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PubMed1999

Management of indigenous North American deer at the end of the 20th century in relation to large predators and primary production.

Five deer species occupy North America: caribou (3.6 x 10(6) individuals), moose (1.1 x 10(6)), white-tailed deer (28.5 x 10(6)), mule deer (5.0 x 10(6)) and wapiti (1.1 x 10(6)). Caribou characterise the north of the boreal forest and the tundra, whereas moose dominate in coniferous and mixed forests growing further south. White-tailed deer are typical of the deciduous forests of the east while mule deer replace them in the mountainous terrain of the west. Wapiti possess the smallest range, mostly adjacent to the prairies to the west. The two large obligate carnivores preying on deer show a reduced distribution: wolves are almost restricted to Canada, and cougar to the mule deer range. We determined the current status of each species with the help of a questionnaire mailed to all jurisdictions harbouring deer. Most reports of threatened populations concerned caribou whereas many jurisdictions declared overabundance of white-tailed deer and wapiti. Hunting was allowed for all species when they abounded in a jurisdiction. Hunters harvested annually 7.0 x 10(6) deer on the continent, 87% being white-tailed deer. The two species that caused most conflicts with humans had the highest harvest rate: 16-17%. In terms of biomass, white-tailed deer and wapiti yielded the highest harvests, with 55 and 39 kg x km-2 of range, respectively. The average standing biomass of deer in winter ranged between 28 kg x km-2 in Nevada to 901 kg x km-2 in Indiana. The lowest standing biomasses occurred in the boreal forest (predators), in the prairies (agriculture) and in the south-west (aridity), and the highest ones in the south-east, where only white-tailed deer is present. The current abundance of deer in North America parallels, in general, the primary production of the landscape (r2 = 0.38; P < 0.0001), but predators and human activity modify this pattern.

Animals↗
PubMed2000

Bovine virus diarrhea virus in free-living deer from Denmark.

Free-living deer are suggested as a possible source of infection of cattle with bovine virus diarrhea (BVD) virus. To examine this hypothesis blood samples from 476 free-living deer were collected during two different periods and tested for BVD virus and antibody in Denmark. In 1995-96, 207 animals were tested. These included 149 roe deer (Capreolus capreolus), 29 fallow deer (Dama dama), 20 red deer (Cervus elaphus) and one sika deer (Cervus sika). For the remaining eight animals no species information was available. In 1998-99, 269 animals were tested including 212 roe deer and 57 red deer. The animals were selected from areas with a relatively high prevalence of cattle herds with a BVD persistent infection status in 1997 and 1998. All 207 samples from 1995-96 were found antibody-negative except two samples from red deer. Only 158 of the 207 samples were tested for virus and were all found negative. Of the 269 samples from 1998-99 all but one were antibody negative. The positive sample was from a red deer. All samples were virus-negative. It appears that BVD infection does not occur in roe deer in Denmark. The presence of antibody in a few red deer from various districts in Jutland probably results from cattle to deer transmission, rather than spread among deer. Hence, the possibility of free-living deer as a source of infection for cattle in Denmark seems to be remote.

Animals↗
PubMed2005

Primary and secondary infection with Ehrlichia chaffeensis in white-tailed deer (Odocoileus virginianus).

