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通过一维凝胶电泳和电荷色谱法对耐药结核分枝杆菌进行蛋白质组学分析。

Proteomic analysis of drug-resistant Mycobacterium tuberculosis by one-dimensional gel electrophoresis and charge chromatography.

作者信息

Yari Shamsi, Hadizadeh Tasbiti Alireza, Ghanei Mostafa, Shokrgozar Mohammad Ali, Fateh Abolfazl, Mahdian Reza, Yari Fatemeh, Bahrmand Ahmadreza

机构信息

Tuberculosis Department, Pasteur Institute of Iran, Tehran, Iran.

Microbiology Research Center (MRC), Pasteur Institute of Iran, Tehran, Iran.

出版信息

Arch Microbiol. 2017 Jan;199(1):9-15. doi: 10.1007/s00203-016-1267-8. Epub 2016 Jul 14.

DOI:10.1007/s00203-016-1267-8
PMID:27417316
Abstract

Multidrug-resistant tuberculosis (MDR-TB) is a form of TB caused by Mycobacterium tuberculosis (M. tuberculosis) that do not respond to, at least, isoniazid and rifampicin, the two most powerful, first-line (or standard) anti-TB drugs. Novel intervention strategies for eliminating this disease were based on finding proteins that can be used for designing new drugs or new and reliable kits for diagnosis. The aim of this study was to compare the protein profiles of MDR-TB with sensitive isolates. Proteomic analysis of M. tuberculosis MDR-TB and sensitive isolates was obtained with ion exchange chromatography coupled with MALDI-TOF-TOF (matrix-assisted laser desorption/ionization) in order to identify individual proteins that have different expression in MDR-TB to be used as a drug target or diagnostic marker for designing valuable TB vaccines or TB rapid tests. We identified eight proteins in MDR-TB isolates, and analyses showed that these proteins are absent in M. tuberculosis-sensitive isolates: (Rv2140c, Rv0009, Rv1932, Rv0251c, Rv2558, Rv1284, Rv3699 and MMP major membrane proteins). These data will provide valuable clues in further investigation for suitable TB rapid tests or drug targets against drug-resistant and sensitive M. tuberculosis isolates.

摘要

耐多药结核病(MDR-TB)是由结核分枝杆菌引起的一种结核病形式,这种细菌至少对两种最有效的一线(或标准)抗结核药物异烟肼和利福平没有反应。消除这种疾病的新干预策略基于寻找可用于设计新药或新型可靠诊断试剂盒的蛋白质。本研究的目的是比较耐多药结核分枝杆菌与敏感菌株的蛋白质谱。为了鉴定在耐多药结核分枝杆菌中表达不同、可作为药物靶点或诊断标志物以设计有价值的结核病疫苗或结核病快速检测方法的单个蛋白质,采用离子交换色谱与基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-TOF)联用技术对结核分枝杆菌耐多药菌株和敏感菌株进行了蛋白质组学分析。我们在耐多药结核分枝杆菌菌株中鉴定出了8种蛋白质,分析表明这些蛋白质在结核分枝杆菌敏感菌株中不存在:(Rv2140c、Rv0009、Rv1932、Rv0251c、Rv2558、Rv1284、Rv3699和主要膜蛋白MMP)。这些数据将为进一步研究针对耐药和敏感结核分枝杆菌菌株的合适结核病快速检测方法或药物靶点提供有价值的线索。

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