Submitted to: Proceedings of the National Academy of Sciences
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 7/13/2005
Publication Date: 8/30/2005
Citation: Li, L., Bannantine, J.P., Zhang, Q., Amonsin, A., May, B.J., Alt, D.P., Banerji, N., Kanjilal, S., Kapur, V. 2005. The Complete Genome Sequence of Mycobacterium avium subsp. paratuberculosis. Proceedings of the National Academy of Sciences. 102:12344-12349. Interpretive Summary: This paper describes the complete genome sequence of Mycobacterium avium subspecies paratuberculosis, the bacterium that causes Johne’s disease. Every nucleotide or DNA base pair has now been defined. Because of this work, we now also know all of the genes encoded by this veterinary pathogen. The genome is large in size for a typical bacterium with over 4.8 million base pairs. This sequence has revealed undiscovered potential virulence genes or genes thought to be responsible for causing Johne’s disease. Furthermore, novel diagnostic targets are expected to emerge from the genome sequence. Collectively, this sequence will be an invaluable reference for researchers studying Johne’s disease for years to come.
Technical Abstract: We describe here the complete genome sequence of a common clone of Mycobacterium avium subsp. partuberculosis (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 open reading frames (ORFs), 45 tRNAs and one rRNA operon. In silico analysis identified over 3,000 genes with homologues to the highly successful human pathogen, M. tuberculosis (Mtb), and 161 unique genomic regions with 39 novel 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 non-synonymous substitution ratio of over 2. Comparative sequence analysis reveal several noteworthy features of the K-10 genome including a relative paucity of the PP/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 genomic 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.