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1.
Toxicon ; 82: 18-25, 2014 May.
Article in English | MEDLINE | ID: mdl-24561121

ABSTRACT

Ureases are multifunctional proteins that display biological activities independently of their enzymatic function, such as induction of exocytosis and insecticidal effects. Rhodnius prolixus, a major vector of Chagas' disease, is a model for studies on the entomotoxicity of jack bean urease (JBU). We have previously shown that JBU induces the production of eicosanoids in isolated tissues of R. prolixus. In insects, the immune response comprises cellular and humoral reactions, and is centrally modulated by eicosanoids. Cyclooxygenase products signal immunity in insects, mainly cellular reactions, such as hemocyte aggregation. In searching for a link between JBU's toxic effects and immune reactions in insects, we have studied the effects of this toxin on R. prolixus hemocytes. JBU triggers aggregation of hemocytes after injection into the hemocoel and when applied to isolated cells. On in vitro assays, the eicosanoid synthesis inhibitors dexamethasone (phospholipase A2 indirect inhibitor) and indomethacin (cyclooxygenase inhibitor) counteracted JBU's effect, indicating that eicosanoids, more specifically cyclooxygenase products, are likely to mediate the aggregation response. Contrarily, the inhibitors esculetin and baicalein were inactive, suggesting that lipoxygenase products are not involved in JBU's effect. Extracellular calcium was also necessary for JBU's effect, in agreement to other cell models responsive to ureases. A progressive darkening of the medium of JBU-treated hemocytes was observed, suggestive of a humoral response. JBU was immunolocalized in the cultured cells upon treatment along with cytoskeleton damage. The highest concentration of JBU tested on cultured cells also led to nuclei aggregation of adherent hemocytes. This is the first time urease has been shown to affect insect hemocytes, contributing to our understanding of the entomotoxic mechanisms of action of this protein.


Subject(s)
Arthropod Vectors/physiology , Canavalia/chemistry , Chagas Disease/transmission , Eicosanoids/toxicity , Hemocytes/drug effects , Rhodnius/physiology , Urease/toxicity , Animals , Canavalia/toxicity , Cell Aggregation/drug effects , Eicosanoids/biosynthesis , Larva , Primary Cell Culture
2.
Biomed Res Int ; 2013: 154542, 2013.
Article in English | MEDLINE | ID: mdl-24380079

ABSTRACT

Lectins are sugar-binding proteins widely distributed in nature with many biological functions. Although many lectins have a remarkable biotechnological potential, some of them can be cytotoxic. Thus, the aim of this study was to assess the toxicity of five lectins, purified from seeds of different species of Canavalia genus. In order to determine the toxicity, assays with Artemia nauplii were performed. In addition, a fluorescence assay was carried out to evaluate the binding of lectins to Artemia nauplii. In order to verify the relationship between the structure of lectins and their cytotoxic effect, structural analysis was carried out to evaluate the volume of the carbohydrate recognition domain (CRD) of each lectin. The results showed that all lectins exhibited different toxicities and bound to a similar area in the digestive tract of Artemia nauplii. Concerning the structural analysis, differences in spatial arrangement and volume of CRD may explain the variation of the toxicity exhibited by each lectin. To this date, this is the first study that establishes a link between toxicity and structure of CRD from Diocleinae lectins.


Subject(s)
Artemia/drug effects , Artemia/metabolism , Lectins/toxicity , Amino Acid Sequence , Animals , Artemia/chemistry , Canavalia/toxicity , Carbohydrates/chemistry , Lectins/chemistry , Lectins/metabolism , Seeds/chemistry
3.
Insect Biochem Mol Biol ; 41(6): 388-99, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21377528

