首页> 美国卫生研究院文献>Infection and Immunity >Evidence for occurrence of the ESAT-6 protein in Mycobacterium tuberculosis and virulent Mycobacterium bovis and for its absence in Mycobacterium bovis BCG.
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Evidence for occurrence of the ESAT-6 protein in Mycobacterium tuberculosis and virulent Mycobacterium bovis and for its absence in Mycobacterium bovis BCG.

机译:有证据表明在结核分枝杆菌和强牛分枝杆菌中存在ESAT-6蛋白而在牛分枝杆菌BCG中不存在。

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摘要

ESAT-6 is a secreted protein present in the short-term culture filtrate of Mycobacterium tuberculosis after growth on a synthetic Sauton medium. ESAT-6 has recently been demonstrated to induce strong T-cell responses in a mouse model of memory immunity after infection with M. tuberculosis. In Western blotting (immunoblotting), the monoclonal antibody HYB76-8, reacting with ESAT-6, gave a 6-kDa region was observed in filtrates from four of eight substrains of M. bovis BCG that produced high levels of MPB64, while no band occurred in the 6-kDa region with any of these BCG substrains. Southern blotting and PCR experiments with genomic mycobacterial DNA showed the presence of the esat-6 gene in reference strains and clinical isolates of M. tuberculosis as well as in virulent M. bovis. The esat-6 gene could not be demonstrated in any of the eight substrains of M. bovis BCG tested by these techniques. Two gene deletions that distinguish M. bovis BCG from virulent M. bovis have thus now been demonstrated. Deletion of mpb64 affects four of the eight substrains tested; deletion of esat-6 affects all of them. The reaction of HYB76-8 AT 26 kDa with four of the BCG substrains was demonstrated to result from cross-reactivity with MPB64. HYB76-8 was also shown to cross-react with the A, B, and C components of the antigen 85 complex and MPT51.
机译:ESAT-6是在合成Sauton培养基上生长后在结核分枝杆菌的短期培养滤液中存在的一种分泌蛋白。在结核分枝杆菌感染后,最近已证明ESAT-6在记忆免疫小鼠模型中诱导强烈的T细胞应答。在Western印迹(免疫印迹)中,与ESAT-6反应的单克隆抗体HYB76-8,在来自牛分枝杆菌BCG的8个亚菌株中的4个亚菌株的滤液中观察到了一个6 kDa的区域,该菌株产生高水平的MPB64,而没有条带这些BCG菌株均在6-kDa区发生。使用基因组分枝杆菌DNA的Southern印迹和PCR实验表明,结核分枝杆菌的参考菌株和临床分离株以及牛分枝杆菌中均存在esat-6基因。 esat-6基因不能在通过这些技术测试的牛分枝杆菌BCG的八个亚菌株中的任何一个中得到证实。因此,现在已经证明了两种区分牛分枝杆菌BCG和强力牛分枝杆菌的基因缺失。删除mpb64会影响所测试的八个亚菌株中的四个。 esat-6的缺失影响所有这些。 HYB76-8 AT 26 kDa与四种BCG菌株的反应被证明是与MPB64的交叉反应所致。还显示HYB76-8与抗原85复合物和MPT51的A,B和C组分发生交叉反应。

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