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Molecular basis of infrared detection by snakes

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Abstract

Snakes possess a unique sensory system for detecting infrared radiation, enabling them to generate a ‘thermal image’ of predators or prey. Infrared signals are initially received by the pit organ, a highly specialized facial structure that is innervated by nerve fibres of the somatosensory system. How this organ detects and transduces infrared signals into nerve impulses is not known. Here we use an unbiased transcriptional profiling approach to identify TRPA1 channels as infrared receptors on sensory nerve fibres that innervate the pit organ. TRPA1 orthologues from pit-bearing snakes (vipers, pythons and boas) are the most heat-sensitive vertebrate ion channels thus far identified, consistent with their role as primary transducers of infrared stimuli. Thus, snakes detect infrared signals through a mechanism involving radiant heating of the pit organ, rather than photochemical transduction. These findings illustrate the broad evolutionary tuning of transient receptor potential (TRP) channels as thermosensors in the vertebrate nervous system.

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Figure 1: Anatomy of the pit organ and comparison of gene expression in snake sensory ganglia.
Figure 2: Expression of TRPA1 and TRPV1 in rattlesnake sensory ganglia.
Figure 3: Functional analysis of snake TRPA1 channels.
Figure 4: Analysis of TRPA1 from python and boa.
Figure 5: Functional analysis of snake sensory neurons.

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Accession codes

Primary accessions

Gene Expression Omnibus

Data deposits

Deep sequencing data are archived under GEO accession number GSE19911. GenBank accession numbers are GU562965 (Python regius TRPA1), GU562966 (Elaphe obsoleta lindheimeri TRPA1), GU562967 (Crotalus atrox TRPA1), GU562968 (Crotalus atrox TRPV1), and GU562969 (Corallus hortulanus TRPA1).

Change history

  • 15 April 2010

    A correction was made to the spelling of an author name (N.T.I.) on 15 April.

References

  1. Bullock, T. H. & Cowles, R. B. Physiology of an infrared receptor: the facial pit of pit vipers. Science 115, 541–543 (1952)

    Article  ADS  CAS  Google Scholar 

  2. Campbell, A. L., Naik, R. R., Sowards, L. & Stone, M. O. Biological infrared imaging and sensing. Micron 33, 211–225 (2002)

    Article  Google Scholar 

  3. Ebert, J. Infrared Sense in Snakes – Behavioural and Anatomical Examinations (Crotalus atrox, Python regius, Corallus hortulanus). Dr rer. nat. thesis, Rheinische Friedrich Wilhelms Univ. Bonn. (2007)

  4. Barrett, R., Maderson, P. F. A. & Meszler, R. M. in Biology of Reptilia (ed. Parsons, T. S.) Ch. 4 277–300 (Academic Press, 1970)

    Google Scholar 

  5. Ebert, J. & Schmitz, A. in Herpetologia Bonnensis II (eds Vences, M. Kohler, J., Ziegler T. & Bohme, W.) 215–217 (2006)

    Google Scholar 

  6. Terashima, S. & Liang, Y. F. Temperature neurons in the crotaline trigeminal ganglia. J. Neurophysiol. 66, 623–634 (1991)

    Article  CAS  Google Scholar 

  7. Amemiya, F., Ushiki, T., Goris, R. C., Atobe, Y. & Kusunoki, T. Ultrastructure of the crotaline snake infrared pit receptors: SEM confirmation of TEM findings. Anat. Rec. 246, 135–146 (1996)

    Article  CAS  Google Scholar 

  8. Bleichmar, H. & De Robertis, E. Submicroscopic morphology of the infrared receptor of pit vipers. Z. Zellforsch. Mikrosk. Anat. 56, 748–761 (1962)

    Article  CAS  Google Scholar 

  9. Hartline, P. H., Kass, L. & Loop, M. S. Merging of modalities in the optic tectum: infrared and visual integration in rattlesnakes. Science 199, 1225–1229 (1978)

    Article  ADS  CAS  Google Scholar 

  10. Newman, E. A. & Hartline, P. H. Integration of visual and infrared information in bimodal neurons in the rattlesnake optic tectum. Science 213, 789–791 (1981)

    Article  ADS  CAS  Google Scholar 

  11. Molenaar, G. J. The sensory trigeminal system of a snake in the possession of infrared receptors. II. The central projections of the trigeminal nerve. J. Comp. Neurol. 179, 137–151 (1978)

    Article  CAS  Google Scholar 

  12. de Cock Buning, T., Terashima, S. & Goris, R. C. Python pit organs analyzed as warm python pit organs analyzed as warm receptors. Cell. Mol. Neurobiol. 1, 271–278 (1981)

    Article  CAS  Google Scholar 

  13. Warren, J. W. & Proske, U. Infrared receptors in the facial pits of the Australian python Morelia spilotes. Science 159, 439–441 (1968)

