Protein expression by a Beijing strain differs from that of another clinical isolate and Mycobacterium tuberculosis H37Rv

被引:44
|
作者
Pheiffer, C
Betts, JC
Flynn, HR
Lukey, PT
van Helden, P
机构
[1] Univ Stellenbosch, Sch Med, Dept Biochem Med, MRC Ctr Mol & Cellular Biol, ZA-7505 Tygerberg, South Africa
[2] GlaxoSmithKline Res & Dev, Stevenage SG1 2NY, Herts, England
来源
MICROBIOLOGY-SGM | 2005年 / 151卷
关键词
D O I
10.1099/mic.0.27518-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Beijing strain family has often been associated with tuberculosis (TB) outbreaks and drug resistance worldwide. In this study the authors have compared the protein expression and antigen recognition profiles of a local Beijing strain with a less prevalent clinical isolate belonging to the family 23 strain lineage, and the laboratory strain Mycobacterium tuberculosis H37Rv. Using two-dimensional electrophoresis, liquid chromatography tandem mass spectrometry and Western blot analysis several proteins were identified as quantitatively increased or decreased in both clinical strains compared to H37Rv. Remarkably, the Beijing strain showed increased expression of alpha-crystallin and decreased expression of Hsp65, PstS1, and the 47 kDa protein compared to the other clinical strain and H37Rv. One- and two-dimensional Western blot analysis of antigens expressed by the three strains, using plasma from TB patients, confirmed differential antigen expression by strains and patient-to-patient variation in humoral immunity. These observed protein differences could aid the elucidation of mechanisms underlying the success of the Beijing strain family, measured by global dissemination, compared to other M. tuberculosis strains.
引用
收藏
页码:1139 / 1150
页数:12
相关论文
共 50 条
  • [41] Assessing the progress of Mycobacterium tuberculosis H37Rv structural genomics
    Fang, Zhuo
    van der Merwe, Ruben Gerhard
    Warren, Robin Mark
    Schubert, Wolf-Dieter
    van Pittius, Nicolaas Claudius Gey
    TUBERCULOSIS, 2015, 95 (02) : 131 - 136
  • [42] The multiple activities of polyphosphate kinase of Mycobacterium tuberculosis H37Rv
    Hwang, M. -R.
    Yoon, J. W.
    Park, S. -K.
    Kim, N. -I.
    Jung, H. -S.
    Kim, H. -Y.
    FEBS JOURNAL, 2008, 275 : 405 - 405
  • [43] Dehalogenation of haloalkanes by Mycobacterium tuberculosis H37Rv and other mycobacteria
    Jesenská, A
    Sedlácek, I
    Damborsky, J
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (01) : 219 - 222
  • [44] MECHANISM OF STREPTOMYCIN ACTION IN MYCOBACTERIUM-TUBERCULOSIS H37RV
    SHAILA, MS
    GOPINATHAN, KP
    RAMAKRISHNAN, T
    JOURNAL OF THE INDIAN INSTITUTE OF SCIENCE, 1975, 57 (09) : 301 - 316
  • [45] OCCURRENCE OF ASCORBIC ACID IN MYCOBACTERIUM-TUBERCULOSIS H37RV
    ALLAUDEE.HS
    RAMAKRIS.T
    INDIAN JOURNAL OF EXPERIMENTAL BIOLOGY, 1971, 9 (02) : 278 - &
  • [46] Evaluation of the expression of cytokines and chemokines in macrophages in response to rifampin-monoresistant Mycobacterium tuberculosis and H37Rv strain
    Ravan, Parvaneh
    Sattari, Taher Nejad
    Siadat, Seyed Davar
    Vaziri, Farzam
    CYTOKINE, 2019, 115 : 127 - 134
  • [47] Aptamer inhibits Mycobacterium tuberculosis (H37Rv) invasion of macrophage
    Fan Chen
    XiaoLian Zhang
    Jing Zhou
    Shengwu Liu
    Junyan Liu
    Molecular Biology Reports, 2012, 39 (3) : 2157 - 2162
  • [48] STUDIES ON MYCOBACTERIUM TUBERCULOSIS H37RV GROWN IN-VIVO
    ARTMAN, M
    BEKIERKUNST, A
    AMERICAN REVIEW OF RESPIRATORY DISEASE, 1961, 83 (01): : 100 - &
  • [49] Different behaviours of promoters in Mycobacterium tuberculosis H37Rv and H37Ra
    Dokladda, Kanchana
    Billamas, Pamaree
    Palittapongarnpim, Prasit
    WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 2015, 31 (02): : 407 - 413
  • [50] Characterization of an acid inducible lipase Rv3203 from Mycobacterium tuberculosis H37Rv
    Gurpreet Singh
    Stuti Arya
    Dominic Narang
    Dipendrasinh Jadeja
    Gurdyal Singh
    U. D. Gupta
    Kashmir Singh
    Jagdeep Kaur
    Molecular Biology Reports, 2014, 41 : 285 - 296