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通过微生物基因组学方法筛选出的肺炎球菌预测蛋白具有血清型交叉反应性,并能与宿主细胞外基质蛋白结合。

Pneumococcal Predictive Proteins Selected by Microbial Genomic Approach Are Serotype Cross-Reactive and Bind to Host Extracellular Matrix Proteins.

作者信息

Argondizzo Ana Paula Corrêa, Rocha-de-Souza Cláudio Marcos, de Almeida Santiago Marta, Galler Ricardo, Reis Joice Neves, Medeiros Marco Alberto

机构信息

Laboratory of Recombinant Technology, Bio-Manguinhos, Brazilian Health Ministry, FIOCRUZ, Rio de Janeiro, Brazil.

Research Laboratory of Hospital Infection, Collection Hospital Origin bacteria cultures, Instituto Oswaldo Cruz, Brazilian Health Ministry, FIOCRUZ, Rio de Janeiro, Brazil.

出版信息

Appl Biochem Biotechnol. 2017 Aug;182(4):1518-1539. doi: 10.1007/s12010-017-2415-6. Epub 2017 Feb 17.

DOI:10.1007/s12010-017-2415-6
PMID:28211009
Abstract

Streptococcus pneumoniae is a colonizer of the human nasopharynx, which accounts for most of the community-acquired pneumonia cases and can cause non-invasive and invasive diseases. Current available vaccines are serotype-specific and the use of recombinant proteins associated with virulence is an alternative to compose vaccines and to overcome these problems. In a previous work, we describe the identification of proteins in S. pneumoniae by reverse vaccinology and the genetic diversity of these proteins in clinical isolates. It was possible to purify a half of 20 selected proteins in soluble form. The expression of these proteins on the pneumococcal cells surface was confirmed by flow cytometry. We demonstrated that some of these proteins were able to bind to extracellular matrix proteins and were recognized by sera from patients with pneumococcal meningitis infection caused by several pneumococcal serotypes. In this context, our results suggest that these proteins may play a role in pneumococcal pathogenesis and might be considered as potential vaccine candidates.

摘要

肺炎链球菌是人类鼻咽部的定植菌,它导致了大多数社区获得性肺炎病例,并且能够引起非侵袭性和侵袭性疾病。目前可用的疫苗是血清型特异性的,使用与毒力相关的重组蛋白是组成疫苗并克服这些问题的一种替代方法。在之前的一项工作中,我们描述了通过反向疫苗学鉴定肺炎链球菌中的蛋白质以及这些蛋白质在临床分离株中的遗传多样性。有可能以可溶形式纯化20种选定蛋白质中的一半。通过流式细胞术证实了这些蛋白质在肺炎球菌细胞表面的表达。我们证明其中一些蛋白质能够结合细胞外基质蛋白,并被由几种肺炎球菌血清型引起的肺炎球菌脑膜炎感染患者的血清所识别。在此背景下,我们的结果表明这些蛋白质可能在肺炎球菌发病机制中起作用,并且可能被视为潜在的疫苗候选物。

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Appl Biochem Biotechnol. 2017 Aug;182(4):1518-1539. doi: 10.1007/s12010-017-2415-6. Epub 2017 Feb 17.
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