Veterinary Sciences最新文献

Uriniferous perinephric pseudocysts (PNPs) are a rare condition in cats, primarily managed by nephrectomy to eliminate persistent urinary leakage. Organ preservation is critical in cases with solitary kidneys. This report describes a cat with congenital absence of the right kidney that developed a uriniferous PNP secondary to abnormal communication between the calyceal diverticulum and subcapsular space. A 6-year-and-11-month-old neutered male Ragdoll cat presented with abdominal distension and lethargy. Ultrasonography revealed an extensive subcapsular perinephric fluid and a cystic lesion adjacent to the renal pelvis. Contrast-enhanced computed tomography with excretory urography directly demonstrated the time-dependent passage of contrast medium from the renal pelvis into the calyceal diverticulum and subsequent leakage into the subcapsular space, allowing precise identification of the renal leakage pathway. Based on these findings, an operation was performed using a non-vascularized free omental plug inserted into the diverticular opening and secured using capsular sutures. Postoperative drainage resolved rapidly, renal function normalized, and no recurrence was detected during long-term follow-up of up to 465 days. To the best of our knowledge, this is the first report to describe an organ-sparing surgical approach that directly addresses the renal leakage pathway in feline uriniferous PNPs.

Captive bird populations in zoological institutions face unique disease risks due to close interspecies contact and human interaction. Vaccination is widely used as a prophylactic measure. However, most available vaccines are developed for poultry and are used off-label in non-domesticated birds, often without species-specific safety and efficacy data. This review provides a comprehensive overview of vaccines reported in zoo-housed birds for major viral, bacterial, and fungal pathogens. This review highlights that for most vaccines, evidence of safety and effectiveness is limited. Vaccine use should therefore be guided by risk assessment, relevant legislation, and institutional priorities, and should integrate species-specific data on vaccine safety and effectiveness, disease susceptibility, and local epidemiology. Extensive research and species-specific validation are essential to improve preventive health strategies in avian conservation programs.

Immune-mediated non-neoplastic bone marrow disorders (NNBMD), including precursor-targeted immune-mediated anemia (PIMA) and myelodysplastic syndrome (MDS), can cause non-regenerative anemia in dogs and often fail to respond to immunosuppressive treatment. Human intravenous immunoglobulin (hIVIG) has been proposed as an immunomodulatory therapy for refractory hematologic disease in humans, but evidence in veterinary patients remains limited. This case report describes the adjunctive use of hIVIG and the associated clinical responses observed in two dogs with refractory NNBMD. A 10-year-old (3.2 kg) spayed female Maltese (case 1) showed persistent non-regenerative anemia, with hematocrit (HCT) 15.6-20.2% and reticulocyte production index (RPI) 0.12-0.69, requiring four transfusions over 10 months, and was diagnosed with PIMA based on bone marrow cytology demonstrating destruction of erythroid precursors. A 7-year-old (9.3 kg) intact female Dachshund (case 2) had sustained non-regenerative anemia (HCT 10.8-20.9%, RPI 0.12-0.40) necessitating eight transfusions over 20 months and was diagnosed with MDS characterized by dyserythropoiesis. Human intravenous immunoglobulin (0.5 g/kg over 6 h) was administered six times in case 1 and seven times in case 2 over a four-month period. After initiating hIVIG therapy, RPI increased (0→1.80 and 0.25→2.10 in cases 1 and 2), and HCT remained above 20% without further transfusions. To our knowledge, this is the first clinical report demonstrating the adjunctive use of hIVIG and associated hematologic improvement in canine NNBMD.

Piglets are highly susceptible to iron deficiency. This randomized clinical trial evaluated the effectiveness of four iron dosing schemes in preventing anemia. Two herds with different farrowing management systems were included. In each herd, 40 litters (6 piglets/litter) were selected on day 3 of age. A 2 × 2 factorial design was applied, combining two intramuscular iron dextran injection schemes [37.5 mg Fe/kg (low injection; LI) or 150 mg Fe/kg (high injection; HI)] with two oral ferrous sulphate feed supplementation schemes [125 mg Fe/kg (low feed; LF) or 200 mg Fe/kg (high feed; HF)]. Blood samples were collected at 4 and 20 days of age, and piglets were weighed at 3 and 20 days. Data were analyzed using linear mixed models, with significance set at p < 0.05. In Herd A, HI-LF piglets showed increased body weight, whereas no growth differences were observed in Herd B. Creep-feed intake did not differ between treatments. HI consistently improved red-cell indices in Herd A, while in Herd B LI piglets initially showed higher values at day 4, but HI piglets surpassed them by day 20. Leukocyte responses were limited. High-dose iron injections were effective in preventing anemia, while oral supplementation had minimal impact.

