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焦磷酸测序干血斑揭示了初治和经验丰富的 HIV 耐药患者之间的药物耐药性差异。

Pyrosequencing dried blood spots reveals differences in HIV drug resistance between treatment naïve and experienced patients.

机构信息

National HIV & Retrovirology Laboratories, National Microbiology Laboratory, Public Health Agency of Canada, Ottawa, Canada.

出版信息

PLoS One. 2013;8(2):e56170. doi: 10.1371/journal.pone.0056170. Epub 2013 Feb 7.

Abstract

Dried blood spots (DBS) are an alternative specimen collection format for HIV-1 genotyping. DBS produce HIV genotyping results that are robust and equivalent to plasma when using conventional sequencing methods. However, using tagged, pooled pyrosequencing, we demonstrate that concordance between plasma and DBS is not absolute and varies according to viral load (VL), duration of HIV infection and antiretroviral therapy (ART) status. The plasma/DBS concordance is the highest when VL is ≥5,000 copies/ml and/or the patient has no ART exposure and/or when the duration of HIV infection is ≤2 years. Stepwise regression analysis revealed that VL is most important independent predictor for concordance of DBS with plasma genotypes. This is the first study to use next generation sequencing to identify discordance between DBS and plasma genotypes. Consideration should be given to VL, duration of infection, and ART exposure when interpreting DBS genotypes produced using next generation sequencing. These findings are of particular significance when DBS are to be used for clinical monitoring purposes.

摘要

干血斑 (DBS) 是 HIV-1 基因分型的另一种替代标本采集格式。当使用传统测序方法时,DBS 产生的 HIV 基因分型结果与血浆结果一样稳健且等效。然而,我们使用标记的、 pooled 焦磷酸测序表明,血浆和 DBS 之间的一致性并非绝对的,并且根据病毒载量 (VL)、HIV 感染持续时间和抗逆转录病毒治疗 (ART) 状况而有所不同。当 VL≥5,000 拷贝/ml 且/或患者未接受 ART 暴露和/或 HIV 感染持续时间≤2 年时,血浆/DBS 一致性最高。逐步回归分析显示,VL 是 DBS 与血浆基因型一致性的最重要独立预测因素。这是第一项使用下一代测序来确定 DBS 和血浆基因型之间不一致性的研究。在解释使用下一代测序产生的 DBS 基因型时,应考虑 VL、感染持续时间和 ART 暴露。当 DBS 用于临床监测目的时,这些发现具有特别重要的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2f9/3567018/654d657aa006/pone.0056170.g001.jpg

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