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  • Review Article
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Toll-like receptors — taking an evolutionary approach

Key Points

  • Toll-like receptors (TLRs) are type-I transmembrane proteins with extracellular leucine-rich repeat (LRR) motifs and an intracellular Toll/interleukin-1R (TIR) domain.

  • TLR genes are restricted to eumetazoans and probably originated at the dawn of animal evolution more than 700 million years ago.

  • With rare exceptions, both TLR and nuclear factor-kappaB (NF-κB) genes are found in sequenced animal genomes, pointing to the ancient origin of the TLR–NF-κB signalling module.

  • Early diversification of TLR structures resulted in two forms of the protein: multiple cysteine cluster TLRs found mostly in protostomes and single cysteine cluster TLRs found mostly in deuterostomes.

  • Three distinct functions of TLRs have been identified: TLRs are essential during host immune responses through NF-κB signalling in insects and vertebrates; they contribute to normal patterning and organogenesis during development through NF-κB signalling in insects; and they contribute to cell adhesion during embryonic development, apparently independently of NF-κB activation in both insects and nematodes.

  • The lack of functional information on TLRs in several lineages such as lophotrocozoans and cnidarians precludes the drawing of a robust evolutionary scenario for the emergence of TLR-mediated immunity or the ancestral function of TLRs. However, two hypotheses can explain the observed similarities and differences in TLR-mediated immunity in vertebrates and insects: an ancient origin of TLR-mediated immunity in the bilaterian ancestor followed by a substantial diversification along the lineages; or a convergent evolution based on the independent recruitment of TLRs to mediate immunity in deuterostomes and insects.

  • The recurrent use of similar protein modules (the TIR domain and LRR motifs) and signalling pathways (NF-κB) in the immune response is observed in phylogenetically distant lineages.

  • Future challenges include analysing TLR function in invertebrate deuterostomes, lophochotrozoan and cnidarian model organisms, and further dissection of the NF-κB-independent role of TLRs during development.

Abstract

The Toll receptor was initially identified in Drosophila melanogaster for its role in embryonic development. Subsequently, D. melanogaster Toll and mammalian Toll-like receptors (TLRs) have been recognized as key regulators of immune responses. After ten years of intense research on TLRs and the recent accumulation of genomic and functional data in diverse organisms, we review the distribution and functions of TLRs in the animal kingdom. We provide an evolutionary perspective on TLRs, which sheds light on their origin at the dawn of animal evolution and suggests that different TLRs might have been co-opted independently during animal evolution to mediate analogous immune functions.

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Figure 1: Toll-like receptors and downstream signalling pathways.
Figure 2: Origins, distribution and functions of Toll-like receptors in the animal kingdom.
Figure 3: Toll-like receptor functions in development.
Figure 4: Toll-like receptor functions in immunity.

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References

  1. Anderson, K. V., Jurgens, G. & Nusslein-Volhard, C. Establishment of dorsal–ventral polarity in the Drosophila embryo: genetic studies on the role of the Toll gene product. Cell 42, 779–789 (1985). This paper describes the initial characterization of Drosophila Toll alleles.

    Article  CAS  PubMed  Google Scholar 

  2. Gerttula, S., Jin, Y. S. & Anderson, K. V. Zygotic expression and activity of the Drosophila Toll gene, a gene required maternally for embryonic dorsal–ventral pattern formation. Genetics 119, 123–133 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Eldon, E. et al. The Drosophila 18 wheeler is required for morphogenesis and has striking similarities to Toll. Development 120, 885–899 (1994).

    CAS  PubMed  Google Scholar 

  4. Akira, S., Uematsu, S. & Takeuchi, O. Pathogen recognition and innate immunity. Cell 124, 783–801 (2006).

    Article  CAS  PubMed  Google Scholar 

  5. Pasare, C. & Medzhitov, R. Toll-like receptors: linking innate and adaptive immunity. Adv. Exp. Med. Biol. 560, 11–18 (2005).

    Article  CAS  PubMed  Google Scholar 

  6. Lemaitre, B., Nicolas, E., Michaut, L., Reichhart, J. & Hoffmann, J. The dorsoventral regulatory gene cassette spätzle/Toll/cactus controls the potent antifungal response in Drosophila adults. Cell 86, 973–983 (1996). This paper describes the first implication of a TLR in host defence.

