A total of 220 random meat samples of different animal species were collected from 50 carcasses consisting 10 carcasses from each of beef, buffalo, camel, sheep and goat, as well20 frozen beef samples. Each carcass represented by four cut samples from neck, shoulder, abdomen and thigh. All samples were collected from random retail and butchers’ shops ofBeni-Suef governorate to assess their microbiological status and compare the levels of contamination among animal species and carcass cuts. This study showed and compared the means of counts (CFU/g) of total aerobicbacteria (mesophilic count and psychrophilic count), coliforms,fecal coliforms,Escherichia coli,Staphylococcusaureus in each of beef, buffalo, camel, sheep and goat carcasses and imported frozen beef as well. Beside the incidence of E.coli, Salmonellaspp, and coagulase positive Staphylococcus aureus. The obtained results clarified that the examined beef, buffalo and mutton samples were more contaminated than those of other kinds of meat. The results were discussed from the hygienic point of view and compared with the national and international standards to assess their reliability for consumption.

Bovine tuberculosis, caused by Mycobacterium bovis, is a zoonotic disease causing approximately 6% of total human deaths. Its economic losses are not only a reduction of 10-20% in milk production and weight, but also infertility and condemnation of meat. Many serological tests are applied for detection of tuberculosis. ELISA test has the highest sensitivity and specificity than the other serological tests for the diagnosis of tuberculosis. Several forms of new technology were brought into the diagnostic approach to mycobacterial infection. The aim of this work was to detect bovine tuberculosis by application of different serological tests. Tuberculin skin test was applied on 2650 cattle, only 63(2.4%) were positive. Forty eight (76.2%) of the slaughtered positive animals showed visible lesions (VL) while the other 15 (23.8%) had non-visible lesions (NVL). The bacteriological examination of the 63 samples revealed isolation of M. bovis from 47 processed samples (74.6%). The results of the immunoassay test have detected 27 out of the tuberculin positive cattle, while the ELISA has detected 34 out of the positive reactor cattle. It was concluded that immunoassay and ELISA tests act as complementary tests for tuberculin skin test especially in anergic cattle.

Ice cream is a delicious dairy product commonly consumed during summer in all age groups. Due to its composition, it can harbor many potent pathogens. Most ice creams become contaminated with microbes during production, transit, and preservation. Such contaminated food product can be responsible for food borne infections in children, elderly people and immune-suppressed patients. Therefore, the study was conducted to evaluate the microbiological quality of street-vended ice creams sold in different areas of Alexandria city, Egypt. One hundred street vended ice cream samples (50 packed and 50 unpacked) randomly collected samples and analyzed for total bacterial count, Enterobacteriaceae count, coliform count, enterococci count and Staphylococcus aureus. The results revealed that the mean value of total viable count, Enterobacteriaceae count, Coliform count, Enterococci count and Staphylococcus aureus in packed and unpacked ice cream samples were 1.9x103±0.3x103, 1.0x106±0.8x106; 2.1x103±0.8x103, 1.9x104±0.8x104; 1.6x103± 0.6x103, 0.8x104±0.6x104; 1.3x103±0.05x103, 7.4x104±5.5x104 and 9.1x102±2.6x102, 0.8x104±0.4x104cfu/ml, respectively. Enterobacter aerogenes, Escherichia coli, Klebsiella pneumoniae and Citrobacter sp. could be isolated and identified from the examined packed and unpacked ice cream samples. Serological identification of E.coli showed that the O111: K58: B4 is the most serotype of E.coli isolated from unpacked ice cream samples while O128: K67: B12 is the most prevalent E.coli serotype isolated from packed ice cream samples. It is recommended to launch awareness programs to minimize the contamination of ice cream products.

A total of 247 intestinal samples from freshly dead broiler and layer chickens were collected from 150 farms in Giza, Sharkia, Qalubia, El-Behera, Daqahlia and Cairo governorates in different seasons. These samples showed different degrees of intestinal lesions from apparently normal to sever necrosis with ulcerations. Clostridium perfringens was isolated from 138 samples with incidence of 55.9%. The incidence of NE was higher in spring and summer than winter and autumn. According to polymerase chain reaction and intradermal injection of guinea pig all isolates were Clostridium perfringens type A. In vitro antibiotic sensitivity tests made for 15 isolates and most of the examined isolates were highly sensitive to amoxicillin, ampicillin, florfenicol, penicillin and metronidazole. Three isolates showed resistance to most of antibiotics were used. Effect of piperazine salt on antibiotic resistance of C. perfringens isolate was studied in this work.

