A proteomic investigation of Streptococcus agalactiae reveals that human serum induces the C protein β antigen and arginine deiminase

被引:11
作者
Yang, Qian [1 ]
Zhang, Meng [1 ]
Harrington, Dean J. [2 ]
Black, Gary W. [1 ]
Sutcliffe, Iain C. [1 ]
机构
[1] Univ Northumbria Newcastle, Sch Life Sci, Newcastle Upon Tyne NE1 8ST, Tyne & Wear, England
[2] Univ Bradford, Div Biomed Sci, Sch Life Sci, Bradford BD7 1DP, W Yorkshire, England
关键词
C protein Beta antigen; Colonisation; Group B Streptococcus; Proteomics; Sepsis; Virulence factors; GROUP-A STREPTOCOCCUS; GROUP-B STREPTOCOCCUS; SYSTEM; VIRULENCE; GROWTH;
D O I
10.1016/j.micinf.2011.03.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Streptococcus agalactiae is a major neonatal pathogen. Disease progression is characterised by bacterial adaptation from commensal maternal vaginal colonisation to environments associated with neonatal disease, including exposure to blood. To explore this adaptation in vitro, we have used proteomics to identify proteins differentially expressed following growth on Todd Hewitt agar in the presence or absence of 10% v/v human serum. Twelve differentially expressed proteins were identified. Notably, the C protein beta antigen and arginine deiminase proteins were upregulated following growth in the presence of human serum, consistent with previous studies implicating these two proteins in the pathogenesis of S. agalactiae disease. (C) 2011 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:757 / 760
页数:4
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