    Article  CAS  PubMed  Google Scholar 

  7. Buchanan, S. G. & Gay, N. J. Structural and functional diversity in the leucine-rich repeat family of proteins. Prog. Biophys. Mol. Biol. 65, 1–44 (1996).

    Article  CAS  PubMed  Google Scholar 

  8. Kobe, B. & Kajava, A. V. The leucine-rich repeat as a protein recognition motif. Curr. Opin. Struct. Biol. 11, 725–732 (2001).

    Article  CAS  PubMed  Google Scholar 

  9. Bell, J. K. et al. The molecular structure of the Toll-like receptor 3 ligand-binding domain. Proc. Natl Acad. Sci. USA 102, 10976–10980 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Choe, J., Kelker, M. S. & Wilson, I. A. Crystal structure of human Toll-like receptor 3 (TLR3) ectodomain. Science 309, 581–585 (2005).

    Article  CAS  PubMed  Google Scholar 

  11. Weber, A. N. et al. Binding of the Drosophila cytokine Spätzle to Toll is direct and establishes signaling. Nature Immunol. 4, 794–800 (2003).

    Article  CAS  Google Scholar 

  12. Mizel, S. B., West, A. P. & Hantgan, R. R. Identification of a sequence in human Toll-like receptor 5 required for the binding of Gram-negative flagellin. J. Biol. Chem. 278, 23624–23629 (2003).

    Article  CAS  PubMed  Google Scholar 

  13. Andersen-Nissen, E., Smith, K. D., Bonneau, R., Strong, R. K. & Aderem, A. A conserved surface on Toll-like receptor 5 recognizes bacterial flagellin. J. Exp. Med. 204, 393–403 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Jin, M. S. et al. Crystal structure of the TLR1–TLR2 heterodimer induced by binding of a tri-acylated lipopeptide. Cell 130, 1071–1082 (2007).

    Article  CAS  PubMed  Google Scholar 

  15. Cornelie, S. et al. Direct evidence that Toll-like receptor 9 (TLR9) functionally binds plasmid DNA by specific cytosine–phosphate–guanine motif recognition. J. Biol. Chem. 279, 15124–15129 (2004).

    Article  CAS  PubMed  Google Scholar 

  16. Rutz, M. et al. Toll-like receptor 9 binds single-stranded CpG–DNA in a sequence- and pH-dependent manner. Eur. J. Immunol. 34, 2541–2550 (2004).

    Article  CAS  PubMed  Google Scholar 

  17. Kufer, T. A., Fritz, J. H. & Philpott, D. J. NACHT-LRR proteins (NLRs) in bacterial infection and immunity. Trends Microbiol. 13, 381–388 (2005).

    Article  CAS  PubMed  Google Scholar 

  18. Martinon, F. & Tschopp, J. NLRs join TLRs as innate sensors of pathogens. Trends Immunol. 26, 447–454 (2005).

    Article  CAS  PubMed  Google Scholar 

  19. DeYoung, B. J. & Innes, R. W. Plant NBS-LRR proteins in pathogen sensing and host defense. Nature Immunol. 7, 1243–1249 (2006).

    Article  CAS  Google Scholar 

  20. Werts, C., Girardin, S. E. & Philpott, D. J. TIR, CARD and PYRIN: three domains for an antimicrobial triad. Cell Death Differ. 13, 798–815 (2006).

    Article  CAS  PubMed  Google Scholar 

  21. Bowie, A. et al. A46R and A52R from vaccinia virus are antagonists of host IL-1 and Toll-like receptor signaling. Proc. Natl Acad. Sci. USA 97, 10162–10167 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Belvin, M. P. & Anderson, K. V. A conserved signaling pathway: the Drosophila Toll–Dorsal pathway. Annu. Rev. Cell Dev. Biol. 12, 393–416 (1996).

    Article  CAS  PubMed  Google Scholar 

  23. Medzhitov, R., Preston-Hurlburt, P. & Janeway, C. A human homologue of the Drosophila Toll protein signals activation of adaptive immunity. Nature 388, 394–397 (1997). This paper shows the first link between TLR- and NF-κB-mediated immune responses in vertebrates.

    Article  CAS  PubMed  Google Scholar 

  24. Xu, Y. et al. Structural basis for signal transduction by the Toll/interleukin-1 receptor domains. Nature 408, 111–115 (2000).

