The present study bases on evaluate the immune responses due to experimental infection of (BALB/c) mice by Salmonella hadar . The experiment was carried out on eighty mice of both genders with age range (6 – 8) weeks old, the mice were divided randomly into three groups (group A:- contain 20 mice were administrated orally with infectious dose (1.5×107C.F.Uml) ,group B:- contain 40 mice were administrated orally with LD50dose (1.5×109 C.F.Uml) and groupC:- contain 20 mice which inoculated orally with 1 ml of PBS (pH=7.2) and consider as control group). The study has noticed that the experimentally infected mice are able to induce humoral immune response which represented by producing antibody against Salmonella hadar and this production was elevated after two weeks of administration and reach the peak after four weeks post infection then decline sharply after passage of six weeks post infection in both groups (A and B) but the titration of the antibodies in group B was higher on that recorded in group A. It is obvious that S. hadar is able to induce cellular immune response during experimental infection with infectious dose and LD50 dose and the results of delayed type hypersensitivity have showed increases in the thickness of the right footpads of the mice of both groups (A and B) and the highest mean of the thickness was after 24 hours post immunization. Finally, we concluded that Salmonella hadar in infected the host was able to induce both humoral and cellular immune responses and these responses are dose dependent.

Chlamydophila abortus (C. abortus) is one of the most important causative agents of enzootic abortion which has been caused a serious economic problem in domesticated and wild ruminants world wide. This study was aimed to diagnose C. abortus infection in aborted goats in Ras Suder Research Station (South Sinai) - Desert Research Center from 2004-2006. Twenty aborted cases from 130 pregnant nannies were recorded and examined serologically using complement fixation test (CFT). Eighty percent (16/20) of the aborted cases were serologically positive and 20% (4/20) randomly collected from apparently healthy pregnant nannies were also had antibodies against C. abortus. Pathological lesions were detected. Ten aborted fetal samples from serologically positive aborted nannies were subjected to diagnosis using Polymerase Chain Reaction (PCR) showed positive results at 119 bp. According to this result, PCR proved to be feasible, reliable, specific and sensitive diagnostic tool in diagnosis of C. abortus infection.

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.

In an attempt to evaluate the possible role of Eimeria stiedae infection on rabbit vaccinated with haemorrhagic septicaemia oil adjuvant vaccine, a total of 60 New-Zealand rabbits were divided into 6 groups (A- F). The first four groups subdivided into two subgroups. The subgroups (A1, A2) vaccinated and infected at time of 1st dose of vaccine, subgroup (B1, B2) vaccinated and infected at 2 weeks post 1st vaccination, subgroup (C1, C2) which vaccinated and infected at the time of 2nd dose of vaccination, finally subgroup (D1, D2) vaccinated and infected at 2 weeks post 2nd dose of vaccine. Group E vaccinated only but the group F left as non vaccinated non infected (control). The results revealed that E. stiedae infection at the time or after 2 weeks from first or second dose of vaccination (A1, B1, C1 and D1) and treated with semduramycine 150 showed slight decrease of the antibody titer in contrast the untreated group (A2, B2, C2 and D2) showed sudden decrease of P. multocida antibody titer measured by indirect haemagglutination and ELISA test. Vaccinated group (E) was the superior one showing the highest antibody titer. The challenge test of all rabbit groups with virulent P. multocida revealed a protective percent of 83.4%, 50%, 100% and 0 % in treated, untreated, vaccinated and control group respectively, but subgroups C2, D2 the protective value was 33.4% this due to challenge concurrency post or at the time of infection. These findings reflect the important to avoid coccidial infection following vaccination programs to obtain better immune response to haemorrhagic septicaemia oil adjuvant pasteurellosis vaccine and high level of protection.

The present study was conducting aiming to throw the light on the retinal structure on the level of both light and electron microscope. Eyeballs of 35 adult clinically healthy goats of both sexes were collected from Beni- Suef abattoir. The eyeballs were clinically examined before they were dissected and fixed in 10% buffed neutral formalin and in Bouin’s solution for 24 hours. The specimens were then processed for light and transmission electron microscope. The retina (pars optica retinae) of the goats extends rostrally to cover the ciliary body as pars ciliaris retinae and the iris as the pars iridis retinae. Pars optica retinae and pars iridis retinae form the light non sensitive parts of the retina, while the sensitive part except at the transition zone; the ora serrata and the optic disc, appeared to be formed of ten layers, named from outward to inward as, retinal pigmented epithelium, rods and cones layer (photoreceptor cell layer), external limiting membrane, outer nuclear layer (cell bodies and nuclei of the photoreceptor cells), outer plexiform layer, inner nuclear layer (contained the horizontal, bipolar, Muller and amacrine cells), inner plexiform layer, ganglionic cell layer, nerve fiber cell layer (unmyelinated nerve fibers) and internal limiting membrane.

