| Literature DB >> 32205346 |
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.Entities:
Keywords: ArgS; antibiotic tolerance; arginine-tRNA synthetase; stringent response
Mesh:
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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