

Severe fever with thrombocytopenia syndrome (SFTS) is an emerging tick‑borne zoonosis in East Asia, yet the contribution of animals to virus maintenance and spillover remains incompletely characterized. This review examines current evidence of SFTS virus (SFTSV) infection across domestic livestock, companion animals, wildlife, and captive species, focusing on host range, geographic distribution, diagnostics, and reports of viral RNA and virus isolation. Available data indicate that SFTSV exposure and infection occur across a broad range of animal hosts, supporting a multi-host ecological framework rather than a simple single-reservoir interpretation. Domestic ruminants frequently exhibit high seroprevalence and may function as sentinels of enzootic activity, while occasional virus isolation from cattle demonstrates that viable virus can be recovered from naturally infected livestock, although this does not establish reservoir or amplification competence. Companion animals are considered a potential interface for interspecies transmission, as some studies have documented severe clinical disease, high viral loads, and cat-associated human transmission events supported by varying levels of epidemiological and genomic evidence. Studies in wildlife further document exposure and natural infection across diverse taxa, although their specific roles in viral maintenance remain unresolved. Interpretation of these findings depends heavily on the diagnostic modality: serology primarily indicates prior exposure, RNA detection supports current or recent infection, and virus isolation demonstrates that viable virus was present in the sampled material. Integrating animal infection data within an ecological framework reveals major knowledge gaps related to reservoir competence, infectious shedding, phylogenetic connections among animal, tick, and human cases, and implications for prevention. The review underscores the need for One Health surveillance that incorporates clinical data from companion animals and applies evidence‑based interpretation to improve recognition of animal–human interfaces associated with potential spillover risk.
Bandavirus dabieense, a single-stranded RNA virus, is the causative agent of severe fever with thrombocytopenia syndrome (SFTS), a disease associated with high fatality rates. Early and accurate diagnosis is essential for improving clinical outcomes, particularly given the limited therapeutic options and high mortality rates associated with SFTS. However, while highly sensitive, conventional diagnostic methods such as PCR and qRT-PCR require specialized laboratory facilities and trained personnel, making them impractical for rapid detection in resource-limited settings. To address these challenges, we developed a rapid and highly sensitive assay for Bandavirus dabieense detection by integrating reverse transcription loop-mediated isothermal amplification (RT-LAMP) with CRISPR/Cas12a technology. LAMP primers and guide RNA sequences were designed to target the L gene, ensuring broad detection across viral genotypes. The optimized assay demonstrated a detection limit of 5 RNA copies per reaction, showing more sensitivity than qRT-PCR, and exhibited 100% concordance with qRT-PCR results in clinical samples. Given its speed, accuracy, and field applicability, this LAMP-CRISPR/Cas12a-based assay represents a promising diagnostic tool for early SFTSV detection, particularly in resource-constrained environments where conventional molecular diagnostics are not readily available.
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