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靶向基因组重复区域测序检测循环无细胞棘球蚴 DNA。

Targeted Sequencing of Genomic Repeat Regions Detects Circulating Cell-free Echinococcus DNA.

机构信息

Institute of Molecular Precision Medicine, Xiangya Hospital, Key Laboratory of Molecular Precision Medicine of Hunan Province, Central South University, Changsha, Hunan, China.

Center for Medical Genetics, Central South University, Changsha, Hunan, China.

出版信息

PLoS Negl Trop Dis. 2020 Mar 10;14(3):e0008147. doi: 10.1371/journal.pntd.0008147. eCollection 2020 Mar.

Abstract

BACKGROUND

Echinococcosis is a chronic zoonosis caused by tapeworms of the genus Echinococcus. Treatment of the disease is often expensive and complicated, sometimes requiring extensive surgery. Ultrasonographic imaging is currently the main technique for diagnosis, while immunological analysis provides additional information. Confirmation still needs pathological analysis. However, these diagnostic techniques generally detect infection in late stages of the disease. An accurate, early and non-invasive molecular diagnostic method is still unavailable.

METHODOLOGY/PRINCIPAL FINDINGS: We sequenced the cell-free DNA (cfDNA) from plasma of echinococcosis patients and confirmed the presence of Echinococcus DNA. To improve detection sensitivity, we developed a method based on targeted next-generation sequencing of repeat regions. Simulation experiments demonstrate that the targeted sequencing is sensitive enough to detect as little as 0.1% of an Echinococcus genome in 1 mL of plasma. Results obtained using patient plasma shows that the Area Under the Curve (AUC) of the method is 0.862, with a detection sensitivity of 62.50% and specificity of 100%, corresponding to a Youden-index of 0.625.

CONCLUSIONS/SIGNIFICANCE: This study provides evidence that hydatid cysts release cfDNA fragments into patient plasma. Using the repeat region targeted sequencing method, highly specific detection of Echinococcus infection was achieved. This study paves a new avenue for potential non-invasive screening and diagnosis of echinococcosis.

摘要

背景

包虫病是一种由棘球属绦虫引起的慢性人畜共患病。该病的治疗通常昂贵且复杂,有时需要广泛的手术。超声成像目前是诊断的主要技术,而免疫分析提供了额外的信息。确诊仍需要进行病理分析。然而,这些诊断技术通常在疾病的晚期才能检测到感染。目前仍缺乏一种准确、早期、非侵入性的分子诊断方法。

方法/主要发现:我们对包虫病患者的血浆中的游离细胞 DNA(cfDNA)进行了测序,并证实了棘球蚴 DNA 的存在。为了提高检测灵敏度,我们开发了一种基于重复区域靶向下一代测序的方法。模拟实验表明,靶向测序足以检测 1 毫升血浆中低至 0.1%的棘球蚴基因组。使用患者血浆获得的结果表明,该方法的曲线下面积(AUC)为 0.862,检测灵敏度为 62.50%,特异性为 100%,对应的约登指数为 0.625。

结论/意义:本研究证明了包虫囊肿会将 cfDNA 片段释放到患者的血浆中。通过使用重复区域靶向测序方法,实现了对棘球蚴感染的高度特异性检测。本研究为包虫病的潜在非侵入性筛查和诊断开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74f/7083330/5ef9851d09a5/pntd.0008147.g001.jpg

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