Lopatkin Allison J, Yang Jason H
Department of Biology, Barnard College, New York, NY, United States.
Department of Ecology, Evolution, and Environmental Biology, Columbia University, New York, NY, United States.
Front Digit Health. 2021 Mar;3. doi: 10.3389/fdgth.2021.583468. Epub 2021 Mar 3.
Nucleotide metabolism plays a central role in bacterial physiology, producing the nucleic acids necessary for DNA replication and RNA transcription. Recent studies demonstrate that nucleotide metabolism also proactively contributes to antibiotic-induced lethality in bacterial pathogens and that disruptions to nucleotide metabolism contributes to antibiotic treatment failure in the clinic. As antimicrobial resistance continues to grow unchecked, new approaches are needed to study the molecular mechanisms responsible for antibiotic efficacy. Here we review emerging technologies poised to transform understanding into why antibiotics may fail in the clinic. We discuss how these technologies led to the discovery that nucleotide metabolism regulates antibiotic drug responses and why these are relevant to human infections. We highlight opportunities for how studies into nucleotide metabolism may enhance understanding of antibiotic failure mechanisms.
核苷酸代谢在细菌生理学中起着核心作用,产生DNA复制和RNA转录所需的核酸。最近的研究表明,核苷酸代谢也积极地促成细菌病原体中抗生素诱导的致死性,并且核苷酸代谢的破坏导致临床上抗生素治疗失败。随着抗菌药物耐药性持续 unchecked 地增长,需要新的方法来研究导致抗生素疗效的分子机制。在此,我们综述了有望改变对临床中抗生素为何可能失效的理解的新兴技术。我们讨论了这些技术如何导致发现核苷酸代谢调节抗生素药物反应,以及为什么这些与人类感染相关。我们强调了关于核苷酸代谢的研究如何可能增进对抗生素失效机制理解的机会。 (注:原文中“unchecked”可能有误,推测可能是“unchecked”,意为“未受抑制的” )