Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Distemper”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 289 records · Page 16Linked to original sources

Retrospective study of testicular degeneration in raccoons with canine distemper infection.

A 6-year (1985-1990) retrospective survey of raccoons with canine distemper infection and an outbreak of the disease in 1988 on South Island, South Carolina, are described. During this epizootic, 3 male raccoons with the clinical disease had gross testicular lesions that, on histopathologic examination, revealed severe diffuse degeneration and mineralization of seminiferous tubules. The testicular pathology of canine distemper in raccoons has not been previously reported.

Animals↗

Comparison of tissue and fluid samples for the early detection of canine distemper virus in experimentally infected dogs.

The clinical utility of various specimens was examined for the early diagnosis of canine distemper (CD). Seven healthy dogs at 17 weeks of age were experimentally infected with a field isolate of canine distemper virus. The RT-PCR was carried out to detect CDV NP gene. Dogs showed mild fever and leukopenia, however, typical clinical signs of CD were not seen through the experimental period. CDV amplicons were detected more, earlier and for longer period in the conjunctival swabs than in the other samples employed. These results suggested that conjunctival swab samples, which are easy to obtain and non-invasive, would be the most suitable and practical specimen for the early antemortem diagnosis of CDV infection.

Animals↗

Mass die-Off of Caspian seals caused by canine distemper virus.

Thousands of Caspian seals (Phoca caspica) died in the Caspian Sea from April to August 2000. Lesions characteristic of morbillivirus infection were found in tissue specimens from dead seals. Canine distemper virus infection was identified by serologic examination, reverse transcriptase- polymerase chain reaction, and sequencing of selected P gene fragments. These results implicate canine distemper virus infection as the primary cause of death.

Animals↗

Canine distemper infection in pet dogs: I. Surveillance in Indiana during a suspected outbreak.

A mail survey of 613 private veterinary practices in Indiana was conducted to determine the prevalence of canine distemper infection in Indiana during 1991 and 1992 and to compare the prevalence in three geographic regions. Of the practices that were contacted, 223 (37%) responded. Canine distemper had been diagnosed by 150 (67%) of the 223 practices. The period prevalence increased significantly from 11.1 to 16.9 cases per 10,000 dog visits. Surveillance of private veterinary practices may be useful to confirm suspected outbreaks of diseases in companion animals.

Animals↗

Canine distemper infection in pet dogs: II. A case-control study of risk factors during a suspected outbreak in Indiana.

The epidemiologic features of an outbreak of canine distemper during 1992 and 1993 in pet dogs in Indiana are described. Risk factors for disease were characterized using hospital records of private veterinary practitioners. The risk of disease for purebred dogs was 85% lower than the risk of disease for mixed-breed dogs. Lack of vaccination was associated with a 350-fold increase in the risk of canine distemper, and 93.8% of all cases could be attributed to the lack of vaccination. For many of the owners, the cost of medical treatment exceeded the cost of a vaccination program.

Age Distribution↗

Tyzzer's disease as a complication of canine distemper in a raccoon.

Intercurrent canine distemper and Tyzzer's disease were diagnosed in a mature raccoon (Procyon lotor) submitted for necropsy. Clinical, gross and microscopic findings characteristic of canine distemper virus (CDV), included ataxia, dyspnea, suppurative conjunctivitis, interstitial pneumonitis and generalized lymphocytolysis. Inclusion bodies typical of CDV infection were present in many epithelial tissues. Acute multifocal hepatic necrosis and acute segmental necrotizing enteritis were attributed to the presence of Bacillus piliformis organisms in these lesions, confirmed by special stains and electron microscopy. This is apparently the first reported case of Tyzzer's disease in a raccoon.

Animals↗

Neutralizing antibodies to phocine distemper virus in Atlantic walruses (Odobenus rosmarus rosmarus) from Arctic Canada.

The first evidence of phocine distemper virus (PDV) infection in Atlantic walruses (Odobenus rosmarus rosmarus) from Nottingham Island, Northwest Territories, Canada, is reported. Blood samples were collected from three male walruses killed by Inuit hunters in the fall of 1990. Differential virus neutralization test for each animal yielded higher titers against PDV than against other members of the Morbillivirus genus including canine distemper, peste des petits ruminants, rinderpest and measles viruses. Thus, PDV infection may be enzootic in walruses of the eastern Canadian Arctic.

Animals↗

Encephalomyelitis induced by canine distemper virus in non-human primates.

