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用于确定新冠病毒转录谱的新型逆转录数字滴度PCR检测方法

Novel RT-ddPCR Assays for determining the transcriptional profile of SARS-CoV-2.

作者信息

Telwatte Sushama, Kumar Nitasha, Vallejo-Gracia Albert, Kumar G Renuka, Lu Chuanyi M, Ott Melanie, Wong Joseph K, Yukl Steven A

机构信息

Department of Medicine, University of California, San Francisco, CA, USA.

Department of Infectious Diseases, San Francisco VA Health Care System, San Francisco, CA, USA.

出版信息

bioRxiv. 2021 Jan 12:2021.01.12.425991. doi: 10.1101/2021.01.12.425991.

Abstract

The exact mechanism of coronavirus replication and transcription is not fully understood; however, a hallmark of coronavirus transcription is the generation of negative-sense RNA intermediates that serve as the templates for the synthesis of positive-sense genomic RNA (gRNA) and an array of subgenomic mRNAs (sgRNAs) encompassing sequences arising from discontinuous transcription. Existing PCR-based diagnostic assays for SAR-CoV-2 are qualitative or semi-quantitative and do not provide the resolution needed to assess the complex transcription dynamics of SARS-CoV-2 over the course of infection. We developed and validated a novel panel of specially designed SARS-CoV-2 ddPCR-based assays to map the viral transcription profile. Application of these assays to clinically relevant samples will enhance our understanding of SARS-CoV-2 replication and transcription and may also inform the development of improved diagnostic tools and therapeutics.

摘要

冠状病毒复制和转录的确切机制尚未完全明确;然而,冠状病毒转录的一个标志是产生负义RNA中间体,这些中间体作为模板用于合成正义基因组RNA(gRNA)和一系列亚基因组mRNA(sgRNA),后者包含来自不连续转录产生的序列。现有的基于PCR的SARS-CoV-2诊断检测方法是定性或半定量的,无法提供评估SARS-CoV-2在感染过程中复杂转录动态所需的分辨率。我们开发并验证了一组新的基于SARS-CoV-2数字滴度PCR(ddPCR)的专门设计检测方法,以绘制病毒转录图谱。将这些检测方法应用于临床相关样本将增进我们对SARS-CoV-2复制和转录的理解,也可能为改进诊断工具和治疗方法的开发提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de9d/7814816/0b7e313dc94d/nihpp-2021.01.12.425991-f0001.jpg

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