    Article  CAS  PubMed  Google Scholar 

  25. Boraschi, D. & Tagliabue, A. The interleukin-1 receptor family. Vitam. Horm. 74, 229–254 (2006).

    Article  CAS  PubMed  Google Scholar 

  26. Miller, D. J. et al. The innate immune repertoire in cnidaria — ancestral complexity and stochastic gene loss. Genome Biol. 8, R59 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Ausubel, F. M. Are innate immune signaling pathways in plants and animals conserved? Nature Immunol. 6, 973–979 (2005).

    Article  CAS  Google Scholar 

  28. Philippe, H., Lartillot, N. & Brinkmann, H. Multigene analyses of bilaterian animals corroborate the monophyly of Ecdysozoa, Lophotrochozoa, and Protostomia. Mol. Biol. Evol. 22, 1246–1253 (2005).

    Article  CAS  PubMed  Google Scholar 

  29. Putnam, N. H. et al. Sea anemone genome reveals ancestral eumetazoan gene repertoire and genomic organization. Science 317, 86–94 (2007).

    Article  CAS  PubMed  Google Scholar 

  30. Sullivan, J. C., Kalaitzidis, D., Gilmore, T. D. & Finnerty, J. R. Rel homology domain-containing transcription factors in the cnidarian Nematostella vectensis. Dev. Genes Evol. 217, 63–72 (2007). This paper describes the initial identification of TLR and NF-κB genes in a cnidarian.

    Article  CAS  PubMed  Google Scholar 

  31. Zheng, L., Zhang, L., Lin, H., McIntosh, M. T. & Malacrida, A. R. Toll-like receptors in invertebrate innate immunity. Invertebrate Survival Journal 2, 105–113 (2005).

    Google Scholar 

  32. Wiens, M. et al. Innate immune defense of the sponge Suberites domuncula against bacteria involves a MyD88-dependent signaling pathway. Induction of a perforin-like molecule. J. Biol. Chem. 280, 27949–27959 (2005).

    Article  CAS  Google Scholar 

  33. Wiens, M. et al. Toll-like receptors are part of the innate immune defense system of sponges (demospongiae: Porifera). Mol. Biol. Evol. 24, 792–804 (2007).

    Article  CAS  PubMed  Google Scholar 

  34. Beutler, B. Innate immunity: an overview. Mol. Immunol. 40, 845–859 (2004).

    Article  CAS  PubMed  Google Scholar 

  35. Imler, J. L. & Zheng, L. Biology of Toll receptors: lessons from insects and mammals. J. Leukoc. Biol. 75, 18–26 (2004).

    Article  CAS  PubMed  Google Scholar 

  36. Luo, C. & Zheng, L. Independent evolution of Toll and related genes in insects and mammals. Immunogenetics 51, 92–98 (2000).

    Article  CAS  PubMed  Google Scholar 

  37. Friedman, R. & Hughes, A. L. Molecular evolution of the NF-κB signaling system. Immunogenetics 53, 964–974 (2002).

    Article  CAS  PubMed  Google Scholar 

  38. Kanzok, S. M. et al. Origin of Toll-like receptor-mediated innate immunity. J. Mol. Evol. 58, 442–448 (2004).

    Article  CAS  PubMed  Google Scholar 

  39. Roach, J. C. et al. The evolution of vertebrate Toll-like receptors. Proc. Natl Acad. Sci. USA 102, 9577–9582 (2005). References 35 to 39 provide phylogenetic data supporting the independent evolution of TLRs in different phyla.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Anderson, K. V. & Nüsslein-Volhard, C. in Pattern Formation: A Primer in Developmental Biology (eds Malacinsky, G. M. & Bryant, S.) 269–289 (MacMillian Publishers Ltd, New York, 1984).

    Google Scholar 

  41. Moussian, B. & Roth, S. Dorsoventral axis formation in the Drosophila embryo — shaping and transducing a morphogen gradient. Curr. Biol. 15, R887–R899 (2005).

    Article  CAS  PubMed  Google Scholar 

  42. Roth, S. The origin of dorsoventral polarity in Drosophila. Phil. Trans. R. Soc. Lond. 358, 1317–1329 (2003).

    Article  CAS  Google Scholar 

  43. Letsou, A., Alexander, S., Orth, K. & Wasserman, S. A. Genetic and molecular characterization of tube, a Drosophila gene maternally required for embryonic dorso-ventral polarity. Proc. Natl Acad. Sci. USA 88, 810–814 (1991).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Halfon, M. S., Hashimoto, C. & Keshishian, H. The Drosophila Toll gene functions zygotically and is necessary for proper motoneuron and muscle development. Dev. Biol. 169, 151–167 (1995).

