Edematogenic and myotoxic activities of the duvernoy’s gland secretion of <i>Philodryas olfersii</i> from the north-east region of Argentina

Philodryas olfersii is found in South America, from Amazonas to Patagonia. It is important to characterize the venom of P. olfersii, who inhabits the North-East region of Argentina, since snake venoms are known to exhibit considerable variability in composition and biological activities. In this work, mice weighing 18-20 g (n = 4 for each experimental group) were used. For the edematogenic activity mice were injected s.c. in the right foot pad with 50 µl of solutions containing different amounts of venom, whereas the left foot pad was injected with 50 µl of PBS. Two hours after injection mice were killed by cervical dislocation and both feet were cut off and weighed individually. For the myotoxic activity mice were injected i.m. with 100 µl of solutions containing 40 µg of venom. Blood samples were extracted after 1, 3, 6, 8, 10, 12, 14, 16 and 24 h of venom injection to determinate serum CPK activity and mice were sacrificed at the same time intervals to obtain the inoculated gastrocnemius muscle. They were fixed with Bouin solution and stained with Hematoxylin-Eosin. Results showed that P. olfersii venom exhibits a high edematogenic activity (MED = 0.31 µg) and a moderate myotoxic activity. Myonecrosis reached its highest level after 12 h of venom injection as shown by plasmatic CPK levels (5,401 ± 330 IU/l) and microscopic assay. It demonstrates the potential toxicity of the venom of P. olfersii, who inhabits the North-East region of Argentina. It also reinforces the original warning concerning the potential danger of bites by colubrids.     

Growth, photosynthesis and cropping of potted grapevines (Vitis vinifera L. cv. Cabernet Sauvignon) in relation to shoot trimming

The present study was conducted to evaluate how changes in leaf area affected vine growth, yield and grape quality of five‐year‐old potted Cabernet Sauvignon grapevines. At the beginning of flowering vines were randomly assigned to the following five treatments: untrimmed (control); shoot trimmed at either node 12 (T12) or node 6 (T6) with laterals either retained (R) or excised (X). Those four manipulations are abbreviated to: T12LR, T12LX, T6LR and T6LX, respectively. Total leaf area per vine was significantly lowered in T12LX and T6LX as compared to the other treatments, whereas lateral formation was able to offset foliage loss due to trimming in T12LR and T6LR with respect to control vines. T6LR also showed a more prolonged lateral node production. Yield per vine and its components did not differ significantly among treatments except for berry size, which was reduced in T6LR and T6LX. Grape ripening was severely retarded in T6LX, as shown by lower Brix, pH, colour and phenolics, and higher TA, tartrate and malate. A maturity delay was also shown in T6LR as lower soluble solids and total anthocyanins per berry in comparison with untrimmed vines. No difference in grape quality versus control was shown by the T12 treatments. Post‐trimming assimilation rates (A) clearly indicated a large compensation capacity of retained main leaves despite their mean age being higher than that calculated for main leaves sampled the same day on control vines. The assimilation rates recorded on lateral leaves increased proportionally with lateral shoot size and inversely to the number of main leaves retained with trimming. Based on present results, both the area and photosynthetic effectiveness of source leaves will drive overall vine responses to shoot trimming. For example, T6LX showed the worst performance with respect to the other treatments, in agreement with lowest leaf area, leaf‐to‐fruit ratio and oldest canopy. However, T6LR had a somewhat retarded ripening despite its non‐limiting leaf‐to‐fruit ratio, relatively young canopy and maximum whole‐canopy photosynthesis and efficiency at veraison. Under such circumstances, duration of growth and possible competition with the berry sugaring process may have played a role.     

