Accuracy of pregnancy diagnosis and prediction of calving date in red deer using real-time ultrasound scanning

One hundred and sixty-two 18-month-old farmed red deer were used to test the accuracy of pregnancy detection and equations for predicting gestational age. Deer ranging from 30 to 110 days gestation were examined by rectal ultrasonography using a 5 MHz transducer while they were standing. Each scan was recorded on video tape for measurements of uterine diameter, amniotic sac diameters, crown-rump length, head length, head diameter, nose length, chest depth, chest width and placentome base-apex length and width. Fetal age was calculated from the mean of the age predictions derived from each dimension measured on individual deer, for 132 deer between 44 and 110 days gestation. All the hinds diagnosed as pregnant produced offspring, and all the hinds diagnosed as not pregnant failed to produce offspring. Between one and six fetal and uterine dimensions were measurable and the number measurable increased with fetal age. The mean error of calving date prediction in 132 deer was 0.97 days. The error of prediction when measurements were made between 44 and 60 days was 0.44 days, whereas between 61 and 80 days and between 81 and 110 days the errors were +0.95 and +4.72 days, respectively. The estimates of calving date were all within 13 days of the calving date.     

茸鹿人工选育品种品系数量性状遗传参数的统计分析

对我国人工选育的梅花鹿和马鹿 6个品种品系的 2 0多个数量性状的遗传参数 ,进行了统计分析 ,结果表明 ,变异系数除鲜茸重的较高之外 ,其他很小 ;公鹿的留种率很低 ,茸重性状的选择差很大 ;遗传力和重复力均较高 ;世代间隔较短 ;鲜茸重的遗传进展和年改进量较大 ;梅花鹿种公鹿的种用年限较短 ,并明显低于马鹿的 ;梅花鹿品种品系间和马鹿亚种间杂交F1茸重性状和繁殖成活率性状的杂种优势率非常显著 (P <0 0 1 )。此项统计分析为茸鹿的优质高效育种、提高纯繁选育速度、杂种优势利用、杂交培育新品种和育种规化及模式提供了科学依据。     

Mycobacteria isolated from deer in New Zealand from 1970–1983

Mycobacterium bovis was isolated from 504 deer from 1970 to 1983. It was first isolated from feral red deer (Cervus elaphus) in New Zealand in 1970, and from farmed deer in 1978. Cervine tuberculosis has emerged as a significant problem in farmed deer and in 1983 M. bovis was found on 40 different farms. Thirty-five isolates of Mycobacterium avium-intracellulare have been cultured from deer but were associated with clinical disease in only four cases. Mycobacterium nonchromogenicum, Mycobacterium diernhoferi, Mycobacterium gastri, Mycobacterium chelonei, Mycobacterium smegmatis and Mycobacterium vaccae were isolated from deer but were not considered to be pathogenic.     

Pharmacokinetics and lung and muscle concentrations of tulathromycin following subcutaneous administration in white‐tailed deer (Odocoileus virginianus)

Respiratory tract infections are common in farmed North American white‐tailed deer (Odocoileus virginianus). Tulathromycin is approved for use in cattle but not deer but is often employed to treat deer. The pharmacokinetic properties and lung and muscle concentrations of tulathromycin in white‐tailed deer were investigated. Tulathromycin was administered to 10 deer, and then, serum, lung, and muscle tulathromycin concentrations were measured using liquid chromatography–mass spectrometry (LC–MS). The mean maximal serum tulathromycin concentration in deer was 359 ng/mL at 1.3 h postinjection. The mean area under the serum concentration–time curve, apparent volume of distribution, apparent clearance, and half‐life was 4883 ng·h/mL, 208 L/kg, 0.5 L/h/kg, and 281 h (11.7 days), respectively. The maximal tulathromycin concentration in lung and muscle homogenate from a single animal was 4657 ng/g (14 days) and 2264 ng/g (7 days), respectively. The minimum concentrations in lung and muscle were 39.4 ng/g (56 days) and 9.1 ng/g (56 days), respectively. Based on similarity in maximal serum concentrations between deer and cattle and high lung concentrations in deer, we suggest the recommended cattle dosage is effective in deer. Tissue concentrations persisted for 56 days, suggesting a need for longer withdrawal times in deer than cattle. Further tissue distribution and depletion studies are necessary to understand tulathromycin persistence in deer tissue; clinical efficacy studies are needed to confirm the appropriate dosage regimen in deer.     