The objective was to determine the accuracy of color Doppler ultrasound for diagnosis of early pregnancy in buffaloes based on the evaluation of corpus luteum blood flow (CLBF) on days 20 and 21 after mating. Local Egyptian buffaloes, (n=12) during 3rd and 4th lactational season were kept in the farm of Animal Reproduction Research Institute (ARRI). The animals were divided into two groups, group A (n=6) was mated naturally by a fertile bull during late estrus phase and group B (n=6) was left. Animals underwent grayscale ultrasonography (US) to locate the CL , then color flow Doppler and power Doppler were activated to evaluate CLBF and pulsed wave Doppler to evaluate uterine blood flow on days 1,5,10,12,14,16,18,19,20,21,23,25,27,30 after mating, using a portable, battery operated color Doppler and B-mode ultrasound scanner equipped with a 10-5MHz, rectal transducer (M-turbo, Fujifilm sonosite, USA). Based on subjective (visual) and objective (Doppler parameters) corpus luteum blood flow (CLBF) evaluation. Animals in group A were classified as pregnant or non- pregnant on day 20 and day 21 after mating depending on CLBF. Blinded from results of the previous diagnosis, we performed a final pregnancy diagnosis using US to visualize the fetal heartbeat on day 30 after mating. Blood samples were collected from jugular vein after examination to determine by ELIZA kits, serum estradiol and progesterone concentration. The final pregnancy outcome on day 30 was retrospectively compared with the CLBF on days 20 and 21 diagnoses and then classified as true positive, true negative, false positive, and false negative. The sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of the CLBF-d20-21 test were calculated using specific equations. The CLBF decreased markedly on days 20-21 in case of non-mated group (CL regression), while it remained constant or slightly increased in case of pregnant animals. Moreover the uterine blood flow markedly increased in case of non-mated group during the same period.

Schistosoma mansoni worms inhabit the portal triad affecting blood elements. Therefore, the current study aimed to compare ameliorative effects of Commiphora molmol extract (Mirazid, MZD) and praziquantel (PZQ) on some biochemical parameters in S. mansoni-infected mice. Accordingly, Swiss albino mice (n=72) were used and were divided into 4 equal groups; 18 mice each. Group (1) was uninfected non-treated control. Mice in infected groups administered 100 S. mansoni cercariae/mouse. Group (2) contained infected non-treated mice. Group (3) was infected and treated with MZD at a dose of 500 mg/kg for 5 successive days. Group (4) was infected and treated with PZQ in a dose of 500 mg/kg for 2 successive days. Treatment started 7 weeks post infection (WPT) by the oral route. Blood samples were collected at the 1st, 2nd and 4th weeks post treatment for liver functions (ALT, AST and ALP), kidney functions tests (blood urea and serum creatinine) and cholinergic function (serum cholinesterase level). PZQ ameliorated activities of serum enzymes; alanine aminotransferase, aspartate aminotransferase and alkaline phosphatase more than MZD compared to infected untreated group. PZQ significantly decreased ALT at 1, 2 and 4 WPT as well as AST and ALP activity at 2 and 4 WPT whereas, MZD resulted in significant reduction in ALT activity at the 1st, 2nd and 4th WPT. AST and ALP activities appeared at the 2nd and 4th WPT. PZQ caused progressive significant reduction in elevated levels of urea and creatinine at the 1st, 2nd and 4th WPT, respectively that produced by MZD. PZQ and MZD induced a significant elevation in the level of AChE. Such effect was early detected MZD, and it was showed at the 2nd and 4th WPT for PZQ. It was concluded that PZQ and MZD were safe drugs with no adverse biochemical effects on S. mansoni-infected treated mice with potential action done by PZQ rather than MZD.

