A Multiplexed Cas13-Based Assay with Point-of-Care Attributes for Simultaneous COVID-19 Diagnosis and Variant Surveillance

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Abstract

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  1. SciScore for 10.1101/2022.03.17.22272589: (What is this?)

    Please note, not all rigor criteria are appropriate for all manuscripts.

    Table 1: Rigor

    Ethicsnot detected.
    Sex as a biological variablenot detected.
    Randomizationnot detected.
    Blindingnot detected.
    Power Analysisnot detected.

    Table 2: Resources

    Recombinant DNA
    SentencesResources
    Gp32 and uvsX were cloned into the pET28a backbone using Type IIS assembly (Engler et al., 2008).
    pET28a
    suggested: RRID:Addgene_139598)
    Plasmid #163912); pET28a- uvsX-H6
    pET28a-
    suggested: None
    (Plasmid #163913); and pET28a-MH6-uvsY (Plasmid #163914).
    pET28a-MH6-uvsY
    suggested: None
    Expression and purification of Cas enzymes: LwaCas13a expression and purification: LwaCas13a was expressed from pC013-His6-Twinstrep-SUMO-LwaCas13a (Addgene: #90097) and purified as previously described (Patchsung et al., 2020).
    pC013-His6-Twinstrep-SUMO-LwaCas13a
    suggested: None
    PsmCas13b expression and purification: Escherichia coli BL21 (DE3) transformed with pC0061-His6-Twinstrep-SUMO-PsmCas13b (Addgene: #115211) were grown in LB media containing 25 µg/mL ampicillin, and the protein expression induced by the addition of 500 µM IPTG at 16 °C for overnight.
    pC0061-His6-Twinstrep-SUMO-PsmCas13b
    suggested: None
    Software and Algorithms
    SentencesResources
    Expression and purification of Cas enzymes: LwaCas13a expression and purification: LwaCas13a was expressed from pC013-His6-Twinstrep-SUMO-LwaCas13a (Addgene: #90097) and purified as previously described (Patchsung et al., 2020).
    Addgene
    suggested: (Addgene, RRID:SCR_002037)
    Four picomoles of the purified dsDNA crRNA template were used in in vitro transcription reactions using RiboMAX Large Scale RNA Production System–T7 (ProMega) or MEGAshortscript™ T7 Transcription Kit (Invitrogen).
    MEGAshortscript™
    suggested: None
    Gels were imaged on ImageQuant™ LAS 4000 (GE Healthcare); quantifications of produced crRNAs were performed by measuring band densitometries using Fiji ImageJ software (Schindelin et al., 2012) and comparing to RNA standards.
    Fiji ImageJ
    suggested: None
    Retrieved sequences were aligned using MAFFT (Katoh & Standley, 2013).
    MAFFT
    suggested: (MAFFT, RRID:SCR_011811)
    The four consensus sequences along with the SARS-CoV- 2 isolate Wuhan-Hu-1 NCBI reference genome (Accession ID NC_045512.2) were re-aligned using MAFFT and visualized in SnapGene software (Insightful Science).
    SnapGene
    suggested: (SnapGene, RRID:SCR_015052)
    Exclusivity evaluation of designed crRNAs: crRNA spacer sequences and their complementary sequences were searched against a BLAST database of Betacoronavirus nucleotide sequences (
    BLAST
    suggested: (BLASTX, RRID:SCR_001653)
    Betacoronavirus BLAST, https://blast.ncbi.nlm.nih.gov/Blast.cgi?PAGE_TYPE=BlastSearch&BLAST_SPEC=Betacoronavirus), with the maximal number of target sequences set to 5000.
    https://blast.ncbi.nlm.nih.gov/Blast.cgi
    suggested: (TBLASTX, RRID:SCR_011823)
    The resulted alignments were visualized and inspected using JalView (Aksamentov et al., 2021).
    JalView
    suggested: (Jalview, RRID:SCR_006459)

    Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).


    Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.

    Results from TrialIdentifier: No clinical trial numbers were referenced.


    Results from Barzooka: We did not find any issues relating to the usage of bar graphs.


    Results from JetFighter: We did not find any issues relating to colormaps.


    Results from rtransparent:
    • Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
    • Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
    • Thank you for including a protocol registration statement.

    Results from scite Reference Check: We found no unreliable references.


    About SciScore

    SciScore is an automated tool that is designed to assist expert reviewers by finding and presenting formulaic information scattered throughout a paper in a standard, easy to digest format. SciScore checks for the presence and correctness of RRIDs (research resource identifiers), and for rigor criteria such as sex and investigator blinding. For details on the theoretical underpinning of rigor criteria and the tools shown here, including references cited, please follow this link.