乙胺丁醇
结核分枝杆菌
肺结核
蛋白质组
微生物学
利福平
生物
医学
药理学
生物化学
病理
作者
Luciana Dias Ghiraldi-Lopes,Paula Aline Zanetti Campanerut-Sá,Geisa Paulino Caprini Evaristo,Jean Eduardo Meneguello,Adriana Fiorini,Vanessa Pietrowski Baldin,Emanuel Maltempi de Souza,Regiane Bertin de Lima Scodro,Vera Lúcia Dias Siqueira,Rosilene Fressatti Cardoso
出处
期刊:Infectious disorders drug targets
[Bentham Science]
日期:2019-02-04
卷期号:19 (1): 73-80
被引量:6
标识
DOI:10.2174/1871526518666180124140840
摘要
In recent years, very few effective drugs against Mycobacterium tuberculosis have emerged, which motivates the research with drugs already used in the treatment of tuberculosis. Ethambutol is a bacteriostatic drug that affects cell wall integrity, but the effects of this drug on bacilli are not fully exploited.Based on the need to better investigate the complex mechanism of action of ethambutol, our study presented the proteome profile of M. tuberculosis after different times of ethambutol exposure, aiming to comprehend the dynamics of bacilli response to its effects. M. tuberculosis was exposed to ½ MIC of ethambutol at 24 and 48 hours. The proteins were identified by MALDI-TOF/TOF.The main protein changes occurred in metabolic proteins as dihydrolipoyl dehydrogenase (Rv0462), glutamine synthetase1 (Rv2220), electron transfer flavoprotein subunit beta (Rv3029c) and adenosylhomocysteinase (Rv3248c).Considering the functions of these proteins, our results support that the intermediary metabolism and respiration were affected by ethambutol and this disturbance provided proteins that could be explored as additional targets for this drug.
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