Publication | Open Access
Adhesion Inhibition of F1C‐Fimbriated <i>Escherichia coli</i> and <i>Pseudomonas aeruginosa</i> PAK and PAO by Multivalent Carbohydrate Ligands
64
Citations
37
References
2003
Year
Antimicrobial Drug DiscoveryAntibioticsMedicineVirulence FactorAdhesion InhibitionLong Spacer ArmsAntibacterial AgentCarbohydrate-protein InteractionMicrobiologyAntimicrobial CompoundAntimicrobial PharmacodynamicsMultivalent Carbohydrate LigandsBacterial PathogensMolecular MicrobiologySpacer ArmsAntimicrobial ResistanceBiomolecular Engineering
Abstract In order to evaluate their inhibition of bacterial adhesion, the carbohydrate sequences GalNAcβ1→4Gal and GalNAcβ1→4Galβ1→4Glc were synthesized. The disaccharide was conjugated to dendrons based on the 3,5‐di‐(2‐aminoethoxy)‐benzoic acid branching unit to yield di‐ and tetravalent versions of these compounds. A divalent compound was also prepared that had significantly longer spacer arms. Relevant monovalent compounds were prepared for comparison. Their anti‐adhesion properties against F1C‐fimbriated uropathogenic Escherichia coli were evaluated in an ELISA‐type assay by using a recombinant strain and also by using Pseudomonas aeruginosa strains PAO and PAK. Adhesion inhibition was observed in all cases, and multivalency effects of up to one order of magnitude were observed. The combination of spacer and multivalency effects led to a 38‐fold increase in the potency of a divalent inhibitor with long spacer arms towards the PAO strain when compared with the free carbohydrate.
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