White-tailed deer (Odocoileus virginianus) are the principal reservoir host for Ehrlichia chaffeensis, causative agent of human monocytic ehrlichiosis (HME). Because white-tailed deer maintain a long-term infection with E. chaffeensis and because deer can be naturally exposed to multiple strains of E. chaffeensis, we evaluated the response to secondary infection of E. chaffeensis in deer. For primary infection, six white-tailed deer were injected with 5.4 x 10(6) DH82 cells infected with the Arkansas strain of E. chaffeensis (Ark) and two control deer were injected with noninfected DH82 cells. On post-infection day 54, three E. chaffeensis (Ark) infected deer and one naive deer were injected with 4.2 x 10(6) cells infected with strain WTD-6045B E. chaffeensis, which differs from the Arkansas strain by number of nucleotide repeats in the variable length PCR target (VLPT) gene; three other Arkansas strain infected deer were injected with noninfected DH82 cells. All animals were monitored for 31 additional days. All deer in the primary infection became positive by PCR amplification of the 16S rRNA or VLPT genes and/or cell culture by DPI-8. PCR amplification of the VLPT gene on whole blood, cell culture, and tissues detected primary and/or secondary strains in all deer exposed to both primary and secondary strains; in one deer, the primary strain was cultured from the lymph node. Our culture results demonstrated that both strains were present; however, PCR detection suggests that the secondary strain may have been circulating in blood at higher levels. In conclusion, this study provides evidence that primary infection of deer with E. chaffeensis does not protect against subsequent exposure and confirms that deer can be simultaneously coinfected with at least two different strains of E. chaffeensis.

Animals↗
PubMed1997

Host defense responses associated with experimental hemorrhagic disease in white-tailed deer.

Our objectives were to examine the immunity conferred by epizootic hemorrhagic disease virus serotype 2 (EHDV-2) infection in white-tailed deer (Odocoileus virginianus) and determine if this immunity was protective during challenge with homologous (EHDV-2) or heterologous (bluetongue virus serotype 10; BTV-10) virus. Trials were conducted in the fall of 1992 and 1993. In the first experiment, naive white-tailed deer were infected intradermally and subcutaneously with EHDV-2 and monitored via physical examinations, complete blood counts, alpha and beta interferon (IFN) assays, viral isolation, and serology. Infected deer had a wide range of clinical signs in response to infection. Eleven of the 16 deer had body temperature elevations > or = 0.5 C between post-infection day (PID) 4 and 8. Infected deer had decreased lymphocyte counts between PID 6 and 10 that returned to normal levels by PID 17. Severely lymphopenic animals had the most severe clinical signs; five of 10 deer with lymphocyte counts less than 1000 cells/microliters succumbed to the infection. Viremia was detected in all 16 EHDV-2 infected animals by PID 4, and peak viremias occurred between PID 4 and PID 10. Three deer remained viremic until PID 56, the study endpoint. Interferon was first detected between PID 2 and 6. Peak alpha and beta IFN levels coincided with peak viremia in 11 deer. Precipitating and neutralizing antibodies were detected in infected deer by PID 10. In the second experiment, convalescent deer were challenged subcutaneously and intradermally with either EHDV-2 or BTV-10 and similarly monitored. Virus was detected in the blood of all four deer challenged with BTV-10, but viremia was not detected in three EHDV-2-challenged deer. Temperature fluctuations, blood cell parameter changes, and IFN and antibody responses seen in BTV-10-challenged deer were similar to those seen in the initial experiment. Deer challenged with EHDV-2 had mildly increased temperatures, but minimal IFN response and lymphocyte alterations.

Acute Disease↗
PubMed1985

Epizootiology of Sarcocystis infections in mule deer fawns in Oregon.

From 1974 to 1977, 62 wild mule deer (Odocoileus hemionus) fawns from Steens Mountain, Ore were euthanatized in autumn (23 deer), winter (21 deer), and spring (18 deer). The number of sarcocysts of Sarcocystis spp was counted in histologic sections of various muscular organs. Sarcocysts were seen in the muscle specimens of 14 of the 23 deer euthanatized in autumn (September to November) and in specimens from all 39 deer euthanatized in winter (December and January) and spring (March and April). The sarcocyst burden was greatest in the spring (736/deer), less in the winter (150/deer), and least in autumn (12/deer). Most sarcocysts collected from 3- to 5-month-old deer in autumn were immature, whereas most sarcocysts collected from 9- and 10-month-old deer in the spring were mature. More sarcocysts were seen in sections of muscles from limbs than in those of tongue, esophagus, and other skeletal muscles; the fewest sarcocysts were seen in the heart. Degenerating sarcocysts were seen in deer examined in the spring, but not in deer examined in autumn and winter. Sarcocystis was the only infectious agent found in unthrifty deer fawns. Of the 18 fawns (6 in autumn, 1974; 6 in winter, 1974; and 6 in spring, 1975) examined for helminths, only mild infections were seen in the deer examined in the spring of 1975. From 1974 to 1977, from the Crooked Creek area of Oregon, 48 mule deer fawns (12 in autumn, 18 in winter, and 18 in spring) were euthanatized and evaluated for Sarcocystis infections.(ABSTRACT TRUNCATED AT 250 WORDS)

