Conserved features of type III secretion

Authors

  • A. P. Tampakaki,

    1. Institute of Molecular Biology and Biotechnology (IMBB), PO Box 1527, GR-71110 Heraklion, Crete, Greece.
    2. Technological and Educational Institute of Crete (TEI), GR-7110 Heraklion, Crete, Greece.
    3. University of Crete, Department of Biology, PO Box 2208, GR-71409 Heraklion, Crete, Greece.
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    • A.P.T. and V.E.F. have equally contributed to this work.

  • V. E. Fadouloglou,

    1. Institute of Molecular Biology and Biotechnology (IMBB), PO Box 1527, GR-71110 Heraklion, Crete, Greece.
    2. University of Crete, Department of Biology, PO Box 2208, GR-71409 Heraklion, Crete, Greece.
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    • A.P.T. and V.E.F. have equally contributed to this work.

  • A. D. Gazi,

    1. Institute of Molecular Biology and Biotechnology (IMBB), PO Box 1527, GR-71110 Heraklion, Crete, Greece.
    2. University of Crete, Department of Biology, PO Box 2208, GR-71409 Heraklion, Crete, Greece.
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  • N. J. Panopoulos,

    1. Institute of Molecular Biology and Biotechnology (IMBB), PO Box 1527, GR-71110 Heraklion, Crete, Greece.
    2. University of Crete, Department of Biology, PO Box 2208, GR-71409 Heraklion, Crete, Greece.
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  • M. Kokkinidis

    Corresponding author
    1. Institute of Molecular Biology and Biotechnology (IMBB), PO Box 1527, GR-71110 Heraklion, Crete, Greece.
    2. University of Crete, Department of Biology, PO Box 2208, GR-71409 Heraklion, Crete, Greece.
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E-mail kokkinid@imbb.forth.gr; Tel. (+30) 812810394455; Fax (+30) 812810394351.

Summary

Type III secretion systems (TTSSs) are essential mediators of the interaction of many Gram-negative bacteria with human, animal or plant hosts. Extensive sequence and functional similarities exist between components of TTSS from bacteria as diverse as animal and plant pathogens. Recent crystal structure determinations of TTSS proteins reveal extensive structural homologies and novel structural motifs and provide a basis on which protein interaction networks start to be drawn within the TTSSs, that are consistent with and help rationalize genetic and biochemical data. Such studies, along with electron microscopy, also established common architectural design and function among the TTSSs of plant and mammalian pathogens, as well as between the TTSS injectisome and the flagellum. Recent comparative genomic analysis, bioinformatic genome mining and genome-wide functional screening have revealed an unsuspected number of newly discovered effectors, especially in plant pathogens and uncovered a wider distribution of TTSS in pathogenic, symbiotic and commensal bacteria. Functional proteomics and analysis further reveals common themes in TTSS effector functions across phylogenetic host and pathogen boundaries. Based on advances in TTSS biology, new diagnostics, crop protection and drug development applications, as well as new cell biology research tools are beginning to emerge.

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