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1.
Acta Vet Scand ; 57: 60, 2015 Sep 26.
Article in English | MEDLINE | ID: mdl-26410386

ABSTRACT

BACKGROUND: Porcine sapovirus, belonging to the family Caliciviridae, is an enteric virus that is widespread in the swine industry worldwide. A total of 14 sapovirus genogroups have been suggested and the most commonly found genogroup in swine is genogroup III (GIII). The goal of the present experiment was to examine the presence of sapovirus in 51 naturally infected pigs at two different time points. The pigs were kept under experimental conditions after weaning. Previous studies on sapovirus have primarily been of a cross sectional nature, typically prevalence studies performed on farms and abattoirs. In the present study, faecal samples, collected from each pig at 5½ weeks and 15-18 weeks of age, were analysed for sapovirus by reverse transciptase polymerase chain reaction and positive findings were genotyped by sequencing. RESULTS: At 5½ weeks of age, sapovirus was detected in the majority of the pigs. Sequencing revealed four different strains in the 5½ week olds-belonging to genogroups GIII and GVII. Ten to 13 weeks later, the virus was no longer detectable from stools of infected pigs. However, at this time point 13 pigs were infected with another GIII sapovirus strain not previously detected in the pigs studied. This GIII strain was only found in pigs that, in the initial samples, were virus-negative or positive for GVII. CONCLUSIONS: At 5 weeks of age 74 % of the pigs were infected with sapovirus. At 15-18 weeks of age all pigs had cleared their initial infection, but a new sapovirus GIII strain was detected in 25 % of the pigs. None of the pigs initially infected with the first GIII strain were reinfected with this new GIII strain, which may indicate the presence of a genogroup-specific immunity.


Subject(s)
Caliciviridae Infections/veterinary , Sapovirus/genetics , Swine Diseases/virology , Viral Proteins/genetics , Animals , Caliciviridae Infections/virology , Feces/virology , Molecular Sequence Data , Phylogeny , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Sapovirus/isolation & purification , Sequence Analysis, DNA/veterinary , Swine , Weaning
2.
Biochem Biophys Res Commun ; 402(2): 247-51, 2010 Nov 12.
Article in English | MEDLINE | ID: mdl-20939999

ABSTRACT

Dialysis related amyloidosis (DRA) is a serious complication to long-term hemodialysis treatment which causes clinical symptoms such as carpal tunnel syndrome and destructive arthropathies. The disease is characterized by the assembly and deposition of ß2-microglobulin (ß2m) predominantly in the musculoskeletal system, but the initiating events leading to ß2m amyloidogenesis and the molecular mechanisms underlying amyloid fibril formation are still unclear. Glycosaminoglycans (GAGs) and metal ions have been shown to be related to the onset of protein aggregation and to promote de novo fiber formation. In this study, we show that fibrillogenesis of a cleavage variant of ß2m, ΔK58-ß2m, which can be found in the circulation of hemodialysis patients and is able to fibrillate at near-physiological pH in vitro, is affected by the presence of copper ions and heparan sulfate. It is found that the fibrils generated when heparan sulfate is present have increased length and diameter, and possess enhanced stability and seeding properties. However, when copper ions are present the fibrils are short, thin and less stable, and form at a slower rate. We suggest that heparan sulfate stabilizes the cleaved monomers in the early aggregates, hereby promoting the assembly of these into fibrils, whereas the copper ions appear to have a destabilizing effect on the monomers. This keeps them in a structure forming amorphous aggregates for a longer period of time, leading to the formation of spherical bodies followed by the assembly of fibrils. Hence, the in vivo formation of amyloid fibrils in DRA could be initiated by the generation of ΔK58-ß2m which spontaneously aggregate and form fibrils. The fibrillogenesis is enhanced by the involvement of GAGs and/or metal ions, and results in amyloid-like fibrils able to promote the de novo formation of ß2m amyloid by a scaffold mechanism.


