An investigation on certain bacterial contaminants of Mortadella produced by three Palestinian factories has been carried out. One sample (2units) was taken monthly (June/1999-may/2000) from each of three local factories (A, B&C). The lowest viable bacterial count recorded was 1x 103 CFU/g. in sample No. C1, while the highest count was 3x107 CFU/g. in sample No. B5. Some bacterial strains were isolated during the course of this study by using specific isolation media. They were identified and distributed as: Salmonella spp. (40%) (S. typhi, 6 strains, S. arizonae, 4 strains and S. infantis, 2 strains), Eschirichia spp. (50%) (E. coli, 8 strains and E. coli O157:H7, 7 strains), anaerobic Streptococcus parvulus (3.3%) (One strain) and Clostridum spp. (6.7%) (Cl. baratii, one strain and Cl. botulinum, 2 strains). Three samples (A1, C3 and B10) were mix contaminated; two pathogenic bacterial strains were isolated from each. All investigated samples were negative for Yersinia spp. and Campylobacter spp. The scientific and medical importance was discussed.

In this study a total of 120 diarrheic buffalo calves were examined clinically and bacteriologically was investigated. The role of E. coli in diarrheic buffalo calves. E. coli, could be isolated from 31 (25.80%) calves. K99 antigen could be detected in (12.90%) isolates. Studying some virulence factors of E. coli isolates revealed that 28 (90.30) isolates showed congored binding, 29 (93.50%) isolates were able to survive in serum and 23 (74.19%) were able to grow in calf serum, 25 (80.64 %) isolates could be proved as enterotoxin producers and caused accumulation of fluids in the intestinal tract of the inoculated mice. In addition, 28 (90.30 %) were able to produce verotoxins. The present study demonstrated the correlation between the presence of different virulence factors in E. coli isolates and its pathogenicity to newborn calves and its role in diarrheic calves

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.

The present study describes the clinical, serological and bacteriolological findings in calves from two beef herds experiencing outbreaks of pneumonia. The clinical signs were nasal discharge, cough, pyrexia and increased respiratory rates. The morbidity and mortality rates over a month period were 40.72% and 15.63% respectively. Laboratory investigations revealed that bovine viral diarrhea virus (BVDV) was involved in and probably initiated both outbreaks as indicated by a significant increase in antibody titers against BVDV in sera of convalescent calves (paired serum samples). No antibodies bovine herpesvirus-1 (BHV-1), bovine respiratory syncytial virus (BRSV) and parainfluenza-3 (BPIV-3) viruses were detected in both acute and convalescent sera. Mycoplasma bovis was concurrently demonstrated in lungs of affected calves as it was isolated from 13 (81.25%) of examined lungs suggesting that there may be a synergism between bovine viral diarrhea virus and Mycoplasma bovis in the pathogenesis of pneumonia. A total of 15 (68.18%) isolates of Mannheimia haemolytica, 5 (22.73%) Pasteurella multocida, 1 (4.54%) Pseudomonase aerugenosa, 3 (13.64%) Staphylococcus aureus, 3 (13.64%) Actinomycis pyogenes, 1 (4.54%) Klebsiella pneumonae, 1 (4.54%) Streptococcus pneumonae, 2 (9.09%) E. coli and 2 (9.09%) Aspergellus fumigatus were recovered from lungs of calves suffering from pneumonia.

Lymph nodes (Ln) are the preferred samples for virus isolation and detection. In the present study, carcass and visceral Ln of apparently healthy cattle were screened for the presence of bovine herpes virus type 1 (BHV-1) and bovine ephemeral fever virus (BEFV) antigens. A total of 198 Ln (114 carcasses Ln and 84 visceral Ln) were collected. Lymph node homogenates were assayed by agar gel precipitation test (AGPT), rapid Staphyloccocal protein A (SPA) agglutination test and Dot-ELISA. The overall results revealed that BHV-1 antigens were detected in 43.9%, 56.1% and in 68.4% of carcass Ln, and in 29.8%, 47.6% and 57.1% of visceral Ln collected from slaughtered cattle by AGPT, SPA agglutination test and Dot-ELISA respectively. On the other hand, BEFV antigens were detected in 5.3%, 38.6% and 52.6% of carcass Ln, and in 6%, 41.7% and 54.8 % of visceral Ln collected from slaughtered animals by AGPT, rapid SPA agglutination test and Dot-ELISA respectively. The results showed high percentage of positive samples with SPA agglutination test and Dot- ELISA in comparison to AGPT for both BHV-1 and BEF.

