ABSTRACT

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Volatile organic compounds (VOCs) emitted from plants in response to insect infestation can function as signals for the attraction of predatory/parasitic insects and/or repulsion of herbivores. VOCs also may play a role in intra- and inter-plant communication. In this work, the kinetics and composition of VOC emissions produced by tomato (Solanum lycopersicum) plants infested with the greenhouse whitefly Trialeurodes vaporariorum was determined within a 14 days period. The VOC emission profiles varied concomitantly with the duration of whitefly infestation. A total of 36 different VOCs were detected during the experiment, 26 of which could be identified: 23 terpenoids, plus decanal, decane, and methyl salicylate (MeSA). Many VOCs were emitted exclusively by infested plants, including MeSA and 10 terpenoids. In general, individual VOC emissions increased as the infestation progressed, particularly at 7 days post-infestation (dpi). Additional tunnel experiments showed that a 3 days exposure to VOC emissions from whitefly-infested plants significantly reduced infection by a biotrophic bacterial pathogen. Infection of VOC-exposed plants induced the expression of a likely tomato homolog of a methyl salicylate esterase gene, which preceded the expression of pathogenesis-related protein genes. This expression pattern correlated with reduced susceptibility in VOC-exposed plants. The observed cross-kingdom effect of plant-plant signaling via VOCs probably represents a generalized defensive response that contributes to increased plant fitness, considering that resistance responses to whiteflies and biotrophic bacterial pathogens in tomato share many common elements.

Cell-surface viral proteins most frequently enter the cell through clathrin or caveolae endocytosis. Respiratory syncytial virus antigen internalization by immune cells is via caveolin, however, uptake of paramyxovirus cell membrane proteins by non-immune cells is done through clathrin-coated pits. In this work, the uptake of respiratory syncytial virus cell surface glycoproteins by non-immune human epithelial cells was investigated through indirect immunofluorescence with polyclonal anti-RSV antibody and confocal lasser-scanner microscopy. Clathrin and caveolae internalization pathways were monitored through specific inhibitors monodansylcadaverine (MDC) and methyl-beta-cyclodextrin (MBCD), respectively. Internalization of RSV antigens was inhibited by MDC but not by MBCD, implying that clathrin-mediated endocytosis is the major uptake route of RSV antigens by an epithelial human cell line.

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BACKGROUND: Intraguild predation (IGP), predation between species that use a common resource, can affect the populations of a pest, of the pest's natural enemy (IG prey) and of the predator of the pest's natural enemy (IG predator). In this study, we determined whether the parasitoid Eretmocerus eremicus (Hymenoptera: Aphelinidae) (IG prey), modifies its foraging behaviour under the risk of IGP by Macrolophus pygmaeus (Hemiptera: Miridae) (IG predator). Parasitoid behaviour was analysed using two bioassays (choice and no-choice) with the following treatments: (i) control, tomato leaf infested with whitefly nymphs; and (ii) PEP, tomato leaf infested with whitefly nymphs and previously exposed to the IG predator; and (iii) PP, tomato leaf infested with whitefly nymphs, with both, the IG predator and the IG prey present. RESULTS:In both bioassays, we found that E. eremicus did not significantly modify the number of ovipositions, time of residence, duration of oviposition or behavioural sequence. However, in the no-choice bioassay, the number of attacks was higher and their duration shorter in the PEP treatment than in the control. CONCLUSION: Our results indicate that the parasitoid may detect IGP risk to a certain extent, but it did not significantly modify its foraging behaviour, suggesting that simultaneous release of the two natural enemies can be successfully employed.

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