A Toll receptor from Chinese shrimp Fenneropenaeus chinensis is responsive to Vibrio anguillarum infection

Fish and Shellfish Immunology

Volumn 24, Issue 5, 2008, Pages 564-574

  Yang, Changjian ^a,b   Zhang, Jiquan ^a   Li, Fuhua ^a   Ma, Hongming ^a   Zhang, Qingli ^a   Jose Priya, T A ^a,b   Zhang, Xiaojun ^a   Xiang, Jianhai ^a  

^a INSTITUTE OF OCEANOLOGY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Innate immunity; Real time PCR; Shrimp; Toll like receptor; Vibrio anguillarum; WSSV

Indexed keywords

BACTERIA (MICROORGANISMS); DECAPODA (CRUSTACEA); FENNEROPENAEUS CHINENSIS; HEXAPODA; INVERTEBRATA; LISTONELLA ANGUILLARUM; SHRIMP WHITE SPOT SYNDROME VIRUS;

EID: 41949106759     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2007.12.012     Document Type: Article

References (83)

1. Flegel T.W., and Alday-Sanz V. The crisis in Asian shrimp aquaculture: current status and future needs. J Appl Ichthyol 14 (1998) 269-273
2. Bachère E., Gueguen Y., Gonzalez M., de Lorgeril J., Garnier J., and Romestand B. Insights into the anti-microbial defense of marine invertebrates: the penaeid shrimps and the oyster Crassostrea gigas. Immunol Rev 198 (2004) 149-168
3. Iwanaga S., and Lee B.L. Recent advances in the innate immunity of invertebrate animals. J Biochem Mol Biol 38 (2005) 128-150
4. Loker E.S., Adema C.M., Zhang S.M., and Kepler T.B. Invertebrate immune systems - not homogeneous, not simple, not well understood. Immunol Rev 198 (2004) 10-24
5. Rinkevich B. Invertebrates versus vertebrates innate immunity: in the light of evolution. Scand J Immunol 50 (1999) 456-460
6. Medzhitov R., and Janeway Jr. C.A. Innate immunity. N Engl J Med 343 (2000) 338-344
7. Janeway Jr. C.A. Approaching the asymptote? Evolution and revolution in immunolgy. Cold Spring Harb Symp Quant Biol 54 (1989) 1-13
8. Meijer A.H., Krens S.F.G., Rodriguez I.A.M., He S.N., Bitter W., Snaar-Jagalska B.E., et al. Expression analysis of the Toll-like receptor and TIR domain adaptor families of zebrafish. Mol Immunol 40 (2004) 773-783
9. Hoffmann J.A., Kafatos F.C., Janeway Jr. C.A., and Ezekowitz R.A.B. Phylogenetic perspectives in innate immunity. Science 284 (1997) 1313-1318
10. Medzhitov R., and Janeway Jr. C.A. Decoding the patterns of self and nonself by the innate immune system. Science 296 (2002) 298-300
11. Medzhitov R., and Janeway Jr. C.A. Innate immunity: the virtues of a nonclonal system of regulation. Cell 91 (1997) 295-298
12. Medzhitov R., and Janeway Jr. C.A. Innate Immunity: the virtues of a nonclonal system of recognition. Curr Biol 13 (2003) 489-492
13. Akira S., Uematsu S., and Takeuchi O. Pathogen recognition and innate immunity. Cell 124 (2006) 783-801
14. Akira S., Takeda K., and Kaisho T. Toll-like receptors: critical proteins linking innate and acquired immunity. Nat Immunol 2 (2001) 675-680
15. Goldstein D.R. Toll-like receptors and other links between innate and acquired alloimmunity. Curr Opin Immunol 16 (2004) 538-544
16. Beutler B. Inferences, questions and possibilities in Toll-like receptor signalling. Nature 430 (2004) 257-263
17. O'Neill L.A. How Toll-like receptors signal: what we know and what we don't know. Curr Opin Immunol 18 (2006) 3-9
18. West A.P., Koblansky A.A., and Ghosh S. Recognition and signaling by Toll-like receptors. Annu Rev Cell Dev Biol 22 (2006) 409-437
19. Baoprasertkul P., Peatman E., Abernathy J., and Liu Z. Structural characterisation and expression analysis of Toll-like receptor 2 gene from catfish. Fish Shellfish Immunol 22 (2007) 418-426
