Following the escape to the mainland of the rabbit hemorrhagic disease virus (RHDV) from Wardang Island off the coast of South Australia, a monitoring program was implemented over a 13 mo period, between October 1995 and October 1996 to determine the activity and rate of spread of the disease in the wild European rabbit (Oryctolagus cuniculus) population. All reports of dead rabbits were investigated. Whenever possible, liver and spleen tissue samples were collected from fresh carcasses and subsequently analysed for the presence of RHDV. Maximum rates of spread of rabbit hemorrhagic disease (RHD) in Australia ranged from 9 km/mo during summer to 414 km/mo in spring. New cases of RHD were moderate during late autumn and winter and peaked in spring. In summer the disease was rarely reported.

An outbreak of rabbit viral hemorrhagic disease (RVHD) and of myxomatosis occurred in a free-living population of rabbits (Oryctolagus cuniculus) near Paris (France) in 1995. Annual mortality rates were 88% in adults and 99% in juveniles. There was no difference in mortality rates between males and females. Since most adults were protected with myxoma antibodies after May, they probably died of RVHD. Mortality lasted throughout the year despite high proportions of rabbits having developed myxomatosis and RVHD antibodies, which suggests that the combination of the two diseases and the immunosuppressive characteristics of myxoma virus could be responsible for the mortality caused by RVHD. The proportion of juveniles with RVHD antibodies increased with their weight. Seroconversion against RVHD occurred in spring and autumn.

Antibodies against rabbit hemorrhagic disease virus (RHDV) from 352 red fox (Vulpes vulpes) sera collected in Germany (Mecklenburg-Vorpommern) in 1993 were tested by a blocking enzyme-linked immunosorbent assay (ELISA) test kit. Ninety samples with positive or suspected results also were analyzed by the hemagglutination inhibition test (HIT). Eighteen serum samples (5%) were positive with the blocking ELISA and eight of these also were positive with HIT. The 18 positive sera also were tested by blocking ELISA for antibodies against European brown hare syndrome virus (EBHSV) and by sandwich ELISA to detect fox antibodies against RHDV and EBHSV antigen. Antibodies were not found against EBHSV using the blocking ELISA. With the sandwich ELISA, six samples were positive against RHDV and also against EBHSV, indicating cross-reactivity between determinants of both viruses. However, antibody titers against RHDV were higher than against EBHSV in five samples, and in one animal titers were similar. In addition, two positive samples were investigated by Western blot immunoassay which showed clear positive reactions with the two main peptide bands of EBHSV and RHDV. Comparison of the areas below the peaks of the bands after immunoblotting indicated that there was a stronger reaction with the two main polypeptides of RHDV than with the two main peptides of EBHSV. This is the first report of calicivirus antibodies in free-ranging red foxes. Based on the specificity of the tests, the antibodies detected against caliciviruses may be induced by RHDV. There is a potential link for RHDV between free-ranging rabbits and foxes.

Two hundred and three sera obtained in 1993–96 from red foxes (Vulpes vulpes), lynx (Lynx lynx), brown bears (Ursus arctos) and wolverines (Gulo gulo) in Fennoscandia (Norway, Sweden, and Finland) were examined for the presence of anti-orthopoxvirus antibodies by a competition enzyme linked immunosorbent assay (ELISA). High prevalences were found for the red foxes in Norway (7/62, 11%) and Finland (7/14, 50%). While only one of 73 (1%) lynx from Finland had anti-orthopoxvirus antibodies, a high prevalence was found in sera from the Sarek National Park in Sweden (5/17, 29%). In addition, anti-orthopoxvirus antibodies were found in one brown bear from the same area (1/45, 2%), whereas none of the 14 wolverines were seropositive. This is the first report of anti-orthopoxvirus antibodies in the brown bear and the lynx, and the first screening for such antibodies in Sweden and Finland. These results indicate that orthopoxviruses are distributed in Sweden and Finland as well as in Norway, and that the red fox and the European lynx may serve as indicator species for the presence of orthopoxviruses in the local populations of small mammals.

