Molecular evolution analysis of three species gyroviruses in China from 2018 to 2019

• Published in: Virus research 2023-03, Vol.326, p.199058-199058, Article 199058
• Main Authors: Yan, Tianxing, Zhao, Manda, Sun, Yufeng, Zhang, Shicheng, Zhang, Xianwen, Liu, Qing, Li, Yubao, Cheng, Ziqiang
• Format: Article
• Language: English
• Subjects: Animals; Chicken anemia virus; Chicken anemia virus - genetics; Chickens; China - epidemiology; Circoviridae Infections; Epidemiology; Evolution; Gyrovirus - genetics; Gyrovirus galga 1; Gyrovirus homsa l; Phylogeny; Poultry Diseases - epidemiology
• ISSN: 0168-1702; 1872-7492
• DOI: 10.1016/j.virusres.2023.199058

•GyVs were widely distributed in China, particularly, co-infection within the three species GyVs in same individual, which had never been reported before.•CAV and GyG1 had similar recombination regions and were associated with viral replication and transcription.•The high substitution rate and recombination were the main factors for the high diversity of GyVs. Gyrovirus (GyV) is a widespread ssDNA virus with a high population diversity, and several of its species, including the chicken anemia virus (CAV), gyrovirus galga 1 (GyG1), and gyrovirus homsa 1 (GyH1), have been shown to be pathogenic to poultry. The evolution of these viruses, however, is still unclear. Our study analyzed epidemiology and molecular evolution of three species of GyVs (CAV, GyG1, and GyH1) from 2018 to 2019 in China. The survey results indicated that GyV was widespread in China. It is vital to consider the coinfections among the three species of GyV. The phylogenetic analysis showed that CAV was divided into three clades and GyG1 and GyH1 were divided into two clades. Based on the recombination analysis, CAV and GyG1 had similar recombination regions associated with viral replication and transcription. Furthermore, the substitution rates for CAV and GyG1 were approximately 6.09 × 10−4 and 2.784 × 10−4 nucleotides per site per year, respectively. The high substitution rate and recombination were the main factors for the high diversity of GyVs. Unfortunately, GyH1 strains have not been discovered in enough numbers to allow evolutionary analysis. The GyVs had several positively selected sites, possibly related to their potential to escape the host immune response. In summary, our study provides insights into the time of origin, evolution rate, and recombination of GyV for assessing their evolutionary process and genetic diversity.