MARATTO

review · Frontiers in Pharmacology

Mechanism of antibacterial resistance, strategies and next-generation antimicrobials to contain antimicrobial resistance: a review

2024107 citationsOpen accessDebre Markos University

In plain language

Bacterial resistance to antibacterial medications presents an ongoing threat to modern healthcare and routine infection management. Resistance develops through diverse biological mechanisms, including the enzymatic inactivation of drugs, structural modifications at drug target sites, reduced drug influx, and the active clearance of compounds via efflux pumps. Bacteria also rely on biofilm formation and horizontal gene transfer to protect themselves and disseminate resistance traits across populations. Addressing this growing challenge requires both systematic intervention programmes and the development of next-generation antimicrobial treatments. By collating evidence on resistance pathways and control measures, the synthesis provides insights intended to assist future research directions and inform antimicrobial stewardship programmes.

Key takeaways

  • Key bacterial resistance mechanisms include target site modifications, reduced compound influx, increased efflux pump activity, and enzymatic inactivation of antibacterial drugs.
  • Biofilm formation and horizontal gene transfer play crucial roles in facilitating bacterial survival and spreading resistance.
  • Containing antimicrobial resistance requires active control measures alongside the development of next-generation antimicrobials.
  • Comprehensive mapping of resistance pathways is necessary to direct future research and guide antimicrobial stewardship efforts.

Why it matters

Antibacterial resistance undermines standard medical treatments by rendering existing drugs ineffective against common bacterial infections. By outlining the primary ways bacteria evade treatments, along with potential countermeasures and emerging therapeutics, this work clarifies the core operational barriers healthcare systems must navigate to sustain effective infection control.

Commercialisation angle

The work synthesises knowledge to inform the development of next-generation antimicrobials and therapeutic interventions. Primary users include pharmaceutical researchers, drug developers, and antimicrobial stewardship teams seeking to bypass mechanisms like efflux pumps, target modifications, or biofilms. As a literature review, it remains at the conceptual and early-stage research level, offering a reference baseline rather than presenting a directly tested product or near-market asset.

AI-generated from the published abstract. Always read the original work before citing.

Abstract

Antibacterial drug resistance poses a significant challenge to modern healthcare systems, threatening our ability to effectively treat bacterial infections. This review aims to provide a comprehensive overview of the types and mechanisms of antibacterial drug resistance. To achieve this aim, a thorough literature search was conducted to identify key studies and reviews on antibacterial resistance mechanisms, strategies and next-generation antimicrobials to contain antimicrobial resistance. In this review, types of resistance and major mechanisms of antibacterial resistance with examples including target site modifications, decreased influx, increased efflux pumps, and enzymatic inactivation of antibacterials has been discussed. Moreover, biofilm formation, and horizontal gene transfer methods has also been included. Furthermore, measures (interventions) taken to control antimicrobial resistance and next-generation antimicrobials have been discussed in detail. Overall, this review provides valuable insights into the diverse mechanisms employed by bacteria to resist the effects of antibacterial drugs, with the aim of informing future research and guiding antimicrobial stewardship efforts.

Research topics

  • Antibiotic Resistance in Bacteria
  • Bacterial biofilms and quorum sensing
  • Pharmaceutical and Antibiotic Environmental Impacts

Sustainable Development Goals

Read the original research

This page summarises published work. The authoritative version sits with the publisher.

DOI: 10.3389/fphar.2024.1444781

Is something wrong with this record? Report it or request removal.

Discussion

Discuss this research

Have you built on this work, tried to replicate it, or seen it applied in practice? Share what you know. Verified researchers and MARATTO™ domain experts can open a discussion, and any member can reply. Contributions are reviewed before they appear.

No discussion yet. Open the first thread.