ABSTRACT
Mexican wolves (Canis lupus baileyi), classified as probably extinct in the wild in Mexico and endangered in the US, were reintroduced into Arizona in 1998. We combined annual serologic testing results from samples collected between 2003 and 2016 from 108 wolves and known survival data from 118 wolves born in the recovery area from 2003 to 2014 to evaluate whether exposure to canine distemper virus (CDV) or canine parvovirus (CPV) was associated with a greater risk of mortality before 2 yr of age. We used mixed-effects logistic regression to estimate the effect of CDV and CPV on the probability of mortality. Annual seroprevalence rates for CDV and CPV ranged from 0% to 62% and from 33% to 100%, respectively (median, 14.2% and 90.3%, respectively). The covariate, age at testing, had a negative effect on mortality, indicating that younger animals had lower survival, whereas sex had little effect on mortality. The best-supported model excluded any effect of CPV or CDV on death before 2 yr old at both the pack and individual level. Although our analysis did not detect an effect of these viruses on mortality before 2 yr old, CDV was later identified as the cause of mortality in two individuals in 2017. Additional information is needed to assess the impact of these diseases on Mexican wolves.
Subject(s)
Distemper Virus, Canine , Distemper/virology , Parvoviridae Infections/veterinary , Parvovirus, Canine , Wolves/virology , Animals , Distemper/epidemiology , Distemper/mortality , Endangered Species , Parvoviridae Infections/epidemiology , Parvoviridae Infections/mortality , Parvoviridae Infections/virology , Seroepidemiologic Studies , United States/epidemiologyABSTRACT
Canine distemper (CD) is the most deadly disease in dogs with mortality rates reaching 50%. The pathological agent, the CD virus (CDV), generally causes a severe systemic disease, although the nervous form can coexist with the acute catarrhal form in the same individual. In this study, we describe an outbreak of 18 cases of CD that occurred in 2015 in a German Shepherd dog population in northwestern Gabon. In addition, we determined the sequence of the CDV genotype associated with this fatal distemper infection in Gabon and compared it with other published CDV sequences. The CDV was detected using RT-PCR on cDNA from RNA of harvested brains and other organs. The identification was confirmed by sequencing amplicons. Moreover, we obtained the whole genome sequence using high-throughput sequencing. Phylogenetic analysis revealed that Gabonese CDV strain clustered with European strains belonging to the Europe genotype. This study provided the first molecular detection of the CDV strain associated with this fatal distemper infection in Central Africa region.
Subject(s)
Distemper Virus, Canine/genetics , Distemper/epidemiology , Genome, Viral , Phylogeny , RNA, Viral/genetics , Animals , Brain/pathology , Brain/virology , DNA, Complementary/genetics , Distemper/mortality , Distemper/transmission , Distemper/virology , Distemper Virus, Canine/isolation & purification , Dogs , Europe/epidemiology , Gabon/epidemiology , Genotype , High-Throughput Nucleotide Sequencing , Sequence Analysis, DNA , Survival Analysis , Whole Genome SequencingABSTRACT
Widespread deaths recently devastated the smallest known population of Ethiopian wolves. Of 7 carcasses found, all 3 tested were positive for rabies. Two wolves were subsequently vaccinated for rabies; 1 of these later died from canine distemper. Only 2 of a known population of 13 wolves survived.
