Suppr超能文献

理解大环内酯类耐药性的演变:一篇小型综述。

Understanding the evolution of macrolides resistance: A mini review.

机构信息

Bacteriology Unit, Infectious Disease Research Centre (IDRC), Institute for Medical Research (IMR), National Institutes of Health, Ministry of Health Malaysia, 40170, Shah Alam, Selangor, Malaysia.

Faculty of Applied Sciences, Universiti Teknologi MARA (UiTM), 40450 Shah Alam, Selangor, Malaysia.

出版信息

J Glob Antimicrob Resist. 2024 Sep;38:368-375. doi: 10.1016/j.jgar.2024.07.016. Epub 2024 Aug 6.

Abstract

BACKGROUND

Macrolides inhibit the growth of bacterial cells by preventing the elongation of polypeptides during protein biosynthesis and include natural, synthetic, and semi-synthetic products. Elongation prevention occurs by blocking the passage of the polypeptide chain as the macrolides bind at the nascent peptide exit tunnel.

OBJECTIVE

Recent data of ribosome profiling via ribo-seq further proves that, other than blocking the polypeptide chain, macrolides are also able to affect the synthesis of individual proteins. Thus, this shows that the mode of action of macrolides is more complex than we initially thought. Since the discovery of macrolides in the 1950s, they have been widely used in veterinary practice, agriculture, and medicine. Due to misuse and overuse of antibiotics, bacteria have acquired resistance against them. Hence, it is of utmost importance for us to fully understand the mode of action of macrolides as well as the mechanisms of resistance against macrolides in order to mitigate antibiotic-resistance issues.

RESULTS

Chemical modifications can be performed to improve macrolide potency if we have a better understanding of their mode of action. Furthermore, a complete and detailed understanding of the mode of action of macrolides has remained vague, as new findings have challenged theories that are already in existence-due to this obscurity, research into macrolide modes of action continues to this day.

CONCLUSION

In this review, we present an overview of macrolide antibiotics, with an emphasis on the latest knowledge regarding the mode of action of macrolides as well as the mechanisms of resistance employed by bacteria against macrolides.

摘要

背景

大环内酯类通过阻止蛋白质生物合成过程中多肽的延伸来抑制细菌细胞的生长,包括天然、合成和半合成产品。通过阻止多肽链的通过,大环内酯类在新生肽出口隧道处结合,从而阻止延伸的发生。

目的

通过核糖体测序的核糖体分析的最新数据进一步证明,除了阻止多肽链外,大环内酯类还能够影响单个蛋白质的合成。因此,这表明大环内酯类的作用模式比我们最初想象的更为复杂。自 20 世纪 50 年代发现大环内酯类以来,它们已广泛应用于兽医实践、农业和医学领域。由于抗生素的滥用和过度使用,细菌已经对它们产生了耐药性。因此,充分了解大环内酯类的作用模式以及细菌对大环内酯类产生耐药性的机制至关重要,以减轻抗生素耐药性问题。

结果

如果我们对大环内酯类的作用模式有更好的了解,就可以进行化学修饰来提高其效力。此外,由于这种模糊性,大环内酯类作用模式的全面和详细的理解仍然模糊不清,因为新的发现挑战了已经存在的理论,因此,对大环内酯类作用模式的研究至今仍在继续。

结论

在这篇综述中,我们介绍了大环内酯类抗生素的概述,重点介绍了大环内酯类作用模式以及细菌对大环内酯类产生耐药性的机制的最新知识。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验