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茶源儿茶素没食子酸酯与细菌病原体的相互作用。

Interactions of Tea-Derived Catechin Gallates with Bacterial Pathogens.

机构信息

School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK.

出版信息

Molecules. 2020 Apr 23;25(8):1986. doi: 10.3390/molecules25081986.

DOI:10.3390/molecules25081986
PMID:32340372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7221614/
Abstract

Green tea-derived galloylated catechins have weak direct antibacterial activity against both Gram-positive and Gram-negative bacterial pathogens and are able to phenotypically transform, at moderate concentrations, methicillin-resistant (MRSA) clonal pathogens from full β-lactam resistance (minimum inhibitory concentration 256-512 mg/L) to complete susceptibility (~1 mg/L). Reversible conversion to susceptibility follows intercalation of these compounds into the bacterial cytoplasmic membrane, eliciting dispersal of the proteins associated with continued cell wall peptidoglycan synthesis in the presence of β-lactam antibiotics. The molecules penetrate deep within the hydrophobic core of the lipid palisade to force a reconfiguration of cytoplasmic membrane architecture. The catechin gallate-induced staphylococcal phenotype is complex, reflecting perturbation of an essential bacterial organelle, and includes prevention and inhibition of biofilm formation, disruption of secretion of virulence-related proteins, dissipation of halotolerance, cell wall thickening and cell aggregation and poor separation of daughter cells during cell division. These features are associated with the reduction of capacity of potential pathogens to cause lethal, difficult-to-treat infections and could, in combination with β-lactam agents that have lost therapeutic efficacy due to the emergence of antibiotic resistance, form the basis of a new approach to the treatment of staphylococcal infections.

摘要

绿茶来源的没食子酰基儿茶素对革兰氏阳性和革兰氏阴性细菌病原体的直接抗菌活性较弱,并且能够在中等浓度下表型转化耐甲氧西林金黄色葡萄球菌(MRSA)克隆病原体,使其从完全β-内酰胺耐药(最小抑菌浓度 256-512mg/L)转变为完全敏感(~1mg/L)。这些化合物插入到细菌细胞质膜中,可逆地转换为敏感性,从而引发与细胞壁肽聚糖合成相关的蛋白质的分散,在存在β-内酰胺抗生素的情况下。这些分子渗透到脂质栅栏的疏水性核心深处,迫使细胞质膜结构重新配置。没食子酸儿茶素诱导的葡萄球菌表型复杂,反映了必需细菌细胞器的扰动,包括预防和抑制生物膜形成、破坏与毒力相关的蛋白质分泌、消除耐盐性、细胞壁增厚、细胞聚集以及细胞分裂期间子细胞分离不良。这些特征与潜在病原体引起致命、难以治疗的感染的能力降低有关,如果与由于抗生素耐药性出现而失去治疗效果的β-内酰胺药物结合使用,可能为治疗葡萄球菌感染提供一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a80f/7221614/81b237704afd/molecules-25-01986-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a80f/7221614/dda89f799590/molecules-25-01986-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a80f/7221614/2b29fa2643d6/molecules-25-01986-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a80f/7221614/81b237704afd/molecules-25-01986-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a80f/7221614/dda89f799590/molecules-25-01986-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a80f/7221614/2b29fa2643d6/molecules-25-01986-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a80f/7221614/81b237704afd/molecules-25-01986-g003.jpg

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