Progress in the study of mefloquine as an antibiotic adjuvant for combination bacterial inhibition treatment

Front Cell Infect Microbiol. 2024 Nov 28:14:1470891. doi: 10.3389/fcimb.2024.1470891. eCollection 2024.

Abstract

Antimicrobial resistance is among the greatest threats to public health globally, and drug repurposing strategies may be advantageous to addressing this problem. Mefloquine, a drug traditionally used to treat malaria, has emerged as a promising antibiotic adjuvant, due to its ability to enhance the effectiveness of conventional antibiotics against resistant bacterial strains. In this paper, we first outline the enhancement properties of mefloquine and its mechanisms of action as an adjuvant antibiotic against multidrug-resistant bacteria. Mefloquine exhibits synergistic bacteriostatic effects when combined with colistin, β-lactams, antituberculosis drugs, quinolones, and linezolid. Potential mechanisms underlying its synergistic effects include inhibition of antibiotic efflux, disruption of bacterial cell membrane integrity, and disturbance of biofilm formation. In addition, we explore the bacteriostatic effects of several mefloquine derivatives against Mycobacterium tuberculosis and some fungi. Further, we summarize the findings of recent studies on other aspects of mefloquine activity, including its antiviral and antitumor effects. Finally, the advantages and challenges of mefloquine use as an antibiotic adjuvant in combination with antibiotics for bacterial inhibition are discussed. Overall, mefloquine shows excellent potential as an antibiotic adjuvant therapy against multidrug-resistant bacteria and is a promising candidate for combination therapy; however, further studies are needed to fully elucidate its mechanism of action and address the challenges associated with its clinical application.

Keywords: antibiotic adjuvant; bacterial cell membrane; biofilm; derivatives; mefloquine; multidrug-resistant bacteria.

Publication types

  • Review

MeSH terms

  • Adjuvants, Pharmaceutic / pharmacology
  • Anti-Bacterial Agents* / pharmacology
  • Bacteria / drug effects
  • Biofilms / drug effects
  • Drug Repositioning
  • Drug Resistance, Multiple, Bacterial / drug effects
  • Drug Synergism*
  • Drug Therapy, Combination
  • Humans
  • Mefloquine* / pharmacology
  • Microbial Sensitivity Tests
  • Mycobacterium tuberculosis / drug effects

Substances

  • Mefloquine
  • Anti-Bacterial Agents
  • Adjuvants, Pharmaceutic

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The author(s) declare financial support was received for the authorship, and/or publication of this article. The authors extend their appreciation to the Gansu Provincial People’s Hospital Subject 21GSSYC-44.