A retrospective study of clinical bovine dermatophilosis outbreaks and cases for the period 1995–2014 was conducted, using data obtained from the Division of Veterinary Services (DVS). A total of 3856 outbreaks and 26 659 cases of dermatophilosis were reported countrywide during this period. The post rainy season accounted for 37.9% of the outbreaks followed by the rainy season (26.7%), cold dry season (22.1%) and the hot dry season (13.2%). A retrospective space–time scan statistic in SaTScanTM was used to detect clusters. From this study, it was evident that dermatophilosis was spreading from the north-west of Zimbabwe through the central to the north-east during the period 2010–2014. Five clusters were identified mainly in the central and north-western regions of Zimbabwe. The primary cluster was centred at Ungwe, Gokwe district in Midlands; the second, third, fourth and fifth likely clusters were centred at Bonga (Mashonaland Central), ARDA (Mashonaland West), Nsenga (Matabeleland North) and Zanda in Gokwe, respectively. The findings of this study suggest the continued spread of dermatophilosis across the country; as such the Department of Livestock and Veterinary Services are advised to develop measures aimed at managing this spread such as dipping, quarantine, movement control and raising farmer awareness.

Contagious ecthyma is a highly contagious disease affecting domestic and wild ruminants such as sheep, goats and camels. The identification and characterisation of a parapoxvirus (PPV) infecting camels is described here. The virus was detected in dromedary camels (Camelus dromedarius) from Kerman and Shiraz in Iran. PPV-specific amplification by polymerase chain reaction (PCR) further confirmed that the disease was associated with PPV infection. Phylogenetic analysis of ORF011 (B2L) gene sequences showed 99.79% and 82.13% similarity of the PPV identified in this study with the Jodhpur isolate and the bovine papular stomatitis virus (BPSV) isolates (CE41), respectively. Moreover, phylogenetic analysis of the ORF045 gene indicated that the Shiraz sample was in all probability closely related to VR634 and to F00.120R and PCPV776. In conclusion, the results suggest that camel PPV (CPPV) is a likely cause of contagious ecthyma in dromedary camels in Iran.

Anthrax is a zoonotic disease caused by the gram-positive, endospore-forming and soil-borne bacterium Bacillus anthracis. When in spore form, the organism can survive in dormancy in the environment for decades. It is a controlled disease of livestock and wild ungulates in South Africa. In South Africa, the two enzootic regions are the Kruger National Park and the Ghaap Plateau in the Northern Cape province. Farms on the Plateau span thousands of hectares comprising of wildlife – livestock mixed use farming. In 2007–2008, anthrax outbreaks in the province led to government officials intervening to aid farmers with control measures aimed at preventing further losses. Because of the ability of the organism to persist in the environment for prolonged periods, an environmental risk or isolation survey was carried out in 2012 to determine the efficacy of control measures employed during the 2007–2008, anthrax outbreaks. No B. anthracis could be isolated from the old carcass sites, even when bone fragments from the carcasses were still clearly evident. This is an indication that the control measures and protocols were apparently successful in stemming the continuity of spore deposits at previously positive carcass sites.

The aim of the study was to determine the species spectrum of ixodid ticks that infest horses and donkeys in South Africa and to identify those species that act as vectors of disease to domestic livestock. Ticks were collected opportunistically from 391 horses countrywide by their owners or grooms, or by veterinary students and staff at the Faculty of Veterinary Science, University of Pretoria. Ticks were also collected from 76 donkeys in Limpopo Province, 2 in Gauteng Province and 1 in North West province. All the ticks were identified by means of a stereoscopic microscope. Horses were infested with 17 tick species, 72.1% with Rhipicephalus evertsi evertsi, 19.4% with Amblyomma hebraeum and 15.6% with Rhipicephalus decoloratus. Rhipicephalus evertsi evertsi was recovered from horses in all nine provinces of South Africa and R. decoloratus in eight provinces. Donkeys were infested with eight tick species, and 81.6% were infested with R. evertsi evertsi, 23.7% with A. hebraeum and 10.5% with R. decoloratus. Several tick species collected from the horses and donkeys are the vectors of economically important diseases of livestock. Rhipicephalus evertsi evertsi is the vector of Theileria equi, the causative organism of equine piroplasmosis. It also transmits Anaplasma marginale, the causative organism of anaplasmosis in cattle. Amblyomma hebraeum is the vector of Ehrlichia ruminantium, the causative organism of heartwater in cattle, sheep and goats, whereas R. decoloratus transmits Babesia bigemina, the causative organism of babesiosis in cattle.

