# Fitness cost and biofilm formation in fosfomycin-resistant clinical Escherichia coli and Klebsiella pneumoniae isolates

**Authors:** Mustafa ÖKEER, Sabire Şöhret AYDEMİR, Bayrı ERAÇ

PMC · DOI: 10.55730/1300-0144.6165 · 2025-12-21

## TL;DR

This study examines how fosfomycin resistance affects bacterial fitness and biofilm formation in E. coli and K. pneumoniae clinical isolates.

## Contribution

The study identifies the fitness cost of fosfomycin resistance and its limited impact on biofilm formation in clinical isolates.

## Key findings

- Fosfomycin resistance was associated with slower growth rates in some isolates.
- Gene expression changes were observed in resistant isolates, but biofilm formation was largely unaffected.
- Resistance to fosfomycin was found in 16.6% of E. coli and 23.5% of K. pneumoniae isolates.

## Abstract

Fosfomycin has regained importance owing to its unique mechanism of action and effectiveness against extended-spectrum β-lactamase-producing Gram-negative bacteria. This study aimed to evaluate the biological fitness cost associated with fosfomycin resistance and its impact on biofilm formation in clinical Enterobacteriaceae isolates.

A total of 78 Escherichia coli and 34 Klebsiella pneumoniae strains isolated from urine samples at Ege University Hospital were analyzed. Fosfomycin minimum inhibitory concentrations (MICs) were determined using the reference agar dilution method. Resistance was induced by exposing two K. pneumoniae strains with a fosfomycin MIC of 4 μg/mL and two E. coli strains susceptible to fosfomycin (MIC ≤ 8 μg/mL) to gradually increasing concentrations of the antibiotic. Biofilm-forming capacities, growth rates, and expression levels of selected virulence genes (fimH and papC in E. coli; entB, mrkD, uge, wabG, and ycfM in K. pneumoniae) were compared between variants with low and high fosfomycin MICs.

Of the 78 E. coli isolates, 13 (16.6%) were resistant to fosfomycin. Additionally, eight (23.5%) of 34 K. pneumoniae isolates exhibited high fosfomycin MICs (MIC > 32 μg/mL). No significant differences in biofilm formation were observed between the variants. However, the expression of the fimH gene decreased in one E. coli resistant variant compared with its susceptible counterpart. While the expression of the uge gene decreased in one K. pneumoniae isolate with a high MIC, the expression of the wabG gene increased. Slower growth rates were observed in two fosfomycin-resistant E. coli strains and one K. pneumoniae strain with a high fosfomycin MIC than in their counterparts.

These findings suggest that, in the examined isolates, decreased susceptibility to fosfomycin was associated with slower growth, whereas biofilm formation ability remained largely unaffected. Continued surveillance of fosfomycin resistance is essential owing to its potential implications for bacterial fitness and pathogenicity.

## Linked entities

- **Genes:** fimH (minor component of type 1 fimbriae) [NCBI Gene 913676], PCDH8 (protocadherin 8) [NCBI Gene 5100], entB (isochorismatase) [NCBI Gene 916993], mrkD (outer membrane usher protein) [NCBI Gene 11639328], UGE (bifunctional UDP-glucose 4-epimerase and UDP-xylose 4-epimerase 1) [NCBI Gene 103433018], ycfM (putative outer membrane lipoprotein) [NCBI Gene 1252725]
- **Chemicals:** fosfomycin (PubChem CID 441029)
- **Species:** Escherichia coli (taxon 562), Klebsiella pneumoniae (taxon 573)

## Full-text entities

- **Genes:** mrkD [NCBI Gene 13982034]
- **Chemicals:** Fosfomycin (MESH:D005578)
- **Species:** Enterobacteriaceae (enterobacteria, family) [taxon 543], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Escherichia coli (E. coli, species) [taxon 562], Klebsiella pneumoniae (species) [taxon 573]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12974299/full.md

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Source: https://tomesphere.com/paper/PMC12974299