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. 1998 May;72(5):3980–3990. doi: 10.1128/jvi.72.5.3980-3990.1998

TABLE 4.

Quadruple verification analysis of SV40 regulatory region sequences of clones recovered from monkey tissues

Animal Prototype virus clonea No. of infectious virus isolates:
Result by viral DNA detection
Recovered from filtratesb
Recovered from DNA lipofectionsb
PCRc
LPCRd
Brain Spleen Brain PBMC Spleen Brain PBMC Spleen Brain Spleen
6593 SV40-6593-1 12 NDe 4 2 ND + + ND 4 ND
SV40-6593-2 2 ND 1 1 ND + + ND 1 ND
SV40-6593-5 4 ND 1 1 ND + + ND 1 ND
H328 SV40-H328-1 6 ND 2 1 ND + + ND 6 ND
SV40-H328-2 0 ND 0 1 ND 0 + ND 0 ND
H491 SV40-H491-1 8 ND 2 0 ND + + ND 6 ND
H388 SV40-H388-1 12 ND 2 2 ND + + ND 3 ND
SV40-H388-2 2 ND 1 1 ND + + ND 2 ND
SV40-H388-16 4 ND 1 1 ND + + ND 2 ND
H822 SV40-H822-1 8 ND 2 ND ND + ND ND 6 ND
I508 SV40-I508-1 8 ND 0 0 ND + + ND 6 ND
K661 SV40-K661-1 8 ND 4 0 ND + + ND 6 ND
T302 SV40-T302-1 8 5 2 ND 3 + ND + 2 1
a

See Fig. 2D for the structure of the regulatory region of each indicated virus clone. 

b

Numbers are the numbers of individual clones verified by DNA sequencing to have identity with the prototype. Additional clones analyzed only by ethidium-bromide gel electrophoresis are not shown. 

c

+, PCR product that comigrated with PCR product amplified from control template (PCR products were not sequenced); 0, no PCR product detected. 

d

Values are numbers of clones analyzed for regulatory region by ethidium-bromide gel electrophoresis. Only the regulatory regions of SV40-H328, SV40-K661, and SV40-T302 LPCR clones were sequenced. 

e

ND, not done.