Intraspecific Differentiation of Francisella tularensis Strains Using Molecular-Genetic Methods. Complex Approach

N. A. Osina, D. A. Sitmbetov, O. A. Morozov, E. G. Bulgakova, A. V. Osin, S. S. Chekmareva, E. V. Sazanova, A. M. Senichkina, O. Lyashova, T. Polunina, Yaroslav M. Krasnov, Z. Devdariani, S. A. Shcherbakova
{"title":"Intraspecific Differentiation of Francisella tularensis Strains Using Molecular-Genetic Methods. Complex Approach","authors":"N. A. Osina, D. A. Sitmbetov, O. A. Morozov, E. G. Bulgakova, A. V. Osin, S. S. Chekmareva, E. V. Sazanova, A. M. Senichkina, O. Lyashova, T. Polunina, Yaroslav M. Krasnov, Z. Devdariani, S. A. Shcherbakova","doi":"10.21055/0370-1069-2024-2-148-156","DOIUrl":null,"url":null,"abstract":"The aim of the study was to develop an algorithm for intraspecific differentiation of tularemia agent strains using a set of approaches based on amplification and sequencing technologies.Materials and methods. 97 strains of Francisella tularensis of various subspecies, biovars and subpopulations from the State Collection of Pathogenic Bacteria of the Russian Research Anti-Plague Institute “Microbe” were used in the work. The intraspecific identification of tularemia agent strains was carried out using the “F. tularensis-4c” system; analysis of the variability of the RD1 differentiation region, the sdhA gene, by applying the disk diffusion method using disks with erythromycin. Fragment Sanger sequencing was performed on a 3500 XL genetic analyzer (Applied Biosystems, USA) taking into account the manufacturer’s recommendations. Sequence homology assessment was conducted using the BLAST algorithm, the GenBank NCBI database, MEGA11 v11.0.13 and Unipro UGENE v50.0 software.Results and discussion. Subspecies- and biovarspecific mutations have been detected in the 23S rRNA gene. Promising regions of this gene for further investigation have been identified using fragment sequencing. A comprehensive scheme for intraspecific differentiation of tularemia microbe strains has been put forward, where at the first stage the subspecies and biovar japonica are determined, and at the second stage, the results are verified based on the determination of mutations in the 23S rRNA gene. The effectiveness of the proposed integrated approach has been confirmed in a study of 97 collection strains of tularemia agent. The conducted research allows for rapid identification of tularemia agent strains of different subspecies and verification of their taxonomic appurtenance using molecular-genetic methods, expanding data on the circulation of various subspecies, biovars and subpopulations of the pathogen in Europe, Asia and other regions of the world.","PeriodicalId":516710,"journal":{"name":"Problems of Particularly Dangerous Infections","volume":" 61","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Problems of Particularly Dangerous Infections","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21055/0370-1069-2024-2-148-156","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The aim of the study was to develop an algorithm for intraspecific differentiation of tularemia agent strains using a set of approaches based on amplification and sequencing technologies.Materials and methods. 97 strains of Francisella tularensis of various subspecies, biovars and subpopulations from the State Collection of Pathogenic Bacteria of the Russian Research Anti-Plague Institute “Microbe” were used in the work. The intraspecific identification of tularemia agent strains was carried out using the “F. tularensis-4c” system; analysis of the variability of the RD1 differentiation region, the sdhA gene, by applying the disk diffusion method using disks with erythromycin. Fragment Sanger sequencing was performed on a 3500 XL genetic analyzer (Applied Biosystems, USA) taking into account the manufacturer’s recommendations. Sequence homology assessment was conducted using the BLAST algorithm, the GenBank NCBI database, MEGA11 v11.0.13 and Unipro UGENE v50.0 software.Results and discussion. Subspecies- and biovarspecific mutations have been detected in the 23S rRNA gene. Promising regions of this gene for further investigation have been identified using fragment sequencing. A comprehensive scheme for intraspecific differentiation of tularemia microbe strains has been put forward, where at the first stage the subspecies and biovar japonica are determined, and at the second stage, the results are verified based on the determination of mutations in the 23S rRNA gene. The effectiveness of the proposed integrated approach has been confirmed in a study of 97 collection strains of tularemia agent. The conducted research allows for rapid identification of tularemia agent strains of different subspecies and verification of their taxonomic appurtenance using molecular-genetic methods, expanding data on the circulation of various subspecies, biovars and subpopulations of the pathogen in Europe, Asia and other regions of the world.
利用分子遗传学方法区分土拉弗氏菌菌株的种内差异。复杂方法
这项研究的目的是利用一套基于扩增和测序技术的方法,开发一种用于区分土拉菌病原体菌株种内差异的算法。研究使用了俄罗斯 "微生物 "抗鼠疫研究所国家病原菌保藏中心保藏的 97 株不同亚种、生物变种和亚群的土拉菌。使用 "F. tularensis-4c "系统对土拉菌病原体菌株进行了种内鉴定;使用含红霉素的磁盘扩散法分析了 RD1 分化区、sdhA 基因的变异性。根据制造商的建议,在 3500 XL 基因分析仪(美国应用生物系统公司)上进行片段桑格测序。使用 BLAST 算法、GenBank NCBI 数据库、MEGA11 v11.0.13 和 Unipro UGENE v50.0 软件进行了序列同源性评估。在 23S rRNA 基因中检测到了亚种和生物种特有的突变。通过片段测序确定了该基因中有望进一步研究的区域。提出了一种用于区分土拉雷病微生物菌株种内差异的综合方案,第一阶段确定亚种和生物种,第二阶段根据 23S rRNA 基因突变的确定结果进行验证。在对 97 个收集的土拉菌病原体菌株进行的研究中,证实了所建议的综合方法的有效性。通过这项研究,可以快速鉴定不同亚种的土拉菌病原体菌株,并利用分子遗传学方法验证它们在分类学上的关联性,从而扩大有关该病原体在欧洲、亚洲和世界其他地区的各种亚种、生物变种和亚群循环的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信