The current study was conducted to investigate the incidence of metritis and endometritis in dairy cows. Moreover, to determine the collective impact of metritis and endometritis in dairy farms on reproductive performance and milk yield. A total number of 246 Holstein cows divided into three groups was included in the current study.One of these groups as control group and the second and the third groups were including those cows diagnosed with acute postpartum metritis and chronic endometritis, respectively. The obtained results showed that endometritis possessed severe negative effects on postpartum reproductive performance of the studied cows compared to normal cows. Moreover, the impact of this disease was higher in premiparous cows in comparison with com their pleuriparous herd-mates. Days to first estrus tended (P=0.06) to be increased in premiparous cows suffering from endometritis (89.19±12.12 days) compared to normal cows (59.45±3.30 days) or those suffering from acute metritis (65.37±4.92 days). While in pleuriparous cows, the negative effects of endometritis did not show any tendency for prolonged days to first estrus, when compared to normal cows. Endometritis had significantly (P<0.01) negative impacts on postpartum cyclicity in premiparous cows (89.19±12.12 days), compared to 56.32±3.15 days in pleuriparous cows. Endometritis, significantly negatively (P<0.05) impacted days to first AI in both premiparous cows (105.63±12.95 days, compared to 65.97±2.63 days for normal cows and pleuriparous cows (76.19±3.64 days). A nearly similar trend was observed for endometritis and metritis regarding their potential negative impacts on number of inseminations per conception in both premiparous and pleuriparous cows. Regarding to, days open, diseases like endometritis was associated with significantly (P<0.01) higher days open in both premiparous and pleuriparous cows. Meanwhile, advancing parity was associated with significantly (P<0.05) higher days open for cows suffering from endometritis only.

Newcastle Disease virus (NDV) and Avian Influenza virus (AI) are represent a great negative significant causing severe economic losses and increased mortalities worldwide. Newcastle disease (ND) and Avian Influenza (AI) vaccination were targeting to lower the losses from mortality, reduce the viral load in the environment as well as eradication of positive cases. Many immunostimulants had been used to improve the immune response of vaccinated chickens. The current study was designed to compare the effect of different immunostimulants on chick's immune response to bivalent ND with AI-H5N1 oil vaccine. One hundred and ten, 1- day old Baladi chicks, At the 1st day of life (0 day) 10 birds were sacrificed to obtained individual blood samples for serum to determine maternal antibodies (MDAbs) to both AI and ND. Rest of birds (100 chicks) were divided into 5 equal groups (1-5); each 20 chicks. All chicken groups were vaccinated against ND with eye drop instillation of HB1 vaccine. While, at the 9th day birds of the groups 1-3 and 5 were given H5N1 vaccine by S.C injection, birds of group 4 were lifted as non AI vaccinated control. The used immune stimulants under test were given to groups 1, 2, and 3 as follows Lector, Superimmune and Imuvral; respectively. All the groups were subjected to daily observation with recording of feed intake, weekly body weight gain and total FCR, Weekly serum samples were collected, for serological examination, and the results showed high antibody titers, low mortality rates and better body performance in the groups treated with immunostimulants than the other groups which were not treated with the immunostimulants

The aim of this study was to investigate the course and distribution of the celiac artery in Hooded crows and to extend our knowledge on the captured crows. Scarce information in the field of veterinary comparative anatomy and the available literature on the celiac artery and its distribution is provided. So, the present study tried to declare the confusion about the course and distribution of the celiac artery in the Hooded crows. Therefore, 10 apparently healthy Hooded crows of different ages and sexes were captured. The birds were anaesthetized by IM injection of 0.5 cc of 2% xylazine HCL (3 mg/kg). Colored gum milk latex (60%) was then injected through the descending aorta. Then, specimens were subjected to fine dissection to demonstrate the origin, course and distribution of the celiac artery. The celiac artery erupted laterally from the right face of the descending aorta opposite to the distance between the 5th and 6th vertebral rib, on a level with the junction of the esophagus and the proventriculus. It proceeded ventrally and slight caudally, where it gave off the esophageal artery after, 5 cm from its origin, the dorsal proventricular artery, splinc arteries and at the middle of spleen then bifurcated into left and right branches. The left branch of the celiac artery gave rise to right hepatic artery, ventral proventricular artery, pyloric branches, ventral gastric artery and then continued as the A. gastrica sinistra. The right branch of the celiac artery released the caudal group of splenic arteries, A. gastrica dextra, then continued as A. pancreaticoduodenalis.

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.

