抗菌药:细菌感染多样化治疗新策略的最新进展。

Advances in microbial physiology Pub Date : 2024-01-01 Epub Date: 2024-03-16 DOI:10.1016/bs.ampbs.2023.12.002
Tegan Hibbert, Zeljka Krpetic, Joe Latimer, Hollie Leighton, Rebecca McHugh, Sian Pottenger, Charlotte Wragg, Chloë E James
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引用次数: 0

摘要

弗莱明发现青霉素 95 年后,人们发现、改造或合成了大量抗生素化合物。靶点的多样化、稳定性的提高和活性谱的改变使抗生素的疗效得以持续,但过度依赖和滥用却加剧了抗菌药耐药性(AMR)在全球的蔓延。据估计,2019 年有 127 万人死于抗生素耐药性细菌,这对现代医学构成了重大威胁。尽管抗生素仍是治疗和控制细菌性疾病的核心策略,但 AMR 的威胁已达到灾难性的程度,迫切需要新的创新。过去十年间,基因组测序、高通量筛选技术和机器学习取得了突破性发展。这些进步为新型抗菌药物的生物勘探打开了新的大门。它们还使人们能够更深入地探索复杂的多微生物感染以及与健康微生物群的相互作用。利用更接近体内感染状态的感染模型,我们现在开始测量抗微生物疗法对宿主/微生物群/病原体相互作用的影响。然而,我们需要新的方法来开发和规范适当的方法,以衡量新型抗菌药物组合在这些情况下的疗效。目前,一系列前景广阔的新型抗菌药物正处于不同的开发阶段,包括共用抑制剂、噬菌体、纳米粒子、免疫疗法、抗生物膜剂和抗病毒剂。这些新型疗法需要多学科合作和新的思维方式,才能将其大规模用于临床。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimicrobials: An update on new strategies to diversify treatment for bacterial infections.

Ninety-five years after Fleming's discovery of penicillin, a bounty of antibiotic compounds have been discovered, modified, or synthesised. Diversification of target sites, improved stability and altered activity spectra have enabled continued antibiotic efficacy, but overwhelming reliance and misuse has fuelled the global spread of antimicrobial resistance (AMR). An estimated 1.27 million deaths were attributable to antibiotic resistant bacteria in 2019, representing a major threat to modern medicine. Although antibiotics remain at the heart of strategies for treatment and control of bacterial diseases, the threat of AMR has reached catastrophic proportions urgently calling for fresh innovation. The last decade has been peppered with ground-breaking developments in genome sequencing, high throughput screening technologies and machine learning. These advances have opened new doors for bioprospecting for novel antimicrobials. They have also enabled more thorough exploration of complex and polymicrobial infections and interactions with the healthy microbiome. Using models of infection that more closely resemble the infection state in vivo, we are now beginning to measure the impacts of antimicrobial therapy on host/microbiota/pathogen interactions. However new approaches are needed for developing and standardising appropriate methods to measure efficacy of novel antimicrobial combinations in these contexts. A battery of promising new antimicrobials is now in various stages of development including co-administered inhibitors, phages, nanoparticles, immunotherapy, anti-biofilm and anti-virulence agents. These novel therapeutics need multidisciplinary collaboration and new ways of thinking to bring them into large scale clinical use.

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