Liver copper, selenium and vitamin B12 concentrations in farmed and feral red deer (Cervus elaphus)

AIM: To compare liver copper, selenium and vitamin B12 concentrations in red deer of farmed and feral origin. METHODS: Liver samples were collected from red deer at a South Island deer slaughter premise and a game packing house in November 2000. The site of origin and age of each animal were recorded. A subsample of 107 livers was selected (n=5-10 per site of origin and age category) from farmed deer from central Canterbury, Nelson and Westland, and from feral deer from north, central and south Westland. Samples were analysed for copper, selenium and vitamin B12 concentrations and reported on a wet-matter basis. RESULTS: Mean liver copper concentrations for farmed and feral yearlings were 267 and 889 micromol/kg, respectively, and for farmed and feral adults were 206 and 677 micromol/kg, respectively. Liver copper concentrations were lower for farmed than for feral deer (p<0.001) and for feral adults than for feral yearlings (p=0.002). Mean liver selenium concentrations in farmed and feral yearlings were 2050 and 1539 nmol/kg, respectively, and in farmed and feral adults were 1938 and 1625 nmol/kg, respectively. Liver selenium concentrations varied significantly between regions and overall, farmed deer had higher liver selenium concentrations than feral deer (p=0.04). Mean liver vitamin B12 concentrations in farmed and feral yearlings were 456 and 742 nmol/kg, and for farmed and feral adults were 428 and 869 nmol/kg, respectively. Liver vitamin B12 concentrations were lower for farmed than for feral deer (p<0.001). CONCLUSION: Feral deer had higher liver copper and vitamin B12 concentrations and lower liver selenium concentrations than farmed deer in the regions studied.     

Omasal Anatomy in New Zealand Red and Fallow Deer: An Exploratory Multivariate Analysis

We measured the weight and volume of omasae, and the number, weight and area of omasal laminae from wild fallow (Cervus dama), and wild and farmed red deer (Cervus elaphus) whose diet, as indicated by rumen content, was known. A multivariate analysis yielded two principal components, interpreted as indices of overall omasal size and laminar leafiness. The second component showed significantly greater variance in wild red deer than in farmed red or wild fallow deer. Deer feeding on a mixed diet of browse and grasses may have greater variability of omasal form than those feeding on grass alone. A relationship is derived by which the laminar area can be estimated from counts of laminae in different size classes.     

Tuberculosis in deer

Extract

It is an intriguing observation on the history of state veterinary medicine that major disease problems of the past usually generated less public debate than many of the minor problems of today; Mycobacterium bovis infection of cattle and farmed deer in New Zealand illustrates this paradox. It took many years of campaigning by a few dedicated individuals before a bovine tuberculosis eradication scheme was established, yet within a few months of the discovery of the same infection in farmed deer there have been numerous demands for government action.     

Impacts of intensification of pastoral agriculture on soils: Current and emerging challenges and implications for future land uses

Abstract

AIM: To find evidence for localisation in the uterus, and fetal infection, of Leptospira spp. in farmed deer in the lower North Island of New Zealand during and shortly after the breeding season.

METHODS: Between February and July 2008, 116 blood samples, 120 kidneys, 120 uteri and 27 fetuses were collected from 120 mixed-age hinds from lines from nine farms, at a deer slaughter premises. Serum samples were tested for antibodies against Leptospira borgpetersenii serovar Hardjo-bovis and Leptospira interrogans serovar Pomona, using the microscopic agglutination test (MAT). For both serovars, a titre of >1:48 was considered positive. Samples from kidneys, uteri and fetal tissue were subjected to bacterial culture, using Ellinghausen-McCullough-Johnson-Harris (EMJH) medium, and real-time PCR, using DNA gyrase subunit B gene primers.

