Mitosis and differentiation in T-cells under cytotoxic action of Echinococcus granulosus hydatid fluid

In the T-cell line, D10, thymidine uptake was used to measure the proportion of cells in S-phase, and the MTT assay to measure the number of viable cells. The effect of Echinococcus granulosus hydatid fluid (HF) on the lymphocytes was assayed in 3-day cultures of the T-cell line, D10, in increasing concentrations of HF. Apparent cytotoxic effects of HF were recorded as a log-linear decline in S-phase activity, which was reduced by the presence of IL-1, IL-2, or a combination of the two. In the presence of IL-2, however, mitogenic treatment with concanavalin A increased the cytotoxic effect in 3-day cultures, while in day-2 cultures, HF itself showed mitogenic effect. HF-induced decline in S-phase activity was not matched by a parallel decline in viable cells, suggesting that the apparent cytotoxicity of HF could result from cell-cycle arrest. Depending on its origin, HF enhanced membrane expression of CD25 and CD38 on human peripheral blood lymphoblasts, and diminished that of CD28. Taken together, these changes suggest that HF can induce T-cell mitosis and reduce co-stimulation with subsequent T-cell anergy or apoptosis.     

POST-OPERATIVE COMPUTED TOMOGRAPHY IN TWO DOGS WITH CEREBRAL MENINGIOMA

Post-operative computed tomography (CT) has been described as a technique for diagnosing incomplete resection or recurrence of cerebral neoplasms in humans. The characteristics of immediate postoperative CT images in dogs with intracranial pathology are unknown. This report describes findings from preoperative, immediate post-operative, and 4 week to 9 month follow-up CT examinations in two dogs with histologically-confirmed cerebral meningiomas. In images of one dog after surgery there was mild contrast enhancement of the tissue surrounding the surgical site. This enhancement had resolved in later images and was probably the result of surgically induced trauma. In post operative images of the other dog there was significant hyperattenuation of the tissues around the surgical site. In post contrast images there was increased enhancement that was evident in later images. These findings, although not supported by necropsy, probably indicate incomplete excision of the tumor.     

Evolution of highly pathogenic H7N3 avian influenza viruses in Mexico

Highly pathogenic H7N3 influenza A viruses have persisted in poultry in Mexico since 2012, diversifying into multiple lineages that have spread to three Mexican states, as of 2016. The H7N3 viruses segregate into three distinct clades that are geographically structured. All 2016 viruses are resistant to adamantane antiviral drugs and have an extended 24‐nucleotide insertion at the HA cleavage site that was acquired from host 28S ribosomal RNA.     

Intrinsic antibiotic resistance in relation to colony morphology in three populations of West African cowpea rhizobia

Rhizobia isolated from cowpeas (Vigna unguiculata (L.) Walp.) grown in three west African soils were examined for intrinsic resistance to five antibiotics and were scored for one of two colony morphologies. Half of the strains tested had a “wet”, slimy colony morphology and half had small discrete “dry”, non-slimy colonies. The populations as a whole were resistant to gentamicin (87%) but varied in their resistance to streptomycin, rifampicin, kanamycin and penicillin. Thirteen patterns of resistance were found for the 128 strains screened and strains within the same pattern usually had the same colony type. The most common pattern (32%) was resistance to all five antibiotics. Associations between resistances were random within populations and colony type. Each population was diverse, expressing from 6 to 8 patterns of resistance, but one population was relatively homogeneous, with 68% of its members exhibiting the same pattern. Correlations between intrinsic antibiotic resistance and colony type were demonstrated both for the west African cowpea rhizobia and for a broader group of cowpea miscellany rhizobia. The method was practical, rapid and reliable for identification of groups within populations.     

Chemometric discrimination among wild and cultured age-0 largemouth bass, black crappies, and white crappies based on fatty acid composition

The potential to distinguish juvenile wild from cultured fishes and to discriminate among juvenile fishes by species based on fatty acid composition was demonstrated. Statistical approaches to data evaluation included analysis of variance, correlation analysis, principal component analysis (PCA), and quadratic discriminant analysis (QDA). Differences were determined between wild and cultured fishes both within and between species and between hatcheries. Fatty acid compositions were compared among individual (not composited) specimens of wild and cultured, age-0, freshwater species: largemouth bass Micropterus salmoides, black crappies Pomoxis nigromaculatus, white crappies P. annularis, and black-nose crappies. Four fatty acids were investigated: linoleic acid (18:2n-6), linolenic acid (18:3n-3), arachidonic acid (20:4n-6), and docosahexaenoic acid (22:6n-3). Linoleic acid was the primary fatty acid used to differentiate juvenile wild from cultured fishes. Concentrations of linoleic acid were significantly different (p < 0.05) in cultured largemouth bass and black crappies from the wild counterparts. Linolenic acid concentrations were not significantly different (p < 0.05) between wild and cultured largemouth bass but were significantly different between wild and cultured black crappies. Wild largemouth bass contained higher concentrations of arachidonic acid than the cultured bass, and concentrations of docosahexaenoic acid were twice as high in wild black crappies than cultured black crappies. On the basis of four signature fatty acids, 90 of 91 juvenile fishes were correctly classified as wild or cultured; 32 of 37 wild juvenile fishes originating from the same reservoir were differentiated by species. Data from the training set were used to classify a test set of fishes as to species, source, or origin with 100% accuracy.     

