...
首页> 外文期刊>MethodsX >A novel approach to minimize the false negative COVID-19 diagnosis by inclusion of specific cell markers and multiple sample collection
【24h】

A novel approach to minimize the false negative COVID-19 diagnosis by inclusion of specific cell markers and multiple sample collection

机译:一种通过包含特定细胞标记和多个样品收集来最小化假阴性Covid-19诊断的新方法

获取原文
   

获取外文期刊封面封底 >>

       

摘要

The SARS-CoV-2 pandemic has caused unpredictable mortality and economic losses globally. With no approved drug for the treatment, the accurate diagnosis of COVID-19 becomes essential. RNA based test takes several hours and require extensive human intervention for RNA extraction and RT-PCR, but it is preferred over the antibody-based detection as the latter does not detect the early stage infections.The RT-PCR being a gold standard of COVID-19 diagnosis offers highly standardized detection of the SARS-CoV-2 RNA, still vulnerable for false-negative diagnosis due to absence of infected cells in the sample or inaccurate RNA extraction. Hence there is a need to develop alternative protocols and methods for the accurate COVID-19 diagnosis. Here we propose two additional steps in RT-PCR based COVID-19 diagnosis to minimize false-negative detection. The first step involves collection of four samples from an individual. Each sample should be collected from nasopharyngeal and oropharyngeal regions on day 01, mixed together followed by RNA extraction and then repeating the same exercise on day 03. The RNA extracted on day 01 and day 03 must be pooled together to be used in the RT-PCR. Second, we propose the inclusion of the control marker genes specific to nasal goblet cell, type-II pneumocyte and absorptive enterocytes to ensure the specificity of the RNA source. Overall, these additional steps in the proposed method would increase the chances of SARS-CoV-2 detection in the infected population and would limit the false-negative diagnosis of COVID-19 and hence the spread of this disease.?RT-PCR based COVID-19 diagnosis is vulnerable to the false-negative results due to inaccurate sample isolation or RNA extraction.?RNA pool of multiple samples from an individual improves the chances of detection of SARS-CoV-2 by RT-PCR.?Inclusion of specific marker genes would ensure the right RNA source from the desired cell.
机译:SARS-COV-2大流行导致全球不可预测的死亡率和经济损失。没有批准的治疗药物,Covid-19的准确诊断变得必不可少。基于RNA的试验需要几个小时,需要大量的人体干预RNA提取和RT-PCR,但是优选在基于抗体的检测中,因为后者未检测到早期感染。RT-PCR是Covid的金标准-19诊断提供了SARS-COV-2 RNA的高度标准化检测,仍然易于由于样品中的存在感染细胞或不准确的RNA提取而导致的假阴性诊断。因此,需要为准确的CoVID-19诊断制定替代协议和方法。在这里,我们提出了另外两步RT-PCR基Covid-19诊断,以最大限度地减少假阴性检测。第一步涉及来自个体的四个样本。应在第01天中从鼻咽癌和口咽区域收集每个样品,混合在一起,然后在第01天重复相同的运动。在第01天和第03天中提取的RNA将合并在一起以便在RT-中使用。 PCR。其次,我们提出包括对鼻腔细胞的对照标记基因,II型肺细胞和吸收性肠细胞,以确保RNA源的特异性。总体而言,这些方法中的这些额外的步骤将增加SARS-COV-2检测在感染的人群中的可能性,并限制Covid-19的假阴性诊断,从而限制该疾病的传播.?Rt- PCR基础的Covid -19诊断易受由于样品分离或RNA提取的不准确的假阴性结果。来自个体的多个样品的池池通过RT-分布通过RT-分布检测SARS-COV-2的可能性。特定标记物基因将确保来自所需细胞的正确RNA源。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号