New Zealand veterinary journal最新文献

Aims: To determine the major causes of mortality in weka (Gallirallus australis), and to investigate associations between causes of mortality and captivity status, age, sex, decade of submission, and season.

Methods: Necropsy records were obtained from the Massey University School of Veterinary Science/Wildbase Pathology database (Palmerston North, NZ) for weka submitted between 1 January 1995 and 22 March 2022. Causes of mortality were classified into categories based on aetiology. Frequency of diagnosis was tested for association with region of submission, captivity status, age, sex, decade, and season of death.

Results: A total of 156 necropsy reports were included in this study, of which 96 (61%) were from wild weka, 57 (36.5%) were captive, and three (1.9%) were of an unspecified captivity status. Weka were submitted from 12 regions across New Zealand. There were 65 (41.7%) adults, 16 (10.3%) juveniles, and 75 (48.1%) weka of an undetermined age among the 156 submissions. Of the weka with a known sex, there was a similar distribution between sexes with 27 (17.3%) males and 29 (18.6%) females. A cause of death was determined in 132/156 (84.6%) cases, with 24/156 (15.4%) cases having an unknown diagnosis. The leading cause of mortality in weka was traumatic injury, which occurred in 65/156 (41.7%), followed by infectious and/or inflammatory diseases in 26/156 (16.7%), and degenerative and/or nutritional conditions affecting 20/156 (12.8%) cases. The distribution of the primary causes of death was found to be dependent on captivity status (p < 0.001). Traumatic and toxic causes of death were more frequent in wild than captive weka. The cause of death was also dependent on season (p < 0.001). There was a significant difference in cause of death between summer and all other seasons (spring p = 0.008; autumn p < 0.001; winter p < 0.001) and between autumn and winter (p = 0.008).

Conclusion: Trauma was identified as the most significant cause of mortality in the free-living weka necropsied. The inherent and uncertain submissions biases, and low case numbers over a long period of time, means that temporal patterns and the effect of captivity status on causes of mortality should be interpreted with caution.

The aim of this scoping review was to investigate the range of methods used to guide veterinarians in their approach to the death of their animal patients with the guiding question: how is this topic addressed in the training of veterinarians? We included studies written in Portuguese or English, with a theme aligned with the objective of the review and which answered the guiding question. Studies not fulfilling these criteria were excluded. A total of 22 complete studies were identified by searching the Scopus, Web of Science, PsycINFO and Pubmed databases/libraries, with no restrictions on the date of publication. Studies from 1989 to 2023 were identified, mostly by North American authors. The results were organised into three major themes: topics in the veterinary curriculum about patient death and its impacts on students and future professionals; teaching methods used to cover this topic; and the extracurricular training available to support veterinarians with their direct experience of this topic. Analysis of these papers indicated that the theme of death appeared in three distinct contexts operating at different stages of veterinarians' training: the hidden curriculum, compulsory training initiatives, and extracurricular training. The review included reflections on the challenges inherent in this theme and inferences from the timeline of publications in this area. Our review clearly indicates that there is increasing recognition of the importance of this subject, as well as a feeling within the profession of being unprepared to manage this aspect of veterinary experience and a perception that teaching in this area needs to be improved.

Aims: To compare the responses of liver Cu concentrations in dairy cows between three forms of injectable Cu supplementation and a negative control group.

Methods: Across two dairy farms in North Canterbury, New Zealand, 80 mid-lactation dairy cows (n = 28 and 52 per farm) were randomly allocated to four treatment groups: (a) 100-mg or (b) 200-mg dose of Cu administered as Ca Cu EDTA; (c) 75-mg dose of Cu as disodium Cu EDTA combined with Se, Zn, and Mn; or (d) no treatment (negative control). Each treatment group contained 20 cows. Groups were balanced for age, plasma Cu and pre-treatment liver Cu concentration. Blood samples and liver biopsies were collected prior to treatment. Six liver biopsies were performed on the same cow over a period of 70 days and the concentration of liver Cu was measured over time and compared to pre-treatment baseline. A mixed, multivariable, linear regression model was constructed to determine the effect of treatment on the change in liver Cu concentration compared to pre-treatment concentrations, accounting for repeated measurements taken from each cow.

Results: There was a difference in the distribution of pre-treatment liver Cu concentration between farms (p = 0.008), with medians of 1,400 (IQR 1,200-1,625) and 1,050 (IQR 805-1,425) µmol/kg on Farms 1 and 2, respectively. There was an interaction between treatment group, study day, and farm, with a treatment effect confirmed only on Farm 2. In the final model, the predicted change in liver Cu concentration (compared to pre-treatment concentrations) among cows on Farm 2 that were treated with 200 mg of Ca Cu EDTA was significantly higher than that of control cows on Days 3, 14, 28 and 42, peaking on Day 14 with a difference of 325.35 (95% CI = 97.00-554.03) µmol/kg. The study found no associations between changes in liver Cu concentration and age or prior plasma Cu concentration. The intraclass correlation coefficient was 0.57 (95% CI = 0.45-0.66), indicating the proportion of variability in changes in liver Cu concentration attributable to inter-cow variation.

