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肺炎链球菌对万古霉素治疗反应的比较蛋白质组学研究。

Comparative Proteomics of Streptococcus pneumoniae Response to Vancomycin Treatment.

机构信息

1 The First Affiliated Hospital of Jinan University , Guangzhou, China .

2 Key Laboratory of Functional Protein Research of Guangdong Higher Education Institutes, Institute of Life and Health Engineering, College of Life Science and Technology, Jinan University , Guangzhou, China .

出版信息

OMICS. 2017 Sep;21(9):531-539. doi: 10.1089/omi.2017.0098. Epub 2017 Sep 1.

DOI:10.1089/omi.2017.0098
PMID:28934029
Abstract

Streptococcus pneumoniae is a gram-positive pathogen that causes otitis media, pneumonia, meningitis, and other serious diseases. Vancomycin is one of the most important drugs currently used for the treatment of gram-positive bacterial infections, representing, importantly, the last line of defense against bacteria that have developed resistance to other antibiotics. While primary efforts of most investigations focused on the antibacterial mechanism of vancomycin, few studies have been performed to assess the tolerance mechanism of bacteria to vancomycin. In this work, whole cellular proteins were extracted from S. pneumoniae D39 with or without vancomycin treatment. Subsequently, differentially expressed proteins (DEPs) were identified with two-dimensional gel electrophoresis coupled with matrix-assisted laser desorption/ionization mass spectrometry (MS)/MS. In total, 27 proteins were upregulated and four proteins were downregulated in vancomycin-treated S. pneumoniae. Gene ontology analysis indicated that these DEPs were mainly involved in the nucleic acid, protein, and carbohydrate biosynthetic processes. Verification experiments with real-time quantitative polymerase chain reaction showed that the gene expression profiles were consistent with proteomic data. These new observations may serve as a valuable resource for future investigations of vancomycin tolerance mechanisms of S. pneumoniae.

摘要

肺炎链球菌是一种革兰阳性病原体,可引起中耳炎、肺炎、脑膜炎和其他严重疾病。万古霉素是目前用于治疗革兰阳性菌感染的最重要药物之一,重要的是,它是对抗对抗生素产生耐药性的细菌的最后一道防线。虽然大多数研究的主要重点是万古霉素的抗菌机制,但很少有研究评估细菌对万古霉素的耐受机制。在这项工作中,用或不用万古霉素处理从肺炎链球菌 D39 中提取全细胞蛋白。随后,通过二维凝胶电泳结合基质辅助激光解吸/电离质谱(MS)/MS 鉴定差异表达蛋白(DEPs)。总共,在万古霉素处理的肺炎链球菌中,有 27 种蛋白上调,4 种蛋白下调。GO 分析表明,这些 DEPs 主要参与核酸、蛋白质和碳水化合物的生物合成过程。实时定量聚合酶链反应的验证实验表明,基因表达谱与蛋白质组学数据一致。这些新的观察结果可能为未来研究肺炎链球菌对万古霉素的耐受机制提供有价值的资源。

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