Avian influenza (AI) significantly threatens poultry health and causes major economic losses in the poultry industry. Vaccination remains crucial for AI prevention and control. The major protective epitopes of influenza viruses are located on hemagglutinin (HA), a surface glycoprotein essential for viral infection. Most influenza vaccines induce neutralizing antibodies against HA to block viral entry. HA maturation requires the HA0 precursor to be proteolytically cleaved at a conserved site by host proteases to yield HA1 and HA2 subunits. A subsequent acidic condition triggers HA conformational changes, enabling viral-host membrane fusion. However, whether HA conformational variations affect immunogenicity remains unclear. In this study, the cleavage site of the HA gene from an H9N2 avian influenza virus was modified to block the proteolytic cleavage of the HA protein. Our results revealed distinct proteolytic patterns of certain mutants, which exhibited either increased or decreased cleavage efficiencies compared to the wild-type (WT) HA. However, none of the mutants exhibited completely abolished HA0 cleavage. To assess the immunogenicity of these variants, BALB/c mice were immunized with DNA vaccines expressing either WT or mutant HA proteins. Strikingly, the mutant HA protein with a 19-amino-acid deletion Dlt5 (P6~P1, P1'~P'13) at the cleavage site exhibited reduced cleavage efficiency and induced significantly higher HI antibody titers compared to the WT. These results offer valuable perspectives for enhancing avian influenza vaccine efficacy through strategic modification of HA cleavage properties.

African swine fever (ASF), caused by the African swine fever virus (ASFV), is a highly contagious and fatal disease. Accurate detection in the early stages of an outbreak relies on molecular methods, but serological monitoring at the population level is also crucial for assessing the extent of exposure and past infections. This experiment developed an indirect enzyme-linked immunosorbent assay (ELISA) to detect antibodies against ASFV, using three ASFV RNA polymerase subunits (H359L, C147L, and D339L) as coating antigens. The recombinant proteins were successfully expressed in Escherichia coli and purified. Using a checkerboard titration method, we systematically optimized key assay parameters, determining the optimal coating conditions to be a mixture of H359L, C147L, and D339L at a volume ratio of 1:2:2, with individual concentrations of 1 μg/mL, 0.4 μg/mL, and 0.5 μg/mL, respectively. Other optimized parameters included a serum dilution of 1:200, a blocking buffer containing 5% skim milk, and specific incubation conditions for the secondary antibody and substrate. The cut-off value was established at 0.430 (x¯ + 4SD) based on 30 negative sera. The established triple-antigen indirect ELISA exhibited high sensitivity (detecting positives at dilutions up to 1:3200) and excellent specificity (no cross-reactivity with antisera against CSFV, PRRSV, PRV, PCV2, and PEDV. Both intra and inter assay repeatability were confirmed, with coefficients of variation ranging from 1.020% to 7.600%. Validation with 123 clinical serum samples demonstrated a 96.75% concordance rate with a commercial kit. In conclusion, the three-antigen indirect ELISA established in this study exhibits high specificity and sensitivity, making it suitable for serological surveillance and exposure assessment of ASFV antibodies. It can be combined with molecular detection for epidemiological investigations and integrated prevention and control measures.

Early recognition of vascular compromise is essential for reconstructive flap survival. In human surgery, local glucose monitoring is widely used as an objective indicator of perfusion, but its application in veterinary patients is still limited. This report describes postoperative glucose measurement as a simple and minimally invasive method for evaluating flap viability in two dogs. This report describes two prospectively observed clinical cases in which local glucose measurement was applied as an adjunctive monitoring tool during postoperative flap management. Local glucose values were measured with a handheld glucometer at predefined flap and control sites. Serial readings were compared with daily assessments of flap color, temperature, turgor, and wound integrity. A previously suggested threshold of 60-62 mg/dL was used as a reference for potential perfusion compromise. In Case 1, a phalangeal fillet flap showed a brief glucose decline on postoperative days 2-3, followed by normalization and uneventful healing. In Case 2, which underwent advancement flap reconstruction after wound dehiscence, glucose values remained persistently below 60 mg/dL and preceded visible ischemia and distal necrosis. Local glucose monitoring provided rapid and clinically meaningful information about flap perfusion. Transient decreases reflected reversible postoperative congestion, whereas persistent hypoglycemia indicated progressive ischemia. These findings support the use of glucose monitoring as an adjunct in small-animal reconstructive surgery.

