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1.
Euro Surveill ; 29(25)2024 Jun.
Article in English | MEDLINE | ID: mdl-38904109

ABSTRACT

Highly pathogenic avian influenza (HPAI) has caused widespread mortality in both wild and domestic birds in Europe 2020-2023. In July 2023, HPAI A(H5N1) was detected on 27 fur farms in Finland. In total, infections in silver and blue foxes, American minks and raccoon dogs were confirmed by RT-PCR. The pathological findings in the animals include widespread inflammatory lesions in the lungs, brain and liver, indicating efficient systemic dissemination of the virus. Phylogenetic analysis of Finnish A(H5N1) strains from fur animals and wild birds has identified three clusters (Finland I-III), and molecular analyses revealed emergence of mutations known to facilitate viral adaptation to mammals in the PB2 and NA proteins. Findings of avian influenza in fur animals were spatially and temporally connected with mass mortalities in wild birds. The mechanisms of virus transmission within and between farms have not been conclusively identified, but several different routes relating to limited biosecurity on the farms are implicated. The outbreak was managed in close collaboration between animal and human health authorities to mitigate and monitor the impact for both animal and human health.


Subject(s)
Animals, Wild , Charadriiformes , Disease Outbreaks , Influenza A Virus, H5N1 Subtype , Influenza in Birds , Phylogeny , Animals , Influenza in Birds/virology , Influenza in Birds/epidemiology , Finland/epidemiology , Influenza A Virus, H5N1 Subtype/genetics , Influenza A Virus, H5N1 Subtype/pathogenicity , Influenza A Virus, H5N1 Subtype/isolation & purification , Animals, Wild/virology , Charadriiformes/virology , Disease Outbreaks/veterinary , Farms , Orthomyxoviridae Infections/veterinary , Orthomyxoviridae Infections/virology , Orthomyxoviridae Infections/mortality , Orthomyxoviridae Infections/epidemiology , Foxes/virology , Birds/virology , Mink/virology
2.
Comp Immunol Microbiol Infect Dis ; 105: 102114, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38142559

ABSTRACT

Modified live canine distemper virus (CDV) vaccines are widely used and considered both safe and effective. Although there are occasional literature reports of suspected vaccine-induced disease, there are none where the vaccine strain has been identified in affected tissues. Here we describe two such cases in different litters. In litter A, five of ten puppies presented with fever, anorexia, vomiting, and diarrhea a few days post-vaccination. Four puppies died or were euthanized, and autopsy revealed atypical necrosis of the lymphoid tissue. In litter B, two of five puppies developed typical neurological signs some months post-vaccination and autopsy revealed encephalitis. In all cases, affected organs tested positive for CDV on immunohistochemistry, and CDV RNA extracted from the lesions confirmed the presence of vaccine strain. Since multiple puppies from each litter were affected, it cannot be excluded without further studies that some undiagnosed inherited immunodeficiency disorder may have been involved.


Subject(s)
Distemper Virus, Canine , Distemper , Dog Diseases , Viral Vaccines , Dogs , Animals , Viral Vaccines/adverse effects , Distemper/diagnosis , Distemper/prevention & control , Vaccination/adverse effects , Vaccination/veterinary , Vaccines, Attenuated/adverse effects , Distemper Virus, Canine/genetics , Dog Diseases/diagnosis
3.
J Comp Pathol ; 188: 52-61, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34686278

ABSTRACT

Atherosclerosis is a chronic inflammatory vascular disease and the leading cause of mortality in humans worldwide. In most domestic animal species, however, primary atherosclerosis is of little clinical relevance. Cats are considered to be atheroresistant and, to our knowledge, spontaneous atherosclerosis has not been reported in cats. Here we report the clinical and histopathological findings in two related cats of the Korat breed that presented with clinical signs of heart failure. In both cases, the clinical signs appeared in adulthood, were progressive and led to death. At necropsy, severe atherosclerotic lesions were present in large and medium-sized arteries and were characterized by the formation of a fibrous cap and a lipid core, which contained a particularly large accumulation of cholesterol crystals, as indicated by the presence of many cholesterol clefts. The lesions closely resembled those of advanced human atherosclerosis. There were no underlying diseases or medical treatments that could have predisposed to the atherosclerosis in these two genetically related cats. A genetic predisposition to human-like atherosclerosis in the local Korat cat population is suspected.


