Abstract: Urinary tract infections (UTIs) are mainly caused by uropathogenic Escherichia coli (UPEC). Acute and recurrent UTIs are commonly treated with antibiotics, the efficacy of which is limited by the emergence of antibiotic resistant strains. The natural sugar d-mannose is considered as an alternative to antibiotics due to its ability to mask the bacterial adhesin FimH, thereby preventing its binding to urothelial cells. Despite its extensive use, the possibility that d-mannose exerts “antibiotic-like” activity by altering bacterial growth and metabolism or selecting FimH variants has not been investigated yet. To this aim, main bacterial features of the prototype UPEC strain CFT073 treated with d-mannose were analyzed by standard microbiological methods. FimH functionality was analyzed by yeast agglutination and human bladder cell adhesion assays. Our results indicate that high d-mannose concentrations have no effect on bacterial growth and do not interfere with the activity of different antibiotics. d-mannose ranked as the least preferred carbon source to support bacterial metabolism and growth, in comparison with d-glucose, d-fructose, and l-arabinose. Since small glucose amounts are physiologically detectable in urine, we can conclude that the presence of d-mannose is irrelevant for bacterial metabolism. Moreover, d-mannose removal after long-term exposure did not alter FimH’s capacity to bind to mannosylated proteins. Overall, our data indicate that d-mannose is a good alternative in the prevention and treatment of UPEC-related UTIs.

d-mannose treatment neither affects uropathogenic Escherichia coli properties nor induces stable FimH modifications / Scribano, Daniela; Sarsharjeryandeh, Meysam; Prezioso, Carla; Lucarelli, Marco; Angeloni, Antonio; Zagaglia, Carlo; Palamara, ANNA TERESA; AMBROSI SACCONI ROSATI, Cecilia. - In: MOLECULES. - ISSN 1420-3049. - 25:2(2020), pp. 1-14. [10.3390/molecules25020316]

d-mannose treatment neither affects uropathogenic Escherichia coli properties nor induces stable FimH modifications

Daniela Scribano
Co-primo
;
Meysam Sarshar
Co-primo
;
Carla Prezioso;Marco Lucarelli;Antonio Angeloni;Carlo Zagaglia;Anna Teresa Palamara;Cecilia Ambrosi
2020

Abstract

Abstract: Urinary tract infections (UTIs) are mainly caused by uropathogenic Escherichia coli (UPEC). Acute and recurrent UTIs are commonly treated with antibiotics, the efficacy of which is limited by the emergence of antibiotic resistant strains. The natural sugar d-mannose is considered as an alternative to antibiotics due to its ability to mask the bacterial adhesin FimH, thereby preventing its binding to urothelial cells. Despite its extensive use, the possibility that d-mannose exerts “antibiotic-like” activity by altering bacterial growth and metabolism or selecting FimH variants has not been investigated yet. To this aim, main bacterial features of the prototype UPEC strain CFT073 treated with d-mannose were analyzed by standard microbiological methods. FimH functionality was analyzed by yeast agglutination and human bladder cell adhesion assays. Our results indicate that high d-mannose concentrations have no effect on bacterial growth and do not interfere with the activity of different antibiotics. d-mannose ranked as the least preferred carbon source to support bacterial metabolism and growth, in comparison with d-glucose, d-fructose, and l-arabinose. Since small glucose amounts are physiologically detectable in urine, we can conclude that the presence of d-mannose is irrelevant for bacterial metabolism. Moreover, d-mannose removal after long-term exposure did not alter FimH’s capacity to bind to mannosylated proteins. Overall, our data indicate that d-mannose is a good alternative in the prevention and treatment of UPEC-related UTIs.
2020
uropathogenic e. coli; cft073; d-mannose; fimh; urinary tract infections (utis); bacterial sugar metabolism
01 Pubblicazione su rivista::01a Articolo in rivista
d-mannose treatment neither affects uropathogenic Escherichia coli properties nor induces stable FimH modifications / Scribano, Daniela; Sarsharjeryandeh, Meysam; Prezioso, Carla; Lucarelli, Marco; Angeloni, Antonio; Zagaglia, Carlo; Palamara, ANNA TERESA; AMBROSI SACCONI ROSATI, Cecilia. - In: MOLECULES. - ISSN 1420-3049. - 25:2(2020), pp. 1-14. [10.3390/molecules25020316]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1416288
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