20. Bilodeau A.L., Peterson B.C., and Bosworth B.G. Response of toll-like receptors, lysozyme, and IGF-I in back-cross hybrid (F1 male (blue × channel) × female channel) catfish challenged with virulent Edwardsiella ictaluri. Fish Shellfish Immunol 20 (2006) 29-39
21. Takano T., Kondo H., Hirono I., Endo M., Saito-Taki T., and Aoki T. Molecular cloning and characterization of Toll-like receptor 9 in Japanese flounder, Paralichthys olivaceus. Mol Immunol 44 (2007) 1845-1853
22. Anderson K.V., and Nüesslein-Volhard C. Information for the dorsal-ventral pattern of the Drosophila embryo is stored as maternal mRNA. Nature 311 (1984) 223-227
23. Nüesslein-Volhard C., Lohs-Schardin M., Sander K., and Cremer C. A dorso-ventral shift of embryonic primordia in a new maternal-effect mutant of Drosophila. Nature 283 (1980) 474-476
24. Lemaitre B., Nicolas E., Michaut L., Reichhart J.M., and Hoffmann J.A. The dorsoventral regulatory gene cassette spätzle/Toll/cactus controls the potent antifungal response in Drosophila adults. Cell 86 (2003) 973-983
25. Rutschmann S., Kilinc A., and Ferrandon D. Cutting edge: the Toll pathway is required for resistance to Gram-positive bacterial infections in Drosophila. J Immunol 168 (2002) 1542-1546
26. Zambon R.A., Nandakumar M., Vakharia V.N., and Wu L.P. The Toll pathway is important for an antiviral response in Drosophila. Proc Natl Acad Sci USA 102 (2005) 7257-7262
27. Belvin M.P., and Anderson K.V. A conserved signaling pathway: the Drosophila Toll-dorsal pathway. Annu Rev Cell Dev Biol 12 (1996) 393-416
28. Takeda K., Kaisho T., and Akira S. Toll-like receptors. Annu Rev Immunol 21 (2003) 335-376
29. Liew F.Y., Xu D., Brint E.K., and O'neil L.A. Negative regulation of Toll-like receptor-mediated immune responses. Nat Rev Immunol 5 (2005) 446-458
30. Gay N.J., Gangloff M., and Weber A.N. Toll-like receptors as molecular switches. Nature 6 (2006) 693-698
31. Weber A.N.R., Tauszig-Delamasure S., Hoffmann J.A., Lelièvre E., Gascan H., Ray K.P., et al. Binding of the Drosophila cytokine spaetzle to Toll is direct and establishes signaling. Nat Immunol 4 (2003) 794-800
32. Hu X., Yagi Y., Tanji T., Zhou S., and Ip Y.T. Multimerization and interaction of Toll and spaetzle in Drosophila. Proc Natl Acad Sci U S A 101 (2004) 9369-9374
33. Arts J.A., Cornelissen F.H.J., Cijsouw T., Hermsen T., Savelkoul H.F.J., and Stet R.J.M. Molecular cloning and expression of a Toll receptor in the giant tiger shrimp, Penaeus monodon. Fish Shellfish Immunol 23 (2006) 504-513
34. Yang L.S., Yin Z.X., Liao J.X., Huang X.D., Guo C.J., Weng S.P., et al. A Toll receptor in shrimp. Mol Immunol 44 (2007) 1999-2008
35. Kumar S., Tamura K., and Nei M. MEGA3: integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief Bioinform 5 (2004) 150-163
36. Zhao J., Song L., Li C., Ni D., Wu L., Zhu L., et al. Molecular cloning, expression of a big defensin gene from bay scallop Argopecten irradians and the antimicrobial activity of its recombinant protein. Mol Immunol 44 (2007) 360-368
37. Yamagata M., Merlie J.P., and Sanes J.R. Interspecific comparisons reveal conserved features of the Drosophila Toll protein. Gene 139 (1994) 223-228
38. Buchanan S.G., and Gay N.J. Structural and functional diversity in the leucine-rich repeat family of proteins. Prog Biophys Mol Biol 65 (1996) 1-44
39. Rothberg J.M., Jacobs J.R., Goodman C.S., and Artavanis-Tsakonas S. Slit: an extracellular protein necessary for development of midline. Gene Dev 4 (1990) 2169-2187
40. Tan E.C., and Lim L. Novel brain-specific bovine cDNA for a developmentally regulated mRNA encoding a putative new member of the leucine-rich glycoprotein (LRG) family. Neurochem Res 17 (1992) 907-916
