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- Publisher Website: 10.1002/adtp.202000084
- Scopus: eid_2-s2.0-85103744538
- WOS: WOS:000543544900001
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Article: Imidazole Type Antifungal Drugs Are Effective Colistin Adjuvants That Resensitize Colistin‐Resistant Enterobacteriaceae
Title | Imidazole Type Antifungal Drugs Are Effective Colistin Adjuvants That Resensitize Colistin‐Resistant Enterobacteriaceae |
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Authors | |
Keywords | colistin adjuvants drug repurposing econazole enterobacteriaceae membrane potentials |
Issue Date | 2020 |
Publisher | John Wiley & Sons Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2366-3987 |
Citation | Advanced Therapeutics, 2020, Epub 2020-06-22, p. article no. 2000084 How to Cite? |
Abstract | The clinical value of the last‐line antibiotic colistin is limited by its toxicity and the increasing prevalence of drug resistance in recent years. These two issues can be tackled by searching for adjuvant compounds that enhance colistin activity and facilitate reduction of treatment dosage. This study identifies a Food and Drug Administration (FDA)‐approved drug, econazole, which can act synergistically with colistin to effectively eradicate colistin‐resistant bacteria both in vitro and in a mouse infection model, and treat infections caused by colistin‐susceptible bacteria in lower doses. Structural analysis shows that econazole exhibits high lipid affinity and acts as an ionophore. Functional assays and microscopy analysis confirm that econazole causes dissipation of transmembrane proton motive force (PMF) and damage to the bacterial cell membrane. Its synergistic effect with colistin might be due to the combination of these two compounds causing further collapse of PMF, arrest of various cellular functions, and eventually cell death. These findings suggest that the econazole and colistin drug combination is highly effective in eradicating colistin‐resistant Gram negative bacterial pathogens regardless of their mechanism of colistin resistance. |
Persistent Identifier | http://hdl.handle.net/10722/284533 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Xu, C | - |
dc.contributor.author | Chen, K | - |
dc.contributor.author | Chan, KF | - |
dc.contributor.author | Chan, EWC | - |
dc.contributor.author | Guo, X | - |
dc.contributor.author | Chow, HY | - |
dc.contributor.author | Zhao, G | - |
dc.contributor.author | Zeng, P | - |
dc.contributor.author | Wang, M | - |
dc.contributor.author | Zhu, Y | - |
dc.contributor.author | Li, X | - |
dc.contributor.author | Wong, KY | - |
dc.contributor.author | Chen, S | - |
dc.date.accessioned | 2020-08-07T08:59:00Z | - |
dc.date.available | 2020-08-07T08:59:00Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Advanced Therapeutics, 2020, Epub 2020-06-22, p. article no. 2000084 | - |
dc.identifier.uri | http://hdl.handle.net/10722/284533 | - |
dc.description.abstract | The clinical value of the last‐line antibiotic colistin is limited by its toxicity and the increasing prevalence of drug resistance in recent years. These two issues can be tackled by searching for adjuvant compounds that enhance colistin activity and facilitate reduction of treatment dosage. This study identifies a Food and Drug Administration (FDA)‐approved drug, econazole, which can act synergistically with colistin to effectively eradicate colistin‐resistant bacteria both in vitro and in a mouse infection model, and treat infections caused by colistin‐susceptible bacteria in lower doses. Structural analysis shows that econazole exhibits high lipid affinity and acts as an ionophore. Functional assays and microscopy analysis confirm that econazole causes dissipation of transmembrane proton motive force (PMF) and damage to the bacterial cell membrane. Its synergistic effect with colistin might be due to the combination of these two compounds causing further collapse of PMF, arrest of various cellular functions, and eventually cell death. These findings suggest that the econazole and colistin drug combination is highly effective in eradicating colistin‐resistant Gram negative bacterial pathogens regardless of their mechanism of colistin resistance. | - |
dc.language | eng | - |
dc.publisher | John Wiley & Sons Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2366-3987 | - |
dc.relation.ispartof | Advanced Therapeutics | - |
dc.rights | Preprint This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Postprint This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | - |
dc.subject | colistin adjuvants | - |
dc.subject | drug repurposing | - |
dc.subject | econazole | - |
dc.subject | enterobacteriaceae | - |
dc.subject | membrane potentials | - |
dc.title | Imidazole Type Antifungal Drugs Are Effective Colistin Adjuvants That Resensitize Colistin‐Resistant Enterobacteriaceae | - |
dc.type | Article | - |
dc.identifier.email | Chow, HY: hchowhy@connect.hku.hk | - |
dc.identifier.email | Li, X: xuechenl@hku.hk | - |
dc.identifier.authority | Li, X=rp00742 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/adtp.202000084 | - |
dc.identifier.scopus | eid_2-s2.0-85103744538 | - |
dc.identifier.hkuros | 311898 | - |
dc.identifier.volume | Epub 2020-06-22 | - |
dc.identifier.spage | article no. 2000084 | - |
dc.identifier.epage | article no. 2000084 | - |
dc.identifier.eissn | 2366-3987 | - |
dc.identifier.isi | WOS:000543544900001 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 2366-3987 | - |