Table 1.

Detection of KSHV genomic DNA in clonogenic colonies derived from infected CD34+ HPCs



KSHV+ colonies/total colonies analyzed

CFU-GM
BFU-E
HPP
KSHV   17% (15 of 90)*  4% (1 of 23)  0% (0 of 20)  
UV-KSHV   1% (1 of 67)  0% (0 of 12)   0% (0 of 17)  
Mock
 
0% (0 of 25)
 
0% (0 of 7)
 
0% (0 of 8)
 


KSHV+ colonies/total colonies analyzed

CFU-GM
BFU-E
HPP
KSHV   17% (15 of 90)*  4% (1 of 23)  0% (0 of 20)  
UV-KSHV   1% (1 of 67)  0% (0 of 12)   0% (0 of 17)  
Mock
 
0% (0 of 25)
 
0% (0 of 7)
 
0% (0 of 8)
 

CD34+ HPCs were exposed to KSHV or UV-irradiated KSHV (10 μW/cm2 for 1 hour). Cells were washed 3 times with PBS and plated into MethoCult H4433. Colonies were visually scored, randomly isolated, and DNA was analyzed by real-time PCR analysis at 12 to 15 days after plating. Experiments were performed 3 times. Colonies with less than 1.0 calculated viral copy per cell were scored as negative for KSHV infection. Colonies demonstrating less than 2 human β-globin copies were excluded from analysis.

*

17 ± 5.6 mean KSHV genomic copies per human cell in positive CFU-GM colonies.

3.3 KSHV genomic copies per human cell in positive BFU-E colony.

2.7 KSHV genomic copies per human cell in positive CFU-GM colony.

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