A Proteomics and Transcriptomics Investigation of the Venom from the Barychelid Spider Trittame loki (Brush-Foot Trapdoor)

Although known for their potent venom and ability to prey upon both invertebrate and vertebrate species, the Barychelidae spider family has been entirely neglected by toxinologists. In striking contrast, the sister family Theraphosidae (commonly known as tarantulas), which last shared a most recent...

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Main Authors: Eivind A. B. Undheim, Kartik Sunagar, Volker Herzig, Laurence Kely, Dolyce H. W. Low, Timothy N. W. Jackson, Alun Jones, Nyoman Kurniawan, Glenn F. King, Syed A. Ali, Agostino Antunes, Tim Ruder, Bryan G. Fry
Format: Article
Language:English
Published: MDPI AG 2013-12-01
Series:Toxins
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Online Access:http://www.mdpi.com/2072-6651/5/12/2488
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spelling doaj-5fcbda661d854c52943cc79d56a0a1782020-11-25T00:49:20ZengMDPI AGToxins2072-66512013-12-015122488250310.3390/toxins5122488toxins5122488A Proteomics and Transcriptomics Investigation of the Venom from the Barychelid Spider Trittame loki (Brush-Foot Trapdoor)Eivind A. B. Undheim0Kartik Sunagar1Volker Herzig2Laurence Kely3Dolyce H. W. Low4Timothy N. W. Jackson5Alun Jones6Nyoman Kurniawan7Glenn F. King8Syed A. Ali9Agostino Antunes10Tim Ruder11Bryan G. Fry12Venom Evolution Lab, School of Biological Sciences, University of Queensland, St. Lucia, Queensland 4072, AustraliaCIMAR/CIIMAR, Centro Interdisciplinar de Investigação Marinha e Ambiental, Universidade do Porto, Rua dos Bragas 177, Porto 4050-123, PortugalInstitute for Molecular Bioscience, University of Queensland, St. Lucia, Queensland 4072, AustraliaVenom Evolution Lab, School of Biological Sciences, University of Queensland, St. Lucia, Queensland 4072, AustraliaVenom Evolution Lab, School of Biological Sciences, University of Queensland, St. Lucia, Queensland 4072, AustraliaVenom Evolution Lab, School of Biological Sciences, University of Queensland, St. Lucia, Queensland 4072, AustraliaInstitute for Molecular Bioscience, University of Queensland, St. Lucia, Queensland 4072, AustraliaCentre for Advanced Imaging, University of Queensland, St. Lucia, Queensland 4072, AustraliaInstitute for Molecular Bioscience, University of Queensland, St. Lucia, Queensland 4072, AustraliaVenom Evolution Lab, School of Biological Sciences, University of Queensland, St. Lucia, Queensland 4072, AustraliaCIMAR/CIIMAR, Centro Interdisciplinar de Investigação Marinha e Ambiental, Universidade do Porto, Rua dos Bragas 177, Porto 4050-123, PortugalVenom Evolution Lab, School of Biological Sciences, University of Queensland, St. Lucia, Queensland 4072, AustraliaVenom Evolution Lab, School of Biological Sciences, University of Queensland, St. Lucia, Queensland 4072, AustraliaAlthough known for their potent venom and ability to prey upon both invertebrate and vertebrate species, the Barychelidae spider family has been entirely neglected by toxinologists. In striking contrast, the sister family Theraphosidae (commonly known as tarantulas), which last shared a most recent common ancestor with Barychelidae over 200 million years ago, has received much attention, accounting for 25% of all the described spider toxins while representing only 2% of all spider species. In this study, we evaluated for the first time the venom arsenal of a barychelid spider, Trittame loki, using transcriptomic, proteomic, and bioinformatic methods. The venom was revealed to be dominated by extremely diverse inhibitor cystine knot (ICK)/knottin peptides, accounting for 42 of the 46 full-length toxin precursors recovered in the transcriptomic sequencing. In addition to documenting differential rates of evolution adopted by different ICK/knottin toxin lineages, we discovered homologues with completely novel cysteine skeletal architecture. Moreover, acetylcholinesterase and neprilysin were revealed for the first time as part of the spider-venom arsenal and CAP (CRiSP/Allergen/PR-1) were identified for the first time in mygalomorph spider venoms. These results not only highlight the extent of venom diversification in this neglected ancient spider lineage, but also reinforce the idea that unique venomous lineages are rich pools of novel biomolecules that may have significant applied uses as therapeutics and/or insecticides.http://www.mdpi.com/2072-6651/5/12/2488venomspidermygalomorphtoxinevolution
