Severe fever with thrombocytopenia syndrome virus (SFTSV) is a tick-borne Phlebovirus with high fatality rates in humans and expanding geographic distribution in East Asia. Companion animals, including dogs and cats, are increasingly recognized as susceptible hosts that may contribute to viral maintenance and spillover. However, genomic information on SFTSV strains circulating in companion animals in Korea remains limited. Between April 2023 and June 2024, 63 SFTSV-positive clinical specimens from dogs and cats were collected across the Republic of Korea. Whole-genome sequencing using a multiplex tiling RT-PCR and next-generation sequencing approach yielded 39 complete viral genomes. Phylogenetic analysis revealed that most viruses clustered within genotype B, including 10 viruses classified as the highly virulent B2 subtype. Five reassortant viruses (12.8%) were identified, comprising four intra-genotypic (B1/B2/B2) and one inter-genotypic (B2/C/B2) reassortants. Multiple amino acid substitutions linked to increased human case fatality, such as RdRp-T1433A (94.9%) and Gn-Q341P (97.4%), were prevalent among companion animal viruses. In addition, mutations within neutralizing antibody epitopes (Y83F, K113R, G218S, P222A, F225L, V323I, and S340N) were detected, several of which significantly reduced antibody binding affinity in silico (G218S, P222A, F225L, and S340N). This study provides nationwide genomic characterization of SFTSV in companion animals in Korea. The detection of highly virulent subtypes, frequent reassortment, and epitope-altering mutations highlights the evolutionary potential of SFTSV in non-human hosts. The close genetic relationship between animal- and human-derived viruses underscores the risk of cross-species transmission. These findings emphasize the need for integrated One Health surveillance systems linking veterinary and human health sectors to enable early detection, risk assessment, and mitigation of emerging SFTSV threats.
Structured evidence records
Evidence records
4 total
Genomic Evolution1 records
Genomic EvolutionExtraction confidence 0.87
Key finding
Phylogenetic analysis showed close genetic relationship between companion animal and human SFTSV strains, suggesting cross-species transmission potential.
Multiple amino acid substitutions linked to increased human case fatality, such as RdRp-T1433A (94.9%) and Gn-Q341P (97.4%), were prevalent among companion animal viruses. In addition, mutations within neutralizing antibody epitopes ... significantly reduced antibody binding affinity in silico.
Method
in silico affinity analysis
Sample type
clinical specimens
Study design
genomic analysis
Transmission direction
molecular mechanism only
Event type
virulence-associated and antibody escape mutations
Recombination Or ReassortmentExtraction confidence 0.90
Key finding
Five SFTSV reassortant viruses, including four intra-genotypic (B1/B2/B2) and one inter-genotypic (B2/C/B2), were detected among companion animal isolates, demonstrating ongoing segment exchange within hosts.
Five reassortant viruses (12.8%) were identified, comprising four intra-genotypic (B1/B2/B2) and one inter-genotypic (B2/C/B2) reassortants.
Method
whole-genome sequencing | phylogenetic analysis
Sample type
clinical specimens
Study design
phylogenetic analysis
Transmission direction
molecular mechanism only
Event type
intra- and inter-genotypic reassortment in animal isolates
Geographic raw
Republic of Korea
Country inferred
KOR
Genes or proteins
L | M | S segments
Mechanism types
reassortment
Zoonotic Surveillance1 records
Zoonotic SurveillanceExtraction confidence 0.95
Key finding
Whole-genome sequencing of SFTSV from dogs and cats across Korea in 2023–2024 revealed genotype B viruses, including highly virulent B2 subtypes and reassortants, indicating active viral circulation in companion animals.
Between April 2023 and June 2024, 63 SFTSV-positive clinical specimens from dogs and cats were collected across the Republic of Korea. Whole-genome sequencing ... revealed that most viruses clustered within genotype B, including 10 viruses classified as the highly virulent B2 subtype. Five reassortant viruses were identified.