Wheeler Paul R, Brosch Roland, Coldham Nicholas G, Inwald Jacqueline K, Hewinson R Glyn, Gordon Stephen V
VLA Weybridge, New Haw, Addlestone KT15 3NB, Surrey, UK.
Institut Pasteur, UP Pathogénomique Mycobactérienne Intégrée, 25, Rue du Dr Roux, 75015 Paris, France.
Microbiology (Reading). 2008 Dec;154(Pt 12):3731-3742. doi: 10.1099/mic.0.2008/022269-0.
Previous work on the population structure of Mycobacterium bovis strains in Great Britain has identified highly successful clones which are expanding across the country. One such clone, designated M. bovis type 17, differs from all other members of the Mycobacterium tuberculosis complex in having a region of deletion, termed RDbovis(d)_0173, of seven genes between Mb1963c and Mb1971. Three of these genes have functions annotated in lipid metabolism. To explore the molecular basis for the success of this clone, we examined the impact of this deletion on lipid metabolism. While type 17 isolates had similar lipid composition to other M. bovis strains, their ability to incorporate propanoate into mycolic acids was remarkably low. When expressed as a reciprocal (the ratio of incorporation of label from acetate : propanoate into mycolic acids) the ratio was higher for all three type 17 field strains tested (mean: 18.90) than the values of 7.30 to 7.61 for other field strains (P < 0.002) and values < 6.50 for all other strains in the M. tuberculosis complex tested. The label from propanoate was diverted to pyruvate, at significantly higher levels in M. bovis type 17 than all other strains (P < 0.021). Complementation of M. bovis type 17 with an integrating cosmid, IE471, carrying the M. tuberculosis orthologues of Mb1963c-Mb1971 resulted in the ability of the recombinant strain to incorporate label from propanoate into mycolic acids in a manner similar to other strains. M. bovis type 17 : : IE471 labelled pyruvate from propanoate about four times more slowly than the parent strain. Thus, RDbovis(d)_0173 results in a profound effect on carbon metabolism, providing the ability to compensate for the inactivation of the ald and pykA genes, involved in pyruvate metabolism, that is seen in M. bovis (but not in M. tuberculosis). This shift in carbon metabolism may be a factor in the extraordinary clonal expansion reported for M. bovis type 17.
此前关于英国牛分枝杆菌菌株群体结构的研究已鉴定出一些在全国范围内不断扩张的非常成功的克隆。其中一个这样的克隆,被命名为牛分枝杆菌17型,与结核分枝杆菌复合群的所有其他成员不同,它在Mb1963c和Mb1971之间有一个由7个基因组成的缺失区域,称为RDbovis(d)_0173。这些基因中的三个在脂质代谢方面有注释功能。为了探究这个克隆成功的分子基础,我们研究了这个缺失对脂质代谢的影响。虽然17型分离株的脂质组成与其他牛分枝杆菌菌株相似,但它们将丙酸盐掺入分枝菌酸的能力非常低。以倒数形式表示(即乙酸盐和丙酸盐标记掺入分枝菌酸的比例),所有三个测试的17型野外菌株的比例(平均值:18.90)高于其他野外菌株的7.30至7.61(P < 0.002),以及所有其他测试的结核分枝杆菌复合群菌株的值< 6.50。丙酸盐的标记被转移到丙酮酸,在牛分枝杆菌17型中的水平显著高于所有其他菌株(P < 0.021)。用携带Mb1963c - Mb1971结核分枝杆菌直系同源物的整合黏粒IE471对牛分枝杆菌17型进行互补,导致重组菌株能够以与其他菌株相似的方式将丙酸盐标记掺入分枝菌酸。牛分枝杆菌17型::IE471从丙酸盐标记丙酮酸的速度比亲本菌株慢约四倍。因此,RDbovis(d)_0173对碳代谢有深远影响,提供了补偿参与丙酮酸代谢的ald和pykA基因失活的能力,这种失活在牛分枝杆菌中可见(但在结核分枝杆菌中不可见)。碳代谢的这种转变可能是牛分枝杆菌17型报道的异常克隆扩张的一个因素。