Age Factors↗
PubMed2002

Novel forages for growth and health in farmed deer.

AIMS: This paper reviews recent research on the use of new forages in deer farming that may be useful for increasing growth in weaner deer for venison production, increasing the trace element status of deer, and for developing systems less reliant on chemical inputs, notably of anthelmintics used to control internal parasites. GROWTH: Grazing on pure swards of red clover (Trifolium pratense) or chicory (Chicorium intybus) increased weaner growth during autumn by 26-47% and during spring by 10-14%, relative to red deer (Cervus elaphus) grazed on perennial ryegrass (Lolium perenne) /white clover (Trifolium repens) pasture (0.8/0.2). Pre-weaning growth during lactation was increased by approximately 20%. These increases were due to increased rate of degradation of feed particles in the rumen, leading to higher digestibility and higher voluntary feed intakes (VFI). Red clover and chicory produce a greater proportion of their total dry matter (DM) during late summer and autumn than perennial ryegrass/white clover pastures, and are therefore better aligned with the seasonal feed requirements of deer. Grazing on the legume, sulla (Hedysarum coronarium), in autumn and spring increased the growth of weaner deer by 33% and 10%, respectively, relative to pasture-fed animals. PARASITES: Plants containing substantial concentrations of secondary compounds such as condensed tannins (CT) show promise for reducing problems caused by internal parasites. CT present in some legumes and the presence of low concentrations of both CT and sesquiterpene lactones in chicory are reviewed. Feeding sulla containing 35g CT /kg DM reduced abomasal nematode establishment and tended to reduce lungworm (Dictyocaulis eckerti) larval counts in faeces. Relative to weaner deer grazing pasture, weaner deer grazing chicory during autumn required fewer anthelmintic treatments without depressing growth rates. CT extracted from a range of legumes, and CT and sesquiterpene lactones extracted from chicory reduced the in vitro motility of both lungworm and gastrointestinal nematode larvae. The beneficial effects of CT-containing forages on the ability of young deer to manage internal parasite infections could be due to: indirect effects of CT resulting in increased amino-acid absorption, better meeting demands of the immune system; direct inhibitory effects of CT on parasite larvae and; taller plant morphology, reducing the ingestion of infective larvae. The effects of CT depend upon both their structure and CT Condensed tannins DM Dry matter L1 First-stage larvae L3 Infective third-stage larvae LWG Liveweight gain ME Metabolisable energy OM Organic matter OMD Organic matter digestibility VFIVoluntary food intake concentration in the plant, which vary between growing conditions, plant varieties and species. TRACE ELEMENTS: Chicory contained higher concentrations of copper and cobalt than perennial ryegrass/white clover pasture grown on the same farm, and deer grazing chicory had higher liver concentrations of both copper and vitamin B12. These forages may contribute to maintaining adequate trace element status in deer. CONCLUSIONS: Grazing systems that include legumes and herbs such as sulla, red clover and chicory can be used to substantially increase the growth of weaner deer for venison production whilst maintaining deer health and reducing requirements for chemical inputs. For maximum plant persistence and animal responses, these plants should be grown and managed as special-purpose forages and not used in seed mixtures with perennial grasses.

