Xu Deshun, Ji Lei, Wu Xiaofang, Chen Liping
Huzhou Center for Disease Control and Prevention, Huzhou, China.
PLoS One. 2025 Feb 11;20(2):e0318742. doi: 10.1371/journal.pone.0318742. eCollection 2025.
Severe fever with thrombocytopenia syndrome (SFTS), a tick-borne emerging infectious disease caused by SFTS virus (SFTSV), is a growing public health threat due to its high mortality rate. To understand the genomic characteristics of SFTSV samples isolated in Huzhou, China, the full-length genomes of Huzhou SFTSV isolates obtained between February 1, 2019 and December 30, 2023 were sequenced, and the gene loci, evolution, and sequence identity of the genome sequences were analyzed using MEGA. The complete genome sequences of seven SFTSV samples were obtained successfully. The full-length genome of each isolate was 11 490 bp in length, composed of a large (L) segment of 6368 bp, medium (M) segment of 3378 bp, and small (S) segment of 1744 bp. The SFTSV samples isolated in Huzhou belonged to multiple genotypes, but were mainly of type D. Each subtype showed nucleotide sequence and amino acid sequence identities of more than 93.67% and 97.18%, respectively, with the syngeneic human host reference strain and more than 93.67% and 97.76%, respectively, with the syngeneic tick-derived host reference strain. Nucleotide sequence analysis of SFTSV isolates from Huzhou showed mutations in genes on all three segments, with those on the M segment showing the highest mutation rate. The nucleotide variations were mainly base transversions. Further studies of the distribution of SFTSV genotypes, sites of nucleotide mutations, and amino acid variations are required.
严重发热伴血小板减少综合征(SFTS)是一种由SFTS病毒(SFTSV)引起的蜱传新发传染病,因其高死亡率而对公共卫生构成日益严重的威胁。为了解在中国湖州分离的SFTSV样本的基因组特征,对2019年2月1日至2023年12月30日期间获得的湖州SFTSV分离株的全长基因组进行了测序,并使用MEGA分析了基因组序列的基因位点、进化和序列同一性。成功获得了7个SFTSV样本的完整基因组序列。每个分离株的全长基因组长度为11490bp,由一个6368bp的大(L)片段、一个3378bp的中(M)片段和一个1744bp的小(S)片段组成。在湖州分离的SFTSV样本属于多个基因型,但主要为D型。每个亚型与同基因人类宿主参考株的核苷酸序列和氨基酸序列同一性分别超过93.67%和97.18%,与同基因蜱源宿主参考株的核苷酸序列和氨基酸序列同一性分别超过93.67%和97.76%。对来自湖州的SFTSV分离株的核苷酸序列分析表明,所有三个片段上的基因均发生了突变,其中M片段上的突变率最高。核苷酸变异主要是碱基颠换。需要进一步研究SFTSV基因型的分布、核苷酸突变位点和氨基酸变异。