Presence of presynaptic neurotoxin complexes in the venoms of Australo-Papuan death adders (Acanthophis spp.)

Australo-papuan death adders (Acanthophis spp.) are a cause of serious envenomations in Papua New Guinea and northern Australia often resulting in neurotoxic paralysis. Furthermore, victims occasionally present with delayed-onset neurotoxicity that sometimes responds poorly to antivenom or anticholi...

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Main Authors: Blacklow, B, Konstantakopoulos, N, Hodgson, WC, Nicholson, GM
Format: Article in Journal/Newspaper
Language:unknown
Published: 2010
Subjects:
Gel
Online Access:http://hdl.handle.net/10453/13801
id ftunivtsydney:oai:opus.lib.uts.edu.au:10453/13801
record_format openpolar
spelling ftunivtsydney:oai:opus.lib.uts.edu.au:10453/13801 2023-05-15T13:52:24+02:00 Presence of presynaptic neurotoxin complexes in the venoms of Australo-Papuan death adders (Acanthophis spp.) Blacklow, B Konstantakopoulos, N Hodgson, WC Nicholson, GM 2010-06-01 application/pdf http://hdl.handle.net/10453/13801 unknown Toxicon 10.1016/j.toxicon.2010.01.007 Toxicon, 2010, 55 (6), pp. 1171 - 1180 0041-0101 http://hdl.handle.net/10453/13801 Toxicology Neuromuscular Junction Animals Chickens Elapidae Receptors Presynaptic Elapid Venoms Neurotoxins Chemical Fractionation Chromatography Gel Muscle Contraction Molecular Weight Phospholipases A2 Journal Article 2010 ftunivtsydney 2022-03-13T13:40:15Z Australo-papuan death adders (Acanthophis spp.) are a cause of serious envenomations in Papua New Guinea and northern Australia often resulting in neurotoxic paralysis. Furthermore, victims occasionally present with delayed-onset neurotoxicity that sometimes responds poorly to antivenom or anticholinesterase treatment. This clinical outcome could be explained by the presence of potent snake presynaptic phospholipase A2 neurotoxin (SPAN) complexes and monomers, in addition to long- and short-chain postsynaptic α-neurotoxins, that bind irreversibly, block neurotransmitter release and result in degeneration of the nerve terminal. The present study therefore aimed to determine within-genus variations in expression of high molecular mass SPAN complexes in the venoms of six major species of Acanthophis, four geographic variants of Acanthophis antarcticus. Venoms were separated by size-exclusion liquid chromatography under non-denaturing conditions and fractions corresponding to proteins in the range of 22 to >60 kDa were subjected to pharmacological characterization using the isolated chick biventer cervicis nerve-muscle (CBCNM) preparation. All venoms, except Acanthophis wellsi and Acanthophis pyrrhus, contained high mass fractions with phospholipase A2 activity that inhibited twitch contractions of the CBCNM preparation. This inhibition was of slow onset, and responses to exogenous nicotinic agonists were not blocked, consistent with the presence of SPAN complexes. The results of the present study indicate that clinicians may need to be aware of possible prejunctional neurotoxicity following envenomations from A. antarcticus (all geographic variants except perhaps South Australia), Acanthophis praelongus, Acanthophis rugosus and Acanthophis. laevis species, and that early antivenom intervention is important in preventing further development of toxicity. © 2010 Elsevier Ltd. All rights reserved. Article in Journal/Newspaper Antarc* antarcticus University of Technology Sydney: OPUS - Open Publications of UTS Scholars
institution Open Polar
collection University of Technology Sydney: OPUS - Open Publications of UTS Scholars
op_collection_id ftunivtsydney
language unknown
topic Toxicology
Neuromuscular Junction
Animals
Chickens
Elapidae
Receptors
Presynaptic
Elapid Venoms
Neurotoxins
Chemical Fractionation
Chromatography
Gel
Muscle Contraction
Molecular Weight
Phospholipases A2
spellingShingle Toxicology
Neuromuscular Junction
Animals
Chickens
Elapidae
Receptors
Presynaptic
Elapid Venoms
Neurotoxins
Chemical Fractionation
Chromatography
Gel
Muscle Contraction
Molecular Weight
Phospholipases A2
Blacklow, B
Konstantakopoulos, N
Hodgson, WC
Nicholson, GM
Presence of presynaptic neurotoxin complexes in the venoms of Australo-Papuan death adders (Acanthophis spp.)
