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. 2003 Mar;77(5):3291–3296. doi: 10.1128/JVI.77.5.3291-3296.2003

TABLE 1.

Genotypes and phenotypes of parental and reassortant viruses used in this study

Virus Parental origin of indicated genome segment (protein)a
Trypsin cleavage of VP4 (EOP)b Neutralization by α-VP4 MAb 2G4c Virion stability during purification (%)d
1 (VP1) 2 (VP2) 3 (VP3) 4 (VP4) 5 (NSP1) 6 (VP6) 7 (NSP3) 8 (NSP2) 9 (VP7) 10 (NSP4) 11 (NSP5)
SA11-4F F F F F F F F F F F F 2.7 × 10−3 Yes 93.3
SA11-C13 S S S S S S S S S S S <6.3 × 10−6 Yes 10.6
B223 B B B B B B B B B B B <1.2 × 10−5 No 0.5
R-A29 S S S F S S S S S S S 1.4 × 10−2 Yes 60.6
R-924 F F F S F F F F F F F NDf Yes 6.9
R-197 B B B F B B B B B B B <8.0 × 10−6e No 8.2
R-202 F F F F F B F F F F F ND ND 65.5
R-600 B B B B B F B B B B B ND ND 1.2
R-004 F F F B F F F F F F F ND Yes 0.5
a

Origin of segments: B, B223; F, SA11-4F; S, SA11-C13. Bold type indicates differing segment.

b

EOP, titer in the absence of trypsin/titer in the presence of trypsin (from reference 2).

c

Neutralization phenotype using VP4-specific MAB 2G4 (from reference 3).

d

Percent initial titer of virus grown in the presence of trypsin recovered by a standard CsCl purification procedure (from reference 4).

e

Unexpected phenotypic expression is shown in bold.

f

ND, not determined.