Toxoplasma gondii and Neospora caninum (Apicomplexa, Sarcocystidae) are protozoan parasites infecting a wide range of intermediate hosts worldwide, including birds. Raptors acquire the infections through the ingestion of both infected preys and oocysts in the environment suggesting they might be used as indicators of the spread of these pathogens. Here, we report an epidemiological survey with the aim of determining the prevalence of T. gondii and N. caninum infections in wild birds of prey, hospitalized in two Wildlife Recovery Centres (WRCs) in Northern Italy. Genomic DNA extracted from brain tissue samples was submitted to Real Time PCR targeting T. gondii B1 and N. caninum Nc5 genes. T. gondii genotyping was then performed by multilocus sequence typing (MLST) analysis, targeting three polymorphic genes (GRA6, BTUB, and altSAG2). T. gondii DNA was found in 35 (62.5%) out of 56 examined samples; concerning genotyping, it was possible to amplify at least one gene for 26 animals, and obtained sequences belonged to Type II. N. caninum DNA was only detected in two (3.6%) common kestrels (Falco tinnunculus), adding a new species to the list of suitable intermediate hosts for this pathogen. Data obtained in the present study thus confirmed the spread of both T. gondiiand N. caninum in wild bird of prey, endorsing the role of WRCs in the epidemiological surveillance of wildlife.
Disorders of the oral cavity represent common conditions in pet reptiles.1 Multiple predisposing factors including immunosuppression, chronic stressful conditions inappropriate husbandry, disruption of normal oral tissue, or systemic disease may lead ultimately to infectious stomatitis. Treatment usually involves correction of environmental parameters, appropriate systemic and topical antimicrobial therapy, and surgical debridement or resection of affected areas.1,2,5 Periodontal disease is another common oral 6 condition, especially in acrodont lizards such as agamids and chameleons.
The aim of this investigation was to assess the clinical use of alfaxalone as a short-acting anaesthetic agent for induction to inhalation anaesthesia in jungle carpet pythons (Morelia spilota cheynei). Ten healthy, captive, sub-adult jungle carpet pythons (1.1±0.32 kg bw) were anaesthetised using a dose of 10mg/kg of alfaxalone, administered intravenously to the ventral tail vein. Heart rate (HR) and respiratory rate (RR) were recorded before administration (T0), and every 5 minutes until the snakes fully recovered from the anaesthesia. The induction time, time of tail-pinch reflex loss, tracheal tube insertion time, interval of deep anaesthesia, and the time of full recovery were recorded. The induction time occurred within 3.1±0.8 minutes. The tail-pinch reflex loss was lost within 5.6±0.7 minutes. The mean tracheal tube insertion time, the interval of deep anaesthesia, and the time of full recovery were 6.9±0.9 minutes, 18.8±4.7 minutes, and 36.7±11.4 minutes, respectively. A prolonged time of full recovery was recorded in two snakes (61.3 and 62.6 minutes, respectively). Their mean heart rate was statistically higher (P<0.05) at T5, T15 and T20 when compared with the basal HR at T0. The respiratory rate of the snakes dropped at T5 and was statistically lower (P<0.05) from T5 until T20 when compared with RR at all other time points. In two snakes apnoea was recorded at T5. Intravenous administration of alfaxalone proved to be a valuable method of induction, suitable for a subsequent inhalation anaesthesia in jungle carpet pythons.
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