Volume 13, Number 10—October 2007
Novel Variant of Tickborne Encephalitis Virus, Russia
We isolated a novel strain of tickborne encephalitis virus (TBEV), Glubinnoe/2004, from a patient with a fatal case in Russia. We sequenced the strain, whose landmark features included 57 amino acid substitutions and 5 modified cleavage sites. Phylogenetically, Glubinnoe/2004 is a novel variant that belongs to the Eastern type of TBEV.
Tickborne encephalitis virus (TBEV) was originally isolated in the Far Eastern region of Russia in 1937 (1). TBEV is defined as a species within the Mammalian tickborne virus group (genus Flavivirus, family Flaviviridae) (2). The TBEV species includes 3 subtypes, Far Eastern (previously RSSE), Siberian (previously West-Siberian), and Western European (previously Central European encephalitis [CEE]) viruses. Recently, taxonomic improvements were proposed, and TBEV were divided into 4 types: Western, Eastern, Turkish sheep, and Louping ill (3). TBEV has been found in nearly 30 countries in Europe and Asia (4), and ≈700 million persons live in areas (excluding the People’s Republic of China) where TBEV infection is endemic. The annual incidence of TBEV infection is estimated to be as many as 14,000 cases (5). Eleven thousand TBE cases occur annually in Russia, but only ≈150 cases are registered in Primorsky District, Russia (6). The Far Eastern subtype is considered to be the most pathogenic for humans, with a mortality rate of >20%. The Western European subtype is less virulent and lethal (7,8). The TBEV genome consists of a single-stranded, positive-sense RNA of ≈11,000 nt that encodes 3 structural and 7 nonstructural proteins (9). The differences in nucleotide sequences encoding protein E between subtypes of TBEV may reach 18%–19%; amino acid sequences are considerably more conserved (10). In 2004, a total of 76 confirmed TBE cases occurred in the spring-summer season in Primorsky District; 10 were fatal. We describe 1 case caused by a novel variant of TBEV.
A 15-year-old boy received 2 tick bites near the village of Glubinnoe, in the northern part of Primorsky District, on May 30 and June 1, 2004, respectively. He had not had any vaccinations against TBEV infection. The first prodromal symptoms developed on June 8. A high fever with strong headache and paresis of cervical muscles developed in the next 2 days. On June 11, the patient was transported by emergency airplane from a local hospital to the Regional Clinical Hospital No. 1 in Vladivostok, where high fever with pronounced meningeal symptoms and complete disorientation in place and time were observed. Coma and acute respiratory dysfunction due to paralysis of respiratory muscles developed the next day, and the patient was put on an automatic respirator. He died of acute cardiovascular insufficiency and heart failure on June 17.
Virus strain Glubinnoe/2004 was isolated from a brain sample from the patient by using pig kidney embryo (PKE) cells. One hundred microliters homogenized brain diluted 1:100 was applied onto PKE cells in minimal essential medium supplemented with 2% fetal calf serum. The cells were incubated at 37°C for 4 days, and cell culture supernatants were used for second passage on PKE cells. The virus for sequencing and immunologic experiments was purified from infected PKE cells on third passage by centrifugation on a sucrose gradient (11). The protocol of study was approved by the Institutional Review Board of the Institute of Epidemiology and Microbiology, Vladivostok. Handling of the infectious material was performed under Biosafety Level 3–4 conditions.
A panel of monoclonal antibodies (MAbs) to TBEV was used for ELISA as described earlier (12). Viral RNA was extracted by using a RIBO-sorb kit (InterLabService Inc., Moscow, Russia); then RNA was transcribed to cDNA and amplified by PCR. The purified cDNA fragment was used for sequencing in a Beckman CEQ2000XL sequencer (Beckman Coulter, Inc., Fullerton, CA, USA). Fifty primers were designed on the basis of the TBEV sequence (GenBank DQ989336), allowing ≈150-bp overlap between adjacent PCR fragments. Each PCR fragment was independently amplified and sequenced 3×. Sequences were aligned with ClustalX (13). Molecular data were statistically processed by using the program MEGA (14). The program PHYLIP version 3.57 (University of Washington, Seattle, WA, USA) or PUZZLE version 4.0.2 (University of Munich, Munich, Germany) was used for constructing a phylogenetic tree.
The nucleotide sequences of the viral isolates were compared with published complete polyprotein sequences of TBEV (Table 1). The complete coding sequence of Glubinnoe/2004 was 10,886 nt. We found profound differences in the nucleotide sequences between listed TBEV strains and the Glubinnoe/2004 strain. The identity with 2 typical Far Eastern strains, 205 and Sofjin-HO, was 95.2% and 94.9%, respectively (Table 1). The complete Glubinnoe/2004 nucleotide sequence was compared with other TBEV sequences available in GenBank. The conservation of the strain’s nucleotide sequences ranged from 82.7% to 95.2%, whereas amino acid sequences’ conservation ranged from 91.0% to 98.4%, depending on the type of TBEV (Table 1). To further delineate the genetic variation, we analyzed polyprotein sequences of 37 other flaviviruses in comparison with Glubinnoe/2004 (Table 2). Fifty-three and 57 amino acid (aa) substitutions were found when Glubinnoe/2004 was compared to strains 205 and Sofjin-HO, respectively, and 14 of these were unique substitutions for all studied flaviviruses. Most substitutions were located in the C-terminal hydrophobic domain (CTHD) of proteins C, NS3, and NS5. The CTHD had 5 substitutions in 20 aa fragment; NS3, 10 substitutions, and NS5,16 substitutions. We also found that 5 putative cleavage sites of polyprotein were modified; the changes were located in viral C/CTHD and anchored C/prM sites. No substitutions were found in well-known features of protein E, such as the 12 cysteine residues, potential N-glycosylation sites, fusion peptide, and DEXH core motif of the NS3 helicase. A cysteine residue in position 4 of NS1 protein was replaced with a glycine; this mutation was described previously only for Sofjin-HO (BAB72162).
