A natural variation in the RNA polymerase of severe fever with thrombocytopenia syndrome virus enhances viral replication and in vivo virulence
Severe 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 sugge...
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creator | Jeon, Kyeongseok Ro, Hyo‐Jin Kang, Jun‐Gu Jeong, Da‐Eun Kim, Joowan Lee, Yebeen Yoon, Ga‐Yeon Kang, Ju‐Il Bae, Joon‐Yong Kim, Jin Il Park, Man‐Seong Lee, Keun Hwa Cho, Hyun‐Soo Kim, Yuri Cho, Nam‐Hyuk |
description | Severe 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. |
doi_str_mv | 10.1002/jmv.29099 |
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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.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.29099</identifier><language>eng</language><publisher>London: Wiley Subscription Services, Inc</publisher><subject>Amino acids ; DNA-directed RNA polymerase ; Fever ; Genetic engineering ; Genomes ; Genotypes ; In vivo methods and tests ; Parasitic diseases ; Replicase ; Replication ; Ribonucleic acid ; RNA ; RNA polymerase ; Segments ; Thrombocytopenia ; Tick-borne diseases ; Variation ; Virology ; Virulence ; Viruses</subject><ispartof>Journal of medical virology, 2023-09, Vol.95 (9), p.e29099-e29099</ispartof><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c325t-63e700a409359028aedf91ce94d60b949bb793f6240c94b934d5ecf17b5bd6923</citedby><cites>FETCH-LOGICAL-c325t-63e700a409359028aedf91ce94d60b949bb793f6240c94b934d5ecf17b5bd6923</cites><orcidid>0000-0002-5452-0998 ; 0000-0001-9600-461X ; 0000-0001-8833-2138</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Jeon, Kyeongseok</creatorcontrib><creatorcontrib>Ro, Hyo‐Jin</creatorcontrib><creatorcontrib>Kang, Jun‐Gu</creatorcontrib><creatorcontrib>Jeong, Da‐Eun</creatorcontrib><creatorcontrib>Kim, Joowan</creatorcontrib><creatorcontrib>Lee, Yebeen</creatorcontrib><creatorcontrib>Yoon, Ga‐Yeon</creatorcontrib><creatorcontrib>Kang, Ju‐Il</creatorcontrib><creatorcontrib>Bae, Joon‐Yong</creatorcontrib><creatorcontrib>Kim, Jin Il</creatorcontrib><creatorcontrib>Park, Man‐Seong</creatorcontrib><creatorcontrib>Lee, Keun Hwa</creatorcontrib><creatorcontrib>Cho, Hyun‐Soo</creatorcontrib><creatorcontrib>Kim, Yuri</creatorcontrib><creatorcontrib>Cho, Nam‐Hyuk</creatorcontrib><title>A natural variation in the RNA polymerase of severe fever with thrombocytopenia syndrome virus enhances viral replication and in vivo virulence</title><title>Journal of medical virology</title><description>Severe 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.</description><subject>Amino acids</subject><subject>DNA-directed RNA polymerase</subject><subject>Fever</subject><subject>Genetic engineering</subject><subject>Genomes</subject><subject>Genotypes</subject><subject>In vivo methods and tests</subject><subject>Parasitic diseases</subject><subject>Replicase</subject><subject>Replication</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA polymerase</subject><subject>Segments</subject><subject>Thrombocytopenia</subject><subject>Tick-borne diseases</subject><subject>Variation</subject><subject>Virology</subject><subject>Virulence</subject><subject>Viruses</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpd0c1KxDAUBeAgCo6jC98g4EYX1Zu0TSfLQfwDURBdlzS9ZTK0SU3ayjyFr2zquHJ1SfjICfcQcs7gmgHwm203XXMJUh6QBQMpEgkFOyQLYJlIhGD5MTkJYQsAK8n5gnyvqVXD6FVLJ-WNGoyz1Fg6bJC-vaxp79pdh14FpK6hASf0SJt50C8zbKLzrquc3g2uR2sUDTtbxyukk_FjoGg3ymoM8zFmeOxbo_cpytZz0mQm94tbjPCUHDWqDXj2N5fk4_7u_fYxeX59eLpdPyc65fmQiBQLAJWBTHMJfKWwbiTTKLNaQCUzWVWFTBvBM9Ayq2Sa1TnqhhVVXtVC8nRJLvfv9t59jhiGsjNBY9sqi24MJV-JTHC2yotIL_7RrRu9jb-bVdxiNLO62ivtXQgem7L3plN-VzIo52rKWE35W036A2KQg8Q</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Jeon, Kyeongseok</creator><creator>Ro, Hyo‐Jin</creator><creator>Kang, Jun‐Gu</creator><creator>Jeong, Da‐Eun</creator><creator>Kim, Joowan</creator><creator>Lee, Yebeen</creator><creator>Yoon, Ga‐Yeon</creator><creator>Kang, Ju‐Il</creator><creator>Bae, Joon‐Yong</creator><creator>Kim, Jin