Evidence map›Paper›PMID 34542686›Full record

ReviewApplied microbiology and biotechnology2021

CRISPR detectives against SARS-CoV-2: a major setback against COVID-19 blowout.

Rahul Gupta, Tawsif Ahmed Kazi, Dhritiman Dey, Arijit Ghosh, V Ravichandiran, Snehasikta Swarnakar, Syamal Roy, Swadesh Ranjan Biswas, Dipanjan Ghosh

Abstract readReview
In one paragraph

Review in Applied microbiology and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Application of CRISPR-Cas system in the diagnosis and therapy of ESKAPE infections.Frontiers in cellular and infection microbiology · 2023
    Review
  9. Review
  10. Cas13d: A New Molecular Scissor for Transcriptome Engineering.Frontiers in cell and developmental biology · 2022
    Review
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Rahul GuptaInfectious Diseases and Immunology Division, CSIR-Indian Institute of Chemical Biology, Kolkata, India.
Tawsif Ahmed KaziDepartment of Botany, Visva-Bharati, Bolpur, India.
Dhritiman DeyNational Institute of Pharmaceutical Education and Research, Kolkata, India.
Arijit GhoshUniversity of Calcutta, Kolkata, India.
V RavichandiranNational Institute of Pharmaceutical Education and Research, Kolkata, India.
Snehasikta SwarnakarInfectious Diseases and Immunology Division, CSIR-Indian Institute of Chemical Biology, Kolkata, India.
Syamal RoyInfectious Diseases and Immunology Division, CSIR-Indian Institute of Chemical Biology, Kolkata, India.
Swadesh Ranjan BiswasDepartment of Botany, Visva-Bharati, Bolpur, India.
Dipanjan GhoshNational Institute of Pharmaceutical Education and Research, Kolkata, India. dipanjan4u@gmail.com.ORCID http://orcid.org/0000-0003-3266-9262

Funding

department of biotechnology , ministry of science and technology BT/PR26301/GET/119/258/2017department of science and technology, government of west bengal BT/P/Budget/RD-74/2017
6 · The paper itself

Abstract

The emergence of SARS-CoV-2 has brought the world to a standstill, and till date, effective treatments and diagnostics against this idiosyncratic pathogen are lacking. As compared to the standard WHO/CDC qPCR detection method, which consumes several hours for detection, CRISPR-based SHERLOCK, DETECTR, and FELUDA have emerged as rapid diagnostic tools for the detection of the RNA genome of SARS-CoV-2 within an hour with 100% accuracy, specificity, and sensitivity. These attributes of CRISPR-based detection technologies have taken themselves one step ahead of available detection systems and are emerging as an inevitable tool for quick detection of the virus. Further, the discovery of Cas13s nucleases and their orthologs has opened a new corridor for exploitation of Cas13s as an antiviral therapy against SARS-CoV-2 and other viral diseases. One such approach is Prophylactic Antiviral CRISPR in huMAN cells (PACMAN), which needs a long haul to bring into therapy. The approval of SHERLOCK as the first CRISPR-based SARS-CoV-2 test kit by the FDA, for emergency diagnosis of COVID-19 patients, has given positive hope to scientists that sooner human trials of CRISPR-based therapy will be ratified. In this review, we have extensively reviewed the present CRISPR-based approaches, challenges, and future prospects in the light of diagnostics and therapeutics against SARS-CoV-2. KEY POINTS: • The discovery of Cas12 and Cas13 siblings allowed scientists to detect the viral genes. • Cas13d's identification aided scientists in precisely cleaving the SARS-CoV-2 ssRNA. • CRISPR-Cas system acts as "molecular detector and antiviral proctor."

Indexed as

COVID-19SARS-CoV-2Antiviral AgentsCRISPR-Cas SystemsHumansReal-Time Polymerase Chain ReactionRNA, ViralAntiviral AgentsRNA, ViralCOVID-19CRISPR/CasDETECTRFELUDAPACMANSARS-CoV-2SHERLOCK

Identifiers

PMID34542686
PMCPMC8450312

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.