Abstract

BackgroundTo date, few peptides in the complex mixture of platypus venom have been identified and sequenced, in part due to the limited amounts of platypus venom available to study. We have constructed and sequenced a cDNA library from an active platypus venom gland to identify the remaining components.ResultsWe identified 83 novel putative platypus venom genes from 13 toxin families, which are homologous to known toxins from a wide range of vertebrates (fish, reptiles, insectivores) and invertebrates (spiders, sea anemones, starfish). A number of these are expressed in tissues other than the venom gland, and at least three of these families (those with homology to toxins from distant invertebrates) may play non-toxin roles. Thus, further functional testing is required to confirm venom activity. However, the presence of similar putative toxins in such widely divergent species provides further evidence for the hypothesis that there are certain protein families that are selected preferentially during evolution to become venom peptides. We have also used homology with known proteins to speculate on the contributions of each venom component to the symptoms of platypus envenomation.ConclusionsThis study represents a step towards fully characterizing the first mammal venom transcriptome. We have found similarities between putative platypus toxins and those of a number of unrelated species, providing insight into the evolution of mammalian venom.

Highlights

  • To date, few peptides in the complex mixture of platypus venom have been identified and sequenced, in part due to the limited amounts of platypus venom available to study

  • A visual representation of Gene Ontology (GO) annotation of 454 read data is shown in Figure S1 in Additional file 1

  • A threshold of three non-venom tissues was chosen so as to limit the number of false negatives; we have previously shown that platypus venom Ornithorhynchus venom defensin-like peptide (OvDLP), Ornithorhynchus venom nerve growth factor (OvNGF) and Ornithorhynchus venom C-type natriuretic peptide (OvCNP) are expressed in some non-venom tissues

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Summary

Introduction

Few peptides in the complex mixture of platypus venom have been identified and sequenced, in part due to the limited amounts of platypus venom available to study. We have constructed and sequenced a cDNA library from an active platypus venom gland to identify the remaining components. Envenomation of humans causes a number of unusual symptoms, including an immediate and excruciating pain that cannot be relieved through normal first-aid practices, including morphine, and generalized ‘whole body’ pain [9]. It causes nausea, gastric pain, cold sweats and lymph node swelling [7]. Blood work reveals high erythrocyte sedimentation and low total protein and serum albumin levels, and symptoms such as localized pain and muscle wasting of the affected limb persist for weeks after envenomation [9]

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