In this study multiplex PCR was used for typing of Clostridium perfringens isolates from soil, clinically healthy and diseased sheep. Clostridium perfringens was isolated from 41 out of 100 soil samples, 12 out of 100 clinically healthy sheep and 118 out of 200 sheep with enterotoxaemia signs. Genotyping of 41 isolates from soil indicated that 29 (70.73%) were type A, 3 (7.31%) were type B and 9 (21.95%) were type D. Of 12 isolates from clinically healthy sheep 6 (50%) were type A and 6(50%) were type D. Of 118 isolates from diseased sheep 42 (35.59%) were type A, 22 (18.64%) were type B and 54 (45.76%) were type D. This result indicates that Clostridium perfringens type A, B and D are the main types causing enterotoxaemia in sheep in Egypt and Clostridium perfringens type A must be included in any vaccine programme to ensure optimum protection.

In this study, 50 vaccinated broiler and one layer flock from Beni-Suef, Fayoum and Minia governorates were investigated. Necropsy lesions were suggestive of LPAI-H9N2 or NDV. Samples of tracheal swabs and organs were subjected for viral isolation and molecular characterization. Specific RT-PCR for the NDV F-gene and the HA gene of the LPAI-H9N2 viruses was used. Virus isolation and primary identification using HI test revealed 37.5 and 43.3-46.2% prevalence for LPAI-H9N2 and NDV viruses, respectively. Phylogenetic analysis of partial sequences of the F gene showed that NDV viruses belong to genotype II and VII-1.1. as indicated by the F0 protein proteolytic cleavage site motifs (aa112-117) of the NDV strains F-gene. The vNDV isolates were 98.7-99.3% and 96.6-98.9% identical to each other based on nucleotide and amino acid identities, respectively. Compared to their counterpart isolates; the lentogenic strains shared 98-99.2% and 96.3-98.1% nucleotide and amino acid identities to the LaSota reference strain. The LPAI-H9N2 phylogeny of the HA gene showed that the 2 isolates obtained in this study are related to each other and related to recent 2016-2018 Egyptian H9N2 strains. Notably, the 2 strains showed higher identity (≥99%) to recent Israeli 2018 isolates with several amino acid changes. The current study revealed wide spread of both NDV and LPAI-H9N2 viruses. The vaccine failure and the mismatch between the vaccine and circulating NDV viruses is the most probable cause of current outbreaks. The LPAI-H9N2 viruses are divergent form their ancestral viruses in Egypt indicating continuous circulation and vaccine pressure induced mutations

During 2005, velogenic Newcastle disease virus (NDV) caused a major outbreak among commercial broiler chicken in Egypt. The outbreak raised concerns regarding the protective immunity of commercially available vaccines for prevention and control of this virus in poultry. The virus was isolated from broiler farm suffered from more than 95% mortalities. The isolate was confirmed not to be avian influenza virus (AIV) by rapid chromatographic strip test, and characterized as NDV using reverse transcription-polymerase chain reaction (RT-PCR) which amplified a portion of the fusion gene of NDV and haemagglutination inhibition (HI) test. This isolate confirmed to be velogenic viscerotropic NDV by mean death time (MDT) test and pathogenicity to 7-week old chickens. We tried to determine whether the existing commercial live NDV La Sota vaccine could provide protection against the isolated virus or not. Birds received a single dose of live La Sota type vaccine at 3 weeks of age and were challenged 2 weeks postvaccination with a lethal dose of NDV. Results indicated that the live vaccine did not protect against morbidity but reduced mortality in comparison to controls. All unvaccinated control chickens challenged with NDV died within 5 days post-challenge (pc). Protection from disease did not correlate with the presence of antibody titers (determined by HI) at day of challenge. These results underscore the need to develop new NDV vaccines and vaccine strategies for use during outbreak situations to protect birds from both disease and infection and to reduce virus shedding.

Feline parvovirus infection (FPV) is one of the serious diseases in Kittens that causes substantial morbidity and death. For the treatment of affected cats and the prevention of disease spread, early diagnosis of FPV infection is critical. To our knowledge, there have been no reports about the disease’s situation in Egypt’s Assiut province. As a result, the goal of this study was to find out how common FPV infection is among ill cats in this province. A total of 30 cats suspected of being infected with FPV were screened using an antigen rapid test to determine whether they were clinically suspicious. To determine the prevalence of FPV, each investigated cat’s age, sex, breed, season, lifestyle (whether kept indoors or outdoors), and immunization were all documented. Overall, 26.7% of examined cats were affected. FPV infection was more common in young, unvaccinated cats who lived outdoor. Epizootiological monitoring of the prevalence rate based on cat breeds and sex revealed no statistically significant differences. In terms of season, spring had the highest infection rate (57.1%), followed by winter (33.3%), and autumn (7.69%). The rapid one-step test is a useful diagnostic tool for detecting FPV, which was found in the research area’s cats.

FMD virus type A/1/ Egypt 2006 was inactivated with 0.1 M of BEI (Binary ethylene imine) formed by cyclization of 2- Bromoethyl-amine hydrobromide (BEA) in 0.2 N NaoH at 37oC with PH 8.0 for 24 hours. The virus was complete inactivated after 15 hours post inactivation. No residual virus particles were detected when inoculated in tissue culture. The inactivation rates are linear with a regular loss of titer ranged from 0.5- 1.0 log10 / hour. Control sample of virus at 37oC without BEI showed only a loss of 1.0 log from the original infectivity titer after 24 hours. The sample of virus which kept at -20oC, without BEI, showed loss 0.3 log10 from its original infectivity titer after 24 hours. There is no change in the complement fixing antigen before and after inactivation process with BEI inactivator and in the CFT 7 dilution of antigen was stable (fixed) pre and post inactivation of virus. Also it was found that the inactivation rate of BEI was higher than the inactivation with pure Ethylenimine (EI) and formalin.