A strain of canine distemper virus was shown to be highly neuro-virulent in non-human primates. Intracerebral inoculation induced in monkeys histological lesions of encephalomyelitis, i.e., degenerative changes consisting mainly of neuronal damage and inflammatory changes such as perivascular cuffings and glial proliferation, in wide areas in the brain and spinal cord. In one monkey observed for 70 days, lesions with a tendency of subacute sclerosing were also noticed. Immunosuppression with cyclophosphamide or antithymocyte serum was found to aggravate the clinical course and to modify the histological lesions in the central nervous system as well as the level of antibody response to the virus in cerebrospinal fluid. Possible application of distemper encephalomyelitis in monkeys as a primate model for analysis of the immune mechanism involved in paramyxovirus-induced encephalomyelitis was discussed.

Animals↗

[Distemper as the cause of death in badgers in Austria].

A canine distemper virus infection of badgers in a hunting range in Austria is described. A badger which was shot after showing symptoms of rabies infection and one which was found dead were examined by gross pathology and parasitological, histological, bacteriological and virological methods. The examination for rabies was negative in both cases. The badger which was found dead histologically showed signs of a non purulent panencephalitis, the shot animal showed hyperaemia and oedema of the brain. No cytoplasmatic or nuclear inclusion bodies could be observed. The aetiologic viral diagnosis was achieved by immunofluorescence. Using two canine distemper-specific conjugates a typical granular fluorescence of different strength could be observed in organ sections. The bacterial examination showed in both cases a secondary infection with opportunistic pathogenic bacteria (haem. E. coli and Pseudomonas aeruginosa).

Animals↗

Fecal incontinence, urinary incontinence, and priapism associated with multifocal distemper encephalomyelitis in a dog.

A 4-year-old castrated mixed-breed dog had atypical signs of chronic distemper encephalomyelitis. The predominant signs were related to visceral rather than somatic dysfunction. The visceral dysfunction was largely attributable to distemper-associated inflammatory lesions in the spinal cord and resulted in fecal incontinence, urinary incontinence, and priapism. Empirical treatment of the dog resulted in transitory improvement prior to euthanasia performed because of the progressive nature of the encephalomyelitis.

Animals↗

[Spontaneous mixed infections with distemper virus and Toxoplasma in dogs].

During a canine distemper epidemic in Switzerland in 1984/85 six cases of spontaneous mixed infections of distemper virus and Toxoplasma spec. were diagnosed. An etiologic diagnosis was made by immunohistological PAP-labelling. Pathological including histopathological findings are reported. The possibilities of histological identification of the organisms (H & E staining) are compared with immunohistology. The importance of spontaneous opportunistic infections involving protozoa is discussed.

Animals↗

Electromyographic analysis of canine distemper myoclonus.

Canine distemper myoclonus was electromyographically analysed to throw more light upon the condition without invasive surgical intervention. Although myoclonus seemed to occur synchronously in many muscles, the onset of myoclonus appeared to be slightly earlier in one or two particular muscles and, furthermore, myoclonus did not arise temporally in descending or ascending order along the neuroaxis. Myoclonus-like discharges were evoked by tendon-tapping and this feature disappeared after cessation of myoclonus. In successive myoclonic bursts, a significant positive correlation was noted between the silent period and the subsequent discharge period, independently of the level of consciousness, i.e., the longer the silent period, the longer the subsequent episode of myoclonus. This correlation was re-established very early after recovery from anesthesia with halothane, when electroencephalograms showed slow waves. These results strongly indicate that the lower motor neurons may be the primary site responsible for the genesis of canine distemper myoclonus.

Animals↗

Serum antibody response to canine parvovirus, canine adenovirus-1, and canine distemper virus in dogs with known status of immunization: study of dogs in Sweden.

Serum antibody titers to canine parvovirus (CPV), canine adenovirus-1 (CAV-1), and canine distemper virus (CDV) were measured in dogs with known immunization status. The dogs represented 3 groups: nonvaccinated dogs less than 12 months old; vaccinated dogs less than 12 months old; and adult dogs greater than 12 months old. For practical reasons, the population from which the specimens were obtained could be considered as free from natural infection with CAV-1 and CDV. In nonvaccinated dogs less than 12 months old, antibodies against all 3 viruses were measured at the time the dogs were given their first vaccination. Altogether, 50.7% of the dogs had titer greater than or equal to 1:10 to CPV, and 26.1 and 46.2% had titer greater than or equal to 1:8 to CAV-1 and CDV, respectively. The concentration of maternal antibody seemed to be of major importance for failure of immunization with use of inactivated CPV vaccine, but not with CAV-1 and CDV vaccination. In dogs less than 12 months old and vaccinated against CPV infection with inactivated virus, only 11.5% had titer greater than or equal to 1:80. In dogs vaccinated against infectious canine hepatitis and canine distemper, 63.2 and 78.3%, respectively, had titer greater than or equal to 1:16. In adult dogs greater than 2 months old and vaccinated against CPV infection, less than 50% had titer greater than or equal to 1:80, regardless of time after vaccination. There was no significant difference in titer between vaccinated and nonvaccinated dogs.(ABSTRACT TRUNCATED AT 250 WORDS)

Adenoviridae↗

[Studies on canine distemper virus. I. Virus cultivation in cell cultures].