A total of 165 cows, 19 buffaloes, 192 sheep and 118 goats were examined for detection of Mycoplasma mastitis. The results revealed that 114 (69.59%) and 6 (31.57%) were clinically mastitic cows and buffaloes respectively while 51 (30.9%) and 13 (68.42%) were apparently healthy cows and buffaloes respectively. On examining the apparently healthy cows and buffaloes, 67 (32.84%) and 18 (34.61%) were subclinically mastitic cows and buffaloes respectively. Mycoplasmas were isolated in percentages of 8.9%, 5.5% from subclinically mastitic cows and buffaloes respectively and in percentages of 12.97%, 12.5% from clinically mastitic cows and buffaloes respectively. M. bovis was isolated from 8 (32%) and M. bovigenitalium from 7 (28%) and 10 (40%) unidentified Mycoplasma. Isolation of Mycoplasma from udder tissue in cows and buffaloes were in a percentage of 28.5% in cows while no Mycoplasma isolates were obtained from buffaloes' udder tissues. Application of PCR technique on these isolates and some of the negative samples was positive 100%. On the other hand, the results revealed that 82 of 192 (42.7%) and 43 of 118 (36.44) of the examined sheep and goats respectively were clinically mastitic. Isolation of Mycoplasma was from 11 (13.41%) and 17 (39.53%) of the examined sheep and goat respectively. Identification of these isolates revealed 8 (29%) M. agalactiae isolates and 20 (71%) unidentified Mycoplasma spp. Application of PCR technique on traditionally identified M. agalactiae isolates revealed negative results on using M. agalactiae specific primer while positive results were obtained for the same 8 isolates (100%) on using M. bovis specific primer.

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.

Female Oreochromis niloticus were exposed to 1/10 LC50 (0.21ppm) of butachlor herbicide for 6 weeks. Weekly specimens were taken for fecundity estimation. Also hormonal and enzymatic levels were determined in addition histopathological alterations in ovaries and liver were detected. Butachlor exerted drastic effects on absolute and relative fecundity. Sex hormones (testosterone "T" and estradiol "E2") dropped significantly. The high significantly decline in Total Ripen Egg Number was assisted by the coagulative necrosis and oocytic atrasia in ovaries. In addition, thrombus formation and hepatoadenocarcinoma were pronounced in the liver and resulted in the significant drop in ALT and total protein levels. So, it is recommended to apply the biological control of pests in substitution to herbicids in rice fields.

he present study was carried out to represent a field problem in squabs of domestic pigeons (columba livia) at Ismailia Province. Squabs were grossly examined and showed typical lesions including yellowish caseous, fibronecrotic patches in mouth due to infection with T. gallinae. Forty squabs were collected and tested individually for the presence of Trichomonas gallinae (T. gallinae). Squabs were divided into equal four groups, the 1st was un-infected control group, the 2nd was T. gallinae infected untreated group, the 3rd and the 4th groups were T. gallinae infected and treated with metronidazole. The obtained results showed that the mortality (%) were 0, 50, 20 and 30 % in 1st, 2nd, 3rd and 4th group, respectively. Body weight was significantly reduced in all groups, although the drugs improved the weight reduction as compared to pre-treatment. Organs' weights were significantly increased after treatment as compared with the control group. Serum biochemical analysis revealed significant elevation in total protein, globulins; β- globulin and γ- globulin but albumin , α-globulin levels and A/G ratio were significantly reduced in infected squabs and increased in treated groups. Serum urea, creatinine and uric acid levels were increased, while, Serum glucose , cholesterol Na, K, Ca, P, Mg and serum iron as well as plasma ChE activity were decreased in both treated and infected groups. Serum AST, ALT, LD, γ -GGT, CK, AP activities were significantly increased in infected groups, Destructive changes in buccal cavity, hyperemia in blood vessels, necrotic changes in the liver with leucocytic infiltration and demylination of brain with preivascular oedema were observed.

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.