RESULTS: Thirty-four of 116 (29.3%) serum samples were positive for serovar Hardjo-bovis, and 13 (11.2%) for serovar Pomona. Seven of 120 kidneys were positive for serovar Hardjo-bovis by culture, and five of these, but no others, were positive by real-time PCR. Of 120 uteri, none was culture- or PCR-positive. None of 27 fetal samples was culture-positive but one was positive by real-time PCR. The dam of the PCR-positive fetus was culture-negative from the kidney, but had an MAT titre of 1:192 for Hardjo-bovis.

CONCLUSIONS: Attempts to isolate Leptospira spp. from the genital tracts and early fetuses of farmed deer were unsuccessful. However, molecular evidence suggested fetal infection in one case. This finding justifies further study of the role of leptospires in the genital tract and fetus and its association with reproductive loss in farmed deer.     

Detection of specific antibodies anti-Neospora caninum in the fallow deer (Dama dama)

Sera from 335 farmed fallow deer (Dama dama) at the breeding station in Kosewo Górne in the Mazurian Lake District, North-East Poland, were investigated for the presence of antibodies against Neospora caninum. The distribution of age groups was as follow: >4 years - 154 animals; 2 years - 76 animals; 1 year - 105 animals. Ten sera with the optical density exceeding 0.159 absorbance units (i.e., cut-off value) in ELISA test were also analyzed by Western blot. Western blot analysis revealed seroreactivity against immunodominant N. caninum antigens of 37, 25, and 16kDa; however, in some sera additional bands were also visible. This is the first screening studies for antibodies against N. caninum in farmed fallow deer in Poland, in the region where neosporosis was confirmed in cattle and in farmed and free-ranging European red deer (Cervus elaphus).     

Congenital contraction of the gastrocnemius and superficial digital flexor muscles in a friesian calf

The red deer (Cervus elaphus) is a host for two louse species, Damalinia longicornis and Solenopotes burmeisteri. Little is known of their prevalence or population dynamics; numbers are likely to peak in winter. Numbers may increase secondarily to malnutrition or disease. Lice are unlikely to seriously affect deer health under most conditions. “Pour-on” insecticides have been used for treatment but their efficacy has not been critically assessed. Animals can be sprayed using garden spray equipment, providing that such equipment has not been used for other toxic chemicals such as weed killers. Little is known of the toxicity of insecticides for deer, so they should be used with care and not used on stressed animals. No lice have been recorded from the fallow deer (Dama dama) in New Zealand.

Dictyocaulus viviparus infects red and fallow deer and can cause high mortalities of young farmed red deer in their first autumn and winter. In clinical cases respiratory signs are seldom obvious but loss of condition and dullness of coat may be evident. Clinical evidence and lung lesions suggest that the pathogenesis of disease may differ from that in cattle. Anthelmintics effective against D. viviparus in cattle are not necessarily effective in deer. Little is known of the significance of lungworm to farmed fallow deer. Research on lungworm in deer is urgently needed.     

Evidence of Mycobacterium avium subsp. paratuberculosis infection in Dutch farmed red deer

Paratuberculosis is a chronic disease in ruminants caused by Mycobacterium avium subsp. paratuberculosis (MAP). Most economic losses due to MAP occur in the dairy industry. However, the infection is not restricted to cattle, but also occurs in other ruminants, such as sheep, goat, and deer. Although deer are of minimal economic importance in The Netherlands, they may constitute a source of infection for the dairy industry. This pilot study was conducted to estimate the prevalence of Johne's disease in farmed red deer in The Netherlands. Serum and faecal samples were collected from 140 animals, originating from 8 different farms. Four of the farms had animals that tested positive for Johne's disease. The within-herd MAP seroprevalence varied between 4.8% and 21.2%. In conclusion, this pilot study provides evidence of MAP infection in the Dutch farmed deer population, and thus there might be a risk of MAP transmission between farmed red deer and dairy cattle.     

