植物酚类抑制病灶粘附激酶,抑制尿路致病性大肠杆菌对宿主细胞的侵袭

IF 2.9 3区 医学 Q3 IMMUNOLOGY
Infection and Immunity Pub Date : 2024-05-07 Epub Date: 2024-03-27 DOI:10.1128/iai.00080-24
Adam J Lewis, Amanda C Richards, Alejandra A Mendez, Bijaya K Dhakal, Tiffani A Jones, Jamie L Sundsbak, Danelle S Eto, Alexis A Rousek, Matthew A Mulvey
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引用次数: 0

摘要

预防和治疗尿路感染(UTI)和其他传染性疾病的传统民间疗法通常包括富含酚类化合物的植物和植物提取物。这些酚类化合物被认为具有多种活性,包括抑制细菌与宿主细胞的相互作用。在这里,我们测试了四种经过充分研究的酚类化合物--咖啡酸苯乙酯(CAPE)、白藜芦醇、儿茶素和表没食子儿茶素没食子酸酯--对宿主细胞粘附和尿路致病性大肠杆菌(UPEC)入侵的影响。这些细菌是尿路感染的主要病因,可通过肌动蛋白依赖过程与膀胱上皮细胞结合并随后侵入。膀胱内的细胞内 UPEC 储库通常不受抗生素和宿主防御系统的影响,很可能导致慢性和复发性感染的发生。在基于细胞培养的试验中,只有白藜芦醇对 UPEC 黏附膀胱细胞有明显的负面影响。然而,CAPE 和白藜芦醇都能显著抑制 UPEC 进入宿主细胞,同时减少宿主肌动蛋白调节因子 Focal Adhesion Kinase(FAK 或 PTK2)的磷酸化,并显著增加病灶粘附结构的数量。我们进一步发现,在小鼠UTI模型中,膀胱内注射白藜芦醇可抑制UPEC对膀胱粘膜的浸润,而且白藜芦醇和CAPE还能破坏其他侵入性病原体进入宿主细胞的能力。这些结果突出了 CAPE 和白藜芦醇等分子的治疗潜力,它们可以通过限制病原体进入细胞内的保护性壁龛来增强抗生素治疗的效果。此外,UTI 的主要致病菌--尿路致病性大肠杆菌(UPEC)可以通过侵入膀胱表面的上皮细胞来避免抗生素暴露和许多宿主防御措施。在这里,我们发现了两种植物萃取的酚类化合物,它们能破坏 UPEC 进入膀胱细胞所需的宿主机制的激活。在小鼠UTI模型中,其中一种化合物白藜芦醇能有效抑制UPEC对膀胱粘膜的侵袭,这两种酚类化合物还能显著减少其他侵袭性病原体进入宿主细胞。这些研究结果表明,精选的酚类化合物可用于补充现有的抗菌疗法,使泌尿病原体无法在宿主细胞和组织中栖息,并有助于解释传统植物药物的一些益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plant phenolics inhibit focal adhesion kinase and suppress host cell invasion by uropathogenic Escherichia coli.

Traditional folk treatments for the prevention and management of urinary tract infections (UTIs) and other infectious diseases often include plants and plant extracts that are rich in phenolic compounds. These have been ascribed a variety of activities, including inhibition of bacterial interactions with host cells. Here, we tested a panel of four well-studied phenolic compounds-caffeic acid phenethyl ester (CAPE), resveratrol, catechin, and epigallocatechin gallate-for the effects on host cell adherence and invasion by uropathogenic Escherichia coli (UPEC). These bacteria, which are the leading cause of UTIs, can bind and subsequently invade bladder epithelial cells via an actin-dependent process. Intracellular UPEC reservoirs within the bladder are often protected from antibiotics and host defenses and likely contribute to the development of chronic and recurrent infections. In cell culture-based assays, only resveratrol had a notable negative effect on UPEC adherence to bladder cells. However, both CAPE and resveratrol significantly inhibited UPEC entry into the host cells, coordinate with attenuated phosphorylation of the host actin regulator Focal Adhesion Kinase (FAK or PTK2) and marked increases in the numbers of focal adhesion structures. We further show that the intravesical delivery of resveratrol inhibits UPEC infiltration of the bladder mucosa in a murine UTI model and that resveratrol and CAPE can disrupt the ability of other invasive pathogens to enter host cells. Together, these results highlight the therapeutic potential of molecules like CAPE and resveratrol, which could be used to augment antibiotic treatments by restricting pathogen access to protective intracellular niches.IMPORTANCEUrinary tract infections (UTIs) are exceptionally common and increasingly difficult to treat due to the ongoing rise and spread of antibiotic-resistant pathogens. Furthermore, the primary cause of UTIs, uropathogenic Escherichia coli (UPEC), can avoid antibiotic exposure and many host defenses by invading the epithelial cells that line the bladder surface. Here, we identified two plant-derived phenolic compounds that disrupt activation of the host machinery needed for UPEC entry into bladder cells. One of these compounds, resveratrol, effectively inhibited UPEC invasion of the bladder mucosa in a mouse UTI model, and both phenolic compounds significantly reduced host cell entry by other invasive pathogens. These findings suggest that select phenolic compounds could be used to supplement existing antibacterial therapeutics by denying uropathogens shelter within host cells and tissues and help explain some of the benefits attributed to traditional plant-based medicines.

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来源期刊
Infection and Immunity
Infection and Immunity 医学-传染病学
CiteScore
6.00
自引率
6.50%
发文量
268
审稿时长
3 months
期刊介绍: Infection and Immunity (IAI) provides new insights into the interactions between bacterial, fungal and parasitic pathogens and their hosts. Specific areas of interest include mechanisms of molecular pathogenesis, virulence factors, cellular microbiology, experimental models of infection, host resistance or susceptibility, and the generation of innate and adaptive immune responses. IAI also welcomes studies of the microbiome relating to host-pathogen interactions.
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