Subject(s)
Disease Outbreaks , Distemper Virus, Canine/pathogenicity , Distemper/epidemiology , Rabies virus/pathogenicity , Rabies/veterinary , Wolves/virology , Animals , Animals, Wild , Distemper/immunology , Distemper/mortality , Distemper/prevention & control , Distemper Virus, Canine/immunology , Distemper Virus, Canine/isolation & purification , Dogs , Endangered Species , Ethiopia/epidemiology , Female , Male , Mortality , Rabies/epidemiology , Rabies/mortality , Rabies/prevention & control , Rabies Vaccines/administration & dosage , Rabies virus/immunology , Rabies virus/isolation & purification , Vaccination , Viral Vaccines/administration & dosageABSTRACT
Distemper disease is an infectious disease reported in several species of domestic and wild carnivores. The high mortality rate of animals infected with canine distemper virus (CDV) treated with currently available therapies has driven the study of new efficacious treatments. Mesenchymal stem cell (MSC)-based therapy is a promising therapeutic option for many degenerative, hereditary, and inflammatory diseases. Therefore, the aim of this study was to characterize stem cells derived from the canine fetal olfactory epithelium and to assess the systemic response of animals infected with CDV to symptomatic therapy and treatment with MSCs. Eight domestic mongrel dogs (N = 8) were divided into two groups: support group (SG) (N = 5) and support group + cell therapy (SGCT) (N = 3), which were monitored over 15 days. Blood samples were collected on days 0, 6, 9, 12, and 15 to assess blood count and serum biochemistry (urea, creatinine, alanine transferase, alkaline phosphatase, gamma-glutamyl transferase, total protein, albumin, and globulin), and urine samples were obtained on days 0 and 15 for urinary evaluation (urine I). The results showed a high mortality rate (SG = 4 and SGCT = 2), providing inadequate data on the clinical course of CDV infection. MSC therapy resulted in no significant improvement when administered during the acute phase of canine distemper disease, and a prevalence of animals with high mortality rate was found in both groups due to the severity of symptoms.
Subject(s)
Antibodies, Viral/blood , Distemper/therapy , Mesenchymal Stem Cell Transplantation , Animals , Distemper/blood , Distemper/mortality , Distemper/virology , Distemper Virus, Canine/pathogenicity , Dogs , Mesenchymal Stem Cells/metabolismABSTRACT
Poaching as well as loss of habitat and prey are identified as causes of tiger population declines. Although some studies have examined habitat requirements and prey availability, few studies have quantified cause-specific mortality of tigers. We used cumulative incidence functions (CIFs) to quantify cause-specific mortality rates of tigers, expanding and refining earlier studies to assess the potential impact of a newly emerging disease. To quantify changes in tiger mortality over time, we re-examined data first collected by Goodrich et al. (; study period 1: 1992-2004) as well as new telemetry data collected since January 2005 (study period 2: 2005-2012) using a total of 57 tigers (27 males and 30 females) monitored for an average of 747 days (range 26-4718 days). Across the entire study period (1992 to 2012) we found an estimated average annual survival rate of 0.75 for all tigers combined. Poaching was the primary cause of mortality during both study periods, followed by suspected poaching, distemper and natural/unknown causes. Since 2005, poaching mortality has remained relatively constant and, if combined with suspected poaching, may account for a loss of 17-19% of the population each year. Canine distemper virus (CDV) may be an additive form of mortality to the population, currently accounting for an additional 5%. Despite this relatively new source of mortality, poaching remains the main threat to Amur tiger survival and, therefore, population growth.
Subject(s)
Distemper/mortality , Tigers , Animals , Cause of Death , Distemper Virus, Canine , Ecosystem , Female , Male , Population DynamicsABSTRACT
Canine distemper virus (CDV) has recently been identified in populations of wild tigers in Russia and India. Tiger populations are generally too small to maintain CDV for long periods, but are at risk of infections arising from more abundant susceptible hosts that constitute a reservoir of infection. Because CDV is an additive mortality factor, it could represent a significant threat to small, isolated tiger populations. In Russia, CDV was associated with the deaths of tigers in 2004 and 2010, and was coincident with a localized decline of tigers in Sikhote-Alin Biosphere Zapovednik (from 25 tigers in 2008 to 9 in 2012). Habitat continuity with surrounding areas likely played an important role in promoting an ongoing recovery. We recommend steps be taken to assess the presence and the impact of CDV in all tiger range states, but should not detract focus away from the primary threats to tigers, which include habitat loss and fragmentation, poaching and retaliatory killing. Research priorities include: (i) recognition and diagnosis of clinical cases of CDV in tigers when they occur; and (ii) collection of baseline data on the health of wild tigers. CDV infection of individual tigers need not imply a conservation threat, and modeling should complement disease surveillance and targeted research to assess the potential impact to tiger populations across the range of ecosystems, population densities and climate extremes occupied by tigers. Describing the role of domestic and wild carnivores as contributors to a local CDV reservoir is an important precursor to considering control measures.
