特克斯巴汀:一种治疗炭疽的抗耐药性抗生素

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
William S. Lawrence*, Jennifer E. Peel, Rosan de Winter, Losee L. Ling, Anthony G. Nitti, Aaron J. Peoples, Rhythm Shukla, Harold D. MacGillavry, Henry S. Heine, Martha E. Hensel, Elbert B. Whorton, Markus Weingarth, Kim Lewis* and Dallas E. Hughes*, 
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引用次数: 0

摘要

抗菌素耐药性危机与数百万人的死亡有关。尤其令人担忧的是以炭疽热为代表的生物武器的威胁。引入新型抗生素有助于减轻抗生素耐药性,但并不能解决带有工程抗性的生物武器的威胁。我们认为,teixobactin是一种没有检测到耐药性的抗生素,是唯一适合应对炭疽武器化挑战的抗生素。Teixobactin结合到不变的目标,细胞壁聚合物的前体。在这里,我们表明teixobactin是高度有效的吸入性炭疽兔模型。吸入炭疽芽孢杆菌的孢子会导致压倒性的发病率和死亡率。兔发病后用teixobactin治疗可迅速消除血液和组织中的病原体,使体温恢复正常,并防止组织损伤。Teixobactin在炭疽杆菌膜表面组装成不可逆的超分子结构,可能有助于其对抗炭疽的异常高效。逃避耐药性的抗生素为抗菌素耐药性和工程生物武器提供了合理的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Teixobactin: A Resistance-Evading Antibiotic for Treating Anthrax

Teixobactin: A Resistance-Evading Antibiotic for Treating Anthrax

The antimicrobial resistance (AMR) crisis has been associated with millions of deaths. Of particular concern is the threat of bioweapons, exemplified by anthrax. Introduction of novel antibiotics helps mitigate AMR, but does not address the threat of bioweapons with engineered resistance. We reasoned that teixobactin, an antibiotic with no detectable resistance, is uniquely suited to address the challenge of weaponized anthrax. Teixobactin binds to immutable targets, precursors of cell wall polymers. Here we show that teixobactin is highly efficacious in a rabbit model of inhalation anthrax. Inhaling spores of Bacillus anthracis causes overwhelming morbidity and mortality. Treating rabbits with teixobactin after the onset of disease rapidly eliminates the pathogen from blood and tissues, normalizes body temperature, and prevents tissue damage. Teixobactin assembles into an irreversible supramolecular structure on the surface of B. anthracis membrane, likely contributing to its unusually high potency against anthrax. Antibiotics evading resistance provide a rational solution to both AMR and engineered bioweapons.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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