Small-molecule inhibitors target Escherichia coli amyloid biogenesis and biofilm formation

小分子抑制剂靶向大肠杆菌淀粉样蛋白的生物合成和生物膜的形成

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作者:Lynette Cegelski, Jerome S Pinkner, Neal D Hammer, Corinne K Cusumano, Chia S Hung, Erik Chorell, Veronica Aberg, Jennifer N Walker, Patrick C Seed, Fredrik Almqvist, Matthew R Chapman, Scott J Hultgren

Abstract

Curli are functional extracellular amyloid fibers produced by uropathogenic Escherichia coli (UPEC) and other Enterobacteriaceae. Ring-fused 2-pyridones, such as FN075 and BibC6, inhibited curli biogenesis in UPEC and prevented the in vitro polymerization of the major curli subunit protein CsgA. The curlicides FN075 and BibC6 share a common chemical lineage with other ring-fused 2-pyridones termed pilicides. Pilicides inhibit the assembly of type 1 pili, which are required for pathogenesis during urinary tract infection. Notably, the curlicides retained pilicide activities and inhibited both curli-dependent and type 1-dependent biofilms. Furthermore, pretreatment of UPEC with FN075 significantly attenuated virulence in a mouse model of urinary tract infection. Curli and type 1 pili exhibited exclusive and independent roles in promoting UPEC biofilms, and curli provided a fitness advantage in vivo. Thus, the ability of FN075 to block the biogenesis of both curli and type 1 pili endows unique anti-biofilm and anti-virulence activities on these compounds.

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