Related Experiment Video
Updated: Jul 6, 2026

Using RNA-interference to Investigate the Innate Immune Response in Mouse Macrophages
Published on: November 3, 2014
Transcriptomic Analysis of Mayaro Virus-Infected Human Macrophages: Effects on Inflammatory and Antiviral Response
Lady Johana Hernández-Sarmiento1, Y S Tamayo-Molina1, Silvio Urcuqui-Inchima1
1Grupo Inmunovirología, Facultad de Medicina, Universidad de Antioquia UdeA, Medellín, Colombia.
Abstract:
Mayaro virus (MAYV) belongs to the Togaviridae family and is the etiologic agent of Mayaro fever, a disease in which inflammatory responses play a critical role in viral pathogenesis. Macrophages are targets of viral infection and key components of innate immunity and antiviral response. This study analyzed an RNA-sequencing (RNA-seq) dataset to gain insights into inflammatory and antiviral responses in monocyte-derived macrophages (MDMs) infected with the MAYV strain (Venezuelan 2010) at a multiplicity of infection (MOI) of 10. The RNA-seq results were validated by real-time quantitative polymerase chain reaction in MDMs infected with the MAYV strain from Brazil (MOI of 2). In addition, the replication capacity of MAYV and the resulting cell death in infected MDMs were assessed using plaque assays and flow cytometry. At 72 hours post-infection, transcriptomic analysis revealed that MAYV promotes a robust proinflammatory response by upregulating the expression of Toll-like receptors, RIG-I-like receptors, and the nuclear factor-κB complex. This strong inflammatory response was accompanied by a robust antiviral response dependent on type I/III interferon and interleukin-27. Both antiviral responses are mediated through the Janus kinase/signal transducer and activator of transcription signaling pathway, leading to the expression of interferon-stimulated genes. Moreover, MAYV-infected MDMs expressed markers of programmed cell death. These findings highlight the inflammatory response and antiviral activity of MDMs at a late stage in MAYV infection, suggesting a critical role of macrophages in MAYV pathogenesis.
Insights
Mayaro virus (MAYV) infection in macrophages triggers strong inflammatory and antiviral responses, involving key immune signaling pathways. This study reveals macrophages
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Mayaro virus (MAYV) causes Mayaro fever, where inflammation is crucial for disease development.
- Macrophages are vital immune cells targeted by MAYV and involved in antiviral defense.
Purpose of the Study:
- To investigate the inflammatory and antiviral responses in human monocyte-derived macrophages (MDMs) infected with MAYV using transcriptomic analysis.
- To validate RNA-sequencing findings and assess MAYV replication, cell death, and immune responses in MDMs.
Main Methods:
- RNA-sequencing (RNA-seq) analysis of MAYV-infected MDMs.
- Validation using real-time quantitative polymerase chain reaction (RT-qPCR).
- Plaque assays and flow cytometry to assess viral replication and cell death.
Main Results:
- MAYV infection induced a significant proinflammatory response, upregulating Toll-like receptors, RIG-I-like receptors, and the nuclear factor-κB complex.
- A robust antiviral response was observed, mediated by type I/III interferons and interleukin-27 via the JAK/STAT pathway, leading to interferon-stimulated gene expression.
- MAYV-infected MDMs exhibited markers of programmed cell death at 72 hours post-infection.
Conclusions:
- Macrophages mount substantial inflammatory and antiviral responses late in MAYV infection.
- These findings underscore the critical role of macrophages in Mayaro virus pathogenesis and immune response.
Related Concept Videos
Immune Response Against Viral Pathogens
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...
Viruses with RNA Genomes
Inhibitors of Viral Protein Synthesis
Inhibitors Of Virion Release
Inhibitors of Virion Maturation and Assembly

