What is type VI secretion doing in all those bugs?

Trends in Microbiology

Volumn 18, Issue 12, 2010, Pages 531-537

  Schwarz, Sandra ^a   Hood, Rachel D ^a   Mougous, Joseph D ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL TOXIN; BACTERIOCIN; VIRULENCE FACTOR;

AMINO ACID SEQUENCE; BACTERIAL GENOME; BACTERIAL INFECTION; BACTERIAL PHENOMENA AND FUNCTIONS; BACTERIAL VIRULENCE; DISEASE COURSE; EVOLUTIONARY ADAPTATION; GENE CLUSTER; GENE FUNCTION; GENETIC CONSERVATION; HOST PATHOGEN INTERACTION; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN STRUCTURE; SHORT SURVEY; TYPE VI SECRETION SYSTEM;

BACTERIA; BACTERIAL INFECTIONS; BACTERIAL PROTEINS; BACTERIAL SECRETION SYSTEMS; GENE EXPRESSION REGULATION, BACTERIAL; HOST-PATHOGEN INTERACTIONS; HUMANS;

BACTERIA (MICROORGANISMS); EUKARYOTA;

EID: 78649326935     PISSN: 0966842X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tim.2010.09.001     Document Type: Short Survey

References (78)

1. Bladergroen M.R., et al. Infection-blocking genes of a symbiotic Rhizobium leguminosarum strain that are involved in temperature-dependent protein secretion. Mol. Plant Microbe Interact. 2003, 16:53-64.
2. Rao P.S., et al. Use of proteomics to identify novel virulence determinants that are required for Edwardsiella tarda pathogenesis. Mol. Microbiol. 2004, 53:573-586.
3. Schwarz S., et al. Burkholderia type VI secretion systems have distinct roles in eukaryotic and bacterial cell interactions. PLoS Pathog. 2010, 6:e1001068.
4. Schell M.A., et al. Type VI secretion is a major virulence determinant in Burkholderia mallei. Mol. Microbiol. 2007, 64:1466-1485.
5. Shalom G., et al. In vivo expression technology identifies a type VI secretion system locus in Burkholderia pseudomallei that is induced upon invasion of macrophages. Microbiology 2007, 153:2689-2699.
6. Bernard C.S., et al. Nooks and crannies in type VI secretion regulation. J. Bacteriol. 2010, 192:3850-3860.
7. Bingle L.E., et al. Type VI secretion: a beginner's guide. Curr. Opin. Microbiol. 2008, 11:3-8.
8. Bonemann G., et al. Tubules and donuts: a type VI secretion story. Mol. Microbiol. 2010, 76:815-821.
9. Boyer F., et al. Dissecting the bacterial type VI secretion system by a genome wide in silico analysis: what can be learned from available microbial genomic resources?. BMC Genomics 2009, 10:104.
10. Ballister E.R., et al. In vitro self-assembly of tailorable nanotubes from a simple protein building block. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:3733-3738.
11. Mougous J.D., et al. A virulence locus of Pseudomonas aeruginosa encodes a protein secretion apparatus. Science 2006, 312:1526-1530.
12. Pell L.G., et al. The phage lambda major tail protein structure reveals a common evolution for long-tailed phages and the type VI bacterial secretion system. Proc. Natl. Acad. Sci. U. S. A. 2009, 106:4160-4165.
13. Kanamaru S. Structural similarity of tailed phages and pathogenic bacterial secretion systems. Proc. Natl. Acad. Sci. U. S. A. 2009, 106:4067-4068.
14. Leiman P.G., et al. Type VI secretion apparatus and phage tail-associated protein complexes share a common evolutionary origin. Proc. Natl. Acad. Sci. U. S. A. 2009, 106:4154-4159.
15. Bonemann G., et al. Remodelling of VipA/VipB tubules by ClpV-mediated threading is crucial for type VI protein secretion. EMBO. J. 2009, 28:315-325.
16. Cascales E. The type VI secretion toolkit. EMBO. Rep. 2008, 9:735-741.
