Staphylococcal Functional Amyloids: Structure, Pathogenic Roles, Biofilm Fortification, and Inhibition Strategies.

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
Nikita Admane, Sumit Biswas
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引用次数: 0

Abstract

Amyloid aggregates, which are hallmarks of various human diseases, show promising roles in almost all life forms. In the past few years, there has been a significant broadening of the diverse roles that bacterial functional amyloids play in nature, expanding the horizons of these fibrillar assemblies. Herein, we provide a review of the current understanding of staphylococcal functional amyloids, their multifaceted roles in pathogenesis, and strengthening biofilm-associated antibiotic resistance. This review aims to explore how staphylococcal biofilm strengthening amyloidogenic proteins and peptides, particularly derived from Staphylococcus aureus and Staphylococcus epidermidis, can act as dual-edged swords supporting pathogenesis in the planktonic stages and triggering infections in biofilms. We outline the different amyloid fibrillar species derived from these proteins/peptides and the molecules that have been discovered to target their amyloid transformation. This review also highlights how the noncanonical structural polymorphisms of these extracellular fibrillar amyloids are responsible for their functional diversity and discusses the techniques that are used recently for exploring staphylococcal amyloid structure assortment.

葡萄球菌功能性淀粉样蛋白:结构、致病作用、生物膜强化和抑制策略。
淀粉样蛋白聚集体是各种人类疾病的标志,在几乎所有的生命形式中都显示出有希望的作用。在过去的几年里,细菌功能性淀粉样蛋白在自然界中扮演的不同角色有了显著的扩大,扩大了这些纤维组装的视野。在此,我们综述了目前对葡萄球菌功能性淀粉样蛋白的理解,它们在发病机制中的多方面作用,以及加强生物膜相关的抗生素耐药性。本文旨在探讨葡萄球菌生物膜增强淀粉样蛋白和肽,特别是来自金黄色葡萄球菌和表皮葡萄球菌的蛋白和肽,如何在浮游阶段支持发病机制并引发生物膜感染的双刃剑。我们概述了来自这些蛋白质/肽的不同淀粉样蛋白纤维种类,以及已经发现的靶向淀粉样蛋白转化的分子。这篇综述还强调了这些细胞外纤维淀粉样蛋白的非典型结构多态性是如何导致其功能多样性的,并讨论了最近用于探索葡萄球菌淀粉样蛋白结构分类的技术。
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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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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