    Article  CAS  PubMed  Google Scholar 

  45. Halfon, M. S. & Keshishian, H. The Toll pathway is required in the epidermis for muscle development in the Drosophila embryo. Dev. Biol. 199, 164–174 (1998).

    Article  CAS  PubMed  Google Scholar 

  46. Rose, D. et al. Toll, a muscle cell surface molecule, locally inhibits synaptic initiation of the RP3 motoneuron growth cone in Drosophila. Development 124, 1561–1571 (1997).

    CAS  PubMed  Google Scholar 

  47. Wang, J. et al. Expression, regulation, and requirement of the Toll transmembrane protein during dorsal vessel formation in Drosophila melanogaster. Mol. Cell Biol. 25, 4200–4210 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Keith, J. & Gay, N. The Drosophila membrane receptor Toll can function to promote cellular adhesion. EMBO J. 9, 4299–4306 (1990).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Tauszig-Delamasure, S., Bilak, H., Capovilla, M., Hoffmann, J. A. & Imler, J. L. Drosophila MyD88 is required for the response to fungal and Gram-positive bacterial infections. Nature Immunol. 3, 91–97 (2002).

    Article  CAS  Google Scholar 

  50. Rutschmann, S., Kilinc, A. & Ferrandon, D. Cutting edge: the Toll pathway is required for resistance to Gram-positive bacterial infections in Drosophila. J. Immunol. 168, 1542–1546 (2002).

    Article  CAS  PubMed  Google Scholar 

  51. De Gregorio, E., Spellman, P. T., Tzou, P., Rubin, G. M. & Lemaitre, B. The Toll and Imd pathways are the major regulators of the immune response in Drosophila. EMBO J. 21, 2568–2579 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Lemaitre, B. & Hoffmann, J. The host defense of Drosophila melanogaster. Annu. Rev. Immunol. 25, 697–743 (2007).

    Article  CAS  PubMed  Google Scholar 

  53. Ferrandon, D., Imler, J. L. & Hoffmann, J. A. Sensing infection in Drosophila: Toll and beyond. Semin. Immunol. 16, 43–53 (2004).

    Article  CAS  PubMed  Google Scholar 

  54. Qiu, P., Pan, P. C. & Govind, S. A role for the Drosophila Toll/Cactus pathway in larval hematopoiesis. Development 125, 1909–1920 (1998).

    CAS  PubMed  Google Scholar 

  55. Sorrentino, R. P., Carton, Y. & Govind, S. Cellular immune response to parasite infection in the Drosophila lymph gland is developmentally regulated. Dev. Biol. 243, 65–80 (2002).

    Article  CAS  PubMed  Google Scholar 

  56. Kambris, Z., Hoffmann, J. A., Imler, J. L. & Capovilla, M. Tissue and stage-specific expression of the Tolls in Drosophila embryos. Gene Expr. Patterns 2, 311–317 (2002).

    Article  CAS  PubMed  Google Scholar 

  57. Kolesnikov, T. & Beckendorf, S. K. 18 wheeler regulates apical constriction of salivary gland cells via the Rho–GTPase-signaling pathway. Dev. Biol. 307, 53–61 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Kleve, C. D., Siler, D. A., Syed, S. K. & Eldon, E. D. Expression of 18 wheeler in the follicle cell epithelium affects cell migration and egg morphology in Drosophila. Dev. Dyn. 235, 1953–1961 (2006).

    Article  CAS  PubMed  Google Scholar 

  59. Seppo, A., Matani, P., Sharrow, M. & Tiemeyer, M. Induction of neuron-specific glycosylation by Tollo/Toll8, a Drosophila Toll-like receptor expressed in non-neural cells. Development 130, 1439–1448 (2003).

    Article  CAS  PubMed  Google Scholar 

  60. Aoki, K. et al. Dynamic developmental elaboration of N-linked glycan complexity in the Drosophila melanogaster embryo. J. Biol. Chem. 282, 9127–9142 (2007).

