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首页> 外文期刊>Tuberculosis >The use of microarray analysis to determine the gene expression profiles of Mycobacterium tuberculosis in response to anti-bacterial compounds.
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The use of microarray analysis to determine the gene expression profiles of Mycobacterium tuberculosis in response to anti-bacterial compounds.

机译:使用微阵列分析来确定结核分枝杆菌响应抗菌化合物的基因表达谱。

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摘要

The response of Mycobacterium tuberculosis to six anti-microbial agents was determined by microarray analysis in an attempt to define mechanisms of innate resistance in M. tuberculosis. The gene expression profiles of M. tuberculosis after treatment at the minimal inhibitory concentration (MIC) for 4 h with isoniazid, isoxyl, tetrahydrolipstatin, SRI#221, SR1#967 and SR1#9190 were compared to untreated M. tuberculosis. A common response to drug exposure was defined, and this expression profile overlapped with a number of other mycobacterial stress responses recently identified by microarray analysis. Compound-specific responses were also distinguished including a number of putative transcriptional regulators and translocation-related genes. These genes may contribute to the intrinsic resistance of M. tuberculosis to anti-microbial compounds. Further investigation into these mechanisms may elucidate novel pathways contributing to mycobacterial drug resistance and influence anti-mycobacterial drug development strategies.
机译:通过微阵列分析确定了结核分枝杆菌对六种抗微生物剂的反应,以试图确定结核分枝杆菌的先天性耐药机制。将异烟肼,异氧基,四氢脂抑素,SRI#221,SR1#967和SR1#9190在最小抑菌浓度(MIC)下处理4小时后的结核分枝杆菌的基因表达谱与未处理的结核分枝杆菌进行了比较。定义了对药物暴露的常见反应,该表达谱与最近通过微阵列分析鉴定的许多其他分枝杆菌应激反应重叠。还区分了化合物特异性应答,包括许多假定的转录调节因子和易位相关基因。这些基因可能有助于结核分枝杆菌对抗微生物化合物的内在抗性。对这些机制的进一步研究可能阐明了导致分枝杆菌耐药性的新途径,并影响了抗分枝杆菌药物的开发策略。

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