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. 2004 Nov;78(21):11678–11685. doi: 10.1128/JVI.78.21.11678-11685.2004

TABLE 2.

Detection of defective and standard genomes in virus from plaques formed by C-S8p260 and C-S8p260p3d

Virus and assaya No. of plaques analyzed Genomes present in the analyzed plaquesb
st Δ417 Δ999 or Δ1017
C-S8p260
    First plaque assay 41 + +
1 +
    Second plaque assay 17 + +
    Third plaque assay 3 + +
C-S8p260p3d plaque assay 5 +
a

The origin of C-S8p260 and C-S8p260p3d and the procedure for the plaque assays are described in Materials and Methods. Three serial plaque assays were done with various plaques from C-S8p260.

b

RT-PCR amplifications used were numbers 9, 10, 13, and 21, to detect Δ417 and 17, 18, 20, and 21, to detect Δ999 or Δ1017 (Fig. 1A); amplification number 29 shown in Table 1 was used to detect standard (st) RNA.

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