首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >The physical state of the negative strand of hepatitis C virus RNA in serum of patients with chronic hepatitis C.
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The physical state of the negative strand of hepatitis C virus RNA in serum of patients with chronic hepatitis C.

机译:慢性丙型肝炎患者血清中丙型肝炎病毒RNA负链的物理状态。

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摘要

Negative strands of the hepatitis C virus (HCV) genome (a positive-stranded RNA virus) have been found in a nuclease-resistant form in the serum of patients with HCV infections. We determined whether a complete negative-strand copy is present in the serum, whether the negative strand is particle-associated, and finally, whether it is virion-associated and encapsidated like the positive (genomic) strand. Isopyknic sucrose and cesium chloride density ultracentrifugation followed by a strand-specific reverse transcription-polymerase chain reaction on the collected fractions was performed to determine whether both positive and negative strands were associated with similar particles. Both strands comigrated to approximately the same density (1.11-1.16 g/cm3) in sucrose. After treatment of the plasma with detergent (0.1% Nonidet P-40) to remove the viral envelope and centrifugation on cesium chloride gradients, the positive strands shifted to a density of 1.35 g/cm3, and the negative strands were not detected. By using antibodies specific for the HCV core or envelope glycoproteins E1 or E2 coated onto the wells of a microtiter plate, it was possible to specifically bind HCV or viral cores to the solid phase. Pelleted virus particles were resuspended in either PBS or PBS with 0.1% Nonidet P-40 to expose the core. These pellets were then incubated in antibody-coated microtiter wells. RNA extracted from the bound and unbound fractions was tested for HCV RNA. The anti-core antibody was able to bind positive strands but not negative strands only in detergent-treated samples. In the nondetergent-treated pellets, the anti-E1 and -E2 bound the positive strand, but only anti-E1 bound the negative strands. These findings indicate that while both strands of HCV RNA can be detected in serum, the positive strand is encapsidated within the enveloped core, and the negative strand appears to be in a membrane particle associated with the viral envelope protein E1 but does not appear to be within the HCV core of circulating virions.
机译:丙型肝炎病毒(HCV)基因组的负链(正链RNA病毒)已在患有HCV的患者血清中以抗核酸酶的形式发现。我们确定血清中是否存在完整的负链拷贝,负链是否与颗粒相关,最后确定它是否与病毒体相关并像正(基因组)链一样被衣壳化。等速蔗糖和氯化铯密度超速离心,然后对收集的馏分进行链特异性逆转录-聚合酶链反应,以确定正链和负链均与相似颗粒相关。两条链在蔗糖中的密度大致相同(1.11-1.16 g / cm3)。用去污剂(0.1%Nonidet P-40)处理血浆以除去病毒包膜并在氯化铯梯度上离心后,正链转移至密度为1.35 g / cm3,而未检测到负链。通过使用特异于HCV核心的抗体或包被在微量滴定板孔中的包膜糖蛋白E1或E2,可以将HCV或病毒核心特异结合至固相。将沉淀的病毒颗粒重悬于PBS或含0.1%Nonidet P-40的PBS中以暴露核心。然后将这些沉淀物在抗体包被的微量滴定孔中孵育。测试了从结合和未结合部分中提取的RNA的HCV RNA。仅在去污剂处理的样品中,抗核心抗体能够结合正链,但不能结合负链。在未经洗涤剂处理的颗粒中,抗E1和-E2结合正链,但只有抗E1结合负链。这些发现表明,虽然可以在血清中检测到HCV RNA的两条链,但正链被包裹在被包裹的核内,而负链似乎在与病毒被膜蛋白E1相关的膜颗粒中,但似乎没有在循环病毒粒子的HCV核心内。

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