The global swine industry suffers persistent economic losses and health challenges due to major viral pathogens such as African swine fever virus (ASFV), porcine reproductive and respiratory syndrome virus (PRRSV), classical swine fever virus (CSFV), and porcine circovirus (PCV). Traditional diagnostic methods, including virus isolation, serology, and quantitative PCR (qPCR), are limited by time, equipment requirements, and field applicability. Recent advances in CRISPR-based diagnostics, particularly those leveraging the collateral cleavage activity of Cas12a and Cas13a, have enabled rapid, sensitive, and field-deployable nucleic acid detection. This review outlines the principles of CRISPR-Cas12a/13a systems, their integration with isothermal amplification techniques, and their application in detecting major swine viruses. Cas12a-based platforms (e.g., DETECTR) and Cas13a-based systems (e.g., SHERLOCK) achieve detection limits as low as single-copy/μL within 25-60 min at 37 °C, offering high specificity and compatibility with visual readouts. Applications include ASFV, PRRSV, CSFV, PCV, foot-and-mouth disease virus (FMDV), porcine rotavirus (PoRV), and porcine parvovirus 7 (PPV7). Despite significant advances, challenges remain, notably the reliance on nucleic acid extraction and the need for fully integrated "sample-in, result-out" systems. Ongoing innovations in extraction-free methods, lyophilized reagents, and multiplex detection will strengthen the role of CRISPR diagnostics in swine disease surveillance and control. From an application standpoint, the technology offers a low-capital, field-adaptable alternative to qPCR, with its value proposition rooted in early outbreak containment and loss prevention. Its adoption pathway is expected to vary across production systems-serving as a sentinel tool in intensive settings, a leapfrogging solution in rapidly intensifying regions, and through shared-service models in resource-limited contexts. However, translation to routine use still requires overcoming standardization hurdles, regulatory validation, and workflow integration.

Although particulate matter (PM) is strongly associated with allergic reactions, the potential risk of the ability of PM derived from poultry houses to induce allergic reactions remains unclear. This study investigated the effects of duck housing PM on allergic reactions in mice. PM samples and fungi were collected from a duck farm. Ovalbumin (OVA) was used as a positive control, with ambient-level concentrations of PM, high-concentration PM (HPM), and fungal experimental groups. Aerosol exposure was performed on the mice. Serum IgE, allergic mediators (histamines and leukotrienes), cytokines, and pulmonary histopathology were analyzed. Furthermore, HPM-induced metabolic profiles in bronchoalveolar lavage fluid were measured. The results revealed that all the treatment groups of mice presented allergic symptoms, including sneezing and coughing; higher concentrations of IgE, His, and LTs in the serum; upregulation of allergic reaction-related cytokines, such as IL4, IL5, and IL33; and microscopic lesions of the lungs characterized by inflammatory cell infiltration were observed in all the treatment groups, indicating that PM and fungi can cause allergic reactions. Notably, allergic reactions were more pronounced in the HPM and fungal groups than in the PM group. In addition, metabolomics analyses revealed that HPM exposure caused metabolic disorders in mouse lungs. The key pathway with the highest correlation to metabolite differences was pyrimidine metabolism, which is associated with allergic reactions. In conclusion, this study demonstrated that exposure to PM in duck houses can cause allergic reactions in mice and significant metabolomic changes in the lungs, especially HPM. Moreover, the contribution of fungal components in the PM cannot be ignored. These findings highlight the potential health risks associated with PM from the poultry industry.

Osteoarthritis (OA) is a degenerative joint disease that affects humans and animals worldwide. Its early diagnosis remains challenging due to subtle clinical signs and late radiographic changes. This study aimed to explore candidate biomarkers associated with spontaneous OA and to investigate their correlation with ultrasonographic scores to support early diagnosis. Clinical, radiographic, and ultrasonographic evaluations were performed on 52 equine metacarpophalangeal joints, with and without OA, allowing joint scoring and classification into osteoarthritis (OAG) and control groups. Synovial fluid samples were analyzed for cartilage degradation (C2C), untargeted ¹H NMR-based metabolomics, and lipid peroxidation (TBARS). Statistical analyses included Student's t-test, Mann-Whitney U test, univariate and multivariate metabolomic analyses, and Spearman's correlation (p < 0.05). Ultrasonography revealed higher scores in the synovial fold, membrane, and fluid, indicating synovitis as the predominant finding in the acute phase. C2C and TBARS concentrations were significantly higher in the OAG. Seven metabolites differed between groups, with citrate and TBARS showing the strongest correlations with ultrasonographic scores. These findings suggest increased metabolic activity and lipid peroxidation in early OA and highlight citrate and TBARS as potential auxiliary biomarkers for early diagnosis associated with synovitis.