17. Jani A.J., Cotter P.A. Type VI secretion: not just for pathogenesis anymore. Cell Host Microbe 2010, 8:2-6.
18. Pukatzki S., et al. The type VI secretion system: translocation of effectors and effector-domains. Curr. Opin. Microbiol. 2009, 12:11-17.
19. Pilatz S., et al. Identification of Burkholderia pseudomallei genes required for the intracellular life cycle and in vivo virulence. Infect. Immun. 2006, 74:3576-3586.
20. Folkesson A., et al. The Salmonella enterica subspecies I specific centisome 7 genomic island encodes novel protein families present in bacteria living in close contact with eukaryotic cells. Res. Microbiol. 2002, 153:537-545.
21. Ma A.T., Mekalanos J.J. In vivo actin cross-linking induced by Vibrio cholerae type VI secretion system is associated with intestinal inflammation. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:4365-4370.
22. Parsons D.A., Heffron F. sciS, an icmF homolog in Salmonella enterica serovar Typhimurium, limits intracellular replication and decreases virulence. Infect. Immun. 2005, 73:4338-4345.
23. Schlieker C., et al. ClpV, a unique Hsp100/Clp member of pathogenic proteobacteria. Biol. Chem. 2005, 386:1115-1127.
24. Suarez G., et al. Molecular characterization of a functional type VI secretion system from a clinical isolate of Aeromonas hydrophila. Microb. Pathog. 2007, 44:344-361.
25. Zheng J., Leung K.Y. Dissection of a type VI secretion system in Edwardsiella tarda. Mol. Microbiol. 2007, 66:1192-1206.
26. Ma A.T., et al. Translocation of a Vibrio cholerae type VI secretion effector requires bacterial endocytosis by host cells. Cell Host Microbe 2009, 5:234-243.
27. Pukatzki S., et al. Type VI secretion system translocates a phage tail spike-like protein into target cells where it cross-links actin. Proc. Natl. Acad. Sci. U. S. A. 2007, 104:15508-15513.
28. Pukatzki S., et al. Identification of a conserved bacterial protein secretion system in Vibrio cholerae using the Dictyostelium host model system. Proc. Natl. Acad. Sci. U. S. A. 2006, 103:1528-1533.
29. Suarez G., et al. A type VI secretion system effector protein VgrG1 from Aeromonas hydrophila that induces host cell toxicity by ADP-ribosylation of actin. J. Bacteriol. 2010, 192:155-168.
30. Wang X., et al. Edwardsiella tarda T6SS component evpP is regulated by esrB and iron, and plays essential roles in the invasion of fish. Fish Shellfish Immunol. 2009, 27:469-477.
31. Dudley E.G., et al. Proteomic and microarray characterization of the AggR regulon identifies a pheU pathogenicity island in enteroaggregative Escherichia coli. Mol. Microbiol. 2006, 61:1267-1282.
32. Robinson J.B., et al. Evaluation of a Yersinia pestis mutant impaired in a thermoregulated type VI-like secretion system in flea, macrophage and murine models. Microb. Pathog. 2009, 47:243-251.
33. Williams S.G., et al. Vibrio cholerae Hcp, a secreted protein coregulated with HlyA. Infect. Immun. 1996, 64:283-289.
34. Lloyd A.L., et al. Genomic islands of uropathogenic Escherichia coli contribute to virulence. J. Bacteriol. 2009, 191:3469-3481.
35. Records A.R., Gross D.C. Sensor kinases RetS and LadS regulate Pseudomonas syringae type VI secretion and virulence factors. J. Bacteriol. 2010, 192:3584-3596.
36. Mattinen L., et al. Microarray profiling of host-extract-induced genes and characterization of the type VI secretion cluster in the potato pathogen Pectobacterium atrosepticum. Microbiology 2008, 154:2387-2396.
