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Polymicrobial infection in cystic fibrosis and future perspectives for improving Mycobacterium abscessus drug discovery

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    Abstract

    Polymicrobial communities inhabit the cystic fibrosis (CF) airway, whereby microbial interactions can occur. One prominent CF pathogen is Mycobacterium abscessus, whose treatment is largely unsuccessful. This creates a need to discover novel antimicrobial agents to treat M. abscessus, however the methods used within antibiotic discovery are typically monomicrobial. This review will discuss this pathogen whilst considering the CF polymicrobial environment, to highlight future perspectives to improve M. abscessus drug discovery.
    Original languageEnglish
    Article number38
    Number of pages12
    Journalnpj Antimicrobials and Resistance
    Volume2
    Issue number1
    Early online date14 Nov 2024
    DOIs
    Publication statusPublished - 14 Nov 2024

    Bibliographical note

    Copyright © The Author(s) 2024. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/

    Funding

    This research was funded by the Engineering and Physical Sciences Research Council (EPSRC) and Science Foundation Ireland (SFI) Centre for Doctoral Training in Engineered Tissues for Discovery, Industry and Medicine [EP/S02347X/1]. EJB is supported by a PhD Studentship funded by LifETIME CDT (EPSRC and SFI). GA is supported by a co-funded PhD studentship between Aston University and Comvita, NZ. The funders had no role in study design, data collection, analysis, decision to publish, or writing of the manuscript.

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