In this study field application of RB51 vaccine combined with the policy of test and slaughter as well as application of hygienic measures for control of bovine brucellosis were carried out and evaluated in a dairy herd of cattle for two years. Serological examination of 1280 cattle using tube agglutination, buffered acidified plate antigen, Rose Bengal plate antigen and Rivanol tests revealed 240 (18.75%) positive animals with a previous history of abortion of 12 cows. Brucella melitensis biovar 3 could be isolated from tissue specimens of slaughtered cows. Animals that tested negative in the first examination were vaccinated with RB 51 vaccine with periodical examination every three weeks and slaughtering of positive cases. New positive cows continued to develop up to the 5th examination then three successive sero-negative tests were obtained with release of the farm from quarantine. Examination of animals 6,12,18 and 24 months post release of quarantine revealed 2, 3, 0 and one positive cases respectively the matter which clarified that the control of the outbreak using RB51 vaccine associated with policy of test and slaughter and application of hygienic measures showed some limitations.

A total of 100 fecal samples from goats were coprologically examined to investigate the main cause of diarrhea. Animals were divided according to the age into 3 groups (7-35 days, 35 days - 6month and over one year). The results revealed that Eimeria species was the most predominant parasite (70%), the parasitic gastroenteritis (28%) and Cryptosporidium species (21%). Ten species of Eimeria were identified from the infected animals, E. hirci, E. arloingi, E. intericata, E. ahsata , E. christenseni, E. marisca, E. crandalis, E. weybridegenesis, E. faurei and E. ovina. Three species of parasitic gastroenteritis (Haemonchus contortus, Ostertagia species and Trichostrongylus species). Cryptosporidium oocysts were found common in young goats

Nasopharyngeal swabs and pnuemonic lung autopsies collected from diseased or slaughtered sheep and goats suffering from respiratory manifestation were subjectedto microbiological sreening. In addition, serum samples were collected from allanimals were investigated. P. hemolytica was the most prevalent recovered bacterialisolates followed by S. aureus and E. coli. On the other hand, Aspergillus fumigatuswas the most prevalent fungus. Aspergillus species and Candida albicans were alsoisolated. Most of the isolated bacterial strains were found sensitive to spectrama andchloramphenicol. Serodiagnosis of P. hemolytica by ELISA using the whole cell antigen gave positive results in 18.3 and 22.5% of diseased sheep and goats respectively and 52% and 42.1% of slaughtered pneumonic sheep and goatsrespectively. Also serodiagnosis of Aspergillus fumigatus by indirect haemagglutinationtest revealed positive results in18.3and 17.5% of diseased sheep and goats respectively and 24% and 21% in sera of slaughtered pneumonic sheep and goatsrespectively. Histopathological changes due to P. haemolytica and Aspergillus fumigatus were recorded.

The anesthetic, biochemical and pathological effects of eugenol were evaluated in the African cat-fish Clarias gariepinus in comparison with MS-222. Aquous exposure of Clarias gariepinus to eugenol at concentration of 62.5 – 250 ) g / ml showed short interval to induction than MS-222. On the other hand, eugenol provided longer time for recovery (8.28 min) at higher concentration (250 )g / ml) than MS-222 (5.26 min) but no differences were observed at lower concentrations between both agents. Mortality rate of 46.5 and 33.3 % was recorded for eugenol and MS-222, respectively at 250 )g / ml. Exposure of fish to 250 )g / ml of eugenol or MS-222 resulted in significant increases in serum levels of creatinine, urea and uric acid and decrease in total protein and albumin. Significant increases in AST, ALT and Ca levels were recorded only on exposure to eugenol 250 )g / ml. Histopathological examinations showed congestion of gill blood vessels, diffuse vacuolar degeneration and necrosis of the epithelium lining of the secondary lamellae of the gill filaments, degeneration and focal necrosis of renal tubules in kidneys, necrosis and deposition of hemosiderin pigment in the macrophages of spleen which is indicative for hemorrhages and hemolysis as well as mild catarrhal enteritis of intestine of fish groups exposed to 250 ) g / ml of both agents. Moreover, massive fatty and degenerative changes in liver were observed only in fish exposed to 250 )g / ml of eugenol. On the other hand, lower concentrations of both agents did not differ from those of control fish. In conclusion, it appears that eugenol at lower and medium concentrations could produce an anesthesia characterized by rapid induction and rational recovery without significant changes in tissues and blood chemistry. Care should be taken on using high concentrations of eugenol as ventilatory failure may occur

