This study aimed to evaluate intramuscularly administered ketamine, intravenously administered ketamine and intravenously administered propofol in diazepam premedicated goats. Nine native female goats divided into three groups (each of 3 goats) were premedicated with diazepam 1 mg/kg intramuscularly. Goats of group I were treated with ketamine (8 mg/kg) intravenously, while those of group II treated with ketamine (10 mg/kg) intramuscularly, and group III injected with propofol (5 mg/kg) intravenously. The mean anesthetic onset, anesthetic duration, and total recovery period were calculated. The mean heart rate (HR), respiratory rate (RR), rectal temperature (RT) and biochemical parameters also were recorded. Satisfactory anesthesia and immobilization (smooth induction, and smooth recovery) needed for surgical interventions of short duration were achieved in all groups. The induction was good and smooth in groups I and III. The quality of recovery was good in groups III and I and recovery is longer in group II. In conclusion, this study indicates that the 3 regimens are associated with acceptable anesthetic characteristics; Propofol IV is superior to ketamine because it provides uneventful onset and recovery which are more rapid than ketamine IV or ketamine IM, so reduces anaesthetic risk while administration of ketamine intravenously is superior to its administration intramuscularly

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 ability of L. monocytogenesas an opportunistic pathogen of humans and animals, to survive and grow under various adverse environmental conditions, makes it a potential health hazard afterthe consumption of contaminated dairy products, it often implicated in several outbreaks of listeriosis. This study was conducted to investigate the survival of L. monocytogenes strain (NCTC13372) when inoculated with a population level of 6.95 log cfu/g and 7.64 logcfu/g and stored at 4ºC for 15 days and 3 months at -18ºC for yoghurt and ice cream respectively. The obtained results indicated that complete inactivation of the tested organism wasn’t achieved till the end of storage periods and the inoculated L. monocytogenes was survived in both yoghurt and ice cream throughout the trial. It is concluded that in the dairy industry, we cannot rely upon either fermentation process and storage at refrigerating temperature or upon storage at freezing temperature during yoghurt and ice cream manufacturing to control L.monocytogenes pathogen in order to provide safe products for consumption.

The aim of this study was to compare the analgesic effect of tramadol, lidocaine and tramadol-lidocaine combination injected in the epidural space in goats. Nine goats were used to compare the epidural analgesic effect of tramadol (3 mg / kg), 2% lidocaine (2.86 mg/kg) and tramadol-lidocaine combination (1 mg /kg and 2.46 mg kg, resp.). Onset time, duration, and degree of analgesia and ataxia were recorded as well as Heart rate (HR), respiratory rate (RR), rectal temperature (RT), and biochemical parameters were recorded. Time to onset and duration of analgesia, were tramadol 10 min and 225 min; lidocaine 4 min and 85 min and tramadol-lidocaine 4 min and 130 min respectively. Onset time and duration were significantly longer with tramadol and tramadol-lidocaine combination than the other treatment. Ataxia was not observed in tramadol and mildly observed in tramadol-lidocaine combination and was severing in lidocaine. Tramadol and tramadol-lidocaine combination might be clinically useful to provide analgesia in goats for long-duration surgical procedures than lidocaine alone.

Lespedeza cuneata (poorman’s lucerne; sericea lespedeza), a tannin-rich perennial legume, was offered as hay to dry Merino ewes in a confined feeding experiment to evaluate the effect on the level of gastrointestinal parasite infection in sheep. Medicago sativa (a low tannin containing perennial legume) was used as the control treatment. Parameters faecal egg count (FEC), FAMACHA© scores and rectal temperatures were used. FECs were substantially lower (p = 0.05) in the Lespedeza group after 35 days, together with a trend of higher rectal temperatures, compared with the Medicago group. Although non-significant (p > 0.05), the higher rectal temperatures suggested a lower level of anaemia in the sheep on the Lespedeza ration and, therefore, a lower parasite-worm burden. However, FAMACHA© scores showed no significant (p > 0.05) differences between treatments despite the differences in FEC that were recorded, indicating that host homeostasis was possibly mediated by improved nutrition as a result of the high protein content of both experimental diets.

Poultry production in South Africa, a so-called developing country, may be seen as a gradient between two extremes with highly integrated commercial enterprises with world-class facilities on one hand and unimproved rural chickens kept by households and subsistence farmers on the other. Although vaccination against Newcastle disease is widely applied to control this devastating infection, epizootics continue to occur. Since the first official diagnosis in 1945, through the sporadic outbreaks of the 1950s and early 1960s, to serious epizootics caused by genotype VIII (late 1960s–2000), genotype VIIb (1993–1999), genotype VIId (2003–2012) and most recently genotype VIIh (2013 to present), South Africa’s encounters with exotic Newcastle disease follow global trends. Importation – probably illegal – of infected poultry, poultry products or exotic birds and illegal swill dumping are likely routes of entry. Once the commercial sector is affected, the disease spreads rapidly within the region via transportation routes. Each outbreak genotype persisted for about a decade and displaced its predecessor.