Journal Article↗
PubMed1999

Novel Ehrlichia organism (Rickettsiales: Ehrlichieae) in white-tailed deer associated with lone star tick (Acari: Ixodidae) parasitism.

Polymerase chain reaction (PCR) evidence of a novel Ehrlichia organism was found recently in wild white-tailed deer, Odocoileus virginianus Zimmermann, and lone star ticks, Amblyomma americanum L., from the southeastern United States. To evaluate whether lone star tick parasitism was associated with the presence of this novel Ehrlichia organism in deer, 2 retrospective studies were conducted using specific nested PCR to test archived deer serum samples. The 1st study of 150 serum samples collected from a single deer population over a 15-yr period examined the temporal association between the presence of the Ehrlichia organism in deer and parasitism by lone star ticks. The deer Ehrlichia was not detected in serum samples collected before 1986, when lone star ticks were absent or rare, but was detected in samples collected in 1986 and every year thereafter, when lone star ticks became increasingly abundant. In the 2nd study, serum samples from 120 deer from 24 sites in 14 southeastern states were tested to evaluate if a site-specific, spatial association existed between the presence of the deer Ehrlichia and lone star ticks. All 60 serum samples from the 12 deer populations without evidence of lone star tick infestation were negative for the deer Ehrlichia, whereas 83% of the 12 populations infested by lone star ticks had PCR evidence of infection. These data suggest that lone star ticks may be a vector of the deer Ehrlichia; however, they do not preclude the involvement of other arthropods in maintaining infection with this organism in deer populations.

Animals↗
PubMed1998

Serologic evidence of a natural infection of white-tailed deer with the agent of human granulocytic ehrlichiosis in Wisconsin and Maryland.

White-tailed deer participate in the maintenance of the Ixodes tick life cycle and are reservoirs for some tick-borne infectious agents. Deer may be useful sentinels for tick-transmitted agents, such as ehrlichiae. In order to determine whether white-tailed deer are markers of natural transmission or are reservoirs for the human granulocytic ehrlichiosis (HGE) agent, we performed indirect immunofluorescent-antibody (IFA) tests and immunoblotting with the HGE agent and Ehrlichia chaffeensis on sera from 43 and 294 deer captured in northwest Wisconsin during 1994 and 1995, respectively, and 12 deer from southern Maryland. According to IFA testing, 47% of 1994 Wisconsin sera, 60% of 1995 Wisconsin sera, and 25% of Maryland sera contained HGE agent antibodies. All IFA-positive deer sera tested reacted with the 44-kDa band which is unique to the Ehrlichia phagocytophila group. Serologic reactions to E. chaffeensis were detected by IFA testing in 15 of 337 (4%) Wisconsin deer and in 10 of 12 (83%) Maryland deer, while 60 and 80% of E. chaffeensis IFA-positive Wisconsin and Maryland deer sera, respectively, reacted with the E. chaffeensis 28- to 29-kDa antigens by immunoblotting. A total of 4% of deer from Wisconsin and 25% of deer from Maryland were found by IFA testing to have antibodies to both the HGE agent and E. chaffeensis; 75% of these were confirmed to contain E. chaffeensis antibodies by immunoblotting. These results suggest that white-tailed deer in diverse geographical regions of the United States are naturally infected with the HGE agent, E. chaffeensis, or both and that these animals, and potentially humans, are exposed to infected ticks at a high frequency in nature.

Animals↗
PubMed1997

Isolation of Ehrlichia chaffeensis from wild white-tailed deer (Odocoileus virginianus) confirms their role as natural reservoir hosts.

