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在单细胞分辨率下检测病毒序列可识别与宿主基因表达变化相关的新型病毒。

Detection of viral sequences at single-cell resolution identifies novel viruses associated with host gene expression changes.

作者信息

Luebbert Laura, Sullivan Delaney K, Carilli Maria, Eldjárn Hjörleifsson Kristján, Viloria Winnett Alexander, Chari Tara, Pachter Lior

机构信息

Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.

Department of Computing and Mathematical Sciences, California Institute of Technology, Pasadena, CA, USA.

出版信息

Nat Biotechnol. 2025 Apr 22. doi: 10.1038/s41587-025-02614-y.

Abstract

The increasing use of high-throughput sequencing methods in research, agriculture and healthcare provides an opportunity for the cost-effective surveillance of viral diversity and investigation of virus-disease correlation. However, existing methods for identifying viruses in sequencing data rely on and are limited to reference genomes or cannot retain single-cell resolution through cell barcode tracking. We introduce a method that accurately and rapidly detects viral sequences in bulk and single-cell transcriptomics data based on the highly conserved RdRP protein, enabling the detection of over 100,000 RNA virus species. The analysis of viral presence and host gene expression in parallel at single-cell resolution allows for the characterization of host viromes and the identification of viral tropism and host responses. We apply our method to peripheral blood mononuclear cell data from rhesus macaques with Ebola virus disease and describe previously unknown putative viruses. Moreover, we are able to accurately predict viral presence in individual cells based on macaque gene expression.

摘要

高通量测序方法在研究、农业和医疗保健领域的使用日益增加,为经济高效地监测病毒多样性以及研究病毒与疾病的相关性提供了契机。然而,现有从测序数据中识别病毒的方法依赖于参考基因组且受限于此,或者无法通过细胞条形码追踪保持单细胞分辨率。我们介绍了一种基于高度保守的RNA依赖的RNA聚合酶(RdRP)蛋白,能在批量和单细胞转录组数据中准确快速检测病毒序列的方法,可检测超过100,000种RNA病毒。在单细胞分辨率下并行分析病毒存在情况和宿主基因表达,有助于表征宿主病毒组,识别病毒嗜性和宿主反应。我们将该方法应用于感染埃博拉病毒病的恒河猴的外周血单核细胞数据,并描述了此前未知的假定病毒。此外,我们能够基于猕猴基因表达准确预测单个细胞中的病毒存在情况。

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