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The neurovirulence and neuroinvasiveness of chimeric tick-borne encephalitis/dengue virus can be attenuated by introducing defined mutations into the envelope and NS5 protein genes and the 3′ non-coding region of the genome
Abstract Tick-borne encephalitis (TBE) is a severe disease affecting thousands of people throughout Eurasia. Despite the use of formalin-inactivated vaccines in endemic areas, an increasing incidence of TBE emphasizes the need for an alternative vaccine that will induce a more durable immunity again...
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Published in: | Virology (New York, N.Y.) N.Y.), 2010-09, Vol.405 (1), p.243-252 |
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description | Abstract Tick-borne encephalitis (TBE) is a severe disease affecting thousands of people throughout Eurasia. Despite the use of formalin-inactivated vaccines in endemic areas, an increasing incidence of TBE emphasizes the need for an alternative vaccine that will induce a more durable immunity against TBE virus (TBEV). The chimeric attenuated virus vaccine candidate containing the structural protein genes of TBEV on a dengue virus genetic background (TBEV/DEN4) retains a high level of neurovirulence in both mice and monkeys. Therefore, attenuating mutations were introduced into the envelope (E315 ) and NS5 (NS5654,655 ) proteins, and into the 3′ non-coding region (Δ30) of TBEV/DEN4. The variant that contained all three mutations (vΔ30/E315 /NS5654,655 ) was significantly attenuated for neuroinvasiveness and neurovirulence and displayed a reduced level of replication and virus-induced histopathology in the brains of mice. The high level of safety in the central nervous system indicates that vΔ30/E315 /NS5654,655 should be further evaluated as a TBEV vaccine. |
doi_str_mv | 10.1016/j.virol.2010.06.014 |
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Despite the use of formalin-inactivated vaccines in endemic areas, an increasing incidence of TBE emphasizes the need for an alternative vaccine that will induce a more durable immunity against TBE virus (TBEV). The chimeric attenuated virus vaccine candidate containing the structural protein genes of TBEV on a dengue virus genetic background (TBEV/DEN4) retains a high level of neurovirulence in both mice and monkeys. Therefore, attenuating mutations were introduced into the envelope (E315 ) and NS5 (NS5654,655 ) proteins, and into the 3′ non-coding region (Δ30) of TBEV/DEN4. The variant that contained all three mutations (vΔ30/E315 /NS5654,655 ) was significantly attenuated for neuroinvasiveness and neurovirulence and displayed a reduced level of replication and virus-induced histopathology in the brains of mice. The high level of safety in the central nervous system indicates that vΔ30/E315 /NS5654,655 should be further evaluated as a TBEV vaccine.</description><identifier>ISSN: 0042-6822</identifier><identifier>EISSN: 1096-0341</identifier><identifier>DOI: 10.1016/j.virol.2010.06.014</identifier><identifier>PMID: 20594569</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>3' Untranslated Regions ; 60 APPLIED LIFE SCIENCES ; ANIMALS ; Animals, Suckling ; ARACHNIDS ; ARTHROPODS ; Brain ; Cercopithecus aethiops ; Dengue virus ; Dengue Virus - genetics ; Dengue Virus - pathogenicity ; DISEASES ; ENCEPHALITIS ; Encephalitis Viruses, Tick-Borne - genetics ; Encephalitis Viruses, Tick-Borne - pathogenicity ; Flavivirus ; Gene Expression Regulation, Viral - physiology ; GENES ; Genome, Viral ; Infectious Disease ; INVERTEBRATES ; Live attenuated vaccine ; MAMMALS ; MICE ; MICROORGANISMS ; MONKEYS ; Mutation ; MUTATIONS ; NERVOUS SYSTEM DISEASES ; Neurovirulence ; ORGANIC COMPOUNDS ; PARASITES ; PRIMATES ; PROTEINS ; RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS ; Reassortant Viruses - genetics ; Reassortant Viruses - pathogenicity ; RODENTS ; Tick-borne encephalitis virus ; TICKS ; VACCINES ; Vero Cells ; VERTEBRATES ; Viral Envelope Proteins - genetics ; Viral Envelope Proteins - metabolism ; Viral Nonstructural