    Article  CAS  PubMed  Google Scholar 

  61. Tauszig, S., Jouanguy, E., Hoffmann, J. A. & Imler, J. L. Toll-related receptors and the control of antimicrobial peptide expression in Drosophila. Proc. Natl Acad. Sci. USA 97, 10520–10525 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. Lazzaro, B. P., Sackton, T. B. & Clark, A. G. Genetic variation in Drosophila melanogaster resistance to infection: a comparison across bacteria. Genetics 174, 1539–1554 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Luo, C., Shen, B., Manley, J. L. & Zheng, L. Tehao functions in the Toll pathway in Drosophila melanogaster: possible roles in development and innate immunity. Insect Mol. Biol. 10, 457–464 (2001).

    Article  CAS  PubMed  Google Scholar 

  64. Ooi, J. Y., Yagi, Y., Hu, X. & Ip, Y. T. The Drosophila Toll9 activates a constitutive antimicrobial defense. EMBO Rep. 3, 82–87 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Rubin, G. M. et al. Comparative genomics of the eukaryotes. Science 287, 2204–2215 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Christophides, G. K. et al. Immunity-related genes and gene families in Anopheles gambiae. Science 298, 159–165 (2002).

    Article  CAS  PubMed  Google Scholar 

  67. Evans, J. D. et al. Immune pathways and defence mechanisms in honey bees Apis mellifera. Insect Mol. Biol. 15, 645–656 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Cheng, T. C. et al. Identification and analysis of Toll-related genes in the domesticated silkworm, Bombyx mori. Dev. Comp. Immunol. (2007).

  69. Waterhouse, R. M. et al. Evolutionary dynamics of immune-related genes and pathways in disease-vector mosquitoes. Science 316, 1738–1743 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  70. Zou, Z. et al. Comparative genomic analysis of the Tribolium immune system. Genome Biol. 8, R177 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  71. Chintapalli, V. R., Wang, J. & Dow, J. A. Using FlyAtlas to identify better Drosophila melanogaster models of human disease. Nature Genet. 39, 715–720 (2007).

    Article  CAS  PubMed  Google Scholar 

  72. Shin, S. W., Bian, G. & Raikhel, A. S. A Toll receptor and a cytokine, Toll5A and Spz1C, are involved in Toll antifungal immune signaling in the mosquito Aedes aegypti. J. Biol. Chem. 281, 39388–39395 (2006). This paper shows a similar role for TLRs in the antifungal immune response in Diptera.

    Article  CAS  PubMed  Google Scholar 

  73. Pujol, N. et al. A reverse genetic analysis of components of the Toll signaling pathway in Caenorhabditis elegans. Curr. Biol. 11, 809–821 (2001). This paper presents a functional analysis of the unique C. elegans TLR.

    Article  CAS  PubMed  Google Scholar 

  74. Tenor, J. L. & Aballay, A. A conserved Toll-like receptor is required for Caenorhabditis elegans innate immunity. EMBO Rep. 9, 103–109 (2008).

    Article  CAS  PubMed  Google Scholar 

  75. Chuang, C. F. & Bargmann, C. I. A Toll-interleukin 1 repeat protein at the synapse specifies asymmetric odorant receptor expression via ASK1 MAPKKK signaling. Genes Dev. 19, 270–281 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  76. Couillault, C. et al. TLR-independent control of innate immunity in Caenorhabditis elegans by the TIR domain adaptor protein TIR-1, an ortholog of human SARM. Nature Immunol. 5, 488–494 (2004).

    Article  CAS  Google Scholar 

  77. Liberati, N. T. et al. Requirement for a conserved Toll/interleukin-1 resistance domain protein in the Caenorhabditis elegans immune response. Proc. Natl Acad. Sci. USA 101, 6593–6598 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  78. Beutler, B. et al. Genetic analysis of host resistance: Toll-like receptor signaling and immunity at large. Annu. Rev. Immunol. 24, 353–389 (2006).

    Article  CAS  PubMed  Google Scholar 

  79. O'Neill, L. A. & Bowie, A. G. The family of five: TIR-domain-containing adaptors in Toll-like receptor signalling. Nature Rev. Immunol. 7, 353–364 (2007).

    Article  CAS  Google Scholar 

  80. Kawai, T. & Akira, S. TLR signaling. Semin. Immunol. 19, 24–32 (2007).

    Article  CAS  PubMed  Google Scholar 

  81. Takeda, K. & Akira, S. Toll-like receptors in innate immunity. Int. Immunol. 17, 1–14 (2005).

    Article  CAS  PubMed  Google Scholar 

  82. Pasare, C. & Medzhitov, R. Toll-like receptors: linking innate and adaptive immunity. Microbes Infect. 6, 1382–1387 (2004).

