Effects of genetic variability of Mycobacterium tuberculosis strains on the presentation of disease

被引:78
作者
Malik, AN
Godfrey-Faussett, P
机构
[1] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Med, London WC1E 7HT, England
[2] Hosp Trop Dis, London NW1 0PE, England
关键词
D O I
10.1016/S1473-3099(05)01310-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The nature of the variability in the clinical and epidemiological consequences of Mycobacterium tuberculosis infection remains poorly understood. Environmental and host factors that contribute to the outcome of infection and disease presentation are well recognised, but the role of bacterial factors has been more elusive. The rapid increase in the understanding of the molecular basis of M tuberculosis over the past decades has revived research into its pathogenesis. DNA fingerprinting techniques have been used to distinguish between strains of M tuberculosis, and efforts to characterise the strains present within populations have led to increased understanding of their global distribution. This research has shown that in certain areas a small number of strains are causing a disproportionate number of cases of the disease. The sequencing of the complete genome of M tuberculosis has accelerated the development of molecular techniques to differentiate strains according to their genetic polymorphisms. Investigation into the reasons why some strains are predominant by genetic strain-typing techniques may clarify which bacterial factors contribute to disease. This knowledge has the potential to influence control and prevention strategies for tuberculosis in the future. However, there are still limitations in these techniques and their results. This review discusses molecular epidemiology and genetic studies, and their contribution to the understanding of the links between genotypic and phenotypic characteristics of M tuberculosis strains.
引用
收藏
页码:174 / 183
页数:10
相关论文
共 105 条
[1]   Spread of strain W, a highly drug-resistant strain of Mycobacterium tuberculosis, across the United States [J].
Agerton, TB ;
Valway, SE ;
Blinkhorn, RJ ;
Shilkret, KL ;
Reves, R ;
Schluter, WW ;
Gore, B ;
Pozsik, CJ ;
Plikaytis, BB ;
Woodley, C ;
Onorato, IM .
CLINICAL INFECTIOUS DISEASES, 1999, 29 (01) :85-92
[2]   Modeling bacterial evolution with comparative-genome-based marker systems:: Application to Mycobacterium tuberculosis evolution and pathogenesis [J].
Alland, D ;
Whittam, TS ;
Murray, MB ;
Cave, MD ;
Hazbon, MH ;
Dix, K ;
Kokoris, M ;
Duesterhoeft, A ;
Eisen, JA ;
Fraser, CM ;
Fleischmann, RD .
JOURNAL OF BACTERIOLOGY, 2003, 185 (11) :3392-3399
[3]  
Anh DD, 2000, EMERG INFECT DIS, V6, P302
[4]   Genetic variation: molecular mechanisms and impact on microbial evolution [J].
Arber, W .
FEMS MICROBIOLOGY REVIEWS, 2000, 24 (01) :1-7
[5]   Tuberculosis transmission in central Los Angeles [J].
Barnes, PF ;
Yang, ZH ;
PrestonMartin, S ;
Pogoda, JM ;
Jones, BE ;
Otaya, M ;
Eisenach, KD ;
Knowles, L ;
Harvey, S ;
Cave, MD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 278 (14) :1159-1163
[6]   The challenges of tuberculosis on antimicrobial resistance [J].
REVISTA DE SAUDE PUBLICA, 2011, 45 (05) :997-1000
[7]   Variations in the Nrampi gene and susceptibility to tuberculosis in West Africans [J].
Bellamy, R ;
Ruwende, C ;
Corrah, T ;
McAdam, KPWJ ;
Whittle, HC ;
Hill, AVS .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (10) :640-644
[8]   TUBERCULOUS MENINGITIS IN PATIENTS INFECTED WITH THE HUMAN-IMMUNODEFICIENCY-VIRUS [J].
BERENGUER, J ;
MORENO, S ;
LAGUNA, F ;
VICENTE, T ;
ADRADOS, M ;
ORTEGA, A ;
GONZALEZLAHOZ, J ;
BOUZA, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (10) :668-672
[9]   Predominace of a novel Mycobacterium tuberculosis genotype in the Delhi region of India [J].
Bhanu, NV ;
van Soolingen, D ;
van Embden, JDA ;
Dar, L ;
Pandey, RM ;
Seth, P .
TUBERCULOSIS, 2002, 82 (2-3) :105-112
[10]   Global dissemination of the Mycobacterium tuberculosis W-Beijing family strains [J].
Bifani, PJ ;
Mathema, B ;
Kurepina, NE ;
Kreiswirth, BN .
TRENDS IN MICROBIOLOGY, 2002, 10 (01) :45-52