Emergence of Third Generation Tetracyclines: New Magic Bullets to Tackle Antibiotic Resistance in the Post-antibiotic Era

Pranitha Jetty, Soni Gaddam, S. Padi
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Abstract

Tetracyclines are broad-spectrum antibiotics effective against a wide variety of microorganisms including bacteria, both Gram-positive and Gram-negative, mycoplasmas, rickettsiae, chlamydiae, and protozoan parasites. Owing to their broad-spectrum antimicrobial activities and inexpensiveness, tetracyclines have been used extensively in both human and animal infections and in animal feed as growth promoters. Owing to this, the global prevalence of antibiotic resistance, particularly of tetracyclines, for Gram-positive methicillin-resistant Staphylococcus aureus (MRSA) and Streptococcus pneumoniae and Gram-negative extended-spectrum β-lactamase-producing Escherichia coli and Klebsiella species is high. Indeed, the acquisition of tetracycline-specific resistance genes, mutations within the ribosomal binding site, and/or chromosomal mutations lead to both class-specific and intrinsic antimicrobial resistance (AMR) mechanisms. As drug resistance increases globally, rendering diseases difficult to manage and eventually to mortality, antibiotics are becoming progressively less effective. Therefore, the discovery and development of novel antibiotics with appropriate indications is of the utmost importance. Among all antibiotics, the tetracyclines have acquired much attention due to the optimization of their chemical structures that paved the way to develop and introduce modern tetracyclines, referred to as third generation, namely tigecycline in the recent past, followed by omadacycline, eravacycline, and sarecycline very recently. Intriguingly, these novel tetracyclines are unique in two ways, first, these are highly effective against pathogens that acquired tetracycline-class resistance, and second, these agents exhibit either narrow or broad spectrum of in vitro activity against Gram-positive, Gram-negative, anaerobic, and atypical pathogens, including many drug-resistant strains lead to approval for limited use and unique indications. These beneficial effects represent a new era in the rational use of newer tetracyclines, the new magic bullets to tackle AMR in the post-antibiotic era. The present review focuses on third-generation tetracyclines emphasizing their safety, efficacy, and therapeutic choices in various clinical conditions of in-patient and out-patient settings.
第三代四环素的出现:解决后抗生素时代抗生素耐药性的新灵丹妙药
四环素是一种广谱抗生素,对多种微生物有效,包括革兰氏阳性和革兰氏阴性细菌、支原体、立克次体、衣原体和原生动物寄生虫。由于其广谱抗菌活性和价格低廉,四环素已广泛用于人类和动物感染以及动物饲料中作为生长促进剂。因此,革兰氏阳性耐甲氧西林金黄色葡萄球菌(MRSA)和肺炎链球菌以及革兰氏阴性产β-内酰胺酶的广谱大肠杆菌和克雷伯氏菌的抗生素耐药性,特别是四环素的全球流行率很高。事实上,四环素特异性耐药基因的获得、核糖体结合位点的突变和/或染色体突变会导致类别特异性和内在抗菌素耐药性(AMR)机制。随着全球耐药性的增加,使疾病难以控制并最终导致死亡,抗生素的效果正逐渐降低。因此,发现和开发具有合适适应症的新型抗生素至关重要。在所有抗生素中,四环素类药物由于其化学结构的优化而备受关注,这为开发和引入现代四环素铺平了道路,被称为第三代,即最近的替加环素,随后是奥马达环素,依拉瓦环素和最近的沙环素。有趣的是,这些新型四环素在两个方面是独特的,首先,这些药物对获得四环素类耐药性的病原体非常有效,其次,这些药物对革兰氏阳性,革兰氏阴性,厌氧和非典型病原体表现出狭窄或广泛的体外活性,包括许多耐药菌株,导致批准有限使用和独特适应症。这些有益效果代表了合理使用新型四环素的新时代,四环素是后抗生素时代应对抗菌素耐药性的新灵丹妙药。目前的回顾重点是第三代四环素,强调其安全性,有效性和治疗选择在各种临床条件下的住院和门诊设置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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