This study was carried out on twelve Holstein dairy cows. Five cows were clinically healthy and considered as control; three cows with left displacement of abomasum (LDA) and four cows with right displacement of abomasum (LDA). Diagnosis of DA based on clinical examinations and confirmed by ultrasonography. The Hb, PCV%, total leucocytic count, neutrophils and abomasal fluid pH were significantly increased (P<0.05) in RDA compared to control. Serum biochemical analysis showed significant reductions of sodium, potassium, chloride and calcium in LDA and RDA and significant increases (P < 0.05) in glucose and total proteins in RDA compared to the control. Moreover, there were significant increases (P<0.001) in ALT, AST, LDH, CPK, urea and creatinine in LDA and RDA compared to control. In conclusion, abomasal displacement produces alterations in the clinical, hematological and biochemical picture compared to control healthy cow and these alterations may vary according to the type of displacement

The present study was carried out in six provinces in both Egypt and Libya throughout the period from January to October 2014. These areas were (Beni-Suef, Ismailia, and Matrouh district) in Egypt and (Tripoli, Zliten, and Zawia district) in Libya. To assess the hygienic quality of underground water sources intended for animal and human drinking and detect the source of pollution. The physicochemical parameters as pH, alkalinity (mg/l), electrical conductivity (μS/cm), total hardness (mg/l), hardness Ca+2 (mg/l), hardness Mg+2 (mg/l), ammonia (mg/l), nitrite (NO2-) (mg/l), nitrate (NO3-) (mg/l) and some heavy metals (Pb, Fe, Cu, Cd, Cr, Zn and Mn) in the underground water were determined. A total of 60 water samples of the underground water were collected from dug wells. Samples were investigated for assessment the physicochemical quality of water destined for human and/or livestock consumption using appropriate instruments for the estimation of metals in the underground water using atomic absorption spectrometer. It has been revealed that a significant increase in mean values of alkalinity (P<0.001) in Ismailia district, Egypt and Zawia district, Libya. Meanwhile, the total hardness showed a significant increase in Tripoli, Zliten and Zawia districts of Libya (367.8±23.73, 345±17.20 and 330±20.19 mg/l, respectively). Mean values of lead (Pb) were higher in Tripoli and Zliten districts, Libya and Matrouh and Ismailia districts, Egypt (0.03±0.1, 0.02±0.3, 0.02±0.07 and 0.02±0.04, respectively). Meanwhile, mean values of cadmium (Cd) were the highest in the three Libyan districts (0.24± 0.003, 0.22±0.07 and 0.012±0.006 mg/l, respectively). In conclusion, the absence of unified system to monitor physicochemical parameters in ground water in the studied areas represented an important task in the evaluation of such water sources and subsequently causing an environmental risk for both animals and humans health.

Four groups of one-day-old SPF chicks were inoculated with the four IBV variants at 1 day old to study the virulence of these isolates. The results at 2 weeks post infection (PI) revealed that all isolates were able to induce serological resposne postinfection, respiratory distress and depression. 20% and 100% mortalities were recorded with isolates 4 and 23; respectively. Assessment of pathogenicity index and pathotyping (at the end of observation period “2wk-PI”), categorized the 4 tested isoaltes (4, 16,18, 23) into three isoaltes of high virulence (4, 18 and 23), and one isolate of intermediate virulence (16). About 50% reduction in body weight was recorded with the four IBV isolates 2 wk PI. Kidney lesions were nephritis-nephrosis with urate deposition in ureters, while microscopic lesions were associated with increase in the amount of rough endoplasmic reticulum (RER). Tracheal lesions recorded as increase the amount of mucin, while microscopic lesions were edema of mucosa and inflammatory cells in the lamina propria. The regime of administering the infectious bronchitis (IB) live commercial H120 vaccine at 1 day old SPF chicks, and the heterologous challenge with four variants (serotypes) at 4 weeks of age, was found to be poorly effective in protecting the respiratory tract of SPF chickens with protection percentages of 8.1%, 55%, 10.5% and 12.6% corresponding to field isolates of IBV 4, 16, 18 and 23; respectively. Protection was measured by assessing ciliary activity of the tracheal epithelium following challenge. It is suggested that the use of the live IB-H120 vaccine will not always broaden the protection against challenge with IB multiple serotypes isolated from Egypt. Therefore it is necessary to develop a new IB vaccines, either locally prepared or imported to overcome any new IB serotype that were emerged, through modifying vaccination strategies to make them appropriate to the field situation.

The current investigation studied an outbreak of lumpy skin disease of cattle in Beni-Suef and Al-Fayium governorates from March up to September 2006. Epidemiological data over a total of 5500 cattle from all ages, breeds and sexes were investigated. Prevalence of lumpy skin antibodies was screened by enzyme-linked immunosorbent assay (ELISA) that revealed high exposure rates; 57% and 51.42% in Beni-Suef and Al Fayium governorates respectively Virus isolation was conducted on chorioallantoic membrane (CAM) of specific pathogen free embryonated chicken egg (SPF-ECE) and MDBK cell culture. The virus identity was confirmed by passive haemagglutination and polymerase chain reaction (PCR) on the infected CAM and MDBK cell culture. Experimental infection of rabbits was successful, demonstrating their possible roles in the epidemiological process of the disease.

During summer 2004, an outbreak of bovine ephemeral fever (BEF) had beenspread among cattle as well as buffaloes in Egypt. The most striking clinical signs incattle were fever of short duration, depression, stiffness, lameness and sometimerecumbency. 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.