Preservation of immunoreactivity and fine structure of adult C. elegans tissues using high-pressure freezing.

The location of a protein labeled by immunogold techniques can be resolved under an electron beam to within nanometers of its epitope, a resolution that makes immunoelectron microscopy a valuable tool for studies of cell biology. However, tissues in the nematode Caenorhabditis elegans are difficult to preserve for immunoelectron microscopic studies. The animal's cuticle slows the diffusion of solutions into the animal and thus makes it difficult to preserve both immunoreactivity and cell morphology. Here we describe a protocol that circumvents these problems. Specifically, we instantly immobilized tissue in vitreous ice by freezing living adult animals under high pressure. Frozen specimens were then chemically fixed, dehydrated, and embedded at low temperatures. As a result, chemical diffusion across the cuticle could occur over an extended period without morphological deterioration. We show that this method is capable of preserving both cell morphology, including fine structures, and immunoreactivity. Therefore, it provides a means to characterize the localization of endogenous proteins and exogenous proteins, such as the green fluorescent protein (GFP), with respect to subcellular compartments in C. elegans tissues by using postembedding immunogold labeling.     

Characterization of cadmium desorption in soils and its relationship to plant uptake and cadmium leaching

Experiments on Cd desorption were conducted with a range of water-to-soil ratios to assess the desorption characteristics of Cd in soils and the availability of Cd for absorption by plant roots and leaching to groundwater, Soil samples were collected from sites contaminated by a former Pb and Zn smelter, by sewage irrigation, or with artificial additions of Cd and sewage sludge. Glasshouse pot experiments were conducted in which the yield and Cd uptake of crop plants were determined. Cadmium leached from soil columns was also studied using soil lysimeters. The soil solution Cd concentration decreased with increasing solution-to-soil ratio and followed a negative power function. Two constants obtained from logarithmic linear regression were identified. The intercept (C₁) was Cd concentration in the soil solution where the solution/soil ratio was equal to 1 and this constant was the intensity factor of the initial element supply in the soil. The slope (a) showed a decreasing trend for Cd concentration in the soil solution which was related to the soil buffering capacity. A corrected concentration (C₁/a) is proposed for expressing soil desorption ability. This combined index was significantly correlated with Cd uptake by plants and also with Cd leached from soil columns.     

How food type and brood influence foraging decisions of Lasius niger scouts

We investigated how the type of food (sucrose or protein) and the presence of brood influence foraging decisions of Lasius niger L. scouts. In particular, we studied whether and how these parameters alter the drinking behaviour of scouts and the allocation of workers to food retrieving and recruiting tasks. We analysed drinking and recruiting behaviour of single scouts from nests with or without brood that encountered a proteinaceous or sucrose droplet. A substantial fraction of scouts encountering a proteinaceous droplet did not ingest it and did not then return to the nest whereas nearly all drank at sugar droplets; brood presence did not influence this decision. Once an ant started drinking, it needed to drink a critical volume before returning to the nest; this critical volume did not depend on the type of food and the presence of brood. Scouts laid a trail only if they returned to the colony. Food type and brood presence altered the proportion of individuals that laid a trail but not the individual trail-laying intensity. We discuss the consequences of this decision system through simple individual assessments and decision rules, with regard to the self-organized foraging patterns of this species and the efficient collective exploitation of natural resources.     

High-yield expression and purification of soluble forms of the anti-apoptotic Bcl-x(L) and Bcl-2 as TolAIII-fusion proteins

A method is presented to produce large amounts of Bcl-2 and Bcl-x_L, two anti-apoptotic proteins of considerable biomedical interest. Expression constructs were prepared in which the Escherichia coli protein TolAIII, known to promote over expression of soluble product, was added to the N-terminus of Bcl-2 or Bcl-x_L proteins, which had their C-terminal hydrophobic anchors deleted. Here the expression of these TolAIII-fusion constructs, followed by a two-step metal-affinity based purification protocol is described. The method delivers at least 20 and 10 mg of more than 90% pure TolAIII-Bcl-x_LΔC and TolAIII-Bcl-2(2)ΔC proteins, respectively, per liter of E. coli cell culture. The proteins are released by proteolysis with thrombin providing >12 mg of Bcl-x_LΔC or >6 mg of Bcl-2(2)ΔC per liter of E. coli cell culture with a purity of more than 95%. Whereas Bcl-x_LΔC is soluble both before and after TolAIII removal, Triton X-100 can significantly increase the extraction of TolAIII- Bcl-2(2)ΔC from the bacterial cells and its subsequent solubility. Far-UV CD spectroscopy demonstrated that they both have an α-helical structure. Fluorescence spectroscopy was used to quantitatively analyze the binding of the respiratory inhibitor antimycin A to recombinant Bcl-2 and Bcl-x_L proteins as well as the displacement of this ligand from the hydrophobic pocket with BH3 Bad-derived peptide. Purified Bcl-x_LΔC and Bcl-2(2)ΔC both protect isolated mitochondria from Bax-induced release of cytochrome c. The ensemble of data shows that the expressed proteins are correctly folded and functional. Therefore, the TolAIII-fusion system provides a convenient tool for functional characterization and structural studies of anti-apoptotic proteins.     

