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.

Nature
|September 27, 2019
PubMed

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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