» Articles » PMID: 35867575

The NS4A Protein of Classical Swine Fever Virus Suppresses RNA Silencing in Mammalian Cells

Overview
Journal J Virol
Date 2022 Jul 22
PMID 35867575
Authors
Affiliations
Soon will be listed here.
Abstract

RNA interference (RNAi) is a significant posttranscriptional gene silencing mechanism and can function as an antiviral immunity in eukaryotes. However, numerous viruses can evade this antiviral RNAi by encoding viral suppressors of RNA silencing (VSRs). Classical swine fever virus (CSFV), belonging to the genus , is the cause of classical swine fever (CSF), which has an enormous impact on animal health and the pig industry. Notably, little is known about how blocks RNAi in their host. In this paper, we uncovered that CSFV NS4A protein can antagonize RNAi efficiently in mammalian cells by binding to double-stranded RNA and small interfering RNA. In addition, the VSR activity of CSFV NS4A was conserved among . Furthermore, the replication of VSR-deficient CSFV was attenuated but could be restored by the deficiency of RNAi in mammalian cells. In conclusion, our studies uncovered that CSFV NS4A is a novel VSR that suppresses RNAi in mammalian cells and shed new light on knowledge about CSFV and other . It is well known that RNAi is an important posttranscriptional gene silencing mechanism that is also involved in the antiviral response in mammalian cells. While numerous viruses have evolved to block this antiviral immunity by encoding VSRs. Our data demonstrated that the NS4A protein of CSFV exhibited a potent VSR activity through binding to dsRNA and siRNA in the context of CSFV infection in mammalian cells, which are a conservative feature among . In addition, the replication of VSR-deficient CSFV was attenuated but could be restored by the deficiency of RNAi, providing a theoretical basis for the development of other important attenuated vaccines.

Citing Articles

hsa-miR-548d-3p: a potential microRNA to target nucleocapsid and/or capsid genes in multiple members of the Flaviviridae family.

Cayatineto H, Hakim S Front Bioinform. 2025; 4:1487292.

PMID: 39877236 PMC: 11772435. DOI: 10.3389/fbinf.2024.1487292.


CSFV restricts necroptosis to sustain infection by inducing autophagy/mitophagy-targeted degradation of RIPK3.

Wu K, Li B, Zhang X, Fang Y, Zeng S, Hu W Microbiol Spectr. 2023; 12(1):e0275823.

PMID: 38100396 PMC: 10782971. DOI: 10.1128/spectrum.02758-23.


Packaging defects in pestiviral NS4A can be compensated by mutations in NS2 and NS3.

Fellenberg J, Dubrau D, Isken O, Tautz N J Virol. 2023; 97(9):e0057223.

PMID: 37695056 PMC: 10537661. DOI: 10.1128/jvi.00572-23.


Immunoinformatic prediction of the pathogenicity of bovine viral diarrhea virus genotypes: implications for viral virulence determinants, designing novel diagnostic assays and vaccines development.

Al-Kubati A, Kandeel M, Hussen J, Hemida M, Al-Mubarak A Front Vet Sci. 2023; 10:1130147.

PMID: 37483297 PMC: 10359904. DOI: 10.3389/fvets.2023.1130147.

References
1.
Thiel H, Stark R, Weiland E, Rumenapf T, Meyers G . Hog cholera virus: molecular composition of virions from a pestivirus. J Virol. 1991; 65(9):4705-12. PMC: 248926. DOI: 10.1128/JVI.65.9.4705-4712.1991. View

2.
Shan G, Li Y, Zhang J, Li W, Szulwach K, Duan R . A small molecule enhances RNA interference and promotes microRNA processing. Nat Biotechnol. 2008; 26(8):933-40. PMC: 2831467. DOI: 10.1038/nbt.1481. View

3.
Dreier S, Zimmermann B, Moennig V, Greiser-Wilke I . A sequence database allowing automated genotyping of Classical swine fever virus isolates. J Virol Methods. 2006; 140(1-2):95-9. DOI: 10.1016/j.jviromet.2006.11.013. View

4.
Karjee S, Minhas A, Sood V, Ponia S, Banerjea A, Chow V . The 7a accessory protein of severe acute respiratory syndrome coronavirus acts as an RNA silencing suppressor. J Virol. 2010; 84(19):10395-401. PMC: 2937820. DOI: 10.1128/JVI.00748-10. View

5.
Li Y, Basavappa M, Lu J, Dong S, Cronkite D, Prior J . Induction and suppression of antiviral RNA interference by influenza A virus in mammalian cells. Nat Microbiol. 2016; 2:16250. PMC: 5488270. DOI: 10.1038/nmicrobiol.2016.250. View