Ten virus isolates were obtained from three species of marine mammals sampled on San Miguel Island (California, USA) and 1,200 km north on Rogue Reef (Oregon, USA) during tagging operations in 1986–87. Seven of these 10 were derived from 30 sampled Steller sea lion (Eumetopias jubatus pups, while two of 10 were isolated from one of 19 sampled California sea lion (Zalophus californianus californianus pups, and the remaining isolate was derived from 30 sampled northern fur seal (Callorhinus ursinus) pups. All 10 isolates were identified as belonging to a single serotype, reptilian calicivirus Crotalus type 1 (RCV Cro-1), previously isolated from both healthy and diseased snakes and frogs in a California zoologie collection. The marine samples also showed that nine of 30 Steller sea lion pups, one of 19 California sea lion pups and zero of 30 fur seal pups were producing type specific neutralizing antibodies to RCV Cro-1. This represents the first reported instance of the isolation from marine sources of a calicivirus originally isolated from a terrestrial species.

A Newcastle disease epidemic in double-crested cormorants (Phalacrocorax auritus) occurred in July and August 1995, during a 1994–96 study of a breeding colony of this species on Doré Lake (Saskatchewan, Canada). Clinical signs and mortality were observed from a tunnel-and-blind system, and moribund and freshly dead birds were examined virologically. Yolks from cormorant eggs and sera from cormorants and other birds were tested for hemagglutination inhibiting antibodies to Newcastle disease virus (NDV). Evidence of Newcastle disease was limited to juvenile double-crested cormorants, despite close contact with other birds, including American white pelicans (Pelecanus erythrorhynchos) and gulls (Larus spp.). Clinical signs included limb, head or neck paralysis, head or body tremors, ataxia, and blindness; pathogenic NDV was isolated from affected birds. The mortality rate of juvenile cormorants was 32 to 64%, which was high relative to overall first-year mortality in years without epidemics. Thirty-seven of 63 (59%) cormorant sera collected during the epidemic tested positive for antibodies to NDV. Antibody status of cormorant egg yolks depended on stage of incubation, likely due to changes in the amount of water in the yolks. The departure of juvenile cormorants from their nests at 4 wk of age, resulting in an increased contact rate among individuals, may have been important in triggering the epidemic.

Studies were conducted to monitor the decline of maternal antibodies to paramyxovirus type 1 (PMV-1) in kori bustard chicks (Ardeotis kori), and to determine the antibody response in birds with low levels of maternally derived immunity (MDI) after being given either one or five times the standard domestic fowl dose of a live PMV-1 La Sota vaccine intranasally. The results confirmed that PMV-1 antibodies were transferred to eggs and chicks derived from kori bustard hens immunized with inactivated vaccine 5 to 8 mo previously. The levels of inherited antibody in chicks varied considerably, with 21% of birds having no detectable antibodies at day 14. Chicks hatched from dams with high hemagglutination inhibition (HI) antibody titers had high titers of MDI. Mean antibody levels in seropositive chicks were log₂ 6.3 and log₂ 2.9 on days 14 and 42, respectively. The rate of decline of detectable antibodies (1 log₂), was estimated to be 5.50 to 6.25 days and 12.25 days in 14 to 21 and 28 to 42 day old chicks, respectively. There was no significant HI antibody response in bustards given a primary vaccination of either one or five times the standard domestic fowl dose of live vaccine intranasally up to 3 wk post-vaccination. High levels of HI antibodies, log₂ 7.4, were detected in birds given a secondary dose of inactivated vaccine, but not in birds given a secondary dose of live vaccine at 2 wk post-vaccination.

Sera from wild geese were tested for antibodies to selected viral pathogens at a resting site for wild waterfowl in Germany. Serum samples from both bean geese (Anser fabalis) and white-fronted geese (Anser albifrons) collected in October 1991 were examined using serological methods licensed for routine diagnosis in domestic poultry. Of 130 sera tested, antibodies to several infectious agents were found including Newcastle disease virus (45%), goose parvovirus (48%), avian reovirus (29%) and avian adenovirus or egg drop syndrome 76 virus (6%). Antibodies against duck hepatitis virus were not detected. Differences in seroprevalences were not detected between the two geese species. While role and significance of wild geese in the epidemiology of avian diseases remains to be determined, it is possible that they could be of some importance as reservoirs and carriers of certain viral diseases of domestic poultry.