Analysis of non-TIR NBS-LRR resistance gene analogs in <Emphasis Type="Italic">Musa acuminata</Emphasis> Colla: Isolation,RFLP marker development,and physical mapping

Background  

Many commercial banana varieties lack sources of resistance to pests and diseases, as a consequence of sterility and narrow genetic background. Fertile wild relatives, by contrast, possess greater variability and represent potential sources of disease resistance genes (R-genes). The largest known family of plant R-genes encode proteins with nucleotide-binding site (NBS) and C-terminal leucine-rich repeat (LRR) domains. Conserved motifs in such genes in diverse plant species offer a means for isolation of candidate genes in banana which may be involved in plant defence.     

Age and experience influence patch assessment for oviposition by an insect predator

Abstract.  1. Dynamic models of optimal foraging predict that an animal's decision to accept or reject a patch depends not only on the environment and patch quality, but also on its internal state. Previous experiments have shown that the two-spot ladybird beetle, Adalia bipunctata (L.), is reluctant to lay eggs in a patch of prey contaminated by the oviposition-deterring pheromone produced by conspecific larvae.
2. An experiment was conducted to test whether the internal state of an A. bipunctata female affects its oviposition response to oviposition-deterring pheromone. Firstly, the oviposition response to oviposition-deterring pheromone of young and old females was compared. Secondly, the oviposition response to oviposition-deterring pheromone of females previously exposed continuously to oviposition-deterring pheromone was compared with that of females of the same age but with no previous experience of oviposition-deterring pheromone.
3. Old females and females with previous experience of oviposition-deterring pheromone were less reluctant to lay eggs in the presence of oviposition-deterring pheromone than young and naive females. These results are consistent with the predictions of optimal foraging theory.     

The Israeli strain IS-98-ST1 of West Nile virus as viral model for West Nile encephalitis in the Old World

West Nile virus (WNV) recently became a major public health concern in North America, the Middle East, and Europe. In contrast with the investigations of the North-American isolates, the neurovirulence properties of Middle-Eastern strains of WNV have not been extensively characterized. Israeli WNV strain IS-98-ST1 that has been isolated from a white stork in 1998, was found to be highly neuroinvasive in adult C57BL/6 mice. Strain IS-98-ST1 infects primary neuronal cells from mouse cortex, causing neuronal death. These results demonstrate that Israeli strain IS-98-ST1 provides a suitable viral model for WNV-induced disease associated with recent WNV outbreaks in the Old World.     

Carbonic anhydrase inhibitors: design of spin-labeled sulfonamides incorporating TEMPO moieties as probes for cytosolic or transmembrane isozymes

A series of spin-labeled sulfonamides incorporating TEMPO moieties were synthesized by a procedure involving the formation of a thiourea functionality between the benzenesulfonamide and free radical fragment of the molecules. The new compounds were tested as inhibitors of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1) and showed efficient inhibition of the physiologically relevant isozymes hCA II and hCA IX (hCA IX being predominantly found in tumors) and moderate to weak inhibitory activity against hCA I. Some derivatives were also selective for inhibiting the tumor-associated isoform over the cytosolic one CA II, and presented significant changes in their ESR signals when complexed to the enzyme active site, being interesting candidates for the investigation of hypoxic tumors overexpressing CA IX by ESR techniques, as well as for imaging/treatment purposes.     

Anterior pituitary pyroglutamyl peptidase II activity controls TRH-induced prolactin release

Ecto-peptidases modulate the action of peptides in the extracellular space. The relationship between peptide receptor and ecto-peptidase localization, and the physiological role of peptidases is poorly understood. Current evidence suggests that pyroglutamyl peptidase II (PPII) inactivates neuronally released thyrotropin-releasing hormone (TRH). The impact of PPII localization in the anterior pituitary on the endocrine activities of TRH is unknown. We have studied whether PPII influences TRH signaling in anterior pituitary cells in primary culture. In situ hybridization (ISH) experiments showed that PPII mRNA was expressed only in 5-6% of cells. ISH for PPII mRNA combined with immunocytochemistry for prolactin, beta-thyrotropin, or growth hormone, showed that 66% of PPII mRNA expressing cells are lactotrophs, 34% somatotrophs while none are thyrotrophs. PPII activity was reduced using a specific phosphorothioate antisense oligodeoxynucleotide or inhibitors. Compared with mock or scrambled oligodeoxynucleotide-treated controls, knock-down of PPII expression by antisense targeting increased TRH-induced release of prolactin, but not of thyrotropin. Similar data were obtained with either a transition-state or a tight binding inhibitor. These results demonstrate that PPII expression in lactotrophs coincides with its ability to control prolactin release. It may play a specialized role in TRH signaling in the anterior pituitary. Anterior pituitary ecto-peptidases may fulfill unique functions associated with their restricted cell-specific expression.