Developing an Amplification Refractory Mutation System-Quantitative Reverse Transcription-PCR Assay for Rapid and Sensitive Screening of SARS-CoV-2 Variants of Concern
Dongyan Xiong,Xiaoxu Zhang,Mengjuan Shi,Nuo Wang,Ping He,Zhuo Dong,Jie Zhong,Jin Luo,Yong Wang,Junping Yu,Hongping Wei +10 more
TL;DR: The ARMS-RT-qPCR assay could be used for screening the two highly concerning variants Alpha and Delta by normal PCR laboratories in airports and in hospitals and other health-related organizations.
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Abstract: The current stage of the pandemic, led by SARS-CoV-2 variants of concern (VOCs), underscores the necessity to develop a cost-effective and rapid molecular diagnosis assay to differentiate the VOCs. In this study, over 1 million SARS-CoV-2 genomic sequences of high quality from GISAID were analyzed and a network of the common mutations of the lineages was constructed. ABSTRACT With the emergence and wide spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs), such as the Delta variant (B.1.617.2 lineage and AY sublineage), it is important to track VOCs for sourcing of transmission. Currently, whole-genome sequencing is commonly used for detecting VOCs, but this is limited by the high costs of reagents and sophisticated sequencers. In this study, common mutations in the genomes of SARS-CoV-2 VOCs were identified by analyzing more than 1 million SARS-CoV-2 genomes from public data. Among them, mutations C1709A (a change of C to A at position 1709) and C56G, respectively, were found in more than 99% of the genomes of Alpha and Delta variants and were specific to them. Then, a method using the amplification refractory mutation system combined with quantitative reverse transcription-PCR (ARMS-RT-qPCR) based on the two mutations was developed for identifying both VOCs. The assay can detect as little as 1 copy/μL of the VOCs, and the results for identifying Alpha and Delta variants in clinical samples by the ARMS-RT-qPCR assay showed 100% agreement with the results using sequencing-based methods. The whole assay can be completed in 2.5 h using commercial fluorescent PCR instruments. Therefore, the ARMS-RT-qPCR assay could be used for screening the two highly concerning variants Alpha and Delta by normal PCR laboratories in airports and in hospitals and other health-related organizations. Additionally, based on the unique mutations identified by the genomic analysis, similar molecular assays can be developed for rapid identification of other VOCs. IMPORTANCE The current stage of the pandemic, led by SARS-CoV-2 variants of concern (VOCs), underscores the necessity to develop a cost-effective and rapid molecular diagnosis assay to differentiate the VOCs. In this study, over 1 million SARS-CoV-2 genomic sequences of high quality from GISAID were analyzed and a network of the common mutations of the lineages was constructed. The conserved unique mutations specific for SARS-CoV-2 VOCs were found. Then, ARMS-RT-qPCR assays based on the two unique mutations of the Alpha and Delta variants were developed for the detection of the two VOCs. Application of the assay in clinical samples demonstrated that the current method is a convenient, cost-effective, and rapid way to screen the target SARS-CoV-2 VOCs.
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Citations
Accessible and Adaptable Multiplexed Real-Time PCR Approaches to Identify SARS-CoV-2 Variants of Concern
Tingbo Yan,Ye Xu,Rongrong Zheng,Xiaohong Zeng,Ze-Jian Chen,Su Lin,Zihan Xia,Yiqun Liao,Yongyou Zhang,Qingge Li +9 more
TL;DR: Two PCR strategies targeting spike protein mutations to identify the Alpha, Delta, and Omicron variants represent an alternative tool capable of identifying current SARS-CoV-2 VOCs, adaptable for emerging variants and accessible for laboratories using existing equipment and personnel.
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An Update on Detection Technologies for SARS-CoV-2 Variants of Concern
TL;DR: A range of research has been reported on detection techniques for VOCs, which is beneficial to prevent the rapid spread of the epidemic, improve the effectiveness of public health and social measures, and reduce the harm to human health and safety as discussed by the authors .
Flap Endonuclease-Induced Steric Hindrance Change Enables the Construction of Multiplex and Versatile Lateral Flow Strips for DNA Detection.
Yinjiao Ma,Xue Ping Ma,Li Bu,Jingwen Shan,Danni Liu,Likun Zhang,Xiemin Qi,Yanan Chu,Hai-Ping Wu,Bingjie Zou,Guohua Zhou +10 more
TL;DR: A multiplex and versatile LFS based on flap endonuclease 1 (FEN1)-induced steric hindrance change (FISH-LFS) that is convenient in operation, simple in instrumentation, specific in genotyping, and very easy in setting up multiplex POCT assays is proposed.
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Asghar Nasir,Uzma Bashir Aamir,Akbar Kanji,Azra Samreen,Zeeshan Ansar,Najia Karim Ghanchi,Ali Raza Bukhari,Kiran Iqbal Masood,Noreen Islam,S. Ghanic,M. A. Syed,M. Wassan,Sahar Mahmood,Zahra Hasan +13 more
TL;DR: It is proposed that a mutation targeted approach can be a rapid, lower cost solution to aid tracking of known VOCs during pandemic waves.
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Rapid assays of SARS-CoV-2 virus and noble biosensors by nanomaterials
Yang Liu,Yilong Li,Yuteng Hang,Lei Wang,Jinghan Wang,Ning Bao,Youngeun Kim,Ho Won Jang +7 more
TL;DR: This critical review discusses the detection principles, fabrication techniques, and applications on the rapid detection of SARS-CoV-2 with three categories: rapid nuclear acid augmentation test, rapid immunoassay test and biosensors.
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