Subject(s)
Atherosclerosis , Cat Diseases , Animals , Atherosclerosis/diagnosis , Atherosclerosis/veterinary , Cat Diseases/diagnosis , Cats , Genetic Predisposition to Disease , Lipids
4.
J Vet Intern Med ; 35(3): 1455-1465, 2021 May.
Article in English | MEDLINE | ID: mdl-33734486

ABSTRACT

BACKGROUND: Shaking puppy syndrome is commonly attributed to abnormal myelination of the central nervous system. HYPOTHESIS/OBJECTIVES: To report the long-term clinical course and the imaging characteristics of hypomyelinating leukodystrophy in German Shepherd dogs. ANIMALS AND METHODS: Three related litters with 11 affected dogs. RESULTS: The 11 affected dogs experienced coarse, side-to-side tremors of the head and trunk, which interfered with normal goal-oriented movements and disappeared at rest. Signs were noticed shortly after birth. Nine dogs were euthanized, 3 dogs underwent pathological examination, and 2 littermates were raised by their breeder. Tremors improved gradually until 6 to 7 months of age. Adult dogs walked with severe residual pelvic limb ataxia. One dog developed epilepsy with tonic-clonic seizures at 15 months of age. Conventional magnetic resonance imaging (MRI) disclosed homogenous hyperintense signal of the entire subcortical white matter in 3 affected 7-week-old dogs and a hypointense signal in a presumably unaffected littermate. Subcortical white matter appeared isointense to gray matter at 15 and 27 weeks of age on repeated MRI. Abnormal white matter signal with failure to display normal gray-white matter contrast persisted into adulthood. Cerebellar arbor vitae was not visible at any time point. Clinical signs, MRI findings, and pathological examinations were indicative of a hypomyelinating leukodystrophy. All parents of the affected litters shared a common ancestor and relatedness of the puppies suggested an autosomal recessive mode of inheritance. CONCLUSION: We describe a novel hypomyelinating leukodystrophy in German Shepherd dogs with a suspected inherited origin.


Subject(s)
Dog Diseases , White Matter , Animals , Ataxia/veterinary , Cerebral Cortex , Dog Diseases/diagnostic imaging , Dogs , Magnetic Resonance Imaging/veterinary , Syndrome , White Matter/diagnostic imaging
5.
Access Microbiol ; 2(11): acmi000168, 2020.
Article in English | MEDLINE | ID: mdl-33294771

ABSTRACT

Rescue dog activity is a heavily increasing form of dog charity. Imported homeless dogs represent a reservoir of zoonotic diseases putting owners, veterinarians and pathologists repeatedly at risk. The clinical signs of tuberculosis in a dog are non-specific and diagnosis is often delayed or dismissed. We present a case of 9 months of possible exposure at home and definite exposure at laparotomy and autopsy to intestinal tuberculosis in a family dog imported from Romania to Finland. Persistent gastrointestinal symptoms started 2 years after the import. Abdominal pain, diarrhoea and vomiting proceeded and led to spontaneous death. Mycobacterium tuberculosis was identified in the liver, lymph nodes and intestine at autopsy. Exposed persons were notified and follow-up was provided, and no further infections were identified within 12 months of follow-up. The heavily increasing import of companion animals presents unexpected public health risks, such as prolonged exposure to tuberculosis, of which the general public is not aware. The dramatic consequences and high costs of tuberculosis could be reduced through accessible information of the risks of imported animals to both the general public and veterinarians, in addition to availability of rapid diagnostics and proper personal protection.

6.
Sci Rep ; 9(1): 973, 2019 01 30.
Article in English | MEDLINE | ID: mdl-30700765

ABSTRACT

Inherited skeletal disorders affect both humans and animals. In the current study, we have performed series of clinical, pathological and genetic examinations to characterize a previously unreported skeletal disease in the Karelian Bear Dog (KBD) breed. The disease was recognized in seven KBD puppies with a variable presentation of skeletal hypomineralization, growth retardation, seizures and movement difficulties. Exome sequencing of one affected dog revealed a homozygous missense variant (c.1301T > G; p.V434G) in the tissue non-specific alkaline phosphatase gene, ALPL. The identified recessive variant showed full segregation with the disease in a cohort of 509 KBDs with a carrier frequency of 0.17 and was absent from 303 dogs from control breeds. In humans, recessive and dominant ALPL mutations cause hypophosphatasia (HPP), a metabolic bone disease with highly heterogeneous clinical manifestations, ranging from lethal perinatal hypomineralization to a relatively mild dental disease. Our study reports the first naturally occurring HPP in animals, resembling the human infantile form. The canine HPP model may serve as a preclinical model while a genetic test will assist in breeding programs.