White‐Tailed Deer (Odocoileus virginianus) as a Potential Sentinel for Human Lyme Disease in Indiana

We assessed the potential of white‐tailed deer (WTD) (Odocoileus virginianus) to be a sentinel for human cases of Lyme disease (LD) in Indiana using location data from a 3‐year survey of approximately 3400 hunted deer with associated tick Ixodes scapularis and Borrelia burgdorferi (Bb) data. Data on human LD cases at the county level were obtained from the Indiana Department of Health. All data were assigned to county centroids to match the resolution of the LD data before creating optimized trend surfaces for LD incidence, hunted deer count, Ixodes scapularis and Bb prevalence. To determine whether LD was spatially associated with the areas of high densities of deer, deer with Ixodes scapularis and deer with ticks infected with Bb, we used spatial analysis with distance indices (SADIE). The SADIE analysis found significant spatial association between LD and the distribution of three organismal predictor variables, that is, WTD, Ixodes ticks and Bb. Lyme disease incident rate varied between 0.08 cases per 10 000 habitants (Johnson county) and 5.9 cases per 10 000 habitants (Warren county). In conclusion, WTD can be used as an accurate and cost‐effective sentinel for human LD. This method will permit public health workers to identify potentially endemic areas independently of human case reports.     

Evaluation of the efficacy of commercial vaccines against bluetongue virus serotypes 1 and 8 in experimentally infected red deer (Cervus elaphus)

Red deer (Cervus elaphus) is a widespread and abundant species susceptible to bluetongue virus (BTV) infection. Inclusion of red deer vaccination among BTV control measures should be considered. Four out of twelve BTV antibody negative deer were vaccinated against serotype 1 (BTV-1), and four against serotype 8 (BTV-8). The remaining four deer acted as unvaccinated controls. Forty-two days after vaccination (dpv), all deer were inoculated with a low cell passage of the corresponding BTV strains. Serological and virological responses were analyzed from vaccination until 28 days after inoculation (dpi). The vaccinated deer reached statistically significant (P<0.05) higher specific antibody levels than the non vaccinated deer from 34 (BTV-8) and 42 (BTV-1) dpv, maintaining stable neutralizing antibodies until 28 dpi. The non vaccinated deer remained seronegative until challenge, showing neutralizing antibodies from 7 dpi. BTV RNA was detected in the blood of the non vaccinated deer from 2 to 28 dpi, whereas no BTV RNA was found in the vaccinated deer. BTV was isolated from the blood of non vaccinated deer from 7 to 28 dpi (BTV-1) and from 9 to 11 dpi (BTV-8). BTV RNA could be identified by RT-PCR at 28 dpi in spleen and lymph nodes, but BTV could not be isolated from these samples. BT-compatible clinical signs were inapparent and no gross lesions were found at necropsy. The results obtained in the present study confirm that monovalent BTV-1 and BTV-8 vaccines are safe and effective to prevent BTV infection in red deer. This finding indicates that vaccination programs on farmed or translocated red deer could be a useful tool to control BTV.     

Use of a polymerase chain reaction to subtype Mycobacterium avium subspecies paratuberculosis, an increasingly important pathogen from farmed deer in New Zealand

AIMS: To review the number of microbiologically-confirmed cases of Johne's disease in farmed deer since 2000, and determine the prevalence of the bovine and ovine subtypes of Mycobacterium avium subsp paratuberculosis (M. paratuberculosis), using a highly specific polymerase chain reaction (PCR) test on samples from infected herds. METHODS: The number of cases of M. paratuberculosis in farmed deer identified by culture or IS900 PCR was documented. A highly specific PCR test was applied to subtype M. paratuberculosis from BACTEC 12B cultures selected on the basis of one culture per deer herd, to give a wide coverage of herds in New Zealand. RESULTS: From January 2001 to October 2005, M. paratuberculosis was isolated from 1,141 farmed deer, and has now been identified by microbiological testing in over 600 deer herds in New Zealand. The bovine subtype of M. paratuberculosis was shown by a highly specific PCR test to be present in 91/95 herds examined; the ovine subtype was found in the remaining four herds. CONCLUSIONS: Since 2000, there has been a substantial increase in both the number of microbiologically-confirmed cases of Johne's disease in farmed deer and the number of infected herds. Johne's disease is now widespread and common in deer herds throughout New Zealand. Whilst the bovine subtype of M. paratuberculosis predominates in deer herds in New Zealand in which Johne's disease has been confirmed, the occasional finding of the ovine subtype highlights the need to consider both sheep and cattle as potential sources of infection for farmed deer.     

