在 1 型糖尿病器官捐献者的胰腺和淋巴组织中检测肠道病毒 RNA

Jutta E Laiho, Sami Oikarinen, Sofia Morfopoulou, Maarit Oikarinen, Ashlie Renner, Daniel Depledge, Matthew C Ross, Ivan C Gerling, Judith Breuer, Joseph F Petrosino, Vincent Plagnol, Alberto Pugliese, Antonio Toniolo, Richard E Lloyd, Heikki Hyoty
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引用次数: 0

摘要

目的/假设 nPOD-Virus 小组合作应用创新技术,对 1 型糖尿病器官捐献者的胰腺和其他组织中的病毒 RNA 进行检测和测序。这些分析涉及迄今为止收集到的最大量的胰腺样本。方法 我们分析了来自以下供体组的胰腺、脾脏、胰腺淋巴结和十二指肠样本:a)1 型糖尿病供体(71 人),含(35 人)或不含(36 人)胰岛素胰岛;b)单或双胰岛自身抗体阳性但无糖尿病的供体(22 人);c)自身抗体阴性但无糖尿病的供体(对照组供体)(74 人)。五家研究实验室参与了此次合作,使用的方法包括无偏见地发现 RNA 病毒(两个 RNA-Seq 平台)、使用 RT-PCR 有针对性地检测肠道病毒 A-D 类型以及检测病毒在细胞培养中的生长情况。结果 直接 RNA-Seq 在胰腺样本中未检测到病毒信号,而 RT-PCR 则在五组供体中的三组胰腺样本中检测到了经测序证实的低量肠道病毒 RNA,这三组供体分别是:含胰岛素胰岛的 1 型糖尿病供体,16%(5/32)呈阳性;单胰岛自身抗体阳性供体,53%(8/15)呈阳性;非糖尿病供体,8%(4/49)呈肠道病毒 RNA 阳性。与胰岛素缺乏的 1 型糖尿病供体(p-value <0.001)和对照组供体(p-value 0.004)相比,单个胰岛自身抗体阳性供体的肠道病毒 RNA 检测率明显更高。一些供体的胰腺淋巴结也呈阳性。RT-PCR 在少数供体的脾脏中也检测到了肠道病毒 RNA,RT-PCR 前在易感细胞系中富集病毒会导致脾脏阳性率更高,尤其是在 1 型糖尿病供体中。有趣的是,检测到的肠道病毒毒株并没有引起典型的溶解性感染,这可能反映了其易持续存在的特性。结论/解释 这是使用多种检测方法检测 1 型糖尿病器官捐献者胰腺中是否存在肠道病毒 RNA 的最大规模协调工作。这些发现与 1 型糖尿病患者和胰岛自身抗体患者的胰腺和淋巴组织中可能携带低水平肠道病毒感染的观点一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of enterovirus RNA in pancreas and lymphoid tissues of organ donors with type 1 diabetes
Aims/hypothesis The nPOD-Virus group collaboratively applied innovative technologies to detect and sequence viral RNA in pancreas and other tissues from organ donors with type 1 diabetes. These analyses involved the largest number of pancreas samples collected to date. Methods We analysed pancreas, spleen, pancreatic lymph nodes, and duodenum samples from the following donor groups: a) donors with type 1 diabetes (n=71), with (n=35) or without (n=36) insulin-containing islets, (b) donors with single or double islet autoantibody positivity without diabetes (n=22) and c) autoantibody-negative donors without diabetes (control donors) (n=74). Five research laboratories participated in this collaborative effort using approaches for unbiased discovery of RNA viruses (two RNA-Seq platforms), targeted detection of Enterovirus A-D species using RT-PCR, and tests for virus growth in cell-culture. Results Direct RNA-Seq did not detect virus signal in pancreas samples, whereas RT-PCR detected enterovirus RNA confirmed by sequencing in low amounts in pancreas samples in three of the five donor groups, namely donors with type 1 diabetes with insulin-containing islets, 16% (5/32) donors being positive, donors with single islet autoantibody positivity with 53% (8/15) donors being positive, and non-diabetic donors with 8% (4/49) being enterovirus RNA positive. Detection of enterovirus RNA was significantly more frequent in single islet autoantibody-positive donors compared to donors with type 1 diabetes with insulin-deficient islets (p-value <0.001) and control donors (p-value 0.004). In some donors, pancreatic lymph nodes were also positive. RT-PCR detected enterovirus RNA also in spleen of a small number of donors and virus enrichment in susceptible cell lines before RT-PCR resulted in much higher rate in spleen positivity, particularly in donors with type 1 diabetes. Interestingly, the enterovirus strains detected did not cause a typical lytic infection, possibly reflecting their persistence-prone nature. Conclusions/interpretation This was the largest coordinated effort to examine the presence of enterovirus RNA in pancreas of organ donors with type 1 diabetes, using a multitude of assays. These findings are consistent with the notion that both the subjects with type 1 diabetes and those with islet autoantibodies may carry a low-grade enterovirus infection in the pancreas and lymphoid tissues.
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