Field and experimental studies have implicated white-tailed deer (Odocoileus virginianus) as probable reservoir hosts for Ehrlichia chaffeensis, the causative agent of human monocytic ehrlichiosis, but natural infection in deer has not been confirmed through isolation of E. chaffeensis. Thirty-five white-tailed deer collected from three Amblyomma americanum-infested populations in Georgia were examined for evidence of E. chaffeensis infection by serologic, molecular, cell culture, and xenodiagnostic methods. Twenty-seven deer (77%) had E. chaffeensis-reactive indirect fluorescent-antibody assay titers of > or = 1:64; and the blood, spleens, or lymph nodes of seven (20%) deer were positive in a nested PCR assay with E. chaffeensis-specific primers. E. chaffeensis was isolated in DH82 cell cultures from the blood of five (14%) deer, including two deer that were PCR negative. Combination of culture and PCR results indicated that six (17%) deer were probably rickettsemic and that nine (26%) were probably infected. Restriction digestion of PCR products amplified from deer tissues and cell culture isolates resulted in a banding pattern consistent with the E. chaffeensis 16S rRNA gene sequence. The sequences of all PCR products from deer tissues or cell culture isolates were identical to the sequence of the Arkansas type strain of E. chaffeensis. Xenodiagnosis with C3H mice inoculated intraperitoneally with deer blood, spleen, or lymph node suspensions was unsuccessful. When viewed in the context of previous studies, these findings provide strong evidence that E. chaffeensis is maintained in nature primarily by a tick vector-vertebrate reservoir system consisting of lone star ticks and white-tailed deer.

Animals↗
PubMed1986

Prevalence of herpesvirus infection in British red deer and investigations of further disease outbreaks.

A serological survey of the prevalence of a new herpesvirus isolated from red deer (Cervus elaphus), tentatively designated herpesvirus of Cervidae type 1 (HVC-1), has shown that the virus is widespread in free-living and farmed red deer. Neutralising antibodies were detected in hill deer culled at three different locations in the north of Scotland, in farmed deer on five of eight Scottish farms and in four of 12 groups of English farmed or park deer. Fifty-eight of 145 (40 per cent) hill deer, 67 of 203 (33 per cent) Scottish farmed deer and 26 of 172 (14 per cent) English deer had antibody, the overall prevalence being 29 per cent. Further outbreaks of ocular disease in farmed red deer calves caused by HVC-1 were investigated. Deer sent to an auction from one farm were found after sale to have been incubating the disease and it was thus spread to seven deer farms. Despite a high incidence of clinical disease in the calves from the original farm, few in-contact deer showed clinical signs.

Animals↗
PubMed1993

Prevalence of Leptospira antibodies in white-tailed deer, Cades Cove, Great Smoky Mountains National Park, Tennessee, USA.

We conducted a study of the population dynamics, movement, and diseases of white-tailed deer (Odocoileus virginianus) in Cades Cove, Great Smoky Mountains National Park, Tennessee (USA) from 1980 to 1984. During the study 590 blood samples were collected from 518 deer, with some deer recaptured one or two times. The estimated percent of the herd sampled each year ranged from 8% to 28%. We also collected serum samples from 56 cattle pastured in Cades Cove. Deer and cattle sera were tested using the microagglutination test for the presence of antibody to the following serovars of Leptospira: pomona, hardjo, grippotyphosa, icterohemorrhagiae, and canicola. One hundred and six deer (21%) were seropositive for only one of the serovars. We found that 57 (11%) of the deer had antibodies to serovar hardjo, 33 (6%) were positive for antibodies to serovar pomona, 15 (3%) were positive for antibodies to serovar icterohemorrhagiae, and one deer had antibodies to serovar canicola. Age class and sex of deer were associated with antibody presence. Adult (> or = 1.5 yr) male deer were more likely to have antibodies than the other age class and sex groups (P = 0.001). In recaptured deer, similar titers were found in samples from one deer taken 807 days apart. Titer declined below the screening dilution level (1:250) after 37 days in one deer.

Age Factors↗
PubMed1998

Genetic analysis of farmed deer hybrids.

