首页> 外文期刊>Archives of virology >Genotypes of TT virus (TTV) compared between liver disease patients and healthy individuals using a new PCR system capable of differentiating 1a and 1b types from others*.
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Genotypes of TT virus (TTV) compared between liver disease patients and healthy individuals using a new PCR system capable of differentiating 1a and 1b types from others*.

机译:使用能够区分1a和1b类型的新PCR系统,比较肝病患者和健康个体之间的TT病毒(TTV)基因型*。

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摘要

TT virus (TTV) lacks obvious pathogenicity; almost all of the infected hosts are symptom-free. A possibility remains, however, that certain strains can cause liver disease while most others are non-pathogenic. Genotypes 1 a and 1 b have been proposed to contain such pathogenic strains. To test this possibility, we constructed a PCR system capable of detecting TTV of the 1 a and 1 b genotypes differentially from the other genotypes, and compared the frequencies of these genotypes between patients with liver disease of unknown etiology (n=42) and healthy individuals (n=50). The assay comprised 3 steps: i) PCR to amplify a 3.2-kb fragment using universal primers; ii) 2nd-round PCR, starting from the 3.2-kb amplicon, for a approximately 280-nt fragment by use of genotype 1-specific primers; and iii) digestion of the approximately 280-nt amplicon with MboI and BanI to discriminate between 1 a and 1 b. Eventually, 40 (95%) of the patients and 47 (94%) of the controls were positive for the 3.2-kb amplicon, and the 1 a, 1 b, 1 a+1 b, and non-1 genotypes of TTV were found in 2 (5%) vs 4 (9 percent), 5 (13%) vs 4 (9%), 1 (3%) vs 1 (2%) and 32 (80%) vs 38 (81%) of the 40 patients and 47 controls, respectively: the distribution was almost identical between the two groups. The hypothesis that the genotype 1 of TTV may be more closely associated with liver disease than other genotypes was not supported by this study.
机译:TT病毒(TTV)缺乏明显的致病性;几乎所有受感染的主机都没有症状。但是,某些菌株仍可能引起肝脏疾病,而其他大多数菌株并非致病性。已经提出基因型1a和1b包含此类致病菌株。为了测试这种可能性,我们构建了一个PCR系统,该系统能够检测与其他基因型不同的1a和1b基因型的TTV,并比较病因未知(n = 42)和健康的肝病患者之间这些基因型的频率个人(n = 50)。该测定包括3个步骤:i)使用通用引物的PCR以扩增3.2kb的片段; ii)使用基因型1特异性引物,从3.2kb的扩增子开始,进行约280nt片段的第二轮PCR; iii)用MboI和BanI消化大约280nt的扩增子,以区分1a和1b。最终,40(95%)的患者和47(94%)的对照的3.2kb扩增子呈阳性,而TTV的1a,1b,1a + 1b和非1基因型为阳性。在2(5%)vs 4(9%),5(13%)vs 4(9%),1(3%)vs 1(2%)和32(80%)vs 38(81%)中发现40例患者和47例对照:两组之间的分布几乎相同。这项研究不支持TTV基因型1可能比其他基因型与肝病更紧密相关的假说。

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