Environmental stress shapes persistence-like phenotypes and genomic changes in Escherichia coli and Morganella morganii: an exploratory study

Introduction Enterobacterales, including E. coli and M. morganii , employ adaptive mechanisms to withstand environmental and host-related stressors, including extreme temperatures, osmotic pressure changes, acidic conditions, and antibiotic pressures. Survival in these conditions can consequently enhance their antibiotic tolerance and persistence. Bacterial persistence contributes to chronic infections and antibiotic treatment failure. This exploratory study investigates the impact of stress conditions (pH, temperature, osmotic, and antibiotic stress) on persistence and genomic adaptations in E. coli and M. morganii . Methods Clinical and environmental M. morganii and E. coli strains from Ghanaian tertiary hospitals were exposed to extreme temperatures (cold ~4 °C, and heat ~45 °C), extreme pH (pH 3, pH 9, pH 10), and hyperosmolarity (1.71M NaCl). Growth kinetics were monitored by OD600 and CFU determinations, and persister-like cell formation was assessed using time-kill assays at 2 × MIC antibiotic conditions. Genomic changes associated with stress recovery including both adaptive mutations and enrichment of pre-existing variants were captured using comparative whole genome sequencing (WGS) of stress-recovered isolates to parental strains. Results Strains exhibited variation in growth kinetics under different stress conditions compared to controls. Temperature, pH, and osmotic stress each affected bacterial growth to varying degrees. Heat stress in particular promoted increased persister-like cell formation in E. coli (with strain-specific differences) and, to a lesser extent, in M. morganii upon exposure to meropenem as observed in the isolates examined in this study. WGS analysis revealed that all four studied strains harbored virulence and resistance genes, with missense mutations detected in stress-recovered variants. Most of the mutated genes encode proteins that may play key roles in metabolic processes, transport functions and transcriptional regulations. Discussion This exploratory study suggests that environmental stress drives both phenotypic and genotypic changes, and that these enhance subsequent survival upon challenge with antibiotics. These adaptive responses may contribute to antibiotic tolerance and chronic infection, emphasizing the need for therapeutic strategies targeting stress response pathways.

Authors

Institutions

Publication Details

Journal
Frontiers in Microbiology
Published
2026-03-17
DOI
https://doi.org/10.3389/fmicb.2026.1749211
Primary Topic
Escherichia coli research studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Environmental stress shapes persistence-like phenotypes and genomic changes in Escherichia coli and Morganella morganii: an exploratory study

Tosin Yetunde Senbadejo, Christina R. Bourne, Samuel Ntiamoah Osei, Elizabeth W. Bugase et al.
Frontiers in Microbiology
Escherichia coli research studies
article

Environmental stress shapes persistence-like phenotypes and genomic changes in Escherichia coli and Morganella morganii: an exploratory study

Tosin Yetunde Senbadejo, Christina R. Bourne, Samuel Ntiamoah Osei, Elizabeth W. Bugase, Abiola Isawumi
article en

Abstract

Introduction Enterobacterales, including E. coli and M. morganii , employ adaptive mechanisms to withstand environmental and host-related stressors, including extreme temperatures, osmotic pressure changes, acidic conditions, and antibiotic pressures. Survival in these conditions can consequently enhance their antibiotic tolerance and persistence. Bacterial persistence contributes to chronic infections and antibiotic treatment failure. This exploratory study investigates the impact of stress conditions (pH, temperature, osmotic, and antibiotic stress) on persistence and genomic adaptations in E. coli and M. morganii . Methods Clinical and environmental M. morganii and E. coli strains from Ghanaian tertiary hospitals were exposed to extreme temperatures (cold ~4 °C, and heat ~45 °C), extreme pH (pH 3, pH 9, pH 10), and hyperosmolarity (1.71M NaCl). Growth kinetics were monitored by OD600 and CFU determinations, and persister-like cell formation was assessed using time-kill assays at 2 × MIC antibiotic conditions. Genomic changes associated with stress recovery including both adaptive mutations and enrichment of pre-existing variants were captured using comparative whole genome sequencing (WGS) of stress-recovered isolates to parental strains. Results Strains exhibited variation in growth kinetics under different stress conditions compared to controls. Temperature, pH, and osmotic stress each affected bacterial growth to varying degrees. Heat stress in particular promoted increased persister-like cell formation in E. coli (with strain-specific differences) and, to a lesser extent, in M. morganii upon exposure to meropenem as observed in the isolates examined in this study. WGS analysis revealed that all four studied strains harbored virulence and resistance genes, with missense mutations detected in stress-recovered variants. Most of the mutated genes encode proteins that may play key roles in metabolic processes, transport functions and transcriptional regulations. Discussion This exploratory study suggests that environmental stress drives both phenotypic and genotypic changes, and that these enhance subsequent survival upon challenge with antibiotics. These adaptive responses may contribute to antibiotic tolerance and chronic infection, emphasizing the need for therapeutic strategies targeting stress response pathways.

Frontiers in MicrobiologyVol. 17
University of Ghana (GH), Africa Center (US), University of Oklahoma (US)
Life in Land
Openalex Percentile: Top 17%
Escherichia coli research studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.