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细菌释放脂蛋白:细菌致病的潜在因素。

Lipoprotein release by bacteria: potential factor in bacterial pathogenesis.

作者信息

Zhang H, Niesel D W, Peterson J W, Klimpel G R

机构信息

Department of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, Texas 77555-1070, USA.

出版信息

Infect Immun. 1998 Nov;66(11):5196-201. doi: 10.1128/IAI.66.11.5196-5201.1998.

Abstract

Lipoprotein (LP) is a major component of the outer membrane of bacteria in the family Enterobacteriaceae. LP induces proinflammatory cytokine production in macrophages and lethal shock in LPS-responsive and -nonresponsive mice. In this study, the release of LP from growing bacteria was investigated by immuno-dot blot analysis. An immuno-dot blot assay that could detect LP at levels as low as 100 ng/ml was developed. By using this assay, significant levels of LP were detected in culture supernatants of growing Escherichia coli cells. During mid-logarithmic growth, approximately 1 to 1.5 microgram of LP per ml was detected in culture supernatants from E. coli. In contrast, these culture supernatants contained 5 to 6 microgram/ml of lipopolysaccharide (LPS). LP release was not unique to E. coli. Salmonella typhimurium, Yersinia enterocolitica, and two pathogenic E. coli strains also released LP during in vitro growth. Treatment of bacteria with the antibiotic ceftazidime significantly enhanced LP release. Culture supernatants from 5-h cultures of E. coli were shown to induce in vitro production of interleukin-6 (IL-6) by macrophages obtained from LPS-nonresponsive C3H/HeJ mice. In contrast, culture supernatants from an E. coli LP-deletion mutant were significantly less efficient at inducing IL-6 production in C3H/HeJ macrophages. These results suggest, for the first time, that LP is released from growing bacteria and that this released LP may play an important role in the induction of cytokine production and pathologic changes associated with gram-negative bacterial infections.

摘要

脂蛋白(LP)是肠杆菌科细菌外膜的主要成分。LP可诱导巨噬细胞产生促炎细胞因子,并在对LPS有反应和无反应的小鼠中引发致死性休克。在本研究中,通过免疫斑点印迹分析研究了生长中的细菌释放LP的情况。开发了一种免疫斑点印迹测定法,该方法能够检测低至100 ng/ml水平的LP。通过使用该测定法,在生长中的大肠杆菌细胞的培养上清液中检测到了显著水平的LP。在对数中期生长阶段,从大肠杆菌的培养上清液中检测到每毫升约1至1.5微克的LP。相比之下,这些培养上清液中含有5至6微克/毫升的脂多糖(LPS)。LP的释放并非大肠杆菌所特有。鼠伤寒沙门氏菌、小肠结肠炎耶尔森氏菌以及两种致病性大肠杆菌菌株在体外生长过程中也释放LP。用抗生素头孢他啶处理细菌可显著增强LP的释放。来自大肠杆菌5小时培养物的培养上清液能够诱导从对LPS无反应的C3H/HeJ小鼠获得的巨噬细胞在体外产生白细胞介素-6(IL-6)。相比之下,来自大肠杆菌LP缺失突变体的培养上清液在诱导C3H/HeJ巨噬细胞产生IL-6方面的效率显著较低。这些结果首次表明,LP是从生长中的细菌释放出来的,并且这种释放的LP可能在诱导细胞因子产生以及与革兰氏阴性菌感染相关的病理变化中发挥重要作用。

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