Recent advances in our knowledge of Mycobacterium bovis:: A feeling for the organism

被引:38
作者
Hewinson, RG [1 ]
Vordermeier, HM [1 ]
Smith, NH [1 ]
Gordon, SV [1 ]
机构
[1] TB Res Grp, Vet Labs Agcy, Weybridge KT15 3NB, Surrey, England
关键词
Mycobacterium bovis; bovine tuberculosis; BCG; genome; evolution; clonal expansion; vaccination; diagnosis; antigen mining; tuberculin test;
D O I
10.1016/j.vetmic.2005.11.050
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Significant and rapid progress has been made in Our knowledge and understanding of Mycobacterium bovis since the last international M. bovis conference 5 years ago. Much of this progress has been underpinned by the completion of the genome sequence. This important milestone has catalysed research into the development of a number of improved tools with which to combat bovine tuberculosis. In this article we will review recent progress made in the development of these tools and in our understanding of the organism, its evolution and spread. Comparison of the genome sequence with those of other members of the Mycobacterium tuberculosis complex has enabled insights into the evolution of M. bovis. This analysis also indicates that the M. tuberculosis complex have the propensity to adapt to new host species. The use of high throughput molecular typing methods has revealed that the recent bovine tuberculosis epidemic in Great Britain is being driven by a number of clonal expansions, which cannot be explained by random Mutation and drift alone. Completion of a number of mycobacterial genome sequences has allowed the development of antigen mining techniques that rapidly identify M. bovis-specific genes. These can then be used as reagents in the gamma interferon assay to increase the specificity of the assay and also to discriminate between Bacillus of Calmette and Guerin (BCG) vaccinated animals and those infected with M. bovis. In the longer term, comparisons between the genomes of M. bovis and BCG will allow insight into how BCG became attenuated following serial passage oil artificial growth media and reveal clues into how to improve the vaccine efficacy of BCG. Crown Copyright (c) 2005 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 139
页数:13
相关论文
共 51 条
  • [1] Diversity in a variable-number tandem repeat from Yersinia pestis
    Adair, DM
    Worsham, PL
    Hill, KK
    Klevytska, AM
    Jackson, PJ
    Friedlander, AM
    Keim, P
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (04) : 1516 - 1519
  • [2] Comparative genomics of BCG vaccines by whole-genome DNA microarray
    Behr, MA
    Wilson, MA
    Gill, WP
    Salamon, H
    Schoolnik, GK
    Rane, S
    Small, PM
    [J]. SCIENCE, 1999, 284 (5419) : 1520 - 1523
  • [3] A Mycobacterium tuberculosis operon encoding ESAT-6 and a novel low-molecular-mass culture filtrate protein (CFP-10)
    Berthet, FX
    Rasmussen, PB
    Rosenkrands, I
    Andersen, P
    Gicquel, B
    [J]. MICROBIOLOGY-UK, 1998, 144 : 3195 - 3203
  • [4] Origin and interstate spread of a New York City multidrug-resistant Mycobacterium tuberculosis clone family
    Bifani, PJ
    Plikaytis, BB
    Kapur, V
    Stockbauer, K
    Pan, X
    Lutfey, ML
    Moghazeh, SL
    Eisner, W
    Daniel, TM
    Kaplan, MH
    Crawford, JT
    Musser, JM
    Kreiswirth, BN
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (06): : 452 - 457
  • [5] ESAT-6 proteins: protective antigens and virulence factors?
    Brodin, P
    Rosenkrands, I
    Andersen, P
    Cole, ST
    Brosch, R
    [J]. TRENDS IN MICROBIOLOGY, 2004, 12 (11) : 500 - 508
  • [6] A new evolutionary scenario for the Mycobacterium tuberculosis complex
    Brosch, R
    Gordon, SV
    Marmiesse, M
    Brodin, P
    Buchrieser, C
    Eiglmeier, K
    Garnier, T
    Gutierrez, C
    Hewinson, G
    Kremer, K
    Parsons, LM
    Pym, AS
    Samper, S
    van Soolingen, D
    Cole, ST
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (06) : 3684 - 3689
  • [7] Buddle BM, 1999, CLIN DIAGN LAB IMMUN, V6, P1
  • [8] Solution structure of the Mycobacterium tuberculosis complex protein MPB70 -: From tuberculosis pathogenesis to inherited human corneal disease
    Carr, MD
    Bloemink, MJ
    Dentten, E
    Whelan, AO
    Gordon, SV
    Kelly, G
    Frenkiel, TA
    Hewinson, RG
    Williamson, RA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (44) : 43736 - 43743
  • [9] CLONAL DIVERSITY OF NEISSERIA-MENINGITIDIS FROM A POPULATION OF ASYMPTOMATIC CARRIERS
    CAUGANT, DA
    KRISTIANSEN, BE
    FROHOLM, LO
    BOVRE, K
    SELANDER, RK
    [J]. INFECTION AND IMMUNITY, 1988, 56 (08) : 2060 - 2068
  • [10] Reduced expression of antigenic proteins MPB70 and MPB83 in Mycobacterium bovis BCG strains due to a start codon mutation in sigK
    Charlet, D
    Mostowy, S
    Alexander, D
    Sit, L
    Wiker, HG
    Behr, MA
    [J]. MOLECULAR MICROBIOLOGY, 2005, 56 (05) : 1302 - 1313