Nasopharyngeal swabs and pnuemonic lung autopsies collected from diseased or slaughtered sheep and goats suffering from respiratory manifestation were subjected to microbiological sreening. In addition, serum samples were collected from all animals were investigated. P. hemolytica was the most prevalent recovered bacterial isolates followed by S. aureus and E. coli. On the other hand, Aspergillus fumigatus was the most prevalent fungus. Aspergillus species and Candida albicans were also isolated. Most of the isolated bacterial strains were found sensitive to spectrama and chloramphenicol. 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 goats respectively. Also serodiagnosis of Aspergillus fumigatus by indirect haemagglutination test revealed positive results in18.3and 17.5% of diseased sheep and goats respectively and 24% and 21% in sera of slaughtered pneumonic sheep and goats respectively. Histopathological changes due to P. haemolytica and Aspergillus fumigatus were recorded.

Samples from medial retropharyngeal, superficial cervical and deep femoral lymph nodes of four camels were fixed in neutral buffered formalin and prepared for light and electron microscopic examination. The camel lymph nodes were formed of stroma and parenchyma. A dense collagenous capsule and trabeculae beside fine reticular framework represented the stroma. The parenchyma was formed of follicular and non-follicular forms of lymphoreticular tissue. The lymphoid follicles were mainly secondary in nature formed of germinal center and outer corona. Afferent and efferent lymph vessels were noticed at the same area of the capsule. Capsular, subcapsular, trabecular, peritrabecular and parenchymal lymph sinuses were noticed in camel lymph nodes.

Fifteen outbreaks with clinical picture and post- mortem lesions similar to that of rabbit haemorrhagic viral disease (RHVD) were investigated in vaccinated flocks during the period between February and July 2005 at Kafr El-Sheikh Governorate. Twelve representative liver homogenate were positive in haemagglutination test (HA) using human type (O) washed RBCs, with titer more than 1/160. Detection of virus particles by electron microscopy, histopathological findings as well as pathogenicity test , confirmed that the outbreaks were RHVD. The possible role of field rats for the transmission and spread of RHVD among rabbitaries was studied. Cross reactivity and cross protection tests were conducted. These tests proved that the newly emerged RHVD isolates were not closely related to classical local vaccinal strain of RHVD and may be a variant strain.

During summer 2004, an outbreak of bovine ephemeral fever (BEF) had been spread among cattle as well as buffaloes in Egypt. The most striking clinical signs in cattle were fever of short duration, depression, stiffness, lameness and sometime recumbency. Young calves, unfattened bulls and dry, lean non-pregnant cows showed only mild signs while fattened calves, mature heavy bulls and high-producing dairy cows and cows at the late stages of pregnancy were severely affected and signs persisted longer. Deaths and other complications accompanied the disease such as subcutaneous emphysema was not recorded in these outbreaks. In buffaloes, the clinical signs were mild and less severe compared with that of cattle. Serological examination of paired serum samples collected from the diseased animals using serum neutralization test revealed rising of the neutralizing antibody titers for BEF virus after 3 weeks from the onset of clinical signs. Blood picture and biochemical analysis of sera of 6 diseased animals, showed anemia represented by significant decrease in RBCS, PCV% and Hb content. The leukogram showed neutrophihia and lymphopenia with normal leukocytic count. There was rise in plasma fibrinogen with drop in calcium and phosphorus values. All of these parameters were more or less improved three weeks post-recovery. Good nursing care with early treatment with non-steroid anti-inflammatory drug (Phenylbutazone) or administration of calcium borogluconate of lame or recumbent animals lead to rapid and prompt recovery.

In the present study, we expected the anti-tumor effect by combined treatment of arsenic trioxide and interferon (IFN)-α on murine Lewis lung carcinoma (LL2) cells through in vivo study. As a experimental model, LL2 cells (1×10∨6/mouse) were injected subcutaneously into the back region of mice. When the tumor volume reached 100 ㎣, mice were treated with 1 mg/kg arsenic trioxide, 50000 IU IFN-α, or arsenic trioxide and IFN-α. The development of tumor cells was significantly inhibited by combined treatment with arsenic trioxide and IFN-α. In arsenic trioxide and IFN-α treated group, apoptotic index was reached a peak valve at 48 hr after the treatment and it was restored to approximately the control level at 8 days.