| Literature DB >> 30104274 |
Mary Kate Alexander1, Anh Miu2, Angela Oh3, Mike Reichelt4, Hoangdung Ho3, Cecile Chalouni4, Sharada Labadie5, Lan Wang5, Jun Liang5, Nicholas N Nickerson6, Huiyong Hu5, Lan Yu7, Miaofen Du7, Donghong Yan8, Summer Park8, Janice Kim8, Min Xu8, Benjamin D Sellers5, Hans E Purkey5, Nicholas J Skelton5, Michael F T Koehler5, Jian Payandeh3, Vishal Verma5, Yiming Xu2, Christopher M Koth3, Mireille Nishiyama1.
Abstract
There is a critical need for new antibacterial strategies to counter the growing problem of antibiotic resistance. In Gram-negative bacteria, the outer membrane (OM) provides a protective barrier against antibiotics and other environmental insults. The outer leaflet of the outer membrane is primarily composed of lipopolysaccharide (LPS). Outer membrane biogenesis presents many potentially compelling drug targets as this pathway is absent in higher eukaryotes. Most proteins involved in LPS biosynthesis and transport are essential; however, few compounds have been identified that inhibit these proteins. The inner membrane ABC transporter MsbA carries out the first essential step in the trafficking of LPS to the outer membrane. We conducted a biochemical screen for inhibitors of MsbA and identified a series of quinoline compounds that kill Escherichia coli through inhibition of its ATPase and transport activity, with no loss of activity against clinical multidrug-resistant strains. Identification of these selective inhibitors indicates that MsbA is a viable target for new antibiotics, and the compounds we identified serve as useful tools to further probe the LPS transport pathway in Gram-negative bacteria.Entities:
Keywords: ABC transporters; Enterobacteriaceae; Escherichia coli; MsbA; lipopolysaccharide; outer membrane
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Year: 2018 PMID: 30104274 PMCID: PMC6201111 DOI: 10.1128/AAC.01142-18
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191