There is paucity of information on the prevalence of leptospirosis in wildlife in Nigeria. This study investigated the prevalence and renal pathology of leptospirosis in wild animals in Southwest Nigeria. One hundred and five kidney samples were examined from 10 different wildlife species (antelope) greater cane rat (GCR), hare, African giant rat (AGR), tree hyrax, civet cat, monitor lizard, python, bushbuck and partridge) using a combination of Ellinghausen McCullough Johnson Harris (EMJH) medium, microscopic agglutination test (MAT), Warthin– Starry silver stain (WSss) and immunohistochemistry. Chi-square test was used with confidence level set at 0.05 to ascertain associations between positive cases and sex and species. Eightytwo (78.1%) samples were culturally positive, while 67.7% (63/93), 57.0% (16/28) and 66.7% (8/12) were WSss, MAT and immunohistochemically positive, respectively. Interstitial nephritis (41.0%) and tubular nephrosis (81.0%) were the most prominent histopathological changes. Pathogenic Leptospira organisms were highest in GCR (32.1%) and antelope (14.3%). Serovars hardjo (11.54%), bratislava (3.9%), canicola (3.9%), icterohaemorrhagiae (15.4%), pomona (7.14%) gripptotyphosa (19.2%) and undetermined isolates were also detected in other animals. The result showed high prevalence of Leptospira infection in the wild and the possibility of domestic animals and humans contracting the disease. This study is the first documentation of evidence of pathogenic Leptospira species in wildlife in Nigeria.

Query (Q) fever is a globally distributed zoonotic disease caused by Coxiella burnetii, a bacterial agent for which ruminants are the most prevalent natural reservoir. Data regarding Q fever infection in camels in Algeria are limited. Therefore, a survey to detect seroprevalence of C. burnetii antibodies was conducted among healthy camel populations in a vast area in southeastern Algeria to determine distribution of the Q fever causative organism and to identify risk factors associated with infection. Between January and March 2016, blood samples were collected from 184 camels and serum samples were subsequently analysed using a commercial Enzyme-Linked Immunosorbent Assay (ELISA) kit. At the time of blood collection, a questionnaire investigating 13 potential predisposing factors associated with C. burnetii seropositivity was completed for every dromedary camel and herd. Results were analysed by a chi-square (χ2) test and multivariate logistic regression. The seroprevalence of C. burnetii at the animal level was 71.2% (95% CI: 65.2–78.3) and 85.3% (95% CI: 72.8–97.8) at the herd level. At the animal level, differences in seroprevalence were observed because of herd size, animal age, animal sex, presence of ticks and contact with other herds. A multivariable logistic regression model identified three main risk factors associated with individual seropositivity: (1) age class > 11 years (OR = 8.81, 95% CI: 2.55–30.41), (2) herd size > 50 head (OR = 4.46, 95% CI: 1.01–19.59) and (3) infestation with ticks (OR 2.2; 95% CI: 1.1–4.5). This study of seroprevalence of C. burnetii infection in camels in Algeria revealed a high seroprevalence of Q fever in camel populations in southeastern Algeria and provided strong evidence that Q fever represents an economic, public health and veterinary concern. Appropriate measures should be taken to prevent the spread of C. burnetii and to reduce the risk of Q fever in farm animals and humans in this agro-ecologically and strategically important region of North Africa.

Sentinel herds and samples submitted by private equine practitioners were used to determine the sero-prevalence and sero-incidence of African horse sickness virus (AHSV) and equine encephalosis virus (EEV) in horse and donkey populations in the Highveld region of Zimbabwe. The sero-prevalence and sero-incidence of antibodies against these viruses were determined using the competitive enzyme-linked immunosorbent assay (ELISA) for the detection of serum antibodies. In donkeys, the median sero-prevalence of AHSV antibodies, across the three rainy seasons under study, was 75% (inter quartile range [IQR] 67–83), with a seasonal median sero-incidence of 45% (IQR 40–63). In horses, the median sero-prevalence of EEV antibodies was 63% (IQR 21–73), with a median seasonal sero-incidence of 10.5% (IQR 10–14), while in donkeys the median sero-prevalence of EEV antibodies was 80% (IQR 67–90), with a median seasonal sero-incidence of 50% (IQR 40–60). This study highlighted the significant levels of exposure of donkeys to AHSV and horses and donkeys to EEV in Zimbabwe despite equine encephalosis remaining unreported by Zimbabwean veterinarians to date. Most seroconversions in sentinel herd animals to AHSV and EEV occurred towards the end of the rainy season in March, April and May corresponding to the time of the year when the Culicoides vectors are in high abundance. In order to determine the clinical significance of these infections, blood and spleen samples, submitted by private equine veterinary practitioners over a 5-year period, from horses showing characteristic clinical signs of African horse sickness were tested for the presence of viral antigen using the antigen capture ELISA. The median sero-prevalence of AHSV antigen in horses recorded from these samples was 38% (IQR 33–88). The predominant AHSV antigen from these samples was serotype 7 (33%) followed by serotype 2 (26%) and serotypes 4 and 8 (16% each). African horse sickness virus serotypes 3 and 9, identified in this study, had not been previously reported in Zimbabwe.

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.