| Literature DB >> 33320883 |
Dan Xiong1, Wenjun Dai2, Jiaojiao Gong2, Guande Li2, Nansong Liu2, Wei Wu1, Jiaqiang Pan2, Chen Chen2, Yingzhen Jiao3, Huina Deng2, Junwei Ye2, Xuanxuan Zhang2, Huiling Huang2, Qianyun Li4, Liang Xue2, Xiuming Zhang1, Guanghui Tang2.
Abstract
The recent outbreak of betacoronavirus Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), which is responsible for the Coronavirus Disease 2019 (COVID-19) global pandemic, has created great challenges in viral diagnosis. The existing methods for nucleic acid detection are of high sensitivity and specificity, but the need for complex sample manipulation and expensive machinery slow down the disease detection. Thus, there is an urgent demand to develop a rapid, inexpensive, and sensitive diagnostic test to aid point-of-care viral detection for disease monitoring. In this study, we developed a clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR associated proteins (Cas) 12a-based diagnostic method that allows the results to be visualized by the naked eye. We also introduced a rapid sample processing method, and when combined with recombinase polymerase amplification (RPA), the sample to result can be achieved in 50 minutes with high sensitivity (1-10 copies per reaction). This accurate and portable detection method holds a great potential for COVID-19 control, especially in areas where specialized equipment is not available.Entities:
Year: 2020 PMID: 33320883 DOI: 10.1371/journal.pbio.3000978
Source DB: PubMed Journal: PLoS Biol ISSN: 1544-9173 Impact factor: 8.029