Why is venom important




















If the evolution of snake venom was driven by natural selection for defence, we would expect to see the same pattern — almost immediate pain that is severe enough to be a deterrent. But is this what happens? There is often severe pain in snakebites , but little was known about the timescale of pain development. If pain occurs long after the bite, it may simply be a side effect of other venom properties, such as tissue damage.

The ideal organism on which to test this idea is a species that is regularly exposed to venomous snakebites from a wide variety of snakes and can communicate precisely the effects of a bite. That model organism is Homo sapiens. In particular, snake keepers, reptile researchers and ecologists who work with them in the field. To tap into the body of collective snakebite experience accumulated by this demographic, Bangor University researcher Harry Ward-Smith designed and distributed a questionnaire asking them about past venomous snakebites, and in particular, how pain developed after a bite.

Respondents were asked to report their pain level on a scale of after one minute and five minutes, and the maximum pain level at any time after the bite.

The purpose was to focus mostly on the timescale of pain development rather than the actual pain levels themselves. The rationale was that while the intensity of pain experienced will vary greatly between people, the timing of when pain develops should be more consistent. Different people may consider a bee sting to be a minor nuisance or unbearable, but everyone agrees that it hurts immediately.

Gutierrez, J. Snakebite envenoming. Primers Phospholipases A2: unveiling the secrets of a functionally versatile group of snake venom toxins. Toxicon 62, 27— Snake venomics and antivenomics: proteomic tools in the design and control of antivenoms for the treatment of snakebite envenoming.

Proteomics 72, — Skeletal muscle degeneration induced by venom phospholipases A2: insights into the mechanisms of local and systemic myotoxicity. Toxicon 42, — Snake venom metalloproteinases: their role in the pathogenesis of local tissue damage. Biochimie 82, — Hemorrhage induced by snake venom metalloproteinases: biochemical and biophysical mechanisms involved in microvessel damage. Gutierrez, V. Crotalphine induces potent antinociception in neuropathic pain by acting at peripheral opioid receptors.

Harel, M. Crystal structure of an acetylcholinesterase-fasciculin complex: interaction of a three-fingered toxin from snake venom with its target. Structure 3, — Harris, J. The neurotoxicity of the venom phospholipases A2, notexin and taipoxin.

Myotoxic activity of the crude venom and the principal neurotoxin, taipoxin, of the Australian taipan, Oxyuranus scutellatus. Secreted phospholipases A2 of snake venoms: Effects on the peripheral neuromuscular system with comments on the role of phospholipases A2 in disorders of the CNS and their uses in industry. Toxins 5, — Harrison, R. The time is now: a call for action to translate recent momentum on tackling tropical snakebite into sustained benefit for victims. Hifumi, T. Venomous snake bites: clinical diagnosis and treatment.

Intensive Care Hite, L. Hoogenboom, H. Selecting and screening recombinant antibody libraries. Jayawardana, S. Chronic musculoskeletal disabilities following snake envenoming in Sri Lanka: a population-based study.

Jia, L. Snake venom metalloproteinases: structure, function and relationship to the ADAMs family of proteins. Toxicon 34, — Juan, H. Comparison of three classes of snake neurotoxins by homology modeling and computer simulation graphics.

Junqueira-De-Azevedo, I. Venom-related transcripts from Bothrops jararaca tissues provide novel molecular insights into the production and evolution of snake venom. Kamiguti, A. Platelets as targets of snake venom metalloproteinases. Kang, T. Enzymatic toxins from snake venom: structural characterization and mechanism of catalysis. Kasturiratne, A. The global burden of snakebite: a literature analysis and modelling based on regional estimates of envenoming and deaths.

PLoS Med. Kessler, P. The three-finger toxin fold: a multifunctional structural scaffold able to modulate cholinergic functions. Kini, R. The intriguing world of prothrombin activators from snake venom. Anticoagulant proteins from snake venoms: structure, function and mechanism. Structure, function and evolution of three-finger toxins: mini proteins with multiple targets. Toxicon 56, — Metalloproteases affecting blood coagulation, fibrinolysis and platelet aggregation from snake venoms: definition and nomenclature of interaction sites.

