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dc.contributor.authorLindqvist, Richard
dc.contributor.authorRosendal, Ebba
dc.contributor.authorWeber, Elvira
dc.contributor.authorAsghar, Naveed
dc.contributor.authorSchreier, Sarah
dc.contributor.authorLenman, Annasara
dc.contributor.authorJohansson, Magnus
dc.contributor.authorDobler, Gerhard
dc.contributor.authorBestehorn, Malena
dc.contributor.authorKröger, Andrea
dc.contributor.authorÖverby, Anna K
dc.identifier.citationJ Neuroinflammation. 2020 Sep 28;17(1):284. doi: 10.1186/s12974-020-01943-w.en_US
dc.description.abstractBackground: Tick-borne encephalitis virus (TBEV) is considered to be the medically most important arthropod-borne virus in Europe. The symptoms of an infection range from subclinical to mild flu-like disease to lethal encephalitis. The exact determinants of disease severity are not known; however, the virulence of the strain as well as the immune status of the host are thought to be important factors for the outcome of the infection. Here we investigated virulence determinants in TBEV infection. Method: Mice were infected with different TBEV strains, and high virulent and low virulent TBEV strains were chosen. Sequence alignment identified differences that were cloned to generate chimera virus. The infection rate of the parental and chimeric virus were evaluated in primary mouse neurons, astrocytes, mouse embryonic fibroblasts, and in vivo. Neutralizing capacity of serum from individuals vaccinated with the FSME-IMMUN® and Encepur® or combined were evaluated. Results: We identified a highly pathogenic and neurovirulent TBEV strain, 93/783. Using sequence analysis, we identified the envelope (E) protein of 93/783 as a potential virulence determinant and cloned it into the less pathogenic TBEV strain Torö. We found that the chimeric virus specifically infected primary neurons more efficiently compared to wild-type (WT) Torö and this correlated with enhanced pathogenicity and higher levels of viral RNA in vivo. The E protein is also the major target of neutralizing antibodies; thus, genetic variation in the E protein could influence the efficiency of the two available vaccines, FSME-IMMUN® and Encepur®. As TBEV vaccine breakthroughs have occurred in Europe, we chose to compare neutralizing capacity from individuals vaccinated with the two different vaccines or a combination of them. Our data suggest that the different vaccines do not perform equally well against the two Swedish strains. Conclusions: Our findings show that two amino acid substitutions of the E protein found in 93/783, A83T, and A463S enhanced Torö infection of neurons as well as pathogenesis and viral replication in vivo; furthermore, we found that genetic divergence from the vaccine strain resulted in lower neutralizing antibody titers in vaccinated individuals.en_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.subjectEnvelope proteinen_US
dc.subjectEuropean subtypeen_US
dc.subjectTick-borne encephalitis virusen_US
dc.titleThe envelope protein of tick-borne encephalitis virus influences neuron entry, pathogenicity, and vaccine protection.en_US
dc.contributor.departmentTWINCORE, Zentrum für experimentelle und klinische Infektionsforschung GmbH,Feodor-Lynen Str. 7, 30625 Hannover, Germany.en_US
dc.identifier.journalJournal of neuroinflammationen_US
dc.source.journaltitleJournal of neuroinflammation

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