Experimental bluetongue disease in white-tailed deer

Nine white-tailed deer and six sheep were experimentally exposed to the California BTV-8 strain of bluetongue virus. The infections were fatal for seven of the nine deer. An additional deer died from exposure to an isolate of bluetongue virus from bighorn sheep. Clinical signs and lesions of bluetongue in deer were described. The incubation period, signs and lesions of bluetongue and epizootic hemorrhagic disease of deer appear to be similar. Virus isolations were made from the blood and a variety of tissues of exposed deer and identified as bluetongue virus. Neutralizing antibodies were detected in all of the convalescent sera.     

Experimental adenovirus hemorrhagic disease in white-tailed deer fawns

Infection with a newly described endotheliotropic adenovirus was the cause of a 1993 epizootic reminiscent of hemorrhagic disease in California mule deer (Odocoileus hemionus columbianus and O. hemionus hemionus). Pulmonary edema and intestinal luminal hemorrhage, or necrotizing stomatitis associated with systemic or localized vasculitis, respectively, were common lesions seen in animals that died during the epizootic. In order to determine if white-tailed deer (Odocoileus virginianus) also are susceptible to infection and fatal disease with the deer adenovirus, eight white-tailed deer fawns (4- to 6-mo-old) were inoculated with purified deer adenovirus. Four were inoculated intravenously and four were inoculated through the mucous membranes. Seven days post-inoculation, one of the fawns inoculated intravenously died. Pulmonary edema and hemorrhagic enteropathy were associated with pulmonary and intestinal vasculitis with systemic multiorgan distribution of endotheliotropic adenovirus as demonstrated by transmission electron microscopy and immunohistochemistry. Adenovirus was reisolated from lung homogenates of the fawn that died of adenovirus hemorrhagic disease.     

Experimental infection of white-tailed deer with rangiferine brucellosis

Experimental infections of white-tailed deer (Odocoileus virginianus) with Brucella suis biovar 4 were evaluated over a period of 6 wk. Five adult male hand-raised white-tailed deer were inoculated with 1 x 10(7) colony forming units of B. suis biovar 4 in the conjunctiva and serologically evaluated over 6 wk by the card test (CARD), rivanol test (RIV), serum agglutination test (SAT), complement fixation test (CFT), particle concentration fluorescence immunoassay (PCFIA), and competitive enzyme linked immunosorbent assay (cELISA), as routinely used for bovine samples. Six weeks postinoculation the animals were euthanized and cultured for B. suis biovar 4. One deer became serologically positive 4 wk postinoculation on CFT, CARD, PCFIA, and cELISA. At 6 wk postinoculation, CFT was positive in four infected deer, CARD was positive in three deer; RIV, SAT, and PCFIA was positive in two deer; and cELISA was positive in one deer. Only the CFT was 100% sensitive. At necropsy B. suis biovar 4 was isolated from four of five deer, and representative colonies were biologically similar to the challenge organism.     

Experimental infection of white-tailed deer with Elaeophora schneideri.

An attempt was made to infect fawn and adult white-tailed deer, Odocoileus virginianus, with Elaeophora schneideri. Experimental infection of fawns caused a relative eosinophilia that persisted. Obstruction of a coronary artery caused death of one fawn, and weakness, dyspnea, and locomotor difficulties were observed in another fawn and an adult. Plaque-like lesions were observed grossly in the intimal lining of carotid arteries, and subintimal thickening and proliferation of fibrous tissue in vessel walls were observed microscopically. Nematodes were recovered from 3 of 4 fawns and 0 of 4 adults, suggesting an age-related resistance in older animals. Microfilariae were recovered via facial skin biopsy of a single fawn. This study suggests that white-tailed deer serve as usual hosts for E. schneideri, although the host-parasite relationship may be tenuous.     

Experimental infection of white-tailed deer with rinderpest virus.

White-tailed deer (Odocoileus virginianus) succumbed to experimental infection with virulent rinderpest (RP) virus that was also lethal to cattle and goats. The deer developed clinical signs typical of RP and died 5 and 6 days post-inoculation. Infection was confirmed by recovery of virus from blood before death, from lymph node tissue after necropsy, and demonstration of specific complement fixing antigen in those tissues. Electron micrographs of infected Vero cell cultures revealed extracellular virions and intracytoplasmic and intranuclear inclusions made of randomly distributed fibrillar strands.     

