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 %.

Two hundred, five-week old chickens were divided into six equal groups (30 chicks/group) and vaccinated with different live NDV vaccines in Nigella sativa oil. The vaccinated birds were bled at one-week interval post-vaccination over six weeks and the collected sera were tested by the HI test. Half of each group was challenged 21-days post-vaccination by intramuscular route of inoculation with 2X105EID50 of the velogenic viscerotropic Newcastle disease virus (VVNDV). Birds were observed for 15 days post-challenge for any clinical signs of Newcastle disease. Deaths within this period were subjected to post mortem examination. The remaining birds in each group were observed after challenge till 42-days post-vaccination.

Seventy-five rats were used to determine the toxic effects of difenoconazole (D) fungicide on haematological, some biochemical parameters and thyroid hormones in adult albino rats of both sexes, as well as possible inhibition of adverse effects by using vitamin E and/or vitamin C as antioxidant drugs. Rats were classified into five groups each of 15 rats. Group (1) served without treatment as negative control, group (2) treated with 1/10 of the LD50 of D (140.3 mg/kg B.wt.), in alternative days for 30 days and cessation of D for further 15 days as a withdrawal period, group (3) treated with vit. E (24 mg/ kg B.wt.) combined with the same dose of D, intubation every other day, group (4) administered vit. C (200 mg/ kg B.wt.) daily per os combined with the same dose of D in alternative days, group (5) taken vit. E, vit. C and D. Vitamins were given daily from the beginning of experiment till the end and at withdrawal period. Samples were collected at 15 and 30 days during D exposure and at the end of withdrawal period. Using analysis of variance, R.B.Cs. count, PCV % and Hb content significantly decreased than negative controls allover the experimental period in D- treated groups, however vit. C alone or combined with vit. E produced gradual improvement in haematological parameters. Marked elevation in W.B.Cs. count and lymphocytes, accompanied by neutropenia were observed in all groups compared to negative controls allover the experiment period. Total protein, triglyceride and high-density lipoprotein levels were significantly reduced in all D-administered groups compared to negative controls. Aspartate aminotransferase, alanine aminotransferase, urea, creatinine, cholesterol and low density lipoprotein showed higher levels in all D-treated groups in comparison to negative controls, meanwhile, administration of vit. E and/or vit. C produces gradual improvement in these parameters. Thyroid hormonal analysis indicated significant decrease in triiodothyronine (T3) and thyroxine (T4) in all D- treated groups, whereas their levels returned to normal in groups given vit. C alone or combined with vit. E at the withdrawal period. In conclusion, these results indicated that D fungicide exposure caused overt disorders in haematological and biochemical parameters as well as thyroid function. These effects could be ameliorated by using vit. E and vit. C as antioxidant drugs. Vit. E and vit. C when combined together produce best results in all tested parameters, however vit. C alone has rapid response than vit. E especially in haematological picture and thyroid function.

The incidence of E. coli O157, Salmonella typhimurium, Listeria monocytogenes, and Yersinia enterocolitica were studied in some locally produced cheeses. Thirty samples of each kind of the cheese were tested for the presence of some pathogens, which are frequently associated with food born disease. E. coli O157: IMS; Listeria monocytogenes were enumerated on modified Oxford agar; Salmonella was enumerated using standard procedures from Dynal manual using anti-Salmonella antibodies. Y. enterocolitica was enumerated on Yersinia selective agar base. Romano and processed cheese were found to be free from all tested pathogens but Kareish and Feta cheese were found to harbor E. coli and Y. entertocolitica. The results indicated the presence of some food borne pathogens in our food supply. Certain types of locally produced cheese still pose a significant health threat for the consumers. The finding of this study warrant the need for educational programs for dairy producers about the risks associated with consumption of certain cheeses manufactured from raw or insufficiently heated milk.

In this study a total of 200 stray dogs housed in Safe Harbor Animal Rescue and Clinic (SHARC), South Florida, USA were clinically and parasitologically examined for intestinal helminthes. In this investigation, dogs were clinically examined and monitored for intestinal parasites for 6 successive weeks, treated with specific drugs and investigated for the possibility of reinfestation with intestinal parasites within the closed quarters of the animal shelter environment. Fecal floatation technique revealed three types of parasitic eggs in fecal samples of 46 (23%) dogs, including Ankylostoma spp. 30 (15%), Toxocara canis 10 (3.5%), and Dipylidium caninum 6 (3%). Clinical examination of investigated dogs revealed bloody diarrhea associated with abdominal pain, anemia, poor hair coat and the presence of segments of tapeworms approximately in the size of grain of rice in the feces of some dogs. Some dogs showed frequent cough. Some dogs that were tested negative for Ankylostoma spp. and Toxocara canis tested positive later indicating definite contamination in the environment of the shelter. Some dogs developed tapeworm infestation during this study indicting the presence of infective flees in contact dogs. Control measures and therapy were discussed.

Forty-eight pathogen free New Zealand rabbits were divided into two groups, the first group contained eighteen rabbits served as normal control and the second group of thirty rabbits were received 1 ml bovine herpesvirus-1 (BHV-1) virus suspension (107 TCID 50) by intraperitoneal route. Rabbits both groups were subjected to hematological, serum biochemical, different serological and histopathological examination 3,7,10,14,21 and 28 days post infection. Clinical observation of infected rabbits showed febrile response and mild conjunctivitis after 24 and 48h. of inoculation, respectively. The hemogram revealed no significant alteration in the erythrogram while leucogram showed leucocytosis accompanied with heterophilia, lymphopenia and monocytopenia at the 3rd and 7th days post infection. Serum biochemical analysis showed significant elevation in the activity of AST, ALT and AP and in blood urea nitrogen and creatinine concentration along the experimental period. Serum total proteins, albumin, :, ; and < globulin significantly increased at different periods of the experiment. BHV-1 antibodies were detected in the sera of infected rabbits by Dot ELISA and ELISA from the first week until the forth week post infection. Histopathological examination revealed that the most affected organs were the trachea, lungs and liver while adrenals, kidneys, and spleen showed mild pathological alterations.

A total of 980 camels were employed in this study for evaluation of some diagnostic procedures used for diagnosis of camel trypanosomiasis. Clinical examination revealed that 180 (18.37%) camels showed sings of illness including, loss of body weight, anemia, abortion, decrease of animal production and edema in some parts of the body. Parasitological examination of camel’s blood smears revealed the presence of Trypanosoma evansi in 57 (5.82%) camels. ELISA detected 99 (63.06%) positive cases while suratex test identified 80 (50.96%) positive cases. Results of mice inoculation test for detection of Trypanosoma evansi among camels showed that 69 (43.95%) camels were positive. The present study clarified that suratex test was 100% sensitive for diagnosis of trypanosomiasis followed by ELISA (98.55%).