Subject(s)
Distemper Virus, Canine/physiology , Distemper/epidemiology , Tigers/virology , Animals , Conservation of Natural Resources , Disease Reservoirs/veterinary , Disease Reservoirs/virology , Distemper/mortality , Distemper/transmission , Population Dynamics , Russia/epidemiologySubject(s)
Animals, Zoo/virology , Disease Outbreaks/veterinary , Distemper Virus, Canine , Distemper/prevention & control , Distemper/transmission , Endangered Species , Ursidae/virology , Animals , Breeding , China , Disease Outbreaks/prevention & control , Distemper/mortality , Dogs , Female , MaleABSTRACT
Persistent organic pollutants are a concern for species occupying high trophic levels since they can cause immunosuppression and impair reproduction. Mass mortalities due to canine distemper virus (CDV) occurred in Caspian seals (Pusa caspica), in spring of 1997, 2000 and 2001, but the potential role of organochlorine exposure in these epizootics remains undetermined. Here we integrate Caspian seal mortality data spanning 1971-2008, with data on age, body condition, pathology and blubber organochlorine concentration for carcases stranded between 1997 and 2002. We test the hypothesis that summed PCB and DDT concentrations contributed to CDV associated mortality during epizootics. We show that age is the primary factor explaining variation in blubber organochlorine concentrations, and that organochlorine burden, age, sex, and body condition do not account for CDV infection status (positive/negative) of animals dying in epizootics. Most animals (57%, n = 67) had PCB concentrations below proposed thresholds for toxic effects in marine mammals (17 µg/g lipid weight), and only 3 of 67 animals had predicted TEQ values exceeding levels seen to be associated with immune suppression in harbour seals (200 pg/g lipid weight). Mean organonchlorine levels were higher in CDV-negative animals indicating that organochlorines did not contribute significantly to CDV mortality in epizootics. Mortality monitoring in Azerbaijan 1971-2008 revealed bi-annual stranding peaks in late spring, following the annual moult and during autumn migrations northwards. Mortality peaks comparable to epizootic years were also recorded in the 1970s-1980s, consistent with previous undocumented CDV outbreaks. Gompertz growth curves show that Caspian seals achieve an asymptotic standard body length of 126-129 cm (n = 111). Males may continue to grow slowly throughout life. Mortality during epizootics may exceed the potential biological removal level (PBR) for the population, but the low frequency of epizootics suggest they are of secondary importance compared to anthropogenic sources of mortality such as fishing by-catch.
