Li Lingling, Bannantine John P, Zhang Qing, Amonsin Alongkorn, May Barbara J, Alt David, Banerji Nilanjana, Kanjilal Sagarika, Kapur Vivek
Department of Microbiology, University of Minnesota, St. Paul, MN 55108, USA.
Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12344-9. doi: 10.1073/pnas.0505662102. Epub 2005 Aug 22.
We describe here the complete genome sequence of a common clone of Mycobacterium avium subspecies paratuberculosis (Map) strain K-10, the causative agent of Johne's disease in cattle and other ruminants. The K-10 genome is a single circular chromosome of 4,829,781 base pairs and encodes 4,350 predicted ORFs, 45 tRNAs, and one rRNA operon. In silico analysis identified >3,000 genes with homologs to the human pathogen, M. tuberculosis (Mtb), and 161 unique genomic regions that encode 39 previously unknown Map genes. Analysis of nucleotide substitution rates with Mtb homologs suggest overall strong selection for a vast majority of these shared mycobacterial genes, with only 68 ORFs with a synonymous to nonsynonymous substitution ratio of >2. Comparative sequence analysis reveals several noteworthy features of the K-10 genome including: a relative paucity of the PE/PPE family of sequences that are implicated as virulence factors and known to be immunostimulatory during Mtb infection; truncation in the EntE domain of a salicyl-AMP ligase (MbtA), the first gene in the mycobactin biosynthesis gene cluster, providing a possible explanation for mycobactin dependence of Map; and Map-specific sequences that are likely to serve as potential targets for sensitive and specific molecular and immunologic diagnostic tests. Taken together, the availability of the complete genome sequence offers a foundation for the study of the genetic basis for virulence and physiology in Map and enables the development of new generations of diagnostic tests for bovine Johne's disease.
我们在此描述了副结核分枝杆菌(Map)K-10菌株常见克隆株的完整基因组序列,该菌株是牛和其他反刍动物中约内氏病的病原体。K-10基因组是一个由4,829,781个碱基对组成的单环染色体,编码4,350个预测的开放阅读框(ORF)、45个转运RNA(tRNA)和一个核糖体RNA(rRNA)操纵子。计算机分析鉴定出超过3000个与人类病原体结核分枝杆菌(Mtb)具有同源性的基因,以及161个独特的基因组区域,这些区域编码39个先前未知的Map基因。与Mtb同源物的核苷酸替换率分析表明,这些共有的分枝杆菌基因中的绝大多数在整体上受到强烈选择,只有68个ORF的同义替换与非同义替换比率大于2。比较序列分析揭示了K-10基因组的几个值得注意的特征,包括:与毒力因子相关且已知在Mtb感染期间具有免疫刺激作用的PE/PPE序列家族相对较少;分枝杆菌素生物合成基因簇中的第一个基因水杨酰-AMP连接酶(MbtA)的EntE结构域发生截短,这可能解释了Map对分枝杆菌素的依赖性;以及可能作为敏感和特异分子及免疫诊断测试潜在靶点的Map特异性序列。总之,完整基因组序列的可得性为研究Map中毒力和生理学的遗传基础提供了基础,并有助于开发新一代牛约内氏病诊断测试。