A number of 50 Ardeola ibis ibis birds were found harboring six nematodes species; Tetrameres species, Microtteramere species, Synhimantus invaginatus, Synhimantus equispeculatus, Ascaridia species, Paracamallanus species,and five species of trematodes; Euclinostomum heterostomum, Nephrostomum ramosum, Apharyngostrigea ibis, Apatemon gracilis and Centrocestus armatus. The most common infection by nematodes was (46%) in which highest infection rate Synhimantus invaginatus recorded (30 %) while the trematode infection was (24 %) and Apatemon gracilis was the most prevalent (16 %). Experimental infection of buff backed heron by encysted metacercaria (EMC) and exysted metacercaria (ExMC) of Clinostomum complanatum from freshwater fish Tilapia nilotica, resulted in adult worms formed after 6 days. Where the infection by EMC recorded higher worm burden (14-18 worm) and hatching percent (78%) while the infection by ExMC gave lower worm burden (7-10 worm / bird ) and hatching (48 %). In the present study, it is worthy to mention that buff backed heron act as final host model for Clinostomum complanatum and this will be helpful in further biological and immunological studies for this trematode to decrease its economic losses in fish intermediate host.Fifty random samples of Kareish cheese were collected from different localities in Bani-suef Governorate. All samples were examined chemically for acidity, salt and moisture percent and bacteriologicaly for the presence of Escherichia coli, Staphylococcus aureus, Enterococci, Bacillus cereus, Clostridium perfringens, Yersinia enterocolitica, Salmonella and Shigella species. The obtained results revealed that the mean values of acidity, salt and moisture % were 1.63 ± 0.095,3.55 ± 0.299 and 58.54 ± 0.599 in the examined kareish cheese samples, respectively.Escherichia coli, Staphylococcus aureus, Enterococci, Bacillus cereus, Clostridium perfringens were recovered from 16 (32%), 12(24%), 46 (92%), 25 (50 %) and 3 (6%) with a mean value of 4.86x102 ±4.21x10 2, 4.84x 10 5 ± 2.91x10 5, 3.74x10 6±1.55x10 6, 7.08x10 4±2.61x10 4 and 9.5x10 1 ± 7.37x10 1 of the examined samples , respectively. Yersinia enterocolitica could be isolated from 12% of the examined samples. Salmonella and Shigella species could not be detected in any of the examined samples. The isolated Escherichia coli were examined for serological identification, Enterotoxigenicity and the susceptibility of the isolated serovars to various chemotherapeutic agents. The public health significance and economical importance of the isolated organisms and the recommendations to be followed in the processing, handling and storage of such dairy product were discussed

Cellulitis is a serious problem for the poultry industry because of increased condemnations, carcass downgrading at processing, and higher labor costs to process affected flocks. In the present study, the prevalence of cellulitis was studied in 240 broiler chickens. The correlation between cellulitis and other systemic lesions of the same bird was investigated also. Moreover, identification of the causative bacterial agents was conducted focusing on E. coli and Salmonella isolates. The prevalence rate of cellulitis in examined broiler chickens was 38.3%. Cellulitis without systemic lesion was observed in 14.2% of birds while 24.2% of birds had cellulitis associated with other systemic lesions in the internal organs while hepatitis was the most frequent. The bacteriological examination revealed that of 253 samples collected, a total of 157 bacterial isolates were recovered (62.1%). Among the recovered isolates, E. coli was the most prevalent (126 isolates; 80.3%) as well as 4 Salmonella species (2.5%), 9 Proteus species (5.7%), 7 Pseudomonas aeruginosa (4.5%), 3 Enterobacter species (1.9%) and 8 Staphylococcus aureus (5.1%). Serogrouping of E. coli isolates revealed that O125 was the most prevalent; 32%, followed by serogroups O158, O55, O78 as 24%, 12%, 10%, respectively, then both O1 and O8; 6% for each, and finally O15; 4%. Antibiogram of E. coli isolates showed a high sensitivity against enrofloxacin only (81%) while they were moderately sensitive to apramycin (65.9%) and colistin sulphate (61.9%) as well as ciprofloxacin and cefotaxime sodium (56.3% and 55.6%, respectively). On the other hand, high moderate degrees of resistances were observed against the other antimicrobials. Salmonella isolates showed complete sensitivities to ciprofloxacin and enrofloxacin while they were completely resistant to most of antimicrbials.

