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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Here, we confirmed the essentiality of ISC in <i>P. aeruginosa</i> under both normal and stress conditions. Moreover, <i>P. aeruginosa</i> ISC restored viability, under balanced growth conditions, to an <i>E. coli</i> strain lacking both ISC and SUF. Reciprocally, the <i>E. coli</i> SUF system sustained growth and [Fe-S] cluster-dependent enzyme activities of ISC-deficient <i>P. aeruginosa</i>. Surprisingly, an ISC-deficient <i>P. aeruginosa</i> strain expressing <i>E. coli</i> SUF showed defects in resistance to H<sub>2</sub>O<sub>2</sub> stress and paraquat, a superoxide generator. Similarly, the <i>P. aeruginosa</i> ISC system did not confer stress resistance to a SUF-deficient <i>E. coli</i> 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, <i>P. aeruginosa</i> shows higher fitness in the face of ROS and iron limitation than <i>E. coli</i>.</p><p><strong>Importance: </strong>ISC and SUF molecular systems build and transfer Fe-S cluster to cellular apo protein clients. The model <i>Escherichia coli</i> 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 <i>E. coli</i> (and related enterobacteria such as Salmonella), most bacteria have only one system, and, in most cases, it is SUF. <i>Pseudomonas aeruginosa</i> fits the general rule of having only one system but stands against the rule by having ISC. This study aims at engineering <i>P. aeruginosa</i> harboring <i>E. coli</i> 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.</p>","PeriodicalId":18315,"journal":{"name":"mBio","volume":" ","pages":"e0120624"},"PeriodicalIF":5.1000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11559095/pdf/","citationCount":"0","resultStr":"{\"title\":\"A molecular comparison of [Fe-S] cluster-based homeostasis in <i>Escherichia coli</i> and <i>Pseudomonas aeruginosa</i>.\",\"authors\":\"Alessandra Lo Sciuto, Francesca D'Angelo, Maria Concetta Spinnato, Pierre Simon Garcia, Shirley Genah, Cervoni Matteo, Emmanuel Séchet, Ehud Banin, Frédéric Barras, Francesco Imperi\",\"doi\":\"10.1128/mbio.01206-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Iron-sulfur [Fe-S] clusters are essential protein cofactors allowing bacteria to perceive environmental redox modification and to adapt to iron limitation. <i>Escherichia coli</i>, 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 <i>Pseudomonas aeruginosa</i> is atypical as it harbors only ISC. Here, we confirmed the essentiality of ISC in <i>P. aeruginosa</i> under both normal and stress conditions. Moreover, <i>P. aeruginosa</i> ISC restored viability, under balanced growth conditions, to an <i>E. coli</i> strain lacking both ISC and SUF. Reciprocally, the <i>E. coli</i> SUF system sustained growth and [Fe-S] cluster-dependent enzyme activities of ISC-deficient <i>P. aeruginosa</i>. Surprisingly, an ISC-deficient <i>P. aeruginosa</i> strain expressing <i>E. coli</i> SUF showed defects in resistance to H<sub>2</sub>O<sub>2</sub> stress and paraquat, a superoxide generator. Similarly, the <i>P. aeruginosa</i> ISC system did not confer stress resistance to a SUF-deficient <i>E. coli</i> 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, <i>P. aeruginosa</i> shows higher fitness in the face of ROS and iron limitation than <i>E. coli</i>.</p><p><strong>Importance: </strong>ISC and SUF molecular systems build and transfer Fe-S cluster to cellular apo protein clients. The model <i>Escherichia coli</i> 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 <i>E. coli</i> (and related enterobacteria such as Salmonella), most bacteria have only one system, and, in most cases, it is SUF. <i>Pseudomonas aeruginosa</i> fits the general rule of having only one system but stands against the rule by having ISC. This study aims at engineering <i>P. aeruginosa</i> harboring <i>E. coli</i> systems and vice versa. 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A molecular comparison of [Fe-S] cluster-based homeostasis in Escherichia coli and Pseudomonas aeruginosa.
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.
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.