2010
DOI: 10.1134/s1022795410030087
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Coding nucleotide sequences of tick-borne encephalitis virus strains isolated from human blood without clinical symptoms of infection

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Cited by 8 publications
(8 citation statements)
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“…Evidence that viral genetic factors may also contribute to the severity of infection was supported by the genetic characterization of different TBEV strains from symptomatic and asymptomatic infections. Mutations affecting the virion proteins, NS3, NS5 proteins, and even the 3= NCR were linked to altered pathogenic properties (93,94). Despite the progress in investigating viral pathogenesis, the background of the TBFV pathomechanism remains poorly understood, especially for less-common TBFVs.…”
Section: Pathogenesismentioning
confidence: 99%
“…Evidence that viral genetic factors may also contribute to the severity of infection was supported by the genetic characterization of different TBEV strains from symptomatic and asymptomatic infections. Mutations affecting the virion proteins, NS3, NS5 proteins, and even the 3= NCR were linked to altered pathogenic properties (93,94). Despite the progress in investigating viral pathogenesis, the background of the TBFV pathomechanism remains poorly understood, especially for less-common TBFVs.…”
Section: Pathogenesismentioning
confidence: 99%
“…Additionally, comparisons of strains isolated from patients infected with TBEV identified several differences in NS5 across strains with varying disease outcomes. Interestingly, two studies identified mutations at position 692, where Ile correlated with high pathogenicity strains while Val was associated with low pathogenicity [ 65 , 66 ]. A third study compared strains isolated from patients with severe TBE found Ile or Thr at position 692; Thr has only been found in European human pathogenic strain Ljublijana I [ 67 ].…”
Section: Effects Of Viral Proteins On Virulencementioning
confidence: 99%
“…The authors speculate this substitution may improve interaction with host replication trans-acting factors. Mutations S634T/Y, R677K, and A724S were also associated with varying degrees of pathogenicity (substitutions associated with high pathogenicity strains are noted first, followed by the residue position and the low pathogenicity substitution), although their role in virulence has not been tested experimentally [ 65 , 66 ]. It should be noted that these mutations also reside within the IFN-I antagonism functional region.…”
Section: Effects Of Viral Proteins On Virulencementioning
confidence: 99%
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