    Article  CAS  PubMed  Google Scholar 

  83. Iwasaki, A. & Medzhitov, R. Toll-like receptor control of the adaptive immune responses. Nature Immunol. 5, 987–995 (2004).

    Article  CAS  Google Scholar 

  84. Sutmuller, R. P., Morgan, M. E., Netea, M. G., Grauer, O. & Adema, G. J. Toll-like receptors on regulatory T cells: expanding immune regulation. Trends Immunol. 27, 387–393 (2006).

    Article  CAS  PubMed  Google Scholar 

  85. Ma, Y. et al. Toll-like receptor 8 functions as a negative regulator of neurite outgrowth and inducer of neuronal apoptosis. J. Cell Biol. 175, 209–215 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  86. Cameron, J. S. et al. Toll-like receptor 3 is a potent negative regulator of axonal growth in mammals. J. Neurosci. 27, 13033–13041 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  87. Rolls, A. et al. Toll-like receptors modulate adult hippocampal neurogenesis. Nature Cell Biol. 9, 1081–1088 (2007). References 85 to 87 report the involvement of mouse TLRs in neurogenesis.

    Article  CAS  PubMed  Google Scholar 

  88. Cook, D. N., Pisetsky, D. S. & Schwartz, D. A. Toll-like receptors in the pathogenesis of human disease. Nature Immunol. 5, 975–979 (2004).

    Article  CAS  Google Scholar 

  89. Bochud, P. Y., Bochud, M., Telenti, A. & Calandra, T. Innate immunogenetics: a tool for exploring new frontiers of host defence. Lancet Infect. Dis. 7, 531–542 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  90. Picard, C. et al. Pyogenic bacterial infections in humans with IRAK4 deficiency. Science 299, 2076–2079 (2003).

    Article  CAS  PubMed  Google Scholar 

  91. Casrouge, A. et al. Herpes simplex virus encephalitis in human UNC-93B deficiency. Science 314, 308–312 (2006).

    Article  CAS  PubMed  Google Scholar 

  92. Zhang, S.-Y. et al. TLR3 Deficiency in patients with herpes simplex encephalitis. Science 317, 1522 (2007).

    Article  CAS  PubMed  Google Scholar 

  93. Ku, C. L. et al. Inherited disorders of human Toll-like receptor signaling: immunological implications. Immunol. Rev. 203, 10–20 (2005).

    Article  CAS  PubMed  Google Scholar 

  94. Berczi, I., Bertok, L. & Bereznai, T. Comparative studies on the toxicity of Escherichia coli lipopolysaccharide endotoxin in various animal species. Can. J. Microbiol. 12, 1070–1071 (1966).

    Article  CAS  PubMed  Google Scholar 

  95. Iliev, D. B., Roach, J. C., Mackenzie, S., Planas, J. V. & Goetz, F. W. Endotoxin recognition: in fish or not in fish? FEBS Lett. 579, 6519–6528 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  96. Ishii, A. et al. Lamprey TLRs with properties distinct from those of the variable lymphocyte receptors. J. Immunol. 178, 397–406 (2007).

    Article  CAS  PubMed  Google Scholar 

  97. van der Sar, A. M. et al. MyD88 innate immune function in a zebrafish embryo infection model. Infect. Immun. 74, 2436–2441 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  98. Rast, J. P., Smith, L. C., Loza-Coll., M., Hibino, T. & Litman, G. W. Genomic insights into the immune system of the sea urchin. Science 314, 952–956 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  99. Hibino, T. et al. The immune gene repertoire encoded in the purple sea urchin genome. Dev. Biol. 300, 349–365 (2006). References 98 and 99 describe and discuss the striking amplification of TLR genes in the sea urchin genome.

    Article  CAS  PubMed  Google Scholar 

  100. Pancer, Z. & Cooper, M. D. The evolution of adaptive immunity. Annu. Rev. Immunol. 24, 497–518 (2006).

    Article  CAS  PubMed  Google Scholar 

  101. Bourlat, S. J. et al. Deuterostome phylogeny reveals monophyletic chordates and the new phylum Xenoturbellida. Nature 444, 85–88 (2006).

