Studies on Normal Haematological and Serum Biochemical Values of the ‘Hijin’ Racing Camels (Camelus dromedarius) in Kuwait

Haematological estimations and serum biochemical analyses were made on 100 samples collected from clinically healthy Hijin racing camels (Camelus dromedarius) in Kuwait. The red blood cell counts, packed cell volume, haemoglobin concentration, mean corpuscular volume, mean corpuscular haemoglobin, mean corpuscular haemoglobin concentration and total white blood cell counts were estimated. In the serum biochemical analyses, sodium, potassium, iron, calcium, phosphorus, magnesium, total bilirubin, blood urea nitrogen, creatinine, glucose, total protein and cholesterol concentrations were measured, as were the alanine aminotransferase, aspartate aminotransferase, -glutamyltransferase, creatine kinase and alkaline phosphatase activities. The results are discussed in relation to other findings reported in camels.     

The pharmacokinetics, metabolism and urinary detection time of etamiphylline in camels after intramuscular administration

The pharmacokinetics of etamiphylline were determined after an intramuscular (i.m.) dose of 3.5 mg/kg body weight in six healthy camels. Furthermore, the metabolites and drug detection time were evaluated. The data obtained median and (range) were as follows: the terminal elimination half-life (t(1/2 beta), h) was 3.04 (2.03-3.62); apparent total body clearance (Cl/F, L/h/kg) was 1.27 (0.74-2.99); the apparent volume of distribution at steady state (V(ss)/F, L/kg) was 4.94 (3.57-12.54); and renal clearance (Cl(r), L/h/kg) determined in two camels was 0.005 and 0.004, respectively. The detection time of etamiphylline in urine after an i.m. dose of 3.5 mg/kg body weight ranged between 12 and 13 days. Three etamiphylline metabolites were tentatively identified in camels urine: The first one desethyletamiphylline was the main metabolite and resulted from N-deethylation of etamiphylline had a molecular weight of 251, and was detected in urine for about 13-14 days. Theophylline (molecular weight 180) was the second metabolite and resulted from ring N-dealkylation of etamiphylline. It was present in small amounts and was detected for about 5 h after drug administration in urine. The third metabolite, possibly resulted from demethylation of etamiphylline, had a molecular weight of m/z 265, and was present in small amounts and was detected in urine for about 5 h after drug administration.     

Prevalence of serotypes G6 and G10 group A rotaviruses in dairy calves in Quebec.

Fecal samples from diarrheic and nondiarrheic dairy calves (1 to 3 weeks old) from 12 regions of Quebec, collected between 1992 and 1994, were screened for group A bovine rotavirus (BRV) using a combination of 2 VP6-specific monoclonal antibodies (MAbs) in an enzyme-linked immunosorbent assay (ELISA). The overall prevalence of BRV infection was 26.4% (107/405). In diarrheic calves, BRV infection reached 74.3% (55/74), but only 15.7% (52/331) in nondiarrheic calves. BRV-positive samples were serotyped by enzyme-linked immunosorbent assay (ELISA) using G6 and G10 specific MAbs. The analysis of 107 field samples revealed that, in diarrheic calves, 34.5% (19/55) were G6, 27.2% (15/55) were G10, 9% (5/55) were G6 and G10 positive, and 29.9% (16/55) were G6 and G10 negative. In nondiarrheic calves, 19.2% (10/52) were G6, 19.2% (10/52) were G10, 7.6% (4/52) were G6 and G10 positive, and 53.6% (28/52) were G6 and G10 negative. Rotavirus dsRNA was extracted from BRV-positive samples and examined by polyacrilamide gel electrophoresis (PAGE). Of 107 samples tested, 74 (69.1%) were positive, and all the samples demonstrated a typical group A rotavirus migration pattern.     

Chromosome locations of leaf rust resistance genes in selected tetraploid wheats through substitution lines

Langdon durum D-genome disomic substitution lines were used to study the chromosome locations of adult-plant leaf rust resistance genes identified from tetraploid wheat accessions. The accessions are 104 (Triticum turgidum subsp. dicoccum var. arras) and 127 (T. turgidum subsp. durum var. aestivum). The complete sets of the substitution lines were crossed as female parents with the accessions and F₁ double monosomic individuals selected at metaphase I. Segregating F₂ individuals were inoculated during the flag leaf stage with pathotype UVPrt2 of Puccinia triticina. The substitution analysis involving accession 104 showed that the gene for leaf rust resistance is located on chromosome 6B. The analysis with accession 127 indicated that chromosome 4A carries a gene for leaf rust resistance. The two novel genes are temporarily designated as Lrac104 and Lrac127, respectively from accessions 104 and 127.     

