Kany Andreas M, Fries Franziska, Seyfert Carsten E, Porten Christoph, Deckarm Selina, Chacón Ortiz María, Dubarry Nelly, Vaddi Swapna, Große Miriam, Bernecker Steffen, Sandargo Birthe, Müller Alison V, Bacqué Eric, Stadler Marc, Herrmann Jennifer, Müller Rolf
Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)-Helmholtz Centre for Infection Research (HZI), Saarbrücken 66123, Germany.
Department of Pharmacy, Saarland University, Saarbrücken 66123, Germany.
ACS Infect Dis. 2024 Dec 13;10(12):4337-4346. doi: 10.1021/acsinfecdis.4c00687. Epub 2024 Nov 20.
In recent years, naturally occurring darobactins have emerged as a promising compound class to combat infections caused by critical Gram-negative pathogens. In this study, we describe the in vivo evaluation of derivative D22, a non-natural biosynthetic darobactin analogue with significantly improved antibacterial activity. We found D22 to be active in vivo against key critical Gram-negative human pathogens, as demonstrated in murine models of thigh infection, peritonitis/sepsis, and urinary tract infection (UTI). Furthermore, we observed the restored survival of -infected embryos in a zebrafish infection model. These in vivo proof-of-concept (PoC) in diverse models of infection against highly relevant pathogens, including drug-resistant isolates, highlight the versatility of darobactins in the treatment of bacterial infections and show superiority of D22 over the natural darobactin A. Together with a favorable safety profile, these findings pave the way for further optimization of the darobactin scaffold toward the development of a novel antibiotic.
近年来,天然存在的达罗巴汀已成为对抗由关键革兰氏阴性病原体引起的感染的一类有前景的化合物。在本研究中,我们描述了衍生物D22的体内评估,D22是一种非天然生物合成的达罗巴汀类似物,其抗菌活性显著提高。我们发现D22在体内对关键的革兰氏阴性人类病原体具有活性,如在大腿感染、腹膜炎/败血症和尿路感染(UTI)的小鼠模型中所证明的那样。此外,我们在斑马鱼感染模型中观察到受感染胚胎的存活率得到恢复。这些在针对包括耐药菌株在内的高度相关病原体的多种感染模型中的体内概念验证(PoC),突出了达罗巴汀在治疗细菌感染方面的多功能性,并显示出D22优于天然达罗巴汀A。连同良好的安全性概况,这些发现为进一步优化达罗巴汀支架以开发新型抗生素铺平了道路。