Structural insights into tecovirimat antiviral activity and poxvirus resistance

Mpox is a zoonotic disease endemic to Central and West Africa. Since 2022, two human-adapted monkeypox virus (MPXV) strains have caused large outbreaks outside these regions. Tecovirimat is the most widely used drug to treat mpox. It blocks viral egress by targeting the viral phospholipase F13; however, the structural details are unknown, and mutations in the F13 gene can result in resistance against tecovirimat, raising public health concerns. Here we report the structure of an F13 homodimer using X-ray crystallography, both alone (2.1 Å) and in complex with tecovirimat (2.6 Å). Combined with molecular dynamics simulations and dimerization assays, we show that tecovirimat acts as a molecular glue that promotes dimerization of the phospholipase. Tecovirimat resistance mutations identified in clinical MPXV isolates map to the F13 dimer interface and prevent drug-induced dimerization in solution and in cells. These findings explain how tecovirimat works, allow for better monitoring of resistant MPXV strains and pave the way for developing more potent and resilient therapeutics.

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Publication Details

Journal
Nature Microbiology
Published
2025-02-12
DOI
https://doi.org/10.1038/s41564-025-01936-6
Citations
32
Primary Topic
Poxvirus research and outbreaks
Type
article
Field-Weighted Citation Impact
33.16

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article

Structural insights into tecovirimat antiviral activity and poxvirus resistance

Pablo Guardado‐Calvo, Alejandro Martínez León, Julian Buchrieser, Françoise Porrot et al.
32 citations
Nature Microbiology
Poxvirus research and outbreaks
33.16
article

Structural insights into tecovirimat antiviral activity and poxvirus resistance

Pablo Guardado‐Calvo, Alejandro Martínez León, Julian Buchrieser, Françoise Porrot, Chetan Poojari, Christopher N. Selverian, Jason Mercer, Maelenn Chevreuil, Olivier Schwartz, Etienne Simon‐Lorière, Jochen S. Hub, Ahmed Haouz, Annalisa Meola, Kartik Chandran, Bertrand Raynal, Riccardo Vernuccio, Florence Guivel-Benhassine, Yakin Jaleta
article en
32 citations

Abstract

Mpox is a zoonotic disease endemic to Central and West Africa. Since 2022, two human-adapted monkeypox virus (MPXV) strains have caused large outbreaks outside these regions. Tecovirimat is the most widely used drug to treat mpox. It blocks viral egress by targeting the viral phospholipase F13; however, the structural details are unknown, and mutations in the F13 gene can result in resistance against tecovirimat, raising public health concerns. Here we report the structure of an F13 homodimer using X-ray crystallography, both alone (2.1 Å) and in complex with tecovirimat (2.6 Å). Combined with molecular dynamics simulations and dimerization assays, we show that tecovirimat acts as a molecular glue that promotes dimerization of the phospholipase. Tecovirimat resistance mutations identified in clinical MPXV isolates map to the F13 dimer interface and prevent drug-induced dimerization in solution and in cells. These findings explain how tecovirimat works, allow for better monitoring of resistant MPXV strains and pave the way for developing more potent and resilient therapeutics.

Nature MicrobiologyVol. 10(3)
Centre National de la Recherche Scientifique (FR), Albert Einstein College of Medicine (US), Institut Pasteur (FR), Université Paris Cité (FR), Immunité et Cancer (FR), University of Birmingham (GB), Saarland University (DE)
Agence Nationale de la Recherche, National Institutes of Health, Horizon 2020 Framework Programme
Good health and well-being
Openalex Percentile: Top 0%
Poxvirus research and outbreaks
33.16
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