# Survival and adaptative strategies of Enterotoxigenic E. coli (ETEC) to the freshwater environment

**Authors:** Åsa Sjöling, Eswari Ashokkumar, Caroline Bjurnemark, Kaisa Thorell, Xue Xiao, Astrid von Mentzer, Yue O. O. Hu, Baoli Zhu, Enrique Joffré

PMC · DOI: 10.21203/rs.3.rs-6252921/v1 · 2025-03-19

## TL;DR

This study explores how Enterotoxigenic E. coli (ETEC) adapts to freshwater environments, revealing survival strategies and antibiotic resistance development.

## Contribution

The study identifies specific transcriptional and physiological adaptations of ETEC to freshwater stress, including colistin tolerance and biofilm formation.

## Key findings

- Over 1,700 genes were differentially expressed in ETEC during freshwater exposure, with early activation of catabolic pathways and membrane reinforcement.
- Prolonged freshwater exposure increased biofilm formation and colistin resistance in ETEC isolates.
- Plasmid gene analysis showed repression of virulence genes and activation of mobilization systems during initial water exposure.

## Abstract

Waterborne pathogenic enterobacteria are adapted for infection of human hosts but can also survive for long periods in water environments. To understand how the human pathogen enterotoxigenic Escherichia coli (ETEC) adapts to acute and long-term hypo-osmotic stress and oligotrophic water conditions, this study aimed to explore the effects of short- and long-term freshwater exposure on ETEC isolates by examining transcriptional responses, survival mechanisms, and antibiotic resistance development. RNA sequencing revealed that over 1,700 genes were differentially expressed, with significant transcriptional reprogramming occurring early within the first two hours of water exposure. Early responses included activation of catabolic pathways for nitrogen and carbon assimilation and downregulation of energy metabolism and anabolic processes to mitigate osmotic stress. Notably, the arnBCADTEF operon was upregulated, facilitating lipid A modification and membrane enforcement which also confers colistin tolerance. ETEC carries virulence genes on large plasmids which cause diarrheal disease in humans. Plasmid gene analysis indicated repression of virulence genes and upregulation of mobilization and toxin-antitoxin systems during the first 48 hours in water, suggesting a shift towards genetic adaptability. Prolonged exposure over weeks enhanced biofilm formation capacity and adherence to human epithelial cells, and ETEC isolates evolved towards increased colistin resistance. These findings stress the significant influence of freshwater on ETEC adaptive strategies, suggesting a role of waterborne transmission for human pathogens in development of persistence, biofilm formation capability and the emergence of antibiotic tolerance.

## Linked entities

- **Chemicals:** colistin (PubChem CID 5311054)
- **Diseases:** diarrheal disease (MONDO:0001673)
- **Species:** Escherichia coli (taxon 562)

## Full-text entities

- **Diseases:** diarrhea (MESH:D003967), infection (MESH:D007239), diarrheal disease (MESH:D004403), Enterotoxigenic E. coli (MESH:D004927)
- **Chemicals:** carbon (MESH:D002244), lipid A (MESH:D008050), nitrogen (MESH:D009584)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11957205/full.md

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Source: https://tomesphere.com/paper/PMC11957205