Morpholinodiazenyl chalcone blocks influenza A virus capsid uncoating by perturbing the clathrin-mediated vesicular trafficking pathway.

4′-morpholinodiazenyl chalcone endocytosis influenza A virus uncoating virus entry

Journal

Archiv der Pharmazie
ISSN: 1521-4184
Titre abrégé: Arch Pharm (Weinheim)
Pays: Germany
ID NLM: 0330167

Informations de publication

Date de publication:
15 Mar 2024
Historique:
revised: 12 02 2024
received: 18 11 2023
accepted: 19 02 2024
medline: 15 3 2024
pubmed: 15 3 2024
entrez: 15 3 2024
Statut: aheadofprint

Résumé

Influenza A virus (IAV) is a highly contagious respiratory pathogen that significantly threatens global health by causing seasonal epidemics and occasional, unpredictable pandemics. To identify new compounds with therapeutic potential against IAV, we designed and synthesized a series of 4'-morpholinodiazenyl chalcones using the molecular hybridization method, performed a high-content screen against IAV, and found that (E)-1-{4-[(E)-morpholinodiazenyl]phenyl}-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one (MC-22) completely neutralized IAV infection. While MC-22 allowed IAV to successfully internalize into the cell and fuse at the acidic late endosomes, it prevented viral capsid uncoating and genome release. Since IAV majorly utilizes clathrin-mediated endocytosis (CME) for cellular entry, we examined whether MC-22 had any effect on CME, using nonviral cargoes that enter cells via clathrin-dependent or -independent pathways. Although MC-22 showed no effect on the uptake of choleratoxin B, a cargo that enters cells majorly via the clathrin-independent pathway, it significantly attenuated the clathrin-dependent internalization of both epidermal growth factor and transferrin. Cell biological analyses revealed a marked increase in the size of early endosomes upon MC-22 treatment, indicating an endosomal trafficking/maturation defect. This study reports the identification of MC-22 as a novel CME-targeting, highly potent IAV entry inhibitor, which is expected to neutralize a broad spectrum of viruses that enter the host cells via CME.

Identifiants

pubmed: 38487979
doi: 10.1002/ardp.202300670
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2300670

Subventions

Organisme : University Grants Commission (UGC), New Delhi
ID : F.540/6/DSA-1/2016/(SAP-1)

Informations de copyright

© 2024 Deutsche Pharmazeutische Gesellschaft.

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Auteurs

Ahammed A Thottasseri (AA)

Department of Chemistry, Pondicherry University, Puducherry, India.

Gaganpreet Kaur (G)

Cellular Virology Lab, Department of Biological Sciences, Indian Institute of Science Education and Research, Mohali (IISER Mohali), Mohali, India.

Deepthi Ramesh (D)

Department of Chemistry, Pondicherry University, Puducherry, India.
Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, USA.

Indranil Banerjee (I)

Cellular Virology Lab, Department of Biological Sciences, Indian Institute of Science Education and Research, Mohali (IISER Mohali), Mohali, India.

Tharanikkarasu Kannan (T)

Department of Chemistry, Pondicherry University, Puducherry, India.

Classifications MeSH