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SARS CoV-2 Delta variant exhibits enhanced infectivity and a minor decrease in neutralization sensitivity to convalescent or post-vaccination sera. | LitMetric

AI Article Synopsis

  • SARS-CoV-2 variants Kappa and Delta have quickly become dominant worldwide, but their infectivity and vaccine response were previously unclear.
  • Research shows that both variants can be neutralized by convalescent sera and post-vaccination sera, although there is some reduction in sensitivity compared to earlier strains.
  • Delta variant demonstrates higher infectivity than Kappa but is still less resistant to vaccines than the Beta variant, while the Delta plus variant shows high resistance similar to Beta, despite having infectivity levels akin to wild-type SARS-CoV-2.

Article Abstract

Since their identification, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Kappa and Delta have rapidly spread to become globally dominant. However, their infectivity and sensitivity to administered vaccines have not been documented. We monitored the neutralization potential of convalescent or BNT162b2 post-vaccination sera against Kappa and Delta SARS-CoV-2 pseudoviruses. We show that both variants were successfully neutralized by convalescent and post-vaccination sera, exhibiting a mild decrease in their neutralization sensitivity. Of the two variants, Delta presented enhanced infectivity levels compared with Kappa or wild-type SARS-CoV-2. Nevertheless, both variants were not as infectious or resistant to post-vaccination sera as the Beta variant of concern. Interestingly, the Delta plus variant (AY.1/B.1.617.2.1) exhibited high resistance to post-vaccination sera, similar to that of the Beta SARS-CoV-2. However, its infectivity levels were close to those of wild-type SARS-CoV-2. These results account for the worldwide prevalence of Delta variant of concern and confirm the efficacy of the BNT162b2 vaccine against circulating other Delta variants.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591850PMC
http://dx.doi.org/10.1016/j.isci.2021.103467DOI Listing

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