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Newly discovered hepatitis C virus minicores circulate in human blood

机译:新发现的丙型肝炎病毒小核在人血中循环

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摘要

Hepatitis C virus (HCV) is one of the most prevalent causes of chronic blood‐borne infections worldwide. Despite developments of highly effective treatments, most infected individuals are unaware of their infection. Approximately 75% of infections are in low‐ and middle‐income countries; therefore, continuing research in HCV molecular virology and the development of vaccines and affordable diagnostics is required to reduce the global burden. Various intracellular forms of the HCV nucleocapsid (core) protein are produced in cell culture; these comprise the conventional p21 core and the newly discovered shorter isoforms (minicores). Minicores lack the N‐terminus of p21 core. This study was conducted to determine if minicores are secreted in cell culture and more importantly if they circulate in the blood of individuals infected with HCV. We also developed a new monoclonal antibody that detects minicores targeting a C‐terminal region common to p21 core and minicores. Direct evidence of minicores requires western blot analysis to distinguish the detection of p21 core from minicores. However, the sensitivity for western blot detection of HCV proteins from blood is nil without their prior purification/enrichment from blood. Therefore, we developed a purification method based on a heparin/Mn+2 precipitation of apolipoprotein B‐containing lipoproteins because HCV is thought to circulate as a hybrid lipoviral particle. Minicores are secreted in culture when cells are grown in the presence of human serum. The heparin/Mn+2 precipitate from HCV‐infected cell culture supernatants and from the blood of 4 patients with high‐titer genotype‐1 HCV contained minicores. Conclusion: Minicores are major newly discovered HCV proteins that are secreted and circulate in blood during natural infections. Minicore proteins have translational potential as targets in diagnostic assays and in vaccine development. (Hepatology Communications 2018;2:21–28)
机译:丙型肝炎病毒(HCV)是全球慢性血液传播感染的最普遍原因之一。尽管已经开发出高效的治疗方法,但大多数感染者仍未意识到其感染。大约75%的感染发生在中低收入国家;因此,为了减少全球负担,需要对HCV分子病毒学进行持续研究,并开发疫苗和负担得起的诊断方法。细胞培养物中会产生多种细胞内形式的HCV核衣壳(核心)蛋白。它们包括常规的p21核心和新发现的较短的同工型(minicores)。迷你核缺乏p21核的N末端。进行这项研究是为了确定微核是否在细胞培养物中分泌,更重要的是,微核是否会在感染HCV的个体的血液中循环。我们还开发了一种新的单克隆抗体,可检测针对p21核心和minicore共有的C末端区域的minicore。 minicores的直接证据需要进行蛋白质印迹分析,以区分p21 core和minicores的检测。然而,如果不事先从血液中纯化/富集,从血液中进行HCV蛋白的蛋白质印迹检测的灵敏度为零。因此,我们开发了一种基于肝素/ Mn +2 沉淀的载脂蛋白B脂蛋白的纯化方法,因为人们认为HCV可以作为杂种脂蛋白颗粒传播。当细胞在人血清存在下生长时,小核在培养中分泌。肝素/ Mn +2 从HCV感染的细胞培养上清液和4名高滴度基因型1 HCV患者的血液中析出的肝素含有minicore。结论:Minicores是新发现的主要HCV蛋白,在自然感染过程中会在血液中分泌并循环。 Minicore蛋白具有翻译潜力,可作为诊断分析和疫苗开发中的靶标。 (肝病通讯2018; 2:21–28)

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