41. Bell J.K., Mullen G.E., Leifer C.A., Mazzoni A., Davies D.R., and Segal D.M. Leucine-rich repeats and pathogen recognition in Toll-like receptors. Trends Immunol 24 (2003) 528-533
42. Lemaitre B. The road to Toll. Nat Rev Immunol 4 (2004) 521-527
43. Lemaitre B., and Hoffmann J. The host defense of Drosophila melanogaster. Annu Rev Immunol 25 (2007) 697-743
44. Tauszig S., Jouanguy E., Hoffmann J.A., and Imler J.L. Toll-related receptors and the control of antimicrobial peptide expression in Drosophila. Proc Natl Acad Sci U S A 97 (2000) 10520-10525
45. Rast J.P., Smith L.C., Loza-Coll M., Hibino T., and Litman G.W. Genomic insights into the immune system of the sea urchin. Science 314 (2006) 952-956
46. Goodson M.S., Kojadinovic M., Troll J.V., Scheetz T.E., Casavant T.L., Soares M.B., et al. Identifying components of the NF-κB pathway in the beneficial Euprymna scolopes-Vibrio fischeri light organ symbiosis. Appl Environ Microbiol 71 (2005) 6934-6946
47. Hoffmann J.A. The immune response of Drosophila. Nature 426 (2003) 33-38
48. Kajava A.V. Structural diversity of leucine-rich repeat proteins. J Mol Biol 277 (1998) 519-527
49. Choe J., Kelker M.S., and Wilson I.A. Crystal structure of human toll-like receptor (TLR3) ectodomain. Science 309 (2005) 581-585
50. Re F., and Strominger J.L. Monomeric recombinant MD-2 binds Toll-like receptor 4 tightly and confers lipopolysaccharide responsiveness. J Biol Chem 277 (2002) 23427-23432
51. Shimazu R., Akashi S., Ogata H., Nagai Y., Fukudome K., Miyake K., et al. MD-2, a molecule that confers lipopolysaccharide responsiveness on Toll-like receptor 4. J Exp Med 189 (1999) 1777-1782
52. Inamori K., Ariki S., and Kawabata S. A Toll-like receptor in horseshoe crabs. Immunol Rev 198 (2004) 106-115
53. Ohnishi T., Muroi M., and Tanamoto K. MD-2 is necessary for the Toll-like receptor 4 protein to undergo glycosylation essential for its translocation to the cell surface. Clin Vaccine Immunol 10 (2003) 405-410
54. Weber A.N.R., Morse M.A., and Gay N.J. Four N-linked glycosylation sites in human Toll-like receptor 2 cooperate to direct efficient biosynthesis and secretion. J Biol Chem 279 (2004) 34589-34594
55. Sun J., Duffy K.E., Ranjith-Kumar C.T., Xiong J., Lamb R.J., Santos J., et al. Structural and functional analyses of the human Toll-like receptor 3: role of glycosylation. J Biol Chem 281 (2006) 11144-11151
56. Andersen-Nissen E., Smith K.D., Bonneau R., Strong R.K., and Aderem A. A conserved surface on Toll-like receptor 5 recognizes bacterial flagellin. J Exp Med 204 (2007) 393-403
57. Xu Y., Tao X., Shen B., Horng T., Medzhitov R., Manley J.L., et al. Structural basis for signal transduction by the Toll/interleukin-1 receptor domains. Nature 408 (2000) 111-115
58. Jebanathirajah J.A., Peri S., and Pandey A. Toll and interleukin-1 receptor (TIR) domain-containing proteins in plants: a genomic perspective. Trends Plant Sci 7 (2002) 388-391
59. O'Neill L.A., and Bowie A.G. The family of five: TIR-domain-containing adaptors in Toll-like receptor signalling. Nat Rev Immunol 7 (2007) 353-364
60. Poltorak A., He X., Smirnova I., Liu M.Y., Van Huffel C., Du X., et al. Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. Science 282 (1998) 2085-2088
61. Fedorova L., and Fedorov A. Introns in gene evolution. Genetica 118 (2003) 123-131
62. Rogers J.H. The role of introns in evolution. FEBS lett 268 (1990) 339-343