The effect of 10 times (10x) overdose of enrofloxacin was studied in broiler chickens. One hundred and eighty chicks were classified in 3 equal groups. The first group received normal theurapeutic dose of enrofloxacin (1x) in drinking water for the first 5 consecutive days of age and repeated again at 24th -28th day of age. The second group received 10x (overdose) at the same ages. The third group was left non-medicated as a control group. Blood samples were taken on the 6th, 14th, 29th and 34th day of age for different laboratory tests. Enrofloxacin at 10x caused a decrease in the value of the following parameters: HI antibody titers to NDV vaccine at the 14th and the 34th day of age, serum albumin at the 10th day of age, hemoglobin at the 29th and the 34th day, lymphocytic count and IBDV ELISA titers at 29th day of age, uric acid at 29th day, phagocytic activity at 34th day, Lactobacillus spp. count in duodenum, feed conversion efficiency and body weight gain. The 10x (overdose) increased serum urea and creatinine at 29th day of age, serum AST and ALT at 29th and 34th day of age, and heterophilic count. Histopathological degeneration in liver, spleen, kidneys, bursa of Fabricius and thymus were demonstrated by 10x (overdose) of enrofloxacin. Challenge with vNDV caused 66.6% mortality in birds received the 10x (overdose) compared with 33.3% in the vaccinated non treated control group.

This study was conducted to evaluate the protective effect of Brucella melitensis Rev.1 and the use of BCG vaccine as immunostimulant by subcutaneous injection in Guinea pigs. Lab. animals were divided into 8 groups: Combined Rev.1 and BCG vaccines injected in the1st group & both vaccines were injected simultaneously in the 2nd group. Three groups sensitized with BCG vaccine then injected with Rev.1 vaccine one week, two week & three weeks intervals respectively. Other two groups were injected with BCG and Rev.1 vaccine individually. The last one was unvaccinated control. All injected animals showed resistance to infection with 16 M strain (90 %, 80 %, 80, 60 %, 70 %, 0 % and 70 % respectively).Thus animals vaccinated with bivalent Rev.1 and BCG vaccines (in one shot) showed the best protective level to infection

The efficacy of four infectious bursal disease virus (IBDV) vaccines including intermediate (D78) and intermediate plus (228E, IBD-Blen and Bursa-Vac+) were compared in priming vaccination of 10 days commercial old male layer chicks. There were different parameters were measured for testing these vaccines including; the immunogenic efficacy, the effect on performance, organ (bursa, spleen, and proventriculus) body weight index as well as histopathological examination of bursa, spleen, proventriculus and thymus. Chick was received a dose of 102 EID50 from one IBDV vaccine out of 228E, IBD-Blen or Bursa-Vac+, while D78 dose was 104 EID50. The results cleared out that all the tested vaccines passed through the maternal derived antibodies 2480.133 + 156.3. All vaccines stimulate antibody formation as measured by ELISA test. The used vaccines not affect markedly body weight and feed intake, as there were no significant differences between the control group and the vaccinated ones in the mean body weight and the feed conversion rate. Furthermore, the bursa: body weight index of vaccinated groups were generally less than those of control one at all intervals, while the spleen and proventriculus: spleen: body weight index of vaccinated groups was higher than control on at the end of the observation period. The used vaccines induced histopathological changes in bursa, spleen , proventriculus and thymus glands. These results indicated that all tested vaccine are of value in vaccination of commercial chicks from vaccinated breeders

Stability study of biological products especially living bacterial vaccines plays an important role for determination of product changes in maintenance period and ensures safety, efficacy and maintenance of biological properties of the vaccines. So, the objective of this study was to establish stability and keeping quality of the local Brucella melitensis Rev-1 vaccine using different types of stabilizers in lyophilization process. A long-term stability study was carried out for four batches of reduced-dose Brucella melitensis Rev-1 vaccine manufactured by veterinary serum and vaccine research institute using four different stabilizers. These stabilizers were (A) sucrose and skimmed milk, (B and C) different concentrations of sucrose, sodium glutamate and gelatin, and (D) casein, sucrose and sodium glutamate. The quality control tests including colony forming unit, purity, dissociation and physicochemical tests on all batches until 12 months post- production were performed. The obtained results indicated that, in spite of collapse (shrinkage) of lyophilized cake in a number of bottles in batches prepared using stabilizer A, the brucella vaccine batches were stable and met the specification recommended by OIE 2012 for 12 months post-production in vaccine batches with stabilizers A and D.