Toxins 8:E Kleggetveit, I. Complex regional pain syndrome following viper-bite. Pain 10, 15— Koivula, K. Konno, K. Crotalphine, a novel potent analgesic peptide from the venom of the South American rattlesnake Crotalus durissus terrificus. Peptides 29, — Konshina, A.

Cardiotoxins: functional role of local conformational changes. Laing, G. Inflammatory pathogenesis of snake venom metalloproteinase-induced skin necrosis. Lauer, M. Circulation , — Lauridsen, L. Exploring the venom of the forest cobra snake: toxicovenomics and antivenom profiling of Naja melanoleuca. Proteomics , 98— Laustsen, A. In vivo neutralization of dendrotoxin-mediated neurotoxicity of black mamba venom by oligoclonal human IgG antibodies.

Li, M. Eggs-only diet: its implications for the toxin profile changes and ecology of the marbled sea snake Aipysurus eydouxii. Lomonte, B. Identification of a heparin-binding and cytolytic toxin region by the use of synthetic peptides and molecular modeling. Snake venom Lys49 myotoxins: from phospholipases A2 to non-enzymatic membrane disruptors. Lynch, M. The evolutionary fate and consequences of duplicate genes. Science , — Lynch, V.

Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A2 genes. BMC Evol. Mackessy, S. Understanding biological roles of venoms among the Caenophidia: the importance of rear-fanged snakes. Madrigal, M. Snake venomics across genus Lachesis.

Ontogenetic changes in the venom composition of Lachesis stenophrys and comparative proteomics of the venoms of adult Lachesis melanocephala and Lachesis acrochorda.

Proteomics 77, — Maduwage, K. Current treatment for venom-induced consumption coagulopathy resulting from snakebite. Mamede, C. Comparative analysis of local effects caused by Bothrops alternatus and Bothrops moojeni snake venoms: enzymatic contributions and inflammatory modulations.

Toxicon , 37— Marchot, P. Inhibition of mouse acetylcholinesterase by fasciculin: crystal structure of the complex and mutagenesis of fasciculin. Toxicon 36, — Markland, F. Snake venoms and the hemostatic system. Snake venom metalloproteinases. Toxicon 62, 3— Marquer, C. Structural model of ligand-G protein-coupled receptor GPCR complex based on experimental double mutant cycle data: MT7 snake toxin bound to dimeric hM1 muscarinic receptor.

McDowell, R. Mambin, a potent glycoprotein IIb-IIIa antagonist and platelet aggregation inhibitor structurally related to the short neurotoxins. Biochemistry 31, — Menaldo, D. Effects of two serine proteases from Bothrops pirajai snake venom on the complement system and the inflammatory response.

Immune cells and mediators involved in the inflammatory responses induced by a P-I metalloprotease and a phospholipase A2 from Bothrops atrox venom. Menezes, M. Sex-based individual variation of snake venom proteome among eighteen Bothrops jararaca siblings.

Modahl, C. Transcriptome-facilitated proteomic characterization of rear-fanged snake venoms reveal abundant metalloproteinases with enhanced activity. Proteomics , — Adaptive evolution of distinct prey-specific toxin genes in rear-fanged snake venom. Mordvintsev, D. Moreira, V. Moura-Da-Silva, A. Evolution of disintegrin cysteine-rich and mammalian matrix-degrading metalloproteinases: gene duplication and divergence of a common ancestor rather than convergent evolution.

Munawar, A. Snake venom peptides: tools of biodiscovery. Toxins E Murakami, M. Thrombomodulin-independent activation of protein C and specificity of hemostatically active snake venom serine proteinases: crystal structures of native and inhibited Agkistrodon contortrix contortrix protein C activator.

Nguyen, T. Cardiotoxin-I: an unexpectedly potent insulinotropic agent. Chembiochem 13, — Nunez, C. Identification of the myotoxic site of the Lys49 phospholipase A2 from Agkistrodon piscivorus piscivorus snake venom: synthetic C-terminal peptides from Lys49, but not from Asp49 myotoxins, exert membrane-damaging activities. Toxicon 39, — O'leary, M. Commercial monovalent antivenoms in Australia are polyvalent.