Genetic Advancement of Newly Developed Wheat Populations Under Drought-Stressed and Non-Stressed Conditions

Journal of Crop Science and Biotechnology - Genetic variation and heritability estimates in early generations are important in identifying superior families that can be targeted for genetic...     

Effect of deficit irrigation on drip-irrigated wheat grown in semi-arid conditions of Upper Egypt

Shortage of water in arid and semi-arid regions increases the need of applying efficient drip irrigation system. A two-year field study in the semi-arid region of Upper Egypt was carried in randomized complete block design with four replicates. Wheat plants were irrigated by 100 or 75% of water requirements (I₁₀₀ = 5,370 and I₇₅ = 4,027 m³ ha^?1). Irrigation of wheat by I₁₀₀ increased growth and uptake of nitrogen, phosphorus, and potassium compared to low irrigation level. I₁₀₀ caused 14 and 5% increase in straw and biological yield, respectively, compared to I₇₅. Grain yield and water use efficiency (WUE) were higher by 20 and 59% in the case of I₇₅ compared to I₁₀₀. The use of deficit irrigation in drip-irrigated wheat under arid conditions is an effective tool to maximize efficiency of water use; moreover, 4,027 m³ ha^?1 is the optimum irrigation rate for maximum WUE and grain yield.     

Yield response and <Emphasis Type="Italic">Stenocarpella</Emphasis> ear rot reaction among selected maize inbred lines and top cross hybrids

Stenocarpella ear rot of maize caused by Stenocarpella maydis (Berk.) Sutton is one of the most important ear rot diseases in South Africa. The objective of this study was to identify suitable maize inbred lines and top cross hybrids with Stenocarpella ear rot resistance and high grain yield. The study was conducted using 54 inbred lines and 54 top crosses with selected standard checks under natural and artificial disease inoculations. A split-plot design was used with three replications. There were considerable variations among tested inbred lines and top crosses for Stenocarpella ear rot resistance and grain yield. Two promising inbred lines GCI-35 and GCI-50 were selected possessing resistance to Stenocarpella ear rot and increased grain yield. Inbred line GCI-35 had a grain yield of 6.31 and 6.27 t/ha under natural and artificial inoculations, respectively. Line GCI-50 yielded 5.8 and 5.7 t/ha when tested under natural and artificial disease infestations, respectively. Two top cross hybrids GCT-14 and GCT-30 were selected with greater grain yield and high level of Stenocarpella ear rot resistance. Top cross entry GCT-14 yielded 7.5 and 9.33 t/ha, respectively, whereas GCT-30 had yield of 7.65 and 9.21 t/ha, respectively. The selected inbred lines and top cross hybrids will be useful in maize improvement for Stenocarpella ear rot resistance and increased grain yield in South Africa or other similar environments.     

New techniques for breeding maize (Zea mays) varieties with fall armyworm resistance and market-preferred traits for sub-Saharan Africa

Deploying maize varieties with fall armyworm (Spodoptera frugiperda [J.E. Smith]; FAW) resistance, desirable product profiles (PPs) and climate resilience is fundamental for food and economic security in sub-Saharan Africa (SSA). This study reviewed and identified challenges and opportunities for effective and accelerated breeding of demand-led maize hybrids with FAW resistance and adaptation to the diverse agro-ecologies of SSA. Lessons were drawn on improving breeding efficiency through adequate genetic variation delivered via prebreeding programmes, speed breeding and a reduced breeding stage plan. Appropriate PPs aligned with demand-led breeding approaches were highlighted as foundations for variety design and commercialization. Challenges to accelerated FAW resistance breeding in maize included inadequate funds and modern tools; poor adaptation of some exotic donor parental lines; lack of information on FAW resistance among local varieties; lack of integration of molecular markers associated with FAW resistance and agronomic traits into selection plans; and limited infrastructure for FAW rearing and germplasm screening. Integration of modern breeding tools and scientific innovations were recommended for accelerated development and release of FAW resistant and market-preferred maize varieties.