Mycobacterial genomics
- 28 February 2002
- journal article
- Published by Oxford University Press (OUP) in Transactions of the Royal Society of Tropical Medicine and Hygiene
- Vol. 96 (1) , 1-6
- https://doi.org/10.1016/s0035-9203(02)90222-1
Abstract
The small size of their genomes made bacteria ideal model organisms for the emerging field of genomics. Elucidating the genome sequences of mycobacteria was particularly attractive owing to the difficulties inherent in their manipulation. The slow growth rate, clumping, and requirement for category III containment make manipulation of Mycobacterium tuberculosis-complex strains laborious. M. leprae presents even greater problems as it has resisted all attempts at axenic culture. Availability of genome sequence data promised to accelerate our knowledge of the fundamental biology of these organisms, and to offer clues to the basis for their virulence, tropism and persistence in the host. This article will focus on what the genome sequences of M. tuberculosis and M. leprae have taught us about these pathogens, and how comparative genomics has exposed some of the fundamental differences between the species.Keywords
This publication has 21 references indexed in Scilit:
- Genomics of Mycobacterium bovisTuberculosis, 2001
- Massive gene decay in the leprosy bacillusNature, 2001
- Granuloma-Specific Expression of Mycobacterium Virulence Proteins from the Glycine-Rich PE-PGRS FamilyScience, 2000
- Analysis of the proteome of Mycobacterium tuberculosis in silicoTubercle and Lung Disease, 1999
- Use of fluorescence induction and sucrose counterselection to identify Mycobacterium tuberculosis genes expressed within host cellsMicrobiology, 1999
- New insertion sequences and a novel repeated sequence in the genome of Mycobacterium tuberculosis H37RvMicrobiology, 1999
- Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequenceNature, 1998
- On the catalase-peroxidase gene, katG, of Mycobacterium leprae and the implications for treatment of leprosy with isoniazidFEMS Microbiology Letters, 1997
- Characterization of the highly abundant polymorphic GC-rich-repetitive sequence (PGRS) present in Mycobacterium tuberculosisArchiv für Mikrobiologie, 1995
- Cloning of an M. tuberculosis DNA fragment associated with entry and survival inside cellsScience, 1993