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Generation of Induced-pluripotent Stem Cells Using Fibroblast-like Synoviocytes Isolated from Joints of Rheumatoid Arthritis Patients
Published on: October 16, 2016
Animal model of arthritis and myositis induced by the Mayaro virus
Franciele Martins Santos1, Roberto Sousa Dias1, Michelle Dias de Oliveira1
1Molecular Immunovirology Laboratory, Department of General Biology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil.
Background:
The Mayaro virus (MAYV) is an endemic arbovirus in South American countries, where it is responsible for sporadic outbreaks of Mayaro fever. Clinical manifestations include fever, headache, ocular pain, rash, myalgia, and debilitating and persistent polyarthralgia. Understanding the mechanisms associated with MAYV-induced arthritis is of great importance due to the potential for its emergence, urbanization and dispersion to other regions.
Methods:
15-day old Balb/c mice were infected by two distinct pathways, below the forelimb and in the rear footpad. Animals were observed for a period of 21 days. During this time, they were monitored every 24 hours for disease signs, such as weight loss and muscle weakness. Histological damage in the muscles and joints was evaluated 3, 7, 10, 15 and 20 days post-infection. The cytokine profile in serum and muscles during MAYV infection was evaluated by flow cytometry at different post-infection times. For pain analysis, the animals were submitted to the von Frey test and titre in different organs was evaluated throughout the study to obtain viral kinetics.
Findings:
Infection by two distinct pathways, below the forelimb and in the rear footpad, resulted in a homogeneous viral spread and the development of acute disease in animals. Clinical signs were observed such as ruffled fur, hunched posture, eye irritation and slight gait alteration. In the physical test, both groups presented loss of resistance, which was associated with histopathological damage, including myositis, arthritis, tenosynovitis and periostitis. The immune response was characterized by a strong inflammatory response mediated by the cytokines TNF-α, IL-6 and INF-γ and chemokine MCP-1, followed by the action of IL-10 and IL-4 cytokines.
Interpretation:
The results showed that Balb/c mice represent a promising model to study mechanisms involved in MAYV pathogenesis and for future antiviral testing.
Insights
Mayaro virus (MAYV) infection in mice caused acute disease with joint and muscle damage. The immune response involved key inflammatory cytokines, establishing a model for MAYV pathogenesis research.
Area of Science:
- Virology
- Immunology
- Pathogenesis research
Background:
- Mayaro virus (MAYV) is an arbovirus endemic to South America, causing Mayaro fever outbreaks.
- Clinical symptoms include fever, headache, rash, myalgia, and persistent polyarthralgia.
- Understanding MAYV-induced arthritis is crucial due to its potential for wider spread.
Purpose of the Study:
- To establish a mouse model for studying Mayaro virus pathogenesis.
- To investigate the mechanisms of MAYV-induced arthritis and associated immune responses.
- To provide a platform for future antiviral testing against MAYV.
Main Methods:
- 15-day old Balb/c mice were infected via two distinct routes (forelimb and footpad).
- Clinical signs, weight, muscle weakness, and viral kinetics were monitored for 21 days.
- Histopathological analysis of muscles and joints, cytokine profiling, and pain assessment were performed.
Main Results:
- Infection led to homogeneous viral spread and acute disease, with clinical signs like ruffled fur and gait alteration.
- Histopathological findings revealed myositis, arthritis, tenosynovitis, and periostitis.
- A strong inflammatory response was observed, mediated by TNF-α, IL-6, INF-γ, MCP-1, IL-10, and IL-4.
Conclusions:
- Balb/c mice infected via distinct routes develop acute MAYV disease with significant musculoskeletal pathology.
- The observed immune response profile provides insights into MAYV pathogenesis.
- This mouse model is suitable for studying MAYV pathogenesis and evaluating antiviral therapies.
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