The present study was designed to investigate trypanosomiasis among one of native freshwater fish breed in Egypt namely catfish (Clarias gariepenus). Fifty fish were collected during summer season from the river Nile at Giza markets. The fish were examined for the presence of trypanosoma in the blood. Trypanosoma were detected in 10 (20%) of the collected fish. The main clinical signs of infected fish with trypanosoma were emaciation, dullness, respiratory distress, loss of escape reflex, mild ascitis and paleness of the gills. Post-mortem examination of infected fish revealed paleness of the internal organs (liver and kidneys) and slight congestion of spleen. Haematological examination of infected fish revealed significant decrease in erythrocytic count, haemoglobin and packed cell volume but significant increase in total leucocytic count accompanied with neutrophilia and eosinophilia. Serum biochemical analysis demonstrated a significant decrease in urea, total protein and albumin while a significant increase in AST, ALT, ALP, creatinine, glucose and 1- globulin were recorded. Microscopic examination of organ histopathological sections revealed cloudy swelling of hepatocytes with activation of kupffer cells, depletion of lymphocytes with thickening of tile trabeculae in spleen. While in kidney, necrobiotic changes of epithelial lining of renal tubules with vacuolation of glomeruli as well as hemorrhages were recorded.

The Pharmacokinetics of florfenicol was studied in buffalo calves following single intravenous and intramuscular administration of 20 mg kg-1 b.wt. Florfenicol concentration in both serum and urine were determined by microbiological assay using Bacillus subtilis (ATCC 6633) as test organism. After intravenous injection the serum florfenicol concentration time course obeys two-compartment open model with distribution (t0.5 ()) and elimination (t0.5 ()) half lives of 0.381 ± 0.004 and 2.89 + 0.263 h., respectively. Total body clearance (CLB) and steady state volume of distribution (Vdss) were 3.6 ± 0.30 ml kg-1 min-1 and 1.70 ± 0.010 l kg-1., respectively. After intramuscular administration the observed mean peak serum concentration (Cmax) was 2.32 ± 0.052 3g ml-1 achieved after maximum time (Tmax) of one hour postinjection. The systemic bioavailability after intramuscular administration was 27.43 % and the plasma protein binding was 13.5 %.

Five species of ixodid ticks were found in a cross-sectional survey in which 200 sheep were examined for ticks in River Nile Province, Sudan. Hyalomma anatolicum anatolicum was the predominant species (73.6 %), whereas ticks belonging to the Rhipicephalus sanguineus group (14.7 %), Rhipicephalus evertsi evertsi (9.1 %), Rhipicephalus simus (2 %) and Hyalomma dromedarii (0.5 %) were also found. The mean tick load was 11.2 per animal. In a subsequent longitudinal survey ticks were collected on a monthly basis from eight sentinel sheep that were introduced into the area. It was found that H. a. anatolicum almost disappeared during the hot period between April and August, whereas it's highest numbers were present in winter between November and February. It is concluded that there is only one generation of H. a. anatolicum per year, which may explain the yearround appearance of clinical cases of malignant ovine theileriosis indicating endemic instability of this disease in River Nile Province.

A conclusive study was conducted for preparation and evaluation of combined inactivated entero-4 vaccine containing bovine rotavirus (BRV), bovine coronavirus (BCV), E. coli K99 and toxoid of C. perfringens type "C". Laboratory and field evaluations were conducted on laboratory animals, calves and late pregnant cows with monitoring the active and passive antibodies in vaccinated cows and their offspring respectively. Laboratory evaluation proved purity, safety and high efficacy of the vaccine without interference between different vaccine ingredients. Field evaluation gave satisfactory results when pregnant cows vaccinated at late stage of pregnancy with high neutralizing antibody titers against BRV, BCV and C. perfringens as well as high E. coli agglutinating titers. Maternal immunity passively protected offspring during the critical period of age and remained protected till the end of sampling time (30th day post parturition).

Beef longissimus dorsi steaks were treated with 10, 25, and 50-kGy gamma irradiation and weekly examined during refrigeration storage at 5ºC to evaluate the changes in their organoleptic, bacteriological, chemical and nutritional quality characteristics as well as deterioration criteria. The signs of spoilage became apparent after 17 days of refrigeration storage in control untreated samples compared with 52 days for 10 kGy treated samples; however, samples treated with 25 or 50 kGy remained without signs of spoilage until the end of storage period (4 months). A characteristic burnt flavor was distinguished in irradiated beef samples, which was intensified with high irradiation dose, but decreased during storage. High doses of irradiation especially 50 kGy resulted in a brownish color of meat surface. Moreover, gamma irradiation resulted in high thiobarbituric acid values after treatments and during storage due to lipid oxidation. Thiamin content of beef was severely reduced and the reduction was dependant on the irradiation dose. Riboflavin was also affected by irradiation, but it was much stable than thiamin. The proximate chemical composition of beef was slightly affected by irradiation.