The author studied the multiplication capacity of 2 avianized strains of canine distemper virus - Onderstepoort and Lederle Encephalitis and 2 country strains - WS-66 and LL-68 in primary cell cultures of chicken embryo fibroblasts and the dog's kidney. The strain Onderstepoort multiplied and caused cytopathological changes in the cell culture of chicken embryo fibroblasts after passaging from villousallantoic membranes of chicken embryos. Maximum titer was found between the 5th and 15th passage in the cell culture and amounted to about 10(5.0) TCID50 or about 10(5.5) EID50. In all 50 passages were carried out. However, multiplication occurred, and cytopathological changes in cell culture of chicken embryo fibroblasts were caused by the strain Lederle Encephalitis only due to the application of initial adsorption and maximum inoculum by 8 successive passages. Maximum TCID50 titre occurred after 40 passages and was about 10(4.5). Both strains preserved their ability to evoke changes on villonsallantoic membranes. Studies on the effect of the inoculum size and incubation time on the virus harvest were carried out Lederle Encephalitis strain on the level of 18-20 passages. In the culture of fibroblasts the most favourable results were obtained by using 10(2.0)-10(2.5) TCID50 inoculum per 10(5.0) cells, harvested after about 96 hr of incubation. Attempts to adapt the strains Onderstepoort and Lederle Encephalitis to cell culture of the dog's kidney gave negative results. Multiplication of the country strains of canine distemper WS-66 and LL-68 was not obtained in the cell culture of the dog's kidney and in that of chicken embryo fibroblasts in the experiment conditions.

Animals↗

Differential diagnosis of granulomatous meningoencephalomyelitis, distemper, and suppurative meningoencephalitis in the dog.

Clinical differences were determined between granulomatous meningoencephalomyelitis, distemper, and suppurative meningoencephalitis in the dog. Dogs with granulomatous meningoencephalomyelitis had "head" signs on examination, which progressed to profound caudal fossa abnormalities, changes in mental status, and tetraparesis. Dogs with distemper had a gradual onset of posterior paresis; tetraparesis and occasional vestibular signs developed later in the course of disease. Dogs with suppurative meningoencephalitis had lethargy and anorexia at the time of examination, which progressed to nuchal rigidity, mental depression, tetraparesis, and profound alterations in consciousness. Analysis of cerebral spinal fluid was useful in distinguishing suppurative meningoencephalitis from the other 2 diseases. Twenty-seven cases of inflammatory disease of the CNS in dogs were reviewed. Comparisons of history, results of physical and neurologic examinations, ancillary data, and response to treatment were made. It appeared that certain clinical and neurologic features contributed to the diagnosis of these diseases.

Animals↗

Contact transmission of distemper virus in ferrets.

Distemper virus was transmitted when infected donor ferrets were placed with susceptible ferrets for various contact periods. Distemper was more likely to be transmitted during the later stages of the disease. A positive correlation was found between the length of contact time and the acquisition of infection.

Animals↗

Canine parvovirus infection potentiates canine distemper encephalitis attributable to modified live-virus vaccine.

Twelve gnotobiotic dogs from 2 litters were allotted to 3 groups. Group A dogs received a modified-live polyvalent (canine distemper, adenovirus type 2, and parainfluenza virus and Leptospira -canicola-icterohemorrhagiae bacterin) vaccine 3 days prior to oral inoculation with canine parvovirus (CPV). Group B dogs received CPV alone. Group C dogs received 1 dose of vaccine only. In none of the 9 CPV-inoculated dogs did clinical signs of CPV infection develop, although high serum antibody titers for CPV developed in all of them. However, in 2 of the 5 CPV-inoculated vaccinates, canine distemper virus encephalomyelitis subsequently developed. The results suggested that CPV exerts an immunomodulating effect on canine immune responses and may be responsible for vaccination failures in dogs.

Animals↗

Canine bladder epithelial cells in culture: susceptibility to canine distemper and measles viruses.

A canine bladder epithelial cell strain was established in culture for the study of canine distemper virus. Epithelial cells were scraped off the bladder with a scalpel and were cultured in enriched Eagle's medium. Cells were enzymatically dispersed and passed over 46 population doublings which covered a period of more than 3 years. The cells were heteroploid when karyotyped at passage level 5 and 42. This cell strain permitted direct isolation of canine distemper virus and also showed susceptibility to laboratory strains of measles virus. Seemingly, establishment of cell strains from canine bladder epithelium can be accomplished without difficulty.

Animals↗