Literature DB >> 32205346

Mutations in ArgS Arginine-tRNA Synthetase Confer Additional Antibiotic Tolerance Protection to Extended-Spectrum-β-Lactamase-Producing Burkholderia thailandensis.

Hyojeong Yi1, Jongwook Park1, Kwang-Hwi Cho2, Heenam Stanley Kim3.   

Abstract

Highly conserved PenI-type class A β-lactamase in pathogenic members of Burkholderia species can evolve to extended-spectrum β-lactamase (ESBL), which exhibits hydrolytic activity toward third-generation cephalosporins, while losing its activity toward the original penicillin substrates. We describe three single-amino-acid-substitution mutations in the ArgS arginine-tRNA synthetase that confer extra antibiotic tolerance protection to ESBL-producing Burkholderia thailandensis This pathway can be exploited to evade antibiotic tolerance induction in developing therapeutic measures against Burkholderia species, targeting their essential aminoacyl-tRNA synthetases.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  ArgS; antibiotic tolerance; arginine-tRNA synthetase; stringent response

Mesh:

Substances:

Year:  2020        PMID: 32205346      PMCID: PMC7269490          DOI: 10.1128/AAC.02252-19

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


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