Subject(s)
Body Constitution/drug effects , Distemper Virus, Canine/pathogenicity , Seals, Earless/virology , Water Pollutants, Chemical/toxicity , Age Factors , Aging , Animals , Biometry , Body Burden , Distemper/mortality , Distemper/pathology , Distemper/virology , Distemper Virus, Canine/genetics , Environmental Exposure , Female , Humans , Hydrocarbons, Chlorinated/toxicity , Male , RNA, Viral/analysis , Reverse Transcriptase Polymerase Chain Reaction , Seals, Earless/anatomy & histology , Seals, Earless/growth & development , Seasons , Sex FactorsABSTRACT
Canine distemper virus (CDV) has recently expanded its host range to nonhuman primates. A large CDV outbreak occurred in rhesus monkeys at a breeding farm in Guangxi Province, China, in 2006, followed by another outbreak in rhesus monkeys at an animal center in Beijing in 2008. In 2008 in Japan, a CDV outbreak also occurred in cynomolgus monkeys imported from China. In that outbreak, 46 monkeys died from severe pneumonia during a quarantine period. A CDV strain (CYN07-dV) was isolated in Vero cells expressing dog signaling lymphocyte activation molecule (SLAM). Phylogenic analysis showed that CYN07-dV was closely related to the recent CDV outbreaks in China, suggesting continuing chains of CDV infection in monkeys. In vitro, CYN07-dV uses macaca SLAM and macaca nectin4 as receptors as efficiently as dog SLAM and dog nectin4, respectively. CYN07-dV showed high virulence in experimentally infected cynomolgus monkeys and excreted progeny viruses in oral fluid and feces. These data revealed that some of the CDV strains, like CYN07-dV, have the potential to cause acute systemic infection in monkeys.
Subject(s)
Disease Outbreaks , Distemper Virus, Canine/isolation & purification , Distemper/epidemiology , Distemper/virology , Primate Diseases/epidemiology , Primate Diseases/virology , Animals , China/epidemiology , Chlorocebus aethiops , Cluster Analysis , Distemper/mortality , Distemper/pathology , Distemper Virus, Canine/classification , Distemper Virus, Canine/genetics , Distemper Virus, Canine/pathogenicity , Feces/virology , Macaca fascicularis , Macaca mulatta , Molecular Sequence Data , Phylogeny , Primate Diseases/mortality , Primate Diseases/pathology , RNA, Viral/genetics , Saliva/virology , Sequence Analysis, DNA , Survival Analysis , Vero Cells , Virus SheddingABSTRACT
Canine distemper virus (CDV) is a highly contagious pathogen of dogs. Vaccination is an effective way to protect dogs from CDV infection, but occasionally fails. In the present study, a wild type (wt) CDV, named XJ2, was isolated from a dead vaccinated dog. The hemagglutinin (H) gene of the XJ2 was amplified and analyzed for the molecular characteristics including N-glycosylation sites, phylogenesis, hydrophobicity and epitopes. The data indicated that XJ2 was a genetic variant strain of CDV. CDV-sero-negative dogs were inoculated intranasally with XJ2, developed severe clinical symptoms and died, suggesting high virulence.
Subject(s)
Distemper Virus, Canine/classification , Distemper Virus, Canine/pathogenicity , Distemper/virology , Genetic Variation , Hemagglutinins, Viral/genetics , Amino Acid Sequence , Animals , China , Chlorocebus aethiops , Distemper/mortality , Distemper/prevention & control , Distemper Virus, Canine/genetics , Distemper Virus, Canine/isolation & purification , Dogs , Hemagglutinins, Viral/chemistry , Molecular Sequence Data , Phylogeny , Sequence Analysis, DNA , Vaccination/veterinary , Vero Cells , VirulenceABSTRACT
Since 2006, canine distemper outbreaks have occurred in rhesus monkeys at a breeding farm in Guangxi, People's Republic of China. Approximately 10,000 animals were infected (25%-60% disease incidence); 5%-30% of infected animals died. The epidemic was controlled by vaccination. Amino acid sequence analysis of the virus indicated a unique strain.
