Novel sub-lineages, recombinants and reassortants of severe fever with thrombocytopenia syndrome virus

被引:25
作者
Lv, Qiang [1 ]
Zhang, Hong [2 ]
Tian, Lei [3 ]
Zhang, Ruiling [1 ]
Zhang, Zhenjie [1 ]
Li, Juan [1 ]
Tong, Yigang [4 ]
Fan, Hang [4 ]
Carr, Michael J. [5 ,6 ]
Shi, Weifeng [1 ]
机构
[1] Taishan Med Coll, Inst Pathogen Biol, Yingshengdonglu 2, Tai An 271000, Shandong, Peoples R China
[2] Taishan Med Univ, Affiliated Hosp, Tai An 271000, Shandong, Peoples R China
[3] 88 Hosp Chinese Peoples Liberat Army, Tai An 271000, Shandong, Peoples R China
[4] Beijing Inst Microbiol & Epidemiol, Beijing 100071, Peoples R China
[5] Hokkaido Univ, Global Stn Zoonosis Control, Global Inst Collaborat Res & Educ GI CoRE, Sapporo, Hokkaido 0010020, Japan
[6] Univ Coll Dublin, Natl Virus Reference Lab, Dublin 4, Ireland
关键词
Severe fever with thrombocytopenia; syndrome virus; Phylogeny; Recombination; Reassortment; TO-PERSON TRANSMISSION; SYNDROME BUNYAVIRUS; RNA VIRUSES; PHYLOGENETIC ANALYSIS; SHANDONG PROVINCE; SFTS BUNYAVIRUS; SOUTH-KOREA; CHINA; IDENTIFICATION; SEQUENCES;
D O I
10.1016/j.ttbdis.2016.12.015
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Severe fever with thrombocytopenia syndrome virus (SFTSV) has been continuously circulating in Eastern Asia in recent years, without the availability of effective vaccines or antiviral drugs, posing a serious threat to public health, particularly in the central-eastern provinces of China. In this study, we isolated and sequenced four new SFTSV strains from Shandong Province identified in 2015. Phylogenetic analysis, with all publicly available L, M and S gene segments, revealed that the four newly described SFTSV strains belonged to genotype C3. In addition, our phylogenetic analyses also identified two potentially novel sub-lineages of SFTSV, tentatively named C6 and J4. Our comprehensive analysis revealed twenty recombination events in fourteen SFTSV genomes and recombination events were found in the S gene segment for the first time. A total of twenty-six strains were probable SFTSV reassortants, including sixteen which were previously unidentified. We further characterised the genetic constellation of these putative reassortants and classified them into twelve different reassortment forms. Our study revealed multiple evolutionary forces acting on SFTSV, responsible for the increasing genetic diversity of this agent, which could potentially alter the antigenicity and pathogenicity of the virus. This calls for an urgent need for intensified surveillance and the development of vaccines and antiviral drugs against this high-consequence pathogen. (C) 2016 Elsevier GmbH. All rights reserved.
引用
收藏
页码:385 / 390
页数:6
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