A co-conserved gene pair supports Caulobacter iron homeostasis during chelation stress.

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Journal of Bacteriology Pub Date : 2025-04-17 Epub Date: 2025-03-14 DOI:10.1128/jb.00484-24
Sergio Hernandez-Ortiz, Kiwon Ok, Thomas V O'Halloran, Aretha Fiebig, Sean Crosson
{"title":"A co-conserved gene pair supports <i>Caulobacter</i> iron homeostasis during chelation stress.","authors":"Sergio Hernandez-Ortiz, Kiwon Ok, Thomas V O'Halloran, Aretha Fiebig, Sean Crosson","doi":"10.1128/jb.00484-24","DOIUrl":null,"url":null,"abstract":"<p><p>Synthetic metal chelators are widely used in industrial, clinical, and agricultural settings, leading to their accumulation in the environment. We measured the growth of <i>Caulobacter crescentus</i>, a soil and aquatic bacterium, in the presence of the ubiquitous chelator ethylenediaminetetraacetic acid (EDTA) and found that it restricts growth by lowering intracellular iron levels. Using barcoded transposon sequencing, we identified an operonic gene pair, <i>cciT-cciO</i>, that is required to maintain iron homeostasis in laboratory media during EDTA challenge. <i>cciT</i> encodes one of four TonB-dependent transporters that are regulated by the ferric uptake repressor (Fur) and stands out among this group of genes in its ability to support <i>Caulobacter</i> growth across diverse media conditions. The function of CciT strictly requires <i>cciO</i>, which encodes a cytoplasmic Fe<sup>II</sup> dioxygenase-family protein. Our results thus define a functional partnership between an outer membrane iron receptor and a cytoplasmic dioxygenase that are broadly co-conserved in Proteobacteria. We expanded our analysis to natural environments by examining the growth of mutant strains in freshwater from two lakes, each with biochemical and geochemical profiles that differ markedly from standard laboratory media. In lake water, <i>Caulobacter</i> growth did not require <i>cciT</i> or <i>cciO</i> and was less affected by EDTA treatment. This result aligns with our observation that EDTA toxicity is influenced by common forms of biologically chelated iron and the spectrum of free cations present in the medium. Our study defines a conserved iron acquisition system in Proteobacteria and bridges laboratory-based physiology studies with real-world conditions.IMPORTANCEMetal-chelating chemicals are widely used across industries, including as preservatives in the food sector, but their full impact on microbial physiology is not well understood. We identified two genes, <i>cciT</i> and <i>cciO</i>, that function together to support <i>Caulobacter crescentus</i> iron balance when cells are exposed to the common synthetic chelator, EDTA. CciT is an outer membrane transporter and CciO is a dioxygenase-family protein that are mutually conserved in many bacteria, including human pathogens where mutations in <i>cciT</i> homologs are linked to clinical resistance to the siderophore antibiotic cefiderocol. This study identifies a conserved genetic system that supports iron homeostasis during chelation stress and illuminates the iron acquisition versatility and stress resilience of <i>Caulobacter</i> in freshwater environments.</p>","PeriodicalId":15107,"journal":{"name":"Journal of Bacteriology","volume":" ","pages":"e0048424"},"PeriodicalIF":2.7000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12004947/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bacteriology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/jb.00484-24","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/14 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Synthetic metal chelators are widely used in industrial, clinical, and agricultural settings, leading to their accumulation in the environment. We measured the growth of Caulobacter crescentus, a soil and aquatic bacterium, in the presence of the ubiquitous chelator ethylenediaminetetraacetic acid (EDTA) and found that it restricts growth by lowering intracellular iron levels. Using barcoded transposon sequencing, we identified an operonic gene pair, cciT-cciO, that is required to maintain iron homeostasis in laboratory media during EDTA challenge. cciT encodes one of four TonB-dependent transporters that are regulated by the ferric uptake repressor (Fur) and stands out among this group of genes in its ability to support Caulobacter growth across diverse media conditions. The function of CciT strictly requires cciO, which encodes a cytoplasmic FeII dioxygenase-family protein. Our results thus define a functional partnership between an outer membrane iron receptor and a cytoplasmic dioxygenase that are broadly co-conserved in Proteobacteria. We expanded our analysis to natural environments by examining the growth of mutant strains in freshwater from two lakes, each with biochemical and geochemical profiles that differ markedly from standard laboratory media. In lake water, Caulobacter growth did not require cciT or cciO and was less affected by EDTA treatment. This result aligns with our observation that EDTA toxicity is influenced by common forms of biologically chelated iron and the spectrum of free cations present in the medium. Our study defines a conserved iron acquisition system in Proteobacteria and bridges laboratory-based physiology studies with real-world conditions.IMPORTANCEMetal-chelating chemicals are widely used across industries, including as preservatives in the food sector, but their full impact on microbial physiology is not well understood. We identified two genes, cciT and cciO, that function together to support Caulobacter crescentus iron balance when cells are exposed to the common synthetic chelator, EDTA. CciT is an outer membrane transporter and CciO is a dioxygenase-family protein that are mutually conserved in many bacteria, including human pathogens where mutations in cciT homologs are linked to clinical resistance to the siderophore antibiotic cefiderocol. This study identifies a conserved genetic system that supports iron homeostasis during chelation stress and illuminates the iron acquisition versatility and stress resilience of Caulobacter in freshwater environments.

一个共保守的基因对在螯合胁迫下支持铁茎杆菌的稳态。
合成金属螯合剂广泛应用于工业、临床和农业环境,导致其在环境中积累。我们在普遍存在的螯合剂乙二胺四乙酸(EDTA)存在的情况下,测量了土壤和水生细菌新月状茎杆菌的生长,发现它通过降低细胞内铁水平来限制生长。利用条形码转座子测序,我们发现了一个操纵子基因对,cciT-cciO,这是在EDTA挑战期间维持实验室培养基中铁稳态所必需的。cciT编码由铁摄取抑制因子(Fur)调节的四种依赖于tonb的转运蛋白之一,在这组基因中,cciT在支持茎状杆菌在不同培养基条件下生长的能力中脱颖而出。CciT的功能严格依赖于cciO, cciO编码细胞质FeII双加氧酶家族蛋白。因此,我们的研究结果定义了外膜铁受体和胞质双加氧酶之间的功能伙伴关系,它们在变形杆菌中广泛共保守。我们将分析扩展到自然环境,通过检查来自两个湖泊的淡水中的突变菌株的生长,每个湖泊的生化和地球化学剖面与标准实验室介质明显不同。在湖水中,茎状杆菌的生长不需要cciT或cciO,受EDTA处理的影响较小。这一结果与我们的观察一致,EDTA毒性受到常见形式的生物螯合铁和存在于培养基中的自由阳离子谱的影响。我们的研究在变形杆菌中定义了一个保守的铁获取系统,并将基于实验室的生理学研究与现实世界的条件联系起来。金属螯合化学物质广泛应用于各行各业,包括食品部门的防腐剂,但它们对微生物生理学的全面影响尚不清楚。我们发现了两个基因,cciT和cciO,当细胞暴露于常见的合成螯合剂EDTA时,它们共同起作用,支持新月状芽孢杆菌的铁平衡。CciT是一种外膜转运蛋白,CciO是一种双加氧酶家族蛋白,它们在许多细菌中相互保守,包括人类病原体,其中CciT同源物的突变与对铁载体抗生素头孢地罗的临床耐药性有关。本研究确定了一个在螯合胁迫下支持铁稳态的保守遗传系统,并阐明了淡水环境中茎状杆菌的铁获取多功能性和应激恢复能力。
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
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
×
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