Berke Z, Dalianis T, Feinstein R, Sandstedt K, Evengard B
Department of Immunology, Microbiology, Pathology and Infectious Diseases, Karolinska Institute, Huddinge Hospital, Stockholm, Sweden.
In Vivo. 1994 May-Jun;8(3):339-42.
C.B-17 mice with the Severe Combined Immune Deficiency (SCID) mutation were infected with the naturally occurring murine polyomavirus. Using the Polymerase Chain Reaction (PCR) technique, persistence of polyomavirus was followed in different tissues of the mice between 24 hours and 2 months post infection (p.i.). Viral DNA appeared by 3-5 days and was detected in all studied organs by 3 weeks p.i. From 4 weeks to 2 months p.i. viral DNA was present at high levels in all studied organs in all of the animals. As controls normal C.B-17 and A/Sn mice were used. Viral DNA appeared by 2-4 days. The infection reached a peak around 1 week p.i. This was followed by a clearing stage and viral DNA was no longer detectable by 4-5 weeks p.i. Most organs studied with PCR were also examined histologically, but no lesions were observed. Consequently persistence and organ distribution of polyomavirus in adult SCID mice differs greatly from that in normal adult mice.
具有严重联合免疫缺陷(SCID)突变的C.B-17小鼠感染了自然发生的鼠多瘤病毒。使用聚合酶链反应(PCR)技术,在感染后(p.i.)24小时至2个月期间,追踪小鼠不同组织中多瘤病毒的持续性。病毒DNA在3 - 5天出现,在感染后3周时在所有研究的器官中都能检测到。从感染后4周至2个月,所有动物的所有研究器官中都存在高水平的病毒DNA。作为对照,使用正常的C.B-17和A/Sn小鼠。病毒DNA在2 - 4天出现。感染在感染后约1周达到峰值。随后是清除阶段,在感染后4 - 5周时病毒DNA不再可检测到。大多数用PCR研究的器官也进行了组织学检查,但未观察到病变。因此,多瘤病毒在成年SCID小鼠中的持续性和器官分布与正常成年小鼠有很大不同。