A total number of 30 buffaloe calves aged between 1-6 months with body weight range of 100- 125 kg and belonged to private farms at Assiut Governorate constituted the materials of this study. Twenty of them showed the classical signs of hypomagnesaemia while the other ten buffaloe calves were proved to be healthy by both clinical and laboratory methods of examinations and used as control.Biochemical analysis of blood sera showed a significant hypomagnesaemia , hypocalcaemia and hypophosphataemia in diseased buffaloe calves when compared with the healthy ones, also fluctuation between the previous studied parameters either pre and post treated animals were evident. Meanwhile, blood serum total protein, albumin, globulin, albumin/globulin ratio and GOT levels were fluctuated in diseased buffaloe calves or treated one when compared with the healthy control animals. Statistical analysis between studies parameters were carried out in buffaloe calves before and after treatment.

The occurrence of cross-resistance among melarsoprol-resistant Trypanosoma brucei rhodesiense isolates was investigated in this study. The isolates, T. b. rhodesiense KETRI 237, 2538, 1992, 2709, 2694 and 3530, had been obtained from sleeping sickness patients in Kenya and Uganda between 1960 and 1985. Five groups consisting of six mice each were inoculated intraperitoneally with 105 parasites of each isolate, and 24 h later treated with either melarsoprol, homidium chloride, diminazene aceturate or isometamidium chloride. The control group comprised infected but untreated mice. The mice were monitored for cure for a period of 60 days post-treatment. The mean prepatent period in the control mice was 5 days while the mean survival period was 22 days. Five of the stabilates, KETRI 237, 2538, 2709, 2694, and 3530, were confirmed to be melarsoprol resistant. Cross-resistance was observed, with the majority of the isolates being resistant to homidium chloride (5/6) and diminazene aceturate (5/6), but all were sensitive to isometamidium chloride (6/6). However T. b. rhodesiense KETRI 1992, which was previously considered as melarsoprol resistant, was sensitive to all the drugs tested. In conclusion, our study has revealed the existence of cross-resistance among the melarsoprol resistant isolates which could only be cured by isometamidium.

Contagious bovine pleuropneumonia (CBPP), caused by Mycoplasma mycoides var. mycoides small colony (MmmSC), is one of the most important diseases of cattle in Africa. The role of innate or acquired cell mediated and humoral immunity in conferring protection against MmmSC infection has not yet been elucidated. On the other hand, the pathological lesions caused by the aetiological agent have been considered indicative of an immunopathological process. In this study ten naïve cattle were exposed to in-contact infection with animals infected by intubation with a strain of MmmSC. Clinical signs, antibody response, IFNg release and pathological changes at necropsy were analysed and compared with the events following in-contact infection of an equal number of animals kept under daily treatment with cyclosporine for the entire observation period of 84 days. Cyclosporine is a suppressor of the immune response related to the T-cell system. Under the conditions of the experiment, cyclosporine appeared to condition the pathogenesis of CBPP by delaying the events that follow infection, bringing further support to the possibility that the immune response may have an impact on the disease outcome.

Seroprevalence of Babesia ovis in sheep and goats was studied in Siwa Oasis between January 2002 and January 2003. A total of 240 blood samples were collected from 108 sheep and 132 goats for preparation of blood smears and for separation of serum samples and tested against B. ovis by using IFAT. B. ovis was detected in 55 (50.92%) and 59 (44.69%) blood smears examined in sheep andgoats, respectively. The overall prevalence of B. ovis infection was 71.3% in sheep and 68.2% in goat using IFAT. The seasonal prevalence of B.ovis peaked in both spring and summer as revealed by blood smear examination and IFAT. A total of 143 ticks were collected from 62 sheep and 81 goats during the study. The ticks examined were Rhipicephalus turanicus (75.52%) and Hyalomma anatolicum (24.48%).

This study was carried out on 180 pregnant ewes located at Ras Sedr research station - desert research center, from 2003 to 2005. Twenty five cases of abortion were recorded and examined serologically by complement fixation test (CFT). 17 (68%) out of these 25, showed positive results against Chlamydophila abortus and 3(15%) out of 20 apparently healthy pregnant ewes were serologically positive. Due to the fact that both clinical signs and pathological findings are not specific in case of chlamydial infection and also due to the fact that CFT is accompanied by false positive reactions due to cross reactivity between chlamydial species, five samples from serologically positive aborted dams were subjected to polymerase chain reaction (PCR). They revealed positive results for Chlamydophila abortus at 119 bp. Therefore, PCR is proven to be reliable, rapid and specific diagnostic technique in thediagnosis of chlamydial infection.