    Article  CAS  PubMed  Google Scholar 

  102. Azumi, K. et al. Genomic analysis of immunity in a urochordate and the emergence of the vertebrate immune system: 'waiting for Godot'. Immunogenetics 55, 570–581 (2003).

    Article  CAS  PubMed  Google Scholar 

  103. Khalturin, K., Panzer, Z., Cooper, M. D. & Bosch, T. C. Recognition strategies in the innate immune system of ancestral chordates. Mol. Immunol. 41, 1077–1087 (2004).

    Article  CAS  PubMed  Google Scholar 

  104. Hughes, A. L. Protein phylogenies provide evidence of a radical discontinuity between arthropod and vertebrate immune systems. Immunogenetics 47, 283–296 (1998).

    Article  CAS  PubMed  Google Scholar 

  105. Boman, H. G. & Hultmark, D. Cell-free immunity in insects. Annu. Rev. Microbiol. 41, 103–126 (1987).

    Article  CAS  PubMed  Google Scholar 

  106. Hultmark, D. Insect lysozymes. EXS 75, 87–102 (1996).

    CAS  PubMed  Google Scholar 

  107. Poltorak, A. et al. Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. Science 282, 2085–2088 (1998).

    Article  CAS  PubMed  Google Scholar 

  108. Hoshino, K. et al. Toll-like receptor 4 (TLR4)-deficient mice are hyporesponsive to lipopolysaccharide: evidence for TLR4 as the Lps gene product. J. Immunol. 162, 3749–3752 (1999).

    CAS  PubMed  Google Scholar 

  109. Qureshi, S. T. et al. Endotoxin-tolerant mice have mutations in Toll-like receptor 4 (TLR4). J. Exp. Med. 189, 615–625 (1999). References 107 to 109 are the first reports of the essential role of TLRs in vertebrate immunity.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  110. Takeuchi, O. et al. Cutting edge: preferentially the R-stereoisomer of the mycoplasmal lipopeptide macrophage-activating lipopeptide-2 activates immune cells through a Toll-like receptor 2- and MyD88-dependent signaling pathway. J. Immunol. 164, 554–557 (2000).

    Article  CAS  Google Scholar 

  111. Takeuchi, O. et al. Discrimination of bacterial lipoproteins by Toll-like receptor 6. Int. Immunol. 13, 933–940 (2001).

    Article  CAS  PubMed  Google Scholar 

  112. Takeuchi, O. et al. Cutting edge: role of Toll-like receptor 1 in mediating immune response to microbial lipoproteins. J. Immunol. 169, 10–14 (2002).

    Article  CAS  PubMed  Google Scholar 

  113. Hayashi, F. et al. The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5. Nature 410, 1099–1103. (2001).

    Article  CAS  PubMed  Google Scholar 

  114. Zhang, D. et al. A Toll-like receptor that prevents infection by uropathogenic bacteria. Science 303, 1522–1526 (2004).

    Article  CAS  PubMed  Google Scholar 

  115. Yarovinsky, F. et al. TLR11 activation of dendritic cells by a protozoan profilin-like protein. Science 308, 1626–1629 (2005).

    Article  CAS  PubMed  Google Scholar 

  116. Alexopoulou, L., Holt, A. C., Medzhitov, R. & Flavell, R. A. Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3. Nature 413, 732–738. (2001).

    Article  CAS  PubMed  Google Scholar 

  117. Hemmi, H. et al. Small anti-viral compounds activate immune cells via the TLR7 MyD88-dependent signaling pathway. Nature Immunol. 3, 196–200 (2002).

    Article  CAS  Google Scholar 

  118. Heil, F. et al. The Toll-like receptor 7 (TLR7)-specific stimulus loxoribine uncovers a strong relationship within the TLR7, 8 and 9 subfamily. Eur. J. Immunol. 33, 2987–2997 (2003).

    Article  CAS  PubMed  Google Scholar 

  119. Hornung, V. et al. Sequence-specific potent induction of IFN-α by short interfering RNA in plasmacytoid dendritic cells through TLR7. Nature Med. 11, 263–270 (2005).

    Article  CAS  PubMed  Google Scholar 

  120. Jurk, M. et al. Human TLR7 or TLR8 independently confer responsiveness to the antiviral compound R-848. Nature Immunol. 3, 499 (2002).

    Article  CAS  Google Scholar 

  121. Heil, F. et al. Species-specific recognition of single-stranded RNA via Toll-like receptor 7 and 8. Science 303, 1526–1529 (2004).

