Abstract
The world is looking towards the development of early diagnosis, treatment, and prevention of Coronavirus disease (COVID-19) caused by SARS-CoV-2 in order to restrict its rapid transmission and mortality among the human population. Globally, more than 5 million cases have been reported with 0.3 million deaths by the end of May 2020. Currently, the World Health Organization (WHO) adopted the screening and diagnosis of SARS-CoV-2 infection with quantitative RT-PCR (qRT-PCR)-based kits; however, the suitability of such kits is restricted due to the requirement of specialized instruments, well-trained personnel, and unavailability in resource-limited areas. The CRISPR-Cas system has recently emerged as a versatile tool for medical research for gene editing, epigenetic control, and disease diagnosis. The use of CRISPR-Cas-based detection of SARS-CoV-2 infection may results in the development of rapid, affordable, and multiplexed point-of-care diagnostic system with high specificity and sensitivity. In this article, we have covered the CRISPR-Cas-based efficient techniques developed for the diagnosis of the SARS-CoV-2 and their suitability for COVID-19 surveillance.
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Abbreviations
- CARMEN:
-
Combinatorial Arrayed Reactions for Multiplexed Evaluation of Nucleic acids
- Cas:
-
CRISPR-associated proteins
- CASLFA:
-
Clustered Regularly Interspaced Short Palindromic Repeats/Cas9-Mediated Lateral Flow Nucleic Acid Assay
- COVID-19:
-
Coronavirus disease
- CRISPR:
-
Clustered regularly interspaced short palindromic repeats
- dCas9:
-
Nuclease-deactivated Cas9
- FELUDA:
-
FnCas9 Editor-Linked Uniform Detection Assay
- FnCas9:
-
Francisella novicida Cas9
- HEPN:
-
Higher eukaryotes and prokaryotes nucleotide-binding domain
- HOLMES:
-
One-hour low-cost multipurpose highly efficient system
- HUDSON:
-
Heating unextracted diagnostic samples to obliterate nucleases
- LAMP:
-
Loop-mediated isothermal amplification
- NASBACC:
-
Nucleic acid sequence-based amplification-CRISPR cleavage
- NHEJ:
-
Non-homologous end joining
- Nsp:
-
Non-structural proteins
- PAM:
-
Protospacer adjacent motif
- PC:
-
Paired dCas9
- RCA:
-
Rolling circle amplification
- RCH:
-
RCA-CRISPR-split-HRP
- RPA:
-
Recombinase polymerase amplification
- RT-qPCR:
-
Quantitative polymerase chain reaction
- SARS-CoV-2:
-
Severe Acute Respiratory Syndrome Coronavirus 2
- sgRNA:
-
Single guide RNA
- SHERLOCK:
-
Specific high sensitivity enzymatic reporter unlocking
- SpCas9:
-
Streptococcus pyogenes Cas9
References
Abudayyeh OO, Gootenberg JS, Konermann S et al (2016) C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector. Science 353:aaf5573
Ackerman CM, Myhrvold C, Thakku SG, et al. (2020) Massively multiplexed nucleic acid detection with Cas13 [published online ahead of print, 2020 Apr 29]. Nature https://doi.org/10.1038/s41586-020-2279-8
Azhar A, Phutela R, Ansari AH et al (2020) Rapid, field-deployable nucleobase detection and identification using FnCas9. bioRxiv. https://doi.org/10.1101/2020.04.07.028167
Bai J, Lin H, Li H, Zhou Y, Liu J, Zhong G (2019) Cas12a-based on-site and rapid nucleic acid detection of African swine fever. Front Microbiol 10(10):2830
Broughton JP, Deng X, Yu G, et al. (2020) CRISPR-Cas12-based detection of SARS-CoV-2 [published online ahead of print, 2020 Apr 16]. Nat Biotechnol https://doi.org/10.1038/s41587-020-0513-4
