Cryptic transmission of SARS-CoV-2 in Washington state
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Abstract
The history of how severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spread around the planet has been far from clear. Several narratives have been propagated by social media and, in some cases, national policies were forged in response. Now that many thousands of virus sequences are available, two studies analyzed some of the key early events in the spread of SARS-CoV-2. Bedford et al. found that the virus arrived in Washington state in late January or early February. The viral genome from the first case detected had mutations similar to those found in Chinese samples and rapidly spread and dominated subsequent undetected community transmission. The other viruses detected had origins in Europe. Worobey et al. found that early introductions into Germany and the west coast of the United States were extinguished by vigorous public health efforts, but these successes were largely unrecognized. Unfortunately, several major travel events occurred in February, including repatriations from China, with lax public health follow-up. Serial, independent introductions triggered the major outbreaks in the United States and Europe that still hold us in the grip of control measures.
Science , this issue p. 571 , p. 564
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SciScore for 10.1101/2020.04.02.20051417: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
NIH rigor criteria are not applicable to paper type.Table 2: Resources
Software and Algorithms Sentences Resources Filtered reads were de novo assembled using SPAdes (30) and contigs were ordered against the reference using BWA-MEM (31). SPAdessuggested: (SPAdes, RRID:SCR_000131)BWA-MEMsuggested: (Sniffles, RRID:SCR_017619)Consensus sequences were annotated using Prokka (32) and deposited to Genbank (accessions pending) Prokkasuggested: (Prokka, RRID:SCR_014732)) bioinformatics pipeline Augur to align genomes via MAFFT v7.4 (33), build maximum likelihood phylogeny via IQTREE v1.6 (34) and reconstruct nucleotide and amino acid changes on the ML tree. MAFFTsuggested: (MAFFT, RRID:SCR_011811)Additionally, … SciScore for 10.1101/2020.04.02.20051417: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
NIH rigor criteria are not applicable to paper type.Table 2: Resources
Software and Algorithms Sentences Resources Filtered reads were de novo assembled using SPAdes (30) and contigs were ordered against the reference using BWA-MEM (31). SPAdessuggested: (SPAdes, RRID:SCR_000131)BWA-MEMsuggested: (Sniffles, RRID:SCR_017619)Consensus sequences were annotated using Prokka (32) and deposited to Genbank (accessions pending) Prokkasuggested: (Prokka, RRID:SCR_014732)) bioinformatics pipeline Augur to align genomes via MAFFT v7.4 (33), build maximum likelihood phylogeny via IQTREE v1.6 (34) and reconstruct nucleotide and amino acid changes on the ML tree. MAFFTsuggested: (MAFFT, RRID:SCR_011811)Additionally, 293 SARS-CoV-2 aligned genomes from the WA1 outbreak clade were analyzed in BEAST (35) to estimate time of common ancestor and rate of epidemic growth. BEASTsuggested: (BEAST, RRID:SCR_010228)Results from OddPub: Thank you for sharing your code and data.
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.
- No protocol registration statement was detected.
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