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Bacterial ageing in the absence of external stressors.

Urszula Łapińska | Georgina Glover | Pablo Capilla-Lasheras | Andrew J Young | Stefano Pagliara
Philosophical transactions of the Royal Society of London. Series B, Biological sciences | 2019

Evidence of ageing in the bacterium Escherichia coli was a landmark finding in senescence research, as it suggested that even organisms with morphologically symmetrical fission may have evolved strategies to permit damage accumulation. However, recent work has suggested that ageing is only detectable in this organism in the presence of extrinsic stressors, such as the fluorescent proteins and strong light sources typically used to excite them. Here we combine microfluidics with brightfield microscopy to provide evidence of ageing in E. coli in the absence of these stressors. We report (i) that the doubling time of the lineage of cells that consistently inherits the 'maternal old pole' progressively increases with successive rounds of cell division until it reaches an apparent asymptote, and (ii) that the parental cell divides asymmetrically, with the old pole daughter showing a longer doubling time and slower glucose accumulation than the new pole daughter. Notably, these patterns arise without the progressive accumulation or asymmetric partitioning of observable misfolded-protein aggregates, phenomena previously hypothesized to cause the ageing phenotype. Our findings suggest that ageing is part of the naturally occurring ecologically-relevant phenotype of this bacterium and highlight the importance of alternative mechanisms of damage accumulation in this context. This article is part of a discussion meeting issue 'Single cell ecology'.

Pubmed ID: 31587633

Research resources used in this publication

None found

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Associated grants

  • Agency: Medical Research Council, United Kingdom
    Id: MC_PC_17189
  • Agency: Biotechnology and Biological Sciences Research Council, United Kingdom
    Id: BB/M009122/1
  • Agency: Biotechnology and Biological Sciences Research Council, United Kingdom
    Id: BB/H022716/1
  • Agency: Wellcome Trust, United Kingdom
    Id: WT097835/Z/11/Z
  • Agency: Medical Research Council, United Kingdom
    Id: MCPC17189

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UniProtKB (tool)

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Central repository for collection of functional information on proteins, with accurate and consistent annotation. In addition to capturing core data mandatory for each UniProtKB entry (mainly, the amino acid sequence, protein name or description, taxonomic data and citation information), as much annotation information as possible is added. This includes widely accepted biological ontologies, classifications and cross-references, and experimental and computational data. The UniProt Knowledgebase consists of two sections, UniProtKB/Swiss-Prot and UniProtKB/TrEMBL. UniProtKB/Swiss-Prot (reviewed) is a high quality manually annotated and non-redundant protein sequence database which brings together experimental results, computed features, and scientific conclusions. UniProtKB/TrEMBL (unreviewed) contains protein sequences associated with computationally generated annotation and large-scale functional characterization that await full manual annotation. Users may browse by taxonomy, keyword, gene ontology, enzyme class or pathway.

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RRID:SCR_008988

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