Conclusions and clinical relevance: This study shows there are differences in response to injectable Cu supplementation at the farm level and wide variation in liver Cu among cows from the same farm. On one farm, a 200-mg dosage of Ca Cu EDTA significantly increased liver Cu concentration for at least 42 days.

Aims: To develop a colourimetric loop-mediated isothermal amplification (LAMP) assay for the detection of Pasteurella multocida in clinical poultry samples and compare the performance of this assay with PCR. A secondary aim was to evaluate a simple DNA extraction method that could enable LAMP-based testing in the field without the need for specialised laboratory equipment.

Methods: Primer sets for both LAMP and PCR were designed to amplify the KMT1 gene of P. multocida. DNA was extracted from 12 P. multocida isolates using a commercial extraction kit, and subjected to analysis using both LAMP and PCR. The analytical specificity of the LAMP assay was evaluated by testing it against a panel of 12 unrelated bacterial species, and the analytical sensitivity (limit of detection) was determined through testing of serial dilutions of the target DNA and compared to that of PCR. Subsequently, cloacal swabs (n = 40) from a commercial turkey flock were subjected to analysis using both LAMP and PCR assays, using a rapid DNA extraction method and a commercial extraction kit. Clinical sensitivity and specificity of the LAMP assay were calculated in comparison to PCR.

Results: A single DNA fragment of the expected size (∼ 200 base pairs), was amplified by PCR from 12 P. multocida isolates, which were also all positive by the LAMP assay. The identity of all PCR amplicons was confirmed by sequencing. Both PCR and LAMP showed similar analytical sensitivity, with a LOD of 20 pg of target DNA. As neither PCR nor LAMP assays produced positive results with 12 non-related bacterial species, the analytical specificity was assessed as 100%. However, LAMP demonstrated lower clinical specificity (94.74%) compared to PCR (100%) when 40 clinical samples were tested. None of the DNA samples extracted using the simplified DNA extraction method were amplified by either LAMP or PCR.

Conclusion: The LAMP assay developed in this study exhibits comparable performance to PCR in detecting P. multocida.

Clinical relevance: The use of a rapid and portable DNA extraction method, in conjunction with LAMP assays, could create opportunities for point-of-care testing for fowl cholera in field settings.

Aims: To investigate the effect of injection of trace mineral supplement (TMS) 14-28 days before calving on white blood cell count (WBCC) and function, serum antioxidant capacity (SAC) and reactive oxygen species (ROS) in pasture-fed cattle after calving.

Methods: On each of two South Island, seasonally calving, pastoral dairy farms,1 month before dry-off, a random sample of 150 multiparous cows predicted to calve within 7 days of the herd's planned start of calving (PSC) were stratified on individual somatic cell count, age, breed and expected calving date. On each farm, 14-24 days before PSC, 60 selected cows were randomly assigned for TMS (Zn, Mn, Se, Cu) injection, and 60 were controls. All 240 cows were contemporaneously injected with hydroxocobalamin, and controls with Se. Blood samples were collected pre-injection and 3, 12 and 40 days after calving. Phagocytic activity, count and proportion of neutrophils, lymphocytes and monocytes, WBCC, ROS, SAC were measured. Plasma concentrations of Se, Cu and glutathione peroxidase (GPx) were monitored from a random subset of animals. Differences attributable to TMS were estimated using mixed-multivariable Bayesian analysis, expressed as mean and highest density interval (HDI).

Results: Three and 40 days after calving, TMS-treated cows had 0.36 (90% HDI = 0.00-0.77) x 10⁹ and 0.25 (90% HDI = 0.00-0.55) x 10⁹ fewer neutrophils/L. Neutrophils comprised 6 (90% HDI = 0-11)% and 4 (90% HDI = 0-8)% less of the WBCC, and the neutrophil count was 14 (90% HDI = 0-27)% and 9 (90% HDI = 0-18)% less than controls. However, 3 days after calving, there were 7 (95% HDI = 2-12)% more cells phagocytosing and 2,900 (95% HDI = 2,600-3,200) more bacteria ingested/cell. Twelve and 40 days after calving, TMS-treated cows had 0.65 (95% HDI = 0.17-1.17) x 10⁹ and 0.28 (95% HDI = 0.00-0.59) x 10⁹ more lymphocytes/L. Lymphocytes comprised 10 (95% HDI = 3-18)% and 5 (95% HDI = 0-9)% more of the WBCC, and the lymphocyte count was 30 (95% HDI = 11-51)% and 9 (95% HDI = 0-9)% more than controls. There were no meaningful differences in ROS, SAC, ROS/SAC, other white blood cells, or WBCC. Plasma Cu, Se and GPx concentrations were above recommended thresholds.