Cascella M, Rajnik M, Cuomo A, et al. (2020) Features, evaluation and treatment Coronavirus (COVID-19). In: StatPearls [Internet]. StatPearls Publishing, Treasure Island (FL)
Chen JS, Ma E, Harrington LB, Da Costa M, Tian X, Palefsky JM, Doudna JA (2018) CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity. Science 360(6387):436–439
Corman VM, Landt O, Kaiser M et al (2020) Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Euro Surveill 25(3):2000045
Gootenberg JS, Abudayyeh OO, Lee JW et al (2017) Nucleic acid detection with CRISPR-Cas13a/C2c2. Science (New York, NY) 356(6336):438–442
Helmy YA, Fawzy M, Elaswad A, Sobieh A, Kenney SP, Shehata AA (2020) The COVID-19 pandemic: a comprehensive review of taxonomy, genetics, epidemiology, diagnosis, treatment, and control. J Clin Med 9(4):1225
Hirano S, Nishimasu H, Ishitani R, Nureki O (2016) Structural basis for the altered PAM specificities of engineered CRISPR-Cas9. Mol Cell 61(6):886–894
Huang Z, Tian D, Liu Y et al (2020) Ultra-sensitive and high-throughput CRISPR-powered COVID-19 diagnosis. Biosens Bioelectron 23:112316
Kellner MJ, Koob JG, Gootenberg JS, Abudayyeh OO, Zhang F (2020) SHERLOCK: nucleic acid detection with CRISPR nucleases. Nat Protoc 15(3):1311
Khailany RA, Safdar M, Ozaslan M (2020) Genomic characterization of a novel SARS-CoV-2 [published online ahead of print, 2020 Apr 16]. Gene Rep 19:100682
Kumar S, Maurya VK, Prasad AK, Bhatt MLB, Saxena SK (2020a) Structural, glycosylation and antigenic variation between 2019 novel coronavirus (2019-nCoV) and SARS coronavirus (SARS-CoV). Virus 31:13–21
Kumar S, Nyodu R, Maurya VK, Saxena SK (2020b) Morphology, genome organization, replication, and pathogenesis of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). In Coronavirus disease 2019 (COVID-19). Springer, Singapore, pp 23–31
Li SY, Cheng QX, Liu JK, Nie XQ, Zhao GP, Wang J (2018) CRISPR-Cas12a has both cis- and trans-cleavage activities on single-stranded DNA. Cell Res 28:491–493
Li L, Li S, Wu N, Wu J, Wang G, Zhao G, Wang J (2019a) HOLMESv2: a CRISPR-Cas12b-assisted platform for nucleic acid detection and DNA methylation quantitation. ACS Synth Biol 8(10):2228–2237
Li Y, Li S, Wang J, Liu G (2019b) CRISPR/Cas systems towards next-generation biosensing. Trends Biotechnol 37:730–743
Liu L, Chen P, Wang M, Li X, Wang J, Yin M et al (2017) C2c1-sgRNA complex structure reveals RNA-guided DNA cleavage mechanism. Mol Cell 65:310–322
Miao F, Zhang J, Li N, Chen T, Wang L, Zhang F (2019) Rapid and sensitive recombinase polymerase amplification combined with lateral flow strip for detecting african swine fever virus. Front Microbiol 15:1004
Notomi T, Okayama H, Masubuchi H, Yonekawa T, Watanabe K, Amino N, Hase T (2000) Loop-mediated isothermal amplification of DNA. Nucleic Acids Res 28:63
Pardee K, Green A, Takahashi MK, Braff D et al (2016) Rapid, low-cost detection of zika virus using programmable biomolecular components. Cell 165:1255–1266
Park GS, Ku K, Baek SH, Kim SJ, Kim SI, Kim BT, Maeng JS (2020) Development of reverse transcription loop-mediated isothermal amplification assays targeting SARS-CoV-2. J Mol Diagn S1525–1578:30090–30098
PDB ID: 5B2O, Hirano H, Gootenberg JS, Horii T et al (2016) Structure and engineering of Francisella novicida Cas9. Cell 164:950–961
