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1.
BMC Vet Res ; 20(1): 270, 2024 Jun 22.
Article in English | MEDLINE | ID: mdl-38909196

ABSTRACT

Equid alphaherpesvirus 1 (EHV-1) is a ubiquitous and significant viral pathogen in horses worldwide, causing a range of conditions, including fever, respiratory disease, abortion in pregnant mares and the severe neurological disease called equine herpes myeloencephalopathy (EHM). Despite that EHV-1 is a notifiable animal disease in Sweden, there is limited knowledge about the circulating strains. This study aimed to analyze the genetic diversity of EHV-1 strains in equine samples from different Swedish outbreaks by partial genome sequencing. Genotyping based on three selected open reading frames ORF11, ORF30, and ORF34 in the viral genome was conducted for 55 outbreaks of EHV-1 spanning from the years 2012 to 2021. The analysis revealed 14 different genovariants, with one prominent genovariant identified in 49% of the outbreaks. Additionally, the study identified seven mutations not previously described. Three new mutations were demonstrated in ORF11, all synonymous, and four new mutations in ORF34, two synonymous, and two non-synonymous. Notably, different EHV-1 genovariants were found in five out of six studied EHM outbreaks, but clonal spreading was shown within the outbreaks. Moreover, the study demonstrated that healthy (recovered) horses that returned from an EHM outbreak at an international meeting in Valencia, Spain (2021), were positive for the virus clone responsible for the severe disease outbreak despite several weeks of quarantine. These findings shed light on the genetic diversity and transmission dynamics of the virus and significantly contribute to better understanding of the epidemiology of EHV-1 in Sweden and globally.


Subject(s)
Disease Outbreaks , Genetic Variation , Herpesviridae Infections , Herpesvirus 1, Equid , Horse Diseases , Animals , Horses , Sweden/epidemiology , Herpesvirus 1, Equid/genetics , Herpesvirus 1, Equid/isolation & purification , Horse Diseases/virology , Horse Diseases/epidemiology , Disease Outbreaks/veterinary , Herpesviridae Infections/veterinary , Herpesviridae Infections/epidemiology , Herpesviridae Infections/virology , Genome, Viral , Genotype , Open Reading Frames
2.
Infect Genet Evol ; 82: 104290, 2020 08.
Article in English | MEDLINE | ID: mdl-32205264

ABSTRACT

Canine respiratory coronavirus (CRCoV) has been identified as a causative agent of canine infectious respiratory disease, an upper respiratory infection affecting dogs. The epidemiology is currently opaque, with an unclear understanding of global prevalence, pathology, and genetic characteristics. In this study, Swedish privately-owned dogs with characteristic signs of canine infectious respiratory disease (n = 88) were screened for CRCoV and 13 positive samples (14.7%, 8.4-23.7% [95% confidence interval (CI)]) were further sequenced. Sequenced Swedish CRCoV isolates were highly similar despite being detected in dogs living in geographically distant locations and sampled across 3 years (2013-2015). This is due to a single introduction into Swedish dogs in approximately 2010, as inferred by time structured phylogeny. Unlike other CRCoVs, there was no evidence of recombination in Swedish CRCoV viruses, further supporting a single introduction. Finally, there were low levels of polymorphisms, in the spike genes. Overall, we demonstrate that there is little diversity of CRCoV which is endemic in Swedish dogs.


Subject(s)
Coronavirus Infections/veterinary , Coronavirus, Canine/genetics , Dog Diseases/virology , Animals , Coronavirus Infections/epidemiology , Coronavirus, Canine/isolation & purification , Dog Diseases/epidemiology , Dogs , Genetic Variation , Genome, Viral , Nasopharynx/virology , Phylogeny , Recombination, Genetic , Sweden/epidemiology
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