This study was carried out in El-Dakahilia governorate on six flocks at different areas 2448 sheep located with varied ages and with history of nervous manifestation. The Prevalence of nervous manifestations was 4.9% (105 /2448). The case fatality rate and mortality rate were 77.14 % and 3.3 % respectively. The percent of Listeria monocytogenes was 26.66% (8/30). Examination of CSF of diseased and control healthy sheep revealed significance elevation of total cell count, total protein and creatinine cytokinase of diseased than control sheep.

Two various kinds of olive mill solid residues (Crude and partly destoned) were used to investigate the adsorbing property of olive mill solid residues (OMSR) to heavy metals. 100 adult albino rats were classified into four groups. One group served as (–ve) control group (10 rats), received balanced ration and supplied tap water; in addition to three equal groups (each of 30 rats) received water polluted with1/100LD50 of either lead, cadmium or copper at concentration levels( 107.2 mg/L, 8.8mg/L or 58.4mg/L respectively). Each main group was divided into 3sub- groups, one (+ve) control and two experimental groups fed either 20 % crude olive mill or 20% partly destoned olive mill. Polluted water administration extended for 1 month, meanwhile feeding 20% crude or partly destoned (OMSR) continued for further 30 days after cessation of polluted water as a withdrawal period. Samples of serum, muscle, liver and kidney were collected at one month of the experiment and at the end of the withdrawal period after one month. Level of metals were determined by atomic absorption spectrophotometer. Results indicate that crude olive mill exhibit higher adsorption capacities to Pb, cd, and cu than partly destoned especially at withdrawal period. In conclusion, the main advantage of this process is the conversion of this waste product to a useful adsorbent material with low coast in minimizing the toxic hazard of environmental pollution with heavy metals.

A total of fifty liver sandwiches served by street vendors and restaurants with different hygienic practices (25 of each), were collected from Giza Governorate. The levels of lead and aluminium residues were determined by using atomic absorption spectrophotometer. The mean values of lead residues in cooked liver sandwiches served by each of street vendors and restaurants were 1.68±0.51 and 0.73±0.2 mg/kg; respectively; as well as, it was constituted 6.2±2.1 and 4.3±1.1 mg/kg for aluminum residues, respectively. The levels of lead and aluminum residues in liver sandwiches served by street vendors were high as compared to that detected in restaurants. The sources of contamination with such elements (lead and aluminium) as well as the public health importance were discussed. The suggestive measures to avoid the contamination with such elements in cooked food were recommended.

The present study has been carried out to investigate the effect of three neurotransmitters (Glutamate, L-Arginine and GABA) on some aspects of the reproductive performance of mature male Albino rats. For this purpose, a total of 100 mature male Albino rats were used. Rats were divided into 4 comparable groups; the first consists of 10 rats, was left as control. The second was administered glutamate 10 mg/ kg, the third group was injected by L- Arginine 20 mg/ kg while the fourth was injected by GABA 1 mg / rat. The results showed that administration of glutamate was concomitant with increase in synthesis and release of pituitary LH causing increase in its serum level as well as decrease serum level of testosterone. On the other hand, prolonged L-Arginine administration led to remarkable elevation in both pituitary and serum LH and significant decrease of serum testosterone. While, GABA administration led to remarkable decrease in pituitary and serum LH with significant decrease in serum testosterone level.

This study was performed in the period February 2009 through January 2010 to determine the role of dairy cattle in transmitting listeriosis to man in Beni-Suef Governorate, Egypt. Individual milk samples and rectal swabs were gathered from 175 dairy cows (125 clinically diseased and 50 apparently healthy). A total of 75 kariesh cheese and 150 dairy shop milk samples were randomly collected from the same localities where the examined cattle were reared. Stool and blood samples were taken from 125 humans comprising 75 individuals residing in close contact with the examined cows and 50 feverish inpatients. The occurrence of Listeria spp. in the examined dairy cattle revealed that 1.14 % of individual milk samples harboured Listeria spp.; L. innocua (0.57 %) and L. seeligeri (0.57 %). None of rectal swabs revealed a positive result. L. monocytogenes could not be recovered from any of the examined cattle samples. Examination of kariesh cheese demonstrated a positive result to L. innocua (1.33 %). Concerning dairy shop milk examined, 5.33 % was Listeria spp.-positive; they were identified as L.monocytogenes (2.67 %), L. innocua (1.33 %) and L.seeligeri (1.33 %). Examination of humans revealed a positive result for L. welshimeri in a stool sample (0.8 %) taken from an apparently healthy woman while all the examined blood sampleswere Listeria-negative. It was concluded that listeriosis in Beni-Suef Governorate appears to be ofsporadic nature and that the potential of human exposure to Listeria spp. and L. monocytogenes from dairy cattle is more likely to exist in dairy shop milk rather than being related to the animal itself.

Fowl and turkey pox viruses were analyzed for their heterogeneity on the basis of protein profile, western blotting, PCR analysis and restriction endonuclease analysis. On the protein level, only a single band with a WM of 115KDa was seen with turkey pox virus but not with the fowl strain, and a band reacted at 10KDa with Turkey but not fowl pox virus in western blotting analysis other protein profiles were nearly the similar. PCR amplification of the lateral terminal repeat (LTR) region of both viruses confirmed a single band migrating about 900 bp with both strains and restriction digestion proved the homology between both strains.