Toxicon 54, — Osipov, A. Gopalakrishnakone, A. Mukherjee, T. Rahmy, C. Ouyang, C. Ownby, C. Cardiotoxin 1 from cobra Naja naja atra venom causes necrosis of skeletal muscle in vivo. Toxicon 31, — Page, M. Serine peptidases: classification, structure and function. Cell Mol. Life Sci. Pawlak, J. Denmotoxin, a three-finger toxin from the colubrid snake Boiga dendrophila Mangrove Catsnake with bird-specific activity. Peng, S. Solution structure of toxin b, a long neurotoxin from the venom of the king cobra Ophiophagus hannah.

Perry, B. Molecular adaptations for sensing and securing prey and insight into amniote genome diversity from the garter snake genome. Genome Biol. Picolo, G. Evaluation of antivenoms in the neutralization of hyperalgesia and edema induced by Bothrops jararaca and Bothrops asper snake venoms.

Pla, D. Snake venomics of Lachesis muta rhombeata and genus-wide antivenomics assessment of the paraspecific immunoreactivity of two antivenoms evidence the high compositional and immunological conservation across Lachesis. Proteomics 89, — What killed Karl Patterson Schmidt? Combined venom gland transcriptomic, venomic and antivenomic analysis of the South African green tree snake the boomslang , Dispholidus typus.

Acta Gen. Rajagopalan, N. Rivel, M. Pathogenesis of dermonecrosis induced by venom of the spitting cobra, Naja nigricollis : an experimental study in mice. Rivera-Torres, I. Discovery and characterisation of a novel toxin from Dendroaspis angusticeps , named Tx, that activates the potassium channel KcsA. Roncolato, E. Phage display as a novel promising antivenom therapy: a review. Toxicon 93, 79— Rong, L.

Hydrogen peroxide detection with high specificity in living cells and inflamed tissues. Rouault, M. Neurotoxicity and other pharmacological activities of the snake venom phospholipase A2 OS2: the N-terminal region is more important than enzymatic activity. Biochemistry 45, — Salinas, M. Binding site and inhibitory mechanism of the mambalgin-2 pain-relieving peptide on acid-sensing ion channel 1a. Schmidt, J. Structure-function studies of waglerin I, a lethal peptide from the venom of Wagler's pit viper, Trimeresurus wagleri.

Toxicon 33, — Toxicon 55, — Seo, Y. Development of complex regional pain syndrome after a snake bite: a case report. Korean J. Pain 27, 68— Serrano, S. The long road of research on snake venom serine proteinases. Toxicon 62, 19— Silva, L. Discovery of human scFvs that cross-neutralize the toxic effects of B. Acta Trop. Six, D. The expanding superfamily of phospholipase A2 enzymes: classification and characterization. Acta , 1— Slagboom, J. Haemotoxic snake venoms: their functional activity, impact on snakebite victims and pharmaceutical promise.

Soares, A. Effects of chemical modifications of crotoxin B, the phospholipase A2 subunit of crotoxin from Crotalus durissus terrificus snake venom, on its enzymatic and pharmacological activities.

Cell Biol. Sribar, J. Understanding the molecular mechanism underlying the presynaptic toxicity of secreted phospholipases A2: an update. Toxicon 89, 9— Stocker, K. Chromogenic assay for the prothrombin activator ecarin from the venom of the saw-scaled viper Echis carinatus. Toxicon 24, 81— Isolation and characterization of Textarin, a prothrombin activator from eastern brown snake Pseudonaja textilis venom. Toxicon 32, — Sunagar, K. Takeda, S.

Tan, C. Antivenom cross-neutralization of the venoms of Hydrophis schistosus and Hydrophis curtus , two common sea snakes in Malaysian waters. Toxins 7, — Tasoulis, T. A review and database of snake venom proteomes. The development of new antivenom is an ongoing struggle, however researchers have found that the toxins found in venoms can also aid in treating other medical conditions and several venom-based drugs are already in use.

Snake venom is a term that covers a wide array of different venoms. Some kill quickly while others take time. Most snakes deliver their poison through fangs that operate in a similar method to a syringe.

The exceptions to this are snakes who spit their venom, like the Mozambique spitting cobra Naja mossambica. Since there is such a variety in the venoms, the potential medical applications differ from snake to snake.

Coronary medical conditions are a field where solutions involving toxins taken from snakes are currently employed. The venom gland of a Komodo dragon works differently to that of a snake. This is why their prey continues to bleed out after the attack.



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