Extensive genetic diversity of severe fever with thrombocytopenia syndrome virus circulating in Hubei Province, China, 2018-2022.

IF 3.8 2区 医学 Q1 Medicine PLoS Neglected Tropical Diseases Pub Date : 2023-09-18 eCollection Date: 2023-09-01 DOI:10.1371/journal.pntd.0011654
Yu-Ting Ren, Hong-Pan Tian, Jia-le Xu, Man-Qing Liu, Kun Cai, Shu-Liang Chen, Xue-Bing Ni, Yi-Rong Li, Wei Hou, Liang-Jun Chen
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Abstract

Severe fever with thrombocytopenia syndrome virus (SFTSV), an etiological agent causing febrile human disease was identified as an emerging tick-borne bunyavirus. The clinical disease characteristics and case fatality rates of SFTSV may vary across distinct regions and among different variant genotypes. From 2018 to 2022, we surveyed and recruited 202 severe fever with thrombocytopenia syndrome (SFTS) patients in Hubei Province, a high-incidence area of the epidemic, and conducted timely and systematic research on the disease characteristics, SFTSV diversity, and the correlation between virus genome variation and clinical diseases. Our study identified at least 6 genotypes of SFTSV prevalent in Hubei Province based on the analysis of the S, M, and L genome sequences of 88 virus strains. Strikingly, the dominant genotype of SFTSV was found to change during the years, indicating a dynamic shift in viral genetic diversity in the region. Phylogenetic analysis revealed the genetic exchange of Hubei SFTSV strains was relatively frequent, including 3 reassortment strains and 8 recombination strains. Despite the limited sample size, SFTSV C1 genotype may be associated with higher mortality compared to the other four genotypes, and the serum amyloid A (SAA) level, an inflammatory biomarker, was significantly elevated in these patients. Overall, our data summarize the disease characteristics of SFTSV in Hubei Province, highlight the profound changes in viral genetic diversity, and indicate the need for in-depth monitoring and exploration of the relationship between viral mutations and disease severity.

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2018-2022年,中国湖北省流行的严重发热伴血小板减少综合征病毒的广泛遗传多样性。
严重发热伴血小板减少综合征病毒(SFTSV)是一种引起发热性人类疾病的病原体,被鉴定为一种新出现的蜱传布尼亚病毒。SFTSV的临床疾病特征和病死率可能因不同地区和不同变异基因型而异。2018年至2022年,我们在疫情高发区湖北省调查招募了202名严重发热伴血小板减少综合征(SFTS)患者,并对疾病特征、SFTSV多样性以及病毒基因组变异与临床疾病的相关性进行了及时、系统的研究。本研究通过对88株病毒的S、M和L基因组序列的分析,确定了湖北省流行的至少6种SFTSV基因型。引人注目的是,SFTSV的显性基因型在这些年中发生了变化,表明该地区病毒遗传多样性发生了动态变化。系统发育分析表明,湖北SFTSV菌株的遗传交换相对频繁,包括3个重组菌株和8个重组菌株。尽管样本量有限,但与其他四种基因型相比,SFTSV C1基因型可能与更高的死亡率相关,并且这些患者的血清淀粉样蛋白A(SAA)水平(一种炎症生物标志物)显著升高。总体而言,我们的数据总结了湖北省SFTSV的疾病特征,突出了病毒遗传多样性的深刻变化,并表明需要深入监测和探索病毒突变与疾病严重程度之间的关系。
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来源期刊
PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases Medicine-Infectious Diseases
CiteScore
7.40
自引率
10.50%
发文量
723
审稿时长
2-3 weeks
期刊介绍: PLOS Neglected Tropical Diseases publishes research devoted to the pathology, epidemiology, prevention, treatment and control of the neglected tropical diseases (NTDs), as well as relevant public policy. The NTDs are defined as a group of poverty-promoting chronic infectious diseases, which primarily occur in rural areas and poor urban areas of low-income and middle-income countries. Their impact on child health and development, pregnancy, and worker productivity, as well as their stigmatizing features limit economic stability. All aspects of these diseases are considered, including: Pathogenesis Clinical features Pharmacology and treatment Diagnosis Epidemiology Vector biology Vaccinology and prevention Demographic, ecological and social determinants Public health and policy aspects (including cost-effectiveness analyses).
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