烟酸-胆酸-肽共轭物是一种潜在的抗生素佐剂,可减轻由革兰氏阴性病原体引起的多微生物感染。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-11-20 DOI:10.1021/acsinfecdis.4c00404
Sayed M Safwan, Devashish Mehta, Amit Arora, Steffi Khatol, Mohit Singh, Kajal Rana, Sonu K Gupta, Yashwant Kumar, Vikas Verma, Varsha Saini, Avinash Bajaj
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引用次数: 0

摘要

由革兰氏阴性菌引起的多微生物伤口感染及相关炎症的处理具有挑战性,因为许多抗生素对这些感染不起作用。利用佐剂重新利用现有抗生素减轻微生物感染是一种可供选择的治疗策略。我们设计并开发了一种烟酸-胆酸-肽共轭物(1),以恢复大环内酯类抗生素对革兰氏阴性病原体的疗效。我们在胆酸的羧基末端共轭了具有抗炎特性的烟酸,并在胆酸的三个羟基末端共轭了二肽(甘氨酸-缬氨酸),从而得到了双亲化合物 1。我们的研究结果表明,两性化合物 1 是一种微生物膜破坏剂,可促进红霉素(ERY)进入细菌细胞。双亲化合物 1 和 ERY 的组合具有杀菌作用,能有效消除单微生物和多微生物革兰氏阴性细菌生物膜。我们进一步证实了将 1 和 ERY 结合使用对单微生物和多微生物伤口感染的抗菌效果。这些发现共同表明,双亲化合物 1 振兴了 ERY 对革兰氏阴性菌的疗效。
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Niacin-Cholic Acid-Peptide Conjugate Act as a Potential Antibiotic Adjuvant to Mitigate Polymicrobial Infections Caused by Gram-Negative Pathogens.

Polymicrobial wound infections caused by Gram-negative bacteria and associated inflammation are challenging to manage, as many antibiotics do not work against these infections. Utilizing adjuvants to repurpose the existing antibiotics for mitigating microbial infections presents an alternative therapeutic strategy. We designed and developed a niacin-cholic acid-peptide conjugate (1) to rejuvenate the therapeutic efficacy of macrolide antibiotics against Gram-negative pathogens. We conjugated niacin with anti-inflammatory properties at the carboxyl terminal of the cholic acid and dipeptide (glycine-valine) at the three hydroxyl terminals of cholic acid to obtain the amphiphile 1. Our findings demonstrated that amphiphile 1 serves as a microbial membrane disruptor that facilitates the entry of erythromycin (ERY) in bacterial cells. The combination of amphiphile 1 and ERY is bactericidal and can effectively eliminate monomicrobial and polymicrobial Gram-negative bacterial biofilms. We further demonstrated the antibacterial effectiveness of combining 1 and ERY against monomicrobial and polymicrobial wound infections. Together, these findings indicate that amphiphile 1 revitalizes the remedial efficacy of ERY against Gram-negative bacteria.

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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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