TY - JOUR
T1 - Biofilm-producing Escherichia coli O104:H4 overcomes bile salts toxicity by expressing virulence and resistance proteins
AU - Moura Machado, Maxsueli Aparecida
AU - Chapartegui Gonzalez, Itziar
AU - Castro, Vinicius Silva
AU - de Souza Figueiredo, Eduardo Eustáquio
AU - Conte-Junior, Carlos Adam
AU - Torres, Alfredo G.
N1 - Publisher Copyright:
© The Author(s) 2024. Published by Oxford University Press on behalf of Applied Microbiology International. All rights reserved.
PY - 2024/4
Y1 - 2024/4
N2 - 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.
AB - 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.
KW - epithelial cells
KW - liquid chromatography-mass spectrometry
KW - OmpC protein
KW - osmotic stress
KW - STEC
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U2 - 10.1093/lambio/ovae032
DO - 10.1093/lambio/ovae032
M3 - Article
C2 - 38573831
AN - SCOPUS:85191845357
SN - 0266-8254
VL - 77
JO - Letters in Applied Microbiology
JF - Letters in Applied Microbiology
IS - 4
M1 - ovae032
ER -