    Article  ADS  CAS  Google Scholar 

  14. Kishida, R., Amemiya, F., Kusunoki, T. & Terashima, S. A new tectal afferent nucleus of the infrared sensory system in the medulla oblongata of Crotaline snakes. Brain Res. 195, 271–279 (1980)

    Article  CAS  Google Scholar 

  15. Kishida, R., de Cock Buning, T. & Dubbeldam, J. L. Primary vagal nerve projections to the lateral descending trigeminal nucleus in boidae (Python molurus and Boa constrictor). Brain Res. 263, 132–136 (1983)

    Article  CAS  Google Scholar 

  16. Noble, G. K. & Schmidt, A. The structure and function of facial and labial pits of snakes. Proc. Am. Phil. Soc. 77, 263–288 (1937)

    Google Scholar 

  17. Pappas, T. C., Motamedi, M. & Christensen, B. N. Unique temperature-activated neurons from pit viper thermosensors. Am. J. Physiol. Cell Physiol. 287, C1219–C1228 (2004)

    Article  CAS  Google Scholar 

  18. Bautista, D. M. et al. TRPA1 mediates the inflammatory actions of environmental irritants and proalgesic agents. Cell 124, 1269–1282 (2006)

    Article  CAS  Google Scholar 

  19. Julius, D. & Basbaum, A. I. Molecular mechanisms of nociception. Nature 413, 203–210 (2001)

    Article  ADS  CAS  Google Scholar 

  20. Molenaar, G. J. An additional trigeminal system in certain snakes possessing infrared receptors. Brain Res. 78, 340–344 (1974)

    Article  CAS  Google Scholar 

  21. Schroeder, D. M. & Loop, M. S. Trigeminal projections in snakes possessing infrared sensitivity. J. Comp. Neurol. 169, 1–13 (1976)

    Article  CAS  Google Scholar 

  22. Eng, S. R., Dykes, I. M., Lanier, J., Fedtsova, N. & Turner, E. E. POU-domain factor Brn3a regulates both distinct and common programs of gene expression in the spinal and trigeminal sensory ganglia. Neural Dev. 2, 3 (2007)

    Article  Google Scholar 

  23. Su, A. I. et al. A gene atlas of the mouse and human protein-encoding transcriptomes. Proc. Natl Acad. Sci. USA 101, 6062–6067 (2004)

    Article  ADS  CAS  Google Scholar 

  24. Woolf, C. J. & Ma, Q. Nociceptors–noxious stimulus detectors. Neuron 55, 353–364 (2007)

    Article  CAS  Google Scholar 

  25. Jordt, S. E. et al. Mustard oils and cannabinoids excite sensory nerve fibres through the TRP channel ANKTM1. Nature 427, 260–265 (2004)

    Article  ADS  CAS  Google Scholar 

  26. Kobayashi, K. et al. Distinct expression of TRPM8, TRPA1, and TRPV1 mRNAs in rat primary afferent neurons with aδ/c-fibers and colocalization with trk receptors. J. Comp. Neurol. 493, 596–606 (2005)

    Article  CAS  Google Scholar 

  27. Tominaga, M. et al. The cloned capsaicin receptor integrates multiple pain-producing stimuli. Neuron 21, 531–543 (1998)

    Article  CAS  Google Scholar 

  28. Bandell, M. et al. Noxious cold ion channel TRPA1 is activated by pungent compounds and bradykinin. Neuron 41, 849–857 (2004)

    Article  CAS  Google Scholar 

  29. Macpherson, L. J. et al. Noxious compounds activate TRPA1 ion channels through covalent modification of cysteines. Nature 445, 541–545 (2007)

    Article  ADS  CAS  Google Scholar 

  30. Hinman, A., Chuang, H. H., Bautista, D. M. & Julius, D. TRP channel activation by reversible covalent modification. Proc. Natl Acad. Sci. USA 103, 19564–19568 (2006)

    Article  ADS  CAS  Google Scholar 

  31. Prober, D. A. et al. Zebrafish TRPA1 channels are required for chemosensation but not for thermosensation or mechanosensory hair cell function. J. Neurosci. 28, 10102–10110 (2008)

    Article  CAS  Google Scholar 

  32. Hamada, F. N. et al. An internal thermal sensor controlling temperature preference in Drosophila . Nature 454, 217–220 (2008)

    Article  ADS  CAS  Google Scholar 

  33. Viswanath, V. et al. Opposite thermosensor in fruitfly and mouse. Nature 423, 822–823 (2003)

    Article  ADS  CAS  Google Scholar 

  34. Krochmal, A. R., Bakken, G. S. & LaDuc, T. J. Heat in evolution’s kitchen: evolutionary perspectives on the functions and origin of the facial pit of pitvipers (Viperidae: Crotalinae). J. Exp. Biol. 207, 4231–4238 (2004)

