Multidrug resistance and lipopolysaccharide remodeling associated with mcr-1 acquisition in Shiga toxin-producing Escherichia coli
4 affiliations
- 1Environmental Health Sciences, School of Public Health, University of Minnesota, St. Paul, Minnesota, USA
- 2Department of Food and Animal Biotechnology, Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul, Republic of Korea
- 3Department of Agricultural Biotechnology, Seoul National University, Seoul, Republic of Korea
- 4Department of Food and Nutrition, Hanyang University, Seoul, Republic of Korea
Abstract
The emergence of plasmid-mediated colistin resistance in Shiga toxin-producing Escherichia coli (STEC) is an important public health concern because these strains can combine antimicrobial resistance with intestinal pathogenic potential. However, although mcr-harboring STEC has been reported from food-related sources, the phenotypic consequences of mcr-1 acquisition in STEC remain poorly understood. In this study, we investigated the prevalence of mcr variants and associated antimicrobial resistance determinants among 144 mcr-harboring STEC isolates and examined the phenotypic impact of mcr-1 in E. coli O157:H7 ATCC 43894. Among the mcr-harboring STEC isolates, mcr-1 was the predominant mcr variant (63.9%), and 88.9% of mcr-1-positive isolates were multidrug-resistant. Notably, genomically predicted fosfomycin resistance determinants were detected in 84.8% of mcr-1-positive isolates. Acquisition of the mcr-1-harboring plasmid in E. coli O157:H7 ATCC 43894 increased adhesion to HEp-2 epithelial cells but reduced swimming motility, biofilm formation, and Galleria mellonella mortality. The reduced G. mellonella mortality may reflect altered innate immune stimulation. These changes were accompanied by remodeling of the lipopolysaccharide profile, with reduced banding in both the O-antigen and core-lipid A regions, reduced endotoxin levels, increased cell surface hydrophobicity, a less negative zeta potential, and reduced autoagglutination, all of which were mcr-1-dependent in knockout and complementation experiments. Collectively, these findings indicate that mcr-1 contributes beyond colistin resistance, converging on a coordinated reshaping of cell surface architecture and host interaction together with co-selection of resistance to other clinically relevant antibiotics, including fosfomycin.
IMPORTANCE: Shiga toxin-producing Escherichia coli is a major foodborne pathogen, but treatment options are limited because some antibiotics increase the risk of severe disease. Mobile colistin resistance genes in this pathogen are therefore concerning, especially alongside resistance to other clinically relevant antibiotics. This study shows that mcr-1 is the predominant colistin resistance gene among mcr-harboring Shiga toxin-producing E. coli and that these isolates frequently carry multidrug resistance determinants, including fosfomycin resistance. We further show that mcr-1 acquisition reshapes the bacterial cell surface and alters host-associated phenotypes in E. coli O157. Despite reduced mortality in Galleria mellonella, increased epithelial cell adhesion suggests that the reduced mortality may reflect altered innate immune stimulation rather than an overall attenuation of host-colonization potential. These findings suggest that mcr-1 is not only a colistin resistance determinant but also a factor associated with broader changes in resistance, surface architecture, and host interaction in foodborne E. coli.
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BibTeX
@article{ahn2026multidrug,
title = {{Multidrug resistance and lipopolysaccharide remodeling associated with mcr-1 acquisition in Shiga toxin-producing Escherichia coli}},
author = {Eunbyeol Ahn and Jinshil Kim and Sangryeol Ryu and Byeonghwa Jeon},
journal = {Microbiology Spectrum},
year = {2026},
month = sep,
doi = {10.1128/spectrum.02034-26},
url = {https://doi.org/10.1128/spectrum.02034-26},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Multidrug resistance and lipopolysaccharide remodeling associated with mcr-1 acquisition in Shiga toxin-producing Escherichia coli
AU - Eunbyeol Ahn
AU - Jinshil Kim
AU - Sangryeol Ryu
AU - Byeonghwa Jeon
PY - 2026
DA - 2026/09/30
JO - Microbiology Spectrum
DO - 10.1128/spectrum.02034-26
UR - https://doi.org/10.1128/spectrum.02034-26
AB - The emergence of plasmid-mediated colistin resistance in Shiga toxin-producing Escherichia coli (STEC) is an important public health concern because these strains can combine antimicrobial resistance with intestinal pathogenic potential. However, although mcr-harboring STEC has been reported from food-related sources, the phenotypic consequences of mcr-1 acquisition in STEC remain poorly understood. In this study, we investigated the prevalence of mcr variants and associated antimicrobial resistance determinants among 144 mcr-harboring STEC isolates and examined the phenotypic impact of mcr-1 in E. coli O157:H7 ATCC 43894. Among the mcr-harboring STEC isolates, mcr-1 was the predominant mcr variant (63.9%), and 88.9% of mcr-1-positive isolates were multidrug-resistant. Notably, genomically predicted fosfomycin resistance determinants were detected in 84.8% of mcr-1-positive isolates. Acquisition of the mcr-1-harboring plasmid in E. coli O157:H7 ATCC 43894 increased adhesion to HEp-2 epithelial cells but reduced swimming motility, biofilm formation, and Galleria mellonella mortality. The reduced G. mellonella mortality may reflect altered innate immune stimulation. These changes were accompanied by remodeling of the lipopolysaccharide profile, with reduced banding in both the O-antigen and core-lipid A regions, reduced endotoxin levels, increased cell surface hydrophobicity, a less negative zeta potential, and reduced autoagglutination, all of which were mcr-1-dependent in knockout and complementation experiments. Collectively, these findings indicate that mcr-1 contributes beyond colistin resistance, converging on a coordinated reshaping of cell surface architecture and host interaction together with co-selection of resistance to other clinically relevant antibiotics, including fosfomycin. IMPORTANCE: Shiga toxin-producing Escherichia coli is a major foodborne pathogen, but treatment options are limited because some antibiotics increase the risk of severe disease. Mobile colistin resistance genes in this pathogen are therefore concerning, especially alongside resistance to other clinically relevant antibiotics. This study shows that mcr-1 is the predominant colistin resistance gene among mcr-harboring Shiga toxin-producing E. coli and that these isolates frequently carry multidrug resistance determinants, including fosfomycin resistance. We further show that mcr-1 acquisition reshapes the bacterial cell surface and alters host-associated phenotypes in E. coli O157. Despite reduced mortality in Galleria mellonella, increased epithelial cell adhesion suggests that the reduced mortality may reflect altered innate immune stimulation rather than an overall attenuation of host-colonization potential. These findings suggest that mcr-1 is not only a colistin resistance determinant but also a factor associated with broader changes in resistance, surface architecture, and host interaction in foodborne E. coli.
SN - 2165-0497
ER -