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Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus

  • Henrique Machado
  • , Yara Seif
  • , George Sakoulas
  • , Connor A. Olson
  • , Ying Hefner
  • , Amitesh Anand
  • , Ying Z. Jones
  • , Richard Szubin
  • , Bernhard O. Palsson
  • , Victor Nizet
  • , Adam M. Feist*
  • *Corresponding author for this work
    • University of California at San Diego

    Research output: Contribution to journal › Journal article › Research › peer-review

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    Abstract

    While microbiological resistance to vancomycin in Staphylococcus aureus is rare, clinical vancomycin treatment failures are common, and methicillin-resistant S. aureus (MRSA) strains isolated from patients after prolonged vancomycin treatment failure remain susceptible. Adaptive laboratory evolution was utilized to uncover mutational mechanisms associated with MRSA vancomycin resistance in a physiological medium as well as a bacteriological medium used in clinical susceptibility testing. Sequencing of resistant clones revealed shared and media-specific mutational outcomes, with an overlap in cell wall regulons (walKRyycHI, vraSRT). Evolved strains displayed similar properties to resistant clinical isolates in their genetic and phenotypic traits. Importantly, resistant phenotypes that developed in physiological media did not translate into resistance in bacteriological media. Further, a bacteriological media-specific mechanism for vancomycin resistance associated with a mutated mprF was confirmed. This study bridges the gap between the understanding of clinical and microbiological vancomycin resistance in S. aureus and expands the number of allelic variants (184 mutations for the top 5 mutated genes) that result in vancomycin resistance phenotypes. Henrique Machado et al. describe mutational mechanisms associated with MRSA vancomycin resistance in Staphylococcus aureus using adaptive laboratory evolution experiments focused on tolerance. Their results reveal environment-dependent mutational strategies to vancomycin tolerization and the impact of mutations in regulatory genes, providing insight into the development of antibiotic resistance under multiple conditions.
    Original languageEnglish
    Article number793
    JournalCommunications Biology
    Volume4
    Issue number1
    Number of pages12
    ISSN2399-3642
    DOIs
    Publication statusPublished - 2021

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