肾综合征出血热(HFRS)患者外泌体microRNA-126和microRNA-218表达谱的研究

I. Gilyazova, G. Khasanova, Elizaveta A. Ivanova, D. Asadullina, Aliya N. Khasanova, A. Izmailov, G. Gilyazova, Guoqing Wang, Honglan Huang, Jiahui Pan, Tong Shao, Haochen Yao, Wenfang Wang, E. Khusnutdinova
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引用次数: 2

摘要

背景:由正汉坦病毒引起的肾综合征出血热(HFRS)是人类自然局灶性疾病中的主要疾病之一,目前尚无准确、灵敏的现代诊断方法。为了改善这种情况,需要更好地了解汉坦病毒的HFRS发病机制。感染期间患者血清或血浆中循环microrna的表达水平使其成为诊断HFRS的潜在治疗性生物标志物。本研究目的:分析HFRS患者不同疾病阶段miR-126和miR-218的表达水平。材料与方法:HFRS患者病情中度组105份RNA样本,重度组99份,重度合并并发症组84份RNA样本。对HFRS患者在发热初期(发病1-4天)、多尿期(发病15-22天)和恢复期三次采集血样用于分子遗传学分析。使用miRNeasy血清/血浆高级试剂盒(Qiagen,德国)进行总RNA分离。采用miRCURY LNA SYBR绿色PCR试剂盒(Qiagen, Germany)和实时PCR产物检测系统LightCycler96 (Roch)进行定量实时PCR。结果:HFRS患者发热期和多尿期miR-126、miR-218表达水平两两比较,无统计学意义(P>0.05)。结论:需要进一步研究各种microrna的靶基因网络,以阐明影响HFRS发生发展的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of the exosomal microRNA-126 and microRNA-218 expression profiles in patients with hemorrhagic fever with renal syndrome (HFRS)
Background: Hemorrhagic fever with renal syndrome (HFRS), caused by orthohantaviruses, occupies one of the leading places among natural focal human diseases, for which there are no modern accurate and highly sensitive diagnostic methods. To improve this situation, a better understanding of the hantavirus pathogenesis of HFRS is required. The expression levels of circulating microRNAs in the serum or plasma of patients during infection make them potential therapeutic biomarkers for the diagnosis of HFRS. The aim of the study: To analyze the expression levels of miR-126 and miR-218 patients with HFRS at different stages of the disease. Materials and methods: The moderate disease severity group of HFRS patients included 105 RNA samples, severe – 99 and severe with complications – 84 RNA samples. Blood samples of HFRS patients for molecular genetic analysis were collected three times – during the initial febrile period (1-4 days of illness), the polyuric period (15-22 days of illness) and during the convalescence period. Total RNA isolation was performed using the miRNeasy Serum/Plasma Advanced Kit (Qiagen, Germany). Quantitative realtime PCR was performed using the miRCURY LNA SYBR Green PCR Kit (Qiagen, Germany) and the real time PCR product detection system LightCycler96 (Roch). Results: A pairwise comparison of miR-126 and miR-218 expression levels in patients with HFRS at the fever stage and at the polyuric stage of HFRS did not reveal statistically significant results (P>0.05). Conclusion: Further studies of the network of genes that are targets of various microRNAs are needed to clarify the molecular mechanisms that can influence the occurrence and development of HFRS.
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