Molecular methods which identify species-specific genetic markers are valuable for identification and genetic analysis of hybrid deer. We have used a variety of molecular techniques to compare Père David's deer Elaphurus davidianus, red deer Cervus elaphus scotticus and North American wapiti C. e. manatobensis. In total, these analyses have identifed over 300 markers in which Père David's deer sires are distinct from farmed red deer and over 100 markers in which wapiti sires differ from red deer. Subsets of these markers have been used to identify hybrids on farms, and to estimate the proportion of red deer and wapiti in hybrid animals. Analysis of the segregation of the species-specific alleles in 352 backcross 1/4 Père David's, 3/4 red deer hybrids has produced a deer genetic linkage map which describes the chromosomal grouping and order of the markers. Correlation of the variability in phenotypic traits with marker segregation in the back-cross hybrids has located genes which influence variation in gestation length, pedicle-initiation, birth weight, growth rate and a variety of morphological traits in Père David's deer x red deer hybrids. Such genetic analyses can now be extended, using new marker technologies, to more closely related taxa, such as farmed red deer and wapiti hybrids, and potentially analyse natural hybrid zones.

Animal Husbandry↗
PubMed2005

Deer ked-induced occupational allergic rhinoconjunctivitis.

BACKGROUND: Deer keds (elk fly) have not previously been described as a cause of respiratory or conjunctival sensitization. OBJECTIVE: To report a case of IgE-mediated allergic rhinoconjunctivitis from occupational exposure to deer ked. METHODS: Skin prick testing (SPT) was performed with pollens, animal danders, mites, molds, and deer ked. The serum deer ked-specific IgE level was examined in ImmunoSpot and radioallergosorbent test assays, and deer ked IgE-binding fractions and their specificities were examined in immunoblot and immunoblot inhibition assays. Nasal provocation testing (NPT) and conjunctival provocation testing (CPT) were performed to detect the association between deer ked sensitization and rhinoconjunctival symptoms. Both SPT and NPT were performed with deer ked whole-body extract, whereas CPT was performed with deer ked wing. RESULTS: The results of SPT, NPT, and CPT were positive for deer ked. In laboratory tests, serum deer ked-specific IgE antibodies were demonstrated in radioallergosorbent test and ImmunoSpot assays. In immunoblot, IgE-binding bands were demonstrated at 17, 33, 70, and 85 kDa, which were clearly inhibited with deer ked extract but not with the control extract. CONCLUSIONS: Occupational IgE-mediated rhinoconjunctival allergy to deer ked was confirmed in this patient.

Adult↗
PubMed2006

White-tailed deer (Odocoileus virginianus) develop spirochetemia following experimental infection with Borrelia lonestari.

Borrelia lonestari is considered a putative agent of southern tick-associated rash illness (STARI) and is known to occur naturally only in lone star ticks (Amblyomma americanum) and white-tailed deer (Odocoileus virginianus). We used a low passage isolate of B. lonestari (LS-1) to inoculate white-tailed deer, C3H mice, Holstein cattle, and beagles. Animals were monitored via examination of Giemsa and acridine orange stained blood smears, polymerase chain reaction (PCR), indirect fluorescent antibody (IFA) test, and/or culture isolation. Spirochetes were visualized in blood smears of both deer on days post-inoculation (DPI) 6, 8, 12 and one deer on DPI 15. Whole blood collected from deer tested PCR positive starting on DPI 4 and remained positive as long as DPI 28. Both deer developed antibody titers of >64, with a maximum IFA titer of 1024. The organism was reisolated from the blood of both deer on DPI 6 and one deer on DPI 12. All isolation attempts from mice, calves, or dogs were negative, although one of seven mice was transiently PCR positive. Mice and dogs developed an IFA titer > or =64, while calves lacked a detectable antibody response. These preliminary experimental infection trials show that white-tailed deer are susceptible to infection with B. lonestari and develop a spirochetemia following needle-inoculation, while C3H mice, calves, and dogs do not. Results suggest that deer may serve as a vertebrate reservoir host. Tick transmission studies are needed to confirm that this organism can be maintained in a natural cycle involving deer and A. americanum.

