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.

Dietary fat and oil is important for many body processes. The present investigation was carried out to determine the concentrations of organochlorine pesticides in butter, olive and corn oil. A total of 125 samples (75 butter, 25 each of olive oil and corn oil) were collected from El Minia Governorate, Egypt. Levels of these compounds were determined by gas chromatography with electron capture detector (GC-ECD). The results indicated that 30.4%(38/125), 24.8%(31/125), 21.6%(27/125), 21.6%(27/125), 16.8%(21/125), 14.4%(18/125), 14.4%(18/125), 12.8%(16/125), 9.6%(12/125), 8.8%(11/125), 8%(10/125), 1.6%(2/125) and 0.8%(1/125) of the examined samples were contaminated with Heptachlor, Endrin, Aldrin, Dichlorodiphenyldichloroethylene(p,p'-DDE), Dichlorodiphenyldichloroethane(p,p'-DDD), Gamma hexachlorocyclohexane(Gamma HCH), Heptachlor epoxide, Dieldrin, Endosulfan, methoxychlor, Alpha hexachlorocyclohexane(Alpha HCH), Delta hexachlorocyclohexane(Delta HCH) and Gamma Chlordane, respectively. None of the examined samples revealed the presence of Dichlorodiphenyltrichloroethane (p,p'-DDT) and 11 samples contained organochlorine residues above European Union maximum residue limits (EU MRL)

Development of environmental, safe and protective vaccines against infectious pathogens remains a challenge. In consequence of its high morbidity and mortality rates canine distemper is one of the most important diseases of young dogs. The object of the present study is to develop a selected method for preparation of an inactivated canine distemper vaccine. This method involved exposure of the virus to different concentrations of binary ethyleneimine (BEI), beta propiolactone (ßPL) and hydrogen peroxide (H2O2). Complete virus inactivation was obtained with BEI (0.003M) for 6 hours, ßPL (1/5000) for 4 hours and H2O2 at a concentration of 3% rapidly inactivated a Vero cell adapted canine distemper virus strain within 3 h of exposure without affecting its antigenicity or immunogenicity. The safety, immunogenicity and potency induced in four groups of puppies were evaluated using the three prepared experimental batches of inactivated canine distemper vaccine. These results revealed that no residual infectious virus was detected in H2O2 inactivated CD vaccine that proved to be safe and effective when compared with the same virus harvest that inactivated with the classical inactivating agents as BEI and βPL. Thus, an alternative inactivation method, such as H2O2 is able to maintain the integrity of the virus protein may be essential for improving the potency of inactivated canine distemper virus vaccine produced sufficient of antibodies which measured by serum neutralization test (SNT) and was protected when challenged with virulent CD virus strain. These findings reinforce the idea that H2O2 can replace BEI and βPL as inactivating agents for canine distemper virus to reduce time and cost of inactivation process.

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.

The objectives of the present study were to validate ultra-sonographic examination (US) as a reliable diagnostic tool for endometritis, as well as to determine the effects of intrauterine infusion (IU) of benzathine cephapirin plus systemic PGF2α as a treatment protocol of endometritis in dairy cows. 260 Holstein cows were included in this study. The affected cows were examined rectally and US. The cows were divided according to the diagnostic method and treatment protocol into 3 groups. Group1: rectally diagnosed and received systemic PGF2α. Group2: diagnosed rectally and received IU benzathine cephapirin plus systemic PGF2α. Group3: diagnosed US and received IU benzathine cephapirin plus systemic PGF2α. Good reproductive indices were recorded for cows examined US and treated with combination of IU benzathine cephapirin plus systemic PGF2α. A highly significant positive correlations were observed between days in milking (DIM) and most of tested reproductive indices. Meanwhile, Daily milk yield was negatively correlated with all tested reproductive parameters. In conclusion, transrectal US could be used as a reliable method for early diagnosis of endometritis. In addition, using a combination of IU application of benzathine cephapirin plus systemic PGF2α was superior treatment protocol in endometritis in comparison with PGF2α.

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.