37. Weber B., et al. Type VI secretion modulates quorum sensing and stress response in Vibrio anguillarum. Environ. Microbiol. 2009, 11:3018-3028.
38. Wu H.Y., et al. Secretome analysis uncovers an Hcp-family protein secreted via a type VI secretion system in Agrobacterium tumefaciens. J. Bacteriol. 2008, 190:2841-2850.
39. Mazurkiewicz P., et al. Signature-tagged mutagenesis: barcoding mutants for genome-wide screens. Nat. Revs. 2006, 7:929-939.
40. Carnell S.C., et al. Role in virulence and protective efficacy in pigs of Salmonella enterica serovar Typhimurium secreted components identified by signature-tagged mutagenesis. Microbiology 2007, 153:1940-1952.
41. Chiang S.L., Mekalanos J.J. Use of signature-tagged transposon mutagenesis to identify Vibrio cholerae genes critical for colonization. Mol. Microbiol. 1998, 27:797-805.
42. Darwin A.J., Miller V.L. Identification of Yersinia enterocolitica genes affecting survival in an animal host using signature-tagged transposon mutagenesis. Mol. Microbiol. 1999, 32:51-62.
43. Dziva F., et al. Identification of Escherichia coli O157: H7 genes influencing colonization of the bovine gastrointestinal tract using signature-tagged mutagenesis. Microbiology 2004, 150:3631-3645.
44. Karlyshev A.V., et al. Application of high-density array-based signature-tagged mutagenesis to discover novel Yersinia virulence-associated genes. Infect. Immun. 2001, 69:7810-7819.
45. Maroncle N., et al. Identification of Klebsiella pneumoniae genes involved in intestinal colonization and adhesion using signature-tagged mutagenesis. Infect. Immun. 2002, 70:4729-4734.
46. Shah D.H., et al. Identification of Salmonella gallinarum virulence genes in a chicken infection model using PCR-based signature-tagged mutagenesis. Microbiology 2005, 151:3957-3968.
47. Goodman A.L., et al. A signaling network reciprocally regulates genes associated with acute infection and chronic persistence in Pseudomonas aeruginosa. Dev. Cell 2004, 7:745-754.
48. Hsu F., et al. TagR promotes PpkA-catalysed type VI secretion activation in Pseudomonas aeruginosa. Mol. Microbiol. 2009, 72:1111-1125.
49. Pieper R., et al. Temperature and growth phase influence the outer-membrane proteome and the expression of a type VI secretion system in Yersinia pestis. Microbiology 2009, 155:498-512.
50. Potvin E., et al. In vivo functional genomics of Pseudomonas aeruginosa for high-throughput screening of new virulence factors and antibacterial targets. Environ. Microbiol. 2003, 5:1294-1308.
51. Hood R.D., et al. A type VI secretion system of Pseudomonas aeruginosa targets a toxin to bacteria. Cell Host Microbe 2010, 7:25-37.
52. Libby S.J., et al. Humanized nonobese diabetic-scid IL2r{gamma}null mice are susceptible to lethal Salmonella Typhi infection. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:15589-15594.
53. Arnoldo A., et al. Identification of small molecule inhibitors of Pseudomonas aeruginosa exoenzyme S using a yeast phenotypic screen. PLoS genetics 2008, 4:e1000005.
54. Gibbs K.A., et al. Genetic determinants of self identity and social recognition in bacteria. Science 2008, 321:256-259.
55. Parsek M.R., Greenberg E.P. Sociomicrobiology: the connections between quorum sensing and biofilms. Trends Microbiol. 2005, 13:27-33.
56. Aschtgen M.S., et al. SciN is an outer membrane lipoprotein required for Type VI secretion in enteroaggregative Escherichia coli. J. Bacteriol. 2008, 190:7523-7531.
57. Aschtgen M.S., et al. The SciZ protein anchors the enteroaggregative Escherichia coli Type VI secretion system to the cell wall. Mol. Microbiol. 2010, 75:886-899.
