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FEMS Microbes· 2026Q1

Copper stress upregulates oxidative stress response, histidine production and iron acquisition genes in E. coli

Hanna Ainelo, Karola Joearu, Andres Ainelo, Angela Ivask

Short summary

Excess copper (2 mM and 8 mM) upregulates oxidative stress response, histidine biosynthesis, and iron acquisition genes in E. coli, with 487 and 364 genes induced, respectively.

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Key points

  • Excess copper (2 mM and 8 mM) induces significant transcriptional changes in E. coli, upregulating 487 and 364 genes, respectively.
  • Key upregulated pathways include oxidative stress defenses, histidine biosynthesis, and iron acquisition systems (e.g., enterobactin).
  • Copper stress represses gene sets related to biofilm formation and anaerobic metabolism at higher concentrations.
  • External iron supplementation did not mitigate copper toxicity.
  • A genome-wide GFP-based promoter library showed limited utility due to low signal-to-noise ratios.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract Copper is widely used as a fast-acting antimicrobial, yet the strategies that allow bacteria to survive copper stress remain incompletely understood. Here, we characterize the transcriptional responses of Escherichia coli MG1655 to excess ionic copper using RNA sequencing and a genome-wide GFP-based promoter library. We applied 2 mM copper, which slows growth, and 8 mM copper, a near-lethal concentration. RNA-seq revealed extensive transcriptome remodeling, with 487 genes upregulated at 2 mM and 364 at 8 mM. Both concentrations strongly induced canonical copper-responsive systems, oxidative stress defenses, histidine biosynthesis, and multiple iron acquisition pathways – including enterobactin biosynthesis and transport – despite external iron failing to reduce copper toxicity. At 2 mM copper, additional pathways were activated, including heat-shock and protein-folding functions as well as lipid A, methionine and arginine biosynthesis. Copper exposure also repressed large gene sets: 486 genes at 2 mM, enriched for biofilm formation and pH elevation, and 217 genes at 8 mM, enriched for anaerobic metabolism. In contrast to the robust RNA-seq results, we investigated the Horizon Discovery E. coli genome-wide GFP based promoter library as an alternative screening tool. However, in our experiments it showed low signal-to-noise ratios, limiting its suitability for large scale gene expression screening.

The authors' abstract, as published at the source. FEMS Microbes, 2026 · DOI ↗

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Field: Nutrition and Dietetics

Nutrition and DieteticsNursing