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人柯萨奇B4病毒分离株的多样性:与病毒诱导的糖尿病的关系

Diversity within a human isolate of coxsackie B4: relationship to viral-induced diabetes.

作者信息

Hartig P C, Madge G E, Webb S R

出版信息

J Med Virol. 1983;11(1):23-30. doi: 10.1002/jmv.1890110104.

Abstract

The ability of different strains of a single virus type to produce different pathogenic expressions is well documented within the picornavirus group. Coxsackievirus, group B, type 4 (CB4) has been associated with viral-induced diabetes in man, but expression of its potential to induce diabetes in experimental animals is variable. Evidence is presented here for one of the primary sources of this variability that could explain resulting contradictory reports offered in support or rejection of its diabetogenic potential. C57B1/6 and SWR mice were infected with the Edwards isolate of CB4 (CB4-Edw) and three of its plaque-purified virion "strains." These were designated Edwards isolate-1 (E1), E2, and E3. CB4-Edw, E1, E2, and E3 were serologically similar by infectivity neutralization tests, had identical plaque morphology, and replicated to a similar level in the pancreas. The most profound difference was the level of virus antigen accumulation in the islet cells as determined by immunoperoxidase localization. CB4-Edw had moderate antigen accumulation in most islet cells of SWR mice but was restricted to only a few specific cells within the periphery islets of C57B1/6 mice. Unlike CB4-Edw all three new isolates accumulated antigen in most islet cells of both mouse strains. Virus isolate (strain) E2 showed the most intense accumulation in islet cells. These observations suggest that the Edwards isolate of CB4, like other human isolates of CB4 virus, probably exists as a heterogeneous population of virion strains. The pathogenic consequences and expression of any diabetogenic potential is, therefore, dependent on virus strain selection. This diversity must be considered when evaluating the pathogenic nature of CB4 viruses in experimental animals and the possible role of the viruses in diabetes of man.

摘要

在微小核糖核酸病毒组中,单一病毒类型的不同毒株产生不同致病表现的能力已有充分记载。B组柯萨奇病毒4型(CB4)与人的病毒诱导性糖尿病有关,但其在实验动物中诱导糖尿病的潜力表现存在差异。本文提供了这种差异的一个主要来源的证据,这可以解释支持或反对其致糖尿病潜力的相互矛盾的报道。将C57B1/6和SWR小鼠感染CB4的爱德华兹分离株(CB4-Edw)及其三个空斑纯化的病毒粒子“毒株”。这些分别命名为爱德华兹分离株-1(E1)、E2和E3。通过感染性中和试验,CB4-Edw、E1、E2和E3在血清学上相似,具有相同的空斑形态,并且在胰腺中的复制水平相似。最显著的差异是通过免疫过氧化物酶定位确定的胰岛细胞中病毒抗原积累的水平。CB4-Edw在SWR小鼠的大多数胰岛细胞中有中等程度的抗原积累,但仅限于C57B1/6小鼠外周胰岛中的少数特定细胞。与CB4-Edw不同,所有三个新分离株在两种小鼠品系的大多数胰岛细胞中都积累了抗原。病毒分离株(毒株)E2在胰岛细胞中的积累最为强烈。这些观察结果表明,CB4的爱德华兹分离株与CB4病毒的其他人类分离株一样,可能以病毒粒子毒株的异质群体形式存在。因此,任何致糖尿病潜力所产生的致病后果和表现取决于病毒毒株的选择。在评估CB4病毒在实验动物中的致病性质以及该病毒在人类糖尿病中可能的作用时,必须考虑这种多样性

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