Subtractive hybridization reveals a type I polyketide synthase locus specific to Mycobacterium ulcerans

被引:20
作者
Jenkin, GA
Stinear, TP
Johnson, PDR
Davies, JK [1 ]
机构
[1] Monash Univ, Dept Microbiol, Bacterial Pathogenesis Res Grp, Clayton, Vic 3800, Australia
[2] Austin & Repatriat Med Ctr, Dept Infect Dis, Heidelberg, Vic, Australia
[3] Inst Pasteur, Unite Genet Mol Bacterienne, Paris, France
关键词
D O I
10.1128/JB.185.23.6870-6882.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mycobacterium ulcerans causes Buruli ulcer, the third most prevalent mycobacterial infection of immunocompetent humans after tuberculosis and leprosy. Recent work has shown that the production by M. ulcerans of mycolactone, a novel polyketide, may partly explain the pathogenesis of Buruli ulcer. To search for the genetic basis of virulence in M. ulcerans, we took advantage of the close genetic relationship between M. ulcerans and Mycobacterium marinum by performing genomic suppressive subtractive hybridization of M. ulcerans with M. marinum. We identified several DNA fragments specific to M. ulcerans, in particular, a type I polyketide synthase locus with a highly repetitive modular arrangement. We postulate that this locus is responsible for the synthesis of mycolactone in M. ulcerans.
引用
收藏
页码:6870 / 6882
页数:13
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