Sequence analysis of proviral DNA of porcine endogenous retroviruses

被引:6
|
作者
Machnik, G
Sypniewski, D
Wydmuch, Z
Cholewa, K
Mazurek, U
Wilczok, T
Smorag, Z
Pacha, J
机构
[1] Med Univ Silesia, Dept Biotechnol & Genet Engn, PL-41200 Sosnowiec, Poland
[2] Med Univ Silesia, Dept Microbiol, PL-41200 Sosnowiec, Poland
[3] Med Univ Silesia, Dept Mol Biol & Med Genet, PL-41200 Sosnowiec, Poland
[4] Natl Res Inst Anim Prod, Dept Physiol & Anim Breeding, Krakow, Poland
关键词
D O I
10.1016/j.transproceed.2005.10.115
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Among all species analyzed, the domestic pig seems to be the most appropriate organ donor for xenotransplantation. Porcine endogenous retroviruses (PERVs) are present in genomes of all pigs and are capable of infecting human cells in vitro thus posing a serious threat for xenotransplantation procedures. Despite the abundant distribution of PERVs integrated with porcine genome, the majority of PERV proviral DNA is not capable of expressing viral proteins unless seriously mutated. The aim of the study was to analyze PERV genome for mutations. The study was performed on blood samples from 146 pigs. Long-range polymerase chain reaction (Long-PCR) was performed with primer sets designed within long terminal repeats (LTRs). Long-PCR products of different molecular weights were obtained: 530 by (33.1% of individuals), 580 by (76.7%), 933 by (100%), and 2900 by (59.8%). Amplimers of 7200 by were absent in 12.8% of individuals, indicating the lack of intact proviral DNA. Sequence analysis showed that most PERV proviral DNA was significantly mutated, thus suggesting the inability to express functional viral RNA; however, it cannot be ruled out that compensatory recombination processes could occur enabling replication of defective proviruses.
引用
收藏
页码:4610 / 4614
页数:5
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