An epidemic of chronic rhinitis in a population of 50 captive spur-thighed tortoises (Testudo graeca graeca) from Palafrugell (Girona, Spain) is described, in which eight animals died and 12 were euthanatized to perform necropsies and post-mortem studies. The main clinical sign was a bilateral, seromucous rhinitis often accompanied by stomatitis and glossitis. Hematology and serum biochemistry were performed in 33 of the 50 ill animals and in 29 healthy tortoises from three disease-free populations. Lymphocyte count, aspartate aminotransferase (AST) activity, and α-globulin levels were significantly higher in the animals from the sick population. The heterophil count was significantly lower in the sick animals. Some of the diseased tortoises also showed a normocytic-normochromic anemia. Lesions were restricted to the respiratory system and oral cavity. Marked epithelial hyperplasia and presence of a severe mixed inflammatory infiltrate in the epithelium of the oral, nasal, and tracheal mucosae were observed. Electron microscopy demonstrated the presence of intracytoplasmic and intranuclear viral particles of the size, shape, and distribution pattern typical of a herpesvirus.

Serodiagnostic tests for detecting green turtle (Chelonia mydas) antibody responses were developed to test the strength of association between exposure to spirorchid trematode antigens or herpesvirus antigens and having green turtle fibropapillomatosis (GTFP). Plasma samples from 46 captive-reared green turtles, including paired pre- and 1-yr post-inoculation samples from 12 turtles with experimentally induced GTFP, were found by enzyme-linked immunosorbent assay (ELISA) to be negative for antibodies to adult spirorchid (Learedius learedi) antigens. In contrast, all 12 turtles that developed experimentally induced GTFP converted within 1 yr from having negative to positive antibody reactivity to GTFP-associated herpesvirus antigens, whereas the three controls and four turtles that failed to develop tumors remained negative. Plasma samples from 104 free-ranging green turtles from two Florida (USA) coastal feeding grounds with different GTFP prevalences were tested by ELISA for antibodies to L. learedi adult antigens; and there was no statistically significant association between antibody prevalence and sampling site. When a low optical density cutoff value (0.15) was used to interpret ELISA results, 98% of the turtles from each site were spirorchid antibody-positive and there was no association between antibody reactivity to spirorchids and GTFP status. When a higher negative cutoff value was used, however, a statistically significant association between antibody reactivity to spirorchids and GTFP-free status was found. These results suggest that spirorchids do not have a role in GTFP pathogenesis. All 20 of the tumor-bearing lagoon turtles had antibodies to herpesvirus antigens whereas only two (10%) of the tumor-free reef turtles had detectable anti-herpesvirus reactivity. The strong association between antibody reactivity to herpesvirus antigens and GTFP status in both captive-reared and free-ranging turtles is consistent with the hypothesis that the transmissible agent that causes GTFP is a herpesvirus.

Twenty-four ill or dead desert tortoises (Gopherus agassizii) were received between March 1992 and July 1995 for necropsies from the Mojave and Colorado deserts of California (USA). Diseases observed in these animals included cutaneous dyskeratosis (n = 7); shell necrosis (n = 2); respiratory diseases (n = 7); urolithiasis (n = 3); and trauma (n = 5). In tortoises with cutaneous dyskeratosis the horn layer of shell was disrupted by multiple crevices and fissures and, in the most severe lesions, dermal bone showed osteoclastic resorption, remodeling, and osteopenia. In tortoises with shell necrosis, multiple foci of necrotic cell debris and heterophilic inflammation within the epidermal horn layer were subtended by necrotic dermal bone colonized by bacteria and fungi. Of the seven tortoises with respiratory disease, five were diagnosed with mycoplasmosis. The diagnosis of mycoplasmosis was based on the presence of chronic proliferative rhinitis and positive serologic tests and/or isolation of Mycoplasma sp. Chronic fungal pneumonia was diagnosed in one tortoise with respiratory disease. In the three tortoises with urolithiasis, two were discovered dead, and the live tortoise had renal and articular gout. Traumatic injuries consisted of one tortoise entombed within its burrow, one tortoise burned in a brush fire, two tortoises struck by moving vehicles, and one tortoise attacked by a predator. While the primary cause of illness could be attributed to one or two major disease processes, lesions were often found in multiple organ systems, and a variety of etiologies were responsible for morbidity and mortality.

