A natural variation in the RNA polymerase of severe fever with thrombocytopenia syndrome virus enhances viral replication and in vivo virulence

Author:

Jeon Kyeongseok12ORCID,Ro Hyo‐Jin12,Kang Jun‐Gu3,Jeong Da‐Eun3,Kim Joowan12,Lee Yebeen12,Yoon Ga‐Yeon4,Kang Ju‐Il5,Bae Joon‐Yong6,Kim Jin Il6ORCID,Park Man‐Seong6,Lee Keun Hwa7ORCID,Cho Hyun‐Soo4,Kim Yuri125,Cho Nam‐Hyuk12589

Affiliation:

1. Department of Microbiology and Immunology Seoul National University College of Medicine Seoul Republic of Korea

2. Department of Biomedical Sciences Seoul National University College of Medicine Seoul Republic of Korea

3. Korea Zoonosis Research Institute Jeonbuk National University Iksan Republic of Korea

4. Department of Systems Biology, College of Life Science and Biotechnology Yonsei University Seoul Republic of Korea

5. Institute of Endemic Disease Seoul National University Medical Research Center Seoul Republic of Korea

6. Department of Microbiology, Vaccine Innovation Center, Institute for Viral Diseases Korea University College of Medicine Seoul Republic of Korea

7. Department of Microbiology and Environmental Biology & Medical Parasitology Hanyang University College of Medicine Seoul Republic of Korea

8. Seoul National University Bundang Hospital Seongnam Gyeonggi‐do Republic of Korea

9. Wide River Institute of Immunology Seoul National University Hongcheon Gangwon‐do Republic of Korea

Abstract

AbstractSevere fever with thrombocytopenia syndrome (SFTS) is an emerging tick‐borne disease with high mortality in Eastern Asia. The disease is caused by the SFTS virus (SFTSV), also known as Dabie bandavirus, which has a segmented RNA genome consisting of L, M, and S segments. Previous studies have suggested differential viral virulence depending on the genotypes of SFTSV; however, the critical viral factor involved in the differential viral virulence is unknown. Here, we found a significant difference in viral replication in vitro and virulence in vivo between two Korean isolates belonging to the F and B genotypes, respectively. By generating viral reassortants using the two viral strains, we demonstrated that the L segment, which encodes viral RNA‐dependent RNA polymerase (RdRp), is responsible for the enhanced viral replication and virulence. Comparison of amino acid sequences and viral replication rates revealed a point variation, E251K, on the surface of RdRp to be the most significant determinant for the enhanced viral replication rate and in vivo virulence. The effect of the variation was further confirmed using recombinant SFTSV generated by reverse genetic engineering. Therefore, our results indicate that natural variations affecting the viral replicase activity could significantly contribute to the viral virulence of SFTSV.

Funder

Korea Health Industry Development Institute

Publisher

Wiley

Subject

Infectious Diseases,Virology

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