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Phosphate starvation decouples cell differentiation from DNA replication control in the dimorphic bacterium Caulobacter crescentus
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. Stockholm University, Science for Life Laboratory (SciLifeLab).ORCID iD: 0000-0001-8602-8095
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. Stockholm University, Science for Life Laboratory (SciLifeLab).ORCID iD: 0000-0001-7025-8558
Stockholm University, Science for Life Laboratory (SciLifeLab). Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.ORCID iD: 0000-0002-2494-1345
Stockholm University, Science for Life Laboratory (SciLifeLab). Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.ORCID iD: 0000-0001-8134-0805
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Number of Authors: 62023 (English)In: PLOS Genetics, ISSN 1553-7390, E-ISSN 1553-7404, Vol. 19, no 11, article id e1010882Article in journal (Refereed) Published
Abstract [en]

Upon nutrient depletion, bacteria stop proliferating and undergo physiological and morphological changes to ensure their survival. Yet, how these processes are coordinated in response to distinct starvation conditions is poorly understood. Here we compare the cellular responses of Caulobacter crescentus to carbon (C), nitrogen (N) and phosphorus (P) starvation conditions. We find that DNA replication initiation and abundance of the replication initiator DnaA are, under all three starvation conditions, regulated by a common mechanism involving the inhibition of DnaA translation. By contrast, cell differentiation from a motile swarmer cell to a sessile stalked cell is regulated differently under the three starvation conditions. During C and N starvation, production of the signaling molecules (p)ppGpp is required to arrest cell development in the motile swarmer stage. By contrast, our data suggest that low (p)ppGpp levels under P starvation allow P-starved swarmer cells to differentiate into sessile stalked cells. Further, we show that limited DnaA availability, and consequently absence of DNA replication initiation, is the main reason that prevents P-starved stalked cells from completing the cell cycle. Together, our findings demonstrate that Ccrescentus decouples cell differentiation from DNA replication initiation under certain starvation conditions, two otherwise intimately coupled processes. We hypothesize that arresting the developmental program either as motile swarmer cells or as sessile stalked cells improves the chances of survival of Ccrescentus during the different starvation conditions.

Place, publisher, year, edition, pages
2023. Vol. 19, no 11, article id e1010882
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Microbiology
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URN: urn:nbn:se:su:diva-227418DOI: 10.1371/journal.pgen.1010882ISI: 001124341600006PubMedID: 38011258Scopus ID: 2-s2.0-85179583488OAI: oai:DiVA.org:su-227418DiVA, id: diva2:1844472
Available from: 2024-03-14 Created: 2024-03-14 Last updated: 2024-03-14Bibliographically approved

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Hallgren, JoelKoonce, KiraFelletti, MicheleMortier, JulienTurco, EloisaJonas, Kristina

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