The red fox (Vulpes vulpes) is a known host for various parasites, including numerous helminths and protozoans. Among these, certain species in the genus Sarcocystis (phylum Apicomplexa) have been documented to possess the capability to infect red foxes as definitive hosts. In South Korea, red foxes have been introduced and released as part of a re-introduction program. However, two months after its release, one of the foxes was found dead because of illegal trapping. The fox was necropsied, and a subsequent coprological study revealed oocysts of Sarcocystis sp. in the intestinal contents. The oocysts were identified as Sarcocystis pilosa based on the 18S rRNA and cytochrome c oxidase subunit 1 (cox1) gene sequences. It exhibited a 99.7–100% identity with 18S rRNA gene sequences and 99.1–99.8% identity with cox1 gene sequences from other previously reported S. pilosa samples. Additionally, it showed identities of 95.4–96.4% and 91.1–91.5% with the cox1 gene sequences of S. hjorti and S. gjerdei, while demonstrating 99.6 and 98.1% identity with the 18S rRNA gene sequences of S. hjorti and S. gjerdei, respectively. This is the first report from mainland Asia, excluding the Japanese archipelago, indicating that the life cycle of S. pilosa persists in South Korea.

Understanding the dietary composition of the Siberian musk deer (Moschus moschiferus) is critical for informing conservation efforts, particularly given the species’ vulnerable status in the Republic of Korea and its limited ecological data. Previous dietary studies have relied on conventional methods with limitations in taxonomic precision, hindering comprehensive insights into their feeding ecology. To address this gap, we used Next-Generation Sequencing to analyze 16 fecal samples collected in April from Gangwon Province, the habitat of M. moschiferus. Our results revealed 213 unique plant species, with Morus, Quercus, and Prunus accounting for the majority of the diet. Notably, nearly half of the identified genera, including Morus, Actinidia, and Viscum, were reported for the first time as dietary plants of M. moschiferus. This study confirms that M. moschiferus is a concentrate feeder that primarily relies on woody plants (98.8%) and may exhibit tree-climbing behavior to access parasitic shrubs like Viscum. These findings provide a foundation for future dietary analysis research and serve as valuable baseline data for the long-term conservation of M. moschiferus.

The Eastern spot-billed duck ( Anas zonorhyncha ) is a common migratory waterfowl widely distributed throughout East Asia. However, the lack of species-specific reference intervals, defined as the normal range of values derived from a healthy population for clinical interpretation, hampers accurate health assessment and clinical diagnostics in this species. This is further complicated by hematologic characteristics of avian blood, such as nucleated red blood cells and thrombocytes, which pose challenges to conventional automated measurement systems optimized for mammals. This study aimed to establish hematological and biochemical reference intervals for juvenile Eastern spot-billed ducks and to evaluate the accuracy of an automated hematology analyzer (XN-1000V, Sysmex, Japan), which newly supports avian blood analysis, compared to traditional manual counting methods. Blood samples were collected from 55 clinically healthy juvenile ducks. The established reference intervals were largely consistent with those reported in related Anas species, though Eastern spot-billed ducks exhibited a heterophil-predominant leukogram. No significant differences were observed between sexes. Comparison between manual and automated methods revealed statistically significant differences in most hematological parameters; however, most of these differences were not clinically relevant, except for thrombocyte counts. Moderate correlations were found for key parameters, including WBC, RBC, hemoglobin, PCV, and MCV, suggesting potential clinical applicability of the automated analyzer with some limitations. This study provides the first species-specific hematologic and biochemical reference intervals for juvenile Eastern spot-billed ducks under semi-captive conditions, offering valuable baseline data for clinical assessments in this subset of the population. Additionally, it highlights the need for further optimization of XN-1000V analyzers for reliable and precise application in avian diagnostics.

Background: Studies are currently being conducted on rabbits requiring serial glucose monitoring. The FreeStyle Libre 2 (FSL2), a serial glucose monitoring device, has been validated in humans, dogs and cats, but not in rabbits.Objectives: This study aimed to evaluate the accuracy of the FSL2 in rabbits.Methods: Six healthy rabbits were used in this study. Interstitial glucose (IG) was measured using the FSL2, and blood glucose (BG) was measured using a portable blood glucose meter (PBGM); their results were compared with those from a clinical chemistry analyser. For the first 3 h, IG and BG were measured at 1‐h intervals. Subsequently, they were measured every 8 h over a 48‐h period. Regular insulin 0.2 U/kg was then administered to the rabbits, and IG and BG were measured every 15 min over a 90‐min period.Results: Before insulin treatment, no measurements fell within the hypoglycaemic range (BG < 100 mg/dL). In the euglycaemic range (BG ≥ 100 mg/dL), the PBGM and FSL2 showed 85.7% and 23.8% accuracies, respectively. After insulin treatment, the PBGM showed 95.5% and 81.3% accuracies in the hypoglycaemic and euglycaemic ranges, respectively. The FSL2 showed 68.1% and 37.5% accuracies in the hypoglycaemic and euglycaemic ranges, respectively. Parkes consensus error grid analysis showed that the PBGM and FSL2 had 100% agreement for Zones A (no effect on clinical action) and B (altered clinical action unlikely to affect outcome) in rabbits with and without insulin treatment.Conclusions: There was limited agreement between the FSL2 and reference standard BG measurements. However, the FSL2 allows clinically acceptable identification of hypoglycaemic states in rabbits.

Osteosarcoma (OSA) is a malignant neoplasm of mesenchymal origin characterized by osteoid or immature bone production and is rarely reported in reptiles. A 3-month-old Argentine black and white tegu presented with a subcutaneous mass on the left flank, approximately 2 months after a dog bite. Physical and radiographic examination revealed no initial internal abnormalities, but follow-up examination revealed a rapidly enlarging soft tissue mass. Ultrasonography confirmed a well-encapsulated mass, while contrast-enhanced computed tomography demonstrated mineralization, rib osteolysis, and multiple bilateral nodules, indicating a malignant process. Histopathological examination of the excised mass demonstrated features consistent with giant cell-rich osteosarcoma, including irregular bony trabeculae, numerous multinucleated giant cells, and peripheral osteoid matrix. This case highlights the diagnostic challenges of OSA in reptiles, the value of integrating diagnostic imaging and histopathology, and the need for species-specific imaging protocols in ectothermic species, thereby expanding the literature on reptilian neoplasia.

Background: Inflammasomes recognize endogenous and exogenous danger signals, and subsequently induce the secretion of IL-1β. Studying inflammasomes in the red fox (Vulpes vulpes) is crucial for wildlife veterinary medicine, as it can help control inflammatory diseases in foxes. Methods: We investigated the activation and intracellular mechanisms of three inflammasomes (NLRP3, AIM2, and NLRC4) in fox peripheral blood mononuclear cells (PBMCs), using established triggers and inhibitors derived from humans and mice. Results: Fox PBMCs exhibited normal activation and induction of IL-1β secretion in response to representative inflammasome triggers (ATP and nigericin for NLRP3, dsDNA for AIM2, flagellin for NLRC4). Additionally, PBMCs showed normal IL-1β secretion when inoculated with inflammasome-activating bacteria. In inhibitors of the inflammasome signaling pathway, fox inflammasome activation was compared with mouse inflammasomes. MCC950, a selective NLRP3 inhibitor, suppressed the secretion of dsDNA- and flagellin-mediated IL-1β in foxes, unlike mice. Conclusions: These findings suggest that NLRP3 may have a common role in dsDNA- and flagellin-mediated inflammasome activation in the red fox. It implies that this fox inflammasome biology can be applied to the treatment of inflammasome-mediated diseases in the red fox.