Niel Christian, Diniz-Mendes Leonardo, Devalle Sylvie
Department of Virology, Oswaldo Cruz Institute, Avenida Brasil 4365, 21040-900 Rio de Janeiro, RJ, Brazil.
J Gen Virol. 2005 May;86(Pt 5):1343-1347. doi: 10.1099/vir.0.80794-0.
Multiply primed rolling-circle amplification is a novel technology that uses bacteriophage phi29 DNA polymerase to amplify circular DNA molecules, without the need for prior knowledge of their sequences. In an attempt to detect Torque teno virus (TTV), rolling-circle amplification was used to amplify DNA extracted from eight human and four pig serum samples. All samples gave high molecular weight (>30 kb) amplification products. By restriction endonuclease digestion, these products generated DNA fragments whose sizes were consistent with those of human TTV (3.8 kb) and swine TTV (Sd-TTV; 2.9 kb) genomes. Two TTV isolates derived from a single AIDS patient, as well as two Sd-TTV isolates derived from a single pig, were characterized by complete nucleotide sequencing. One of the Sd-TTV isolates showed very low (43-45 %) nucleotide sequence similarity to the other Sd-TTV isolate and to the prototype isolate Sd-TTV31, and could be considered the prototype of a novel genogroup.
多重引物滚环扩增是一种新技术,它利用噬菌体phi29 DNA聚合酶扩增环状DNA分子,而无需事先了解其序列。为了检测细小病毒(TTV),采用滚环扩增法对从8份人血清样本和4份猪血清样本中提取的DNA进行扩增。所有样本均产生了高分子量(>30 kb)的扩增产物。通过限制性内切酶消化,这些产物产生的DNA片段大小与人TTV(3.8 kb)和猪TTV(Sd-TTV;2.9 kb)基因组的大小一致。对来自一名艾滋病患者的两株TTV分离株以及来自一头猪的两株Sd-TTV分离株进行了全核苷酸测序。其中一株Sd-TTV分离株与另一株Sd-TTV分离株以及原型分离株Sd-TTV31的核苷酸序列相似性非常低(43-45%),可被视为一个新基因组群的原型。