Unity Makes Strength : Exploring Intraspecies and Interspecies Toxin Synergism between Phospholipases A2 and Cytotoxins
(2020) In Frontiers in Pharmacology 11.- Abstract
Toxin synergism is a complex biochemical phenomenon, where different animal venom proteins interact either directly or indirectly to potentiate toxicity to a level that is above the sum of the toxicities of the individual toxins. This provides the animals possessing venoms with synergistically enhanced toxicity with a metabolic advantage, since less venom is needed to inflict potent toxic effects in prey and predators. Among the toxins that are known for interacting synergistically are cytotoxins from snake venoms, phospholipases A2 from snake and bee venoms, and melittin from bee venom. These toxins may derive a synergistically enhanced toxicity via formation of toxin complexes by hetero-oligomerization. Using a human... (More)
Toxin synergism is a complex biochemical phenomenon, where different animal venom proteins interact either directly or indirectly to potentiate toxicity to a level that is above the sum of the toxicities of the individual toxins. This provides the animals possessing venoms with synergistically enhanced toxicity with a metabolic advantage, since less venom is needed to inflict potent toxic effects in prey and predators. Among the toxins that are known for interacting synergistically are cytotoxins from snake venoms, phospholipases A2 from snake and bee venoms, and melittin from bee venom. These toxins may derive a synergistically enhanced toxicity via formation of toxin complexes by hetero-oligomerization. Using a human keratinocyte assay mimicking human epidermis in vitro, we demonstrate and quantify the level of synergistically enhanced toxicity for 12 cytotoxin/melittin-PLA2 combinations using toxins from elapids, vipers, and bees. Moreover, by utilizing an interaction-based assay and by including a wealth of information obtained via a thorough literature review, we speculate and propose a mechanistic model for how toxin synergism in relation to cytotoxicity may be mediated by cytotoxin/melittin and PLA2 complex formation.
(Less)
- author
- publishing date
- 2020-05-07
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- cytotoxicity, cytotoxins, melittin, phospholipase A, toxin complexes, toxin interactions, toxin synergism, venom
- in
- Frontiers in Pharmacology
- volume
- 11
- article number
- 611
- publisher
- Frontiers Media S. A.
- external identifiers
-
- pmid:32457615
- scopus:85085085522
- ISSN
- 1663-9812
- DOI
- 10.3389/fphar.2020.00611
- language
- English
- LU publication?
- no
- id
- 03b4fc46-56d2-4b28-9c75-602c4625461b
- date added to LUP
- 2020-06-16 16:58:27
- date last changed
- 2024-09-19 23:56:09
@article{03b4fc46-56d2-4b28-9c75-602c4625461b, abstract = {{<p>Toxin synergism is a complex biochemical phenomenon, where different animal venom proteins interact either directly or indirectly to potentiate toxicity to a level that is above the sum of the toxicities of the individual toxins. This provides the animals possessing venoms with synergistically enhanced toxicity with a metabolic advantage, since less venom is needed to inflict potent toxic effects in prey and predators. Among the toxins that are known for interacting synergistically are cytotoxins from snake venoms, phospholipases A<sub>2</sub> from snake and bee venoms, and melittin from bee venom. These toxins may derive a synergistically enhanced toxicity via formation of toxin complexes by hetero-oligomerization. Using a human keratinocyte assay mimicking human epidermis in vitro, we demonstrate and quantify the level of synergistically enhanced toxicity for 12 cytotoxin/melittin-PLA<sub>2</sub> combinations using toxins from elapids, vipers, and bees. Moreover, by utilizing an interaction-based assay and by including a wealth of information obtained via a thorough literature review, we speculate and propose a mechanistic model for how toxin synergism in relation to cytotoxicity may be mediated by cytotoxin/melittin and PLA<sub>2</sub> complex formation.</p>}}, author = {{Pucca, Manuela B. and Ahmadi, Shirin and Cerni, Felipe A. and Ledsgaard, Line and Sørensen, Christoffer V. and McGeoghan, Farrell T.S. and Stewart, Trenton and Schoof, Erwin and Lomonte, Bruno and auf dem Keller, Ulrich and Arantes, Eliane C. and Çalışkan, Figen and Laustsen, Andreas H.}}, issn = {{1663-9812}}, keywords = {{cytotoxicity; cytotoxins; melittin; phospholipase A; toxin complexes; toxin interactions; toxin synergism; venom}}, language = {{eng}}, month = {{05}}, publisher = {{Frontiers Media S. A.}}, series = {{Frontiers in Pharmacology}}, title = {{Unity Makes Strength : Exploring Intraspecies and Interspecies Toxin Synergism between Phospholipases A<sub>2</sub> and Cytotoxins}}, url = {{http://dx.doi.org/10.3389/fphar.2020.00611}}, doi = {{10.3389/fphar.2020.00611}}, volume = {{11}}, year = {{2020}}, }