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牛分枝杆菌卡介苗(Mycobacterium bovis BCG)与强毒力牛分枝杆菌之间遗传差异的分子分析

Molecular analysis of genetic differences between Mycobacterium bovis BCG and virulent M. bovis.

作者信息

Mahairas G G, Sabo P J, Hickey M J, Singh D C, Stover C K

机构信息

Laboratory of Tuberculosis and Molecular Microbiology, PathoGenesis Corp., Seattle, Washington 98119, USA.

出版信息

J Bacteriol. 1996 Mar;178(5):1274-82. doi: 10.1128/jb.178.5.1274-1282.1996.

Abstract

The live attenuated bacillus Calmette-Guérin (BCG) vaccine for the prevention of disease associated with Mycobacterium tuberculosis was derived from the closely related virulent tubercle bacillus, Mycobacterium bovis. Although the BCG vaccine has been one of the most widely used vaccines in the world for over 40 years, the genetic basis of BCG's attenuation has never been elucidated. We employed subtractive genomic hybridization to identify genetic differences between virulent M. bovis and M. tuberculosis and avirulent BCG. Three distinct genomic regions of difference (designated RD1 to RD3) were found to be deleted from BCG, and the precise junctions and DNA sequence of each deletion were determined. RD3, a 9.3-kb genomic segment present in virulent laboratory strains of M. bovis and M. tuberculosis, was absent from BCG and 84% of virulent clinical isolates. RD2, a 10.7-kb DNA segment containing a novel repetitive element and the previously identified mpt-64 gene, was conserved in all virulent laboratory and clinical tubercle bacilli tested and was deleted only from substrains derived from the original BCG Pasteur strain after 1925. Thus, the RD2 deletion occurred after the original derivation of BCG. RD1, a 9.5-kb DNA segment found to be deleted from all BCG substrains, was conserved in all virulent laboratory and clinical isolates of M. bovis and M. tuberculosis tested. The reintroduction of RD1 into BCG repressed the expression of at least 10 proteins and resulted in a protein expression profile almost identical to that of virulent M. bovis and M. tuberculosis, as determined by two-dimensional gel electrophoresis. These data indicate a role for RD1 in the regulation of multiple genetic loci, suggesting that the loss of virulence by BCG is due to a regulatory mutation. These findings may be applicable to the rational design of a new attenuated tuberculosis vaccine and the development of new diagnostic tests to distinguish BCG vaccination from tuberculosis infection.

摘要

用于预防与结核分枝杆菌相关疾病的减毒活卡介苗(BCG)源自密切相关的强毒结核杆菌——牛分枝杆菌。尽管卡介苗在40多年来一直是世界上使用最广泛的疫苗之一,但其减毒的遗传基础从未得到阐明。我们采用消减基因组杂交技术来鉴定强毒牛分枝杆菌与结核分枝杆菌以及无毒卡介苗之间的遗传差异。发现卡介苗缺失了三个不同的基因组差异区域(命名为RD1至RD3),并确定了每个缺失区域的精确连接点和DNA序列。RD3是一个9.3kb的基因组片段,存在于强毒的牛分枝杆菌和结核分枝杆菌实验室菌株中,卡介苗以及84%的强毒临床分离株中均不存在该片段。RD2是一个10.7kb的DNA片段,包含一个新的重复元件和先前鉴定的mpt-64基因,在所有测试的强毒实验室和临床结核杆菌中均保守,仅在1925年后源自原始卡介苗巴斯德菌株的亚菌株中缺失。因此,RD2缺失发生在卡介苗原始衍生之后。RD1是一个9.5kb的DNA片段,发现所有卡介苗亚菌株均缺失该片段,在所测试的所有强毒牛分枝杆菌和结核分枝杆菌实验室及临床分离株中均保守。将RD1重新引入卡介苗可抑制至少10种蛋白质的表达,通过二维凝胶电泳测定,其蛋白质表达谱几乎与强毒牛分枝杆菌和结核分枝杆菌相同。这些数据表明RD1在多个基因位点的调控中起作用,提示卡介苗毒力丧失是由于调控突变所致。这些发现可能适用于新型减毒结核疫苗的合理设计以及开发新的诊断测试以区分卡介苗接种与结核感染。

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