logo
ResearchBunny Logo
SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion

Medicine and Health

SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion

P. Mlcochova, S. A. Kemp, et al.

The B.1.617.2 (Delta) variant of SARS-CoV-2 poses a significant challenge as it exhibits reduced sensitivity to neutralizing antibodies and increased replication efficiency. Conducted by a diverse team of authors, including Petra Mlcochova and Steven A. Kemp, this research highlights the urgent need for continued infection control measures to combat the Delta variant's immune evasion strategies.

00:00
00:00
~3 min • Beginner • English
Abstract
The B.1.617.2 (Delta) variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first identified in the state of Maharashtra in late 2020 and spread throughout India, outcompeting pre-existing lineages including B.1.617.1 (Kappa) and B.1.1.7 (Alpha)¹. B.1.617.2 is sixfold less sensitive to serum neutralizing antibodies from recovered individuals, and B.1.617.2 showed reduced neutralization with monoclonal antibodies, compared with wild-type viruses. The spike's additional mutations exhibited compromised sensitivity to monoclonal antibodies due to steric hindrance at the amino-terminal domain. B.1.617.2 demonstrates higher replication efficiency than B.1.1.7 in both airway organoids and in various experimental systems, associated with B.1.617.2 spike being in a predominantly cleaved state compared with B.1.1.7 spike. The B.1.617.2 spike protein is able to mediate highly efficient syncytium formation that was less sensitive to inhibition by neutralizing antibody, compared with that of wild-type spike. We also observed that B.1.617.2 had higher receptor binding and spike-mediated entry than B.1.617.1, potentially explaining the B.1.617.2 dominance. In an analysis of more than 1,130 SARS-CoV-2-infected health care workers across three trends in India during a period of mixed lineage circulation, we observed reduced ChAdOx vaccine effectiveness against B.1.617.2 relative to non-B.1.617.2, with the caveat of possible residual confounding. Compromised vaccine effectiveness against the highly fit and immune-evasive B.1.617.2 Delta variant warrants continued infection control measures in the post-vaccination era.
Publisher
Nature
Published On
Jul 28, 2021
Authors
Petra Mlcochova, Steven A. Kemp, Mahesh Shankar Dhar, Guido Papa, Bo Meng, Isabella A. T. M. Ferreira, Rawlings Dati, Dana M. Collier, Anna Albeck, Sujeet Singh, Rajesh Pandey, Jonathan Brown, Jie Zhou, Niiuka Goonawardena, Swapnil Mishra, Charles Whittaker, Thomas Mellan, Robin Marwal, Meena Datt, Shantanu Sengupta, Kalaiarasuan Ponnuswamy, Venkataraman Srinivasan Radhakrishnan, Adam Abdullah, Oscar Charles, Partha Chattopadhyay, Priti Devi, Daniela Caputo, Tom Peacock, Chand Watstal, Neeraj Goel, Ambrish Satwik, Raj Vaishya, Meenakshi Agarwal, The Indian SARS-CoV-2 Genomics Consortium (INSACOG), The Complete to Phenotype Japan (G2P-Japan) Consortium, The CTIID-NIHR BioResource COVID-19 Collaboration, Antriksh Mavcousiãn, Joo Hyoen Lee, Jessica Bassi, Chiara Silacci-Fregni, Christian Saliba, Dora Pinto, Takashi Irie, Isao Yoshida, William L. Hamilton, Kei Sato, Samir Bhatt, Seth Flaxman, Leo C. James, Davide C. Lucco, Wendy S. Barclay, Partha Rakshit, Anurag Agarwal, Ravindra K. Gupta
Tags
SARS-CoV-2
Delta variant
neutralizing antibodies
vaccine effectiveness
infection control
immune evasion
replication efficiency
Listen, Learn & Level Up
Over 10,000 hours of research content in 25+ fields, available in 12+ languages.
No more digging through PDFs, just hit play and absorb the world's latest research in your language, on your time.
listen to research audio papers with researchbunny