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外膜囊泡可诱导对毒力蛋白的免疫反应,并预防产肠毒素大肠杆菌的定植。

Outer membrane vesicles induce immune responses to virulence proteins and protect against colonization by enterotoxigenic Escherichia coli.

作者信息

Roy Koushik, Hamilton David J, Munson George P, Fleckenstein James M

机构信息

Department of Medicine, University of Tennessee Health Sciences Center, Memphis, Tennessee, USA.

出版信息

Clin Vaccine Immunol. 2011 Nov;18(11):1803-8. doi: 10.1128/CVI.05217-11. Epub 2011 Sep 7.

Abstract

Enterotoxigenic Escherichia coli (ETEC) strains are a heterogeneous group of pathogens that produce heat-labile (LT) and/or heat-stable (ST) enterotoxins. Collectively, these pathogens are responsible for hundreds of thousands of deaths annually in developing countries, particularly in children under the age of 5 years. The heterogeneity of previously investigated molecular targets and the lack of complete sustained protection afforded by antitoxin immunity have impeded progress to date toward a broadly protective vaccine. Many pathogens, including ETEC, have the capacity to form outer membrane vesicles (OMV), which often contain one or more virulence proteins. Prompted by recent studies that identified several immunogenic virulence proteins in outer membrane vesicles of ETEC, we sought to examine the immunogenicity and protective efficacy of these structures in a murine model of infection. Here we demonstrate that immunization with OMV impairs ETEC colonization of the small intestine and stimulates antibodies that recognize the heat-labile toxin and two additional putative virulence proteins, the EtpA adhesin and CexE. Similar to earlier studies with EtpA, vaccination with LT alone also inhibited intestinal colonization. Together, these findings suggest that OMV could be exploited to deliver protective antigens relevant to development of ETEC vaccines.

摘要

产肠毒素大肠杆菌(ETEC)菌株是一类异质性病原体,可产生不耐热(LT)和/或耐热(ST)肠毒素。总体而言,这些病原体每年在发展中国家导致数十万人死亡,尤其是5岁以下儿童。先前研究的分子靶点的异质性以及抗毒素免疫提供的不完全持续保护阻碍了迄今为止在广泛保护性疫苗方面的进展。许多病原体,包括ETEC,都有能力形成外膜囊泡(OMV),其通常含有一种或多种毒力蛋白。受近期研究的启发,这些研究在ETEC的外膜囊泡中鉴定出了几种免疫原性毒力蛋白,我们试图在小鼠感染模型中研究这些结构的免疫原性和保护效果。在此我们证明,用OMV免疫可损害ETEC在小肠的定植,并刺激识别不耐热毒素和另外两种假定毒力蛋白(EtpA黏附素和CexE)的抗体产生。与早期关于EtpA的研究相似,单独用LT疫苗接种也能抑制肠道定植。这些发现共同表明,OMV可用于递送与ETEC疫苗开发相关的保护性抗原。

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