PDB: 5XWY, Liu L, Li X, Ma J et al (2017) The molecular architecture for RNA-guided RNA cleavage by Cas13a. Cell 170:714–726.e10
PDB: 6GTC, Stella S, Mesa P, Thomsen J et al (2018) Conformational activation promotes CRISPR-Cas12a catalysis and resetting of the endonuclease activity. Cell 175:1856–1871.e21
Rauch JN, Valois E, Solley SC et al (2020) A scalable, easy-to-deploy, protocol for cas13-based detection of SARS-CoV-2 genetic material. bioRxiv. https://doi.org/10.1101/2020.04.20.052159
Rostron P, Pennance T, Bakar F et al (2019) Development of a recombinase polymerase amplification (RPA) fluorescence assay for the detection of Schistosoma haematobium. Parasit Vectors 12:514
Smargon AA, Shi YJ, Yeo GW (2020) RNA-targeting CRISPR systems from metagenomic discovery to transcriptomic engineering. Nat Cell Biol 22:143–150
Swarts DC, van der Oost J, Jinek M (2017) Structural basis for guide RNA processing and seed-dependent DNA targeting by CRISPR-Cas12a. Mol Cell 66:221–233e4
Stella S, Mesa P, Thomsen J, Paul B, Alcón P, Jensen SB, Saligram B, Moses ME, Hatzakis NS, Montoya G (2018) Conformational activation promotes CRISPR-Cas12a catalysis and resetting of the endonuclease activity. Cell 175(7):1856–1871.e21
Wang X, Xiong E, Tian T et al (2020a) Clustered regularly interspaced short palindromic repeats/Cas9-mediated lateral flow nucleic acid assay. ACS Nano 4:2497–2508
Wang R, Zhao X, Chen X et al (2020b) Rolling circular amplification (RCA)-assisted CRISPR/Cas9 cleavage (RACE) for highly specific detection of multiple extracellular vesicle MicroRNAs. Anal Chem 92:2176–2185
Wiedenheft B, Sternberg SH, Doudna JA (2012) RNA-guided genetic silencing systems in bacteria and archaea. Nature 482:331–338
Yan F, Wang W, Zhang J (2019) CRISPR-Cas12 and Cas13: the lesser known siblings of CRISPR-Cas9. Cell Biol Toxicol 35:489–492
Yinhua Zhang NO, Xiong J, Sun L et al (2020) Rapid molecular detection of sars-cov-2 (covid-19) virus RNA using colorimetric LAMP. medRxiv. https://doi.org/10.1101/2020.02.26.20028373
Yu L, Wu S, Hao X et al (2020) Rapid detection of COVID-19 coronavirus using a reverse transcriptional loop-mediated isothermal amplification (RT-LAMP) diagnostic platform [published online ahead of print, 2020 Apr 21]. Clin Chem:hvaa102
Zhang F, Abudayyeh OO, Gootenberg JS. (2020) A protocol for detection of COVID-19 using CRISPR diagnostics. A protocol for detection of COVID-19 using CRISPR diagnostics. p 8
Zhou L, Peng R, Zhang R, Li J (2018a) The applications of CRISPR/Cas system in molecular detection. J Cell Mol Med 22:5807–5815
Zhou W, Hu L, Ying L et al (2018b) A CRISPR–Cas9-triggered strand displacement amplification method for ultrasensitive DNA detection. Nat Commun 9:5012
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Srivastava, A., Gupta, T., Kumar, S., Saxena, S.K. (2020). Next-Generation Rapid Advanced Molecular Diagnostics of COVID-19 by CRISPR-Cas. In: Chandra, P., Roy, S. (eds) Diagnostic Strategies for COVID-19 and other Coronaviruses. Medical Virology: From Pathogenesis to Disease Control. Springer, Singapore. https://doi.org/10.1007/978-981-15-6006-4_9
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DOI: https://doi.org/10.1007/978-981-15-6006-4_9
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