Suppr超能文献

基质辅助激光解吸电离飞行时间质谱分析用于直接检测鼻咽拭子中的 SARS-CoV-2。

Matrix-Assisted Laser Desorption and Ionization Time-of-Flight Mass Spectrometry Analysis for the Direct Detection of SARS-CoV-2 in Nasopharyngeal Swabs.

机构信息

Division of Microbiology, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki City, Kanagawa 210-9501, Japan.

Laboratory of Microbiology, Department of Veterinary Medicine, Azabu University, 1-17-71 Fucihnobe, Chuo-ku, Sagamihara, Kanagawa 252-5201, Japan.

出版信息

Anal Chem. 2022 Mar 15;94(10):4218-4226. doi: 10.1021/acs.analchem.1c04328. Epub 2022 Mar 3.

Abstract

The most common diagnostic method used for coronavirus disease-2019 (COVID-19) is real-time reverse transcription polymerase chain reaction (PCR). However, it requires complex and labor-intensive procedures and involves excessive positive results derived from viral debris. We developed a method for the direct detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in nasopharyngeal swabs, which uses matrix-assisted laser desorption and ionization time-of-flight mass spectrometry (MALDI-ToF MS) to identify specific peptides from the SARS-CoV-2 nucleocapsid phosphoprotein (NP). SARS-CoV-2 viral particles were separated from biological molecules in nasopharyngeal swabs by an ultrafiltration cartridge. Further purification was performed by an anion exchange resin, and purified NP was digested into peptides using trypsin. The peptides from SARS-CoV-2 that were inoculated into nasopharyngeal swabs were detected by MALDI-ToF MS, and the limit of detection was 10 viral copies. This value equates to 10 viral copies per swab and is approximately equivalent to the viral load of contagious patients. Seven NP-derived peptides were selected as the target molecules for the detection of SARS-CoV-2 in clinical specimens. The method detected between two and seven NP-derived peptides in 19 nasopharyngeal swab specimens from contagious COVID-19 patients. These peptides were not detected in four specimens in which SARS-CoV-2 RNA was not detected by PCR. Mutated NP-derived peptides were found in some specimens, and their patterns of amino acid replacement were estimated by accurate mass. Our results provide evidence that the developed MALDI-ToF MS-based method in a combination of straightforward purification steps and a rapid detection step directly detect SARS-CoV-2-specific peptides in nasopharyngeal swabs and can be a reliable high-throughput diagnostic method for COVID-19.

摘要

用于 2019 冠状病毒病(COVID-19)的最常见诊断方法是实时逆转录聚合酶链反应(PCR)。然而,它需要复杂且劳动密集的程序,并且涉及来自病毒碎片的过多阳性结果。我们开发了一种直接检测鼻咽拭子中严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的方法,该方法使用基质辅助激光解吸电离飞行时间质谱(MALDI-ToF MS)来识别 SARS-CoV-2 核衣壳磷蛋白(NP)的特定肽。SARS-CoV-2 病毒粒子通过超滤膜从鼻咽拭子中的生物分子中分离出来。进一步通过阴离子交换树脂进行纯化,并用胰蛋白酶将纯化的 NP 消化成肽。将接种到鼻咽拭子中的 SARS-CoV-2 病毒粒子用 MALDI-ToF MS 检测,检测限为 10 个病毒拷贝。这个值相当于每个拭子 10 个病毒拷贝,大约相当于传染性患者的病毒载量。选择 7 个 NP 衍生肽作为检测临床标本中 SARS-CoV-2 的靶分子。该方法在 19 份来自传染性 COVID-19 患者的鼻咽拭子标本中检测到 2 到 7 个 NP 衍生肽。在通过 PCR 未检测到 SARS-CoV-2 RNA 的 4 个标本中未检测到这些肽。在一些标本中发现了突变的 NP 衍生肽,并通过精确质量估计了其氨基酸替换模式。我们的结果表明,开发的 MALDI-ToF MS 方法结合了简单的纯化步骤和快速检测步骤,可以直接检测鼻咽拭子中的 SARS-CoV-2 特异性肽,是 COVID-19 的一种可靠高通量诊断方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6be3/8928148/80d213cd4497/ac1c04328_0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验