Animals↗
PubMed1999

High prevalence of antibodies to Neospora caninum in white-tailed deer (Odocoileus virginianus).

Serum samples of 400 white-tailed deer (Odocoileus virginianus) from 16 preserves in northeastern Illinois were tested for Neospora caninum antibodies in the N. caninum agglutination test using mouse-derived N. caninum tachyzoites and mercaptoethanol. Antibodies were found in 162 deer with titres of 1:40 (47 deer), 1:80 (32 deer), 1:160 (17 deer), 1:200 (eight deer), 1:400 (19 deer), 1:800 (17 deer) and > or = 1:1600 (22 deer). There were no significant differences in prevalence between age or sex of the deer. The high prevalence of N. caninum infection in deer is consistent with a sylvatic cycle of N. caninum.

Animals↗
PubMed2000

Genetic influences on reproduction of female red deer (Cervus elaphus) (2) seasonal and genetic effects on the superovulatory response to exogenous FSH.

This study evaluated the influences of seasons and genotype on the superovulatory response to a standardised oFSH regimen in red deer (Cervus elaphus scoticus) and its hybrids with either wapiti (C.e. nelsoni) or Père David's (PD) deer (Elaphurus davidianus). Adult red deer (n=9), F(1) hybrid wapiti x red deer (n=6), and maternal backcross hybrid PD x red deer (i.e., 14 PD hybrid; n=9) were kept together in the presence of a vasectomised stag for 13 months. At 6 weekly intervals, all hinds received a standardised treatment regimen used routinely to induce a superovulatory response in red deer hinds, with 10 consecutive treatments spanning an entire year. This involved synchronisation with intravaginal progesterone devices and delivery of multiple injections of oFSH (equivalent to 72 units NIH-FSH-S(1)). Laparoscopy to assess ovarian response was performed 6-7 days after the removal of the devices. Both season and genotype had significant effects on ovulation rate (OR) and total follicular stimulation (TFS) (P<0.05). For all the three genotypes, ovarian responses were highest from March to November (breeding season) and lowest in the period from December to January, inclusive. Mean OR for red deer hinds ranged from 3.7 to 1.8 during the breeding season, with no observable trend. All red deer hinds were anovulatory during December and January. A similar pattern occurred for 14 PD hybrids, although mean OR during the breeding seasons were twofold lower than for the red deer. For F(1) wapiti hybrids, the first two treatments in March and April resulted in the highest mean OR observed (15.6 and 11.7, respectively). Thereafter, mean values ranged between 6.3 and 4.7 for the remainder of the breeding season. Furthermore, mean OR of 3.0 and 0.5 were recorded in December and January, respectively. For the red deer and F(1) wapiti hybrids, between-hind variation in OR was not randomly distributed across the treatment dates, indicating that the individuals varied significantly in their ability to respond to oFSH, at least within a given season.In conclusion, the study has shown that relative to red deer, F(1) wapiti hybrid hinds exhibit a higher sensitivity to oFSH, whereas 14 PD hybrid hinds have a lower sensitivity. However, individual variation within genotype was very marked. A seasonal effect was apparent for all genotypes, although some F(1) wapiti hybrid hinds exhibited ovulatory responses throughout the year.

Administration, Intravaginal↗
PubMed2005

Impact of molybdenum on the copper status of red deer (Cervus elaphus).

