[抑制减法杂交鉴定结核分枝杆菌H37Rv与减毒菌株H37Ra的差异基因组基因]。

Zhi-Hong Xiong, Yu-Hui Zhuang, Guo-Li Li
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引用次数: 0

摘要

为了研究结核分枝杆菌毒力相关基因,我们采用抑制减法杂交技术克隆结核分枝杆菌毒力菌株H37Rv与减毒菌株H37Ra的差异基因组基因。对54个不同基因进行克隆、测序和Southern-blotting分析。H37Ra中两个不同的DNA片段是迄今为止的新基因,并获得新的基因库编号AY534505和AY560011。在H37Rv中获得了8个不同的DNA片段。一个是编码毒力因子mce的基因片段;一个片段属于编码purC合成酶的基因;一个为PE家族蛋白;其余4个片段为推定基因;最后一个是非编码片段。PCR分析表明,其中2个基因只存在于临床毒株和H37Rv中,而不存在于临床无毒毒株和H37Ra中。这些新的差异基因可能为研究结核分枝杆菌的发病机制提供重要线索。
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[Identification of differential genomic genes of Mycobacterium tuberculosis H37Rv and attenuated strain H37Ra by suppression subtractive hybridization].

To study the virulence-related genes in Mycobacterium tuberculosis, we used suppression subtractive hybridization to clone the differential genomic genes between Mycobacterium tuberculosis virulence strain H37Rv and attenuated strain H37Ra. All of 54 different genes were cloned, sequenced and analyzed by Southern-blotting. Two different DNA fragments in H37Ra are new genes so far, and get the new Genbank number AY534505 and AY560011. Eight different DNA fragments in H37Rv were obtained. One is the fragment of a gene coding virulence factor mce; one fragment belongs to the gene coding for purC synthenzyme; one for PE family protein; the other 4 fragments for putative gene; and the last one is a non-coding fragment. PCR analysis indicated that 2 of the different genes were present exclusively in the clinical virulent strain and in H37Rv, but not in the clinical avirulent strain and in H37Ra. The novel differential genes may provide an important clue for studying the mechanism of M. tuberculosis pathogenesis.

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