This study aimed to evaluate the effect of Ca soap of palm oil fatty acids (CSFA), as a protected fat, on milk composition and the performance of both ewes and lambs. Thirty-three crossbred ewes aged 2-3 years and weighed 41-44 kg were allocated in three unequal groups for A, B &C (10, 12 &11 ewes, respectively). Group A was fed a diet free from protected fat and kept as a control. Group B was fed a diet containing 4 % fat and group C was given a diet containing 8 % fat. The ewes were in the last month of pregnancy and the experiment extended till the end of late lactation (4.5 months). Milk composition was tested, and body change in ewes and nursing lambs was traced. Moreover, the effect of fat addition on dry matter intake of ewes was analyzed. Results revealed a decrease in dry matter intake in the late gestation and an increase in early lactation, with no significant differences in the late lactation. The effect followed the amount of fat added. There was no effect on ewe’s body weight change or lamb’s growth rate from birth to weaning. On milk composition, there was an increase in fat %, higher in group B and total solids%, while percentage of protein was decreased. Concerning fat supplementation, no effect on lactose, urea milk nitrogen, and somatic cell counts was detected. There was a decreased level of solids-not-fat in group B, while group C showed no detectable alterations. In conclusion CSFA supplementation was effective to increase the fat % and yield in milk of sheep especially at the rate of 4% of addition.

Fungal diseases of poultry have become problematic as bacterial and viral diseases. Therefore, this study was designed to investigate the prevalence of fungal agents in broiler chickens suffering from respiratory disorders. The prevalence rate of fungal isolation was 53.1% including mycelia fungi (42%) and yeast isolates (11.1%). Mould isolates were identified as Aspergillus fumigatus (21.7%), Aspergillus flavus (8.4%), Aspergillus niger (8.4%), Aspergillus nidulans (1.3%), Cladosporium spp. (0.4%) and Penicillium spp. (1.8%). Concerning yeast isolates, Candida spp. was the most predominant which were identified as C. albicans, C. pseudotropicalis (2.7% each), C. krusei, C. regosa (2.2% each), and C. stellatoidea (0.4%). Moreover, one Cryptococcus sp. was recovered and identified as C. neoformans (0.9%). PCR assay using oligonucleotide primer amplifying a 570 bp fragment based on ITS region gene was conducted on randomly selected 9 isolates including 6 Aspergillus spp. (A. flavus, A. niger, A. fumigates; 2 each) as well as 3 yeast isolates (two isolates of C. albicans and one isolate of C. neoformans). All tested isolates had positive reactions.

Broiler chickens are frequently infected with Escherichia coli (E.coli), which often results in disease and high economic losses. Poultry of all ages are susceptible to infections with E.coli, but the most affected are birds of 4-5 weeks. In our study Serotypes O78 and O187 were chosen as they were the most prevalent isolated serotypes from diseased broiler chicken with respiratory affections specially CRD, one hundred chicks of different ages, sex and breeds (cobb, native, sasso) were used in this study. The samples were collected from privately owned poultry farms at EL Mina, Fayoum, Giza and Beni-Suef governorates, all sampled chicks showed clinical signs characteristic for E. coli affections including respiratory distress with or without diarrhea, Swabs from internal organs of 60 diseased chicks were subjected to bacterial examination. Out of 53 oxidase negative strains, 40 E. coli isolates were recovered, other Enterobacteriaceae including, Proteus vulgaris and Pseudomonas aeruginosa. Out of 40 E.coli isolates, E. coli O78 was the most predominant serotype isolated (23) with an incidence of 57.5 % followed by E. coli O187 (12) isolates with an incidence of 30 % and E. coli O115 (5) isolates at percentage of 12.5%, The pre-prepared vaccine against E.coli serotype O used in this study was designed vaccine as it contains an E. coli strain that has been genetically-modified by the deletion of the aroA gene responsible for the biosynthesis of amino acids in the virulent E. coli parent strain (The GMO is named aroA- PTA-5094). The aroA gene-deleted vaccine can trigger a protective immunity in poultry against infection and disease from wild, virulent E. coli bacteria found in the environment. However, because the aroA gene is deleted, the live vaccine bacterium becomes a-virulent and unable to form a self-sustaining population since the vaccine strain has lost the capability to synthesize the amino acids necessary for its survival. The E. coli vaccine dosages were calculated according to a titer of 5.0x106 cfu per dose, one hundred one day old chicks were divided into 5 groups each one 20chicks,group 1, control negative and groups 4 and 5 control positive for serotype O78 and serotype O178 ,while group 2 vaccinated at one day and challenged with E.coli O78 at age of 25 day old, also group 3 vaccinated at 5 day old and challenged with E.coli O178 at age of 25 day old, Two findings, the average lesion scores of air sacs in the groups 4 and 5,four and 3 birds died in the positive control at two days post challenge with E. coli O78 and O178 respectively. The birds were found to have acute, severe septicemia and E. coli could be isolated from the livers. The mortality and morbidity rates of the birds vaccinated with E. coli aroA-live vaccine was great better significant difference from the positive control group showing no mortalities and low pathological picture. There were significant differences in the FCR among the 3 groups significantly less than those of the positive control groups; the body weight was higher in vaccinated groups. Our conclusion, vaccination improves health and FCR and ABW of broiler chicks

