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探索功能基因组学以开发抗结核病的新型干预策略。

Exploring functional genomics for the development of novel intervention strategies against tuberculosis.

作者信息

Rachman Helmy, Kaufmann Stefan H E

机构信息

Department of Immunology, Max Planck Institute for Infection Biology, Schumannstr. 21/22, D-10117 Berlin, Germany.

出版信息

Int J Med Microbiol. 2007 Nov;297(7-8):559-67. doi: 10.1016/j.ijmm.2007.03.003. Epub 2007 Apr 27.

Abstract

Tuberculosis (TB) remains a serious threat to humankind, and humans have encountered the causative agent of TB, Mycobacterium tuberculosis (MTB), for more than 10,000 years. Despite rapid advances in technology, efforts to besiege this robust pathogen seem to fail. The availability of genome sequences of several MTB complex strains open a new era of MTB research, the functional genomics, which will provide guidelines for novel control measures. In recent years, a series of methods have been developed to explore the mechanisms employed by MTB to persist and cause disease in the host. DNA array technology enables us to perform comparative genomics of different MTB strains and to examine the gene expression profiles of MTB growing under diverse living conditions. The generated transcriptome data can be exploited for design of new drugs, especially against multidrug-resistant (MDR) strains, development of more efficient vaccines, and identification of biomarkers for better diagnosis.

摘要

结核病(TB)仍然是对人类的严重威胁,人类与结核病的病原体结核分枝杆菌(MTB)已经抗争了一万多年。尽管技术取得了飞速进步,但围剿这种顽强病原体的努力似乎都失败了。几种MTB复合菌株基因组序列的可得性开启了MTB研究的新时代——功能基因组学,它将为新的控制措施提供指导。近年来,已经开发出一系列方法来探究MTB在宿主体内持续存在并致病所采用的机制。DNA芯片技术使我们能够对不同的MTB菌株进行比较基因组学研究,并检测MTB在不同生活条件下生长时的基因表达谱。所产生的转录组数据可用于新药设计,特别是针对耐多药(MDR)菌株的药物设计、开发更有效的疫苗以及识别用于更好诊断的生物标志物。

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