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Multiplexed Isothermal Amplification Based Diagnostic Platform to Detect Zika, Chikungunya, and Dengue 1
Published on: March 13, 2018
FHL1 is a major host factor for chikungunya virus infection
Laurent Meertens1, Mohamed Lamine Hafirassou2, Thérèse Couderc3
1INSERM U944, CNRS UMR 7212, Genomes & Cell Biology of Disease Unit, Institut de Recherche Saint-Louis, Université de Paris, Hôpital Saint-Louis, Paris, France. laurent.meertens@inserm.fr.
Abstract:
Chikungunya virus (CHIKV) is a re-emerging alphavirus that is transmitted to humans by mosquito bites and causes musculoskeletal and joint pain1,2. Despite intensive investigations, the human cellular factors that are critical for CHIKV infection remain unknown, hampering the understanding of viral pathogenesis and the development of anti-CHIKV therapies. Here we identified the four-and-a-half LIM domain protein 1 (FHL1)3 as a host factor that is required for CHIKV permissiveness and pathogenesis in humans and mice. Ablation of FHL1 expression results in the inhibition of infection by several CHIKV strains and o'nyong-nyong virus, but not by other alphaviruses and flaviviruses. Conversely, expression of FHL1 promotes CHIKV infection in cells that do not normally express it. FHL1 interacts directly with the hypervariable domain of the nsP3 protein of CHIKV and is essential for the replication of viral RNA. FHL1 is highly expressed in CHIKV-target cells and is particularly abundant in muscles3,4. Dermal fibroblasts and muscle cells derived from patients with Emery-Dreifuss muscular dystrophy that lack functional FHL15 are resistant to CHIKV infection. Furthermore, CHIKV infection is undetectable in Fhl1-knockout mice. Overall, this study shows that FHL1 is a key factor expressed by the host that enables CHIKV infection and identifies the interaction between nsP3 and FHL1 as a promising target for the development of anti-CHIKV therapies.
Insights
The four-and-a-half LIM domain protein 1 (FHL1) is crucial for Chikungunya virus (CHIKV) infection. Blocking FHL1 inhibits CHIKV, offering a new therapeutic target for this mosquito-borne illness.
Area of Science:
- Virology
- Molecular Biology
- Immunology
Background:
- Chikungunya virus (CHIKV) is a re-emerging alphavirus causing significant musculoskeletal and joint pain.
- Understanding host factors critical for CHIKV infection is essential for developing effective therapies.
Purpose of the Study:
- To identify human cellular factors essential for CHIKV permissiveness and pathogenesis.
- To investigate the role of the four-and-a-half LIM domain protein 1 (FHL1) in CHIKV infection.
Main Methods:
- Gene silencing to ablate FHL1 expression in human and mouse cells.
- Infection assays with various alphaviruses and flaviviruses.
- Protein interaction studies between FHL1 and CHIKV nsP3.
- Analysis of CHIKV infection in FHL1-deficient cells and Fhl1-knockout mice.
Main Results:
- Ablation of FHL1 inhibited infection by CHIKV and o'nyong-nyong virus, but not other alphaviruses or flaviviruses.
- FHL1 expression promoted CHIKV infection in normally resistant cells.
- FHL1 directly interacts with CHIKV nsP3 and is essential for viral RNA replication.
- CHIKV infection was undetectable in Fhl1-knockout mice and FHL1-deficient patient-derived cells.
Conclusions:
- FHL1 is a critical host factor enabling CHIKV infection and pathogenesis.
- The interaction between CHIKV nsP3 and FHL1 represents a promising target for anti-CHIKV therapeutic development.
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