topic_facet Toxicology
Neuromuscular Junction
Animals
Chickens
Elapidae
Receptors
Presynaptic
Elapid Venoms
Neurotoxins
Chemical Fractionation
Chromatography
Gel
Muscle Contraction
Molecular Weight
Phospholipases A2
description Australo-papuan death adders (Acanthophis spp.) are a cause of serious envenomations in Papua New Guinea and northern Australia often resulting in neurotoxic paralysis. Furthermore, victims occasionally present with delayed-onset neurotoxicity that sometimes responds poorly to antivenom or anticholinesterase treatment. This clinical outcome could be explained by the presence of potent snake presynaptic phospholipase A2 neurotoxin (SPAN) complexes and monomers, in addition to long- and short-chain postsynaptic α-neurotoxins, that bind irreversibly, block neurotransmitter release and result in degeneration of the nerve terminal. The present study therefore aimed to determine within-genus variations in expression of high molecular mass SPAN complexes in the venoms of six major species of Acanthophis, four geographic variants of Acanthophis antarcticus. Venoms were separated by size-exclusion liquid chromatography under non-denaturing conditions and fractions corresponding to proteins in the range of 22 to >60 kDa were subjected to pharmacological characterization using the isolated chick biventer cervicis nerve-muscle (CBCNM) preparation. All venoms, except Acanthophis wellsi and Acanthophis pyrrhus, contained high mass fractions with phospholipase A2 activity that inhibited twitch contractions of the CBCNM preparation. This inhibition was of slow onset, and responses to exogenous nicotinic agonists were not blocked, consistent with the presence of SPAN complexes. The results of the present study indicate that clinicians may need to be aware of possible prejunctional neurotoxicity following envenomations from A. antarcticus (all geographic variants except perhaps South Australia), Acanthophis praelongus, Acanthophis rugosus and Acanthophis. laevis species, and that early antivenom intervention is important in preventing further development of toxicity. © 2010 Elsevier Ltd. All rights reserved.
format Article in Journal/Newspaper
author Blacklow, B
Konstantakopoulos, N
Hodgson, WC
Nicholson, GM
author_facet Blacklow, B
Konstantakopoulos, N
Hodgson, WC
Nicholson, GM
author_sort Blacklow, B
title Presence of presynaptic neurotoxin complexes in the venoms of Australo-Papuan death adders (Acanthophis spp.)
title_short Presence of presynaptic neurotoxin complexes in the venoms of Australo-Papuan death adders (Acanthophis spp.)
title_full Presence of presynaptic neurotoxin complexes in the venoms of Australo-Papuan death adders (Acanthophis spp.)
title_fullStr Presence of presynaptic neurotoxin complexes in the venoms of Australo-Papuan death adders (Acanthophis spp.)
title_full_unstemmed Presence of presynaptic neurotoxin complexes in the venoms of Australo-Papuan death adders (Acanthophis spp.)
title_sort presence of presynaptic neurotoxin complexes in the venoms of australo-papuan death adders (acanthophis spp.)
publishDate 2010
url http://hdl.handle.net/10453/13801
genre Antarc*
antarcticus
genre_facet Antarc*
antarcticus
op_relation Toxicon
10.1016/j.toxicon.2010.01.007
Toxicon, 2010, 55 (6), pp. 1171 - 1180
0041-0101
http://hdl.handle.net/10453/13801
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