Type VI secretion requires a dynamic contractile phage tail-like structure

被引:519
作者
Basler, M. [2 ]
Pilhofer, M. [1 ,3 ]
Henderson, G. P. [1 ]
Jensen, G. J. [1 ,3 ]
Mekalanos, J. J. [2 ]
机构
[1] CALTECH, Div Biol, Pasadena, CA 91125 USA
[2] Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Boston, MA 02115 USA
[3] CALTECH, Howard Hughes Med Inst, Pasadena, CA 91125 USA
关键词
ENTEROAGGREGATIVE ESCHERICHIA-COLI; PSEUDOMONAS-AERUGINOSA; PROTEIN SECRETION; TARGET-CELLS; SYSTEM; TOMOGRAPHY; APPARATUS; ALIGNMENT; BACTERIA; ACTIN;
D O I
10.1038/nature10846
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Type VI secretion systems are bacterial virulence-associated nanomachines composed of proteins that are evolutionarily related to components of bacteriophage tails. Here we show that protein secretion by the type VI secretion system of Vibrio cholerae requires the action of a dynamic intracellular tubular structure that is structurally and functionally homologous to contractile phage tail sheath. Time-lapse fluorescence light microscopy reveals that sheaths of the type VI secretion system cycle between assembly, quick contraction, disassembly and re-assembly. Whole-cell electron cryotomography further shows that the sheaths appear as long tubular structures in either extended or contracted conformations that are connected to the inner membrane by a distinct basal structure. These data support a model in which the contraction of the type VI secretion system sheath provides the energy needed to translocate proteins out of effector cells and into adjacent target cells.
引用
收藏
页码:182 / U78
页数:6
相关论文
共 36 条
[1]   Markov random field based automatic image alignment for electron tomography [J].
Amat, Fernando ;
Moussavi, Farshid ;
Comolli, Luis R. ;
Elidan, Gal ;
Downing, Kenneth H. ;
Horowitz, Mark .
JOURNAL OF STRUCTURAL BIOLOGY, 2008, 161 (03) :260-275
[2]   SciN Is an Outer Membrane Lipoprotein Required for Type VI Secretion in Enteroaggregative Escherichia coli [J].
Aschtgen, Marie-Stephanie ;
Bernard, Christophe S. ;
De Bentzmann, Sophie ;
Lloubes, Roland ;
Cascales, Eric .
JOURNAL OF BACTERIOLOGY, 2008, 190 (22) :7523-7531
[3]   Anchoring the type VI secretion system to the peptidoglycan TssL, TagL, TagP, ... what else? [J].
Aschtgen, Marie-Stephanie ;
Thomas, Mark S. ;
Cascales, Eric .
VIRULENCE, 2010, 1 (06) :535-540
[4]   The SciZ protein anchors the enteroaggregative Escherichia coli Type VI secretion system to the cell wall [J].
Aschtgen, Marie-Stephanie ;
Gavioli, Marthe ;
Dessen, Andrea ;
Lloubes, Roland ;
Cascales, Eric .
MOLECULAR MICROBIOLOGY, 2010, 75 (04) :886-899
[5]   In vitro self-assembly from a simple protein of tailorable nanotubes building block [J].
Ballister, Edward R. ;
Lai, Angela H. ;
Zuckermann, Ronald N. ;
Cheng, Yifan ;
Mougous, Joseph D. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (10) :3733-3738
[6]   Vibrio cholerae tolC is required for bile resistance and colonization [J].
Bina, JE ;
Mekalanos, JJ .
INFECTION AND IMMUNITY, 2001, 69 (07) :4681-4685
[7]   Remodelling of VipA/VipB tubules by ClpV-mediated threading is crucial for type VI protein secretion [J].
Boenemann, Gabriele ;
Pietrosiuk, Aleksandra ;
Diemand, Alexander ;
Zentgraf, Hanswalter ;
Mogk, Axel .
EMBO JOURNAL, 2009, 28 (04) :315-325
[8]   Nucleoid occlusion factor SlmA is a DNA-activated FtsZ polymerization antagonist [J].
Cho, Hongbaek ;
McManus, Heather R. ;
Dove, Simon L. ;
Bernhardt, Thomas G. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (09) :3773-3778
[9]   MOLECULAR EPIDEMIOLOGICAL-STUDIES OF UNITED-STATES GULF-COAST VIBRIO-CHOLERAE STRAINS - INTEGRATION SITE OF MUTATOR VIBRIOPHAGE VCA-3 [J].
GOLDBERG, S ;
MURPHY, JR .
INFECTION AND IMMUNITY, 1983, 42 (01) :224-230
[10]   TIGHT REGULATION, MODULATION, AND HIGH-LEVEL EXPRESSION BY VECTORS CONTAINING THE ARABINOSE P-BAD PROMOTER [J].
GUZMAN, LM ;
BELIN, D ;
CARSON, MJ ;
BECKWITH, J .
JOURNAL OF BACTERIOLOGY, 1995, 177 (14) :4121-4130