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儿童肺炎球菌性脑膜炎脑脊液的定量蛋白质组学研究。

Quantitative Proteomics of Cerebrospinal Fluid in Paediatric Pneumococcal Meningitis.

机构信息

Centre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, United Kingdom.

Department of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, United Kingdom.

出版信息

Sci Rep. 2017 Aug 1;7(1):7042. doi: 10.1038/s41598-017-07127-6.

DOI:10.1038/s41598-017-07127-6
PMID:28765563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5539295/
Abstract

Streptococcus pneumoniae is responsible for diseases causing major global public health problems, including meningitis, pneumonia and septicaemia. Despite recent advances in antimicrobial therapy, pneumococcal meningitis remains a life-threatening disease. Furthermore, long-term sequelae are a major concern for survivors. Hence, a better understanding of the processes occurring in the central nervous system is crucial to the development of more effective management strategies. We used mass spectrometry based quantitative proteomics to identify protein changes in cerebrospinal fluid from children with Streptococcus pneumoniae infection, compared with children admitted to hospital with bacterial meningitis symptoms but negative diagnosis. Samples were analysed, by label free proteomics, in two independent cohorts (cohort 1: cases (n = 8) and hospital controls (n = 4); cohort 2: cases (n = 8), hospital controls (n = 8)). Over 200 human proteins were differentially expressed in each cohort, of which 65% were common to both. Proteins involved in the immune response and exosome signalling were significantly enriched in the infected samples. For a subset of proteins derived from the proteome analysis, we corroborated the proteomics data in a third cohort (hospital controls (n = 15), healthy controls (n = 5), cases (n = 20)) by automated quantitative western blotting, with excellent agreement with our proteomics findings. Proteomics data are available via ProteomeXchange with identifier PXD004219.

摘要

肺炎链球菌可引起多种严重的全球公共卫生问题,包括脑膜炎、肺炎和败血症。尽管抗菌治疗近年来取得了进展,但肺炎球菌性脑膜炎仍然是一种危及生命的疾病。此外,长期后遗症是幸存者的主要关注点。因此,更好地了解中枢神经系统中发生的过程对于开发更有效的治疗策略至关重要。我们使用基于质谱的定量蛋白质组学方法,比较了患有肺炎链球菌感染的儿童与因细菌性脑膜炎症状但诊断为阴性而住院的儿童的脑脊液中的蛋白质变化。通过无标记蛋白质组学分析了两个独立队列的样本(队列 1:病例(n=8)和医院对照组(n=4);队列 2:病例(n=8),医院对照组(n=8))。每个队列中都有超过 200 种人类蛋白质表达差异,其中 65%在两个队列中都存在。感染样本中明显富集了参与免疫反应和外泌体信号转导的蛋白质。对于从蛋白质组分析中得到的一组蛋白质,我们通过自动定量 Western 印迹在第三个队列(医院对照组(n=15)、健康对照组(n=5)、病例(n=20))中对蛋白质组学数据进行了验证,结果与我们的蛋白质组学发现非常吻合。蛋白质组学数据可通过 ProteomeXchange 以标识符 PXD004219 获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/7d422d41a7a1/41598_2017_7127_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/cd60b00fc23a/41598_2017_7127_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/9ff534ebba6c/41598_2017_7127_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/16df00dd9b0e/41598_2017_7127_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/42bd3b7ca085/41598_2017_7127_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/277f242d12b6/41598_2017_7127_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/7d422d41a7a1/41598_2017_7127_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/cd60b00fc23a/41598_2017_7127_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/9ff534ebba6c/41598_2017_7127_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/16df00dd9b0e/41598_2017_7127_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/42bd3b7ca085/41598_2017_7127_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/277f242d12b6/41598_2017_7127_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4561/5539295/7d422d41a7a1/41598_2017_7127_Fig6_HTML.jpg

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