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Updated: Dec 5, 2025

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
Published on: October 7, 2011
Mx GTPases: efficient host defense against viral intruders
Sébastien Soubies1, Otto Haller2
1Unité de virologie, immunologie et parasitologie aviaires et cunicoles/Avian and Rabbit Virology Immunology and Parasitology Unit (VIPAC), Zoopole, rue des Fusillés, BP 53, 22440 Ploufragan, France.
Abstract:
Mx proteins are interferon-induced members of the dynamin superfamily of large GTPases. They inhibit a wide range of viruses by blocking early steps in the viral replication cycle. Recent evidence suggests that the human MxA (MX1) protein provides a barrier against zoonotic introduction of influenza A viruses into the human population, whereas the related human MxB (MX2) protein is an inhibitor of HIV-1 and other primate lentiviruses. Structural and functional data suggest that Mx proteins target the nucleocapsids of Mx-sensitive viruses and thereby inhibit their transcriptional and replicative function. Evolutionary studies revealed that Mx GTPases are subject to recurrent arms races with viral targets that shape their specificity determinants while the overall architecture is conserved. Here we briefly review the most salient features of Mx GTPases and their antiviral action as molecular machines.
Insights
Mx proteins are interferon-induced GTPases that block viral replication. Human MxA inhibits influenza A, while MxB targets HIV-1, acting as molecular machines against viruses.
Area of Science:
- Molecular Biology
- Virology
- Immunology
Background:
- Mx proteins are interferon-induced dynamin superfamily GTPases.
- They are crucial in innate immunity, inhibiting viral replication.
- Human MxA (MX1) and MxB (MX2) have distinct antiviral specificities.
Purpose of the Study:
- To review the antiviral functions of Mx GTPases.
- To highlight their role as molecular machines targeting viral nucleocapsids.
- To discuss evolutionary aspects of Mx protein-virus interactions.
Main Methods:
- Review of existing structural and functional data.
- Analysis of evolutionary studies on Mx GTPase specificity.
- Examination of antiviral mechanisms at the molecular level.
Main Results:
- Mx proteins inhibit viruses by targeting nucleocapsids, blocking replication.
- Human MxA acts as a barrier against zoonotic influenza A.
- Human MxB inhibits HIV-1 and other primate lentiviruses.
Conclusions:
- Mx GTPases are conserved molecular machines with potent antiviral activity.
- Their specificity is shaped by co-evolutionary arms races with viruses.
- Mx proteins represent a key defense mechanism against viral infections.
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