Microbial Populations and Enzyme Activities in Soil Treated with Pesticides

The effect of soil treatment with brominal (a herbicide) and theinsecticide selecron (the equivalent field rates and five-fold) on population counts of bacteria, actinomycetes and celluloyticfungi in soil was tested throughout 10 weeks incubation at28 °C. Also, tested their effect on four soil enzymes:cellulase, acid phosphatase, alkaline phosphatase andarylsulphatase. Bacterial and actinomycetes populations in soiltreated with the two pesticides were promoted at fieldapplication rates and inhibited at higher levels. The twopesticides significantly decreased the total number ofcellulolytic fungi and most fungal species after most incubationperiods either by one or the two used levels but the effect ofselecron was more pronounced.Cellulase activity in soil treated with brominal and selecronwas inhibited after most incubation periods. The effect of soiltreatment with the two pesticides on acid phosphatase waspromotive at field application rates after some incubationperiods but the enzyme activity was delayed at the higherapplication doses. Alkaline phosphatase activity in treated soilwas accelerated with both pesticides even at the higherapplication rates, suggesting a direct role of alkaline soil pHin increasing resistance of alkaline phosphatase to pesticides.The effect of soil treatment with pesticides on arylsulphataseactivity fluctuated between promotion and inhibition, butinhibition was predominant.     

Comparison of the chemical composition of extracts from Scutellaria lateriflora using accelerated solvent extraction and supercritical fluid extraction versus standard hot water or 70% ethanol extraction

The aqueous extract of American skullcap (Scutellaria lateriflora L. (S. lateriflora), Lamiaceae) has been traditionally used by North American Indians as a nerve tonic and for its sedative and diuretic properties. Recent reports stated that flavonoids and possibly amino acids are responsible for the anxiolytic activity. As a part of our search for environmentally friendly solvents to extract the active components from medicinal plants, we used S. lateriflora in a comparison of accelerated solvent extraction (ASE) using water, and supercritical fluid extraction (SFE) using CO2 and 10% EtOH as modifier, at different temperatures. Flavonoids and amino acids were quantified by HPLC-UV and HPLC-MS, respectively. The flavonoid content was compared with conventional extraction methods (hot water extraction and 70% ethanol). The use of ASE at 85 degrees C with water as solvent gave the best results for flavonoid glycosides and amino acids, whereas SFE gave higher yields of flavonoid aglycones. However, the results obtained for total flavonoids were not significatively superior to hot water extraction or 70% aqueous EtOH extract.     

Identification of the Egyptian species of Fasciola.

Reports on the species of Fasciola present in the Nile Delta, Egypt, appear controversial. Some authors reported the presence of both Fasciola gigantica and Fasciola hepatica, others reported F. gigantica only and mentioned that F. hepatica was found only in imported animals.This study was an attempt to identify the species of Fasciola flukes collected from locally bred animals. Morphologic, morphoanatomic, morphometric, and chemotaxonomic criteria of the fluke isolates were studied. Speciation based on morphologic and morphometric data was not decisive due to overlap in the values of most measurements. Morphoanatomic data proved the presence of both the species, and isoelectric focusing (IEF) of fluke soluble protein confirmed the presence of both F. gigantica and F. hepatica in Egypt.     

Immunity to Toxocara vitulorum repeated infections in a rabbit model.