Between August 1992 and November 1995, 31 moribund or dead common loons (Gavia immer) found in the three Maritime provinces of Canada (New Brunswick, Nova Scotia, Prince Edward Island) were necropsied. Eight of these birds were in good body condition and died acutely from drowning or trauma. The remaining 23 birds were in poor body condition and had either chronic lead poisoning, respiratory mycosis, or oil contamination of their plumage. Loons in poor body condition had significantly higher numbers of intestinal trematodes and significantly higher levels of total renal mercury than loons in good body condition. Therefore, poor body condition in many loons was associated with two or more concurrent potential disease processes, although we could not establish a cause-effect relationship among these processes in individual birds. These results suggest that mortality in chronically ill wild animals can result from synergism among several potentially debilitating agents present in their environment.

Between June 1986 and May 1997, chronic wasting disease (CWD) was the only natural cause of adult mortality among captive Rocky Mountain elk (Cervus elaphus nelsoni) held at a wildlife research facility near Fort Collins, Colorado (USA). Of 23 elk that remained in this herd >15 mo, four (17%) developed CWD. All affected elk were unrelated females from the founding cohort, captured as neonates and raised in 1986. The index case was diagnosed in 1989; time intervals between subsequent cases ranged from 13 to 32 mo. Initial age at onset of clinical signs ranged from about 2.9 to 8.1 yr; duration of clinical disease ranged from 5 to 12 mo (mean = 7.5 mo) prior to death. Intraspecific lateral transmission of CWD seemed the most plausible explanation for the epidemic pattern observed; neither periparturient nor maternal transmission appeared necessary to sustain this outbreak. Early detection and elimination of incubating or clinical individuals may have aided in reducing exposure or infection rates as compared to a previous outbreak in the same facility. Transmission routes and rates, pathogenesis, antemortem diagnostic tools, and the potential role of reservoirs or environmental contamination in perpetuating CWD epidemics warrant further investigation.

Immunocontraception using porcine zona pellucida (PZP) vaccines is being explored as a nonlethal method of solving the problems of locally overabundant wildlife populations. This study characterized the immunological response of captive elk (Cervus elaphus nelsoni) to PZP challenge using 18 3-yr-old cows and was conducted from 14 September 1994 to 13 December 1995. All animals were given a single PZP inoculation and 1 mo later six of these animals were randomly chosen and received a booster inoculation. Blood samples were drawn from all animals at the time of the initial inoculation and 1, 2, 4, 6, 10, and 15 mo later. Immunological response was assessed by measuring anti-PZP antibody levels in serum. All animals demonstrated a strong immune response with no evidence that the booster enhanced antibody levels. Antibody levels rose from between 0 and 4 at the time of the initial injection to peak levels of 85 to 163 within 2 to 6 mo, followed by a noticeable decline by 15 mo post-vaccination. Limited data suggest that antibody levels >100 may be required to effect contraception. High individual variability in immune response observed in this study suggests it may be difficult to predict the proportion of animals effectively treated. Disruption of seasonal synchrony in calving also could occur if antibody levels in individuals fall below effective levels while animals are still cycling. These results indicate that immunocontraception using PZP vaccines is possible for elk. However, carefully controlled population experiments will be required in order to assess the potential and limitations for management applications of this technique.

A surgical approach was developed for implantation of transmitters to monitor heart rate of bighorn sheep (Ovis canadensis) with an objective of discrete long-term, long-range data collection. We surgically implanted Telonics model HR400 transmitters on the dorsolateral thorax of 15 captive adult bighorn sheep ewes in April-May and October-November 1995. No complications or marked impairment of function were associated with the surgery; however, a transmitter was passively expelled from one ewe 19.5 mo post-implantation. Twelve of 15 transmitters remained functional ≥1 yr, while three failed 3.5 to 4.5 mo following implantation. Heart rate data collected from the transmitters using a Lotek SRX_400 telemetry receiver/datalogger equipped with W9 EVENT_LOG accurately reflected heart rate as measured with electrocardiogram tracings. Line of sight signal range was at least 800 m in 95% (37/39) of collections made from standing ewes, while data could be collected reliably (74% 29/39) to 600 m from bedded ewes. When a reliable long-lasting inconspicuous telemetry system is required, we believe that this approach holds promise for success in free-ranging as well as captive ungulates.

