Biofilm-producing Escherichia coli O104: H4 overcomes bile salts toxicity by expressing virulence and resistance proteins.
Maxsueli Aparecida Moura MachadoItziar Chapartegui-GonzálezVinicius Silva CastroEduardo Eustáquio de Souza FigueiredoCarlos Adam Conte JuniorAlfredo G TorresPublished in: Letters in applied microbiology (2024)
We investigated bile salts' ability to induce phenotypic changes in biofilm production and protein expression of pathogenic Escherichia coli strains. For this purpose, 82 pathogenic E. coli strains isolated from humans (n = 70), and animals (n = 12), were examined for their ability to form biofilms in the presence or absence of bile salts. We also identified bacterial proteins expressed in response to bile salts using sodium dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-electrophoresis) and Liquid Chromatography-Mass Spectrometry (LC-MS/MS). Lastly, we evaluated the ability of these strains to adhere to Caco-2 epithelial cells in the presence of bile salts. Regarding biofilm formation, two strains isolated from an outbreak in Republic of Georgia in 2009 were the only ones that showed a high and moderate capacity to form biofilm in the presence of bile salts. Further, we observed that those isolates, when in the presence of bile salts, expressed different proteins identified as outer membrane proteins (i.e. OmpC), and resistance to adverse growth conditions (i.e. F0F1, HN-S, and L7/L12). We also found that these isolates exhibited high adhesion to epithelial cells in the presence of bile salts. Together, these results contribute to the phenotypic characterization of E. coli O104: H4 strains.
Keyphrases
- escherichia coli
- biofilm formation
- ionic liquid
- pseudomonas aeruginosa
- candida albicans
- staphylococcus aureus
- mass spectrometry
- liquid chromatography
- klebsiella pneumoniae
- emergency department
- high resolution
- genetic diversity
- high intensity
- capillary electrophoresis
- antimicrobial resistance
- cell adhesion
- high performance liquid chromatography
- atomic force microscopy