Rapid and accurate nucleobase detection using FnCas9 and its application in COVID-19 diagnosis

被引:100
作者
Azhar, Mohd [1 ,2 ]
Phutela, Rhythm [1 ,2 ]
Kumar, Manoj [1 ,2 ]
Ansari, Asgar Hussain [1 ,2 ]
Rauthan, Riya [1 ,2 ]
Gulati, Sneha [1 ]
Sharma, Namrata [1 ]
Sinha, Dipanjali [1 ,2 ]
Sharma, Saumya [1 ,2 ]
Singh, Sunaina [1 ]
Acharya, Sundaram [1 ,2 ]
Sarkar, Sajal [1 ]
Paul, Deepanjan [1 ]
Kathpalia, Poorti [1 ]
Aich, Meghali [1 ,2 ]
Sehgal, Paras [1 ,2 ]
Ranjan, Gyan [1 ,2 ]
Bhoyar, Rahul C. [1 ]
Singhal, Khushboo [1 ,2 ]
Lad, Harsha [3 ]
Patra, Pradeep Kumar [3 ]
Makharia, Govind [4 ]
Chandak, Giriraj Ratan [5 ]
Pesala, Bala [7 ]
Chakraborty, Debojyoti [1 ,2 ]
Maiti, Souvik [1 ,2 ,6 ]
机构
[1] CSIR Inst Genom & Integrat Biol, Mathura Rd, New Delhi 110025, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
[3] Chhattisgarh Inst Med Sci, CSIR Sickle Cell Anemia Mission Lab, Bilaspur 495001, Chhattisgarh, India
[4] All India Inst Med Sci, New Delhi 110029, India
[5] CSIR Ctr Cellular & Mol Biol, Uppal Rd, Hyderabad 500007, Telangana, India
[6] CSIR Natl Chem Lab, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India
[7] CSIR Cent Elect Engn Res Inst, Chennai, Tamil Nadu, India
关键词
CRISPRDx; FnCas9; SARS-CoV2; SNV detection; FELUDA; LFA; AMPLIFICATION;
D O I
10.1016/j.bios.2021.113207
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Rapid detection of DNA/RNA pathogenic sequences or variants through point-of-care diagnostics is valuable for accelerated clinical prognosis, as witnessed during the recent COVID-19 outbreak. Traditional methods relying on qPCR or sequencing are tough to implement with limited resources, necessitating the development of accurate and robust alternative strategies. Here, we report FnCas9 Editor Linked Uniform Detection Assay (FELUDA) that utilizes a direct Cas9 based enzymatic readout for detecting nucleobase and nucleotide sequences without transcleavage of reporter molecules. We also demonstrate that FELUDA is 100% accurate in detecting single nucleotide variants (SNVs), including heterozygous carriers, and present a simple web-tool JATAYU to aid end-users. FELUDA is semi-quantitative, can adapt to multiple signal detection platforms, and deploy for versatile applications such as molecular diagnosis during infectious disease outbreaks like COVID-19. Employing a lateral flow readout, FELUDA shows 100% sensitivity and 97% specificity across all ranges of viral loads in clinical samples within 1hr. In combination with RT-RPA and a smartphone application True Outcome Predicted via Strip Evaluation (TOPSE), we present a prototype for FELUDA for CoV-2 detection closer to home.
引用
收藏
页数:8
相关论文
共 47 条
[41]   Unique and conserved features of genome and proteome of SARS-coronavirus, an early split-off from the coronavirus group 2 lineage [J].
Snijder, EJ ;
Bredenbeek, PJ ;
Dobbe, JC ;
Thiel, V ;
Ziebuhr, J ;
Poon, LLM ;
Guan, Y ;
Rozanov, M ;
Spaan, WJM ;
Gorbalenya, AE .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 331 (05) :991-1004
[42]   Continuous and Discontinuous RNA Synthesis in Coronaviruses [J].
Sola, Isabel ;
Almazan, Fernando ;
Zuniga, Sonia ;
Enjuanes, Luis .
ANNUAL REVIEW OF VIROLOGY, VOL 2, 2015, 2 :265-288
[43]   CDetection: CRISPR-Cas12b-based DNA detection with sub-attomolar sensitivity and single-base specificity [J].
Teng, Fei ;
Guo, Lu ;
Cui, Tongtong ;
Wang, Xin-Ge ;
Xu, Kai ;
Gao, Qingqin ;
Zhou, Qi ;
Li, Wei .
GENOME BIOLOGY, 2019, 20 (1)
[44]  
Wu F, 2020, NATURE, V580, pE7
[45]   Beware of the second wave of COVID-19 [J].
Xu, Shunqing ;
Li, Yuanyuan .
LANCET, 2020, 395 (10233) :1321-1322
[46]   Cas13d Is a Compact RNA-Targeting Type VI CRISPR Effector Positively Modulated by a WYL-Domain-Containing Accessory Protein [J].
Yan, Winston X. ;
Chong, Shaorong ;
Zhang, Huaibin ;
Makarova, Kira S. ;
Koonin, Eugene V. ;
Cheng, David R. ;
Scott, David A. .
MOLECULAR CELL, 2018, 70 (02) :327-+
[47]   Isothermal Amplification of Nucleic Acids [J].
Zhao, Yongxi ;
Chen, Feng ;
Li, Qian ;
Wang, Lihua ;
Fan, Chunhai .
CHEMICAL REVIEWS, 2015, 115 (22) :12491-12545