Schleicher Sabine B, Flehmig Bertram F
Children's Hospital, Department I, University of Tübingen, Tübingen, Germany.
J Med Virol. 2003 Oct;71(2):226-32. doi: 10.1002/jmv.10474.
GB virus C (GBV-C) is a virus that has been proposed as a member of the Flaviviridae family, distantly related to hepatitis C virus (HCV). The virus is able to infect humans parenterally and perinatally, although its true pathogenicity remains unknown. The 5' terminal region of GBV-C is the most highly conserved region of the virus genome. Comparison of 5' untranslated region (5' UTR) sequences from GBV-C infected individuals shows that variation is limited to particular sites that are often covariant and associated with different virus genotypes. Extensive sequence analysis of the GBV-C genome provides evidence for the existence of at least five major genotypes, some of which can be further divided into subtypes. For genotyping by restriction fragment length polymorphism (RFLP), it is essential to identify genomic positions that not only reflect genotype differences, but that also harbor restriction sites that allow recognition of these differences. Restriction site analysis of type-specific sequence motifs predicted that endonucleases BsmFI, HaeII, HinfI, and ScrFI could be used for the identification all known genotypes (types 1-5) with 99.6% accuracy. The method was applied to serum samples from 46 chronic GBV-C carriers of heterogeneous geographical and ethnic origin, comparing observed cleavage patterns of GBV-C variants amplified by reverse transcriptase-polymerase chain reaction (RT-PCR) of the 5' UTR with the RFLP predicted from sequences deposited in GenBank database. cDNA sequencing and subsequent alignment of the 46 GBV-C isolates confirmed RFLP profiles predicted theoretically. The observed geographical distribution of genotypes is also in agreement with previous reports. This method may be useful for rapid and reliable characterization of GBV-C isolates when either epidemiological or transmission studies are carried out.
GB病毒C(GBV-C)是一种被提议归入黄病毒科的病毒,与丙型肝炎病毒(HCV)亲缘关系较远。该病毒能够通过肠道外和围产期途径感染人类,但其真正的致病性尚不清楚。GBV-C的5'末端区域是病毒基因组中保守性最高的区域。对GBV-C感染个体的5'非翻译区(5'UTR)序列进行比较发现,变异仅限于特定位点,这些位点通常是协变的,并且与不同的病毒基因型相关。对GBV-C基因组进行的广泛序列分析为至少五种主要基因型的存在提供了证据,其中一些基因型还可进一步分为亚型。对于通过限制性片段长度多态性(RFLP)进行基因分型,必须确定不仅能反映基因型差异,而且含有能识别这些差异的限制性位点的基因组位置。对型特异性序列基序的限制性位点分析预测,内切酶BsmFI、HaeII、HinfI和ScrFI可用于以99.6%的准确率鉴定所有已知基因型(1-5型)。该方法应用于来自不同地理和种族背景的46名慢性GBV-C携带者的血清样本,将通过5'UTR的逆转录聚合酶链反应(RT-PCR)扩增的GBV-C变异体的观察到的切割模式与从GenBank数据库中存入的序列预测的RFLP进行比较。对46株GBV-C分离株进行cDNA测序及后续比对,证实了理论上预测的RFLP图谱。观察到的基因型地理分布也与先前的报道一致。当进行流行病学或传播研究时,该方法可能有助于快速、可靠地表征GBV-C分离株。