Subject(s)
Distemper Virus, Canine/genetics , Distemper/epidemiology , Macaca mulatta/virology , Monkey Diseases/epidemiology , Animal Husbandry , Animals , China/epidemiology , Disease Outbreaks/veterinary , Distemper/mortality , Distemper/prevention & control , Distemper/virology , Distemper Virus, Canine/classification , Distemper Virus, Canine/immunology , Distemper Virus, Canine/isolation & purification , Dogs , Incidence , Monkey Diseases/prevention & control , Monkey Diseases/virology , Viral Vaccines/administration & dosage , Viral Vaccines/immunologyABSTRACT
Phocine distemper virus (PDV) has caused two mass mortalities of European harbour seals (Phoca vitulina) in recent decades. Levels of mortality varied considerably among European populations in both the 1988 and 2002 epidemics, with higher mortality in continental European populations in comparison to UK populations. High levels of genetic differentiation at neutral makers among seal populations allow for the possibility that there could be potential genetic differences at functional loci that may account for some of the variation in mortality. Recent genome sequencing of carnivore species and development of genomic tools have now made it possible to explore the possible contribution of variation in candidate genes from harbour seals in relation to the differential mortality patterns. We assessed variation in eight genes (CD46, IFNG, IL4, IL8, IL10, RARa, SLAM and TLR2) encoding key proteins involved in host cellular interactions with Morbilliviruses and the relationship of variants to disease status. This work constitutes the first genetic association study for Morbillivirus disease susceptibility in a non-model organism, and for a natural mortality event. We found no variation in harbour seals from across Europe in the protein coding domains of the viral receptors SLAM and CD46, but SNPs were present in SLAM intron 2. SNPs were also present in IL8 p2 and RARa exon 1. There was no significant association of SLAM or RARa polymorphisms with disease status implying no role of these genes in determining resistance to PDV induced mortality, that could be detected with the available samples and the small number of polymorphisms indentified. However there was significant differentiation of allele frequencies among populations. PDV and other morbilliviruses are important models for wildlife epidemiology, host switches and viral evolution. Despite a negative result in this case, full sequencing of pinniped and other 'non-model' carnivore genomes will help in refining understanding the role of host genetics in disease susceptibility for these viruses.
Subject(s)
Distemper Virus, Phocine/pathogenicity , Distemper/genetics , Distemper/immunology , Phoca/genetics , Phoca/immunology , Animals , Antigens, CD/genetics , Base Sequence , Case-Control Studies , DNA Primers/genetics , Distemper/mortality , Distemper/virology , Europe/epidemiology , Genes, MHC Class II , Genetic Association Studies , Genetic Predisposition to Disease , Genetic Variation , Genetics, Population , Host-Pathogen Interactions/genetics , Host-Pathogen Interactions/immunology , Phoca/virology , Polymorphism, Single Nucleotide , Receptors, Cell Surface/genetics , Receptors, Virus/genetics , Signaling Lymphocytic Activation Molecule Family Member 1ABSTRACT
In 2006 and 2007, elevated numbers of deaths among seals, constituting an unusual mortality event, occurred off the coasts of Maine and Massachusetts, United States. We isolated a virus from seal tissue and confirmed it as phocine distemper virus (PDV). We compared the viral hemagglutinin, phosphoprotein, and fusion (F) and matrix (M) protein gene sequences with those of viruses from the 1988 and 2002 PDV epizootics. The virus showed highest similarity with a PDV 1988 Netherlands virus, which raises the possibility that the 2006 isolate from the United States might have emerged independently from 2002 PDVs and that multiple lineages of PDV might be circulating among enzootically infected North American seals. Evidence from comparison of sequences derived from different tissues suggested that mutations in the F and M genes occur in brain tissue that are not present in lung, liver, or blood, which suggests virus persistence in the central nervous system.
