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Tytuł pozycji:

Deubiquitinating Enzyme Inhibitors Block Chikungunya Virus Replication.

Tytuł:
Deubiquitinating Enzyme Inhibitors Block Chikungunya Virus Replication.
Autorzy:
López LS; Grupo de Virología, Universidad El Bosque, Bogotá 110121, Colombia.
Calvo EP; Grupo de Virología, Universidad El Bosque, Bogotá 110121, Colombia.
Castellanos JE; Grupo de Virología, Universidad El Bosque, Bogotá 110121, Colombia.
Źródło:
Viruses [Viruses] 2023 Feb 09; Vol. 15 (2). Date of Electronic Publication: 2023 Feb 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: Basel, Switzerland : MDPI
MeSH Terms:
Chikungunya Fever*/drug therapy
Chikungunya virus*/drug effects
Deubiquitinating Enzymes*/antagonists & inhibitors
Enzyme Inhibitors*/pharmacology
Enzyme Inhibitors*/therapeutic use
Virus Replication*/drug effects
Humans ; HEK293 Cells ; RNA, Viral
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Contributed Indexing:
Keywords: chikungunya virus; deubiquitinase inhibitor; deubiquitinating enzymes; infection; replication; ubiquitination
Substance Nomenclature:
EC 3.4.19.12 (Deubiquitinating Enzymes)
0 (Enzyme Inhibitors)
0 (RNA, Viral)
Entry Date(s):
Date Created: 20230228 Date Completed: 20230307 Latest Revision: 20230410
Update Code:
20240105
PubMed Central ID:
PMC9966916
DOI:
10.3390/v15020481
PMID:
36851696
Czasopismo naukowe
Ubiquitination and deubiquitination processes are widely involved in modulating the function, activity, localization, and stability of multiple cellular proteins regulating almost every aspect of cellular function. Several virus families have been shown to exploit the cellular ubiquitin-conjugating system to achieve a productive infection: enter the cell, promote genome replication, or assemble and release viral progeny. In this study, we analyzed the role of deubiquitinating enzymes (DUBs) during chikungunya virus (CHIKV) infection. HEK293T, Vero-E6, and Huh-7 cells were treated with two DUB inhibitors (PR619 or WP1130). Then, infected cells were evaluated by flow cytometry, and viral progeny was quantified using the plaque assay method. The changes in viral proteins and viral RNA were analyzed using Western blotting and RT-qPCR, respectively. Results indicate that treatment with DUB inhibitors impairs CHIKV replication due to significant protein and viral RNA synthesis deregulation. Therefore, DUB activity may be a pharmacological target for blocking CHIKV infection.
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