Spread dynamics of SARS-CoV-2 epidemic in China: a phylogenetic analysis

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Abstract

Background

Since December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused a pandemic and infected millions of people. As the first country proclaimed the SARS-CoV-2 outbreak, China implemented travel ban measure, and curbed the epidemic quickly. We performed a phylogenetic analysis to reveal the spread dynamics detail of SARS-CoV-2 in China and the impact of travel ban on SARS-CoV-2.

Method

Focusing on SARS-CoV-2 sequences collected from China in public database released as of March 31, 2020, we performed a Bayesian inference phylogenetic analyses to estimate the effective population size ( Ne ) curve of SARS-CoV-2 epidemic. Furthermore, we displayed the geographic spread mode of SARS-CoV-2 among different China regions by using Bayesian stochastic search variable selection (BSSVS) method.

Results

The most recent common ancestor (tMRCA) of SARS-CoV-2 in China was traced back to December 9, 2019. According the Ne estimation and geographic spread reconstruction, January 25, 2020 was considered as the crucial time point during the SARS-CoV-2 epidemic in China,which was 2 days after the travel ban implemented. On the point, the tendency of viral population size changed from ascending to decreasing, and the cross-regional spread paths were blocked.

Conclusions

Travel ban is an effective measure to intervene in the spread of SARS-CoV-2, It is necessary to continue efforts in research for prevention and control measures.

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  1. SciScore for 10.1101/2020.05.20.20107854: (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
    SentencesResources
    A multiple alignment was performed by CLUSTAL X program(7) and trimmed into full-length S gene with 3822nt.
    CLUSTAL X
    suggested: (Clustal X , RRID:SCR_017055)
    General Time Reversible (GTR) was selected as the nucleotide substitution model by calculated AIC score using jModeltest v1.9.1 program(10).
    jModeltest
    suggested: (jModelTest, RRID:SCR_015244)
    The output files generated by bayesian computing were discarded the first 10% as burn-in and then combined by LogCombiner tool in BEAST v1.10.4 packages.
    BEAST
    suggested: (BEAST, RRID:SCR_010228)
    Tracer software v1.7.1(17) was used to diagnose MCMCs output and estimate Ne curve with additional 10% burn-in.
    Tracer
    suggested: (Tracer, RRID:SCR_019121)
    We displayed the discrete geographical phylogenetic MCC trees in FigTree v1.4.3 and generated a visual kml file by spreaD3 v0.9.7(19), which was viewed in Google Earth v7.1.8.
    FigTree
    suggested: (FigTree, RRID:SCR_008515)

    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.
    • No protocol registration statement was detected.

    About SciScore

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