ABSTRACT
Cyanobacteria are sometimes widespread in lakes and can produce potent toxins, which can be dangerous for animals that drink the water, e.g. cattle and dogs. If the toxins are taken up by fish and other organisms in the food chain, or occur in drinking-water, they may pose a problem also for humans. Microcystin-LR, a hepatotoxic cyclic peptide, is one of the most frequently found cyanobacterial toxins. Data on the genotoxic potential of microcystin-LR and other cyanobacterial toxins are contradictory. Here we report results of the micronucleus assay carried out in vivo and in vitro with these toxins. To increase the sensitivity, we used the flow cytometry-based micronucleus assay in the mouse. In this study both pure microcystin-LR and cyanobacterial extracts originating from four different lakes in Sweden were analysed. Although doses up to near lethality were used and an average of 200,000 young erythrocytes, polychromatic erythrocytes, were analysed from each animal, no genotoxic effect was observed, nor could any effect be shown in the in vitro micronucleus study, using human lymphocytes. These results show that the low concentration of microcystins that now and then occur in drinking-water does not increase the cancer risk through chromosome breaks or mal-distribution of chromosomes.
Subject(s)
Bacterial Toxins/toxicity , Cyanobacteria/metabolism , Microcystins/toxicity , Micronucleus Tests , Water Microbiology , Animals , Flow Cytometry , Humans , Marine Toxins/toxicity , Mice , Micronucleus Tests/methods , SwedenABSTRACT
Forty-one outbreaks of mortality in wild finches were reported in southern Norway, Sweden, and Finland in the second half of 2008 (n = 40) and in February 2009 (n = 1). Greenfinches (Carduelis chloris) and occasional chaffinches (Fringilla coelebs) primarily were affected. Forty-eight greenfinches, eight chaffinches, one hawfinch (Coccothraustes coccothraustes), and one blue tit (Parus caeruleus) from 22 incidents were examined postmortem. Birds were in poor nutritional condition and had necrotizing ingluvitis, esophagitis, and/or oropharyngitis. Viable trichomonads with morphology consistent with Trichomonas gallinae were demonstrated successfully in 65% and 71% of fresh carcasses examined by culture and wet mount, respectively. No primary bacterial pathogens were detected. To our knowledge, this is the first report of epizootic trichomoniasis in wild finches in Europe outside of the UK.
Subject(s)
Bird Diseases/epidemiology , Finches , Trichomonas Infections/veterinary , Animals , Bird Diseases/parasitology , Disease Outbreaks/veterinary , Finland/epidemiology , Norway/epidemiology , Sweden/epidemiology , Trichomonas Infections/epidemiology , Trichomonas Infections/pathologyABSTRACT
Highly pathogenic avian influenza (HPAI) subtype H5N1 is an infectious systemic viral disease that results in high morbidity and mortality in poultry, and has been reported in a wide range of wild bird species during the last few years. An outbreak of HPAI H5N1 occurred in wild birds in Sweden in 2006 that affected several duck species, geese, swans, gulls, and raptors. Tufted ducks (Aythya fuligula) accounted for the largest number of positive cases and, therefore, were selected for more in-depth histologic and immunohistochemical evaluations. The main histologic lesions associated with the presence of avian influenza antigen were found in the brain, pancreas, and upper respiratory tract. Other tissues in which influenza antigen was variably found included liver, lung, adrenal glands, kidneys, and peripheral nerve ganglia. The current study describes the pathology and viral tissue targeting of H5N1 by using histology, polymerase chain reaction, and immunohistochemistry, and highlights the range and variation in the presentation of the natural disease in tufted ducks.
Subject(s)
Influenza A Virus, H1N1 Subtype/pathogenicity , Influenza in Birds/virology , Animals , Animals, Wild/virology , Antigens, Viral/analysis , Brain/pathology , Brain/virology , Cloaca/pathology , Cloaca/virology , Ducks/virology , Immunohistochemistry , Influenza A Virus, H1N1 Subtype/genetics , Influenza in Birds/epidemiology , Influenza in Birds/pathology , Liver/pathology , Liver/virology , Neurons/pathology , Neurons/virology , Polymerase Chain Reaction , RNA, Viral/genetics , RNA, Viral/isolation & purification , Reverse Transcriptase Polymerase Chain Reaction , Sweden/epidemiologyABSTRACT
Proventriculitis and chronic respiratory disease were diagnosed in two flocks of gray partridges (Perdix perdix) on unrelated Swedish game bird farms. Affected birds showed loss of condition, respiratory signs, and flock mortality rates of 50 and 98%, respectively. The proventricular lesions were associated closely with fungal organisms that were microscopically indistinguishable from the ascomycetous yeast Macrorhabdus ornithogaster (former provisional name "megabacterium"). At necropsy, the proventriculi were swollen and hyperemic, and viscous mucus adhered to the mucosa. Proventricular hemorrhages were commonly detected, and one bird had proventricular rupture and peritonitis. Microscopically, mild to severe subacute to chronic lymphoplasmacytic proventriculitis, microabscesses, necrosis, epithelial metaplasia, disrupted koilin, ulcers, and hemorrhages were observed. Transmission electron microscopy of the proventricular microorganisms revealed a membrane-bound nucleus, vacuoles, ribosomes, microtubules in parallel arrays, and a two-layered cell wall but no mitochondria. Scanning electron microscopy of the proventricular epithelium demonstrated masses of organisms with occasional constrictions in parallel arrangement. Many of the birds also suffered from concurrent respiratory bacterial infections and/or gastrointestinal candidiasis. The clinical course and gross and microscopic proventricular lesions were similar to those described in psittacine and passerine pet birds colonized by M. ornithogaster-like microorganisms but differed from published case reports and experimental infections of chickens in which the clinical signs and lesions have been considerably milder. The findings presented in this paper suggest that mycotic proventriculitis, presumably associated with M. ornithogaster, may be a serious but possibly opportunistic, although unusual, disease problem in gray partridges on game farms.
