Literature detail

Genomic and phylogenetic characterization of severe fever with thrombocytopenia syndrome virus in companion animals in Korea, 2023-2024.

Dong-Yeop Lee1 Hong-Jae Lee2 Hwi-Yeon Choi2 Jason S Park2 Dong-Hun Lee1
Affiliations 2 institutions
  1. Wildlife Health Laboratory, College of Veterinary Medicine, Konkuk University, Seoul, Republic of Korea.
  2. Green Vet, Yongin, Republic of Korea.
PMID 42241469 2026 PLoS Negl Trop Dis eng aheadofprint
PubMed DOI Browse context

Article

Publication summary

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
1 records
Extraction confidence 0.87
Key finding

Phylogenetic analysis showed close genetic relationship between companion animal and human SFTSV strains, suggesting cross-species transmission potential.

Virus
Location
Supporting text

The close genetic relationship between animal- and human-derived viruses underscores the risk of cross-species transmission.

Method
phylogenetic analysis
Sample type
clinical specimens
Study design
phylogenetic analysis
Transmission direction
unknown
Event type
animal-human phylogenetic relationship indicating cross-species potential
Geographic raw
Republic of Korea
Country inferred
KOR
Mechanism types
phylogenetic similarity
1 records
Extraction confidence 0.93
Key finding

Companion animal SFTSV genomes contained virulence-associated substitutions RdRp-T1433A and Gn-Q341P, and epitope mutations G218S, P222A, F225L, and S340N predicted to reduce antibody binding.

Virus
Location
Supporting text

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
Geographic raw
Republic of Korea
Country inferred
KOR
Genes or proteins
RdRp | Gn | antibody epitopes
Mutations
RdRp-T1433A | Gn-Q341P | Y83F | K113R | G218S | P222A | F225L | V323I | S340N
Mechanism types
virulence-associated mutation | antibody escape
1 records
Extraction 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.

Virus
Location
Supporting text

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
1 records
Extraction 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.

Virus
Location
Supporting text

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.

Method
whole-genome sequencing | multiplex tiling RT-PCR | next-generation sequencing | phylogenetic analysis
Sample type
clinical specimens
Study design
genomic surveillance
Transmission direction
animal reservoir only
Event type
genomic surveillance of companion animals
Geographic raw
Republic of Korea
Country inferred
KOR