The experiment applied on four groups of calves, each of four calves. Three calves from each group were vaccinated with one of the following attenuated vaccines: Lumpy skin disease vaccine (LSD), Romanian sheep pox (RSP) vaccine, Held goat pox (HGP) vaccine and dual (bivalent) vaccine of SPV and GPV. All vaccines were evaluated by estimating the cellular immunity using lymphocyte blastogenesis measured by XTT assay, and humeral immunity using serum neutralization and ELISA tests of vaccinated calves. The NI coincided with the ELISA antibody results and corroborated the results of cell mediated immunity which demonstrated the capacity of LSD and dual vaccines to induce immune response higher than SP vaccine and GP vaccines. In conclusion, the current study proved that the LSD and dual vaccines were highly immunogenic than the RSP and HGP vaccines, and dual vaccine could be safely used for vaccination of cattle against lumpy skin disease.

Brucellosis is considered an economically important highly contagious and zoonotic bacterial disease of water buffaloes. Control of brucellosis in buffaloes is very important for public health. The efficacy of control program depends on the detection and eradication of infected animals coupled with vaccination and application of biosecurity. This study was carried out to control the brucellosis in buffalo farm in Assuit Governorate, Egypt during the period from April 2015 to August 2016. Out of 620 unvaccinated buffaloes, 87 (14.03%) aborted. Moreover, 90/620(14.51%), 82/620(13.22%), 82/620(13.22%), and 80/620 (12.9%) buffaloes were serologically positive by BAPA, RBPT, m SAT and Riv.T, respectively. Three isolates were differentiated as Brucella melitensis, biovar 3, one strain isolated from one vaginal swap out of 10 Riv.T. positive recently aborted buffaloes (10%) and two strains were isolated out of ten milk samples of Riv.T. positive buffaloes (20%). Eighty serological positive buffaloes to Riv.T were culled from the herd, while 60 serological negative heifers were vaccinated by Brucella abortus S 19 vaccine, with a dose of 3-8×109 cfu/5ml and monitored for serological titer for 240 days. After 6 months of vaccination, the number of serologically positive calves declined marginally to 50 (83.33%), 40 (66.67%), 50 (83.33%), 0 (0%), 40 (66.67%) and 0 (0%) by BAPA, RBPT, mSAT, CFT, iELISA and cELISA, respectively. Three successive serological tests every three weeks were done by screening tests, BAPA and RBPT and confirmed by Riv.T. At the end of the control program, all examined buffaloes were serologically negative. Application of biosecurity in the farm was applied by the sanitary disposal of aborted material and application of proper disinfectants at its recommended work strength and contact time.

The objective of the study was to record the tick species collected from three species of tortoise, each in a different province of South Africa. Ticks were collected from leopard tortoises, Stigmochyles pardalis, in the southern region of the Kruger National Park, Mpumalanga province; from hingeback tortoises, Kinixys zombensis, in the Enseleni Nature Reserve, KwaZulu-Natal province and from angulate tortoises, Chersina angulata, in the West Coast National Park, Western Cape province. Of the 63 leopard tortoises examined, 58 were infested with Amblyomma marmoreum and 49 with Amblyomma hebraeum, and all stages of development of both species were recovered. Amblyomma nuttalli was collected from 25 hingeback tortoises, and all stages of development were present. All 24 angulate tortoises examined were infested with Amblyomma sylvaticum, and large numbers of larvae, nymphs and adults were collected. Three snake species and a sand lizard were also infested with A. sylvaticum. The adults of A. marmoreum, A. nuttalli and A. sylvaticum were identified as specific parasites of the family Testudinidae, whereas all stages of development of A. hebraeum were classified as generalists.

Coagulase negative Staphylococci are the most prevalent cause of bovine subclinical mastitis. The current study were designed to study their occurrence, antibiogram and their ability to form biofilms. A total number of 95 CNS isolates were recovered from 400 lactating. S. xylosus (36.84%), S. chromogenes (12.63%), S. epidermidis (10.53%), S. saprophyticus (8.42%), S. haemolyticus (7.38%) were the most common recovered species. Disk diffusion method against 14 antimicrobials discs was used to detect their antibiogram. 100% were sensitive to Imipenem, 96.84% were sensitive to Enrofloxacin, 85.26% to Chlramphenicol and 84.21% to Vancomycin. But, 95.79% were resistant to Ampicillin, 77.9% resistant to Cefoxitin, 35.8% resistant to Cefuroxime, 32.63% resistant to Amoxycillin and 18.95% resistant to Clindamycin. Cultivation on Congo Red Agar (CRA) was carried out to detect biofilm formation. 47.37% were positive and S. epidermidis was the most biofilm positive species on CRA by the percentage of 70%. Haemolysins were studied by cultivating CNS on sheep blood agar. 25.26% were β-haemolytic, 71.57% (n=68) were γ-haemolytic and 3.15% were α- haemolytic.