Subject(s)
Ascomycota/isolation & purification , Bird Diseases/diagnosis , Galliformes/microbiology , Mycoses/veterinary , Proventriculus/microbiology , Stomach Diseases/veterinary , Animals , Ascomycota/pathogenicity , Bird Diseases/mortality , Female , Immunohistochemistry/veterinary , Male , Microscopy, Electron, Scanning/veterinary , Mycoses/diagnosis , Mycoses/mortality , Stomach Diseases/diagnosis , Stomach Diseases/mortalityABSTRACT
BACKGROUND: Tularemia is a zoonosis caused by the bacterium Francisella tularensis. It has a wide host range, which includes mammals, birds and invertebrates. F. tularensis has often been isolated from various species of small rodents, but the pathology in naturally infected wild rodent species has rarely been reported. CASE PRESENTATION: Herein, we describe the pathology of tularemia in two naturally infected wild yellow-necked mice (Apodemus flavicollis). To visualize F. tularensis subsp. holarctica, indirect immunofluorescence and immunohistochemistry were applied on tissue sections. Real time polymerase chain reaction detected the bacterium in samples from liver and spleen in both mice. The only finding at necropsy was splenomegaly in one of the mice. Histological examination revealed necrotic foci in the liver associated with mild inflammation in both mice. Immunohistochemistry and indirect immunofluorescence showed bacteria disseminated in many organs, in the cytoplasm of macrophages, and intravascularly. CONCLUSIONS: The two yellow-necked mice died of an acute disease caused by tularemic infection disseminated to many organs. Further investigations of naturally infected small rodents are important to better understand the variability in pathological presentation caused by infection by F. tularensis subsp. holarctica, as well to elucidate the importance of small rodents as transmitters and/or reservoirs.
Subject(s)
Francisella tularensis/isolation & purification , Murinae , Rodent Diseases/pathology , Tularemia/veterinary , Animals , Liver/microbiology , Male , Rodent Diseases/microbiology , Spleen/microbiology , Sweden , Tularemia/microbiology , Tularemia/pathologyABSTRACT
The Baltic Sea population of the common eider (Somateria mollissima) has declined dramatically during the last two decades. Recently, widespread episodic thiamine (vitamin B1) deficiency has been demonstrated in feral birds and suggested to contribute significantly to declining populations. Here we show that the decline of the common eider population in the Baltic Sea is paralleled by high mortality of the pulli a few days after hatch, owing to thiamine deficiency and probably also thereby associated abnormal behaviour resulting in high gull predation. An experiment with artificially incubated common eider eggs collected in the field revealed that thiamine treatment of pulli had a therapeutic effect on the thiamine status of the brain and prevented death. The mortality was 53% in untreated specimens, whereas it was only 7% in thiamine treated specimens. Inability to dive was also linked to brain damage typical for thiamine deficiency. Our results demonstrate how thiamine deficiency causes a range of symptoms in the common eider pulli, as well as massive die-offs a few days after hatch, which probably are the major explanation of the recent dramatic population declines.
Subject(s)
Ducks/metabolism , Thiamine Deficiency/metabolism , Thiamine/metabolism , Animals , Baltic States , Birds , Eggs , Reproduction/drug effectsABSTRACT
Serum samples from 106 Eurasian lynx (Lynx lynx) from across Sweden, found dead or shot by hunters in 1993-99, were investigated for presence of antibodies to feline parvovirus (FPV), feline coronavirus, feline calicivirus, feline herpesvirus, feline immunodeficiency virus, Francisella tularensis, and Anaplasma phagocytophila, and for feline leukemia virus antigen. In addition, tissue samples from 22 lynx submitted in 1999 were analyzed by real-time polymerase chain reaction (PCR) to detect nucleic acids specific for viral agents and A. phagocytophila. Except for FPV antibodies in one lynx and A. phagocytophila in four lynx, all serology was negative. All PCR results also were negative. It was concluded that free-ranging Swedish lynx do not have frequent contact with the infectious agents considered in this study.