Proteins - genetics ; Viral Nonstructural Proteins - metabolism ; Virulence ; Virus Replication ; VIRUSES</subject><ispartof>Virology (New York, N.Y.), 2010-09, Vol.405 (1), p.243-252</ispartof><rights>2010</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-722aff6276fb95deffc6ad253cdd2f81f4f47a6ebf3db288d68e2112ef74a5f63</citedby><cites>FETCH-LOGICAL-c573t-722aff6276fb95deffc6ad253cdd2f81f4f47a6ebf3db288d68e2112ef74a5f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20594569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/21416180$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Engel, Amber R</creatorcontrib><creatorcontrib>Rumyantsev, Alexander A</creatorcontrib><creatorcontrib>Maximova, Olga A</creatorcontrib><creatorcontrib>Speicher, James M</creatorcontrib><creatorcontrib>Heiss, Brian</creatorcontrib><creatorcontrib>Murphy, Brian R</creatorcontrib><creatorcontrib>Pletnev, Alexander G</creatorcontrib><title>The neurovirulence and neuroinvasiveness of chimeric tick-borne encephalitis/dengue virus can be attenuated by introducing defined mutations into the envelope and NS5 protein genes and the 3′ non-coding region of the genome</title><title>Virology (New York, N.Y.)</title><addtitle>Virology</addtitle><description>Abstract Tick-borne encephalitis (TBE) is a severe disease affecting thousands of people throughout Eurasia. Despite the use of formalin-inactivated vaccines in endemic areas, an increasing incidence of TBE emphasizes the need for an alternative vaccine that will induce a more durable immunity against TBE virus (TBEV). The chimeric attenuated virus vaccine candidate containing the structural protein genes of TBEV on a dengue virus genetic background (TBEV/DEN4) retains a high level of neurovirulence in both mice and monkeys. Therefore, attenuating mutations were introduced into the envelope (E315 ) and NS5 (NS5654,655 ) proteins, and into the 3′ non-coding region (Δ30) of TBEV/DEN4. The variant that contained all three mutations (vΔ30/E315 /NS5654,655 ) was significantly attenuated for neuroinvasiveness and neurovirulence and displayed a reduced level of replication and virus-induced histopathology in the brains of mice. The high level of safety in the central nervous system indicates that vΔ30/E315 /NS5654,655 should be further evaluated as a TBEV vaccine.</description><subject>3' Untranslated Regions</subject><subject>60 APPLIED LIFE SCIENCES</subject><subject>ANIMALS</subject><subject>Animals, Suckling</subject><subject>ARACHNIDS</subject><subject>ARTHROPODS</subject><subject>Brain</subject><subject>Cercopithecus aethiops</subject><subject>Dengue virus</subject><subject>Dengue Virus - genetics</subject><subject>Dengue Virus - pathogenicity</subject><subject>DISEASES</subject><subject>ENCEPHALITIS</subject><subject>Encephalitis Viruses, Tick-Borne - genetics</subject><subject>Encephalitis Viruses, Tick-Borne - pathogenicity</subject><subject>Flavivirus</subject><subject>Gene Expression Regulation, Viral - physiology</subject><subject>GENES</subject><subject>Genome, Viral</subject><subject>Infectious Disease</subject><subject>INVERTEBRATES</subject><subject>Live attenuated vaccine</subject><subject>MAMMALS</subject><subject>MICE</subject><subject>MICROORGANISMS</subject><subject>MONKEYS</subject><subject>Mutation</subject><subject>MUTATIONS</subject><subject>NERVOUS SYSTEM DISEASES</subject><subject>Neurovirulence</subject><subject>ORGANIC COMPOUNDS</subject><subject>PARASITES</subject><subject>PRIMATES</subject><subject>PROTEINS</subject><subject>RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS</subject><subject>Reassortant Viruses - genetics</subject><subject>Reassortant Viruses - pathogenicity</subject><subject>RODENTS</subject><subject>Tick-borne encephalitis virus</subject><subject>TICKS</subject><subject>VACCINES</subject><subject>Vero Cells</subject><subject>VERTEBRATES</subject><subject>Viral Envelope Proteins - genetics</subject><subject>Viral Envelope Proteins - metabolism</subject><subject>Viral Nonstructural Proteins - genetics</subject><subject>Viral Nonstructural Proteins - metabolism</subject><subject>Virulence</subject><subject>Virus Replication</subject><subject>VIRUSES</subject><issn>0042-6822</issn><issn>1096-0341</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFks1u1DAUhSMEoqXwBEjIEgtWmdpO4iQLKqGKP6mCRYvEznLs6xlPE3uwnUiz45l4I3gS7E6pgE1XVu499_O58SmK5wSvCCbsdLtajHfjiuJUwWyFSf2gOCa4ZyWuavKwOMa4piXrKD0qnoSwxem7bfHj4ojipq8b1h8XP682gCzM3iXYPIKVgIRVh5KxiwhmAQshIKeR3JgJvJEoGnldDs5bQHlitxGjiSacKrDrGVBGBSSFRUOixQh2FhEUGvbI2OidmqWxa6RAG5vK0xxFNM6G3HUobjJ1gdHtDl4-XTZo510EY9E6m7mpZln16_sPZJ0tpVOZ6GGdONlq7iatm-Bp8UiLMcCz2_Ok-PLu7dX5h_Li8_uP528uStm0VSxbSoXWjLZMD32TrGnJhKJNJZWiuiO61nUrGAy6UgPtOsU6oIRQ0G0tGs2qk-LswN3NwwRKQtpUjHznzST8njth-L8dazZ87RZOe1InUAK8PABciIYHaSLIjXTWgoycJg0jHU6qV7fXePdthhD5ZIKEcRQW3Bx429Rdzxgh9yuTkLaEZuvVQSm9C8GDvnNNMM9Z41t-kzWes8Yx4ylraerF3wvfzfwJVxK8Pggg_fbFgM9L5bwo4_NOypl7Ljj7b16OxhopxmvYQ9i62dv0opzwQDnmlznuOe0kBb3q2dfqN0iKBAc</recordid><startdate>20100915</startdate><enddate>20100915</enddate><creator>Engel, Amber R</creator><creator>Rumyantsev, Alexander A</creator><creator>Maximova, Olga A</creator><creator>Speicher, James M</creator><creator>Heiss, Brian</creator><creator>Murphy, Brian R</creator><creator>Pletnev, Alexander G</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope><scope>7U9</scope><scope>C1K</scope><scope>F1W</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>OTOTI</scope><scope>5PM</scope></search><sort><creationdate>20100915</creationdate><title>The neurovirulence and neuroinvasiveness of chimeric tick-borne encephalitis/dengue virus can be attenuated by introducing defined mutations into the envelope and NS5 protein genes and the 3′ non-coding region of the genome</title><author>Engel, Amber R ; 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Despite the use of formalin-inactivated vaccines in endemic areas, an increasing incidence of TBE emphasizes the need for an alternative vaccine that will induce a more durable immunity against TBE virus (TBEV). The chimeric attenuated virus vaccine candidate containing the structural protein genes of TBEV on a dengue virus genetic background (TBEV/DEN4) retains a high level of neurovirulence in both mice and monkeys. Therefore, attenuating mutations were introduced into the envelope (E315 ) and NS5 (NS5654,655 ) proteins, and into the 3′ non-coding region (Δ30) of TBEV/DEN4. The variant that contained all three mutations (vΔ30/E315 /NS5654,655 ) was significantly attenuated for neuroinvasiveness and neurovirulence and displayed a reduced level of replication and virus-induced histopathology in the brains of mice. The high level of safety in the central nervous system indicates that vΔ30/E315 /NS5654,655 should be further evaluated as a TBEV vaccine.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20594569</pmid><doi>10.1016/j.virol.2010.06.014</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3' Untranslated Regions 60 APPLIED LIFE SCIENCES ANIMALS Animals, Suckling ARACHNIDS ARTHROPODS Brain Cercopithecus aethiops Dengue virus Dengue Virus - genetics Dengue Virus - pathogenicity DISEASES ENCEPHALITIS Encephalitis Viruses, Tick-Borne - genetics Encephalitis Viruses, Tick-Borne - pathogenicity Flavivirus Gene Expression Regulation, Viral - physiology GENES Genome, Viral Infectious Disease INVERTEBRATES Live attenuated vaccine MAMMALS MICE MICROORGANISMS MONKEYS Mutation MUTATIONS NERVOUS SYSTEM DISEASES Neurovirulence ORGANIC COMPOUNDS PARASITES PRIMATES PROTEINS RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS Reassortant Viruses - genetics Reassortant Viruses - pathogenicity RODENTS Tick-borne encephalitis virus TICKS VACCINES Vero Cells VERTEBRATES Viral Envelope Proteins - genetics Viral Envelope Proteins - metabolism Viral Nonstructural Proteins - genetics Viral Nonstructural Proteins - metabolism Virulence Virus Replication VIRUSES |
title | The neurovirulence and neuroinvasiveness of chimeric tick-borne encephalitis/dengue virus can be attenuated by introducing defined mutations into the envelope and NS5 protein genes and the 3′ non-coding region of the genome |
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