Eleven rabbits were infected with 10 embryonated eggs of Toxocara vitulorum per g body weight on Days 0, 35 and 72. Embryonated eggs and larvae were enumerated in feces on Days 1-3 after each infection. Two rabbits were killed and larvae were enumerated in small intestine, liver, lungs, skeletal muscles, heart, kidney, brain, eye, uterus, and mammary glands on Days 5, 15, 30, 65 and 101. Serum was obtained on Days 0, 5, 15, 30, 42, 50, 65, 78, 86 and 101 to perform enzyme-linked immunosorbent assays (ELISAs) and Western blots against an extract of embryonated eggs. Between 4 and 10% of the administered parasites, almost all embryonated eggs, were found in the feces after the first or second infection, but 32% (27% of them larvae) after the third. Yields of tissue parasites were 4.1% of the administered dose on Day 5, 2% on Day 15, and 0.8% on Day 30 of the first infection, 0.1% on Day 30 of the second infection, and 0.06% on Day 30 of the third. Larvae were found only in liver, lungs and muscle, including heart. Larva content declined steadily in liver and lungs from Day 5 to 30 of the first infection, was absent in the liver at Day 30 of the second, and in both organs at Day 30 of the third. Muscle larva content increased from Day 15 to 30 of the first infection, and persisted throughout the third infection. Production of IgM antibody was minimal, IgG and the sum of IgMGA antibodies increased slightly or moderately after the first and second infections, but dramatically after the third. Western blots revealed the first antigens (12) by Day 15 of the first infection. Their total number increased with time and number of infections, but some antigens disappeared, whereas new antigens appeared in the course of the observations. Four antigens (32,500-41,000 mol.wt.) may be related to protection. Comparison of the Western blot patterns of two rabbits showed differences in the antigens, recognizable for each rabbit.     

Additional details of the life history of the chicken coccidium Eimeria mitis Tyzzer, 1929

Four asexual generations of Eimeria mitis were identified. The first three developed above the epithelial cell nuclei, but the fourth developed above and below. Meronts measured 13.8 x 16.4 microns, 16.1 x 16.4 microns, 12.1 x 14.6 microns, and 9.5 x 12.4 microns, respectively, of generations 1, 2, 3, and 4. They matured at 36, 67, 72, and 88 hr postinoculation (PI) and contain 20-24, 16-20, 10-14, and 7-10 merozoites, respectively. Merozonts measured 7.2 x 1.9 microns, 8.5 x 2.5 microns, 9.6 x 2.0 microns, and 6.75 x 2.75 microns, respectively. The first two types of meronts were deep in the crypts and epithelial cells. The third and fourth types of meronts were along the side and tip of the villi. Gametocytes developed from third and fourth generation. Gamonts were usually below the nuclei of the epithelial cells. Parasitism was primarily in the ileum, ceca, and rectum and also in the yolk-sac diverticulum.     

Pathophysiology of hepatic coccidiosis in rabbits

Four groups of 5 40-day-old, Eimeria stiedai-naive, New Zealand rabbits were infected with 0 (Group A), 10² (B), 10³ (C) and 10⁴ (D) sporulated oocysts of E. stiedai and observed for 50 days. Serum glutamic pyruvic (GPT) and glutamic oxalacetic (GOT) transaminases, bilirubinemia, lipemia, proteinemia, glycemia, oocyst output, body, carcass and liver weights, and mortality were recorded. Four physiopathological events were identified: (1) a phase of indirect damage to the hepatocytes that takes place during the first 2 weeks of infection and is characterized by increased transaminases; (2) a cholestatic period consequent to the production of oocysts that begins suddenly in the 3rd week, diminishes gradually towards the 7th week, and is characterized by a rise of bilirubinemia and lipemia; (3) a stage of metabolic dysfunction that begins in the 3rd–4th week, intensifies for the next 3 weeks and starts to recover during the 7th week. It is characterized by hypoproteinemia and hypoglycemia; (4) a period of immunodepression characterized by the inability of the heavily infected host to inhibit oocyst production. Apart from the cholestatic phase, the respective pathogenic mechanisms remains to be studied.     

Protection of Brucella abortus RB51 revaccinated cows, introduced in a herd with active brucellosis, with presence of atypical humoral response

It is a dogma, that RB51 vaccination does not induce antibodies that interfere with Brucellosis diagnosis, therefore any animal positive to serological test is considered as an infected animal. To determine protection against Brucellosis virulent field strain, 35 pregnant cows from a free-Brucellosis herd, previously vaccinated as calves with 1 x 10(10) CFU of RB51, were revaccinated with RB51 reduced dose, and then introduced into a herd with an active outbreak. Seventeen cows resulted positive in card test after revaccination. All 35 pregnant revaccinated cows had normal parturition; nevertheless, RB51 vaccine strain was isolated from milk and vaginal exudates from two cows after delivery at day 120 post-revaccination. At 150 days post-revaccination, two cows were positives to card and rivanol test and the field virulent strain was isolated. Revaccination with a reduced dose of RB51 in endemic zones did not cause abortion and protected 94% of animals against field infection, but caused an atypical response to conventional serological tests.     

