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Nonlethal deleterious mutation-induced stress accelerates bacterial aging.

Maryam Kohram1, Amy E Sanderson1, Alicia Loui1

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Summary
This summary is machine-generated.

Loss-of-function mutations in Escherichia coli trigger stress responses for adaptation. Certain mutations, like in ATP synthase, cause slower growth but reveal an "aging cost" in individual cells, impacting population resilience.

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Area of Science:

  • Microbiology
  • Genetics
  • Cell Biology

Background:

  • Microbial adaptation relies on random mutagenesis, often causing gene loss.
  • Deleterious mutations trigger cellular stress responses (allostasis) for survival.

Purpose of the Study:

  • To investigate the effects of 65 gene deletions on E. coli growth in varied environments.
  • To analyze transcriptome changes and single-cell phenotypes in specific mutants, including ATP synthase subunit deletions.

Main Methods:

  • Systematic screening of 65 single-gene deletion mutants in E. coli across three environments.
  • Transcriptome profiling of select mutants, focusing on adenosine triphosphate (ATP) synthase subunit deletions.
  • Single-cell analysis of growth, proliferation, and senescence in ATP synthase alpha-subunit deleted (ΔatpA) cells.

Main Results:

  • Mutants showed environment- and gene-specific transcriptome reorganization.
  • ΔatpA cells exhibited higher metabolic rates but slower growth than wild-type.
  • Single ΔatpA cells displayed early senescence and a post-replicative state, despite normal proliferation.

Conclusions:

  • Bacterial adaptation involves a trade-off between population resilience and individual cell