The objective of this work was to estimate the lead (Pb), Cadmium (Cd), Copper (Cu), Zinc (Zn), Iron (Fe) and Manganese (Mn) levels in drinking water, layer feed and muscle samples were collected during winter season from two layer farms which present at two different areas, non industrial area (Integrated poultry project in El-Azab) and industrial area (Kom Oshim) in Tamia district in El-Fayoum province, Egypt. All samples will be analyzed to determine the translocations of heavy metals from water and feed to the bird's muscle. The results explained that the mean metal concentrations in the different samples of selected poultry farms are Pb (1.1034±0.097, 1.173±0.129), (2.891±0.194, 3.182±0.28) and (0.071±0.03, 0.099±0.0396 ppm). Cd (0.419±0.004, 0.389±0.017), (0.508±0.017, 0.5854±0.003) and (0.005±0.0013, 0.0125±0.003 ppm). Cu (5.9±2.1, 0.8596±0.054), (9.15±1.202, 14.75±0.417) and (0.0442±0.0075, 0.03032±0.004 ppm). Zn (14.50±1.285, 13.628±1.053), (57.605±3.06, 58.319±0.73) and (0.0668±0.018, 0.016±0.00498 ppm). Fe (171.011±79.6, 186.74±72.65), (153.58±15.3, 124.12±3.26) and (0.013±0.008 ppm, ND). And Mn (3.187±1.539, 1.398±0.768), (84.98±5.676, 85.884±1.07) and (0.0056±0.0037ppm, ND) for muscle, layer feeds and drinking water which were collected from non industrial area and industrial area in ElFayoum province, Egypt, respectively. These data indicated that Pb and Cd in muscle, layer feeds and drinking water collected from industrial area were higher than that collected from non industrial area. Also these metals residual concentrations particularly in layer muscle and drinking water were more than the permissible limits.

The objective of the study was to establish the baseline values for blood and coagulation parameters in normal and healthy rusa deer (Rusa timorensis) of different ages and sexes. The samplepopulation consists of 40 rusa deer, divided into four groups of (i) juvenile males (ii) juvenile females (iii) adult males and (iv) adult females. The findings showed significant (p<0.05) higher values in erythrocyte count, calcium concentration and prothrombin time in the adult males compared to adult female rusa deer. On the other hand, the total protein concentration was significantly higher in adult females than adult male deer. No significant differences in blood or coagulation parameters were observed between sexes in the juvenile deer. Between age group, the adult deer had significantly higher mean cell volume, plasma protein and globulin concentration than juvenile rusa deer. Thus, it is necessary to take into account the age and sex of the rusa deer when using blood reference values for the diagnosis of diseases or health assessment.

A total of 23,322 specimens collected between 2014 and 2017, froma total of 2,592 cases, were received in Veterinary Research Institute, Ipoh (VRI) from various states in Malaysia and testedfor common bacterial, viral, and parasitic diseases in pigs. The highest occurrence of isolated bacteria from 771 samples whichtested positive were Salmonella (47.38%) and Escherichia coli (15.68%), followed by Staphylococcus (6.62%), Streptococcus (5.57%), Klebsiella pneumonia (4.88%), Pseudomona (3.38%), Acinetobacter (3.14%), Aeromonas (2.79%), Enterobacter (2.44%), one each of Bacillus and Pasteurella multocida (1.74%), Enterococcus (1.39%) and Corynebacterium (1.05%). 1.74% of each bacteria detected were Moxarella, Aspergillus, Burkholderia andChromobacterium. Positive samples tested by ELISA was Japanese encephalitis virus (JEV) (9.15%), Aujezsky disease virus (ADV)(5.37%), porcine cirvo-virus-2 (PCV2) (5.09%) and porcine reproductive and respiratory syndrome virus (PRRSV) (4.52%). Positive amples tested by the molecular test wasPCV2 (1.62%), PRRSV (1.32%) and classical swine fever virus (CSFV) (0.4%). Serology tests were conducted on 11,305 samplesand reported positive for Brucella suis (15.32%), Brucella abortus (0.62%), Brucella melitensis (0.85%), and melioidosis (0.05%). Parasitology analyses on 99 samples. revealed presence of 10.1% coccidia and 1% each of helminths and Sarcocystis. Within the 4-year period, there were no positive samples for porcine parvovirus (PPV), Nipah virus, swine influenza virus (SIV), and bacteria of Johne’s disease and leptospirosis. Continuous assessment is required to establish a comprehensive baseline data of swine diseases in Malaysia.

Multiple ovulation and embryo transfer is one of the reproductivetechnologies which is important to increase animal production. In this case report, four cows were selected as donors while elevencows were selected as recipients. Both donors and recipients had undergone the same procedures and steps for multiple ovulation and embryo transfer (MOET), such as cow preparation, synchronisation and where only donor cows follow the superovulation protocol. Cows were artificially inseminated and the embryos were flushed and graded. Out of four selected cows for donor, one of them was pregnant and only two cows actuallyproduced the embryos. The recovery rate for the embryo collection was 70.1%, and from 13 embryos (including unfertilised ova), 84.6% of the embryos was classified as good quality and suitable for embryo transfer. The overall results showed that out of eight recipients, five cows were detected pregnant, a 62.5% pregnancy rate. The aim of this report is to describe the procedures aswell as the factors that affect the successful of the MOET programme.