Kuddus Ruhul H, Gandhi Chandrashekhar R, Rehman Khaja K, Guo Fengli, Watkins Simon C, Valdivia Luis A, Fung John J
Thomas E Starzl Transplantation Institute, Department of Surgery, University of Pittsburgh Medical Center, PA 15261, USA.
Genome. 2003 Oct;46(5):858-69. doi: 10.1139/g03-064.
A major concern in using porcine organs for transplantation is the potential of transmission of porcine endogenous retrovirus (PERV). To investigate the long-term effects of PERV infection on human cells, human embryonic kidney cell line HEK-293 infected with PERV PK-15 was maintained for up to 72 passages and samples were harvested at intervals for use in morphological, growth, and genomic analyses. Morphology, DNA content/cell, and doubling time of uninfected and infected cells were similar. Restriction fragment length polymorphism (RFLP) analysis of PCR-amplified nearly full-length PERV genome showed no alterations in band pattern. RFLP analysis of the long terminal repeats (LTR) showed some changes in band pattern, but not in length. Southern blot analysis of genomic DNA of infected cells indicated random integration of PERV without structural alterations in proviral genome. Semi-quantitative PCR demonstrated a gradual increase of proviral load in the infected cells. Sequence analysis of the LTR region of PERV from infected cells indicated a relatively low rate (6.0 x 10(-4)/bp or about 2 x 10(-6)/bp/generation) of mutation. There were also indications of recombination of PERV strains A and B. Finally, PERV infection had no effect on transcription of human endogenous retrovirus-K (HERV-K) genes. Together, no significant effect attributable to PERV infection was evident on chronically PERV-infected HEK-293 cells.
使用猪器官进行移植的一个主要担忧是猪内源性逆转录病毒(PERV)传播的可能性。为了研究PERV感染对人类细胞的长期影响,将感染了PERV PK-15的人胚肾细胞系HEK-293维持培养多达72代,并定期采集样本用于形态学、生长和基因组分析。未感染和感染细胞的形态、DNA含量/细胞以及倍增时间相似。对PCR扩增的近乎全长的PERV基因组进行限制性片段长度多态性(RFLP)分析,结果显示条带模式没有改变。对长末端重复序列(LTR)的RFLP分析显示条带模式有一些变化,但长度没有改变。对感染细胞的基因组DNA进行Southern印迹分析表明,PERV随机整合,前病毒基因组没有结构改变。半定量PCR显示感染细胞中前病毒载量逐渐增加。对感染细胞中PERV的LTR区域进行序列分析表明,突变率相对较低(6.0×10⁻⁴/bp或约2×10⁻⁶/bp/代)。也有PERV A和B株重组的迹象。最后,PERV感染对人类内源性逆转录病毒-K(HERV-K)基因的转录没有影响。总体而言,对于长期感染PERV的HEK-293细胞,未发现PERV感染有明显的显著影响。