TY - JOUR
T1 - Otilonium bromide boosts antimicrobial activities of colistin against Gram-negative pathogens and their persisters
AU - Xu, Chen
AU - Liu, Chenyu
AU - Chen, Kaichao
AU - Zeng, Ping
AU - Chan, Edward Wai Chi
AU - Chen, Sheng
N1 - Funding Information:
This research was supported by the Research Impact Fund (R5011-18F) from the Research Grant Council of Hong Kong Government.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/6/21
Y1 - 2022/6/21
N2 - Colistin is the last-line antibiotic against Gram-negative pathogens. Here we identify an FDA-approved drug, Otilonium bromide (Ob), which restores the activity of colistin against colistin-resistant Gram-negative bacteria in vitro and in a mouse infection model. Ob also reduces the colistin dosage required for effective treatment of infections caused by colistin-susceptible bacteria, thereby reducing the toxicity of the drug regimen. Furthermore, Ob acts synergistically with colistin in eradicating multidrug-tolerant persisters of Gram-negative bacteria in vitro. Functional studies and microscopy assays confirm that the synergistic antimicrobial effect exhibited by the Ob and colistin involves permeabilizing the bacterial cell membrane, dissipating proton motive force and suppressing efflux pumps, resulting in membrane damages, cytosol leakage and eventually bacterial cell death. Our findings suggest that Ob is a colistin adjuvant which can restore the clinical value of colistin in combating life-threatening, multidrug resistant Gram-negative pathogens.
AB - Colistin is the last-line antibiotic against Gram-negative pathogens. Here we identify an FDA-approved drug, Otilonium bromide (Ob), which restores the activity of colistin against colistin-resistant Gram-negative bacteria in vitro and in a mouse infection model. Ob also reduces the colistin dosage required for effective treatment of infections caused by colistin-susceptible bacteria, thereby reducing the toxicity of the drug regimen. Furthermore, Ob acts synergistically with colistin in eradicating multidrug-tolerant persisters of Gram-negative bacteria in vitro. Functional studies and microscopy assays confirm that the synergistic antimicrobial effect exhibited by the Ob and colistin involves permeabilizing the bacterial cell membrane, dissipating proton motive force and suppressing efflux pumps, resulting in membrane damages, cytosol leakage and eventually bacterial cell death. Our findings suggest that Ob is a colistin adjuvant which can restore the clinical value of colistin in combating life-threatening, multidrug resistant Gram-negative pathogens.
UR - http://www.scopus.com/inward/record.url?scp=85132296215&partnerID=8YFLogxK
U2 - 10.1038/s42003-022-03561-z
DO - 10.1038/s42003-022-03561-z
M3 - Journal article
C2 - 35729200
AN - SCOPUS:85132296215
SN - 2399-3642
VL - 5
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 613
ER -