A molecular comparison of [Fe-S] cluster-based homeostasis in Escherichia coli and Pseudomonas aeruginosa.

IF 5.1 1区 生物学 Q1 MICROBIOLOGY mBio Pub Date : 2024-11-13 Epub Date: 2024-10-03 DOI:10.1128/mbio.01206-24
Alessandra Lo Sciuto, Francesca D'Angelo, Maria Concetta Spinnato, Pierre Simon Garcia, Shirley Genah, Cervoni Matteo, Emmanuel Séchet, Ehud Banin, Frédéric Barras, Francesco Imperi
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Abstract

Iron-sulfur [Fe-S] clusters are essential protein cofactors allowing bacteria to perceive environmental redox modification and to adapt to iron limitation. Escherichia coli, which served as a bacterial model, contains two [Fe-S] cluster biogenesis systems, ISC and SUF, which ensure [Fe-S] cluster synthesis under balanced and stress conditions, respectively. However, our recent phylogenomic analyses revealed that most bacteria possess only one [Fe-S] cluster biogenesis system, most often SUF. The opportunist human pathogen Pseudomonas aeruginosa is atypical as it harbors only ISC. Here, we confirmed the essentiality of ISC in P. aeruginosa under both normal and stress conditions. Moreover, P. aeruginosa ISC restored viability, under balanced growth conditions, to an E. coli strain lacking both ISC and SUF. Reciprocally, the E. coli SUF system sustained growth and [Fe-S] cluster-dependent enzyme activities of ISC-deficient P. aeruginosa. Surprisingly, an ISC-deficient P. aeruginosa strain expressing E. coli SUF showed defects in resistance to H2O2 stress and paraquat, a superoxide generator. Similarly, the P. aeruginosa ISC system did not confer stress resistance to a SUF-deficient E. coli mutant. A survey of 120 Pseudomonadales genomes confirmed that all but five species have selected ISC over SUF. While highlighting the great versatility of bacterial [Fe-S] cluster biogenesis systems, this study emphasizes that their contribution to cellular homeostasis must be assessed in the context of each species and its own repertoire of stress adaptation functions. As a matter of fact, despite having only one ISC system, P. aeruginosa shows higher fitness in the face of ROS and iron limitation than E. coli.

Importance: ISC and SUF molecular systems build and transfer Fe-S cluster to cellular apo protein clients. The model Escherichia coli has both ISC and SUF and study of the interplay between the two systems established that the ISC system is the house-keeping one and SUF the stress-responding one. Unexpectedly, our recent phylogenomic analysis revealed that in contrast to E. coli (and related enterobacteria such as Salmonella), most bacteria have only one system, and, in most cases, it is SUF. Pseudomonas aeruginosa fits the general rule of having only one system but stands against the rule by having ISC. This study aims at engineering P. aeruginosa harboring E. coli systems and vice versa. Comparison of the recombinants allowed to assess the functional versatility of each system while appreciating their contribution to cellular homeostasis in different species context.

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大肠杆菌和铜绿假单胞菌基于[Fe-S]簇的稳态分子比较。
铁硫[Fe-S]簇是重要的蛋白质辅助因子,可使细菌感知环境氧化还原修饰并适应铁限制。作为细菌模型的大肠杆菌含有两个[Fe-S]簇生物发生系统,即ISC和SUF,它们分别确保[Fe-S]簇在平衡和应激条件下的合成。然而,我们最近的系统发生组分析表明,大多数细菌只拥有一个[Fe-S]簇生物发生系统,最常见的是 SUF。铜绿假单胞菌(Pseudomonas aeruginosa)是一种非典型的机会主义人类病原体,因为它只拥有 ISC。在这里,我们证实了铜绿假单胞菌在正常和应激条件下 ISC 的重要性。此外,在平衡生长条件下,铜绿假单胞菌 ISC 恢复了同时缺乏 ISC 和 SUF 的大肠杆菌菌株的活力。反过来,大肠杆菌 SUF 系统也能维持 ISC 缺乏的铜绿假单胞菌的生长和[Fe-S]簇依赖性酶活性。令人惊讶的是,表达大肠杆菌 SUF 的 ISC 缺陷铜绿微囊藻菌株对 H2O2 压力和百草枯(一种超氧化物生成物)的抗性存在缺陷。同样,铜绿假单胞菌的 ISC 系统也没有赋予大肠杆菌 SUF 缺失突变体以抗逆性。对 120 个假单胞菌基因组的调查证实,除 5 个物种外,其他所有物种都选择了 ISC 而不是 SUF。这项研究强调了细菌[Fe-S]簇生物发生系统的多功能性,同时也强调必须根据每个物种及其自身的应激适应功能来评估它们对细胞平衡的贡献。事实上,尽管铜绿假单胞菌只有一个 ISC 系统,但它在面对 ROS 和铁限制时比大肠杆菌表现出更高的适应能力:重要意义:ISC 和 SUF 分子系统可构建 Fe-S 簇并将其转移到细胞的载脂蛋白客户中。大肠杆菌模型同时具有 ISC 和 SUF,对这两个系统之间相互作用的研究表明,ISC 系统是看家系统,而 SUF 系统是应激反应系统。意想不到的是,我们最近的系统发生组分析发现,与大肠杆菌(以及沙门氏菌等相关肠杆菌)不同,大多数细菌只有一种系统,而且在大多数情况下是 SUF。铜绿假单胞菌符合只有一种系统的一般规则,但却拥有 ISC 系统,从而违反了这一规则。本研究的目的是对铜绿假单胞菌进行工程改造,使其携带大肠杆菌系统,反之亦然。通过比较重组子,可以评估每个系统的功能多样性,同时了解它们在不同物种背景下对细胞平衡的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
期刊最新文献
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