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细菌脂多糖的结构修饰促进革兰氏阴性菌逃避宿主固有免疫。

Structural Modifications of Bacterial Lipopolysaccharide that Facilitate Gram-Negative Bacteria Evasion of Host Innate Immunity.

机构信息

Department of Microbiology, Graduate School of Medicine, Kyoto University Kyoto, Japan.

出版信息

Front Immunol. 2013 May 24;4:109. doi: 10.3389/fimmu.2013.00109. eCollection 2013.

Abstract

Bacterial lipopolysaccharide (LPS), a cell wall component characteristic of Gram-negative bacteria, is a representative pathogen-associated molecular pattern that allows mammalian cells to recognize bacterial invasion and trigger innate immune responses. The polysaccharide moiety of LPS primary plays protective roles for bacteria such as prevention from complement attacks or camouflage with common host carbohydrate residues. The lipid moiety, termed lipid A, is recognized by the Toll-like receptor 4 (TLR4)/MD-2 complex, which transduces signals for activation of host innate immunity. The basic structure of lipid A is a glucosamine disaccharide substituted by phosphate groups and acyl groups. Lipid A with six acyl groups (hexa-acylated form) has been indicated to be a strong stimulator of the TLR4/MD-2 complex. This type of lipid A is conserved among a wide variety of Gram-negative bacteria, and those bacteria are easily recognized by host cells for activation of defensive innate immune responses. Modifications of the lipid A structure to less-acylated forms have been observed in some bacterial species, and those forms are poor stimulators of the TLR4/MD-2 complex. Such modifications are thought to facilitate bacterial evasion of host innate immunity, thereby enhancing pathogenicity. This hypothesis is supported by studies of Yersinia pestis LPS, which contains hexa-acylated lipid A when the bacterium grows at 27°C (the temperature of the vector flea), and shifts to contain less-acylated forms when grown at the human body temperature of 37°C. This alteration of lipid A forms following transmission of Y. pestis from fleas to humans contributes predominantly to the virulence of this bacterium over other virulence factors. A similar role for less-acylated lipid A forms has been indicated in some other bacterial species, such as Francisella tularensis, Helicobacter pylori, and Porphyromonas gingivalis, and further studies to explore this concept are expected.

摘要

细菌脂多糖(LPS)是革兰氏阴性细菌细胞壁的特征成分,是一种代表性的病原体相关分子模式,使哺乳动物细胞能够识别细菌入侵并触发先天免疫反应。LPS 的多糖部分主要发挥保护细菌的作用,例如防止补体攻击或与常见的宿主碳水化合物残基伪装。脂质部分,称为脂质 A,被 Toll 样受体 4(TLR4)/MD-2 复合物识别,该复合物传递信号以激活宿主先天免疫。脂质 A 的基本结构是带有磷酸基团和酰基的葡萄糖胺二糖。具有六个酰基的脂质 A(六酰化形式)已被证明是 TLR4/MD-2 复合物的强刺激物。这种类型的脂质 A 在广泛的革兰氏阴性细菌中是保守的,这些细菌很容易被宿主细胞识别,从而激活防御性先天免疫反应。在一些细菌物种中观察到脂质 A 结构向较少酰化形式的修饰,这些形式是 TLR4/MD-2 复合物的较差刺激物。这种修饰被认为有助于细菌逃避宿主先天免疫,从而增强致病性。这种假设得到了鼠疫耶尔森氏菌 LPS 的研究支持,当细菌在 27°C(媒介跳蚤的温度)下生长时,其含有六酰化脂质 A,而当在 37°C 下生长时,其含有较少酰化形式。这种从跳蚤到人类传播的 Y. pestis 脂质 A 形式的改变主要导致该细菌比其他毒力因子更具毒力。在其他一些细菌物种中,如土拉弗朗西斯菌、幽门螺杆菌和牙龈卟啉单胞菌,已经表明较少酰化的脂质 A 形式具有类似的作用,预计将进一步研究探索这一概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d11/3662973/67eb756ce113/fimmu-04-00109-g001.jpg

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