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. 2007 Oct 31;82(2):871–879. doi: 10.1128/JVI.01626-07

TABLE 1.

Tumor development in Syrian golden hamsters following i.p. inoculation with SV40 parental strains and recombinant virusesa

Viral isolate No. of tumors/no. of animals % Tumors Median time to tumors (wk) (range)
Parental viruses
    776(1E) 5/16 31 33 (29-46)
    776(2E) 3/30 10 27 (24-41)
    Baylor(1E) 10/12 83 27 (21-30)
    Baylor(2E) 1/17 6 23
    777 5/19 26 35 (21-39)
    SVCPCb 18/33 54 32 (15-52)
    VA45-54(2E)b 3/13 23 26 (23-30)
    SVPML 0/16 0
Subtotal 45/156 29
Recombinant viruses
    776-CPC(2E) 1/15 7 27
    776-Baylor(2E) 5/15 33 28 (17-52)
    776-VA(2E) 4/31 13 32 (26-41)
    776-PML(2E) 1/18 6 36
    CPC-776(1E) 6/17 35 30 (15-46)
    CPC-Baylor(1E) 7/19 37 30 (17-40)
    CPC-VA(1E) 4/17 24 36 (22-48)
    CPC-PML(1E) 11/19 58 37 (25-51)
Subtotal 39/151 26
Controls
    TC7 cell lysate 0/109 0
    Uninoculated 0/78 0
a

A total of 1 × 107 PFU of each virus was inoculated i.p. into 21-day-old weanling hamsters, and animals were observed for 1 year. Only autopsy-proven tumors are reported; if an animal died and no autopsy was performed, that animal was removed from the group count.

b

Some animals of the SVCPC and VA45-54 groups were described previously (50).