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首页> 外文期刊>Proteomics >Identification of vaccine candidate antigens of an ESBL producing Klebsiella pneumoniae clinical strain by immunoproteome analysis.
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Identification of vaccine candidate antigens of an ESBL producing Klebsiella pneumoniae clinical strain by immunoproteome analysis.

机译:通过免疫蛋白质组分析鉴定产生ESBL的肺炎克雷伯菌临床株的疫苗候选抗原。

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摘要

Klebsiella pneumoniae is an opportunistic pathogen which causes pneumoniae, urinary tract infections and septicemia in immunocompromised patients. Hospital outbreaks of multidrug-resistant K. pneumoniae, especially those in neonatal wards, are often caused by strains producing the extended-spectrum-beta-lactamases (ESBLs). An immunoproteome based approach was developed to identify candidate antigens of K. pneumoniae for vaccine development. Sera from patients with acute K. pneumoniae infections (n = 55) and a control group of sera from healthy individuals (n = 15) were analyzed for reactivity by Western blot against ESBL K. pneumoniae outer membrane proteins separated by 2-DE. Twenty highly immunogenic protein spots were identified by immunoproteomic analysis. The immunogenic proteins that are most frequently recognized by positive K. pneumoniae sera were OmpA, OmpK36, FepA, OmpK17, OmpW, Colicin I receptor protein and three novel proteins. Two of the vaccine candidate genes, OmpA (Struve et al. Microbiology 2003, 149, 167-176) and FepA (Lai, Y. C. et al.. Infect Immun 2001, 69, 7140-7145), have recently been shown to be essential in colonization and infection in an in vivo mouse model. Hence, these two immunogenic proteins could serve as potential vaccine candidates.
机译:肺炎克雷伯菌是一种机会病原体,可在免疫力低下的患者中引起肺炎,尿路感染和败血病。多药耐药的肺炎克雷伯菌的医院暴发,特别是在新生儿病房,通常是由产生超广谱β-内酰胺酶(ESBLs)的菌株引起的。开发了一种基于免疫蛋白质组学的方法来鉴定肺炎克雷伯菌的候选抗原用于疫苗开发。通过Western印迹分析了被2-DE分离的ESBL肺炎克雷伯菌外膜蛋白的反应性,分析了急性肺炎克雷伯菌感染患者(n = 55)和健康个体血清的对照组(n = 15)的反应性。通过免疫蛋白质组学分析鉴定出二十个高免疫原性蛋白斑点。肺炎克雷伯菌阳性血清最常识别的免疫原性蛋白是OmpA,OmpK36,FepA,OmpK17,OmpW,Colicin I受体蛋白和三种新型蛋白。最近已证明两个疫苗候选基因OmpA(Struve等,Microbiology 2003,149,167-176)和FepA(Lai,YC等。InfectImmun 2001,69,7140-7145)是必不可少的。在体内小鼠模型中的定植和感染。因此,这两种免疫原性蛋白质可用作潜在的疫苗候选物。

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