Seroprevalence and Risk Factors for Leptospira Seropositivity in Beef Cattle,Sheep and Deer Farmers in New Zealand

Leptospirosis is a global zoonosis that in New Zealand affects primarily people occupationally exposed to livestock. The objective of this study was to estimate the seroprevalence of five Leptospira serovars in farmers working on cattle, sheep and deer farms that had the serological status of animals previously assessed and to identify risk factors for farmer seropositivity. A total of 178 farmers from 127 properties participated in the study. Blood samples were tested using the microscopic agglutination test (MAT) for the presence of antibodies to Leptospira. Samples with a MAT titre ≥48 were considered seropositive. Using Bayesian statistical analysis, the median seroprevalence of Leptospira, all serovars combined, was estimated to be 6.6% (95% probability interval (PI) 3.6–10.9%). Risk factors associated with seropositivity were assisting deer or cattle calving, farming deer, having ≥25% of flat terrain and high abundance of wild deer on farm, while high possum abundance on farm was negatively associated with seropositivity. No association was observed between farmer serostatus and previously recorded livestock serology. Leptospira seropositivity was associated with influenza‐like illness of farmers (RR = 1.7; 95% PI 1.0–2.5). Assuming a causal relationship, this suggested an annual risk of 1.3% (95% PI 0.0–3.0%) of influenza‐like illnesses due to Leptospira infection in the population of farmers. The association between seropositivity and disease can be used to estimate the public health burden of leptospirosis in New Zealand. Identifying and understanding risk factors for Leptospira seropositivity can inform preventive measures, hence contributing to the reduction of leptospirosis incidence in farmers.     

马鹿特异性SNP分子标记的验证

试验旨在对基于基因分型测序（genotyping by sequencing,GBS）技术筛选出的马鹿特异性SNPs位点的准确性进行验证,为梅花鹿、马鹿及其杂交后代的鉴别提供可靠的分子遗传标记。随机选取30个马鹿特异性SNPs位点,根据SNPs位点前后各200 bp的序列,利用Primer Premier 6.0软件设计特异性引物,以随机选取的验证样本DNA作为模板进行PCR扩增,并进行Sanger测序,对测序结果利用BioEdit软件进行峰图的观察,利用Mega 6.0软件对测序得到的序列进行比对分析并观察每个特异性SNP位点在不同验证群体中的基因型,对每一个马鹿特异性位点的峰图和比对信息进行统计分析。结果表明,30个马鹿特异性位点中有28个和前期研究结果一致,其中1个SNP位点（SNP3）中G等位基因在梅花鹿中的基因频率为0.05,而G等位基因在马鹿中的基因频率为1,G等位基因在马鹿个体中的基因频率比在梅花鹿个体中高,同时,利用SPSS 22.0进行统计分析发现,该位点在马鹿和梅花鹿中基因型分布表现出显著性差异（P<0.05）;另外1个SNP位点（SNP5）中T等位基因在梅花鹿的基因频率为0.15,而在马鹿中的基因频率为1,且这个SNP位点在梅花鹿和马鹿中基因型分布差异显著（P<0.05）,所以这2个位点仍然可以作为马鹿的特异性SNPs位点。研究结果说明了GBS测序筛选出的马鹿特异性SNPs可以作为鉴定的分子标记,对梅花鹿、马鹿及其杂交后代的鉴别奠定了理论基础。     

Lack of effects of an equine chorionic gonadotropin (eCG) administration between days 9 and 15 postpartum on reproductive performance in a Holstein dairy herd