Subject(s)
Distemper Virus, Phocine/genetics , Distemper Virus, Phocine/isolation & purification , Distemper/epidemiology , Distemper/virology , Phoca/virology , Amino Acid Sequence , Animals , Chlorocebus aethiops , Distemper/mortality , Distemper Virus, Phocine/classification , Maine , Massachusetts , Molecular Sequence Data , Mutation , RNA, Viral/genetics , Sequence Alignment , Sequence Analysis, DNA , United States , Vero Cells , Viral Proteins/geneticsABSTRACT
In 2007, disease related mortality occurred in one African wild dog (Lycaon pictus) pack close to the north-eastern boundary of the Serengeti National Park, Tanzania. Histopathological examination of tissues from six animals revealed that the main pathologic changes comprised interstitial pneumonia and suppurative to necrotizing bronchopneumonia. Respiratory epithelial cells contained numerous eosinophilic intracytoplasmic inclusion bodies and multiple syncytial cells were found throughout the parenchymal tissue, both reacting clearly positive with antibodies against canine distemper virus (CDV) antigen. Phylogenetic analysis based on a 388 nucleotide (nt) fragment of the CDV phosphoprotein (P) gene revealed that the pack was infected with a CDV variant most closely related to Tanzanian variants, including those obtained in 1994 during a CDV epidemic in the Serengeti National Park and from captive African wild dogs in the Mkomazi Game Reserve in 2000. Phylogenetic analysis of a 335-nt fragment of the fusion (F) gene confirmed that the pack in 2007 was infected with a variant most closely related to one variant from 1994 during the epidemic in the Serengeti National Park from which a comparable fragment is available. Screening of tissue samples for concurrent infections revealed evidence of canine parvovirus, Streptococcus equi subsp. ruminatorum and Hepatozoon sp. No evidence of infection with Babesia sp. or rabies virus was found. Possible implications of concurrent infections are discussed. This is the first molecular characterisation of CDV in free-ranging African wild dogs and only the third confirmed case of fatal CDV infection in a free-ranging pack.
Subject(s)
Animals, Wild/virology , Distemper Virus, Canine/physiology , Distemper/virology , Animals , Coccidia/physiology , Coccidiosis/complications , Coccidiosis/veterinary , Distemper/complications , Distemper/epidemiology , Distemper/mortality , Distemper/pathology , Distemper Virus, Canine/genetics , Distemper Virus, Canine/isolation & purification , Dog Diseases/microbiology , Dog Diseases/parasitology , Dogs , Ecosystem , Lung/pathology , Molecular Sequence Data , Phosphoproteins/genetics , Phylogeny , Streptococcal Infections/complications , Streptococcal Infections/veterinary , Streptococcus equi/physiology , Tanzania/epidemiology , Viral Fusion Proteins/geneticsABSTRACT
Fifteen 8-month-old fennec foxes imported from Sudan showed fever, mucopurulent ocular discharge, diarrhea, severe emaciation, seizures, and generalized ataxia, and died. Three of the 15 animals were presented for diagnostic investigation. Severe dehydration, brain congestion, and gastric ulcers were observed in all animals. In one animal, the lungs had failed to collapse and were multifocally dark red in appearance. Histopathologically, there were lymphohistiocytic meningoencephalitis with malacia, mild interstitial pneumonia, lymphoid depletion of lymphoid tissues and organs, and intestinal villous atrophy with intralesional coccidia. There were many intracytoplasmic and/or intranuclear inclusion bodies in the epithelial cells of the medullary velum, lungs, liver, kidneys, trachea, pancreas, stomach, gall bladder, urinary bladder, and ureters, and in macrophages of malacia foci and lymphocytes and macrophages of lymphoid organs. Additionally, intestinal coccidia were confirmed to be Isospora species by a fecal test. To our knowledge, this is the first report of canine distemper with intestinal coccidiosis in fennec fox.
