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基于熔解曲线的检测方法作为准确检测新型冠状病毒的替代技术

Melting Curve-based Assay as an Alternative Technique for the Accurate Detection of SARS-CoV-2.

作者信息

Aboutalebian Shima, Mirzaaghaei Somaye, Fakhim Hamed, Faramarzi Sama, Mousavi Somayeh, Ghafel Safiyeh, Gholipour Sahar, Farhang Armin, Mirhendi Hossein, Nikaeen Mahnaz

机构信息

Department of Medical Parasitology and Mycology, School of Medicine, & Research Core Facilities Laboratory, Isfahan University of Medical Sciences, Isfahan, Iran.

Infectious Diseases and Tropical Medicine Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Adv Biomed Res. 2022 May 30;11:37. doi: 10.4103/abr.abr_87_21. eCollection 2022.

Abstract

BACKGROUND

Early and cost-effective diagnosis and monitoring of the infection caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are critically important to anticipate and control the disease. We aimed to set up a SYBR Green-based one-step real-time polymerase chain reaction (PCR) as a lower-cost alternative method to detect the virus.

MATERIALS AND METHODS

An in-house SYBR Green-based PCR assay targeting the envelope (E) and RNA-dependent RNA polymerase (RdRp) genes, was set up to diagnose the infection, and was compared with the reference probe-based PCR method.

RESULTS

When the commercial probe-based assay was considered as the reference method, SYBR Green-based PCR had a slightly lower sensitivity (81.98% and 86.25% for E and RdRp targets, respectively) and a good specificity (100% and 94.44% for E and RdRp targets, respectively). For both gene targets, three different melting temperature (Tm) patterns were found in the PCRs of the nasopharyngeal/oropharyngeal swab samples, but no size polymorphism was seen in agarose gel electrophoresis.

CONCLUSION

Further studies to improvement of the assay are needed to make it an inexpensive and reliable tool for the diagnosis of COVID-19.

摘要

背景

对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的感染进行早期且经济高效的诊断和监测对于预测和控制该疾病至关重要。我们旨在建立一种基于SYBR Green的一步法实时聚合酶链反应(PCR),作为检测该病毒的低成本替代方法。

材料与方法

建立了一种针对包膜(E)基因和RNA依赖性RNA聚合酶(RdRp)基因的基于SYBR Green的内部PCR检测方法用于诊断感染,并与基于探针的参考PCR方法进行比较。

结果

当将基于商业探针的检测方法视为参考方法时,基于SYBR Green的PCR敏感性略低(E和RdRp靶标的敏感性分别为81.98%和86.25%),但特异性良好(E和RdRp靶标的特异性分别为100%和94.44%)。对于这两个基因靶标,在鼻咽/口咽拭子样本的PCR中发现了三种不同的解链温度(Tm)模式,但在琼脂糖凝胶电泳中未观察到大小多态性。

结论

需要进一步研究改进该检测方法,使其成为诊断新型冠状病毒肺炎(COVID-19)的廉价且可靠的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3280/9259445/02c7eadf5666/ABR-11-37-g001.jpg

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