58. Enos-Berlage J.L., et al. Genetic determinants of biofilm development of opaque and translucent Vibrio parahaemolyticus. Mol. Microbiol. 2005, 55:1160-1182.
59. Vaysse P.J., et al. Proteomic analysis of Marinobacter hydrocarbonoclasticus SP17 biofilm formation at the alkane-water interface reveals novel proteins and cellular processes involved in hexadecane assimilation. Res. Microbiol. 2009, 160:829-837.
60. Sauer K., et al. Pseudomonas aeruginosa displays multiple phenotypes during development as a biofilm. J. Bacteriol. 2002, 184:1140-1154.
61. Southey-Pillig C.J., et al. Characterization of temporal protein production in Pseudomonas aeruginosa biofilms. J. Bacteriol. 2005, 187:8114-8126.
62. Mattinen L., et al. Host-extract induced changes in the secretome of the plant pathogenic bacterium Pectobacterium atrosepticum. Proteomics 2007, 7:3527-3537.
63. de Berardinis V., et al. A complete collection of single-gene deletion mutants of Acinetobacter baylyi ADP1. Mol. Syst. Biol. 2008, 4:174.
64. Chow J., Mazmanian S.K. A pathobiont of the microbiota balances host colonization and intestinal inflammation. Cell Host Microbe 2010, 7:265-276.
65. Kim H.S., et al. Bacterial genome adaptation to niches: divergence of the potential virulence genes in three Burkholderia species of different survival strategies. BMC Genomics 2005, 6:174.
66. Gross R., et al. Resemblance and divergence: the "new" members of the genus Bordetella. Med. Microbiol. Immunol. 2010, 199:155-163.
67. Mattoo S., Cherry J.D. Molecular pathogenesis, epidemiology, and clinical manifestations of respiratory infections due to Bordetella pertussis and other Bordetella subspecies. Clin. Microbiol. Rev. 2005, 18:326-382.
68. Parkhill J., et al. Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica. Nat. Genet. 2003, 35:32-40.
69. Riley M.A., Wertz J.E. Bacteriocins: evolution, ecology, and application. Ann. Rev. Microbiol. 2002, 56:117-137.
70. Gillor O., et al. The dual role of bacteriocins as anti- and probiotics. Appl. Microbiol. Biotechnol. 2008, 81:591-606.
71. Blondel C.J., et al. Comparative genomic analysis uncovers 3 novel loci encoding type six secretion systems differentially distributed in Salmonella serotypes. BMC Genomics 2009, 10:354.
72. Kurazono H., et al. Characterization of a putative virulence island in the chromosome of uropathogenic Escherichia coli possessing a gene encoding a uropathogenic-specific protein. Microb. Pathog. 2000, 28:183-189.
73. Parret A.H., De Mot R. Escherichia coli's uropathogenic-specific protein: a bacteriocin promoting infectivity?. Microbiology 2002, 148:1604-1606.
74. Suarez G., et al. A type VI secretion system effector protein VgrG1 from Aeromonas hydrophila that induces host cell toxicity by ADP-ribosylation of actin. J. Bacteriol. 2009, 192:155-168.
75. Shaevitz, J.W. and Gitai, Z. (2010) The structure and function of bacterial actin homologs. Cold Spring Harbor perspectives in biology, Volume 2, a000364, doi:10.1101/cshperspect.a000364.
76. Brogden K.A., et al. Human polymicrobial infections. Lancet 2005, 365:253-255.
77. Reid G., et al. Can. bacterial interference prevent infection?. Trends Microbiol. 2001, 9:424-428.
78. Kudryashov D.S., et al. Connecting actin monomers by iso-peptide bond is a toxicity mechanism of the Vibrio cholerae MARTX toxin. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:18537-18542.