63. Fedorov A., Merican A.F., and Gibert W. Large-scale comparison of intron positions among animal, plant, and fungal genes. Proc Natl Acad Sci U S A 99 (2002) 16128-16133
64. Rogozin I.B., Wolf Y.I., Sorokin A.V., Mirkin B.G., and Koonin E.V. Remarkable interkingdom conservation of intron positions and massive, lineage-specific intron loss and gain in eukaryotic evolution. Curr Biol 13 (2003) 1512-1517
65. Shapiro M.B., and Senapathy P. RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression. Nucleic Acids Res 15 (1987) 7155-7174
66. Roy S.W., and Gilbert W. Complex early genes. Proc Natl Acad Sci U S A 102 (2005) 1986-1991
67. Luo C., and Zheng L. Independent evolution of Toll and related genes in insects and mammals. Immunogenetics 51 (2000) 92-98
68. Luna C., Hoa N.T., Zhang J., Kanzok S.M., Brown S.E., Imler J.L., et al. Characterization of three Toll-like genes from mosquito Aedes aegypti. Insect Mol Biol 12 (2003) 67-74
69. Qiu L., Song L., Xu W., Ni D., and Yu Y. Molecular cloning and expression of a Toll receptor gene homologue from Zhikong Scallop, Chlamys farreri. Fish Shellfish Immunol 22 (2007) 451-466
70. Clavero-Salas A., Sotelo-Mundo R.R., Gollas-Galván T., Hernández-López J., Peregrino-Uriarte A.B., Muhlia-Almazán A., et al. Transcriptome analysis of gills from the white shrimp Litopenaeus vannamei infected with white spot syndrome virus. Fish Shellfish Immunol 23 (2007) 459-472
71. Hasson K.W., Lightner D.V., Mohney L.L., Redman R.M., and White B.M. Role of lymphoid organ spheroids in chronic Taura syndrome virus (TSV) infections in Penaeus vannamei. Dis Aquat Organ 38 (1999) 93-105
72. Martin G.G., Quintero M., Quigley M., and Khosrovian H. Elimination of sequestered material from the gills of decapod crustaceans. J Crust Biol 20 (2000) 209-217
73. van de Braak C.B.T., Botterblom M.H.A., Taverne N., van Muiswinkel W.B., Rombout J., and van der Knaap W.P.W. The roles of haemocytes and the lymphoid organ in the clearance of injected Vibrio bacteria in Penaeus monodon shrimp. Fish Shellfish Immunol 13 (2002) 293-309
74. Anggraeni M.S., and Owens L. The haemocytic origin of lymphoid organ spheroid cells in the penaeid prawn Penaeus monodon. Dis Aquat Organ 40 (2000) 85-92
75. Gerold G., Zychlinsky A., and Juana L. What is the role of Toll-like receptors in bacterial infections?. Semin Immunol 19 (2007) 41-47
76. Bachère E. Shrimp immunity and disease control. Aquaculture 191 (2000) 3-11
77. Liu Y.C., Li F.H., Dong B., Wang B., Luan W., Zhang X.J., et al. Molecular cloning, characterization and expression analysis of a putative C-type lectin (Fclectin) gene in Chinese shrimp Fenneropenaeus chinensis. Mol Immunol 44 (2007) 598-607
78. Williams M.J., Rodriguez A., Kimbrell D.A., and Eldon E.D. The 18-wheeler mutation reveals complex antibacterial gene regulation in Drosophila host defense. EMBO 16 (1997) 6120-6130
79. Ooi J.Y. The Drosophila Toll-9 activates a constitutive antimicrobial defense. EMBO 3 (2002) 82-87
80. Ao J.-q., Ling E., and Yu X.-Q. A Toll receptor from Manduca sexta is in response to Escherichia coli infection. Mol Immunol 45 (2008) 543-552
81. Lightner D.V. Epizootiology, distribution and the impact on international trade of two penaeid shrimp viruses in the Americas. Rev Sci Tech OIE 15 (1996) 579-601
82. Ma T.H., Tiu S.H., He J.G., and Chan S.M. Molecular cloning of a C-type lectin (LvLT) from the shrimp Litopenaeus vannamei: early gene down-regulation after WSSV infection. Fish Shellfish Immunol 23 (2007) 430-437
83. Bettencourt R., Tanji T., Yagi Y., and Ip Y.T. Toll and Toll-9 in Drosophila innate immune response. J Endotoxin Res 10 (2004) 261-268