Subject(s)
Distemper Virus, Canine/pathogenicity , Distemper/diagnosis , Animals , Atrophy , DNA Primers , Dehydration/pathology , Dehydration/veterinary , Dehydration/virology , Distemper/mortality , Distemper/pathology , Distemper Virus, Canine/genetics , Distemper Virus, Canine/isolation & purification , Dogs , Emaciation/pathology , Emaciation/veterinary , Emaciation/virology , Eye Diseases/pathology , Eye Diseases/veterinary , Eye Diseases/virology , Female , Foxes , Genome, Viral , Lymphoid Tissue/pathology , Lymphoid Tissue/virology , Male , Reverse Transcriptase Polymerase Chain Reaction , SudanABSTRACT
The island fox (Urocyon littoralis catalinae) population on Santa Catalina Island, California, USA declined precipitously in 1999 with an approximate 95% reduction on their eastern range, an area representing 87% of the island. During this investigation, between October 1999 and April 2000, evidence of live foxes dramatically decreased. The only carcass recovered during the decline succumbed to a co-infection of canine distemper virus (CDV) and toxoplasmosis. Sequence analysis of the viral P gene, derived by polymerase chain reaction, indicated that the virus was closely related to CDV from a mainland USA raccoon (Procyon lotor). Nine of 10 foxes trapped in 1999-2000, on the eastern portion of the island after the decline, had serologic evidence of exposure to CDV, whereas only four of 19 foxes trapped in this region in 1998 had antibodies reactive against CDV. The confirmation of CDV in one deceased fox, evidence of exposure to CDV in east-end foxes in 1999-2000 compared to 1998, and documentation of raccoon introductions to the island, implicates canine distemper as the cause of the population decline.
Subject(s)
Antibodies, Viral/blood , Distemper Virus, Canine/immunology , Distemper/epidemiology , Distemper/mortality , Foxes , Animals , California/epidemiology , Demography , Distemper/pathology , Distemper/transmission , Distemper Virus, Canine/isolation & purification , Female , Foxes/virology , Health Status , Male , Polymerase Chain Reaction/veterinary , Seroepidemiologic Studies , Toxoplasmosis, Animal/epidemiology , Toxoplasmosis, Animal/mortality , Toxoplasmosis, Animal/pathology , Toxoplasmosis, Animal/transmissionABSTRACT
In 2002, the northern European harbour seal (Phoca vitulina) population experienced an epidemic of phocine distemper virus (PDV) in which 22,000 seals died. Clinical signs were recorded in 20 harbour seal pups admitted to the Seal Rehabilitation and Research Centre with clinical disease, and they were diagnosed PDV infection-positive by RT-PCR postmortem. All 20 had respiratory signs, 14 had conjunctivitis and 10 had neurological signs. Severe neurological signs were one of the criteria for euthanasia during the epidemic, and many pups that were euthanased were not included in this study owing to the lack of complete datasets. Neurological signs were therefore among the most prevalent signs of fatal PDV infection in harbour seal pups. The lymphoid depletion reported in dead seals during the epidemic was not reflected in the total mononuclear leucocyte count of the seal pups, but they had an absolute granulocytosis, thrombocytosis, anaemia, and high total white blood cell counts. When first examined, 11 of the pups had a positive serum IgG titre, and four had a positive serum IgM titre. High levels of PDV-specific serum IgG antibodies were not correlated with an absence of clinical signs or longer survival.
Subject(s)
Distemper Virus, Phocine , Distemper/complications , Nervous System Diseases/veterinary , Phoca/microbiology , Animals , Disease Outbreaks/veterinary , Distemper/blood , Distemper/diagnosis , Distemper/mortality , Distemper Virus, Phocine/genetics , Distemper Virus, Phocine/immunology , Distemper Virus, Phocine/isolation & purification , Euthanasia, Animal , Immunoglobulin G/blood , Immunohistochemistry/veterinary , Nervous System Diseases/virology , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Vaccination/veterinaryABSTRACT
The European mink, Mustela lutreola, has suffered a dramatic decline in Europe during the 20th century and is one of the most endangered carnivores in the world. The subpopulation of European mink from Navarra, Spain, estimated to number approximately 420, represents approximately two thirds of the total number of mink in Spain. Aleutian Disease Virus (ADV) is a parvovirus with a high degree of variability that can infect a broad range of mustelid hosts. The pathogenesis of this virus in small carnivores is variable and can be influenced by both host factors (e.g., species, American mink genotype, and immune status) and viral strain. A cross-sectional study was conducted during the pre-reproductive period of February-March 2004 and 2005 and the postreproductive period of September-December 2004. Mink were intensively trapped along seven rivers that were representative of the European mink habitat in Navarra. Antibody counter immunoelectrophoresis against ADV was performed on 84 European mink blood samples. All the samples were negative. Protein electrophoresis was performed on 93 plasma samples. Nine of those samples (9.6%) had gamma globulin levels exceeding 20% of the total plasma protein. Complete necropsies were performed on 23 cadavers of European mink collected in the area between 2000 and 2005. Seventeen of the mink (74%) had traumatic and hemorrhagic lesions compatible with vehicular impact injuries. Although there were no histopathologic lesions associated with ADV, this study documents the first description of a naturally occurring canine distemper virus infection in a European mink. In addition, pulmonary adiaspiromycosis in three European mink from Spain was reported.
