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Massively parallel combination screen reveals small molecule sensitization of antibiotic-resistant Gram-negative ESKAPE pathogens.

Megan W TseMeilin ZhuBenjamin PetersEfrat HamamiJulie ChenKathleen P DavisSamuel NitzJuliane WellerThulasi WarrierDiana K HuntYoelkys MoralesTomohiko KawateJeffrey L GaulinJon H ComeJuan Hernandez-BirdWenwen HuoIsabelle NeisewanderLaura L KiesslingDeborah T HungJoan MecsasBree B AldridgeRalph R IsbergPaul C Blainey
Published in: bioRxiv : the preprint server for biology (2024)
. We generated P2-56-3, a more potent derivative of P2-56, and found that it likely potentiates rifampin by compromising the outer membrane integrity. Our study demonstrates a high-throughput strategy for identifying antibiotic potentiators against multidrug-resistant bacteria.
Keyphrases
  • gram negative
  • multidrug resistant
  • high throughput
  • small molecule
  • drug resistant
  • acinetobacter baumannii
  • klebsiella pneumoniae
  • protein protein
  • pseudomonas aeruginosa
  • cystic fibrosis