Studies of the mechanism of action of asulam in plants. Part I: Antagonistic interaction of asulam and 4-aminobenzoic acid

Studies have been carried out on the herbicidal action of asulam [methyl (4-aminophenylsulphonyl)carbamate] and sulphanilamide, alone or in association either with 4-aminobenzoic acid (4ABA) or 4, 6-diamino-1-(3, 4-dichlorophenyl)-1, 2-dihydro-2, 2-dimethyl-1,3,5-triazine (DCDT). The soaking of wheat seeds (Triticum estivum L.) for 12 h at 30°C in asulam and DCDT in a 10:1 ratio doubled the inhibition of root growth produced by soaking in asulam alone; the addition of 4ABA partially reversed the activity of asulam. Foliar applications of a mixture of asulam + DCDT (1.1 + 0.55 kg ha^?1) markedly increased the activity of asulam in susceptible wheat, wild oat (Avena fatua L.), tolerant flax (Linum usitatissimum L.), and in Stellaria media L. The activity of asulam at 1.1 kg ha^?1 was reversed by 4ABA at 2.2 kg ha^?1 by about 50% in wheat and wild oat, 82% in flax and 100% in S. media. The results indicate that asulam and sulphanilamide act by similar mechanisms in apparently inhibiting the biosynthesis of folic acid.     

Molecular Mapping of the Stb4 Gene for Resistance to Septoria tritici Blotch in Wheat

ABSTRACT Breeding wheat for resistance is the most effective means to control Septoria tritici blotch (STB), caused by the ascomycete Mycosphaerella graminicola (anamorph Septoria tritici). At least eight genes that confer resistance to STB in wheat have been identified. Among them, the Stb4 locus from the wheat cv. Tadinia showed resistance to M. graminicola at both seedling and adult-plant stages. However, no attempt has been made to map the Stb4 locus in the wheat genome. A mapping population of 77 F10 recombinant-inbred lines (RILs) derived from a three-way cross between the resistant cv. Tadinia and the susceptible parent (Yecora Rojo x UC554) was evaluated for disease resistance and molecular mapping. The RILs were tested with Argentina isolate I 89 of M. graminicola for one greenhouse season in Brazil during 1999, with an isolate from Brazil (IPBr1) for one field season in Piracicaba (Brazil) during 2000, and with Indiana tester isolate IN95-Lafayette-1196-WW-1-4 in the greenhouse during 2000 and 2001. The ratio of resistant:susceptible RILs was 1:1 in all three tests, confirming the single-gene model for control of resistance to STB in Tadinia. However, the patterns of resistance and susceptibility were different between the Indiana isolate and those from South America. For example, the ratio of RILs resistant to both the Indiana and Argentina isolates, resistant to one but susceptible to the other, and susceptible to both isolates was approximately 1:1:1:1, indicating that Tadinia may contain at least two genes for resistance to STB. A similar pattern was observed between the Indiana and Brazil isolates. The gene identified with the Indiana tester isolate was assumed to be the same as Stb4, whereas that revealed by the South American isolates may be new. Bulked-segregant analysis was used to identify amplified fragment length polymorphism (AFLP) and microsatellite markers linked to the presumed Stb4 gene. The AFLP marker EcoRI-ACTG/MseI-CAAA5 and microsatellite Xgwm111 were closely linked to the Stb4 locus in coupling at distances of 2.1 and 0.7 centimorgans (cM), respectively. A flanking marker, AFLP EAGG/ M-CAT10, was 4 cM from Stb4. The Stb4 gene was in a potential supercluster of resistance genes near the centromere on the short arm of wheat chromosome 7D that also contained Stb5 plus five previously identified genes for resistance to Russian wheat aphid. The microsatellite marker Xgwm111 identified in this study may be useful for facilitating the transfer of Stb4 into improved cultivars of wheat.