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filingDate 2007-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2013-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101478985-B
titleOfInvention Virulence determinant within E2 structural glycoprotein of classical swine fever virus
abstract In swine, Classical Swine Fever Virus (CSFV) E2 glycoprotein is a major inducer of neutralizing antibodies and protective immunity. E2 mediates virus is adsorbed to the target cell, and harbors genetic determinants associated with virus virulence. CSFV E2 also comprises a discrete epitope (TAVSPTTLR) which is recognized by monoclonal antibody (mAb) WH303 between residues 829 and 837, and is used to differentiate CSFV from related Pestiviruses Bovine Viral Diarrhea Virus (BVDV) and Border Disease Virus (BDV). In the report, a CSFV infectious clone of the virulent Brescia isolate (BICv) is used to progressively mutate the mAb WH303 epitope of CSFV E2 to the homologous amino acid sequence of BVDV strain NADL E2 (TSFNMDTLA). While the resulting virus mutants T1v (TSFSPTTLR), T2v (TSFNPTTLR), T3v (TSFNMTTLR) demonstrate in vitro growth characteristics similar to those of parental BICv, mutants T4v (TSFNMDTLR) and T5v (TSFNMDTLA) exhibit a decrease of 10 times in virus yield and a significant decrease in plaque size relative to the parental BICv. Immunohistochemical reactivity pointing against WH303 is lost only in T3v, T4v and T5v.
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