Parasitoid assemblages of soybean defoliator Lepidoptera in north-western Buenos Aires province, Argentina

1 The objective of this study was to examine the structure of parasitoid assemblages attacking soybean defoliator Lepidoptera in north-western Buenos Aires province, Argentina. 2 Through larvae sampling from 1992 to 1996, and laboratory data plus the known biology of the species recorded during the study, parasitoid species composition, richness, number of guilds per host species, and levels of parasitism, were determined. 3 Total species richness was 23, all species were primary endoparasitoids, and categorized as koinobionts. They belonged to Hymenoptera (11 species) and Diptera (12 species). Rachiplusia nu (Noctuidae) hosted the highest number of parasitoid species. 4 Four parasitoid guilds were recorded for R. nu (egg–prepupal endoparasitoid, early larval endoparasitoid, late larval endoparasitoid, and larval–pupal endoparasitoid); two for Spilosoma virginica (Arctiidae) (late larval endoparasitoid and larval–pupal endoparasitoid) and Colias lesbia (Pieridae) (early larval endoparasitoid and larval–pupal endoparasitoid); and one for Anticarsia gemmatalis (Noctuidae) and Loxostege biffidalis (Pyralidae) (early larval endoparasitoid). 5 Only four out of seven potential parasitoid guilds defined for Lepidoptera were recorded in a soybean agroecosystem located in north-western Buenos Aires province, suggesting that potential host niches were not totally utilized. 6 Soybean lepidopteran defoliators supported a mean species richness of 4.8 parasitoids, a result that is similar to that reported for exophytic hosts in the Neotropics. 7 Parasitoid assemblages from each host differed in species composition, richness, number of guilds, and levels of parasitism.     

Regulation of Newly Evolved Enzymes. III Evolution of the ebg Repressor during Selection for Enhanced Lactase Activity

The evolution of lactose utilization by lacZ deletion strains of E. coli occurs via mutations in the ebg genes. We show that one kind of mutation in the regulatory gene ebgR results in a repressor which retains the ability to repress synthesis of ebg enzymes, but which permits 4.5-fold more ebg enzyme synthesis during lactose induction than does the wild-type repressor. A comparison between the growth rate of various ebg+ strains on lactose and the amount of ebg enzyme synthesized by these strains shows that the rate of enzyme synthesis permitted by the wild-type repressor is insufficient for growth on lactose as a sole carbon source by a cell with the most active ebg lactase yet isolated. We conclude, therefore, that the evolution of lactose utilization requires both a structural and a regulatory mutation.     

Enhanced alternative oxidase and antioxidant enzymes under Cd<Superscript>2+</Superscript> stress in <Emphasis Type="Italic">Euglena</Emphasis>

To identify some of the mechanisms involved in the high resistance to Cd²⁺ in the protist Euglena gracilis, we studied the effect of Cd²⁺ exposure on its energy and oxidative stress metabolism as well as on essential heavy metals homeostasis. In E. gracilis heterotrophic cells, as in other organisms, CdCl₂ (50 μM) induced diminution in cell growth, severe oxidative stress accompanied by increased antioxidant enzyme activity and strong perturbation of the heavy metal homeostasis. However, Cd²⁺ exposure did not substantially modify the cellular respiratory rate or ATP intracellular level, although the activities of respiratory complexes III and IV were strongly decreased. In contrast, an enhanced capacity of the alternative oxidase (AOX) in both intact cells and isolated mitochondria was determined under Cd²⁺ stress; in fact, AOX activity accounted for 69-91% of total respiration. Western blotting also revealed an increased AOX content in mitochondria from Cd²⁺-exposed cells. Moreover, AOX was more resistant to Cd²⁺ inhibition than cytochrome c oxidase in mitochondria from control and Cd²⁺-exposed cells. Therefore, an enhanced AOX seems to be a relevant component of the resistance mechanism developed by E. gracilis against Cd²⁺-stress, in addition to the usual increased antioxidant enzyme activity, that enabled cells to maintain a relatively unaltered the energy status.     

Nuclear Ca2+ regulates cardiomyocyte function.

