Genomic and Transcriptomic Diversification of Flagellin Genes Provides Insight into Environmental Adaptation and Phylogeographic Characteristics in Aeromonas hydrophila

IF 3.3 3区 生物学 Q2 ECOLOGY Microbial Ecology Pub Date : 2024-05-02 DOI:10.1007/s00248-024-02373-4
HyeongJin Roh, Dhamotharan Kannimuthu
{"title":"Genomic and Transcriptomic Diversification of Flagellin Genes Provides Insight into Environmental Adaptation and Phylogeographic Characteristics in Aeromonas hydrophila","authors":"HyeongJin Roh, Dhamotharan Kannimuthu","doi":"10.1007/s00248-024-02373-4","DOIUrl":null,"url":null,"abstract":"<p><i>Aeromonas hydrophila</i> is an opportunistic motile pathogen with a broad host range, infecting both terrestrial and aquatic animals. Environmental and geographical conditions exert selective pressure on both geno- and phenotypes of pathogens. Flagellin, directly exposed to external environments and containing important immunogenic epitopes, may display significant variability in response to external conditions. In this study, we conducted a comparative analysis of ~ 150 <i>A. hydrophila</i> genomes, leading to the identification of six subunits of the flagellin gene (<i>fla-1</i> to <i>fla-4</i>, <i>flaA</i>, and <i>flaB</i>). Individual strains harbored different composition of flagellin subunits and copies. The composition of subunits showed distinct patterns depending on environmental sources. Strains from aquatic environments were mainly comprised of <i>fla-1</i> to <i>fla-4</i> subunits, while terrestrial strains predominated in groups harboring <i>flaA</i> and <i>flaB</i> subunits. Each flagellin showed varying levels of expression, with <i>flaA</i> and <i>flaB</i> demonstrating significantly higher expression compared to others. One of the chemotaxis pathways that control flagellin movement through a two-component system was significantly upregulated in <i>flaA</i>(+ 1)/<i>flaB</i>(+ 1) group, whereas <i>flaA</i> and <i>flaB</i> showed different transcriptomic expressions. The genes positively correlated with <i>flaA</i> expression were relevant to biofilm formation and bacterial chemotaxis, but <i>flaB</i> showed a negative correlation with the genes in ABC transporters and quorum sensing pathway. However, the expression patterns of <i>fla-2</i> to <i>fla-4</i> were identical. This suggests various types of flagellin subunits may have different biological functions. The composition and expression levels of flagellin subunits could provide valuable insights into the adaptation of <i>A. hydrophila</i> and the differences among strains in response to various external environments.</p>","PeriodicalId":18708,"journal":{"name":"Microbial Ecology","volume":"98 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2024-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial Ecology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00248-024-02373-4","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Aeromonas hydrophila is an opportunistic motile pathogen with a broad host range, infecting both terrestrial and aquatic animals. Environmental and geographical conditions exert selective pressure on both geno- and phenotypes of pathogens. Flagellin, directly exposed to external environments and containing important immunogenic epitopes, may display significant variability in response to external conditions. In this study, we conducted a comparative analysis of ~ 150 A. hydrophila genomes, leading to the identification of six subunits of the flagellin gene (fla-1 to fla-4, flaA, and flaB). Individual strains harbored different composition of flagellin subunits and copies. The composition of subunits showed distinct patterns depending on environmental sources. Strains from aquatic environments were mainly comprised of fla-1 to fla-4 subunits, while terrestrial strains predominated in groups harboring flaA and flaB subunits. Each flagellin showed varying levels of expression, with flaA and flaB demonstrating significantly higher expression compared to others. One of the chemotaxis pathways that control flagellin movement through a two-component system was significantly upregulated in flaA(+ 1)/flaB(+ 1) group, whereas flaA and flaB showed different transcriptomic expressions. The genes positively correlated with flaA expression were relevant to biofilm formation and bacterial chemotaxis, but flaB showed a negative correlation with the genes in ABC transporters and quorum sensing pathway. However, the expression patterns of fla-2 to fla-4 were identical. This suggests various types of flagellin subunits may have different biological functions. The composition and expression levels of flagellin subunits could provide valuable insights into the adaptation of A. hydrophila and the differences among strains in response to various external environments.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
鞭毛蛋白基因的基因组和转录组多样性为了解嗜水气单胞菌的环境适应性和系统地理学特征提供了线索
嗜水气单胞菌(Aeromonas hydrophila)是一种机会性运动病原体,宿主范围广泛,可感染陆生和水生动物。环境和地理条件对病原体的基因型和表型产生选择性压力。鞭毛蛋白直接暴露于外部环境,含有重要的免疫原表位,可能会对外部条件产生显著的反应变异。在这项研究中,我们对大约 150 个嗜水蝇基因组进行了比较分析,从而确定了鞭毛蛋白基因的六个亚基(fla-1 至 fla-4、flaA 和 flaB)。不同菌株含有不同的鞭毛蛋白亚基和拷贝。亚基的组成因环境来源不同而呈现出不同的模式。水生环境中的菌株主要由 fla-1 至 fla-4 亚基组成,而陆生环境中的菌株则以携带 flaA 和 flaB 亚基的群体为主。每种鞭毛蛋白都有不同程度的表达,其中 flaA 和 flaB 的表达量明显高于其他鞭毛蛋白。通过双组分系统控制鞭毛蛋白运动的趋化途径之一在 flaA(+ 1)/flaB(+ 1)组中明显上调,而 flaA 和 flaB 则表现出不同的转录组表达。与 flaA 表达正相关的基因与生物膜形成和细菌趋化有关,但 flaB 与 ABC 转运体和法定量感应途径中的基因呈负相关。然而,fla-2 至 fla-4 的表达模式是相同的。这表明不同类型的鞭毛蛋白亚基可能具有不同的生物学功能。鞭毛蛋白亚基的组成和表达水平可为了解嗜水青虫的适应性以及不同菌株对各种外部环境的反应差异提供有价值的信息。
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 去求助
来源期刊
Microbial Ecology
Microbial Ecology 生物-海洋与淡水生物学
CiteScore
6.90
自引率
2.80%
发文量
212
审稿时长
3-8 weeks
期刊介绍: The journal Microbial Ecology was founded more than 50 years ago by Dr. Ralph Mitchell, Gordon McKay Professor of Applied Biology at Harvard University in Cambridge, MA. The journal has evolved to become a premier location for the presentation of manuscripts that represent advances in the field of microbial ecology. The journal has become a dedicated international forum for the presentation of high-quality scientific investigations of how microorganisms interact with their environment, with each other and with their hosts. Microbial Ecology offers articles of original research in full paper and note formats, as well as brief reviews and topical position papers.
期刊最新文献
Influences of Community Coalescence on the Assembly of Bacterial Communities of the Small-Scale Complex Aquatic System from the Perspective of Bacterial Transmission, Core Taxa, and Co-occurrence Patterns. Wild-Type Domestication: Loss of Intrinsic Metabolic Traits Concealed by Culture in Rich Media. Fungus Fighters: Wood Ants (Formica polyctena) and Their Associated Microbes Inhibit Plant Pathogenic Fungi. Biological Nitrification Inhibitors with Antagonistic and Synergistic Effects on Growth of Ammonia Oxidisers and Soil Nitrification. Seasonal and Spatial Dynamics of Fungal Leaf Endophytes in Eucalyptus crebra (Narrow-Leaved Ironbark).
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1