In vivo genetic analysis of bacterial virulence

被引:163
作者
Chiang, SL [1 ]
Mekalanos, JJ
Holden, DW
机构
[1] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Shipley Inst Med, Boston, MA 02115 USA
[3] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Dept Infect Dis, London W12 0NN, England
基金
英国惠康基金;
关键词
in vivo expression technology; signature-tagged mutagenesis; differential fluorescence induction; pathogenesis; GAMBIT;
D O I
10.1146/annurev.micro.53.1.129
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In vitro assays contribute greatly to our understanding of bacterial pathogenesis, but they frequently cannot replicate the complex environment encountered by pathogens during infection. The information gained from such studies is therefore limited. In vivo models, on the other hand, can be difficult to use, and this has to some extent diminished the incentive to perform studies in living animals. However, several recently developed techniques permit in vivo examination of many genes simultaneously. Most of these methods fall into two broad classes: in vivo expression technology and signature-tagged mutagenesis. In vivo expression technology is a promoter-trap strategy designed to identify genes whose expression is induced in a specific environment, typically that encountered in a host. Signature-tagged mutagenesis uses comparative hybridization to isolate mutants unable to survive specified environmental conditions and has been used to identify genes critical for survival in the host. Both approaches have so far been used exclusively for investigating pathogen-host interactions, but they should be easily adaptable to the study of other processes.
引用
收藏
页码:129 / 154
页数:26
相关论文
共 72 条
  • [1] Akerley B.J., 1998, AM SOC MICR GEN M 98
  • [2] ECTOPIC EXPRESSION OF THE FLAGELLAR REGULON ALTERS DEVELOPMENT OF THE BORDETELLA HOST INTERACTION
    AKERLEY, BJ
    COTTER, PA
    MILLER, JF
    [J]. CELL, 1995, 80 (04) : 611 - 620
  • [3] Systematic identification of essential genes by in vitro mariner mutagenesis
    Akerley, BJ
    Rubin, EJ
    Camilli, A
    Lampe, DJ
    Robertson, HM
    Mekalanos, JJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) : 8927 - 8932
  • [4] FPTA, THE FE(III)-PYOCHELIN RECEPTOR OF PSEUDOMONAS-AERUGINOSA - A PHENOLATE SIDEROPHORE RECEPTOR HOMOLOGOUS TO HYDROXAMATE SIDEROPHORE RECEPTORS
    ANKENBAUER, RG
    QUAN, HN
    [J]. JOURNAL OF BACTERIOLOGY, 1994, 176 (02) : 307 - 319
  • [5] SALMONELLA-TYPHIMURIUM ACTIVATES VIRULENCE GENE-TRANSCRIPTION WITHIN ACIDIFIED MACROPHAGE PHAGOSOMES
    ARANDA, CMA
    SWANSON, JA
    LOOMIS, WP
    MILLER, SI
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) : 10079 - 10083
  • [6] THE ROLE OF TOXIN-COREGULATED PILI IN THE PATHOGENESIS OF VIBRIO-CHOLERAE-O1 EL-TOR
    ATTRIDGE, SR
    VOSS, E
    MANNING, PA
    [J]. MICROBIAL PATHOGENESIS, 1993, 15 (06) : 421 - 431
  • [7] Survival of FimH-expressing enterobacteria in macrophages relies on glycolipid traffic
    Baorto, DM
    Gao, ZM
    Malaviya, R
    Dustin, ML
    vanderMerwe, A
    Lublin, DM
    Abraham, SN
    [J]. NATURE, 1997, 389 (6651) : 636 - 639
  • [8] FURTHER CHARACTERIZATION OF THE PHOP REGULON - IDENTIFICATION OF NEW PHOP-ACTIVATED VIRULENCE LOCI
    BELDEN, WJ
    MILLER, SI
    [J]. INFECTION AND IMMUNITY, 1994, 62 (11) : 5095 - 5101
  • [9] Bennish Michael L., 1994, P229
  • [10] Specific binding of the Listeria monocytogenes transcriptional regulator PrfA to target sequences requires additional factor(s) and is influenced by iron
    Bockmann, R
    Dickneite, C
    Middendorf, B
    Goebel, W
    Sokolovic, Z
    [J]. MOLECULAR MICROBIOLOGY, 1996, 22 (04) : 643 - 653