Aphid feeding deterrency of ellagitannins, their phenolic hydrolysis products and related phenolic derivatives

Feeding deterrent activities of ellagic acid, two ellagitannins, gallic acid, pyrogallol, and several gallic acid derivatives towards three species of aphids were determined. The most sensitive species tested was Schizaphis graminum (Rondani), the least sensitive was Acyrthosiphon pisum (Harris). Myzus persicae (Sulzer) was of intermediate sensitivity. Ellagic acid (ED₅₀=15 ppm) and n-decyl gallate (ED₅₀=16 ppm) were particularly potent against S. graminum, while n-octyl gallate was the most active compound tested against A. pisum (ED₅₀=182 ppm) and M. persicae (ED₅₀=56 ppm). The ellagitannins, geraniin and pedunculagin, were active against S. graminum and M. persicae, but not against A. pisum. Methylation of the free hydroxyl groups of gallic acid resulted in a large decrease in activity, while esterification of its carboxyl group with alkyl chains of increasing length resulted in increasing activity against S. graminum. Against A. pisum and M. persicae, ellagic acid, gallic acid and 3,4,5-trimethoxybenzoic acid were inactive, whereas pyrogallol and the gallate esters were at least moderately active as feeding deterrents.

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Résumé L'examen a porté sur l'action répulsive, lors de l'alimentation de trois espèces de pucerons, de l'acide ellgique, de deux ellagitanins, de l'acide gallique, du pyrogallol et de plusieurs dérivés de l'acide gallique. Schizaphis graminum Rondani a été l'espèce la plus sensible, tandis que Acyrthosiphon pisum. Harris a été la moins sensible; la sensibilité de Myzus persicae Sulzer était intermédiaire. L'acide ellagic (ED₅₀=15 ppm) et le n-décyl gallate (ED₅₀=16 ppm) ont été particulièrement actifs contre S. graminum, tandis que le n-octyl gallate a été le produit le plus actif contre A. pisum (ED₅₀=182 ppm) et M. persicae (ED₅₀=56 ppm). Les ellagitanins, géraniine et pédunculagine ont été actifs contre S. graminum et M. persicae, mais pas contre A. pisum. La méthylation des groupes hydroxyl libres de l'acide gallique a réduit fortement l'activité, tandis qu l'estérification de son groupe carboxyl avec des chaînes alkyl de longuers croissantes a augmenté l'activité contre S. graminum. Les acides ellagique, gallique et 3,4,5-triméthoxybenzoïque ont été inactifs contre A. pisum et M. persicae, tandis que le pyrogallol et les esters de gallate on été pour le moins des répulsifs modérément actifs au cours de l'alimentation.

     

Expression of type I interferon by splenic macrophages suppresses adaptive immunity during sepsis

Early during Gram-negative sepsis, excessive release of pro-inflammatory cytokines can cause septic shock that is often followed by a state of immune paralysis characterized by the failure to mount adaptive immunity towards secondary microbial infections. Especially, the early mechanisms responsible for such immune hypo-responsiveness are unclear. Here, we show that TLR4 is the key immune sensing receptor to initiate paralysis of T-cell immunity after bacterial sepsis. Downstream of TLR4, signalling through TRIF but not MyD88 impaired the development of specific T-cell immunity against secondary infections. We identified type I interferon (IFN) released from splenic macrophages as the critical factor causing T-cell immune paralysis. Early during sepsis, type I IFN acted selectively on dendritic cells (DCs) by impairing antigen presentation and secretion of pro-inflammatory cytokines. Our results reveal a novel immune regulatory role for type I IFN in the initiation of septic immune paralysis, which is distinct from its well-known immune stimulatory effects. Moreover, we identify potential molecular targets for therapeutic intervention to overcome impairment of T-cell immunity after sepsis.     

HSC73-tubulin complex formation during low-flow ischemia in the canine myocardium

Canine myocardium was exposed to bouts of low-flow ischemia to identify the interactions that develop between the microtubule-based cytoskeleton and the heat shock protein 70 (HSP70) family of heat shock proteins in viable cardiomyocytes. "Moderate" or "severe" low-flow ischemia was produced in chronically instrumented dogs by reducing circumflex coronary flow by 50% for 2 h or by 75% for 5 h followed by reperfusion for 2 and 24 h, respectively. Electron and immunofluorescence microscopy demonstrated either partial or nearly complete depolymerization of the intermyofibrillar microtubules in areas of myofibril disruption and partial dissolution of the perinuclear microtubule girdle. In contrast, centrosomal tubulin arrays appeared to remain intact following low-flow ischemia. In cardiomyocytes displaying myofibril disruption, constitutively expressed HSP73 (HSC73) colocalized with intact but not disrupted microtubules and with perinuclear and centrosomal tubulin following moderate ischemia. Microtubule depolymerization and high molecular weight tubulin-HSC73 complexes were present in more severely ischemic tissue. These results suggest that HSC73 directly interacts with tubulin and may protect selected elements of the microtubule network and limit myofibril disruption during reversible low-flow ischemia.     