Il</creator><creator>Park, Man‐Seong</creator><creator>Lee, Keun Hwa</creator><creator>Cho, Hyun‐Soo</creator><creator>Kim, Yuri</creator><creator>Cho, Nam‐Hyuk</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5452-0998</orcidid><orcidid>https://orcid.org/0000-0001-9600-461X</orcidid><orcidid>https://orcid.org/0000-0001-8833-2138</orcidid></search><sort><creationdate>20230901</creationdate><title>A natural variation in the RNA polymerase of severe fever with thrombocytopenia syndrome virus enhances viral replication and in vivo virulence</title><author>Jeon, Kyeongseok ; Ro, Hyo‐Jin ; Kang, Jun‐Gu ; Jeong, Da‐Eun ; Kim, Joowan ; Lee, Yebeen ; Yoon, Ga‐Yeon ; Kang, Ju‐Il ; Bae, Joon‐Yong ; Kim, Jin Il ; Park, Man‐Seong ; Lee, Keun Hwa ; Cho, Hyun‐Soo ; Kim, Yuri ; Cho, Nam‐Hyuk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c325t-63e700a409359028aedf91ce94d60b949bb793f6240c94b934d5ecf17b5bd6923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino acids</topic><topic>DNA-directed RNA polymerase</topic><topic>Fever</topic><topic>Genetic engineering</topic><topic>Genomes</topic><topic>Genotypes</topic><topic>In vivo methods and tests</topic><topic>Parasitic diseases</topic><topic>Replicase</topic><topic>Replication</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA polymerase</topic><topic>Segments</topic><topic>Thrombocytopenia</topic><topic>Tick-borne diseases</topic><topic>Variation</topic><topic>Virology</topic><topic>Virulence</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeon, Kyeongseok</creatorcontrib><creatorcontrib>Ro, Hyo‐Jin</creatorcontrib><creatorcontrib>Kang, Jun‐Gu</creatorcontrib><creatorcontrib>Jeong, Da‐Eun</creatorcontrib><creatorcontrib>Kim, Joowan</creatorcontrib><creatorcontrib>Lee, Yebeen</creatorcontrib><creatorcontrib>Yoon, Ga‐Yeon</creatorcontrib><creatorcontrib>Kang, Ju‐Il</creatorcontrib><creatorcontrib>Bae, Joon‐Yong</creatorcontrib><creatorcontrib>Kim, Jin Il</creatorcontrib><creatorcontrib>Park, Man‐Seong</creatorcontrib><creatorcontrib>Lee, Keun Hwa</creatorcontrib><creatorcontrib>Cho, Hyun‐Soo</creatorcontrib><creatorcontrib>Kim, Yuri</creatorcontrib><creatorcontrib>Cho, Nam‐Hyuk</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeon, Kyeongseok</au><au>Ro, Hyo‐Jin</au><au>Kang, Jun‐Gu</au><au>Jeong, Da‐Eun</au><au>Kim, Joowan</au><au>Lee, Yebeen</au><au>Yoon, Ga‐Yeon</au><au>Kang, Ju‐Il</au><au>Bae, Joon‐Yong</au><au>Kim, Jin Il</au><au>Park, Man‐Seong</au><au>Lee, Keun Hwa</au><au>Cho, Hyun‐Soo</au><au>Kim, Yuri</au><au>Cho, Nam‐Hyuk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A natural variation in the RNA polymerase of severe fever with thrombocytopenia syndrome virus enhances viral replication and in vivo virulence</atitle><jtitle>Journal of medical virology</jtitle><date>2023-09-01</date><risdate>2023</risdate><volume>95</volume><issue>9</issue><spage>e29099</spage><epage>e29099</epage><pages>e29099-e29099</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><abstract>Severe 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.</abstract><cop>London</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/jmv.29099</doi><orcidid>https://orcid.org/0000-0002-5452-0998</orcidid><orcidid>https://orcid.org/0000-0001-9600-461X</orcidid><orcidid>https://orcid.org/0000-0001-8833-2138</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids DNA-directed RNA polymerase Fever Genetic engineering Genomes Genotypes In vivo methods and tests Parasitic diseases Replicase Replication Ribonucleic acid RNA RNA polymerase Segments Thrombocytopenia Tick-borne diseases Variation Virology Virulence Viruses |
title | A natural variation in the RNA polymerase of severe fever with thrombocytopenia syndrome virus enhances viral replication and in vivo virulence |
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