In the heart, cytosolic Ca(2+) signals are well-characterized events that participate in the activation of cell contraction. In contrast, nuclear Ca(2+) contribution to cardiomyocyte function remains elusive. Here, we examined functional consequences of buffering nuclear Ca(2+) in neonatal cardiomyocytes. We report that cardiomyocytes contain a nucleoplasmic reticulum, which expresses both ryanodine receptor (RyR) and inositol 1,4,5-trisphosphate receptor (InsP(3)R), providing a possible way for active regulation of nuclear Ca(2+). Adenovirus constructs encoding the Ca(2+) buffer protein parvalbumin were targeted to the nucleus with a nuclear localization signal (Ad-PV-NLS) or to the cytoplasm with a nuclear exclusion signal (Ad-PV-NES). A decrease in the amplitude of global Ca(2+) transients and RyR-II expression, as well as an increase in cell beating rate were observed in Ad-PV-NES and Ad-PV-NLS cells. When nuclear Ca(2+) buffering was imposed nuclear enlargement, increased calcineurin expression, NFAT translocation to the nucleus and subcellular redistribution of atrial natriuretic peptide were observed. Furthermore, prolongation of action potential duration occurred in adult ventricular myocytes. These results suggest that nuclear Ca(2+) levels underlie the regulation of specific protein targets and thereby modulate cardiomyocyte function. The local nuclear Ca(2+) signaling and the structures that control it constitute a novel regulatory motif in the heart.     

VuNIP1 (NOD26-like) and VuHSP17.7 gene expression are regulated in response to heat stress in cowpea nodule

In tropical areas, high soil temperatures frequently limit biological nitrogen fixation (BNF) activity in a number of legumes species. In contrast with other legumes growing under BNF, cowpea (Vigna unguiculata) nodules are very resistant to high-temperature stress. However, the molecular basis of nodule heat tolerance remains unclear. In order to identify genes involved in the heat stress response in cowpea nodules a cDNA library was screened with cDNA-AFLP derived probes. Two full-length cDNAs corresponding to a small heat shock protein (VuHSP17.7) and to a Nodulin 26 (VuNIP1) were isolated and characterized. VuHSP17.7 encodes a sHSP family class I protein, and VuNIP1 corresponds to a NOD26-like protein, member of NIP subfamily of plant membrane intrinsic protein (MIP). VuHSP17.7 was highly induced by high-temperature stress in nodule, leaves, flower, and bud flower, and VuNIP1 was repressed in nodule after heat stress. Moreover, the spatial expression pattern of VuNIP1 and VuHSP17.7 differs significantly indicating that distinct signaling pathways under heat stress may regulate the expression of these genes.     

Activation of phosphatidylcholine signalling during oxidative stress in synaptic endings

The purpose of the present study was to investigate the involvement of phosphatidylcholine (PC) signalling in synaptic endings incubated under oxidative stress conditions. Synaptosomes purified from adult rats (4 months old) cerebral cortex were exposed to oxidative insult (FeSO₄, 50 μM) or vehicle, and diacylglycerol (DAG) generation and free fatty acid (FFA) release were subsequently evaluated using exogenous [¹⁴C]PC as substrate. DAG formation increased after 5, 30, and 60 min of Fe²⁺-exposure with respect to the control conditions. The contribution of PC-specific phospholipase C (PC-PLC) and phospholipase D (PLD) pathways to DAG generation was evaluated using ethanol in the enzyme assays. Phosphatidylethanol (PEth) production was measured as a marker of PLD activity. In the presence of ethanol (2%) iron significantly stimulated DAG and PEth production at all times assayed. FFA release from PC, however, was inhibited after 5 and 60 min of iron exposure. Similar results were observed in aged animals (28 months old) when compared with adult animals. DAG generation from PC was also evaluated in the presence of the tyrosine kinase inhibitors genistein and herbimycin A. Inhibition of tyrosine kinase activity did not modify the stimulatory effect exerted by iron on PC-PLC and PLD activities. Moreover, the presence of LY294002 (a specific PI3K inhibitor) did not alter DAG production. Our results demonstrate that oxidative stress induced by free iron stimulates the generation of the lipid messenger DAG from PC in synaptic endings in adult and aged rats.