# Phylogenetic analysis and biological characteristics of an Akabane virus isolated in China

**Authors:** Gan Li, Shikai Cai, Xiyu Liu, Hairui Li, Limei Qin, Dengshuai Zhao, Junjie Huang, Ping Li, Yuanhang Zhang, Yajie Zheng, Miaomiao Zhang, Han Gao, Wenqiang Tang, Xialing Zhao, Bin Shi, Wanxiang Qi, Mengmeng Zhao, Keshan Zhang

PMC · DOI: 10.3389/fvets.2025.1691476 · Frontiers in Veterinary Science · 2025-10-27

## TL;DR

This study analyzes a newly isolated Akabane virus in China, examining its genetic makeup and pathogenic effects on mice.

## Contribution

The study provides new insights into the genetic variation and pathogenicity of an Akabane virus strain in China.

## Key findings

- The FS202301 strain has a high viral titer and causes severe central nervous system damage in mice.
- The virus belongs to genogroup Ia with significant variation in the M segment and fewer antigenic epitopes in the Gc protein.

## Abstract

Akabane virus (AKAV) is an arbovirus that can cause miscarriage, premature birth, congenital malformations, and encephalomyelitis in young livestock. It is currently widely prevalent in China. Vero and MDBK cells were utilized to determine the virus titer and growth curve of the AKAV FS202301 strain in this study. Subsequently, the viral solution was intracranially (IC) or intraperitoneally (IP) inoculated into 8-day-old suckling mice, and the pathogenicity was explored by observing clinicopathological changes, and hematoxylin–eosin (HE) staining. Additionally, the S, M, and L segment sequences of the FS202301 strain were analyzed, phylogenetic trees were constructed, and antigenic epitopes were predicted to investigate its genetic variation. The results revealed that the viral titer of strain FS202301 was 106 TCID50/mL, with the number of viral copies peaking 24 h post-infection (hpi). This strain predominantly induced damage to the central nervous system, culminating in the death of suckling mice. It was classified as belonging to the genogroup Ia, exhibiting the highest degree of variation in the M segment, lower degrees of variation in the S and L segments, and no recombination events in any of the genes. The Gc protein encoded by the M segment contains more amino acid mutation sites and predicts a greater number of antigenic epitopes. This study aims to enhance the understanding of AKAV genetic variation in China and to establish a theoretical foundation for the future prevention and control of AKAV epidemics.

## Linked entities

- **Genes:** S (Star) [NCBI Gene 33281], m (miniature) [NCBI Gene 44835], L (Lobe) [NCBI Gene 36609], GC (GC vitamin D binding protein) [NCBI Gene 2638]
- **Proteins:** GC (GC vitamin D binding protein)
- **Diseases:** encephalomyelitis (MONDO:0005156)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** premature birth (MESH:D047928), congenital malformations (OMIM:163000), miscarriage (MESH:D000022), encephalomyelitis (MESH:D004679)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Akabane virus (no rank) [taxon 70566]
- **Cell lines:** MDBK — Bos taurus (Bovine), Spontaneously immortalized cell line (CVCL_0421), Vero — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0059)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12597804/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12597804/full.md

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Source: https://tomesphere.com/paper/PMC12597804