Immobilization was studied in 202 free-ranging two-toed sloths (Choloepus didactylus). All the sloths were in good condition with a body weight >2 kg, and were anesthetized for a variety of minor clinical procedures. Intramuscular anesthetic combinations included 0.1 mg/kg acepromazine 10 mg/kg ketamine (A/K, n = 30), 1 mg/kg xylazine 10 mg/kg ketamine (X/K, n = 89), 10 mg/kg tiletamine/zolazepam (T/Z, n = 37), and 0.04 mg/kg medetomidine 3 mg/kg ketamine (M/K, n = 46) antagonized by 0.2 mg/kg atipamezole. The animals were quiet during the induction stage and complete recumbency was reached in (mean ± SD) 2.5 ± 2.0 min with A/K, 2.7 ± 1.7 min with X/K, 1.8 ± 0.6 min with T/Z, and 2.5 ± 5 with M/K. Utilization of A/K was not satisfactory because of poor anesthetic level and lack of muscle relaxation. T/Z induced immobilization was characterized by deep anesthesia and good myorelaxation, but often was associated with irregular respiration and low relative oxyhemoglobin saturation values (SpO₂). Ketamine in combination with alpha₂-agonists, xylazine or medetomidine, provided suitable anesthesia, with good to excellent muscular relaxation, good analgesia, high SpO₂ values, moderate bradycardia, but strong bradypnea with medetomidine. Anesthesia with M/K was reversed after 41.6 min of immobilization with atipamezole. Calm recoveries were obtained and the animals were able to hang up after 10.0 ± 7.9 min. The first signs of arousal were observed within an average of 43 to 51 min after the injection of the three other combinations. Recoveries from X/K immobilization were quiet; sloths held on after 34 min. With T/Z, recovery duration was long and very irregular at 76.7 ± 31.3 min, some animals required 3 hr before being able to hang up. Finally, ketamine in association with an alpha₂-agonist appeared to give the best chemical immobilization in wild two-toed sloths for 40 min procedures including minor surgery.

Four wild African ruminants, eland (Taurotragus oryx), giraffe (Giraffa camelopardalis), kudu (Tragephalus strepsiceros strepsiceros), and blue wildebeest (Connochaetes taurinus), were experimentally infected with the rickettsia Cowdria ruminantium, the tickborne agent causing heartwater in domestic ruminants. The infections were established, and C. ruminantium was transmitted to naive small ruminants by the vector Amblyomma hebraeum when transmission attempts were made at days 128 (eland and wildebeest), 85 (giraffe), and 24 (kudu) post infection. These wild ruminants, which are natural hosts for the tick vector, and which commonly occur within heartwater-endemic areas of Africa, are likely to play important roles in the epidemiology of heartwater as reservoirs of C. ruminantium infection. These findings also demonstrate that considerable risks are associated with the translocation of wild ruminants from heartwater-endemic areas to heartwater-free areas such as the northern and southern American mainlands, which have large populations of susceptible domestic and wild ruminant hosts and tick species that are capable of transmitting the disease.

Leptospira interrogans serovar balcanica is a potential vector being investigated for spreading a biological control agent among introduced brushtail possums (Trichosurus vulpecula) in New Zealand. As previous studies have shown that possums are unlikely to contract leptospirosis through a contaminated environment alone, the objective was to determine whether L. interrogans serovar balcanica could be transmitted between sexually mature, socially housed possums. Possums were infected experimentally with L. interrogans serovar balcanica and housed in pairs or groups with uninfected possums for either 70 or 140 days, during the breeding or non-breeding seasons. No transmission occurred between any infected and uninfected possums during the non-breeding season. However, transmission occurred between females that had been socially housed in pairs or groups in the breeding season. Mixed sex transmission also occurred in pairs and groups, both from males to females and from females to males. Mixed sex transmission usually occurred rapidly (<44 days) and was not associated with the production of offspring. No transmission occurred between males during the breeding or the non-breeding seasons. Transmission probably occurs as a result of affiliative or sexual behaviour, but is unlikely to occur through fighting. The social transmission pathways determined in this study suggest that L. interrogans serovar balcanica may have the transmission attributes desired in a vector for biological control.

