy Osobo Opasnykh Infektsii
Problemy Osobo Opasnykh Infektsii Medicine-Infectious Diseases
CiteScore
1.90
自引率
0.00%
发文量
79
审稿时长
12 weeks
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