Recently, it has been demonstrated that administration of equine chorionic gonadotropin (eCG) in the postpartum period in dairy cows can enhance follicle growth, reduce the interval from calving to first ovulation and increase plasma estradiol concentrations, and, thus, could enhance reproductive performance in a dairy herd when administered on day 6 postpartum. The aim of this study was to investigate the effects of a single dose of eCG between days 9 and 15 postpartum on parameters of reproductive performance in dairy cows. German Holstein cows (n = 1937; primiparous cows: n = 748; pluriparous cows: n = 1189) in a commercial dairy farm were randomly assigned to three experimental groups. Animals within the group eCG received a single dose of 600 IU eCG intramuscularly (i.m.) between days 9 and 15 postpartum followed by an i.m. administration of 500 μg cloprostenol after 14 days. Those of treatment group PG received cloprostenol only between days 23 and 29 postpartum. Cows of the control group remained untreated. Starting on day 49 postpartum, cows were subjected to a Presynch‐Ovsynch protocol and inseminated artificially. The impact of application time (days postpartum) of eCG on the intervals calving to first service and calving to conception was statistically not significant. Outcomes of reproductive performance (i.e. first service conception rate, proportion of pregnant cows until 100 and 150 days in milk [DIM], number of inseminations until 150 DIM, calving to first service interval and calving to conception interval) did not differ significantly between treatment group eCG and group PG compared to control group. Regarding postpartum eCG administration, significant interactions between treatment and parity, season, milk yield, and early puerperal disorders, respectively, could not be shown. In conclusion, an eCG treatment of dairy cows between days 9 and 15 postpartum to increase reproductive performance cannot be recommended under the given circumstances.     

Chemical composition, palatability and physical characteristics of venison from farmed deer

The quality of venison from farmed deer were evaluated based on chemical composition, palatability scores, W-B shear force, ultimate pH, and color. The samples of venison were derived from javan rusa ( Cervus timorensis russa ), moluccan rusa ( Cervus timorensis moluccensis ), sambar ( Cervus unicolor brookei ), fallow ( Dama dama ) and imported red deer ( Cervus elaphus ). Moluccan rusa and red deer were fed grass. Javan rusa, sambar and fallow deer were fed concentrate. The venison obtained from grazing deer (grass-fed) gave higher moisture content (75.3%) than concentrate-fed or confinement-raised deer (74.4%) and imported venison (70.62%). Fat content in venison shows some differences between muscles and species. The concentrate-fed animals had a higher ( P  < 0.05) fat content in the venison than the grazing deer. Temperate deer (fallow and red deer) showed higher ( P  < 0.05) fat content than tropical deer (rusa and sambar deer). Venison obtained from concentrate-fed deer showed normal ultimate pH values (pH ≤ 6.0) and more reddish in color than grass-fed deer. The concentrate-fed venison produced slightly higher ( P  > 0.05) palatability scores than grass-fed venison. Feeding regimens (grass-fed vs. concentrate-fed) significantly ( P  < 0.05) influenced fat composition in the venison of farmed deer in this study.     

Seroprevalence of Toxoplasma gondii in wild boar and deer in Brandenburg,Germany

Consumption of game in Germany has increased during the past 10 years. Wild boar (Sus scrofa), roe deer (Capreolus capreolus) and red deer (Cervus elaphus) are the most frequently hunted and consumed game animals in Germany, yet information on the occurrence of zoonotic pathogens in these animal species is scarce. To better estimate the public health risk emanating from handling and consumption of game, this study investigated seroprevalences of Toxoplasma gondii in game hunted in the German federal state of Brandenburg during two hunting seasons from 2017 to 2019. Toxoplasma gondii‐specific antibodies were detected in 24.4% (44/180, 95% CI: 18.4%–31.4%) of wild boar, 12.8% (16/125, 95% CI: 7.5%–20%) of roe deer and 6.4% (3/47, 95% CI: 1.3%–17.5%) of red deer using a commercial ELISA kit. Seroprevalences were similar in the two hunting seasons. Correlation between sex and seropositivity could not be observed. A rise in seroprevalence was seen with increasing age in all studied game species. Observed seroprevalences suggest that T. gondii is endemic in the sylvatic environment in the German federal state of Brandenburg and imply that game could represent a relevant source for human T. gondii infection.     

Observations on the eruption of the permanent incisor teeth of farmed Javan rusa deer (Cervus timorensis russa) in New Caledonia

The eruption of the permanent incisor teeth of 14 farmed Javan rusa deer (Cervus timorensis russa) of known birth date and their live weights were observed about every 2 weeks from 12 to 30 months of age. The permanent incisor pattern was 11, 14-17 months; 12, 18-23 months; 13, 20-26 months; and 14, 22-27 months. There was no significant relationship between body weight and timing of permanent incisor eruption.