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      SARS-CoV-2 variant transition dynamics are associated with vaccination rates, number of co-circulating variants, and convalescent immunity

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          Abstract

          Background

          Throughout the COVID-19 pandemic, the SARS-CoV-2 virus has continued to evolve, with new variants outcompeting existing variants and often leading to different dynamics of disease spread.

          Methods

          In this paper, we performed a retrospective analysis using longitudinal sequencing data to characterize differences in the speed, calendar timing, and magnitude of 16 SARS-CoV-2 variant waves/transitions for 230 countries and sub-country regions, between October 2020 and January 2023. We then clustered geographic locations in terms of their variant behavior across several Omicron variants, allowing us to identify groups of locations exhibiting similar variant transitions. Finally, we explored relationships between heterogeneity in these variant waves and time-varying factors, including vaccination status of the population, governmental policy, and the number of variants in simultaneous competition.

          Findings

          This work demonstrates associations between the behavior of an emerging variant and the number of co-circulating variants as well as the demographic context of the population. We also observed an association between high vaccination rates and variant transition dynamics prior to the Mu and Delta variant transitions.

          Interpretation

          These results suggest the behavior of an emergent variant may be sensitive to the immunologic and demographic context of its location. Additionally, this work represents the most comprehensive characterization of variant transitions globally to date.

          Funding

          doi 10.13039/100007000, Laboratory Directed Research and Development; (LDRD), doi 10.13039/100008902, Los Alamos National Laboratory; .

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          Most cited references27

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          mice: Multivariate Imputation by Chained Equations inR

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            Tracking changes in SARS-CoV-2 Spike: evidence that D614G increases infectivity of the COVID-19 virus

            Summary A SARS-CoV-2 variant carrying the Spike protein amino acid change D614G has become the most prevalent form in the global pandemic. Dynamic tracking of variant frequencies revealed a recurrent pattern of G614 increase at multiple geographic levels: national, regional and municipal. The shift occurred even in local epidemics where the original D614 form was well established prior to the introduction of the G614 variant. The consistency of this pattern was highly statistically significant, suggesting that the G614 variant may have a fitness advantage. We found that the G614 variant grows to higher titer as pseudotyped virions. In infected individuals G614 is associated with lower RT-PCR cycle thresholds, suggestive of higher upper respiratory tract viral loads, although not with increased disease severity. These findings illuminate changes important for a mechanistic understanding of the virus, and support continuing surveillance of Spike mutations to aid in the development of immunological interventions.
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              A global panel database of pandemic policies (Oxford COVID-19 Government Response Tracker)

              COVID-19 has prompted unprecedented government action around the world. We introduce the Oxford COVID-19 Government Response Tracker (OxCGRT), a dataset that addresses the need for continuously updated, readily usable and comparable information on policy measures. From 1 January 2020, the data capture government policies related to closure and containment, health and economic policy for more than 180 countries, plus several countries' subnational jurisdictions. Policy responses are recorded on ordinal or continuous scales for 19 policy areas, capturing variation in degree of response. We present two motivating applications of the data, highlighting patterns in the timing of policy adoption and subsequent policy easing and reimposition, and illustrating how the data can be combined with behavioural and epidemiological indicators. This database enables researchers and policymakers to explore the empirical effects of policy responses on the spread of COVID-19 cases and deaths, as well as on economic and social welfare.
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                Author and article information

                Journal
                eBioMedicine
                EBioMedicine
                eBioMedicine
                The Author(s). Published by Elsevier B.V.
                2352-3964
                31 March 2023
                May 2023
                31 March 2023
                : 91
                : 104534
                Affiliations
                [a ]Statistical Sciences, Los Alamos National Laboratory, Los Alamos, NM, USA
                [b ]Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, NM, USA
                [c ]Information Systems and Modeling, Los Alamos National Laboratory, Los Alamos, NM, USA
                [d ]Space Data Science and Systems, Los Alamos National Laboratory, Los Alamos, NM, USA
                [e ]Center for Nonlinear Studies, Los Alamos National Laboratory, Los Alamos, NM, USA
                [f ]The New Mexico Consortium, Los Alamos, NM, USA
                Author notes
                []Corresponding author.
                [g]

                These authors contributed equally to this work.

                Article
                S2352-3964(23)00099-3 104534
                10.1016/j.ebiom.2023.104534
                10065418
                37004335
                1d53bb18-3a64-432f-8d50-679fcb8d2606
                © 2023 The Author(s)

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 22 November 2022
                : 6 March 2023
                : 8 March 2023
                Categories
                Articles

                sars-cov-2,covid-19,variant transition,gisaid
                sars-cov-2, covid-19, variant transition, gisaid

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