6533b7d0fe1ef96bd125a4ca

RESEARCH PRODUCT

Haemolytic activity and characterization of nematocyst venom fromPelagia noctiluca(Cnidaria: Scyphozoa)

Maria MaisanoVincenzo ParrinoAntonino NatalottoGigliola BenenatiMaria Rosa TrapaniAngela MauceriAlessia D'agataMatteo CammarataMaria Giovanna ParisiTiziana Cappello

subject

biologyVenomScyphozoaAnatomybiology.organism_classificationPelagia noctilucaHaemolysischemistry.chemical_compoundBiochemistrychemistryCrude venom; haemolysis; HPLC analysis; nematocysts; Pelagia noctilucaCrude venom haemolysis HPLC analysis nematocysts Pelagia noctilucaAnimal Science and ZoologyNematocystCnidocyteSodium dodecyl sulfatePolyacrylamide gel electrophoresis

description

We investigated the haemolytic capacity of the crude venom extracted from isolated nematocysts of Pelagia noctiluca (Cnidaria: Scyphozoa), and evidenced the proteic fractions responsible for this activity. The nematocyst venom was used at various concentrations to evaluate the haemolytic activity and the lysosomal membrane stability of red blood cells of two teleostean species treated with the extract. The nematocyst extract was assayed against erythrocytes of the two teleostean species living in different environments, Carassius auratus as a common freshwater species, and Liza aurata as a representative of seawater species. Experiments on the haemolytic activity of P. noctiluca in the presence of lipid components of erythrocyte membranes showed that sphyngomyelin strongly inhibited this activity. The crude venom was analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis SDS-PAGE and high performance liquid chromatography (HPLC) to detect the proteic composition, and it was found that the active haemolytic components of this venom are distributed in at least four protein fractions. The results of our experiments indicated that Pelagia noctiluca venom induces haemolysis and lysosomal membrane destabilisation in both species and that Carassius auratus was more susceptible to jellyfish venom than was Liza aurata. No significant differences in glutathione (GSH) levels were observed between control and treatments; consequently the toxins do not cause the oxidative stress but likely recognize specific targets (i.e. sphyngomyelin) in the plasmatic membrane of red blood cells.

https://doi.org/10.1080/11250003.2012.758782