One hundred milk samples were collected from camel’s milk for the isolation of Staphylococcus aureus. Thirty-one isolates were S. aureus, 45 were other forms of staphylococci and 24 represented other bacteria. Five isolates from S. aureus were methicillin resistant S. aureus (MRSA) and 26 samples were methicillin susceptible S. aureus (MSSA). The whole genome sequence of S. aureus was annotated and visualised by rapid annotation using subsystem technology (RAST) which is a fully-automated service for annotating complete or nearly complete bacterial genomes. Four isolates from MSSA strains were subjected to multi-locus sequence typing (MLST). Three multilocus sequences types or sequence types (MLST/ST) were found, namely ST15, ST1153 and ST130. The phylogenetic analysis of the concatenated sequences of the seven genes forming the MLST profile of S. aureus classification revealed a high degree of similarity and close relationship between the ST15 and ST1153 while the third ST (ST130) was located in a different cluster.

Chicken anemia virus (CAV) is the causative agent of chicken infectious anemia CIA). Studying CAV isolates in Egypt and their genetic diversity and its potential role in vaccination failure recently noticed in broiler flocks, is lacking in Egypt. So, the present study aimed to characterize CAV isolate-collected from a commercial broiler flock suffered from severe anemia and high mortality based on sequence and phylogenetic analysis of partial VP1 gene as well as to study pathogenicity and immunosuppressive potential in one day-old SPF chicks. The CAV isolate proved to be positive by PCR. The PCR product was sequenced and submitted to the gene bank under the accession number KX171350 and the CAV strain was designated as CLEVB-Zag2. Phylogenetic analysis at the nucleotide and amino acids level classify CLEVB-Zag2 CAV under group III (genotype III) of CAVs. On the other hand, the CLEVB-Zag2 CAV was found to be highly pathogenic for the experimentally inoculated SPF- chicks showing depression, severe anemia in almost all chicks in two infected groups beginning at the 7th day post infection (PI) and reached the peak of severity at the 14th day (hematocrit value, hemoglobin conc. and RBCs counts) are significantly reduced in chicks of the infected group. Blue wings were observed in few chicks in each infected group at the 14th day PI. Macroscopic lesions consisting of subcutaneous and muscular hemorrhages are observed with pale bone marrow, significant atrophy of thymus, spleen and bursa, hepatomegally with mottled liver and paleness of the carcasses were detected 7 days PI Those findings were evident and increased in severity until the day 14 PI. Concerning the CLEVB-Zag2 CAV, it was found to be highly immunosuppressive in the infected SPFchicks vaccinated with a commercial potent inactivated H5N1 vaccine as manifested by a significant reduction (protection 50%). The variance in the titer of the shieded challenge H5N1 virus was 1.45 log10 and the mean HI titer at the 4th week post vaccination was 1.5 log2 compared with the non-infected vaccinated group where these values were 90%, 2.35 log10 and 5.3 log2; respectively. In conclusion, the present study revealed that the CLEVB-Zag2 CAV isolate is highly pathogenic and immunosuppressive.

Staphylococcus aureus(S. aureus) is a major cause of mastitis in dairy animals and a serious pathogen affecting human health. The current study was designed to investigate the extent of S.aureus in milk samples collected from dairy animals as well as human clinical samples,beside determination of its antimicrobial susceptibility pattern. Also, the prevalence of both mecA and vanA genes among some selected methicillin-resistant isolates was investigated. Out of 120 milk samples obtained from different animals (cows, buffaloes, sheep, and goats), 81 (67.5%) samples reacted positive for S. aureus, whereas 67 (74%) out of 90 human samples were found positive for S. aureus. Disk diffusion susceptibility testing revealed that S.aureus isolates of humans were more resistant than thoseof animals against all tested antimicrobials except for clindamycin. A high rate of multi-drug resistance (MDR) and mecA gene was recorded in S. aureusof both animals and humans. Surprisingly,vanAgene, which is responsible for vancomycin resistance was detected only in S. aureus isolated from animal milk. To the best of ourknowledge, it is the first record of vanA gene in S. aureus recovered from animals.