| Literature DB >> 29914946 |
Anna Vickers1, Shazad Mushtaq1, Neil Woodford1, Michel Doumith1, David M Livermore2,3.
Abstract
Pyrrolocytosines RX-04A to -D are designed to bind to the bacterial 50S ribosomal subunit differently from currently used antibiotics. The four analogs had broad anti-Gram-negative activity: RX-04A-the most active analog-inhibited 94.7% of clinical Enterobacteriaceae, Acinetobacter baumannii, and Pseudomonas aeruginosa at 0.5 to 4 μg/ml, with no MICs of >8 μg/ml. MICs for multidrug-resistant (MDR) carbapenemase producers were up to 2-fold higher than those for control strains; values were highest for one Serratia isolate with porin and efflux lesions. mcr-1 did not affect MICs. © Crown copyright 2018.Entities:
Keywords: 50S ribosomal subunit; blasticidin; mcr-1; pyrrolocytosine
Mesh:
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Year: 2018 PMID: 29914946 PMCID: PMC6105809 DOI: 10.1128/AAC.00689-18
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191