Thirty samples of freshly slaughtered broiler frame with skin were obtained from small scale poultry processing plant in Cairo and Giza markets. Samples of neck and breast skin were examined for Total colony count, Psychrotrophic count, Staphylococcus aureus count, Coliform Count, presumptive E. coli count and total yeast and mould count. In addition isolation of Salmonella spp. and thermotolerant Campylobater were performed. Lower bacterial counts were recorded in cooked samples, with mean value of 7.6 ± 0.18, 5.68 ± 0.16, 5.12 ± 0.14, 3.6 ± 0.3, 2.3 ± 0.39 and 6.85 ± 0.37 log10 cfu /g in raw samples and 0.91 ± 0.27, 0.74 ± 0.21, 0.56 ± 0.19, 1.1 ± 0.13, < 3 and 2.44 ± 0.12 log10 cfu/g in cooked samples respectively. The incidence of S. aureus, Salmonella and Campylobater jejuni in raw skin samples were 66.7%, 20%, and 56.6%, respectively. While S. aureus was unexpectedly isolated from cooked samples. Fat content was estimated by using Sohexelt method and fatty acids content of methylester were determined.

In this study we used one reference Climson University (CU) strain and 3 virulentfield strains isolated from naturally infected chicken and identified as P. Multocida.DNA was extracted from all strains and subjected to restriction endonuclease analysis, using EcoRI, HpaII and Hind III revealing that, great similarity between either the reference or local virulent field isolates. The obtained results indicated that the most differentiable restriction endonuclease enzyme was the Hind III, which showed different band patterns between different strains.

Twenty-five samples of canned fish (tuna and mackerel), frozen fish (mackerel and mazelli) as well as smoked fish (herring); five samples of each were randomly collected from different localities of Alexandria city. Collected samples were subjected to biogenic amine examination. Histamine and Tyramine were determined by HPLC. The highest average value (mg/100g) for histamine was 6.94 (canned tuna) and the lowest was 0.76 (Frozen Mazelli), the respective values for Tyramine were 1.63 (canned tuna) and 0.06 (frozen mazelli) mg/100g. For improvement the quality of raw fish (fresh sardine, 10 kg) during preparation the fresh sardine prior chilling or freezing was dipped into crude potato extract (as protease inhibitor) to reduce biogenic amines production. In order to test the effect of heat treatment on the concentration of the biogenic amines in fish (Frozen mackerel and sardine) were subjected to oven baking at 1506 C for 20 min. This showed high reduction in the percentage of biogenic amine production due to heat treatment. The public health significance of the biogenic amines as well as the suggested measures for improving the quality of produced products has been discussed

Rhizome extracts of Gunnera perpensa are used in traditional remedies in South Africa to treat endometritis both in humans and animals. An investigation was undertaken to determine whether this plant possesses antibacterial activity, which may explain its efficacy. Gunnera perpensa rhizome extracts were prepared serially with solvents of increasing polarity and tested for antibacterial activity. Test bacteria included the Gram-positive Enterococcus faecalis and Staphylococcus aureus and the Gram-negative Escherichia coli and Pseudomonas aeruginosa. A moderate to weak level of antibacterial activity in most of the extracts resulted, with the best minimal inhibitory concentration (MIC) value of 2.61 mg ml-1 shown by the acetone extract against S. aureus. The extracts were also submitted to the brine shrimp assay to detect possible toxic or pharmacological effects. All the extracts were lethal to the brine shrimp larvae at a concentration of 5 mg ml-1. The acetone extract was extremely toxic at 1 mg ml-1, with some toxicity evident at 0.1 mg ml-1. The remainder of the extracts generally displayed little activity at concentrations lower than 5 mg ml-1. In summary, the results indicate that although the extracts demonstrated a level of pharmacological activity, the relatively weak antibacterial activity is unlikely to justify the use of G. perpensa rhizomes in the traditional treatment of endometritis. Rather, the slightly antibacterial nature of the rhizomes may contribute to an additive effect, along with their known uterotonic activity, to the overall efficacy of the preparation.

Serum samples from 20 out of 180 (11.1 %) apparently healthy Nigerian indigenous chickens were negative for antibodies against chicken anaemia virus using the enzyme-linked immunosorbent assay (ELISA). Of the 160 positive sera (88.9 %), 12 (7.5 %) had titres ranging from 1 500-3 000, 46 (28.8 %) had titres from 3 000-5 000 while 102 (63.8 %) had titres between 5 000-11 000. The overall mean titre value was 5 845 + 2 402. This appears to be evidence of a natural outbreak of the infection since the chickens had no history of vaccination against any poultry disease.

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 %.