Demonstration of persistent enterovirus in the pancreas of diabetic mice by in situ polymerase chain reaction

M.M Berger , D.M See , M Aymard , B Lina
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引用次数: 12

Abstract

Background: Although Enterovirus (EV) do not persist in the tissue, which is essential to maintain autoimmunity, they have been associated as the cause of chronic autoimmunity in some cases of insulin dependent diabetes mellitus (IDDM). Convincing reports, demonstrating persistent EV infections in the pancreases, are rare.

Objectives: To determine the role of EV in IDDM, a mouse model was tested and in situ polymerase chain reaction (ISPCR) developed. The major problem of ISPCR are the high amounts of non-specific staining. In the current study we developed an ISPCR protocol which minimised non-specific staining and allowed the accurate localisation of the viral RNA in the tissue.

Study design: Five mice were infected with coxsackievirus group B4, sacrificed 7 weeks later and the pancreases were harvested. The EV nucleic acid were localised and detected in the pancreases by ISPCR.

Results: In the current study non-specific staining of ISPCR, due to DNA repair and diffuse artefacts, were minimised and the EV nucleic acids were localised in the β cells of the endocrine pancreases in all five diabetogenic mice.

Conclusion: This study demonstrates an association of viral RNA with the development of diabetes in mice and the usefulness of ISPCR to determine the role of EV in IDDM.

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用原位聚合酶链反应证明糖尿病小鼠胰腺中肠病毒的持久性
背景:虽然肠病毒(EV)不能在组织中持续存在,而这是维持自身免疫所必需的,但在一些胰岛素依赖型糖尿病(IDDM)患者中,它们被认为是慢性自身免疫的原因。令人信服的报告显示,胰腺持续的EV感染是罕见的。目的:为了确定EV在IDDM中的作用,我们建立了小鼠模型,并建立了原位聚合酶链反应(ISPCR)。ISPCR的主要问题是大量的非特异性染色。在目前的研究中,我们开发了一种ISPCR方案,该方案最大限度地减少了非特异性染色,并允许在组织中准确定位病毒RNA。研究设计:5只感染柯萨奇病毒B4组的小鼠,7周后处死,取胰腺。用ISPCR方法定位并检测胰腺中EV核酸。结果:在目前的研究中,由于DNA修复和弥漫性伪影,ISPCR的非特异性染色被最小化,EV核酸被定位在所有5只糖尿病小鼠的内分泌胰腺的β细胞中。结论:本研究证明了病毒RNA与小鼠糖尿病的发展之间的关联,以及ISPCR在确定EV在IDDM中的作用方面的有效性。
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