Subject(s)
Accidents, Traffic , Aleutian Mink Disease Virus/immunology , Aleutian Mink Disease/epidemiology , Antibodies, Viral/blood , Distemper/epidemiology , Mink , Aleutian Mink Disease/mortality , Animals , Animals, Wild/microbiology , Animals, Wild/virology , Cause of Death , Conservation of Natural Resources , Cross-Sectional Studies , Distemper/mortality , Distemper Virus, Canine , Female , Male , Mycoses/epidemiology , Mycoses/mortality , Mycoses/veterinary , Seasons , Seroepidemiologic Studies , Spain/epidemiologyABSTRACT
Extreme climatic conditions may alter historic host-pathogen relationships and synchronize the temporal and spatial convergence of multiple infectious agents, triggering epidemics with far greater mortality than those due to single pathogens. Here we present the first data to clearly illustrate how climate extremes can promote a complex interplay between epidemic and endemic pathogens that are normally tolerated in isolation, but with co-infection, result in catastrophic mortality. A 1994 canine distemper virus (CDV) epidemic in Serengeti lions (Panthera leo) coincided with the death of a third of the population, and a second high-mortality CDV epidemic struck the nearby Ngorongoro Crater lion population in 2001. The extent of adult mortalities was unusual for CDV and prompted an investigation into contributing factors. Serological analyses indicated that at least five "silent" CDV epidemics swept through the same two lion populations between 1976 and 2006 without clinical signs or measurable mortality, indicating that CDV was not necessarily fatal. Clinical and pathology findings suggested that hemoparsitism was a major contributing factor during fatal epidemics. Using quantitative real-time PCR, we measured the magnitude of hemoparasite infections in these populations over 22 years and demonstrated significantly higher levels of Babesia during the 1994 and 2001 epidemics. Babesia levels correlated with mortalities and extent of CDV exposure within prides. The common event preceding the two high mortality CDV outbreaks was extreme drought conditions with wide-spread herbivore die-offs, most notably of Cape buffalo (Syncerus caffer). As a consequence of high tick numbers after the resumption of rains and heavy tick infestations of starving buffalo, the lions were infected by unusually high numbers of Babesia, infections that were magnified by the immunosuppressive effects of coincident CDV, leading to unprecedented mortality. Such mass mortality events may become increasingly common if climate extremes disrupt historic stable relationships between co-existing pathogens and their susceptible hosts.
Subject(s)
Climate , Distemper/epidemiology , Lions , Africa/epidemiology , Animals , Distemper/complications , Distemper/mortalityABSTRACT
European harbour seal (Phoca vitulina) populations decreased substantially during the phocine distemper virus (PDV) outbreaks of 1988 and 2002. Different hypotheses have stated that various seals and terrestrial carnivore species might be the source of infection. To further analyse these hypotheses, grey (Halichoerus grypus) and ringed (Phoca hispida) seals, polar bears (Ursus maritimus) and minks (Mustela lutreola) were sampled from the North Sea and East Greenland coasts between 1988 and 2004 and investigated by RT-PCR using a panmorbillivirus primer pair. However, all samples were negative for morbillivirus nucleic acid.