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Development and validation of Mayaro virus with luciferase reporter genes as a tool for antiviral assays.

作者信息

Marinho Mikaela Dos Santos, Zhang Ya-Nan, Cassani Natasha Marques, Santos Igor Andrade, Costa Oliveira Ana Laura, Dos Santos Pereira Anna Karla, Corbi Pedro Paulo, Zhang Bo, Jardim Ana Carolina Gomes

机构信息

Laboratory of Antiviral Research, Institute of Biomedical Science, Federal University of Uberlândia (UFU), Uberlândia, MG, Brazil.

Key Laboratory of Virology and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, 430071, China.

出版信息

Heliyon. 2024 Jul 2;10(13):e33885. doi: 10.1016/j.heliyon.2024.e33885. eCollection 2024 Jul 15.


DOI:10.1016/j.heliyon.2024.e33885
PMID:39071632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11283106/
Abstract

Arboviruses are etiological agents in an extensive group of emerging diseases with great clinical relevance in Brazil, due to the wide distribution of their vectors and the favorable environmental conditions. Among them, the Mayaro virus (MAYV) has drawn attention since its emergence as the etiologic agent of Mayaro fever, a highly debilitating disease. To study viral replication and identify new drug candidates, traditional antiviral assays based on viral antigens and/or plaque assays have been demonstrating low throughput, making it difficult to carry out larger-scale assays. Therefore, we developed and characterized two DNA-launched infectious clones reporter viruses based on the MAYV strain BeAr 20290 containing the reporter genes of and designated as MAYV- and MAYV-, respectively. The viruses replicated efficiently with similar properties to the parental wild-type MAYV, and luminescence expression levels reflected viral replication. Reporter genes were also preserved during passage in cell culture, remaining stably expressed for one round of passage for MAYV- and three rounds for MAYV- Employing the infectious clone, we described the effect of Rimantadine, an FDA-approved Alzheimer's drug, as a repurposing agent for MAYV but with a broad-spectrum activity against Zika virus infection. Additionally, we validated MAYV- as a tool for antiviral drug screening using the compound EIDD-2749 (4'-Fluorouridine), which acts as an inhibitor of alphavirus RNA-dependent RNA polymerase.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/2c5986ad37a6/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/727c0211c933/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/ae92fcfb1085/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/c11809685af5/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/3f95e4acefea/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/46e07862b7ab/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/2c5986ad37a6/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/727c0211c933/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/ae92fcfb1085/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/c11809685af5/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/3f95e4acefea/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/46e07862b7ab/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa00/11283106/2c5986ad37a6/gr6.jpg

相似文献

[1]
Development and validation of Mayaro virus with luciferase reporter genes as a tool for antiviral assays.

Heliyon. 2024-7-2

[2]
Development of a rapid antiviral screening assay based on eGFP reporter virus of Mayaro virus.

Antiviral Res. 2019-5-29

[3]
Antiviral activity of silymarin against Mayaro virus and protective effect in virus-induced oxidative stress.

Antiviral Res. 2018-8-1

[4]
Repurposing Drugs for Mayaro Virus: Identification of EIDD-1931, Favipiravir and Suramin as Mayaro Virus Inhibitors.

Microorganisms. 2021-3-31

[5]
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[6]
Targeting Host PIM Protein Kinases Reduces Mayaro Virus Replication.

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[7]
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[8]
An update on the development of antiviral against Mayaro virus: from molecules to potential viral targets.

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[9]
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Acta Trop. 2024-4

[10]
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引用本文的文献

[1]
Development of viral infectious clones and their applications based on yeast and bacterial artificial chromosome platforms.

Mol Biomed. 2025-4-29

[2]
In Vitro Evaluation of the Antiviral Activity of Polyphenol (-)-Epigallocatechin-3-Gallate (EGCG) Against Mayaro Virus.

Viruses. 2025-2-14

本文引用的文献

[1]
Suitable Promoter for DNA Vaccination Using a pDNA Ternary Complex.

Pharmaceutics. 2024-5-17

[2]
4'-Fluorouridine inhibits alphavirus replication and infection and .

mBio. 2024-6-12

[3]
Effect of proteins isolated from Brazilian snakes on enterovirus A71 replication cycle: An approach against hand, foot and mouth disease.

Int J Biol Macromol. 2023-6-30

[4]
Roles of Bothrops jararacussu toxins I and II: Antiviral findings against Zika virus.

Int J Biol Macromol. 2023-2-1

[5]
A study of the MAYV replication cycle: Correlation between the kinetics of viral multiplication and viral morphogenesis.

Virus Res. 2023-1-2

[6]
A high-throughput screening assay to identify inhibitory antibodies targeting alphavirus release.

Virol J. 2022-10-29

[7]
Generation of a DNA-launched classical swine fever virus infectious clone packaged in bacterial artificial chromosome.

Virus Res. 2023-1-2

[8]
Monitoring SARS-CoV-2 Infection Using a Double Reporter-Expressing Virus.

Microbiol Spectr. 2022-10-26

[9]
Climate Change and Cascading Risks from Infectious Disease.

Infect Dis Ther. 2022-8

[10]
Construction and characterization of two SARS-CoV-2 minigenome replicon systems.

J Med Virol. 2022-6

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