This investigation was carried out on 5457 animals; among which, 3916 cows, 1531 buffaloes and 10 she-camels in Beni-Suef and Fayoum provinces. Animals were subjected to clinical examination to study the congenital and acquired udder and teat surgical affections. Clinical findings of affected animals were recorded. It has been found that the prevalence of teat and udder affections were: in cattle (19.87%; 778/3916), 141 (3.6%) had congenital anomalies, (hyperthelia 2.17%, leaker 0.38%, athelia 0.26%, pendulous udder 0.20%, hypermastia 0.26%, hypoplasia of mammary gland 0.13%, hyperplasia of teat 0.08%, teat obstruction 0.08% and fistula 0.05%)and 637 (16.267%) suffered from acquired affections (fibrosis 6.26%, mastitis 3.29%, pendulous udder 1.18%, edema 1.15%, fistula/wound 0.84%, teat obstruction 0.66%, teat stenosis 0.66%, ulcer/crack 0.64%, abscess 0.54%, hematoma 0.26%, seborrhea 0.23%, impetigo 0.18%, neoplastic growths 0.18%, udder gangrene 0.15% and teat gangrene 0.05%). In buffaloes (11.43%; 175/1531), 11 (0.72%) had congenital anomalies (hypermastia 0.59%, hyperthelia 0.07% and fistula 0.07%), and 164 (10.71%) had acquired affections (fibrosis 2.81%, ulcer/cracks 2.09%, mastitis 1.89%, seborrhea 1.44%, obstruction 0.91%, edema 0.46%, hematoma 0.33%, fistula/wound 0.26%, teat gangrene 0.26%, stenosis 0.13%, abscess 0.07% and impetigo 0.07%). In shecamels, no congenital anomalies were recorded with only one animal showed an acute mastitis and other had a teat orifice obstruction.

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.

A study was conducted to investigate the pathogenicity and the median lethal dose (LD50) of Aeromonas hydrophila isolated from clinically diseased catfish against apparently healthy homologous fish to evaluate the lethality of extra-cellular products (ECPs) of the isolated strain in vivo. For pathogenicity experiment, five different concentrations of Aeromonas hydrophila strain BNS 01614 including 3× 108, 1.5 × 108, 1.5 × 107, 1.5 × 106 and 1.5 × 105 CFU/fish used via intra peritoneal. The results revealed that pathogenicity of BNS 01614 was confirmed by the mortality of 30 % to 100 % of all tested fish within 4 to 12 days with LD50 1.5 × 107 CFU/fish. The Concentrated extracellular products (ECPs) of the selected bacterium were prepared and confirmed to be toxic in Clarias garipineus with LC50 of 20µg.

African animal trypanosomiasis causes significant economic losses in sub-Saharan African countries because of livestock mortalities and reduced productivity. Trypanosomes, the causative agents, are transmitted by tsetse flies (Glossina spp.). In the current study, we compared and contrasted the virulence characteristics of five Trypanosoma congolense and Trypanosoma brucei isolates using groups of Swiss white mice (n = 6). We further determined the vectorial capacity of Glossina pallidipes, for each of the trypanosome isolates. Results showed that the overall pre-patent (PP) periods were 8.4 ± 0.9 (range, 4–11) and 4.5 ± 0.2 (range, 4–6) for T. congolense and T. brucei isolates, respectively (p < 0.01). Despite the longer mean PP, T. congolense–infected mice exhibited a significantly (p < 0.05) shorter survival time than T. brucei–infected mice, indicating greater virulence. Differences were also noted among the individual isolates with T. congolense KETRI 2909 causing the most acute infection of the entire group with a mean ± standard error survival time of 9 ± 2.1 days. Survival time of infected tsetse flies and the proportion with mature infections at 30 days post-exposure to the infective blood meals varied among isolates, with subacute infection–causing T. congolense EATRO 1829 and chronic infection–causing T. brucei EATRO 2267 isolates showing the highest mature infection rates of 38.5% and 23.1%, respectively. Therefore, our study provides further evidence of occurrence of differences in virulence and transmissibility of eastern African trypanosome strains and has identified two, T. congolense EATRO 1829 and T. brucei EATRO 2267, as suitable for tsetse infectivity and transmissibility experiments.

Lumpy skin disease (LSD) is an endemic infectious disease of cattle in Egypt. This survey aimed to define the prevalence of clinical and sub-clinical LSD virus (LSDV) infection among cattle and investigate their contact with water buffaloes (Bubalus bubalis) in order to improve the understanding of LSD epidemiology. Cattle and buffalo were examined owing to the appearance of skin lesions. Because clinical signs were consistent with LSDV infection, samples from cattle in a non-grazing dairy farm (n = 450) were submitted for LSDV testing together with those from the in-contact buffaloes (n = 100). Results revealed that the intra-herd percentage of cattle infected with LSDV varied with the detection method. This ranged from 22.4% to 65.4% by virus isolation (VI) and polymerase chain reaction (PCR), respectively, in clinical cattle samples, compared to 0% and 10% by VI and PCR in non-clinical cases. Using the neutralising index (NI), LSDV antibodies were found in 100% (n = 100) of the tested cow’s sera (NI = > 2.0 and ≥ 3.0), whereas buffalo’s sera (n = 34) displayed little increase in antibody level (NI ≥ 1.5). None of the buffalo were positive for LSDV by VI and PCR. In addition, there were no significant differences in LSD prevalence among the cattle with regard to age and sex. In conclusion, the occurrence of LSD in cattle warrants a further epidemiological study of the spread of the disease in the area and adoption of control and prevention strategies. In addition, the PCR assay was confirmed to be useful in the diagnosis of LSDV and for wider epidemiological studies.