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.

The pharmacokinetic aspects of tulathromycin(2.5 mg/kg) administered alone and in combination with flunixin meglumine (2.2 mg/kg) after a single subcutaneous (SC) administration, werestudied in clinically healthy goats. The animals were divided into two groups: the 1st group was given tulathromycin alone and the 2nd group was given tulathromycin concurrently with flunixin meglumine. Serum concentrations of tulathromycin were determined using microbiological assay method. Tulathromycin was rapidly absorbed with a half-life of absorption (t(0.5)ab) of 0.54 h and the peak plasma concentration (Cmax) was 3.7ug/ml was attained after 0.98 h (Tmax). Flunixin significantly altered the pharmacokinetics of tulathromycin by increasing its absorption and delay its elimination from body where t0.5(ab)were 0.54 and0.34 h and the elimination half-lives (t0.5(el)) were 1.35 and 1.8 h, for alone and combination groups, respectively. Significant decreases (39.8%) in the area under the curve (AUC) and (22.6%) in the elimination rate constant (Kel) from the central compartment were found following coadministration with flunixin compared with administration of tulathromycin alone. It was concluded that the combination of tulathromycin and flunixin negatively altered the kinetics of tulathromycin.

A total of 100 random muscle samples of Oreochromis niloticus, Claries lazera, imported Mugil cephalus and Scomber scombrus fish (25 of each) were collected from different markets in Fayoum City for determination of lead, cadmium, copper and mercury residual levels to ascertain whether these levels exceeded the prescribed legal limits. The mean mercury level in the edible muscles tissues of fish species were ranged from below detectable level to 0.29 ppm in local fish and to 0.28 ppm in imported fish. The residual levels were not exceeded the prescribed legal limits of the European Commission Regulation (EC). The highest mean levels of cadmium were recorded in Mackerel (0.119 ± 0.060, ppm) which exceeded the permitted values stipulated by European Commission (EC). The samples in this study contained copper within of the general guideline limit for copper in food. The highest mean levels of lead were also recorded in Mackerel (0.477±0.073 ppm) which exceeded the permitted value stipulated by European Commission (EC). The results were evaluated according to International standards of WHO and EC. The provisional tolerable weekly intakes used in this study to assess the relative safety of marketed in Fayoum. The public health significance of heavy metal residues in fishes were also discussed.

This study was carried out to detect the efficiency of different concentrations of medicinal herbal extract as decontaminant agent on broiler carcasses. Therefore, a total of twelve broiler carcasses treated with sumac extract (4% and 8% w/v) and rosemary extract (0.3% and 0.5% w/v) and stored at 0±1°C. All treated carcasses were sensory and microbiologically analyzed. It has been found that there were no changes in color and odor of treated carcasses, either by sumac extract (8% w/v) or rosemary extract (0.5% w/v), however, a reduction in the total bacterial count, coliforms count, E. coli count and Staphylococcus spp. count one/two log less than control samples and shelf-life of broiler carcasses was noticed and extended three to six days more than the control. From the present study, it could be concluded that sumac extract (8% w/v) and rosemary extract (0.5% w/v) are effective as broiler meat decontaminant and preservative.

