• Newer variant of COVID-19-causing virus

    From ScienceDaily@1337:3/111 to All on Thu Jul 2 21:35:30 2020
    Newer variant of COVID-19-causing virus dominates global infections
    Virus with D614G change in Spike out-competes original strain, but may
    not make patients sicker

    Date:
    July 2, 2020
    Source:
    DOE/Los Alamos National Laboratory
    Summary:
    New research shows that a specific change in the SARS-CoV-2
    coronavirus virus genome, previously associated with increased
    viral transmission and the spread of COVID-19, is more infectious
    in cell culture.



    FULL STORY ========================================================================== [Coronavirus illustration | Credit: (c) dottedyeti / stock.adobe.com] Coronavirus illustration (stock image).

    Credit: (c) dottedyeti / stock.adobe.com [Coronavirus illustration |
    Credit: (c) dottedyeti / stock.adobe.com] Coronavirus illustration
    (stock image).

    Credit: (c) dottedyeti / stock.adobe.com Close Research out today in the journal Cell shows that a specific change in the SARS-CoV-2 coronavirus
    virus genome, previously associated with increased viral transmission
    and the spread of COVID-19, is more infectious in cell culture.

    The variant in question, D614G, makes a small but effective change in
    the virus's 'Spike' protein, which the virus uses to enter human cells.


    ========================================================================== Bette Korber, a theoretical biologist at Los Alamos National Laboratory
    and lead author of the study, noted, "The D614G variant first came to
    our attention in early April, as we had observed a strikingly repetitive pattern. All over the world, even when local epidemics had many cases of
    the original form circulating, soon after the D614G variant was introduced
    into a region it became the prevalent form." Geographic information from samples from the GISAID COVID-19 viral sequence database enabled tracking
    of this highly recurrent pattern, a shift in the viral population from
    the original form to the D614G variant. This occurred at every geographic level: country, subcountry, county, and city.

    Two independent lines of experimental evidence that support these initial results are included in today's paper. These additional experiments, led
    by Professor Erica Ollmann Saphire, Ph.D., at the La Jolla Institute, and
    by Professor David Montefiori, Ph.D., at Duke University, showed that the
    D614G change increases the virus's infectivity in the laboratory. These
    new experiments, as well as more extensive sequence and clinical data and improved statistical models, are presented in the Cell paper. More in vivo
    work remains to be done to determine the full implications of the change.

    The SARS-CoV-2 virus has a low mutation rate overall (much lower than the viruses that cause influenza and HIV-AIDS). The D614G variant appears as
    part of a set of four linked mutations that appear to have arisen once and
    then moved together around the world as a consistent set of variations.

    "It's remarkable to me," commented Will Fischer of Los Alamos, an author
    on the study, "both that this increase in infectivity was detected by
    careful observation of sequence data alone, and that our experimental colleagues could confirm it with live virus in such a short time."
    Fortunately, "the clinical data in this paper from Sheffield showed
    that even though patients with the new G virus carried more copies of
    the virus than patients infected with D, there wasn't a corresponding
    increase in the severity of illness," said Saphire, who leads the Gates Foundation-supported Coronavirus Immunotherapy Consortium (CoVIC).



    ========================================================================== Korber noted, "These findings suggest that the newer form of the virus
    may be even more readily transmitted than the original form -- whether
    or not that conclusion is ultimately confirmed, it highlights the value
    of what were already good ideas: to wear masks and to maintain social distancing." Research partners from Los Alamos National Laboratory,
    Duke University, and the University of Sheffield initially published
    work on this analysis on the bioRxiv site in an April 2020 preprint. That
    work also included observations of COVID-19 patients from Sheffield that suggested an association of the D614G variant with higher viral loads
    in the upper respiratory tract.

    "It is possible to track SARS-CoV-2 evolution globally because researchers worldwide are rapidly making their viral sequence data available through
    the GISAID viral sequence database," Korber said. Currently tens of
    thousands of sequences are available through this project, and this
    enabled Korber and the research team to identify the emergence of the
    D614G variant.

    GISAID was established to encourage collaboration among influenza
    researchers, but early in the epidemic the consortium established a
    SARS-CoV-2 database, which soon became the de facto standard for sharing outbreak sequences among researchers worldwide.

    The study, "Tracking changes in SARS-CoV-2 Spike: evidence that D614G
    increases infectivity of the COVID-19 virus" was supported by the
    Medical Research Council (MRC) part of UK Research & Innovation (UKRI the National Institute of Health Research (NIHR); Genome Research Limited, operating as the Wellcome Sanger Institute; CoVIC, INV-006133 of the
    COVID-19 Therapeutics Accelerator, supported by the Bill and Melinda
    Gates Foundation, Mastercard, Wellcome; private philanthropic support,
    as well as the Overton family; a FastGrant, from Emergent Ventures,
    in aid of COVID-19 research; and the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health
    and Human Services, under Interagency Agreement No. AAI12007-001-00000,
    and the Los Alamos Laboratory Directed Research and Development program.

    Additional study authors included S. Gnanakaran, H. Yoon, J. Theiler, W.

    Abfalterer, N. Hengartner, E.E. Giorgi, T. Bhattacharya, B. Foley,
    K.M. Hastie, M.D. Parker, D.G. Partridge, C.M. Evans, T.M. Freeman,
    T.I. de Silva, C.

    McDanal, L.G. Perez, H. Tang, A. Moon-Walker, S.P. Whelan, C.C. LaBranche.


    ========================================================================== Story Source: Materials provided by
    DOE/Los_Alamos_National_Laboratory. Note: Content may be edited for
    style and length.


    ========================================================================== Journal Reference:
    1. B. Korber, W.M. Fischer, S. Gnanakaran, H. Yoon, J. Theiler, W.

    Abfalterer, N. Hengartner, E.E. Giorgi, T. Bhattacharya, B. Foley,
    K.M.

    Hastie, M.D. Parker, D.G. Partridge, C.M. Evans, T.M. Freeman,
    T.I. de Silva, C. McDanal, L.G. Perez, H. Tang, A. Moon-Walker,
    S.P. Whelan, C.C.

    LaBranche, E.O. Saphire, D.C. Montefiori, on behalf of theSheffield
    COVID-19 Genomics Group. Tracking changes in SARS-CoV-2 Spike:
    evidence that D614G increases infectivity of the COVID-19
    virus. Cell, July 2, 2020; DOI: 10.1016/j.cell.2020.06.043 ==========================================================================

    Link to news story: https://www.sciencedaily.com/releases/2020/07/200702144054.htm

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