Buzz Kill: Function and Proteomic Composition of Venom from the Giant Assassin Fly <i>Dolopus genitalis</i> (Diptera: Asilidae)

Assassin flies (Diptera: Asilidae) inject paralysing venom into insect prey during hunting, but their venoms are poorly characterised in comparison to those produced by spiders, scorpions, or hymenopteran insects. Here we investigated the composition of the venom of the giant Australian assassin fly...

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Main Authors: Andrew A. Walker, James Dobson, Jiayi Jin, Samuel D. Robinson, Volker Herzig, Irina Vetter, Glenn F. King, Bryan G. Fry
Format: Article
Language:English
Published: MDPI AG 2018-11-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/10/11/456
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spelling doaj-7ede63c09dd44caa865609b7a8e8a6832020-11-24T20:56:59ZengMDPI AGToxins2072-66512018-11-01101145610.3390/toxins10110456toxins10110456Buzz Kill: Function and Proteomic Composition of Venom from the Giant Assassin Fly <i>Dolopus genitalis</i> (Diptera: Asilidae)Andrew A. Walker0James Dobson1Jiayi Jin2Samuel D. Robinson3Volker Herzig4Irina Vetter5Glenn F. King6Bryan G. Fry7Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, AustraliaVenom Evolution Lab, School of Biological Sciences, The University of Queensland, St Lucia, QLD 4072, AustraliaInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, AustraliaInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, AustraliaInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, AustraliaInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, AustraliaInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, AustraliaVenom Evolution Lab, School of Biological Sciences, The University of Queensland, St Lucia, QLD 4072, AustraliaAssassin flies (Diptera: Asilidae) inject paralysing venom into insect prey during hunting, but their venoms are poorly characterised in comparison to those produced by spiders, scorpions, or hymenopteran insects. Here we investigated the composition of the venom of the giant Australian assassin fly <i>Dolopus genitalis</i> using a combination of insect microinjection assays, calcium imaging assays of mammalian sensory neurons, proteomics and transcriptomics. Injection of venom into blowflies (<i>Lucilia cuprina</i>) produced rapid contractile paralysis (PD<sub>50</sub> at 1 min = 3.1 &#956;g per fly) followed by death, and also caused immediate activation of mouse dorsal root ganglion neurons (at 50 ng/&#956;L). These results are consistent with venom use for both prey capture and predator deterrence. Paragon searches of tandem mass spectra of venom against a translated thoracic gland RNA-Seq database identified 122 polypeptides present in the venom, including six linear and 21 disulfide-rich peptides. Some of these disulfide-rich peptides display sequence homology to peptide families independently recruited into other animal venoms, including inhibitor cystine knots, cystine-stabilised &#945;/&#946; defensins, Kazal peptides, and von Willebrand factors. Numerous enzymes are present in the venom, including 35 proteases of the S1 family, proteases of the S10, C1A, M12A, M14, and M17 families, and phosphatase, amylase, hydrolase, nuclease, and dehydrogenase-like proteins. These results highlight convergent molecular evolution between the assassin flies and other venomous animals, as well as the unique and rich molecular composition of assassin fly venom.https://www.mdpi.com/2072-6651/10/11/456venompeptidedefensinAsilidaeDipterainsect venomAsilidininhibitor cystine knotextra-oral digestion
collection DOAJ
language English
format Article
sources DOAJ
author Andrew A. Walker
James Dobson
Jiayi Jin
Samuel D. Robinson
Volker Herzig
Irina Vetter
Glenn F. King
Bryan G. Fry
spellingShingle Andrew A. Walker
James Dobson
Jiayi Jin
Samuel D. Robinson
Volker Herzig
Irina Vetter
Glenn F. King
Bryan G. Fry
Buzz Kill: Function and Proteomic Composition of Venom from the Giant Assassin Fly <i>Dolopus genitalis</i> (Diptera: Asilidae)
Toxins
venom
peptide
defensin
Asilidae
Diptera
insect venom
Asilidin
inhibitor cystine knot
extra-oral digestion
author_facet Andrew A. Walker
James Dobson
Jiayi Jin
Samuel D. Robinson
Volker Herzig
Irina Vetter
Glenn F. King
Bryan G. Fry
author_sort Andrew A. Walker
title Buzz Kill: Function and Proteomic Composition of Venom from the Giant Assassin Fly <i>Dolopus genitalis</i> (Diptera: Asilidae)
title_short Buzz Kill: Function and Proteomic Composition of Venom from the Giant Assassin Fly <i>Dolopus genitalis</i> (Diptera: Asilidae)
title_full Buzz Kill: Function and Proteomic Composition of Venom from the Giant Assassin Fly <i>Dolopus genitalis</i> (Diptera: Asilidae)
title_fullStr Buzz Kill: Function and Proteomic Composition of Venom from the Giant Assassin Fly <i>Dolopus genitalis</i> (Diptera: Asilidae)
title_full_unstemmed Buzz Kill: Function and Proteomic Composition of Venom from the Giant Assassin Fly <i>Dolopus genitalis</i> (Diptera: Asilidae)
title_sort buzz kill: function and proteomic composition of venom from the giant assassin fly <i>dolopus genitalis</i> (diptera: asilidae)
publisher MDPI AG
series Toxins
issn 2072-6651
publishDate 2018-11-01
description Assassin flies (Diptera: Asilidae) inject paralysing venom into insect prey during hunting, but their venoms are poorly characterised in comparison to those produced by spiders, scorpions, or hymenopteran insects. Here we investigated the composition of the venom of the giant Australian assassin fly <i>Dolopus genitalis</i> using a combination of insect microinjection assays, calcium imaging assays of mammalian sensory neurons, proteomics and transcriptomics. Injection of venom into blowflies (<i>Lucilia cuprina</i>) produced rapid contractile paralysis (PD<sub>50</sub> at 1 min = 3.1 &#956;g per fly) followed by death, and also caused immediate activation of mouse dorsal root ganglion neurons (at 50 ng/&#956;L). These results are consistent with venom use for both prey capture and predator deterrence. Paragon searches of tandem mass spectra of venom against a translated thoracic gland RNA-Seq database identified 122 polypeptides present in the venom, including six linear and 21 disulfide-rich peptides. Some of these disulfide-rich peptides display sequence homology to peptide families independently recruited into other animal venoms, including inhibitor cystine knots, cystine-stabilised &#945;/&#946; defensins, Kazal peptides, and von Willebrand factors. Numerous enzymes are present in the venom, including 35 proteases of the S1 family, proteases of the S10, C1A, M12A, M14, and M17 families, and phosphatase, amylase, hydrolase, nuclease, and dehydrogenase-like proteins. These results highlight convergent molecular evolution between the assassin flies and other venomous animals, as well as the unique and rich molecular composition of assassin fly venom.
topic venom
peptide
defensin
Asilidae
Diptera
insect venom
Asilidin
inhibitor cystine knot
extra-oral digestion
url https://www.mdpi.com/2072-6651/10/11/456
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