Conclusions: Pre-calving TMS injection was associated with differences in white blood cell population and function that may reduce the risk of disease.

Abbreviations: BHOB: Beta-hydroxybutyrate; GPx: Glutathione peroxidase; HDI: Highest density interval; MESF: Molecules of equivalent soluble fluorophore; OSi: Oxidative stress index; PSC: Planned start of calving; ROPE: Region of probable equivalence; ROS: Reactive oxygen species; SAC: Serum antioxidant capacity; THI: Temperature humidity index; TMS: Trace mineral supplement; WAIC: Widely applicable information criterion; WBCC: White blood cell count.

Aims: To describe rates of and reasons for culling and mortality of ewes between breeding and mid-lactation on New Zealand sheep farms; to investigate associations of these variables with farm demographic variables; and to describe rates of and reasons for culling of ewes at weaning.

Methods: Participants were a convenience sample of 34 farms from across New Zealand. Demographic data were initially collected for each farm via a questionnaire administered in-person to the flock owner or manager. During approximately 8 months from breeding to mid-lactation, ewe tally, culling and mortality data were collected and used to calculate various parameters related to flock performance and to investigate associations. During the main ewe-culling event at weaning, ewe-culling data were collected from 29/34 flocks participating in the study.

Results: There was considerable variation between flocks, but the between-flock mean replacement percentage was 29.2 (SD 5.0)%. Overall, a between-flock mean of 10.5 (SD 4.6)% of ewes presented for breeding were culled or dead/missing by mid-lactation and thus did not rear any lambs. Additionally, from 27 flocks that reported data on ewes' success at rearing lambs, a between-flock mean of 3.9 (SD 2.5)% of ewes that remained alive at mid-lactation failed to rear any lambs, resulting in an overall between-flock mean loss of 23.1 (SD 6.3) potential lambs per 100 ewes. Two-thirds of ewe mortalities between breeding and mid-lactation occurred during the lambing period. Model results showed flocks with higher pregnancy scanning percentages had lower rates of culling and mortality between breeding and mid-lactation. However, apart from farm contour, from breeding to mid-lactation there were no associations for culling and mortality with farm size, flock size, number of ewes per labour unit, whether ewe hoggets (7-9 months of age) were presented for breeding, or duration of the breeding period. A between-flock mean of 16.5 (SD 8.3)% of ewes present at weaning were culled, and among mixed-age ewes, the most common reasons for culling at this time were age, incisor teeth defects and udder defects.

Conclusions: To reduce unnecessary ewe culling and mortality, attention should be focused on maximising conception rates, ensuring judicious culling decisions, optimising body condition score, and identifying farm-specific causes of death over the lambing period to facilitate targeted intervention strategies.

Clinical relevance: Identifying why and when ewes exit flocks, and comparing it with the data presented here, will facilitate the development of flock-specific interventions to reduce ewe culling and mortality.

Aim: To assess whether the fluoride concentration in the humeri of first-lactation, 2-year-old dairy cows with a spontaneous humeral fracture is significantly different from that of first-lactation, 2-year-old dairy cows without a humeral fracture.

Methods: Two studies were conducted, the first with nine bone samples from 2-year-old, first-calving dairy cows with a humeral fracture (all from the Waikato region) age-matched with seven control bone samples from the Waikato, Bay of Plenty and Manawatū-Whanganui regions. The second study used 26 bone samples from 2-year-old, first-lactation dairy cows with a humeral fracture (from the Otago, Canterbury, Southland, West Coast, Waikato and Manawatū-Whanganui regions) age-matched with 14 control bone samples (all from the Manawatū-Whanganui region or unknown). Control bone samples were from first-lactation, 2-year-old dairy cows that did not have humeral fractures. Bone fluoride concentration was quantified for all samples.

Results: The median fluoride concentration of humeri from first-lactation, 2-year-old dairy cows with a humeral fracture was significantly higher than humeri from unaffected control cows in both studies. In Study 1, the median bone fluoride concentration was 599 (IQR 562.7-763.5) mg/kg from case cows and 296.6 (IQR: 191.2-391.7) mg/kg from control cows (p < 0.001), and in Study 2 the median bone fluoride concentration from case and control cows was 415 (IQR: 312.5-515) mg/kg and 290 (IQR: 262.5-410) mg/kg (p = 0.04) respectively.

Conclusions and clinical relevance: Although there are limitations to this study due to the unbalanced regional distribution of cases and controls, the results indicate that sub-clinical fluoride toxicosis may be linked to spontaneous humeral fractures in first-lactation dairy cows in New Zealand. Further research is required to determine if bone fluoride concentrations play a role in the pathogenesis of these fractures.

