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Assessing in Vitro Resistance Development in Enterovirus A71 in the Context of Combination Antiviral Treatment

  • Kristina Lanko
  • , Chenyan Shi
  • , Shivaprasad Patil
  • , Leen Delang
  • , Jelle Matthijnssens
  • , Carmen Mirabelli
  • , Johan Neyts*
  • *Corresponding author for this work
  • KU Leuven

Research output: Contribution to journalArticleAcademicpeer-review

14 Citations (Scopus)

Abstract

There are currently no antivirals available to treat infection with enterovirus A71 (EV-A71) or any other enterovirus. The extensively studied capsid binders rapidly select for drug-resistant variants. We here explore whether the combination of two direct-acting enterovirus inhibitors with a different mechanism of action may delay or prevent resistance development to the capsid binders. To that end, the in vitro dynamics of resistance development to the capsid binder pirodavir was studied either alone or in combination with a viral 2C-targeting compound (SMSK_0213), a viral 3C-protease inhibitor (rupintrivir) or a viral RNA-dependent RNA polymerase inhibitor (7DMA). We demonstrate that combining pirodavir with either rupintrivir or 7DMA delays the development of resistance to pirodavir and that no resistance to the protease or polymerase inhibitor develops. The combination of pirodavir with the 2C inhibitor results in a double-resistant virus population, where only the minority carries the resistant mutation.

Original languageEnglish
Pages (from-to)2801-2806
Number of pages6
JournalACS Infectious Diseases
Volume7
Issue number10
DOIs
Publication statusPublished - 8 Oct 2021
Externally publishedYes

Bibliographical note

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UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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