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黑猩猩丙型肝炎病毒感染的早期事件。

Early events in hepatitis C virus infection of chimpanzees.

作者信息

Shimizu Y K, Weiner A J, Rosenblatt J, Wong D C, Shapiro M, Popkin T, Houghton M, Alter H J, Purcell R H

机构信息

Department of Enteroviruses, National Institute of Health, Tokyo, Japan.

出版信息

Proc Natl Acad Sci U S A. 1990 Aug;87(16):6441-4. doi: 10.1073/pnas.87.16.6441.

Abstract

The cytoplasmic antigen and ultrastructural changes we described previously for chimpanzees (Pan troglodytes) infected with hepatitis C virus (HCV) or with hepatitis D virus have recently been shown to be indirect measures of viral replication and appear to represent a host response to the expression or action of interferon. The time of appearance of these changes in hepatocytes during HCV infection, when compared with similar changes in hepatitis D virus infection, suggests a very early replicative phase for HCV. To investigate the early events in HCV infection, we infected two chimpanzees with HCV and obtained blood and liver biopsy samples from them daily during the first 10 days of infection. The early stage of infection with regard to HCV replication, antigen expression, and ultrastructural changes was similar in both chimpanzees. When tested by cDNA/polymerase chain reaction, HCV sequences became detectable in the serum as early as 3 days after inoculation and remained positive through the peak of aminotransferase elevations. In one chimpanzee the peak of virus production appeared to be 7 weeks after inoculation, which was coincident with rising enzyme values. The cytoplasmic antigen, detected by immunofluorescence, and ultrastructural changes, detected by electron microscopy, became positive in hepatocytes 3 and 6 days, respectively, after HCV sequences were first detected in serum. Circulating anti-HCV appeared 13 weeks and 32 weeks after inoculation, respectively, in the chimpanzees. These data indicate a very early replicative phase for HCV and a potentially long period of infectivity before the appearance of anti-HCV.

摘要

我们先前描述的感染丙型肝炎病毒(HCV)或丁型肝炎病毒的黑猩猩(Pan troglodytes)的细胞质抗原和超微结构变化,最近已被证明是病毒复制的间接指标,似乎代表了宿主对干扰素表达或作用的反应。与丁型肝炎病毒感染时肝细胞中这些变化的出现时间相比,HCV感染时这些变化在肝细胞中出现的时间表明HCV有一个非常早期的复制阶段。为了研究HCV感染的早期事件,我们用HCV感染了两只黑猩猩,并在感染的前10天每天从它们身上获取血液和肝活检样本。两只黑猩猩在HCV复制、抗原表达和超微结构变化方面的感染早期阶段相似。通过cDNA/聚合酶链反应检测,接种后3天血清中即可检测到HCV序列,并且在转氨酶升高的高峰期一直呈阳性。在一只黑猩猩中,病毒产生的高峰期似乎在接种后7周,这与酶值升高同时出现。通过免疫荧光检测到的细胞质抗原和通过电子显微镜检测到的超微结构变化,在血清中首次检测到HCV序列后,分别在肝细胞中于3天和6天变为阳性。在黑猩猩中,循环抗-HCV分别在接种后13周和32周出现。这些数据表明HCV有一个非常早期的复制阶段,并且在抗-HCV出现之前有一个潜在的长时间传染性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ec/54550/1d8a31f1b8ed/pnas01041-0444-a.jpg

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