This study was conducted in the period July 2009 through June 2010 to determine the role of commensal rodents in transmitting bacterial pathogens to man in Beni-Suef Governorate, Egypt. A total of 50 rats of various species were selected from both urban and rural areas at different localities. In the laboratory, rodent species were identified and bacteriological examination was performed. Seven types of samples were cultured from external and internal body parts of each rat. The identified rodent spp. included Rattus norvegicus (16%), Rattus rattus rattus (42%) and Rattus rattus frugivorus (42%). The results demonstrated that S. aureus, S. lentus, S. sciuri and S. xylosus were isolated from the examined rats at percentages of 8, 2, 6 and 6 %, respectively. Moreover, E. durans (2%), E. faecalis (12%), E. faecium (24%), E. gallinarum (4%), Aerococcus viridans (12%) and S. porcinus (2%) in addition to Lc. lactis lactis (4%), Leuconostoc sp. (2%) and Corynebacterium kutscheri (8%) were also harbored by the screened rodents. On the other hand, S. arizonae, E. coli, E. cloacae and E. sakazakii were isolated from the examined rats at percentages of 4, 8, 4 and 6 %, respectively. Besides, Proteus mirabilis (6%), Proteus vulgaris (2%), Providencia rettgeri (6%), P. aeruginosa (4%), Burkholderia cepacia (2%) and V. fluvialis (2%) were also recovered from the investigated rodents. It was concluded that considerable bacterial pathogens could be harbored in/on different body parts of the examined rodents and that commensal rodents prevalent in Beni-Suef Governorate supply multiple potentials through which they may act as sources of infection and occasionally represent a serious threat to the public health.

Three vaccination regimes based on Clostridium perfringens (C. perfringens) type A, C or combined AC toxoids were evaluated to detect if toxoid vaccines can prevent necrtotic enteritis (NE) caused by clostridial infection in broilers. The vaccines were administered two times at two weeks interval, then the birds were challenged with virulent strains of C. perfringens type A, C or combined AC. Blood samples were taken after both first and second vaccination doses as well as after challenge. Evaluating parameters included clinical signs, gross intestinal lesions, hemogram [red blood cell count (RBCs), packed cell volume (PCV), hemoglobin (Hb), total leukocytic count (TLC) and differential leukocytic count],serum biochemical assays [total protein (TP), albumin (Alb), globulin (Glob), albumin globulin ratio (A/G), serum activities of alanine amino transferase (ALT), aspartate amino transferase (AST), alkaline phosphatase (ALP) and uric acid (UA) values] and ELISA test for detecting serum antibody titers. Results revealed that affected birds showed marked depression, anorexia, reluctance to move, ruffled feathers and diarrhea. Numbers of chickens with intestinal lesions in immunized challenged groups were greatly fewer than the infected non immunized ones. There was an increase in RBCs, PCV and Hb. TLC decreased in infected non immunized birds and increased in vaccinated ones. Heterophils were increased in infected groups while, lymphocytes decreased. Prominent lymphocytosis was observed in immunized birds. Results of biochemical assays showed that there was a significant increase in TP, Alb, Glob, ALP, ALT, AST and UA and decrease in A/G. Results of ELISA test showed that there was a significant increase in antibody titer after immunization paricularly after the second dose of vaccination. The combined AC toxoid provided the greater antibody titer and best protection followed by toxoid A and finally toxoid C. We concluded that results provide an evidence that immunization of broilers with toxoid vaccines paricularly the combined type AC is safe, welltolerated and can protect broiler chickens against NE after the second booster dose of the vaccine.

The pharmacokinetic aspects of cephradine were studied after intravenous (IV), intramuscular (IM), subcutaneous (SC) and oral administration of a single dose of 50 mg kg-1 b.wt. in chickens. Tissue distribution and residues of cephradine after repeated oral administration for 5 consecutive days were also estimated. After IV injection of cephradine in a dose of 50 mg kg-1 b.wt., the serum concentration time curves were best described by a two compartment-open model. The drug was rapidly distributed with a distribution half-life (t0.5(α)) of 0.120 h and apparent volume of distribution (Vdss) was 2.187 L kg-1. The drug was rapidly eliminated with a half-life of elimination (t0.5(β)) of 1.047 h and the body clearance (ClB) was 2.35 L kg-1 h-1. The drug was rapidly absorbed after IM, SC and oral administration as indicated by short half-lives of absorption (t0.5(ab)) of 0.154, 0.364 and 0.65 h., respectively. While the elimination half-lives (t0.5(el)) and systemic bioavailabilities were 0.859, 2.652, 1.74 h and 59.386, 84.5, 97.97 %, respectively. Repeated oral administration of cephradine (50 mg kg-1 b.wt twice daily) for 5 consecutive days caused no change in serum enzyme activities of ALT and AST but induced a significant increase in serum uric acid concentration at 72 to 120 hours post administration.

Twenty five isolates of IBV were isolated from 36 broiler and layer chicken farms collected from 13 governorates during 2 years started from January 2003. All the examined farms were vaccinated using the commercial live IB-H120 vaccine in addition to the IB-inactivated vaccine in the layer farm. The viruses were isolated and identified previously by chicken embryo, CEK cell culture inoculation. Isolates subjected to RT-PCR. Four isolates; three broiler farms and one from layer farm were genotyped using S1 partial gene sequencing. Typing of the four isolates using S1 partial gene sequencing, revealed that the isolated IBV strains showed homology to Asia, Europe, USA and Middle East strains.