Subject(s)
Alkaline Phosphatase/genetics , Dog Diseases/enzymology , Dog Diseases/genetics , Dogs/genetics , Hypophosphatasia/genetics , Hypophosphatasia/veterinary , Mutation, Missense/genetics , Alkaline Phosphatase/chemistry , Amino Acid Sequence , Animals , Breeding , Calcification, Physiologic/genetics , Conserved Sequence , Dog Diseases/urine , Ethanolamines/urine , Female , Homozygote , Hypophosphatasia/diagnostic imaging , Hypophosphatasia/physiopathology , Male , Osteogenesis/genetics , Pedigree , Protein Domains , Exome Sequencing
7.
J Wildl Dis ; 54(4): 838-842, 2018 10.
Article in English | MEDLINE | ID: mdl-29889007

ABSTRACT

Rabbit hemorrhagic disease (RHD) was detected in European rabbits ( Oryctolagus cuniculus) for the first time ever in Finland in 2016. Reports of dead feral rabbits in Helsinki started to accumulate from April 2016. The Finnish Food Safety Authority Evira received the first animals in late April, and the main necropsy finding was severe, acute necrotizing hepatitis. Genetic material from RHD virus (RHDV) was detected in the liver and was further characterized as RHDV2. The Finnish virus did not group with RHDV strains from a concurrent outbreak in neighboring Sweden, suggesting another origin. The outbreak peaked in May and lasted until August, after which sightings of both live and dead rabbits became rare. No major outbreaks in domestic rabbits were observed, although infection in one pet rabbit was confirmed.


Subject(s)
Caliciviridae Infections/veterinary , Disease Outbreaks/veterinary , Hemorrhagic Disease Virus, Rabbit , Rabbits/virology , Animals , Caliciviridae Infections/epidemiology , Caliciviridae Infections/virology , Finland/epidemiology
8.
Acta Vet Scand ; 59(1): 62, 2017 Sep 25.
Article in English | MEDLINE | ID: mdl-28946904

ABSTRACT

European bat lyssavirus type 2 (EBLV-2) was detected in Finland in a Daubenton's bat (Myotis daubentonii) found in the municipality of Inkoo (60°02'45″N, 024°00'20″E). The bat showed neurological signs and was later found dead. The laboratory analysis revealed the presence of lyssavirus, and the virus was characterized as EBLV-2. This isolation of EBLV-2 was the second time that the virus has been detected in a Daubenton's bat in Finland. This provides additional proof that EBLV-2 is endemic in the Finnish Daubenton's bat population.


Subject(s)
Chiroptera , Lyssavirus/isolation & purification , Rhabdoviridae Infections/veterinary , Animals , Female , Finland , Lyssavirus/classification , Phylogeny , Rhabdoviridae Infections/virology
9.
Acta Vet Scand ; 56: 84, 2014 Dec 10.
Article in English | MEDLINE | ID: mdl-25492266

ABSTRACT

BACKGROUND: Leishmania spp. are zoonotic protozoans that infect humans and other mammals such as dogs. The most significant causative species in dogs is L. infantum. In dogs, leishmaniosis is a potentially progressive, chronic disease with varying clinical outcomes. Autochthonous cases of canine leishmaniosis have not previously been reported in the Nordic countries. RESULTS: In this report we describe the first diagnosed autochthonous cases of canine leishmaniosis in Finland, in which transmission via a suitable arthropod vector was absent. Two Finnish boxers that had never been in endemic areas of Leishmania spp., had never received blood transfusions, nor were infested by ectoparasites were diagnosed with leishmaniosis. Another dog was found with elevated Leishmania antibodies. A fourth boxer dog that had been in Spain was considered to be the source of these infections. Transmission occurred through biting wounds and semen, however, transplacental infection in one of the dogs could not be ruled out. Two of the infected dogs developed a serious disease and were euthanized and sent for necropsy. The first one suffered from membranoproliferative glomerulonephritis and the second one had a chronic systemic disease. Leishmania sp. was detected from tissues by PCR and/or IHC in both dogs. The third infected dog was serologically positive for Leishmania sp. but remained free of clinical signs. CONCLUSIONS: This case report shows that imported Leishmania-infected dogs may pose a risk for domestic dogs, even without suitable local arthropod vectors.


Subject(s)
Dog Diseases/transmission , Leishmania/isolation & purification , Leishmaniasis/veterinary , Animals , Dog Diseases/parasitology , Dogs , Female , Finland , Leishmaniasis/parasitology , Leishmaniasis/transmission , Male , Polymerase Chain Reaction/veterinary , Spain
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