Functional and Structural Characterization of Treatment-Emergent Nirmatrelvir Resistance Mutations at Low Frequencies in the Main Protease (Mpro) Reveals a Unique Evolutionary Route for SARS-CoV-2 to Gain Resistance - Takeaways - MDSpire

Functional and Structural Characterization of Treatment-Emergent Nirmatrelvir Resistance Mutations at Low Frequencies in the Main Protease (Mpro) Reveals a Unique Evolutionary Route for SARS-CoV-2 to Gain Resistance

  • By

  • Natalie M Deschenes

  • Jimena Pérez-Vargas

  • Zoe Zhong

  • Merrilee Thomas

  • Calem Kenward

  • Wesley A Mosimann

  • Liam J Worrall

  • Nicholas Waglechner

  • Angel XinLiu Li

  • Finlay Maguire

  • Patryk Aftanas

  • Jason R Smith

  • Jared Lim

  • Robert N Young

  • Artem Cherkasov

  • Lubna Farooqi

  • Adnan Moinuddin

  • Lina Siddiqi

  • Imaan Malik

  • Maxime Lefebvre

  • Mark Paetzel

  • Natalie C J Strynadka

  • François Jean

  • Allison McGeer

  • Robert A Kozak

  • June 3, 2025

  • 0 min

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  • 1

    The study identified low-frequency resistance mutations in the main protease (Mpro) of SARS-CoV-2 in patients treated with nirmatrelvir-ritonavir.

  • 2

    Two novel Mpro variants were discovered: D48D/L58F/P132H and D48D/L67V/K90R/P132H, which impact nirmatrelvir resistance without affecting Mpro activity.

  • 3

    Mutations were found in the Mpro N-terminal domain, disrupting substrate binding site structure and dynamics, potentially reducing protein stability.

  • 4

    This research highlights a unique evolutionary pathway for SARS-CoV-2 resistance, including cross-resistance to different Mpro inhibitors.

  • 5

    The findings emphasize the need for ongoing surveillance of low-frequency resistance mutations in clinical samples to inform therapeutic strategies.

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