Subject(s)
Antibodies, Bacterial/blood , Antibodies, Viral/blood , Bacterial Infections/veterinary , Lynx/microbiology , Virus Diseases/veterinary , Animals , Animals, Wild/microbiology , Animals, Wild/virology , Bacterial Infections/epidemiology , Female , Lynx/parasitology , Lynx/virology , Male , Polymerase Chain Reaction/methods , Polymerase Chain Reaction/veterinary , Scabies/epidemiology , Scabies/immunology , Scabies/veterinary , Seroepidemiologic Studies , Sweden/epidemiology , Virus Diseases/epidemiologyABSTRACT
We describe tularaemia in a Norwegian dog caused by Francisella tularensis subspecies holarctica. A Hamilton Hound and his owner developed tulaeremia after hunting an infected mountain hare (Lepus timidus). The dog showed signs of lethargy, anorexia and fever during a period two to four days after hunting and thereafter fully recovered. Its antibody titers increased 32-fold from one to three weeks post exposure. Thereafter, the titer declined and leveled off at moderate positive values up to one year after exposure (end of study). This is believed to be the first case report of clinical F. tularensis subspecies holarctica infection in a European dog. In 2011, enormous numbers of Norway lemmings (Lemmus lemmus) occurred in Finnmark, the northernmost county of Norway and many dogs caught and swallowed lemmings. Some of these dogs developed non-specific signs of disease and the owners consulted a veterinary surgeon, who suspected tularaemia. In order to investigate this hypothesis, serum samples from 33 dogs were examined for antibodies to F. tularensis. The dogs were allocated into three groups: Dogs from Finnmark that became sick (Group 1) or remained healthy following contact with lemmings (Group 2), and healthy control dogs from Oslo without known contact with lemmings (Group 3). All the serum samples were analyzed with a tube agglutination assay. Among dogs exposed to lemmings, 10/11 and 3/12 were antibody positive in Group 1 and Group 2, respectively, whereas none of the control dogs (n=10) were positive for antibodies against F. tularensis. These results strongly indicate that the non-specific disease seen in the dogs in Finnmark was linked to F. tularensis infection acquired through contact with lemmings.
Subject(s)
Dog Diseases/microbiology , Dog Diseases/transmission , Francisella tularensis/immunology , Hares/microbiology , Tularemia/veterinary , Zoonoses/pathology , Agglutination Tests , Animals , Antibodies, Bacterial/blood , Arvicolinae/microbiology , Dogs , Humans , Immunohistochemistry/veterinary , Norway , Pilot Projects , Tularemia/transmissionABSTRACT
Recently, a novel mec gene conferring beta-lactam resistance in Staphylococcus aureus has been discovered. This gene, mecC, is situated on a SCCmec XI element that has to date been identified in clonal complexes 49, 130, 425, 599 and 1943. Some of the currently known isolates have been identified from animals. This, and observations of mecA alleles that do not confer beta-lactam resistance, indicate that mec genes might have a reservoir in Staphylococcus species from animals. Thus it is important also to screen wildlife isolates for mec genes. Here, we describe mecC-positive Staphylococcus aureus (ST130-MRSA-XI) and the lesions related to the infection in two diseased free-ranging European hedgehogs (Erinaceus europaeus). One was found dead in 2003 in central Sweden, and suffered from S. aureus septicaemia. The other one, found on the island of Gotland in the Baltic Sea in 2011, showed a severe dermatitis and was euthanised. ST130-MRSA-XI isolates were isolated from lesions from both hedgehogs and were essentially identical to previously described isolates from humans. Both isolates carried the complete SCCmec XI element. They lacked the lukF-PV/lukS-PV and lukM/lukF-P83 genes, but harboured a gene for an exfoliative toxin homologue previously described from Staphylococcus hyicus, Staphylococcus pseudintermedius and other S. aureus of the CC130 lineage. To the best of our knowledge, these are the first reported cases of CC130-MRSA-XI in hedgehogs. Given that one of the samples was taken as early as 2003, this was the earliest detection of this strain and of mecC in Sweden. This and several other recent observations suggest that CC130 might be a zoonotic lineage of S. aureus and that SCCmec XI/mecC may have originated from animal pathogens.