Mastitis is the most common and most expensive disease that impacts dairy farms in Egypt. In this study, we investigated bacterial mastitis cases that did not respond to antimicrobial treatment from buffaloes and cows. Milk samples (11) were collected from diseased animals (5 buffaloes and 6 cows). The samples were tested microbiologically to isolate and identify the causative bacteria and antimicrobial susceptibility. The antimicrobial sensitivity of the isolated bacteria was tested by using minimum inhibitory concentration technique according to the clinical national laboratory standards.  The total number of bacterial isolates from the cases was 15 isolates. Staphylococcus aureus (S. aureus) was isolated alone in two cases (13.33% of the isolates), and S. aureus isolated in combination with Arcanobacterium pyogenes (A. pyogenes) in one case (6.67%), and S. aureus isolated in combination with both A. pyogenes and Streptococcus agalactiae (S. agalactiae) in two cases (13.33%), and Coagulase negative staphylococci (CNS) isolated alone in one case (6.67%), and CNS isolated in combination with Klebsiella pneumoniae in one case (6.67%), and A. pyogenes isolated alone in two cases (13.33%). In two cases were not able to isolate any bacterial pathogen. In terms of susceptibility to antibiotics, the isolated strains were sensitive to clindamycin with MICs ranging from 0.125 to <0.03125 µM. The same isolates exhibited medium sensitivity to gentamicin and ciprofloxacin with MICs ranging from 0.5 to 8 µM. Most S. aureus isolates were resistant to oxytetracycline with a MIC of 128 µM. Most of the isolated bacteria were resistant to polymyxin B with a MIC > 128 µM. With the exception of the A. pyogenes isolates, all the isolated bacteria were sensitive to enrofloxacin with a MIC <1 µM.

To determine whether the immunization using commercially available living Escherichia coli-O78 aroA deleted vaccine (Poulvac®E. coli) is protective against APEC challenges or not. Ninety chicks were divided into six groups (15 birds/each); two groups were vaccinated at day 1 by spray and drinking routes then challenged intratracheally with homologous E. coli O78 at day 21, the other two groups were similar to the previously mentioned groups but challenged with heterologous E. coli O1 in parallel with the four challenged-vaccinated groups there were two positive control (challenged-not vaccinated) groups; one challenged with O78 and the other one with O1 at day 21 using intratacheal route. The best obtained results were recorded to the vaccinated-challenged group with the homologous strain and vaccinated by spraying method which exhibited decreases in organ lesion scores in comparison to the other groups (non-vaccinated challenged chickens and groups of chickens either homologous challenged-vaccinated through drinking water or heterologous challenged-vaccinated groups). These findings suggest that vaccine is a suitable for minimizing lesion scores against homologous challenge using spraying method that could lead to minimizing the time for treatment and cases of condemnation in processing plants.

O gambá (Didelphis spp.) é um marsupial onívoro nativo das Américas que apresenta comportamento sinantrópico em áreas urbanas. Apesar da sua proximidade com animais domésticos e o homem, o conhecimento da sua participação na epidemiologia de alguns agentes zoonóticos é fundamental. Este estudo objetivou determinar a presença de anticorpos contra Toxoplasma gondii, Neospora spp. e Leptospira spp. em amostras de sangue colhidas de gambás de 18 municípios do estado de São Paulo, Brasil, entre 2003 e 2008. Foram obtidas amostras sanguíneas de 343 gambás: Didelphis aurita (n = 256) e Didelphis albiventris (n = 87). As amostras foram testadas para detecção de anticorpos contra T. gondii, utilizando o teste de aglutinação modificado (TAM-Toxo; ponto de corte ≥ 25); Neospora spp., utilizando a reação de imunofluorescência indireta (RIFI; ponto de corte ≥ 25); e Leptospira spp., utilizando a soroaglutinação microscópica (SAM-Lepto; ponto de corte ≥ 100). As frequências de anticorpos contra T. gondii, Neospora spp. e Leptospira spp. foram 22,7%, 1,5% e 3,5%, respectivamente. Os sorogrupos-sorovares de Leptospira spp. que apresentaram soropositividade foram: Autumnalis-Butembo; Mini-Mini; Ballum-Castellonis; Icterohaemorrhagiae-Icterohaemorrhagiae; Icterohaemorrhagiae-Copenhageni e Grippotyphosa-Grippotyphosa ou Bananal. Esse estudo demonstrou que esses agentes estão circulando em populações de gambás no estado de São Paulo. Desta forma, investigações que visam determinar o papel dos marsupiais na epidemiologia de cada doença devem ser conduzidas, especialmente visando o entendimento do comportamento desses animais como hospedeiros dessas zoonoses.