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Evaluation of 3D Human Intestinal Organoids as a Platform for EV-A71 Antiviral Drug Discovery

Enteroviruses are a leading cause of upper respiratory tract, gastrointestinal, and neurological infections. Management of enterovirus-related diseases has been hindered by the lack of specific antiviral treatment. The pre-clinical and clinical development of such antivirals has been challenging, ca...

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Autores principales: Masmoudi, Fatma, Santos-Ferreira, Nanci, Pajkrt, Dasja, Wolthers, Katja C., DeGroot, Jeroen, Vlaming, Maria L. H., Rocha-Pereira, Joana, Buti, Ludovico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136548/
https://www.ncbi.nlm.nih.gov/pubmed/37190047
http://dx.doi.org/10.3390/cells12081138
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author Masmoudi, Fatma
Santos-Ferreira, Nanci
Pajkrt, Dasja
Wolthers, Katja C.
DeGroot, Jeroen
Vlaming, Maria L. H.
Rocha-Pereira, Joana
Buti, Ludovico
author_facet Masmoudi, Fatma
Santos-Ferreira, Nanci
Pajkrt, Dasja
Wolthers, Katja C.
DeGroot, Jeroen
Vlaming, Maria L. H.
Rocha-Pereira, Joana
Buti, Ludovico
author_sort Masmoudi, Fatma
collection PubMed
description Enteroviruses are a leading cause of upper respiratory tract, gastrointestinal, and neurological infections. Management of enterovirus-related diseases has been hindered by the lack of specific antiviral treatment. The pre-clinical and clinical development of such antivirals has been challenging, calling for novel model systems and strategies to identify suitable pre-clinical candidates. Organoids represent a new and outstanding opportunity to test antiviral agents in a more physiologically relevant system. However, dedicated studies addressing the validation and direct comparison of organoids versus commonly used cell lines are lacking. Here, we described the use of human small intestinal organoids (HIOs) as a model to study antiviral treatment against human enterovirus 71 (EV-A71) infection and compared this model to EV-A71-infected RD cells. We used reference antiviral compounds such as enviroxime, rupintrivir, and 2′-C-methylcytidine (2′CMC) to assess their effects on cell viability, virus-induced cytopathic effect, and viral RNA yield in EV-A71-infected HIOs and cell line. The results indicated a difference in the activity of the tested compounds between the two models, with HIOs being more sensitive to infection and drug treatment. In conclusion, the outcome reveals the value added by using the organoid model in virus and antiviral studies.
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spelling pubmed-101365482023-04-28 Evaluation of 3D Human Intestinal Organoids as a Platform for EV-A71 Antiviral Drug Discovery Masmoudi, Fatma Santos-Ferreira, Nanci Pajkrt, Dasja Wolthers, Katja C. DeGroot, Jeroen Vlaming, Maria L. H. Rocha-Pereira, Joana Buti, Ludovico Cells Article Enteroviruses are a leading cause of upper respiratory tract, gastrointestinal, and neurological infections. Management of enterovirus-related diseases has been hindered by the lack of specific antiviral treatment. The pre-clinical and clinical development of such antivirals has been challenging, calling for novel model systems and strategies to identify suitable pre-clinical candidates. Organoids represent a new and outstanding opportunity to test antiviral agents in a more physiologically relevant system. However, dedicated studies addressing the validation and direct comparison of organoids versus commonly used cell lines are lacking. Here, we described the use of human small intestinal organoids (HIOs) as a model to study antiviral treatment against human enterovirus 71 (EV-A71) infection and compared this model to EV-A71-infected RD cells. We used reference antiviral compounds such as enviroxime, rupintrivir, and 2′-C-methylcytidine (2′CMC) to assess their effects on cell viability, virus-induced cytopathic effect, and viral RNA yield in EV-A71-infected HIOs and cell line. The results indicated a difference in the activity of the tested compounds between the two models, with HIOs being more sensitive to infection and drug treatment. In conclusion, the outcome reveals the value added by using the organoid model in virus and antiviral studies. MDPI 2023-04-12 /pmc/articles/PMC10136548/ /pubmed/37190047 http://dx.doi.org/10.3390/cells12081138 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Masmoudi, Fatma
Santos-Ferreira, Nanci
Pajkrt, Dasja
Wolthers, Katja C.
DeGroot, Jeroen
Vlaming, Maria L. H.
Rocha-Pereira, Joana
Buti, Ludovico
Evaluation of 3D Human Intestinal Organoids as a Platform for EV-A71 Antiviral Drug Discovery
title Evaluation of 3D Human Intestinal Organoids as a Platform for EV-A71 Antiviral Drug Discovery
title_full Evaluation of 3D Human Intestinal Organoids as a Platform for EV-A71 Antiviral Drug Discovery
title_fullStr Evaluation of 3D Human Intestinal Organoids as a Platform for EV-A71 Antiviral Drug Discovery
title_full_unstemmed Evaluation of 3D Human Intestinal Organoids as a Platform for EV-A71 Antiviral Drug Discovery
title_short Evaluation of 3D Human Intestinal Organoids as a Platform for EV-A71 Antiviral Drug Discovery
title_sort evaluation of 3d human intestinal organoids as a platform for ev-a71 antiviral drug discovery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136548/
https://www.ncbi.nlm.nih.gov/pubmed/37190047
http://dx.doi.org/10.3390/cells12081138
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