SYSTEMIC INSECTICIDAL ACTION OF AZADIRACHTIN, NEEM SEED AND CHINABERRY SEED EXTRACTS APPLIED AS SOIL DRENCHES TO POTTED PLANTS

Abstract  The systemic insecticidal activities of: 1) azadirachtin, a potent insect antifeedant and growth regulator isolated from seeds of the neem tree, Azadirachta indica , 2) a neem seed extract containing 0. 30 quantitative fraction of azadirachtin, and 3) a methanolic extract of seeds from the chinaberry tree, Melia azedarach , a close relative of neem were determined. Soil drenches of azadirachtin or the neem seed extract at 1 and 2. 5 mg to potted potato ( Solanum tuberosum ) and tomato ( Lycopersicon esculentum ), remarkably retarded the growth of Manduca sexta larvae and strongly disrupted the pupation of Leptinotarsa decemlineata larvae, respectively. However, five to ten times as much azadirachtin or neem seed extract was needed to reduce the amount of tomato and potato foliage consumed. On sorghum ( Surghum biocolor ), much higher quantity (≥25 mg) of azadirachtin or the neem seed extract was necessary to slow the population growth of Schizaphis graminum , and prolong the survival of treated plants. But methanolic extracts of chinaberry seeds ( M. azedarach ) from two sources (Guangdong, PRC and Hurricane, Utah, USA) at 150 mg per pot were ineffective in reducing aphid population growth and preventing plant damage.     

Effects of cotton condensed tannin on feeding and digestion in the cotton pest, Heliothis zea

Condensed tannin of cotton incorporated into an artificial diet caused growth inhibition in H. zea larvae whose susceptibility was dependent upon the concentration of the dietary tannin, and also upon the size of the feeding larvae.Larvae feeding on tannin-treated diet exhibited both decreased protease and invertase activities in the midgut caecal wall, as well as lowered total protein and sugar levels in the haemolymph as compared to controls. These differences, however, had no effect on assilimation and efficiency of conversion of digested matter into animal biomass and therefore may be secondary effects. Ultimately, inhibition of growth is attributed to a reduction in food consumption.     

Heterologous expression of enterocin A, a bacteriocin from Enterococcus faecium, fused to a cellulose-binding domain in Escherichia coli results in a functional protein with inhibitory activity against Listeria

The genes for the bacteriocins enterocin A and B were isolated from Enterococcus faecium ATB 197a. Using the pET37b(+) vector, the enterocin genes were fused to an Escherichia coli specific export signal sequence, a cellulose-binding domain (CBD_cenA) and a S-tag under the control of a T7lac promotor. The constructs were subsequently cloned into E. coli host cells. The expression of the recombinant enterocins had different effects on both the host cells and other Gram-positive bacteria. The expression of entA in Esc. coli led to the synthesis and secretion of functional active enterocin A fusion proteins, which were active against some Gram-positive indicator bacteria, but did not influence the viability of the host cells. In contrast, the expression of enterocin B fusion proteins led to a reduced viability of the host cells, indicating a misfolding of the protein or interference with the cellular metabolism of Esc. coli. Indicator strains of Gram-positive bacteria were not inhibited by purified enterocin B fusion proteins. However, recombinant enterocin B displayed inhibitory activity after the proteolytic cleavage of the fused peptides.     

Measurement of S-nitrosothiols in extracellular fluids from healthy human volunteers and rheumatoid arthritis patients, using electron paramagnetic resonance spectrometry

In human tissues, S-nitrosothiols (RSNOs) are generated by the nitric oxide (NO.)-dependent S-nitrosation of thiol-containing species. Here, a novel electron paramagnetic resonance spectrometry assay for RSNOs is described, together with its application to studies of human health and disease. The assay involves degrading RSNOs using N-methyl-d-glucamine dithiocarbamate (MGD) at high pH and spin trapping the NO. released using (MGD)2-Fe2+. Because dietary nitrate might contribute to tissue RSNOs, the assay was used to monitor the effect of Na15NO3 ingestion on plasma and gastric juice RSNOs in healthy human volunteers. Na15NO3 ingestion (2 mmol) increased gastric RS15NO concentrations (p<0.01), but there was no significant effect on plasma RS15NO concentrations. Having established that dietary nitrate was not a confounding factor, we applied the RSNO assay to matched plasma and knee-joint synovial fluid (SF) from rheumatoid arthritis (RA) patients, with healthy subjects as controls. Clinical markers of RA inflammatory disease activity were quantified, as were plasma and SF NO2- and NO3-. Median RSNO concentrations were 0 (interquartile range 68) nM, 109 (282) nM, and 309 (470) nM in normal plasma, RA plasma, and SF, respectively. The median RSNO concentration was significantly elevated in RA SF compared with RA plasma (p<0.05) and in RA plasma compared with normal plasma (p<0.05). SF RSNO concentrations correlated positively with SF neutrophil counts (rs=0.55, p<0.05) and inversely with blood hemoglobin concentrations (rs=-0.52, p<0.05), but not with NO2- or NO3-. Thus the raised levels of RSNOs in RA SF correlate with some established markers of inflammation, suggesting the described RSNO assay may have applications in rapid clinical monitoring of NO metabolism in human inflammatory conditions.