    Article  Google Scholar 

  35. Safer, A. B. & Grace, M. S. Infrared imaging in vipers: differential responses of crotaline and viperine snakes to paired thermal targets. Behav. Brain Res. 154, 55–61 (2004)

    Article  Google Scholar 

  36. Kishida, R., Goris, R. C., Terashima, S. & Dubbeldam, J. L. A suspected infrared-recipient nucleus in the brainstem of the vampire bat, Desmodus rotundus . Brain Res. 322, 351–355 (1984)

    Article  CAS  Google Scholar 

  37. Jordt, S. E., McKemy, D. D. & Julius, D. Lessons from peppers and peppermint: the molecular logic of thermosensation. Curr. Opin. Neurobiol. 13, 487–492 (2003)

    Article  CAS  Google Scholar 

  38. Komatsu, H., Mori, I., Rhee, J. S., Akaike, N. & Ohshima, Y. Mutations in a cyclic nucleotide-gated channel lead to abnormal thermosensation and chemosensation in C. elegans . Neuron 17, 707–718 (1996)

    Article  CAS  Google Scholar 

  39. Ramot, D., MacInnis, B. L. & Goodman, M. B. Bidirectional temperature-sensing by a single thermosensory neuron in C. elegans . Nature Neurosci. 11, 908–915 (2008)

    Article  CAS  Google Scholar 

  40. Story, G. M. et al. ANKTM1, a TRP-like channel expressed in nociceptive neurons, is activated by cold temperatures. Cell 112, 819–829 (2003)

    Article  CAS  Google Scholar 

  41. Caspani, O. & Heppenstall, P. A. TRPA1 and cold transduction: an unresolved issue? J. Gen. Physiol. 133, 245–249 (2009)

    Article  CAS  Google Scholar 

  42. Wang, G. et al. Anopheles gambiae TRPA1 is a heat-activated channel expressed in thermosensitive sensilla of female antennae. Eur. J. Neurosci. 30, 967–974 (2009)

    Article  Google Scholar 

  43. Matsuura, H., Sokabe, T., Kohno, K., Tominaga, M. & Kadowaki, T. Evolutionary conservation and changes in insect TRP channels. BMC Evol. Biol. 9, 228 (2009)

    Article  Google Scholar 

  44. Dong, S. & Kumazawa, Y. Complete mitochondrial DNA sequences of six snakes: phylogenetic relationships and molecular evolution of genomic features. J. Mol. Evol. 61, 1432 (2005)

    Article  Google Scholar 

  45. Liman, E. R. Use it or lose it: molecular evolution of sensory signaling in primates. Pflugers Arch. 453, 125–131 (2006)

    Article  CAS  Google Scholar 

  46. Myers, B. R., Sigal, Y. M. & Julius, D. Evolution of thermal response properties in a cold-activated TRP channel. PLoS One 4, e5741 (2009)

    Article  ADS  Google Scholar 

  47. Chuang, H. H., Neuhausser, W. M. & Julius, D. The super-cooling agent icilin reveals a mechanism of coincidence detection by a temperature-sensitive TRP channel. Neuron 43, 859–869 (2004)

    Article  CAS  Google Scholar 

  48. DeCoursey, T. E. & Cherny, V. V. Temperature dependence of voltage-gated H+ currents in human neutrophils, rat alveolar epithelial cells, and mammalian phagocytes. J. Gen. Physiol. 112, 503–522 (1998)

    Article  CAS  Google Scholar 

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Acknowledgements

We thank A. Priel for advice and assistance with calcium imaging and electrophysiology, C. Chu for help with sequencing, J. Poblete for technical assistance, and the staff of the Natural Toxins Research Center serpentarium for animal husbandry. We thank P. Garrity for providing the dTrpA1 cDNA. This work was supported by a Ruth L. Kirschstein National Research Service Award (GM080853) (N.T.I.), a NIH Institutional Research Service Award in Molecular and Cellular Basis of Cardiovascular Disease (A.T.C.), the Howard Hughes Medical Institute (J.S.W.), and grants from the National Institutes of Health, including NCRR Viper grant P40 RR018300-06 (E.E.S. and J.C.P.), P01 AG010770 (J.S.W.) and NS047723 and NS055299 (D.J.).

Author Contributions E.O.G., J.F.C.-M. and N.T.I. designed and performed experiments and analysed data. N.T.I. and J.S.W. developed analytical tools and analysed data. Y.M.K., G.H. and A.T.C. performed experiments and/or provided reagents and analysed data. E.E.S. and J.C.P. supervised snake husbandry and handling. E.O.G., Y.M.K., J.F.C.-M. and D.J. wrote the manuscript with discussion and contributions from all authors. J.S.W. and D.J. provided advice and guidance throughout. D.J. initiated and supervised the project.

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Correspondence to David Julius.

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Gracheva, E., Ingolia, N., Kelly, Y. et al. Molecular basis of infrared detection by snakes. Nature 464, 1006–1011 (2010). https://doi.org/10.1038/nature08943

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