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dc.date.accessioned 2013-09-20T14:20:30Z
dc.date.available 2013-09-20T14:20:30Z
dc.date.issued 2013
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/29550
dc.description.abstract Although most eggs are intensely predated, the aerial egg clutches from the aquatic snail Pomacea canaliculata have only one reported predator due to unparalleled biochemical defenses. These include two storage-proteins: ovorubin that provides a conspicuous (presumably warning) coloration and has antinutritive and antidigestive properties, and PcPV2 a neurotoxin with lethal effect on rodents. We sequenced PcPV2 and studied whether it was able to withstand the gastrointestinal environment and reach circulation of a potential predator. Capacity to resist digestion was assayed using small-angle X-ray scattering (SAXS), fluorescence spectroscopy and simulated gastrointestinal proteolysis. PcPV2 oligomer is antinutritive, withstanding proteinase digestion and displaying structural stability between pH 4.0-10.0. cDNA sequencing and protein domain search showed that its two subunits share homology with membrane attack complex/perforin (MACPF)-like toxins and tachylectin-like lectins, a previously unknown structure that resembles plant Type-2 ribosome-inactivating proteins and bacterial botulinum toxins. The protomer has therefore a novel AB toxin combination of a MACPF-like chain linked by disulfide bonds to a lectin-like chain, indicating a delivery system for the former. This was further supported by observing PcPV2 binding to glycocalix of enterocytes in vivo and in culture, and by its hemaggutinating, but not hemolytic activity, which suggested an interaction with surface oligosaccharides. PcPV2 is able to get into predator's body as evidenced in rats and mice by the presence of circulating antibodies in response to sublethal oral doses. To our knowledge, a lectin-pore-forming toxin has not been reported before, providing the first evidence of a neurotoxic lectin in animals, and a novel function for ancient and widely distributed proteins. The acquisition of this unique neurotoxic/antinutritive/storage protein may confer the eggs a survival advantage, opening new perspectives in the study of the evolution of animal defensive strategies. en
dc.language en es
dc.subject Caracoles es
dc.subject predadores es
dc.subject Neurotoxinas es
dc.subject defensa bioquímica es
dc.title Novel animal defenses against predation: a snail egg neurotoxin combining lectin and pore-forming chains that resembles plant defense and bacteria attack toxins en
dc.type Articulo es
sedici.identifier.uri http://www.plosone.org/article/comments/info%3Adoi%2F10.1371%2Fjournal.pone.0063782 es
sedici.identifier.other eid:2-s2.0-84878550608
sedici.identifier.other https://doi.org/10.1371/journal.pone.0063782
sedici.identifier.issn 1932-6203 es
sedici.creator.person Dreon, Marcos Sebastián es
sedici.creator.person Frassa, María Victoria es
sedici.creator.person Ceolín, Marcelo Raúl es
sedici.creator.person Ituarte, Santiago es
sedici.creator.person Qiu, Jian-Wen es
sedici.creator.person Sun, Jin es
sedici.creator.person Fernández, Patricia Elena es
sedici.creator.person Heras, Horacio es
sedici.subject.materias Ciencias Veterinarias es
sedici.subject.materias Ciencias Médicas es
sedici.description.fulltext true es
mods.originInfo.place Facultad de Ciencias Veterinarias es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution 2.5 Argentina (CC BY 2.5)
sedici.rights.uri http://creativecommons.org/licenses/by/2.5/ar/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle PLoS ONE es
sedici.relation.journalVolumeAndIssue vol. 8, no. 5 es


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Creative Commons Attribution 2.5 Argentina (CC BY 2.5) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution 2.5 Argentina (CC BY 2.5)