A. N. Al Khalaf helminthes , Egret , Egretta alba , Saudi ArabiaExamination of the alimentary tracts of 9 Great Egret (Egretta alba) found freshly died in their inland places around Al-Qassim area during migration season in September and October revealed infection by 6 species of helminths. The extracted parasites were include two cestode worms, three nematodes and one acanthocephala. They were identified as Uniciuna species, Choano-taenia, Subulura species, Contrac-aecum species, Syphacia species and Polymorphus species. None of any examined carcass appears free from infection. The rate of distribution of the parasite in the examined birds was varied between 66.6%, 11.1%, 44.4%, 44.4%, 66.6% and 2.2 % for the previous parasites respectively. The rate of Parasite burden for each species was moderate to low, as it was 3.4, 2.0, 2.65, 3.25, 5.16 and 4.5 from the previous parasites respectively. None of these parasites was published previously in Saudi Arabia as infect this type of Egret. Their morphological characters and their distribution were described in detail

Polyclonal hyperimmune serum against Pasteurella multocida type A:5, A:8 and A:9 was prepared in boskat rabbits. The indirect haemagglutination test (IHT) showed that such serum had an antibody titer of 1114. The immunoglobulins in the prepared antiserum were precipitated using saturated ammonium sulphate solution. Its concentration was adjusted to be 18mg/ml in normal saline then it was conjugated with horse radish peroxidase and evaluated through the application of double sandwich ELISA. It was successful to detect Pasteurella multocida antibodies in positive serum samples with strong positive reactions up to a dilution of 1:100 ofthe prepared conjugate.In the present study, polymerase chain reaction (PCR) using random primer (E-20) was used to characterize and identify strains included in this study. Strains included 4 vaccinal reference strains of Pasteurella multocida, CU strain and 4 field isolates of Pasteurella multocida isolated from diseased turkeys which were identified biochemically and serologically as A:1, A:3, A3x4 and D:11. The obtained results revealed that all strains were reacted positively and in different manner with the E20 primer except the 2 field isolates. The results of these reactions demonstrated in terms of bands of different molecular weight specific to each strain. This can be used as a base for characterization and differentiation of strains involved in the present study as the 2 field strains A:1 and A:3 react with primer. Mouse protection test was performed by vaccination of mice with local fowl cholera oil adjuvant vaccine then challenge with virulent field strains A:1, A:3, D:12 and untypable isolates. Results revealed that the local fowl cholera adjuvant vaccine could protect mice against virulent challenge with A:1, A:3 and D:12 field strains but it could not be protect mice against untypable isolates

Two experiments were carried out to evaluate the efficacy of the administration of active dry yeast and/or lactobacillus preparation (AVI-BAC), either before or after the infection with antibiotic resistant field strain of Escherichia coli O127 (E. coli O127) in controlling the severity of infection in quail chicks. The quail chicks of the different experimental groups were infected orally for two successive days with 3x107 CFU of E. coli O-127 as an individual dose. The used field strain proved to be highly pathogenic for quails. Probiotics were supplemented in the drinking water for the different treatment groups at a dose level of 0.5 gm/L. The results revealed that the inclusion of lactobacilli or active dry yeast before E. coli infection has been highly effective in reducing mortality rate, organ invasion and the number of E. coli positive quail chicks. In addition, it decreased the severity of macroscopic and microscopic lesions in different organs in the probiotic treated groups as comparedto the infected controls. Lactobacilli preparations were more efficient in controlling the severity of the infection. On the other hand, the administration of yeast and /or lactobacilli after inducing E. coli infection reduced the mortality rate and the severity of lesion score in different organs but probiotics failed to protect quail chicks against the infection. It has been proved that the two probiotics have synergistic effect in controlling collibacillosis in quails.

Lumpy skin disease virus (LSDV) was isolated, from naturally infected cattle that have a history of previous vaccination with live attenuated sheep pox virus (SPV) vaccine. The virus was isolated on chorio-allantoic membrane (CAM) of specific pathogen free (SPF) embryonated chicken eggs (ECE) and identified by agar gel precipitation test (AGPT) and neutralization test using specific hyperimmune serum against LSDV and SPV. Characteristic intracytoplasmic inclusion bodies was detected in trypsenized cell of infected CAM stained with H&E. Laboratory studies for characterization of isolated LSDV revealed that it was stable at a wide range of pH, but it was inactivated by exposure to 56 0C for 15 minutes. Treatment of isolated LSDV with lipid solvents (20% ethyle ether and chloroform) reduced the virus titer 3.2 and 4.4 log respectively after 24 hrs at 4 0C .On cross neutralization testcomplete neutralization of isolated LSDV was obtained with both reference LSDV and SPV antisera. Cattle vaccinated with live attenuated SPV vaccine under experimental condition found to be protected against natural field infection with LSDV.

Thirty samples of Mozzarella cheese (15 made traditionally from raw milk in Tripoli city (Libya) and other 15 imported samples sold in markets related to different brand names) were examined bacteriologically for their total bacterial count, psychrophilic count, coliform count (MPN/g), presumptive Staphylococcus aureus count, as well as enterococci count. Higher counts were found in locally manufactured Mozzarella cheese. Salmonellae were absent in all examined samples for both types, while Escherichia coli were isolated from 3 samples (20%) of locally made samples. According to the suggested Libyan Standards of such samples, most of examined locally manufactured Mozzarella cheese samples were found unacceptable.