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BRIEF RESEARCH REPORT article

Front. Vet. Sci.

Sec. Veterinary Infectious Diseases

Volume 12 - 2025 | doi: 10.3389/fvets.2025.1691476

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

Provisionally accepted
Gan  LiGan Li1Shikai  CaiShikai Cai1Hairui  LiHairui Li1Limei  QinLimei Qin1Dengshuai  ZhaoDengshuai Zhao1Junjie  HuangJunjie Huang1Ping  LiPing Li1Yuanhang  ZhangYuanhang Zhang1Yajie  ZhengYajie Zheng1Miaomiao  ZhangMiaomiao Zhang1Han  GaoHan Gao1Wenqiang  TangWenqiang Tang2Xialing  ZhaoXialing Zhao2Bin  ShiBin Shi2Wanxiang  QiWanxiang Qi2Mengmeng  ZhaoMengmeng Zhao1*Keshan  ZhangKeshan Zhang1*
  • 1Foshan University, Foshan, China
  • 2Xizang Academy of Agricultural and Animal Husbandry Sciences, Lhasa 850009, China, Institute of Animal Science, Xizang Academy of Agricultural and Animal Husbandry Sciences, China

The final, formatted version of the article will be published soon.

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.

Keywords: Akabane virus, Genetic Variation, phylogeny, Antigenic epitope, pathogenicity

Received: 23 Aug 2025; Accepted: 25 Sep 2025.

Copyright: © 2025 Li, Cai, Li, Qin, Zhao, Huang, Li, Zhang, Zheng, Zhang, Gao, Tang, Zhao, Shi, Qi, Zhao and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Mengmeng Zhao, mengmengzhao2021@fosu.edu.cn
Keshan Zhang, zks0009@126.com

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