Impact of a glossy collard trap crop on diamondback moth adult movement, oviposition, and larval survival

One component of developing a systematic approach for deployment of trap crops is to understand how the trap crop modifies pest behavior. Glossy‐leafed collards, Brassica oleracea L. var. acephala (Brassicaceae), were evaluated as a potential trap crop for diamondback moth, Plutella xylostella (L.) (Lepidoptera: Plutellidae), because they are attractive to P. xylostella adults and are a poor host for P. xylostella larvae compared to cabbage, Brassica oleracea L. var. capitata. We used large field plots to measure the changes in adult, egg, and larval P. xylostella densities in cabbage when the trap crop was planted in the field. Furthermore, we planted the trap crop in dispersed and concentrated spatial arrangements to determine the impact of trap crop arrangement on the behavior of P. xylostella. In 2002, results showed that the presence of collards within a cabbage field reduced larval density on cabbage. In 2003, neither trap crop arrangement had a significant impact on P. xylostella larval density on cabbage. Adult moths aggregated in proximity to collards in 2002, but not in 2003. Egg and larval data in both years in all treatments showed that total oviposition was highest near a central release point, indicating that females lay many eggs before dispersing very far when suitable host plants are available. The mean direction of P. xylostella movement and oviposition from a central release point was not consistent or correlated to wind direction. Plant size of the trap crop in relation to the main crop and environmental factors may have been responsible for the inconsistent effectiveness of the trap crop.     

Differential binding of lectins IL-2 and CSL to candida albicans and cancer cells

The demonstration that interleukin 2 (IL-2) is a lectin specific for oligomannosides allows to understand a new function for this cytokine: as a bifunctional molecule when bound to its receptor ss, IL-2 associates the latter which the CD3/TCR complex, interacting with oligosaccharides of CD3 through its carbohydrate-recognition domain (Zanetta et al. , 1996, Biochem. J., 318, 49-53). This induces the tyrosine phosphorylation of the IL-2R beta by ++p56(lck) , the first step of the IL-2-dependent signaling. Since this specific association is disrupted in vitro by oligomannosides with five and six mannose residues, we made the hypothesis that pathogenic cells or microorganisms could bind IL-2, consequently disturbing the IL-2- dependent response. This study shows that the pathogenic yeast Candida albicans (in contrast with nonpathogenic yeasts) binds high amounts of IL-2 as did cancer cells. In contrast with cancer cells, yeasts do not bind the Man6GlcNAc2-specific lectin CSL, an endogenous "amplifier of activation signals" (Zanetta et al. , 1995, Biochem. J., 311, 629-636).