Analysis of production levels of InlA and InlB invasion factors in Listeria monocytogenes isolates collected in the Russian Federation

E. Kalinin, Y. Chalenko, P. Safarova, V. A. Fedorova, S. Ermolaeva
{"title":"Analysis of production levels of InlA and InlB invasion factors in Listeria monocytogenes isolates collected in the Russian Federation","authors":"E. Kalinin, Y. Chalenko, P. Safarova, V. A. Fedorova, S. Ermolaeva","doi":"10.36233/0372-9311-397","DOIUrl":null,"url":null,"abstract":"Background. Listeria monocytogenes is characterized by the presence of epidemic hypervirulent clones. A key feature of L. monocytogenes is its capacity to invade non-professional phagocytic cells. Hypervirulent clones are strongly associated with the increased production and/or the presence of certain isoforms of invasion factors InlA and InlB. The purpose of the study is to create a test system for InlA and InlB detection and to measure the InlA and InlB production levels in L. monocytogenes isolates belonging to clonal groups with different virulence potential. Materials and methods. The study was performed using 32 L. monocytogenes strains belonging to epidemic clones ECII, ECIV, ECVII (clonal complexes CC1, CC2, CC7) and hypovirulent clonal complex CC9. Sequencing of inlA and inlB genes was performed. The indirect enzyme-linked immunosorbent assay was used to analyze the production levels of InlA and InlB proteins. Results. The variability of InlA was revealed among strains belonging to the same clonal complex: 3 InlA isoforms were identified among strains belonging to CC7; out of 8 strains belonging to CC9, one strain had a stop codon in the inlA gene, leading to the loss of function of the InlA protein. The differences between inlB alleles correlated with the specificity of strains belonging to a certain clonal complex. Differences in production levels of invasion factors were measured. In strains belonging to CC9, the InlA production level was 2.5 times as low compared to strains belonging to CC1, CC2, and CC7. In strains belonging to phylogenetically related CC1 and CC2, the InlB production level was on average 4 times as high compared to strains belonging to CC7 and CC9. Conclusion. The obtained results confirm the variability of major invasion factors both among clonal complexes and strains of the same complex. The increased production of invasion factors InlA and InlB correlates with the potential virulence of strains.","PeriodicalId":508236,"journal":{"name":"Journal of microbiology, epidemiology and immunobiology","volume":"17 17","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of microbiology, epidemiology and immunobiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36233/0372-9311-397","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

Background. Listeria monocytogenes is characterized by the presence of epidemic hypervirulent clones. A key feature of L. monocytogenes is its capacity to invade non-professional phagocytic cells. Hypervirulent clones are strongly associated with the increased production and/or the presence of certain isoforms of invasion factors InlA and InlB. The purpose of the study is to create a test system for InlA and InlB detection and to measure the InlA and InlB production levels in L. monocytogenes isolates belonging to clonal groups with different virulence potential. Materials and methods. The study was performed using 32 L. monocytogenes strains belonging to epidemic clones ECII, ECIV, ECVII (clonal complexes CC1, CC2, CC7) and hypovirulent clonal complex CC9. Sequencing of inlA and inlB genes was performed. The indirect enzyme-linked immunosorbent assay was used to analyze the production levels of InlA and InlB proteins. Results. The variability of InlA was revealed among strains belonging to the same clonal complex: 3 InlA isoforms were identified among strains belonging to CC7; out of 8 strains belonging to CC9, one strain had a stop codon in the inlA gene, leading to the loss of function of the InlA protein. The differences between inlB alleles correlated with the specificity of strains belonging to a certain clonal complex. Differences in production levels of invasion factors were measured. In strains belonging to CC9, the InlA production level was 2.5 times as low compared to strains belonging to CC1, CC2, and CC7. In strains belonging to phylogenetically related CC1 and CC2, the InlB production level was on average 4 times as high compared to strains belonging to CC7 and CC9. Conclusion. The obtained results confirm the variability of major invasion factors both among clonal complexes and strains of the same complex. The increased production of invasion factors InlA and InlB correlates with the potential virulence of strains.
分析俄罗斯联邦收集的李斯特菌分离物中 InlA 和 InlB 侵袭因子的产生水平
背景。单核细胞增生李斯特菌的特点是存在流行性高病毒克隆。单核细胞增多性李斯特氏菌的一个主要特征是它有能力侵入非专业吞噬细胞。高侵袭性克隆与侵袭因子 InlA 和 InlB 的某些异构体的产生和/或存在增加密切相关。 本研究的目的是建立一个检测 InlA 和 InlB 的测试系统,并测量属于不同毒力克隆组的单核细胞增多性球菌分离物中 InlA 和 InlB 的产生水平。 材料和方法。研究使用了 32 株单核细胞增多性酵母菌株,它们分别属于流行性克隆 ECII、ECIV、ECVII(克隆复合体 CC1、CC2、CC7)和低病毒性克隆复合体 CC9。对 inlA 和 inlB 基因进行了测序。采用间接酶联免疫吸附试验分析 InlA 和 InlB 蛋白的生成水平。 结果发现在属于同一克隆复合体的菌株中发现了 InlA 的变异性:在属于 CC7 的菌株中发现了 3 种 InlA 异构体;在属于 CC9 的 8 个菌株中,有一个菌株的 inlA 基因有一个终止密码子,导致 InlA 蛋白失去功能。inlB等位基因之间的差异与属于某一克隆复合体的菌株的特异性有关。对入侵因子产生水平的差异进行了测量。在属于CC9的菌株中,InlA的产生水平是属于CC1、CC2和CC7的菌株的2.5倍。在系统发育相关的 CC1 和 CC2 菌株中,InlB 的产生水平平均是 CC7 和 CC9 菌株的 4 倍。 结论研究结果证实,主要入侵因子在克隆复合体之间和同一复合体的菌株之间存在变异。入侵因子 InlA 和 InlB 产量的增加与菌株的潜在毒力有关。
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:481959085
Book学术官方微信