Exploring Structure–Activity Relationships of Niclosamide-Based Colistin Potentiators in Colistin-Resistant Gram-Negative Bacteria

Author:

Berry Liam1,Neale Quinn1,Arora Rajat1ORCID,Ramirez Danyel1,Brizuela Marc1,Domalaon Ronald1,Arthur Gilbert2,Schweizer Frank13ORCID

Affiliation:

1. Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada

2. Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E 3N4, Canada

3. Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, MB R3E 0J9, Canada

Abstract

Colistin is primarily used as a last resort antibiotic against highly resistant Gram-negative bacteria (GNB). Rising rates of colistin resistance, however, may limit future use of this agent. The anthelmintic drug niclosamide has been shown to enhance colistin activity in combination therapy, but a detailed structure–activity relationship (SAR) for niclosamide against GNB has yet to be studied. A series of niclosamide analogs were synthesized to perform an SAR, leading to the discovery of a lead compound that displayed comparable colistin-potentiating activity to niclosamide with reduced cytotoxicity. Overall, this work provides important insights into synthetic strategies for the future development of new niclosamide derivatives and demonstrates that toxicity to mammalian cells can be reduced while maintaining colistin potentiation.

Funder

Natural Sciences and Engineering Research Council of Canada

University of Manitoba

Publisher

MDPI AG

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