Subject(s)
Amyloid/metabolism , Glycosaminoglycans/metabolism , beta 2-Microglobulin/metabolism , Amyloid/ultrastructure , Amyloidosis/metabolism , Copper/metabolism , Copper/pharmacology , Glycosaminoglycans/pharmacology , Heparitin Sulfate/metabolism , Humans , Renal Dialysis/adverse effects
3.
J Clin Virol ; 46(3): 265-9, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19695950

ABSTRACT

BACKGROUND: Sapoviruses are known to cause gastroenteritis mainly in young children. OBJECTIVES: To establish a collection of sapoviruses and to gain knowledge about the genetic diversity and epidemiology of sapoviruses circulating in children in Denmark. STUDY DESIGN: During a 24-month period in 2005-2007 samples from 1104 children, aged 0-3 years, submitted for acute gastroenteritis diagnostics, were analysed for sapoviruses by real-time PCR. Genotyping of positive findings was carried out by sequencing part of the capsid gene, and in several cases also part of the polymerase gene. RESULTS: Sapoviruses were detected in stool samples from 97 children (9%), with the highest prevalence in the 7-18 months age group. Viruses from three genogroups and seven genotypes were found. Genotype I.1 was demonstrated in half of the positive samples and was observed throughout the study period. The less common types seemed to appear during shorter periods, often in succession of each other. Positive samples were detected throughout the study period. The only months, in both years studied, with high proportions of positive samples were September, November and February. CONCLUSIONS: Sapoviruses were commonly found in children with gastroenteritis in Denmark. No clear seasonal pattern could be seen. Genotype I.1 was clearly the most common genotype found, but several other genotypes circulated during shorter periods.


Subject(s)
Caliciviridae Infections/virology , Gastroenteritis/virology , Sapovirus/genetics , Capsid Proteins/genetics , Child, Preschool , Denmark , Female , Genotype , Humans , Infant , Infant, Newborn , Male , Molecular Epidemiology , Phylogeny , Prevalence , Prospective Studies
4.
Biochem Biophys Res Commun ; 381(2): 187-91, 2009 Apr 03.
Article in English | MEDLINE | ID: mdl-19232323

ABSTRACT

Beta2-microglobulin (beta2m) deposits as amyloid in dialysis-related amyloidosis (DRA), predominantly in joints. The molecular mechanisms underlying the amyloidogenicity of beta2m are still largely unknown. In vitro, acidic conditions, pH < 4.5, induce amyloid fibrillation of native beta2m within several days. Here, we show that amyloid fibrils are generated in less than an hour when a cleavage variant of beta2m--found in the circulation of many dialysis patients--is exposed to pH levels (pH 6.6) occurring in joints during inflammation. Aggregation and fibrillation, including seeding effects with intact, native beta2m were studied by Thioflavin T fluorescence spectroscopy, turbidimetry, capillary electrophoresis, and electron microscopy. We conclude that a biologically relevant variant of beta2m is amyloidogenic at slightly acidic pH. Also, only a very small amount of preformed fibrils of this variant is required to induce fibrillation of native beta2m. This may explain the apparent lack of detectable amounts of the variant beta2m in extracts of amyloid from DRA patients.


Subject(s)
Amyloid/metabolism , Arthritis/metabolism , beta 2-Microglobulin/metabolism , Acids/metabolism , Amyloid/chemistry , Humans , Hydrogen-Ion Concentration , Joints/metabolism , Protein Stability , beta 2-Microglobulin/chemistry , beta 2-Microglobulin/genetics
5.
J Virol Methods ; 134(1-2): 92-8, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16417929

ABSTRACT

It is possible to visualize rapidly viral particles by electron microscopy (EM) in patient samples and in cell cultures, and characterize the particles on the basis of their size and morphology. In many instances, EM has contributed to the diagnosis of specific infectious agents. Four different types of viruses with different characteristics of particle size, capsid structure, the presence or absence of an envelope, genomic content and stability outside the host were screened and diagnosed by EM at the level of family/genus. The results were confirmed at the species level by elution of the sample material from the grids used for EM examination and nucleic acid amplification. This approach could be valuable in situations where the immediate diagnosis is unclear, or when new infectious agents appear.