Characterization of humic acids extracted from sewage sludge-amended oxisols by electron paramagnetic resonance

In tropical soils, the high turnover rate and mineralization of organic matter (OM) associated with intensive agricultural use, generally leads to faster soil degradation than that observed in temperate climatic zones. The application of sewage sludge to the soils is one proposed method of maintaining soil organic matter, and is also an alternative method of disposing of this waste product. As well as containing large quantities of OM, sludge is also a significant source of supplementary nitrogen, phosphorus and other essential nutrients for plant growth. However, it is necessary to understand the qualitative and quantitative changes that take place in the OM in soil treated with sewage sludge. The approach of the present study was intended to identify possible structural changes caused by sewage sludge applications on soil humic acids (HAs). The HAs extracted from a Typic Achrortox under sewage sludge applications were characterized by electron paramagnetic resonance (EPR) spectroscopy. The soil samples were collected from a field experiment designed to evaluate the effects of different doses of sewage sludge on corn growth and development in Brazil. The sewage sludge originated from urban waste treated at the sewage sludge treatment station in the city of Franca, state of Sao Paulo, Brazil. The following soil treatments were studied: control (non-cultivated soil under natural vegetation (NC)), control soil amended with NPK (conventional corn fertilization) and four treatments N1, N2, N4 and N8 with applications of 3.5, 7, 14 and 28 Mg ha⁻¹ of sewage sludge (dry matter), respectively. HAs were extracted from the surface layer using the methodology of the International Humic Substance Society (IHSS). Fe³⁺ and VO²⁺ ions complexed with HAs, and also semiquinone-type free radical (SFR) at concentrations of approximately 2.0 × 10¹⁸ spins g⁻¹ HA were identified in EPR spectra. The levels of SFR were lower for treatments where the applied sewage sludge doses were equivalent to four and eight times the normal doses of N mineral fertilization, reaching values of 1.7 × 10¹⁸ and 1.24 × 10¹⁸ spins g⁻¹ HA, respectively. The observed decrease in SFR content as sewage sludge dose was increased, was probably associated with the incorporation of less aromatic components into HAs originating from the sewage sludge.     

Analysis of coffee for the presence of acrylamide by LC-MS/MS

A variety of popular instant, ground, and brewed coffees were analyzed using a modified liquid chromatography-tandem mass spectrometry (LC-MS/MS) method specifically developed for the determination of acrylamide in foods. Coffee test portions were spiked with 13C3-labeled acrylamide as an internal standard prior to their extraction and cleanup. Ground coffees (1 g) and instant coffees (0.5 g) were extracted by shaking with 9 mL of water for 20 min. Brewed coffee test portions (9 mL) were taken through the cleanup procedure without further dilution with extraction solvent. Coffee test portions were cleaned up by passing 1.5 mL first through an Oasis HLB (hydrophilic/lipophilic copolymer sorbent) solid phase extraction (SPE) cartridge and then a Bond Elut-Accucat (cation and anion exchange sorbent) SPE cartridge. The cleaned up extracts were analyzed by positive ion electrospray LC-MS/MS. The MS/MS data was used to detect, confirm, and quantitate acrylamide. The limit of quantitation of the method was 10 ng/g for ground and instant coffees and 1.0 ng/mL for brewed coffee. The levels of acrylamide ranged from 45 to 374 ng/g in unbrewed coffee grounds, from 172 to 539 ng/g in instant coffee crystals, and from 6 to 16 ng/mL in brewed coffee.     

Chemical and microbiological parameters for the characterisation of the stability and maturity of pruning waste compost

Composting of pruning waste, leaves and grass clippings was monitored by different parameters. A windrow composting pile, having the dimensions 2.5 m (height) x 30 m (length) was establish. The maturation of pruning waste compost was accompanied by a decline in NH₄ ⁺-N concentration, water soluble C (WSC) and an increase in NO₃ ^–-N content. Both organic matter (OM) content and total N (TN) losses during composting followed a first-order kinetic equation. These results were in agreement with the microbiological activity measured either by the CO₂ respiration or dehydrogenase (DH-ase) activity during the process. Statistically significant correlations were found between DH-ase activity, easily biodegradable organic C forms, NH₄ ⁺-N and NO₃ ^–-N concentrations and organic matter content and N losses. For this reason, DH-ase activity and the CO₂ evolution could be used as good indicators of pruning waste compost maturity. In contrast, humification parameters data from the organic matter fractionation did not agree with the initially expected values and did not contribute to the assessment of compost maturity. Neither the cation exchange capacity nor the germination index showed a clear tendency during the composting time, suggesting that these parameters are not suitable for evaluating the dynamics of the process.