Reproductive procedures for cattle were adapted to American bison (Bison bison) to evaluate the potential preservation of germ plasm from bison infected with Brucella abortus without transmission of the pathogen to the recipient or offspring. Two of four experimentally inoculated bison bulls excreted B. abortus in the semen. Four healthy calves were produced from non-infected, un-vaccinated bison cows by natural breeding with a bison bull excreting B. abortus in the semen. There was no seroconversion of the cows or their calves. Two culture negative bison calves were produced by superovulation of infected bison donor cows followed by artificial insemination and embryo transfer without transmitting B. abortus to recipient cows or calves. These limited data indicate that embryo manipulatory procedures and natural breeding in bison may facilitate preservation of valuable germ plasm from infected bison while reducing the risk of transmission of B. abortus to recipients and progeny.

Members of the family Columbidae are hosts for the sarcomastigophoran, Trichomonas gallinae, the causative agent of trichomoniasis. Birds of prey are susceptible to the disease when they ingest infected prey. Doves are a major dietary component of urban nesting Cooper's hawks (Accipiter cooperii) in Tucson, Arizona (USA). During the breeding seasons of 1995 and 1996, we clinically evaluated 89 breeding age and 223 nestling Cooper's hawks from urban and exurban (i.e., undeveloped natural area) areas for infection of T. gallinae. There was no difference in the rate of infection between breeding age Cooper's hawks in urban and exurban locations; only one bird tested positive for T. gallinae. However, prevalence of T. gallinae was significantly greater among urban nestlings (85%) than exurban nestlings (9%). There also was a difference between the prevalence in breeding age and nestling Cooper's hawks in urban areas, but not in exurban areas. Trichomonas gallinae was present in at least one nestling at 98% of urban nests tested (n = 51), but only 13% of exurban nests tested (n = 23). The patterns we found probably are caused by three factors; doves are hosts for the parasite, they are present in large numbers in Tucson, and they are the primary prey of urban Cooper's hawks at that locality.

Macroscopic gastrointestinal sarcocysts were detected in 36 of 270 (13%) Tasmanian pademelons (Thylogale billardierii) and 47 of 292 (16%) Bennetts wallabies (Macropus rufogriseus) from January 1995 to March 1996 at onshore and offshore study sites in Tasmania (Australia). The sarcocysts were characterized using light and electron microscopy. The ultrastructure of the primary cyst wall was consistent with that of Sarcocystis mucosa, an apicomplexan parasite commonly found in macropodid marsupials. Although conventional statistical tests were not applied to data, there were apparent differences in the prevalence of infection in macropodid marsupials inhabiting onshore (19%) versus offshore (0%) sites. These differences were attributed to the presence or absence of medium-sized dasyurid marsupials. The results of this study provide strong circumstantial evidence that these dasyurid marsupials are the probable definitive hosts for S. mucosa in free-ranging Tasmanian macropodids.

The clinical response of red foxes (Vulpes vulpes) to the mange mite, Sarcoptes scabiei, was characterized by infection of five, 4-mo-old red foxes with S. scabieioriginally isolated from a wild red fox. The infected foxes and three uninfected control foxes were monitored with weekly complete blood counts and biweekly serum chemistry profiles, hypersensitivity tests, and evaluation of skin biopsies. After 7 wk, the foxes were treated and held free of infection for 2 mo. Six foxes, three previously infected and three with no history of exposure, were then infected with the same isolate of S. scabiei and followed for another 7 wk; two additional previously infected foxes were held as treatment controls, and two foxes with no history of exposure as naive controls. All infected foxes developed significant immediate (Type I) hypersensitivity reactions to a S. scabiei mite extract within 2 wk of exposure and maintained this reaction as long as 4 mo after clearance of mites. Pronounced mast cell hyperplasia and infiltration with eosinophils were the earliest inflammatory cell responses noted in biopsy samples from infected foxes and were maintained throughout infection. Infected foxes also showed significant increases in white blood cell counts, due primarily to increases in numbers of circulating neutrophils and eosinophils. Clinical response, severity of disease, and relative numbers of mites per cm² of skin of previously infected foxes and foxes undergoing their first infection did not differ. These results show that red foxes develop strong immediate hypersensitivity reactions to S. scabieibut, under our experimental conditions, did not exhibit resistance to reinfection.