Subject(s)
Adenoviridae/isolation & purification , Cytomegalovirus/isolation & purification , Influenza A virus/isolation & purification , Microscopy, Electron, Transmission , Norovirus/isolation & purification , Nucleic Acid Amplification Techniques , Adenoviridae/genetics , Adenoviridae/ultrastructure , Adenoviridae Infections/diagnosis , Adenoviridae Infections/virology , Animals , Caliciviridae Infections/diagnosis , Caliciviridae Infections/virology , Cytomegalovirus/genetics , Cytomegalovirus/ultrastructure , Cytomegalovirus Infections/diagnosis , Cytomegalovirus Infections/virology , DNA, Viral/genetics , Eye/virology , Feces/virology , Humans , Influenza A virus/genetics , Influenza A virus/ultrastructure , Influenza, Human/diagnosis , Influenza, Human/virology , Norovirus/genetics , Norovirus/ultrastructure , RNA, Viral/genetics , Sensitivity and Specificity , Species Specificity , Tissue Embedding , Trachea/virology , Urine/virology
6.
Scand J Infect Dis ; 36(11-12): 840-7, 2004.
Article in English | MEDLINE | ID: mdl-15764171

ABSTRACT

In 2000, a large enterovirus (EV) outbreak was seen in Denmark; the number of patients with a verified EV infection was 3-fold higher compared to previous y. Echovirus 30 (E30) was the dominant EV type and was detected in 31% of all 306 EV positive patients and in 61% of the 155 patients in whom typing was successful. The outbreak started in February and peaked in June, which is unusually early in a temperate climate and not registered before in Denmark. The age distribution of the patients also differed from previous y with a significantly higher proportion of older children and adults being affected. The patients had mainly symptoms consistent with aseptic meningitis. A phylogenetic analysis based upon a part of the VP1 structural gene of 21 E30 isolates showed that the Danish isolates belonged to the E30 genotype which has prevailed in Europe during the last few years. However, they constituted a separated cluster compared with 2 other outbreaks in other parts of Europe in 2000.


Subject(s)
Enterovirus Infections/epidemiology , Enterovirus/genetics , Meningitis, Aseptic/virology , Molecular Epidemiology , Adolescent , Adult , Age Distribution , Child , Child, Preschool , Denmark/epidemiology , Disease Outbreaks , Enterovirus/isolation & purification , Enterovirus/pathogenicity , Enterovirus Infections/physiopathology , Female , Humans , Infant , Infant, Newborn , Male , Meningitis, Aseptic/epidemiology , Phylogeny , Seasons
7.
Vet Immunol Immunopathol ; 96(1-2): 13-8, 2003 Nov 15.
Article in English | MEDLINE | ID: mdl-14522130

ABSTRACT

CCL27 (also named CTACK, ALP, ILC and ESkine) is a CC chemokine primarily expressed by keratinocytes of the skin. The cognate receptor of CCL27 named CCR10 (GPR-2), is also expressed in skin-derived cells, and in addition by a subset of peripheral blood T-cells and in a variety of other tissues. In this paper, we report the cloning of porcine CCL27 cDNA and investigation of CCL27 mRNA expression in Staphylococcus hyicus infected piglets. At the protein level, 77 and 74% homology was found to human and mouse CCL27 sequences, respectively. The results of the expression analyses show that CCL27 mRNA is upregulated in the skin of infected piglets and to a lesser extent in piglets recovered from disease and without clinical signs of infection, indicating a role for CCL27 both during inflammation and after recovery from an infection.


Subject(s)
Chemokines, CC/genetics , Epidermitis, Exudative, of Swine/immunology , Staphylococcal Skin Infections/veterinary , Staphylococcus/immunology , Amino Acid Sequence , Animals , Base Sequence , Biopsy/veterinary , Chemokine CCL27 , Chemokines, CC/biosynthesis , Chemokines, CC/immunology , Concanavalin A/immunology , Epidermitis, Exudative, of Swine/microbiology , Exfoliatins/immunology , Gene Expression Regulation , Interleukin-12/genetics , Interleukin-12/immunology , Molecular Sequence Data , Phytohemagglutinins/immunology , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Sequence Alignment , Staphylococcal Skin Infections/immunology , Staphylococcal Skin Infections/microbiology , Swine
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