collection DOAJ
language English
format Article
sources DOAJ
author Eivind A. B. Undheim
Kartik Sunagar
Volker Herzig
Laurence Kely
Dolyce H. W. Low
Timothy N. W. Jackson
Alun Jones
Nyoman Kurniawan
Glenn F. King
Syed A. Ali
Agostino Antunes
Tim Ruder
Bryan G. Fry
spellingShingle Eivind A. B. Undheim
Kartik Sunagar
Volker Herzig
Laurence Kely
Dolyce H. W. Low
Timothy N. W. Jackson
Alun Jones
Nyoman Kurniawan
Glenn F. King
Syed A. Ali
Agostino Antunes
Tim Ruder
Bryan G. Fry
A Proteomics and Transcriptomics Investigation of the Venom from the Barychelid Spider Trittame loki (Brush-Foot Trapdoor)
Toxins
venom
spider
mygalomorph
toxin
evolution
author_facet Eivind A. B. Undheim
Kartik Sunagar
Volker Herzig
Laurence Kely
Dolyce H. W. Low
Timothy N. W. Jackson
Alun Jones
Nyoman Kurniawan
Glenn F. King
Syed A. Ali
Agostino Antunes
Tim Ruder
Bryan G. Fry
author_sort Eivind A. B. Undheim
title A Proteomics and Transcriptomics Investigation of the Venom from the Barychelid Spider Trittame loki (Brush-Foot Trapdoor)
title_short A Proteomics and Transcriptomics Investigation of the Venom from the Barychelid Spider Trittame loki (Brush-Foot Trapdoor)
title_full A Proteomics and Transcriptomics Investigation of the Venom from the Barychelid Spider Trittame loki (Brush-Foot Trapdoor)
title_fullStr A Proteomics and Transcriptomics Investigation of the Venom from the Barychelid Spider Trittame loki (Brush-Foot Trapdoor)
title_full_unstemmed A Proteomics and Transcriptomics Investigation of the Venom from the Barychelid Spider Trittame loki (Brush-Foot Trapdoor)
title_sort proteomics and transcriptomics investigation of the venom from the barychelid spider trittame loki (brush-foot trapdoor)
publisher MDPI AG
series Toxins
issn 2072-6651
publishDate 2013-12-01
description Although known for their potent venom and ability to prey upon both invertebrate and vertebrate species, the Barychelidae spider family has been entirely neglected by toxinologists. In striking contrast, the sister family Theraphosidae (commonly known as tarantulas), which last shared a most recent common ancestor with Barychelidae over 200 million years ago, has received much attention, accounting for 25% of all the described spider toxins while representing only 2% of all spider species. In this study, we evaluated for the first time the venom arsenal of a barychelid spider, Trittame loki, using transcriptomic, proteomic, and bioinformatic methods. The venom was revealed to be dominated by extremely diverse inhibitor cystine knot (ICK)/knottin peptides, accounting for 42 of the 46 full-length toxin precursors recovered in the transcriptomic sequencing. In addition to documenting differential rates of evolution adopted by different ICK/knottin toxin lineages, we discovered homologues with completely novel cysteine skeletal architecture. Moreover, acetylcholinesterase and neprilysin were revealed for the first time as part of the spider-venom arsenal and CAP (CRiSP/Allergen/PR-1) were identified for the first time in mygalomorph spider venoms. These results not only highlight the extent of venom diversification in this neglected ancient spider lineage, but also reinforce the idea that unique venomous lineages are rich pools of novel biomolecules that may have significant applied uses as therapeutics and/or insecticides.
topic venom
spider
mygalomorph
toxin
evolution
url http://www.mdpi.com/2072-6651/5/12/2488
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