Aims: To assess the feasibility and safety of a locking cortical pearl plate system for the repair of lumbar vertebral fractures and luxation in cats using an ex vivo feline model.

Methods: This cadaveric study of the lumbar vertebral column (L1-L7) involved 28 Domestic Short-hair cats without vertebral column pathology. Surrounding soft tissue was removed, except for the paravertebral musculature, joint capsules, and ligaments associated with the L1-L7 vertebrae. To determine whether the application of a 2.0-mm, 69-mm-long, 12-hole locking cortical pearl plate (LCPP) and screws was feasible, the dimensions of the feline lumbar vertebral bodies (length, width, and height) were measured using CT imaging. Width and height were evaluated at five locations along the length of the vertebrae with implant corridors (cor 1-cor4) located in between. Following CT, plates were applied to the vertebral columns. After implantation, another CT scan was performed to evaluate plate positions, screw trajectories, screw implantation angles, and vertebral canal breaching. Implantation was classified according to the modified Zdichavsky scoring system for vertebral canal penetration and grade I and IIa defined as acceptable.

Results: A total of 371 screws were inserted into the lumbar vertebral bodies, and breaching occurred in 32 cases (8.6%), of which 29 (90.6%) were at L6 and L7. The median angle of inserted screws was 61.6° (min 53.4°, max 76.3°). Aside from one location, no significant angle deviations were observed between breaching (median 62.8°; min 53.4°, max 76.3°) and non-breaching (median 61.2°; min 53.8°, max 74.7°) screws. All 267 screws implanted in L1-L5 were graded I or IIa (acceptable). In contrast, low rates of acceptable implantation were achieved for L6 (52/60; 86.7%) and L7 (24/44; 54.4%), caused by clustering of breachings in corridor 3 of the two vertebrae.

Conclusions: Application of the LCPP immediately proximal to the transverse processes and ventral to the pedicles with a screw implantation angle of 60° is feasible and appears safe for L1-L5, resulting in a low number of vertebral canal breaches and a high rate of acceptable implantations.

Clinical relevance: The 2.0-mm, 69-mm-long, 12-hole LCPP can be considered an acceptable option for treating feline vertebral fractures and luxations of L1-L5. It cannot be recommended for use in corridor 3 of L6 or L7 due to the high risk of breaching the vertebral canal.

Aims: To investigate the effect of preservation by addition of yoghurt starter, potassium sorbate and citric acid on counts of aerobic bacteria, Lactobacillus spp., Streptococcus thermophilus and coliforms, Brix percentage, pH, protein, fat and anhydrous lactose concentrations at 0, 7 and 14 days after collection for colostrum stored at ambient temperature.

Method: Approximately 2 L of first milking colostrum was collected from 10 farms in the Waikato region. Following mixing, it was split into five 400-mL sub-samples and allocated randomly to a control (two sub-samples), or treatment with yoghurt, potassium sorbate, or citric acid preservative. Throughout the trial samples remained in the laboratory at ambient temperature with the lids slightly ajar, and were stirred daily for 15-30 seconds using a sterile spatula. Sub-samples were tested on Days 0, 7 and 14. On Days 0 and 14 aerobic bacteria (by aerobic plate count (APC)), Lactobacillus spp., coliforms and Streptococcus thermophilus counts, pH, Brix percentage, protein, fat and anhydrous lactose were measured. On Day 7 only bacterial counts were completed.The data were analysed using non-parametric clustered bootstrap sampling to estimate the effect of treatment, time, and their interaction on the outcome variables.

Results: Compared to control samples, on Day 7 the APC for potassium sorbate (1.0 (90% CI = 0.6-1.6) × 10⁸ cfu/mL) was approximately seven-fold lower than for yoghurt (7.3 (90% CI = 4.1-11) × 10⁸ cfu/mL), and approximately three-fold lower than citric acid (3.2 (90% CI = 0.2-4.3) × 10⁸ cfu/mL) remaining low to Day 14. All preservatives reduced coliform growth compared to control samples at Day 7 but growth was lower for potassium sorbate than the other preservatives. For Lactobacillus spp., at Day 7, samples with yoghurt preservative had greater counts than the other two preservatives. Potassium sorbate reduced growth of S. thermophilus compared to the other treatments, especially at Day 7, with 7-10 times fewer S. thermophilus per mL compared to the other three groups. All groups showed an obvious acidification over time, with very little variation within days and treatment groups. There was no evidence for change in fat or protein percentage over time regardless of treatment.

Conclusion and clinical relevance: Aerobic and coliform bacteria proliferate extensively in unpreserved colostrum. All preservatives decreased coliform counts compared to un-preserved colostrum, but potassium sorbate was more effective at decreasing both coliforms and aerobic bacteria than either yoghurt or citric acid.