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Identification of N‐Arylated NH125 Analogues as Rapid Eradicating Agents against MRSA Persister Cells and Potent Biofilm Killers of Gram‐Positive Pathogens
Author(s) -
Abouelhassan Yasmeen,
Basak Akash,
Yousaf Hussain,
Huigens Robert W.
Publication year - 2017
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.201600622
Subject(s) - biofilm , multidrug tolerance , microbiology and biotechnology , enterococcus faecium , staphylococcus aureus , staphylococcus epidermidis , biology , methicillin resistant staphylococcus aureus , antibiotics , chemistry , bacteria , genetics
Abstract Bacterial biofilms housing dormant persister cells are innately tolerant to antibiotics and disinfectants, yet several membrane‐active agents are known to eradicate tolerant bacterial cells. NH125, a membrane‐active persister killer and starting point for development, led to the identification of two N‐arylated analogues ( 1 and 2 ) that displayed improved biofilm eradication potencies compared to the parent compound and rapid persister‐cell‐killing activities in stationary cultures of methicillin‐resistant Staphylococcus aureus (MRSA). We found 1 and 2 to be superior to other membrane‐active agents in biofilm eradication assays, with 1 demonstrating minimum biofilm eradication concentrations (MBEC) of 23.5, 11.7, and 2.35 μ m against MRSA, methicillin‐resistant Staphylococcus epidermidis (MRSE), and vancomycin‐resistant Enterococcus faecium (VRE) biofilms, respectively. We tested our panel of membrane‐active agents against MRSA stationary cultures and found 1 to rapidly eradicate MRSA stationary cells by 4 log units (99.99 %) in 30 min. The potent biofilm eradication and rapid persister‐cell‐killing activities exhibited by N‐arylated NH125 analogues could have significant impact in addressing biofilm‐associated problems.