OBJECTIVE To determine effects of diurnal variation and anesthetic agents on intraocular pressure (IOP) in Syrian hamsters (Mesocricetus auratus). ANIMALS 90 healthy adult Syrian hamsters (45 males and 45 females). PROCEDURES IOP was measured with a rebound tonometer. In phase 1, IOP was measured in all hamsters 3 times during a 24-hour period (7 am, 3 pm, and 11 pm). In phase 2, hamsters were assigned to 5 groups (18 animals [9 males and 9 females]/group). Each group received an anesthetic agent or combination of anesthetic agents (ketamine hydrochloride, xylazine hydrochloride, diazepam, ketamine-diazepam [KD], or ketamine-xylazine [KX] groups) administered via the IP route. The IOP was measured before (time 0 [baseline]) and 10, 30, 60, 90, 120, and 150 minutes after administration of drugs. RESULTS Mean ± SD IOP values were 2.58 ± 0.87 mm Hg, 4.46 ± 1.58 mm Hg, and 5.96 ± 1.23 mm Hg at 7 am, 3 pm, and 11 pm, respectively. Mean baseline IOP was 6.25 ± 0.28 mm Hg, 6.12 ± 0.23 mm Hg, 5.75 ± 0.64 mm Hg, 5.12 ± 1.40 mm Hg, and 4.50 ± 1.30 mm Hg for the ketamine, xylazine, diazepam, KD, and KX groups, respectively. A significant decrease in IOP, compared with baseline IOP, was detected in only the KX group at 30, 60, and 90 minutes after drug administration. CONCLUSIONS AND CLINICAL RELEVANCE Maximum IOP in Syrian hamsters was detected at night. The ketamine-xylazine anesthetic combination significantly decreased IOP in Syrian hamsters.

OBJECTIVE To quantify plasma fentanyl concentrations (PFCs) and evaluate antinociceptive and respiratory effects following application of transdermal fentanyl patches (TFPs) and assess cerebrospinal μ-opioid receptor mRNA expression in ball pythons (compared with findings in turtles). ANIMALS 44 ball pythons (Python regius) and 10 turtles (Trachemys scripta elegans). PROCEDURES To administer 3 or 12 μg of fentanyl/h, a quarter or whole TFP (TFP-3 and TFP-12, respectively) was used. At intervals after TFP-12 application in snakes, PFCs were measured by reverse-phase high-pressure liquid chromatography. Infrared heat stimuli were applied to the rostroventral surface of snakes to determine thermal withdrawal latencies after treatments with no TFP (control [n = 16]) and TFP-3 (8) or TFP-12 (9). Breathing frequency was measured in unrestrained controls and TFP-12–treated snakes. μ-Opioid receptor mRNA expression in brain and spinal cord tissue samples from snakes and turtles (which are responsive to μ-opioid receptor agonist drugs) were quantified with a reverse transcription PCR assay. RESULTS Mean PFCs were 79, 238, and 111 ng/mL at 6, 24, and 48 hours after TFP-12 application, respectively. At 3 to 48 hours after TFP-3 or TFP-12 application, thermal withdrawal latencies did not differ from pretreatment values or control treatment findings. For TFP-12–treated snakes, mean breathing frequency significantly decreased from the pretreatment value by 23% and 41% at the 24- and 48-hour time points, respectively. Brain and spinal cord tissue μ-opioid receptor mRNA expressions in snakes and turtles did not differ. CONCLUSIONS AND CLINICAL RELEVANCE In ball pythons, TFP-12 application resulted in high PFCs, but there was no change in thermal antinociception, indicating resistance to μ-opioid-dependent antinociception in this species.

OBJECTIVE To develop a spasticity scale for dogs with chronic deficits following severe spinal cord injury (SCI) for use in clinical assessment and outcome measurement in clinical trials. ANIMALS 20 chronically paralyzed dogs with a persistent lack of hind limb pain perception caused by an acute SCI at least 3 months previously. PROCEDURES Spasticity was assessed in both hind limbs via tests of muscle tone, clonus, and flexor and extensor spasms adapted from human scales. Measurement of patellar clonus duration and flexor spasm duration and degree was feasible. These components were used to create a canine spasticity scale (CSS; overall score range, 0 to 18). Temporal variation for individual dogs and interrater reliability were evaluated. Gait was quantified with published gait scales, and CSS scores were compared with gait scores and clinical variables. Owners were questioned regarding spasticity observed at home. RESULTS 20 dogs were enrolled: 18 with no apparent hind limb pain perception and 2 with blunted responses; 5 were ambulatory. Testing was well tolerated, and scores were repeatable between raters. Median overall CSS score was 7 (range, 3 to 11), and flexor spasms were the most prominent finding. Overall CSS score was not associated with age, SCI duration, lesion location, or owner-reported spasticity. Overall CSS score and flexor spasm duration were associated with gait scores. CONCLUSIONS AND CLINICAL RELEVANCE The CSS could be used to quantify hind limb spasticity in dogs with chronic thoracolumbar SCI and might be a useful outcome measure. Flexor spasms may represent an integral part of stepping in dogs with severe SCI.

A recombinase polymerase amplification (RPA)-based method was developed for rapid and specific detection of African swine fever virus (ASFV), the etiologic agent of African swine fever, a devastating disease of swine. Primers and the exo probe targeting the conserved region of the P72 gene of ASFV were designed and the reaction was run on the Genie III scanner device. Using recombinant plasmid DNA containing the P72 gene as template, we showed that the amplified product could be detected in less than 10 min and that the detection limit was 102 copies DNA/reaction [same detection limit as real-time polymerase chain reaction (PCR)]. The RPA assay did not cross-detect CSFV, PCV-2, PRV, PRRSV, or FMDV, common viruses seen in pigs. Tests of recombinant plasmid-spiked serum samples revealed that RPA and real-time PCR had the same diagnostic rate. The RPA assay, which is simple, cost-effective, and fast, is a promising alternative to real-time PCR for ASFV detection.