Abstract |
Venoms are excellent model systems for studying evolutionary processes associated with predator-prey interactions. Here, we present the discovery of a peptide toxin, MIITX2-Mg1a, which is a major component of the venom of the Australian giant red bull ant Myrmecia gulosa and has evolved to mimic, both structurally and functionally, vertebrate epidermal growth factor ( EGF) peptide hormones. We show that Mg1a is a potent agonist of the mammalian EGF receptor ErbB1, and that intraplantar injection in mice causes long-lasting hypersensitivity of the injected paw. These data reveal a previously undescribed venom mode of action, highlight a role for ErbB receptors in mammalian pain signaling, and provide an example of molecular mimicry driven by defensive selection pressure.
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Authors | David A Eagles, Natalie J Saez, Bankala Krishnarjuna, Julia J Bradford, Yanni K-Y Chin, Hana Starobova, Alexander Mueller, Melissa E Reichelt, Eivind A B Undheim, Raymond S Norton, Walter G Thomas, Irina Vetter, Glenn F King, Samuel D Robinson |
Journal | Proceedings of the National Academy of Sciences of the United States of America
(Proc Natl Acad Sci U S A)
Vol. 119
Issue 7
(02 15 2022)
ISSN: 1091-6490 [Electronic] United States |
PMID | 35131940
(Publication Type: Journal Article)
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Copyright | Copyright © 2022 the Author(s). Published by PNAS. |
Chemical References |
- Ant Venoms
- Toxins, Biological
- Epidermal Growth Factor
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Topics |
- Amino Acid Sequence
- Animals
- Ant Venoms
(chemistry)
- Ants
(physiology)
- Drug Hypersensitivity
- Epidermal Growth Factor
(chemistry)
- Insect Bites and Stings
- Mice
- Molecular Mimicry
- Toxins, Biological
(chemistry)
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