Sera obtained from 66 free-ranging Florida black bears (Ursus americanus floridanus) from three geographic areas of Florida (USA) between November 1993 and August 1995 were tested for antibodies to 13 disease agents. Antibody prevalences were 3 positive of 37 tested (8%) Coxiella burnetii, 37 of 66 (56%) Toxoplasma gondii, 3 of 61 (5%) blue-tongue virus/epizootic hemorrhagic disease virus (BTV/EHDV), 4 of 66 (6%) canine adenovirus-type l, 5 of 66 (8%) canine distemper virus (CDV), 10 of 62 (16%) canine parvovirus (CPV), 7 of 66 (11%) eastern equine encephalitis virus, 4 of 66 (6%) western equine encephalitis virus, 2 of 66 (3%) Venezuelan equine encephalitis virus, and 11 of 66 (17%) St. Louis encephalitis virus. No samples had serologic evidence of exposure to. Brucella spp. (n = 37), Francisella tularensis (n = 40), or pseudorabies virus (n = 37). This is the first known published report of antibodies to B1V/EHDV, CDV, and CPV in black bears.

Diagnostic findings on 51 red foxes (Vulpes vulpes) from the southeastern United States examined from 1967 to 1995 were reviewed. Etiologic diagnoses included sarcoptic mange (n = 33), traumatic injury and associated complications (n = 5), suspected canine distemper (n = 2), capture myopathy (n = 1), congenital absence of guard hairs (n = 1), intradermal tick infestation (n = 1), otodectic mange (n = 1), and toxicosis (n = 1). The cause of morbidity was not determined for three of the foxes, and three others were classified as normal animals. Sarcoptic mange was diagnosed in 65% of the red foxes, was found in foxes submitted from four of the eight southeastern states represented, and was seen in 19 of 29 yr covered by this study.

An emaciated, moribund, male blue jay (Cyanocitta cristata) was collected in Georgia (USA) and died shortly after capture. Necropsy revealed nine large nematodes identified as Diplotriaena tricuspis in the thoracic and abdominal air sacs and within the pericardial sac. Multiple mycotic granulomas also were observed in the lungs and air sacs, and fungal culture of these lesions yielded pure growth of Aspergillus fumigatus. Histologic examination of the lungs revealed disseminated granulomatous inflammation containing both larvated nematode eggs and abundant fungal hyphae. This is the first description of concomitant A. fumigatus and D. tricuspis infection in a bird.

A stranded bottlenose dolphin (Tursiops truncatus gilli) succumbed to a pulmonary infection of Coccidioides immitis. The dolphin initially presented with mild inspiratory dyspnea that rapidly worsened over 48 hr to include buoyancy abnormalities and finally death. At necropsy, caseous nodules were observed throughout the lungs and perihilar lymph nodes. On histological examination of tissues, double walled organisms containing endospores characteristic of C. immitis were observed in lung, perihilar lymph nodes, and brain. Pyogranulomatous infiltrates were observed in the lung and perihilar lymph nodes only. A DNA Gen-Probe test performed on a purified isolate confirmed infection by C. immitis. Serum was positive for antibodies to C. immitis at a titer of 1:128 and was negative for all known marine morbilliviruses. Although there have been reports of C. immitis infections in free ranging marine wildlife, including California sea lions (Zalophus californianus) and sea otters (Enhydra lutris), this is the first reported case of coccidioidomycosis in a cetacean.

During a survey for tuberculosis in wild carnivores and omnivores, Mycobacterium bovis was cultured from pooled lymph nodes of three adult female coyotes (Canis latrans) harvested by hunters in Michigan (USA). No gross or histologic lesions suggestive of tuberculosis were seen in these animals. One coyote was taken from Montmorency county and two coyotes from Alcona county located in the northeastern portion of Michigan's Lower Peninsula where free-ranging white-tailed deer (Odocoileus virginianus) have been found infected with bovine tuberculosis. It is thought that these coyotes became infected with M. bovis through the consumption of tuberculous deer. Other species included in the survey were the opossum (Didelphis virginiana), raccoon (Procyonlotor), red fox (Vulpes vulpes), bobcat (Felis rufus), and badger (Taxidea taxus).

