medRxiv · 2021 · 157 citations · 42 references
Life SciencesImmunologyInfectious DiseasesEmerging Infectious DiseasesMolecular VirologyVirologyEmerging Viral DiseasesVaccinationVaccines For Emerging PathogensAntibody-mediated Disease ResistanceHost Transmission DynamicsLineage ReplacementSars-cov-2 Antiviral ResistanceSars-cov-2 InfectionSpatial Transmission DynamicsVariant Emergence StudiesVariants Of Concern
SARS‑CoV‑2 has surged globally, with spike mutations such as E484K and N501Y threatening vaccine and antibody efficacy and leading to widespread emergence of lineages like B.1.526 across the United States and other countries. The study reports the emergence and rapid dominance of the E484K‑bearing B.1.526 lineage in New York City during early 2021. B.1.526, which resists certain therapeutic monoclonal antibodies and shows reduced neutralization by convalescent plasma or vaccinee sera, rapidly displaced earlier lineages in New York with a 35 % transmission advantage, but its growth slowed as B.1.1.7 and other variants rose.
Recent months have seen surges of SARS-CoV-2 infection across the globe with considerable viral evolution 1-3 . Extensive mutations in the spike protein may threaten efficacy of vaccines and therapeutic monoclonal antibodies 4 . Two signature mutations of concern are E484K, which plays a crucial role in the loss of neutralizing activity of antibodies, and N501Y, a driver of rapid worldwide transmission of the B.1.1.7 lineage. Here, we report the emergence of variant lineage B.1.526 that contains E484K and its alarming rise to dominance in New York City in early 2021. This variant is partially or completely resistant to two therapeutic monoclonal antibodies in clinical use and less susceptible to neutralization by convalescent plasma or vaccinee sera, posing a modest antigenic challenge. The B.1.526 lineage has now been reported from all 50 states in the US and numerous other countries. B.1.526 rapidly replaced earlier lineages in New York upon its emergence, with an estimated transmission advantage of 35%. Such transmission dynamics, together with the relative antibody resistance of its E484K sub-lineage, likely contributed to the sharp rise and rapid spread of B.1.526. Although SARS-CoV-2 B.1.526 initially outpaced B.1.1.7 in the region, its growth subsequently slowed concurrent with the rise of B.1.1.7 and ensuing variants.
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Nextstrain: real-time tracking of pathogen evolution
James Hadfield, Colin Megill, Sidney M. Bell et al. · Bioinformatics · 2018 · 3.4K citations · Full text
Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody
Dora Pinto, Young‐Jun Park, Martina Beltramello et al. · Nature · 2020 · 2.2K citations · Full text