Highly conserved PenI-type class A β-lactamase in pathogenic members of 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 This pathway can be exploited to evade antibiotic tolerance induction in developing therapeutic measures against species, targeting their essential aminoacyl-tRNA synthetases.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269490 | PMC |
http://dx.doi.org/10.1128/AAC.02252-19 | DOI Listing |
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