A flexible, image-based, high-throughput platform encompassing in-depth cell profiling to identify broad-spectrum coronavirus antivirals with limited off-target effects.

Antivirals Coronavirus Drug discovery High throughput High-content imaging Phenotypic screening

Journal

Antiviral research
ISSN: 1872-9096
Titre abrégé: Antiviral Res
Pays: Netherlands
ID NLM: 8109699

Informations de publication

Date de publication:
27 Dec 2023
Historique:
received: 25 09 2023
revised: 14 12 2023
accepted: 21 12 2023
medline: 2 1 2024
pubmed: 2 1 2024
entrez: 29 12 2023
Statut: aheadofprint

Résumé

The recent pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) posed a major threat to global health. Although the World Health Organization ended the public health emergency status, antiviral drugs are needed to address new variants of SARS-CoV-2 and future pandemics. To identify novel broad-spectrum coronavirus drugs, we developed a high-content imaging platform compatible with high-throughput screening. The platform is broadly applicable as it can be adapted to include various cell types, viruses, antibodies, and dyes. We demonstrated that the antiviral activity of compounds against SARS-CoV-2 variants (Omicron BA.5 and Omicron XBB.1.5), SARS-CoV, and human coronavirus 229E could easily be assessed. The inclusion of cellular dyes and immunostaining in combination with in-depth image analysis enabled us to identify compounds that induced undesirable phenotypes in host cells, such as changes in cell morphology or in lysosomal activity. With the platform, we screened ∼900K compounds and triaged hits, thereby identifying potential candidate compounds carrying broad-spectrum activity with limited off-target effects. The flexibility and early-stage identification of compounds with limited host cell effects provided by this high-content imaging platform can facilitate coronavirus drug discovery. We anticipate that its rapid deployability and fast turnaround can also be applied to combat future pandemics.

Identifiants

pubmed: 38158129
pii: S0166-3542(23)00267-X
doi: 10.1016/j.antiviral.2023.105789
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105789

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: JD, IH, KT, PV, AD, SJ, MB, DP, MVL, AK, CB, MVG, and EVD are employees of Janssen Pharmaceutica NV, part of Johnson and Johnson, and some of the authors hold shares or share options from Johnson and Johnson as part of their employee remuneration. NVdB, VR, JP, KK, and MC are employees of Charles River Laboratories, which is a contractor of Janssen Pharmaceutica NV.

Auteurs

Jordi Doijen (J)

Global Public Health R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: JDoijen@its.jnj.com.

Inha Heo (I)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: IHeo@its.jnj.com.

Koen Temmerman (K)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: KTemmer2@ITS.JNJ.com.

Peter Vermeulen (P)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: PVERMEUL@its.jnj.com.

Annick Diels (A)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: ADIELS@its.jnj.com.

Steffen Jaensch (S)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: SJAENSCH@its.jnj.com.

Mark Burcin (M)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: MBurcin@ITS.JNJ.com.

Nick Van den Broeck (N)

Charles River Laboratories, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: NVanden6@ITS.JNJ.com.

Valerie Raeymaekers (V)

Charles River Laboratories, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: VRaeymae@ITS.JNJ.com.

Joren Peremans (J)

Charles River Laboratories, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: jpereman@ITS.JNJ.com.

Katrien Konings (K)

Charles River Laboratories, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: KKoning1@ITS.JNJ.com.

Maxime Clement (M)

Charles River Laboratories, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: mcleme12@its.jnj.com.

Danielle Peeters (D)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: DPEETER1@its.jnj.com.

Marnix Van Loock (M)

Global Public Health R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: mvloock@its.jnj.com.

Anil Koul (A)

Global Public Health R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: AKOUL@its.jnj.com.

Christophe Buyck (C)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: CBUYCK@its.jnj.com.

Michiel Van Gool (M)

Therapeutics Discovery R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: mvgool2@its.jnj.com.

Ellen Van Damme (E)

Global Public Health R&D, Janssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium. Electronic address: evandamm@its.jnj.com.

Classifications MeSH