In this study a total of 14 infected sheep and 6 lactating albino goats were used. These animals were proved to be brucellosis seropositive using TAT, MET, BAPAT, RBPT and rivanol test as well as bacteriologically positive by isolation of Brucella melitensis biovar 3 from their milk. These animals were subjected to trials of treatment using three different methods. Goats treated by antibiotics combined with BCG showed the highest recovery rate (on bacteriological basis), followed by animals treated with antibiotics only and finally animals treated with antibiotics combined ID. The recovered treated animals were placed under careful investigation for 2 years with no evidence of Brucella infection neither in them nor in their newborns.

Considerable difficulties are associated with the isolation of Yersinia enterocolitica from food particularly milk and milk products. Most methods are time consuming require enrichment steps and are unable to differentiate pathogenic isolates from non pathogenic ones. The purpose of this study was to evaluate the detection of Yersinia enterocolitica in milk by both polymerase chain reaction (PCR) and conventional culturing methods. Fifty milk samples were collected from Shami goats in North Sinai governorate. Two primers (DG26 and DG63) were used in PCR and the size of the PCR-product was 440bp. The results obtained by PCR technique were in good agreement with that obtained by conventional culturing method. Five samples (10%) were positive by PCR while 4 samples were positive by conventional culturing method. Interestingly, PCR results are obtained within few hours. Moreover, it solved the problem of interpretation of classical biochemical and serological typing in one step without necessity of using additional examinations. This makes diagnosis in food control laboratories much faster and more efficient.

The lectin-binding characteristics of the epithelial lining of the thoracic air sacs of the chicken were determined. Con A, LCA and PSA bound to the apical membrane as well as to the cytoplasm distal to the nucleus of the surface epithelium, indicated the presence of a-linked mannose as well as Nacetylchitobiose- linked a-fucose residues in the glycoproteins. GSL I bound to the apical membrane and cytoplasm distal to the nucleus, but not to the cilia of the epithelium, where-as MPL, DBA and RCA120 bound to the apical membrane, cilia and cytoplasm, indicated the presence of a-linked Nacetylgalactosamine residues. However, neither SJA or SBA showed any binding, indicating the absence of b anomers of galactosyl (b1.3)N-acetylgalactosamine and b-linked N-acetylgalactosamine residues. UEA I bound to the apical membrane and cilia, as well as to the cytoplasm of a few cells, indicated the presence of a-linked fucose residues. PNA bound to the apical membrane of some, but not all, surface epithelium cells, indicated the presence of galactosyl (b1.3)N-acetylgalactosamine residues. WGA bound to the apical membrane and cilia, as well as to the cytoplasm of a few cells, indicated the presence of neuraminic acid residues.

Poisoning with cardiac glycoside-containing plants is collectively the most important plant-associated poisoning of livestock in southern Africa. As a diagnosis of this significant poisoning is currently based on circumstantial evidence, a practical chemical procedure indicating the presence of cardiac glycosides in plants and animal specimens would be of considerable benefit. The fluorescence polarization immunoassay (FPIA) method, used to determine digoxin plasma levels in humans and dogs, was adapted to estimate cardiac glycoside levels in known cardiac-glycoside- containing plants as well as in the rumen and organs of dosed sheep. Positive FPIA values were obtained with bufadienolide-containing plants, while negative results were obtained with plants not known to contain cardiac glycosides. The FPIA has aided in the diagnosis of cardiac glycoside poisoning in livestock and game in 30 outbreaks examined at the Division of Toxicology, Onderstepoort Veterinary Institute. Each outbreak is briefly described. As a result of this assay, a better understanding of cardiac glycoside poisoning has been reached.

The concentration of organochlorines (OCs) such as organochlorine pesticides and polychlorinated biphenyls were measured in adipose tissue collected from 14 male hippopotami at Mfuwe in the southern part of the Luangwa National Park, Zambia. The samples contained low levels of OCs, and the concentrations of OCs were comparable to or lower than reported for wild herbivores studied in other parts of the world.