Ultrastructure of the ovariole sheath in <i>Diatraea saccharalis</i> (Lepidoptera: Pyralidae)

The ultrastructure of the ovariole sheath along the Diatraea saccharalis ovariole was studied by scanning and transmission electron microscopy. Each ovariole is surrounded by an epithelial sheath, a tunica propria and scattered lumen cells. These three components of the ovariole sheath show different ultrastructural features along the ovariole, in the germarium or in the vitellarium; these differences are more evident in the epithelial sheath cells. The epithelial sheath is composed by two layers of cells, the external one running longitudinally and the internal one running circularly in the ovariole. These cells, in vitellarium, present cytoplasmic bundles of myofilaments that are arranged parallel to the long axis of the cells; these myofilaments are apparently related to the contraction movements of the follicles within the ovariole. The acellular tunica propria, composed of finely filamentous material, is attached to the adjacent follicle cells by adhesive dense plates. Between the epithelial sheath and the tunica propria there is a population of lumen cells, with morphological features of secretory activity     

Fractions of a chloroform extract of ajenjo leaves (<i>Artemisia mendozana</i> DC. var. <i>mendozana</i>) inhibit the proliferation,viability and clonogenicity of B16-F0 melanoma cells

The ajenjo, Artemisia mendozana DC. var. mendozana (Asteraceae), grows in the Andean foothills of Mendoza and San Juan, Argentina, and is used as a medicinal plant for its antispasmodic and antifungal properties. The aim of this work was to obtain fractions of a chloroform extract of ajenjo leaves and to evaluate the in vitro effects on proliferation, viability and clonogenicity of B16-F0 melanoma cells. Using a silica gel chromatography column, 120 fractions were collected and grouped according to the chromatographic profile in 9 main fractions (F1–F9). Their major compounds identified were: terpenes (F1), terpenes and sesquiterpene lactones (F2–F3), sesquiterpenes (F4–F6) and phenols and sesquiterpenes (F7-9). B16-F0 cells were incubated for 72 h with DMSO (vehicle) or 0.1 mg/ml F1–F9. At 72 h of culture, F1 decreased both the growing index (GI) and cell viability. F2 and F3 both decreased GI and only F3 decreased clonogenic activity. F4 and F5 both decreased GI. Only F5 decreased cell viability and F4 decreased clonogenicity. Consequently, fractions F6–F8 did not affect any of the cell parameters assayed, while F9 decreased cell viability and inhibited clonogenicity.     

A simple and rapid antibody-capture ELISA for the detection of staphylococcal enterotoxin A in food including a simple extraction step

A sensitive and precise ELISA for the detection of staphylococcal enterotoxin A in food has been developed, using specific IgG anti-toxin antibodies purified from immunized rabbits. an antibody capture format was found to be the most useful following cross-reaction and sensitivity studies. the ELISA was used to investigate concentration of staphylococcal enterotoxin A from food samples by polyethylene glycol dialysis. the procedure was shown to be inefficient and highly variable, as well as time-consuming. Direct analysis of aqueous food extracts without a concentration step was found to be possible. With an assay time of 140 min, the ELISA detection limit was 12.5 pg of toxin (corresponding to a sensitivity of 0.5 ngg^-1 of food sample.     

Interleukin-1β regulates metalloproteinase activity and leptin secretion in a cytotrophoblast model

Implantation is one of the most regulated processes in human reproduction, by endocrine and immunological systems. Cytokines are involved in embryo-maternal communication and an impaired balance could result in pregnancy loss. Here we investigated the effect of interleukin 1-β on the activity of two important metalloproteinases (MMP-2 and MMP-9) that are involved in extracellular matrix remodeling as well as the secretion of leptin, one of the reproductive hormones actively regulating their activity and secretion. We found that IL-1β activates matrix metalloproteinase activity as well as increases leptin secretion. We propose that this interleukin, through the regulation of leptin, in turn activates matrix metalloproteinases which results in an increased cytotrophoblast invasion.     

Secondary zoospores in the algal endoparasite <i>Maullinia ectocarpii</i> (Plasmodiophoromycota)

The present paper deals with the ultrastructure of zoospores produced by the plasmodiophorid Maullinia ectocarpii, living in the marine algal host Ectocarpus siliculosus. The zoospores described here are very similar to secondary zoospores of Polymyxa graminis and Phagomyxa sp. (the latter an algal endoparasite, also). Our results indicate that M. ectocarpii produces two types of plasmodia, and suggest that is a species with a complete life cycle, as it is known for all the Plasmodiophormycota that have been studied. Sporogenic and sporangial plasmodia produce, respectively, primary zoospores with parallel flagella within thick walled resting sporangia, and secondary zoospores with opposite flagella within thin walled sporangia.