We also performed phylogenetic analysis of the fully sequenced TBEV strains and Glubinnoe/2004 (Figure 1) and analyzed 100 different protein E gene sequences available in GenBank (data not shown). Both phylogenetic trees clearly demonstrated that Glubinnoe/2004 belonged to the Eastern type and formed a separate clade (branch or group) within the type. The time of divergence of Glubinnoe/2004 from the Oshima-Sofjin and Senzhang groups was calculated by using the average substitution rate analysis (15). We estimate that Glubinnoe/2004 and Senzhang group diverged 300–470 years ago and Glubinnoe/2004 and Oshima-Sofjin group, 320–490 years ago. Our findings suggest that parallel evolution of different genetic groups of TBEV occurred in the relatively small Far Eastern region of Russia.
The growth curves for Glubinnoe/2004 and 205 viruses in PKE cells at 37°C are shown in Figure 2. The virus yield rapidly increased 9–18 h after infection and then stabilized. The maximum difference in virus yields (in 50% tissue culture infective doses [TCID50]/mL) between Glubinnoe/2004 and 205 viruses was 2.1 TCID50/mL at 12 h postinfection and nearly 10× from 15 to 36 h. By 72 h postinfection, PKE cells infected by Glubinnoe/2004 and 205 were completely lysed. We also evaluated the replication of viruses by directly measuring viral E protein levels by using 2 MAbs. E protein level rapidly increased 15–24 h postinfection and was similar for both strains. This finding correlated with a production rate of infectious virions with delay close to 6 h, which demonstrates that the Glubinnoe/2004 strain may produce more infectious virions in the early stage of infection of a PKE cell. The discovered mutations in 4 of 5 cleavage sites in viral polyprotein are required for cleavage of structural viral proteins. This finding may explain the more robust formation of infectious virions in the early stages of infection.
Serologic data demonstrate that strain Glubinnoe/2004 has epitopes well recognized by 14 anti-TBEV MAbs (data not shown). Based on these data, we concluded that all protein E epitopes of strain 205 virus are also present on Glubinnoe/2004 virions and are not affected by 4 aa substitutions found in protein E. This would suggest that modern vaccines against TBE and diagnostic immunologic kits will be effective against this novel variant.
We have genetically characterized TBEV isolate Glubinnoe/2004 by determining its complete coding nucleotide sequence and comparing it with most of the available TBEV sequences. We found 53 and 57 aa substitutions in comparison with strains 205 and Sofjin-HO, respectively, and 14 of these were unique for 37 flaviviruses. Most substitutions were located in the CTHD of proteins C, NS3, and NS5. Phylogenetic analysis showed that Glubinnoe/2004 appears to be a separate lineage within the Eastern type of TBEV. We estimate that strain Glubinnoe/2004 diverged from Eastern TBEV in Senzhang group ≈300–470 years ago and from viruses in the Oshima-Sofjin group ≈320–490 years ago.
Five putative cleavage sites of the viral polyprotein were changed, including 4 sites responsible for processing of structural proteins. Strain Glubinnoe/2004 replicated more effectively in PKE cells than did strain 205. These data suggest that Glubinnoe/2004 could be used for production of vaccines, instead of strains 205 and Sofjin, and for development of diagnostic kits. This conclusion is supported by immunologic data with anti-TBEV MAbs, which demonstrated that viral glycoprotein E has a conserved antigenic structure typical of the Eastern type of TBEV.
Dr Ternovoi is head of the Section for Molecular Diagnostic, Department Molecular Virology for Flaviviruses and Viral Hepatitis, State Research Center of Virology and Biotechnology “VECTOR,” Koltsovo, Russia. His current research interests are associated with genetic diagnosis of viral infection, mechanisms of gene expression, and the role of viral polypeptides in the development of immune response for the prevention of viral infection.
We thank the medical personnel of the Neurology and Pathology Divisions of the Regional Clinical Hospital No. 1, Vladivostok, for collaboration in studying the tickborne encephalitis cases, and Tatyana Bondarenko for technical assistance in our experiments.
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- Figure 1. Phylogenetic tree, based on complete polyprotein sequences of tickborne encephalitis virus (TBEV). Original names of TBEV are presented. The multiple sequence alignments were obtained with ClustalX, and the tree...
- Figure 2. Growth curves and E protein synthesis of Glubinnoe/2004 and 205 in pig kidney embryo (PKE) cells: monolayer of PKE cells were infected with Glubinnoe/2004 and 205 of tickborne encephalitis...
- Table 1. Tickborne encephalitis virus (TBEV) strains used in the study and comparison of identify for full-length polyprotein sequences with strains Glubinnoe/2004 of TBEV
- Table 2. Individual amino acid substitutions of Glubinnoe/2004 and 205/Sofjin-HO viruses and unique substitutions in comparison with 37 flaviviruses, determined by polyprotein alignment†
Suggested citation for this article: Ternovoi VA, Protopopova EV, Chausov EV, Novikov DV, Leonova GN, Netesov SV, et al. Novel variant of tickborne encephalitis virus, Russia. Emerg Infect Dis [serial on the Internet]. 2007 Oct [date cited]. Available from http://wwwnc.cdc.gov/eid/article/13/10/07-0158
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Valery B. Loktev, State Research Center of Virology and Biotechnology “VECTOR,” Koltsovo, Novosibirsk Oblast, 630559, Russia;
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