    Article  CAS  PubMed  Google Scholar 

  122. Hemmi, H. et al. A Toll-like receptor recognizes bacterial DNA. Nature 408, 740–745 (2000).

    Article  CAS  PubMed  Google Scholar 

  123. Lund, J., Sato, A., Akira, S., Medzhitov, R. & Iwasaki, A. Toll-like receptor 9-mediated recognition of herpes simplex virus-2 by plasmacytoid dendritic cells. J. Exp. Med. 198, 513–520 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  124. Coban, C. et al. Toll-like receptor 9 mediates innate immune activation by the malaria pigment hemozoin. J. Exp. Med. 201, 19–25 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  125. Goodson, M. S. et al. Identifying components of the NF-κB pathway in the beneficial Euprymna scolopesVibrio fischeri light organ symbiosis. Appl. Environ. Microbiol. 71, 6934–6946 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  126. Qiu, L., Song, L., Xu, W., Ni, D. & Yu, Y. Molecular cloning and expression of a Toll receptor gene homologue from Zhikong Scallop, Chlamys farreri. Fish Shellfish Immunol. 22, 451–466 (2007).

    Article  CAS  PubMed  Google Scholar 

  127. Matsuo, K., Yoshida, H. & Shimizu, T. Differential expression of caudal and dorsal genes in the teloblast lineages of the oligochaete annelid Tubifex tubifex. Dev. Genes Evol. 215, 238–247 (2005).

    Article  CAS  PubMed  Google Scholar 

  128. Goldstein, B., Leviten, M. W. & Weisblat, D. A. Dorsal and snail homologs in leech development. Dev. Genes Evol. 211, 329–337 (2001).

    Article  CAS  PubMed  Google Scholar 

  129. Carty, M. et al. The human adaptor SARM negatively regulates adaptor protein TRIF-dependent Toll-like receptor signaling. Nature Immunol. 7, 1074–1081 (2006).

    Article  CAS  Google Scholar 

  130. Adoutte, A. et al. The new animal phylogeny: reliability and implications. Proc. Natl Acad. Sci. USA 97, 4453–4456 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We are grateful to B. Prud'homme, J. Bangham, J. Casanova and colleagues at the Centre de Génétique Moléculaire for discussions and insights on our manuscript. We apologise to the many authors whose work has not been directly cited because of space limitation.

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Glossary

Metazoans

Heterotrophic multicellular organisms (that is, animals).

Deuterostomes

Animal taxon including all animal species in which the blastopore forms the anus.

Eumetazoans

The clade comprising all major animal groups except sponges (that is, cnidarians to vertebrates).

Protostomes

Animal taxon including all animal species in which the blastopore forms the mouth.

Bilaterians

Animals with bilateral symmetry.

Fat body

The functional equivalent, in insects, of the mammalian liver.

Haemolymph

Insect blood.

Avoidance behaviour

C. elegans worms that are fed on bacterial lawn in experimental conditions have the capacity to discriminate between bacterial species and avoid pathogenic bacteria such as Serratia marcescens, while being attracted by non-pathogenic species such as Escherichia coli.

Paneth cells

Specialized epithelial cells of the small intestine, which provide host defence against microorganisms.

Endotoxin shock

A medical condition that is caused by decreased tissue perfusion and oxygen delivery as a result of lipopolysaccharide contamination of the blood stream.

Morpholinos

A synthetic molecule used to modify gene expression.

Coelomocytes

Circulating cells that are present in the body cavity (coelome) of sea urchins and other invertebrates.

Adaptive immune system

The long-lasting host defence response to infection, which is acquired during the life of the host.

Chordates

The phylum of animals that is defined by the presence of a notochord.

Complement system

A complex system of proteins that interact in a proteolytic cascade, leading to pathogen clearance in the serum.

Innate immune response

The first line of defence against invading organisms, which is inherited.

Clade

A taxonomic group of organisms comprising a single common ancestor and all the descendants of that ancestor.

Convergent evolution

The process whereby organisms that are not closely related (not monophyletic) independently evolve similar traits as a result of having to adapt to similar environments or ecological niches.

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Leulier, F., Lemaitre, B. Toll-like receptors — taking an evolutionary approach. Nat Rev Genet 9, 165–178 (2008). https://doi.org/10.1038/nrg2303

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