ABSTRACT

Jackbean (Canavalia ensiformis) ureases are entomotoxic upon the release of internal peptides by insect's digestive enzymes. Here we studied the digestive peptidases of Oncopeltus fasciatus (milkweed bug) and its susceptibility to jackbean urease (JBU). O. fasciatus nymphs fed urease showed a mortality rate higher than 80% after two weeks. Homogenates of midguts dissected from fourth instars were used to perform proteolytic activity assays. The homogenates hydrolyzed JBU in vitro, yielding a fragment similar in size to known entomotoxic peptides. The major proteolytic activity at pH 4.0 upon protein substrates was blocked by specific inhibitors of aspartic and cysteine peptidases, but not significantly affected by inhibitors of metallopeptidases or serine peptidases. The optimal activity upon N-Cbz-Phe-Arg-MCA was at pH 5.0, with complete blockage by E-64 in all pH tested. Optimal activity upon Abz-AIAFFSRQ-EDDnp (a substrate for aspartic peptidases) was detected at pH 5.0, with partial inhibition by Pepstatin A in the pH range 2-8. Fluorogenic substrates corresponding to the N- and C-terminal regions flanking a known entomotoxic peptide within urease sequence were also tested. While the midgut homogenate did not hydrolyze the N-terminal peptide, it cleaved the C-terminal peptide maximally at pH 4.0-5.0, and this activity was inhibited by E-64 (10 µM). The midgut homogenate was submitted to ion-exchange chromatography followed by gel filtration. A 22 kDa active fraction was obtained, resolved in SDS-PAGE (12%), the corresponding band was in-gel digested by trypsin, the peptides were analyzed by mass spectrometry, retrieving a cathepsin L protein. The purified cathepsin L was shown to have at least two possible cleavage sites within the urease sequence, and might be able to release a known insecticidal peptide in a single or cascade event. The results suggest that susceptibility of O. fasciatus nymphs to jackbean urease is, like in other insect models, due mostly to limited proteolysis of ingested protein and subsequent release of entomotoxic peptide(s) by cathepsin-like digestive enzymes.


Subject(s)
Canavalia/toxicity , Insecticides/metabolism , Nymph/drug effects , Plant Proteins/metabolism , Protein Precursors/metabolism , Urease/metabolism , Amino Acid Sequence , Animals , Base Sequence , Canavalia/enzymology , Cathepsin L/chemistry , Cathepsin L/metabolism , Chromatography, Ion Exchange , Coumarins/pharmacology , Cysteine Proteinase Inhibitors/pharmacology , Digestion , Dipeptides/pharmacology , Electrophoresis, Polyacrylamide Gel , Heteroptera/drug effects , Heteroptera/enzymology , Hydrogen-Ion Concentration , Hydrolysis/drug effects , Insecticides/chemistry , Insecticides/isolation & purification , Insecticides/toxicity , Leucine/analogs & derivatives , Leucine/pharmacology , Molecular Sequence Data , Nymph/enzymology , Peptide Fragments/analysis , Plant Proteins/chemistry , Plant Proteins/isolation & purification , Plant Proteins/toxicity , Protein Precursors/chemistry , Protein Precursors/isolation & purification , Protein Precursors/toxicity , Urease/chemistry , Urease/isolation & purification , Urease/toxicity
4.
Vet Hum Toxicol ; 45(1): 10-3, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12583688

ABSTRACT

The effect of raw jackbean (Canavalia ensiformis) or limabean (Phaseolus lunatus) seeds at 0, 250 or 500 g/kg in broiler chick diets for 28 d on performance and cytopathological changes in internal organs was evaluated. Relative pancreas weight increased significantly (P < 0.05) and the lungs had severe atelectasis, thickening of the alveolar septa and bronchiolar epithelial hyperplasia. Slight hemorrhages were in the intestinal walls of growing chicks fed 250 g/kg or 500 g/kg of jackbean and limabean, respectively. The livers had marked congestion of the sinusoids and centrolobular veins, while the kidneys had distension of the capillary vessels with numerous thrombi. The structural alterations in the internal organs of chicks fed the plant seeds were attributed to allelochemicals in the seeds.


Subject(s)
Canavalia/toxicity , Chickens , Phaseolus/toxicity , Animal Feed/toxicity , Animals , Kidney/drug effects , Liver/drug effects , Lung/drug effects , Pancreas/drug effects , Seeds
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