AIM: To determine the effect of increasing molybdenum (Mo) intakes on serum and liver copper (Cu) concentrations and growth rates of grazing red deer (Cervus elaphus). METHODS: Molybdenum- and Cu-amended fertilisers were applied to six 1.1-ha paddocks in a 3 x 2 design. Three levels of Mo were applied on two paddocks at each level in mid April (designated Day 1); levels were: none (control), 0.5 (medium) and 1.0 (high) kg Mo/ha as sodium molybdate. In late May (Day 39), two levels of Cu (none and 3.0 kg Cu/ha, as copper sulphate) were applied to each of the three levels of Mo-treated paddocks. Pasture Mo, Cu and sulphur (S) concentrations were measured at about fortnightly intervals. In late June (Day 74), ten 6-month-old red deer hinds were placed on the six experimental pastures, and serum and liver Cu concentrations were monitored at about monthly intervals for 102 days. The hinds were weighed on four occasions during the trial. RESULTS: Mean pasture Mo concentrations on Day 56 were 2, 4.6 and 11.3 mg/kg dry matter (DM) for the untreated control, medium and high Mo-treated pastures, respectively. Pasture Cu concentration was 95 mg/kg DM on Day 59, 53 mg/kg DM on Day 90, and 9 mg/kg DM by Day 153. Mean S concentration in pasture was 3.3 (range 3.03-3.45) g/kg DM. Copper application to pasture had no significant effect on serum and liver Cu concentrations in deer so data were pooled within Mo treatment. Mean initial (Day 74) serum Cu concentration was 9.2 micromol/L. In the deer grazing the control Mo pasture, this increased to 10.3 micromol/L on Day 112, before decreasing to 6.4 micromol/L on Day 176. In deer grazing the medium and high Mo-treated pastures, mean serum Cu concentrations were 3.8 and 3.9 micromol/L, respectively, on Day 112, and 2.5 and 3.3 micromol/L, respectively, on Day 176. Mean initial (Day 74) liver Cu concentration was 131 micromol/kg fresh tissue. In the deer grazing the control Mo pasture, this declined to 120 and 52 micromol/kg on Days 112 and Day 176, respectively. In deer grazing the medium and high Mo-treated pastures, liver Cu concentrations decreased to 55 and 52 micromol/kg fresh tissue, respectively, on Day 112, and 21 and 20 micromol/kg fresh tissue, respectively, on Day 176. Mean serum and liver Cu concentrations were not significantly different between deer grazing the medium and high Mo-treated pastures, and were lower (serum p=0.003, liver p<0.001) in those groups than in deer grazing the untreated control pastures. No clinical signs of Cu deficiency associated with lameness were observed. Deer grazing pastures that had Mo concentrations >10 mg/kg DM had lower (p=0.002) growth rates (100 vs 130 g/day) than those on pastures containing <2.4 mg Mo/kg DM. CONCLUSION: Increasing pasture Mo concentrations from 2 mg/kg DM to > or =4.6 mg/kg DM significantly reduced serum and liver Cu concentrations in grazing deer. Reduced growth rate was observed at pasture Mo concentrations >10 mg/kg DM.

Animal Feed↗
PubMed1989

Suitability of white-tailed deer as hosts for cattle fever ticks (Acari: Ixodidae).

White-tailed deer (Odocoileus virginianus L.) were evaluated as an alternate host for the cattle fever tick, Boophilus annulatus (Say). The total of adult female ticks recovered and associated reproductive parameters were compared between deer and bovine hosts. Significantly fewer ticks were recovered from deer than from cattle; this was attributed to the grooming behavior of the deer. The mean weight of ticks taken from deer (243.5 mg) was significantly less than that of ticks recovered from cattle (344.5 mg) with about 15% of the ticks from deer prematurely detached. Egg mass weight from the ticks recovered from deer (129.4 mg) was significantly less than that of ticks from cattle (172.1 mg). A significant difference was observed between the percentage hatch of the eggs of ticks from deer (63.1%) and ticks from cattle (76.7%). The index of reproduction was about 20 times greater for the ticks from the cattle than for the ticks from the deer. When the larval progeny of the ticks recovered from deer were reared on cattle, significantly fewer adult females were recovered than when larvae of ticks recovered from cattle were reared on cattle. This indicates a possible reduction in viability. All other parameters were comparable between the two groups. Thus, deer are biologically suitable hosts for B. annulatus, but significantly fewer ticks complete engorgement and those that complete engorgement have reduced fecundity.

Animals↗