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鉴定人血清抗体识别的无乳链球菌分离株中的高免疫反应性蛋白。

Identification of high immunoreactive proteins from Streptococcus agalactiae isolates recognized by human serum antibodies.

机构信息

Department of Bacteriology, Microbial Ecology and Parasitology, Jagiellonian University Medical College, Krakow, Poland.

出版信息

FEMS Microbiol Lett. 2013 Dec;349(1):61-70. doi: 10.1111/1574-6968.12292. Epub 2013 Oct 24.

Abstract

The aim of the studies was to identify immunogenic proteins of Streptococcus agalactiae (group B streptococcus; GBS) isolates. Investigation of the immunoreactivity with human sera allowed us to determine major immunogenic proteins which might be potential candidates for the development of vaccine. For the study, we have selected 60 genetically different, well-characterized GBS clinical isolates. The proteins immunoreactivity with 24 human sera from patients with GBS infections, carriers, and control group without GBS was detected by SDS-PAGE and Western blotting. As a result, some major immunogenic proteins were identified, of which four proteins with molecular masses of about 45 to 50 kDa, which exhibited the highest immunoreactivity features, were analyzed by LC-MS/MS. The proteins were identified by comparative analysis of peptides masses using MASCOT and statistical analysis. The results showed known molecules such as enolase (47.4 kDa), aldehyde dehydrogenase (50.6 kDa), and ones not previously described such as trigger factor (47 kDa) and elongation factor Tu (44 kDa). The preliminary results indicated that some GBS proteins that elicit protective immunity hold promise not only as components in a vaccine as antigens but also as carriers or adjuvants in polysaccharide conjugate vaccines, but more studies are needed.

摘要

本研究旨在鉴定无乳链球菌(B 组链球菌;GBS)分离株的免疫原性蛋白。用人类血清进行免疫反应性研究,有助于确定可能成为疫苗开发潜在候选物的主要免疫原性蛋白。为此,我们选择了 60 株遗传上不同、特征明确的 GBS 临床分离株。通过 SDS-PAGE 和 Western blot 检测了 24 份来自 GBS 感染患者、携带者和无 GBS 对照组的人类血清与这些分离株的免疫反应性。结果鉴定出一些主要的免疫原性蛋白,其中 4 种相对分子质量约为 45 至 50 kDa 的蛋白表现出最高的免疫反应性特征,并用 LC-MS/MS 进行了分析。通过 MASCOT 和统计分析对肽质量进行比较分析来鉴定蛋白。结果表明,存在一些已知分子,如烯醇酶(47.4 kDa)、醛脱氢酶(50.6 kDa),以及一些以前未描述的分子,如触发因子(47 kDa)和延伸因子 Tu(44 kDa)。初步结果表明,一些引发保护性免疫的 GBS 蛋白不仅有望作为疫苗抗原的成分,而且还可作为多糖结合疫苗的载体或佐剂,但是还需要进一步研究。

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