A serological survey detected antibodies against Babesia ovis in mouflon sheep (Ovis musimon) from two different reserves located in Catalonia in northeastern Spain. An indirect fluorescent antibody test (IFAT) was developed using a B. ovis isolate of ovine origin as the antigen. Of 50 sera tested, six (12%) showed titres between 1:160 and 1:640 and were considered positive. These results indicate that exposure of mouflon to Babesia ovis is common in this region.

Hematozoan parasites were not found on blood smears fron any of 82 Griffon vultures (Gyps fulvus) examined from Spain. These vultures represented samples of diverse temporal and spatial origin, and there was a great disparity in host ages (nestlings to >5-yr-old adults) and physiological condition (growing, food-stressed, injured, and healthy birds).

The liver fluke Platynosomum fastosum was identified upon necropsy of three ex-captive orangutans (Pongo pygmaeus) which had been part of a rehabilitation program for reintroduction to the wild. This trematode has not been reported in orangutans previously and is commonly found in cats in Southeast Asia. Cross infection from cats via intermediate hosts, to orangutans kept in captivity as pets, could explain their presence in the latter. Although P. fastosum caused intrahepatic and bile duct damage, death of the hosts could not be attributed solely to the presence of the liver fluke infection.

During 1993, the Ontario Ministry of Natural Resources, Rabies Research Unit, conducted experiments to develop a bait that would be attractive to raccoons (Procyon lotor) and serve as a vehicle to deliver oral rabies vaccine to that species. Testing of six candidate baits on captive and wild raccoons revealed that the best baits in terms of attractiveness to raccoons were a sugar-vanilla bait and a cheese powder bait. Further testing of those two baits containing miniature radio-transmitters indicated there was no preference between the baits, with respect to acceptance by raccoons; however, as there were fewer problems in mass producing the sugar-vanilla bait, it was selected for larger scale experiments.

Blood sampling in manually restrained or ketamine (15 mg/kg given intramuscularly) treated saker falcons (Falco cherrug) induced an increased concentration in plasma corticosterone. Elevated plasma progesterone, oestradiol 17β, and testosterone concentrations also were observed in some of these birds. An inverse relationship was demonstrated between levels of corticosterone and progesterone, but not with the levels of other hormones. It is suggested that progesterone measurement should be taken into consideration when studying the influence of stressors in falcons.

The morbillivirus epizootic during 1990 to 1992 in Mediterranean striped dolphins (Stenella coeruleoalba) off the Mediterranean coast of Spain diminished these populations directly through mortalities, and indirectly through loss of normal fecundity. High levels of polychlorinated biphenyls (PCB's) also were detected in stranded animals. In addition to high numbers of abortions during the epidemic, unusual cystic structures were noted in the ovaries of several morbillivirus-infected dolphins with high PCB levels. These structures were identified as multiple luteinized cysts from their gross and histomorphologic characteristics. No morbillivirus antigens were detected in the lesions by immunohistochemistry. Because luteinized cysts occur when ovulation is impeded, either an effect of morbillivirus or PCB's on hypothalamic/pituitary function or an effect of PCB's on ovarian responsiveness are proposed as pathogenic mechanisms. These cysts may impede population recovery from the epidemic if similar cysts occurred on surviving dolphins.

Progressive ataxia, delayed growth, dementia and tremors were noted in a female African lion (Panthera leo) cub at the Tel-Aviv Ramat-Gan Zoological Center (Israel). The lioness was 3-mo-old when clinical signs were first noticed. Repeated neurological evaluations and blood tests were conducted in an attempt to establish a diagnosis. A congenital abnormality was suspected and the lioness died 6 mo later. Post mortem examination revealed an Arnold-Chiari malformation. The abnormality was classified as a Chiari type 2 malformation, based on the herniation of the cerebellar vermis and paravermis and the slight caudal displacement of the medulla, combined with lack of displacement in other parts of the brainstem.