The objectives of the study were to determine the species composition of ticks infesting white and black rhinoceroses in southern Africa as well as the conservation status of those tick species that prefer rhinos as hosts. Ticks were collected opportunistically from rhinos that had been immobilised for management purposes, and 447 white rhinoceroses (Ceratotherium simum) and 164 black rhinoceroses (Diceros bicornis) were sampled in South Africa, 61 black rhinos in Namibia, 18 white and 12 black rhinos in Zimbabwe, and 24 black rhinos in Zambia. Nineteen tick species were recovered, of which two species, Amblyomma rhinocerotis and Dermacentor rhinocerinus, prefer rhinos as hosts. A. rhinocerotis was collected only in the northeastern KwaZulu-Natal reserves of South Africa and is endangered, while D. rhinocerinus is present in these reserves as well as in the Kruger National Park and surrounding conservancies. Eight of the tick species collected from the rhinos are ornate, and seven species are regularly collected from cattle. The species present on rhinos in the eastern, moister reserves of South Africa were amongst others Amblyomma hebraeum, A. rhinocerotis, D. rhinocerinus, Rhipicephalus maculatus, Rhipicephalus simus and Rhipicephalus zumpti, while those on rhinos in the Karoo and the drier western regions, including Namibia, were the drought-tolerant species, Hyalomma glabrum, Hyalomma rufipes, Hyalomma truncatum and Rhipicephalus gertrudae. The species composition of ticks on rhinoceroses in Zambia differed markedly from those of the other southern African countries in that Amblyomma sparsum, Amblyomma tholloni and Amblyomma variegatum accounted for the majority of infestations.

Campylobacter spp. are common pathogenic bacteria in both veterinary and human medicine. Infections caused by Campylobacter spp. are usually treated using antibiotics. However, the injudicious use of antibiotics has been proven to spearhead the emergence of antibiotic resistance. The purpose of this study was to detect the prevalence of antibiotic resistance genes in Campylobacter spp. isolated from chickens and human clinical cases in South Africa. One hundred and sixty one isolates of Campylobacter jejuni and Campylobacter coli were collected from chickens and human clinical cases and then screened for the presence of antimicrobial resistance genes. We observed a wide distribution of the tetO gene, which confers resistance to tetracycline. The gyrA genes that are responsible quinolone resistance were also detected. Finally, our study also detected the presence of the blaOXA-61, which is associated with ampicillin resistance. There was a higher (p < 0.05) prevalence of the studied antimicrobial resistance genes in chicken faeces compared with human clinical isolates. The tetO gene was the most prevalent gene detected, which was isolated at 64% and 68% from human and chicken isolates, respectively. The presence of gyrA genes was significantly (p < 0.05) associated with quinolone resistance. In conclusion, this study demonstrated the presence of gyrA (235 bp), gyrA (270 bp), blaOXA-61 and tetO antimicrobial resistance genes in C. jejuni and C. coli isolated from chickens and human clinical cases. This indicates that Campylobacter spp. have the potential of resistance to a number of antibiotic classes.

he present study aimed to prepare a combined inactivated vaccine containing bovine viral diarrhea genotype-1(BVD-1),bovine viral diarrhea genotype-2 (BVD-2), infectious bovine rhinotracheitis (IBR),parainfluenza-3 (PI-3) and bovine respiratory syncytial virus(BRSV) and adjuvanted with montanide oil ISA 206. Quality control results proved that the pneumo-5 vaccine was pure and completely safe to be used in calves without abnormalities. Potency test was performed on two groups of calves three for each group, where the first group was vaccinated with pneumo-5 vaccine adjuvant with montanide oil ISA 206 and the second group was left as non-vaccinated control group. In group (1), serum neutralization test revealed that the serum neutralizing antibody titers in BVD-1 and BVD-2 developed more higher than the minimal acceptable titer of the protective level (log10 0.9), while log10 0.6 was protective against IBR, PI-3 and BRS viruses at one month of vaccination and remained protective till the end of experiment compared to group (2) that showed no neutralizing antibody response. The prepared vaccine proved to be highly potent as the developed BVD-1, BVD-2, IBR, PI-3 and BRSV antibodies remained within the protective level for 9 months post vaccination.