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%).

Hyalomma anatolicum anatolicum nymphs were collected from two localities in the Sudan: Eddamer in Northern Sudan and Wad-Medani in Central Sudan. They were allowed to moult to adult ticks, which were assessed for Theileria infection in their salivary glands using Feulgen stain. At Eddamer, 49.6 % of 123 ticks examined were infected with Theileria and the mean intensity of infection was 1.3 (i.e. the number of infected acini / number of infected ticks). At Wad-Medani, 8.6 % of 162 ticks were infected and the mean intensity of infection was 7.9. The prevalence of infection was higher in female than in male ticks at both localities. When adult H. a. anatolicum were applied onto two susceptible calves, both animals developed the severe form of theileriosis.

A single-tube duplex nested polymerase chain reaction (sdn-PCR) was developed for the detection of and discrimination between ovine herpesvirus-2 (OvHV-2) and alcelaphine herpesvirus-1 (AlHV-1). These viruses respectively cause sheep- and wildebeest-associated malignant catarrhal fever (SAMCF and WA-MCF). In the first step of the sdn-PCR, two primers with high annealing temperatures based on conserved regions of the tegument genes were used for DNA amplification. In the second step, two primer sets based on variable regions of the respective OvHV-2 and AlHV-1 genes and with annealing temperatures > 11 °C below the primers used in the first step, were used. Internal regions of different sizes from amplicons produced in the first step were amplified. This single-tube test obviates the need for two separate assays to detect both viral types, thereby reducing time, labour and cost.

An experimental study was conducted on 14 donkeys. The animals were classified into two main groups. The first group included 5 donkeys that are used for induction of duodenal, obstruction for determination of the different clinical and biochemical changes and for determination of the mean survival time after obstruction. The second group contained 9 donkeys that were used for the determination of proper time for surgical intervention. Results revealed that mean survival time after obstruction was 20-35 h and the critical time for surgery was 14-35 h.

In this study, Brucella abortus RB51 could be detected in the vaginal exudates of 5 out of 26 aborted cows following vaccination of three dairy cattle herds of 3810 animals including heifers and pregnant and non-pregnant cows by RB51 vaccine. Abortion associated with isolation of RB51 vaccinal strain from recently vaccinated cows in this study served as evidence that the vaccinal RB51 strain was the cause of abortion due to extensive bacterial multiplication and colonization in the uterus of vaccinated pregnant cows

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.

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.

In this study, two methods for determination of formalin amount were applied on samples of inactivated vaccines representing local or foreign companies. The first method; matching method was conducted by using phenyl hydrazine while in the other method is; spectrophotometry phloroglucinol was used. Spectrophotometrical method was found more sensitive and more accurate than the matching one. At the same time, the spectrophotometry method could be used for determination of formalin in all inactivated vaccines either bacterial or viral vaccines.

The challenge virus standard (CVS-11) strain of fixed rabies virus was propagated in weaning mice brains and in suckling mice brains. It was also propagated on baby hamster kidney cell line (BHK-21) with use of diethylaminoethyl-dextran (DEAEDextran). These passages were titerated in 3-4 weeks old white Swiss mice using mouse inoculation test (MIT). The virus harvest was concentrated using zinc acetate method , inactivated by beta-propiolactone (BPL) and adjuvanted with combination of vitamin E and selenium. The prepared adjuvanted inactivated tissue culture rabies vaccine was subjected to quality control tests as safety, sterility and potency using National Institute of Health (NIH) test against reference vaccine.