Abstract 2117 Potential of established and novel antibacterials against Acinetobacter baumannii gyrase and topoisomerase IV

Acinetobacter baumannii is a health-care associated infection that has major therapeutic challenges due to extensive antibacterial resistance. Most A. baumannii infections are resistant to fluoroquinolones (FQs), a class of gyrase/topoisomerase IV poisons. Therefore, we assessed the effects of two novel antibacterials, gepotidacin (a triazaacenaphthelene) and zoliflodacin (a spiropyrimidinetrione), on the activities of A. baumannii gyrase and topoisomerase IV. FQ-resistance is associated with single-amino acid mutations in the proteins that disrupt the interaction between FQs and the enzyme.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-05-01
DOI
https://doi.org/10.1016/j.jbc.2025.109055
Primary Topic
Synthesis of β-Lactam Compounds
Type
article
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Abstract 2117 Potential of established and novel antibacterials against Acinetobacter baumannii gyrase and topoisomerase IV

Jo Ann W. Byl, Neil Osheroff, Samika Joshi
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Journal of Biological Chemistry
Synthesis of β-Lactam Compounds
article

Abstract 2117 Potential of established and novel antibacterials against Acinetobacter baumannii gyrase and topoisomerase IV

Jo Ann W. Byl, Neil Osheroff, Samika Joshi
article en

Abstract

Acinetobacter baumannii is a health-care associated infection that has major therapeutic challenges due to extensive antibacterial resistance. Most A. baumannii infections are resistant to fluoroquinolones (FQs), a class of gyrase/topoisomerase IV poisons. Therefore, we assessed the effects of two novel antibacterials, gepotidacin (a triazaacenaphthelene) and zoliflodacin (a spiropyrimidinetrione), on the activities of A. baumannii gyrase and topoisomerase IV. FQ-resistance is associated with single-amino acid mutations in the proteins that disrupt the interaction between FQs and the enzyme.

Journal of Biological ChemistryVol. 301(5)
Emory University (US), Vanderbilt University (US)
Zero hunger
Openalex Percentile: Top 90%
Synthesis of β-Lactam Compounds
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