Anthrax epizootic in white-tailed deer

Bacillus anthracis caused high mortality among white-tailed deer (Odocoileus virginianus) on Beulah Island, Desha County, Arkansas. Sixty-seven carcasses were located and the total loss was estimated between 200 and 300 deer. Range conditions indicated that the deer herd had greatly exceeded carrying capacity. Lesions in deer were similar to those ascribed to anthrax in domestic cattle, sheep, and goats.     

Salmonellosis in white-tailed deer fawns

Experimental infection of white-tailed deer fawns with Salmonella meleagridis was accomplished. The fawns suffered clinical illness, similar to spontaneous cases observed in the field. This disease may be an important factor in fawn survival in wild herds based on the frequency with which Salmonellae could be isolated in wild fawns. The clinical disease was acute, characterized by rapid depression and dehydration. Death ensued in three of eight experimental cases. The survivors suffered clinical illness.     

Parelaphostrongyliasis in white-tailed deer in Missouri

The heads of 137 white-tailed deer (Odocoileus virginianus) were collected on the opening day of the 1996 Missouri (USA) fire-arms deer season and surveyed for the presence of meningeal worm (Parelaphostrongylus tenuis). Eighteen percent of the deer examined were infected. Mean intensity of infection was 2.0 (range 1-7). There were no significant differences of infection or mean intensity when deer were classified and compared according to sex or age class.     

Fertility control in female white-tailed deer

Silastic rods containing either melengestrol acetate (MGA) or levonorgestrel (LN) were placed in anestrous white-tailed deer (Odocoileus virginianus borealis) does to evaluate the contraceptive efficacy of the implants over a 2 yr period. Implants of MGA were placed in five does during mid-pregnancy to evaluate the effect of this treatment on pregnancy, parturition and lactation. Pregnancies were not observed in the five animals implanted with MGA during anestrus. Three of five does implanted with LN became pregnant in the first season. Pregnancy was not interrupted in the five pregnant does implanted with MGA and it was necessary to remove the implants and treat the does with an estrogen to achieve parturition. One of five fawns was delivered alive and was raised by the doe. MGA was effective for 2 yr as a contraceptive in white-tailed deer, LN was ineffective as used, and MGA placed in pregnant does delayed or prevented normal parturition and thus should not be used in pregnant deer.     

Persistent Ehrlichia chaffeensis infection in white-tailed deer

Four white-tailed deer (Odocoileus virginianus) were inoculated intravenously with a deer-origin isolate (15B-WTD-GA) of Ehrlichia chaffeensis. The course of infection was monitored using indirect fluorescent antibody (IFA), polymerase chain reaction (PCR), and culture over a 9 m period. All deer became rickettsemic within 24 days post inoculation (DPI), and all developed antibody titers >1:64 to E. chaffeensis by 17 DPI. Titers in all deer fell below 1:64 during 87 to 143 DPI. One deer exhibited a second period of seropositivity (peak titer of 1:256) from 207 to 271 DPI but was culture and PCR negative during this period. Rickettsemia was confirmed by reisolation of E. chaffeensis as late as 73 to 108 DPI in three deer. Positive PCR results were obtained from femur bone marrow of one deer and from rumenal lymph node of another (leer at 278 DPI. None of the deer developed clinical signs, hematologic abnormalities, or gross or microscopic lesions attributable to E. chaffeensis. Two uninoculated control deer were negative on all tests through 90 DPI at which time they were removed from the study. Herein we confirm that white-tailed deer become persistently infected with E. chaffeensis, have initial rickettsemias of several weeks duration and may experience recrudescence of rickettsemia, which reaffirm the importance of deer in the epidemiology of E. chaffeensis.     

Hepatic fatty cirrhosis in Texas white-tailed deer

Hepatic fatty cirrhosis (HFC) has been known to occur in certain domestic livestock species since 1931. Early studies in Texas indicated that HFC was restricted to five western counties. Recently HFC was identified in white-tailed deer (Odocoileus virginianus texanus) in South Texas for the first time. Of the deer examined, 25% were affected. The etiology of HFC was not determined.     

Xylazine and ketamine-induced glycosuria in white-tailed deer

This study documents glycosuria effects of xylazine and ketamine in eight captive and 19 free-ranging white-tailed deer (Odocoileus virginianus) from January to April 1985. Mean urinary glucose:creatinine ratios in two groups of deer fed high protein-high energy and low protein-low energy diets and in free-ranging deer were 1,000, 719, and 259, respectively. Glucose did not occur in urine of deer immobilized by physical restraint. Glucose:creatinine increased with the time interval between xylazine injection and urine collection in the two groups of captive deer.