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乙肝亚病毒颗粒的形态计量分析表明,丝状体比例和长度与临床分期和基因型无关。

A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype.

机构信息

INSERM U1259 MAVIVH, Université de Tours and CHRU de Tours, Tours, France.

Plate-Forme IBiSA de Microscopie Electronique, Université de Tours and CHRU de Tours, Tours, France.

出版信息

J Viral Hepat. 2022 Sep;29(9):719-726. doi: 10.1111/jvh.13712. Epub 2022 Jun 7.

Abstract

It was recently suggested that the composition of circulating hepatitis B subviral particles (SVPs) could be used to differentiate the various stages in chronic hepatitis B virus (HBV) infection, with significantly lower proportions of L and M proteins in inactive carriers than in individuals with chronic hepatitis. L protein is abundant in virions and filamentous SVPs but almost absent from spherical SVPs. We, therefore, performed a morphometric analysis of SVPs in these two groups of patients, by conducting a retrospective analysis on sera from 15 inactive carriers and 11 patients with chronic hepatitis infected with various HBV genotypes. Subviral particles were concentrated by centrifugation on a sucrose cushion, with monitoring by transmission electron microscopy. The percentage of filamentous SVPs and filament length for 100 SVPs was determined with a digital camera. The L protein PreS1 promoter was sequenced from viral genomes by the Sanger method. No marked differences were found between patients, some of whom had only spherical SVPs, whereas others had variable percentages of filamentous SVPs (up to 28%), of highly variable length. High filament percentages were not associated with a particular sequence of the L protein promoter, HBV genotype or even disease stage. High levels of circulating filamentous SVPs are probably more strongly related to individual host factors than to viral strain characteristics or disease stage.

摘要

最近有人提出,循环乙型肝炎亚病毒颗粒 (SVPs) 的组成可用于区分慢性乙型肝炎病毒 (HBV) 感染的各个阶段,非活动携带者中的 L 和 M 蛋白比例明显低于慢性肝炎患者。L 蛋白在病毒粒子和丝状 SVPs 中含量丰富,但在球形 SVPs 中几乎不存在。因此,我们对这两组患者的 SVPs 进行了形态计量分析,对 15 名非活动携带者和 11 名患有慢性乙型肝炎的患者的血清进行了回顾性分析。通过在蔗糖垫上离心浓缩亚病毒颗粒,并通过透射电子显微镜进行监测。使用数码相机确定 100 个 SVPs 中的丝状 SVPs 的百分比和丝状长度。通过 Sanger 法从病毒基因组中对 L 蛋白 PreS1 启动子进行测序。未发现患者之间存在明显差异,其中一些患者只有球形 SVPs,而另一些患者则具有不同比例的丝状 SVPs(高达 28%),长度变化很大。高丝状百分比与 L 蛋白启动子的特定序列、HBV 基因型甚至疾病阶段无关。高水平的循环丝状 SVPs 可能与个体宿主因素的关系更为密切,而与病毒株特征或疾病阶段的关系不大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/686b/9541738/a816f071825d/JVH-29-719-g003.jpg

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