Subject(s)
Bacterial Proteins/metabolism , Hedgehogs , Methicillin-Resistant Staphylococcus aureus/genetics , Staphylococcal Infections/veterinary , Animals , Base Sequence , Fatal Outcome , Methicillin-Resistant Staphylococcus aureus/metabolism , Microarray Analysis , Microbial Sensitivity Tests , Molecular Sequence Data , Multilocus Sequence Typing , Polymerase Chain Reaction , Sequence Analysis, DNA , Species Specificity , Staphylococcal Infections/microbiology , Staphylococcal Infections/pathology , SwedenABSTRACT
BACKGROUND: Serological surveys for disease investigation of wild animal populations require obtaining blood samples for analysis, which has logistic, ethic and economic difficulties. Applying serological test to fluids collected from dead animals is an alternative. The aim of this study was to assess if antibodies could be detected in two types of fluids collected from 56 carcasses of red foxes (Vulpes vulpes): pleural fluid and lung extract. FINDINGS: In 22 (39%) foxes antibodies against Sarcoptes scabiei were detected in both fluid types by ELISA and Western blot. In 46 (82%) foxes, antibodies against Toxoplasma gondii were detected in pleural fluid and in 41 (73%) in lung extract applying a Toxo-screen test (DAT). Antibodies were still detectable in the same fluids kept at room temperature for 28 days, although in fewer foxes (16 and 14 foxes tested for T. gondii in lung extract and pleural fluid respectively; and 1 and 4 tested for S. scabiei in lung extract and pleural fluid respectively. CONCLUSIONS: These results indicate the potential utility of using fluids from carcasses for antibody screening of wild animals at the population level.
Subject(s)
Agglutination Tests/methods , Antibodies/analysis , Enzyme-Linked Immunosorbent Assay/methods , Foxes/parasitology , Scabies/epidemiology , Toxoplasmosis, Animal/epidemiology , Agglutination Tests/veterinary , Animals , Antibodies, Protozoan/analysis , Body Fluids/chemistry , Body Fluids/immunology , Body Fluids/parasitology , Enzyme-Linked Immunosorbent Assay/veterinary , Female , Foxes/immunology , Lung/immunology , Lung/parasitology , Male , Prevalence , Sarcoptes scabiei/immunology , Sweden/epidemiology , Thoracic Cavity/immunology , Thoracic Cavity/parasitology , Time Factors , Toxoplasma/immunologyABSTRACT
The bladderworm Pearsonema (syn Capillaria) plica affects domestic dogs and wild carnivores worldwide. A high prevalence in red foxes (Vulpes vulpes) has been reported in many European countries. P. plica inhabits the lower urinary tract and is considered to be of low pathogenic significance in dogs mostly causing asymptomatic infections. However, a higher level of pathogenicity has been reported in foxes. A severe cystitis associated with numerous bladderworms was found in a captive arctic fox (Vulpes lagopus) originating from the endangered Fennoscandian arctic fox population. To our knowledge this is the first description of P. plica infection in an arctic fox.
Subject(s)
Capillaria/pathogenicity , Cystitis/veterinary , Enoplida Infections/veterinary , Foxes/parasitology , Helminthiasis, Animal/parasitology , Animals , Animals, Wild , Cystitis/parasitology , Cystitis/pathology , Enoplida Infections/parasitology , Enoplida Infections/pathology , Female , Finland , Helminthiasis, Animal/pathology , Norway , Species Specificity , Sweden , Urinary Bladder/pathologyABSTRACT
BACKGROUND: During the past decade, Chorioptes mites occupying the outer ear canals have been a common finding at routine necropsies of moose (Alces alces) in Sweden, but neither the taxonomy of the mites nor lesions from the infestation have been investigated. In this study, the mites are characterized by morphological and molecular techniques, and the histopathology of the skin of the outer ear canal is described. METHODS: External auditory meatuses from 53 necropsied moose were examined for the presence of Chorioptes, and samples from outer ear canals were taken for histopathological and microbiological examination. A proportion of the mites from each moose was identified to species. The DNA was extracted from mites from three moose, and their ITS-2 sequences were determined; these sequences were compared phylogenetically to sequences from other Chorioptes taxa. RESULTS: Chorioptes mites were found in 43 (81%) of the 53 moose. The mites had morphological and genetic characteristics distinct from those of C. texanus and C. bovis, the two species generally accepted within the genus. Morphology also did not argue for a diagnosis as C. crewei, C. mydaus or C. panda. On histopathology, lesions were characterized by a hyperplastic perivascular to interstitial dermatitis with epidermal hyperkeratosis and crust formation. Dermal inflammatory infiltrates were composed of mixed T- and B-lymphocytes, plasma cells and macrophages, whereas eosinophils were notably uncommon. Staphylococcus aureus was grown from the infested epidermis of five of 14 examined moose. CONCLUSION: Chorioptes mite infestation was frequently detected in the outer ear canals of moose in Sweden. The mites were evidently pathogenic, being associated with inflammatory lesions of the external auditory meatus. Our studies indicate infestations with a previously undescribed Chorioptes species.