Several nucleic acid-based assays have been developed for detecting Anaplasma marginale and Anaplasma centrale in vectors and hosts, making the choice of method to use in endemic areas difficult. We evaluated the ability of the reverse line blot (RLB) hybridisation assay, two nested polymerase chain reaction (nPCR) assays and a duplex real-time quantitative polymerase chain reaction (qPCR) assay to detect A. marginale and A. centrale infections in cattle (n = 66) in South Africa. The lowest detection limits for A. marginale plasmid DNA were 2500 copies by the RLB assay, 250 copies by the nPCR and qPCR assays and 2500, 250 and 25 copies of A. centrale plasmid DNA by the RLB, nPCR and qPCR assays respectively. The qPCR assay detected more A. marginale- and A. centrale-positive samples than the other assays, either as single or mixed infections. Although the results of the qPCR and nPCR tests were in agreement for the majority (38) of A. marginale-positive samples, 13 samples tested negative for A. marginale using nPCR but positive using qPCR. To explain this discrepancy, the target sequence region of the nPCR assay was evaluated by cloning and sequencing the msp1β gene from selected field samples. The results indicated sequence variation in the internal forward primer (AM100) area amongst the South African A. marginale msp1β sequences, resulting in false negatives. We propose the use of the duplex qPCR assay in future studies as it is more sensitive and offers the benefits of quantification and multiplex detection of both Anaplasma spp.

Stability study of biological products especially living bacterial vaccines plays an important role for the 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. 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 postproduction 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, 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.

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)

This study was carried out to assess the effect of storage conditions on the sensory, quality parameters and microbiological status of beef from the muscle “Semitendinosus”. The experiment was design into 4 groups of beef samples, the first was control and the others were unpacked, aerobic packed and vacuum packed chilled meat. The obtained results showed that the mean values of mesophilic counts were 6×10⁷±5×10⁶, 3×10⁷±3×10⁶, 3×10⁷±2×10⁶ and 5×10⁷±5×10⁶ CFU/g, while those of psychrophilic count were 5×10⁷±5×10⁶, 3×10⁶±3×10⁵, 4×10⁶±3×10⁵ and 7×10⁶±7×10⁵ CFU/g, whereas the mean values of coliforms MPN were 10⁵±10⁴, 10⁵±10⁴, 2×10⁴±10³ and 4×10⁷±2×10⁶ MPN/g, the mean values of fecal coliforms MPN were 2×10³±2×10², 4×10⁴±3×10³, 2×10³±10² and 10⁷±10⁶ MPN/g, the mean values of E. coli MPN were 9×10²±9×10, 6×10±6×10², 6×10³±10² and 2×10³±10² MPN/g and the mean values of Staphylococcus count were (9×10⁵±9×10⁴, 10⁶±10⁵, 2×10⁶±10⁵ and 2×10⁶±2×10⁵ CFU/g) for control, unpacked, aerobic packed and vacuum packed chilled stored beef, respectively. The unpacked meat showed increase in shelf life time till four days as the sensory evaluation become excellent till four days also, increased pH, drip, water holding capacity (WHC) and cooking loss at four days. Staphylococcus reach to unsatisfactory level. Area packed meat increase in shelf life time till six days showing excellent sensory evalution at six day, decreasd drip, water holding capacity and cooking loss and slowly increased in bacterial count. Anaerobic meat have the longest shelf life time till 10 days as vacuum packing reduce drip, WHC and cooking loss. Also decrease mesophilic, fecal coliform growth. The quality assurance of cold storage was discussed as well as the vacuum packaged chilled beef has long shelf –life time than aerobic packed and fresh meat. This attributed to that package and cold storage reduce microbiological and physio-chemical alterations in meat. The recommendations to extension of shelf life time were discussed.

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.

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.