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Updated: Jan 7, 2026

Highly Sensitive Assay for Measurement of Arenavirus-cell Attachment
Published on: March 2, 2016
Enterovirus D68 receptor usage: from static attachment to dynamic entry
Dongxue Liu1,2, Zhilin Ji3, Xiangyu Zheng4,5
1Institute of Virology and AIDS Research, The First Hospital of Jilin University, Changchun, Jilin, China.
Abstract:
Enterovirus D68 (EV-D68) is a globally reemerging respiratory pathogen of notable clinical concern due to its association with severe respiratory disease and the paralytic complication acute flaccid myelitis (AFM). Viral tropism and pathogenesis are critically dictated by interactions with host cell receptors. Our understanding of this process has evolved from a simple model of sialic acid dependence to a dynamic paradigm involving a repertoire of attachment factors and proteinaceous entry receptors. This review synthesizes the evolving landscape of EV-D68 receptor usage. We detail the well-established role of α2,6-linked sialic acid as an attachment factor and uncoating trigger for historical strains. We further discuss the discovery of intracellular adhesion molecule-5 (ICAM-5) as a neuron-specific receptor that provides a molecular explanation for neurotropism in AFM. A pivotal recent advance is the identification of major facilitator superfamily domain-containing 6 (MFSD6) as an essential entry receptor for a broad range of EV-D68 strains in both respiratory and neuronal cells. We explore the implications of this receptor versatility, whereby the virus can switch between or co-opt sialic acid, ICAM-5, and MFSD6, a plasticity that influences tissue tropism and viral evolution. Finally, we highlight how these mechanistic insights, particularly the characterization of the MFSD6 interface, are paving the way for novel therapeutic strategies, such as engineered decoy receptors, and outline key future directions in the field.
Insights
Enterovirus D68 (EV-D68) uses multiple receptors, including sialic acid, ICAM-5, and MFSD6, to infect cells. This receptor plasticity explains its spread in respiratory and nervous systems, guiding new therapeutic development.
Area of Science:
- Virology
- Molecular Biology
- Immunology
Background:
- Enterovirus D68 (EV-D68) is a reemerging pathogen causing severe respiratory illness and acute flaccid myelitis (AFM).
- Viral entry mechanisms are key to understanding EV-D68 tropism and pathogenesis.
- Previous models focused on sialic acid, but recent discoveries reveal a more complex receptor landscape.
Purpose of the Study:
- To review the evolving understanding of EV-D68 receptor usage.
- To synthesize current knowledge on viral attachment factors and entry receptors.
- To explore the implications of receptor versatility for viral evolution and therapeutic strategies.
Main Methods:
- Literature review of studies on EV-D68 receptor interactions.
- Analysis of established and newly identified viral receptors.
- Discussion of the functional significance of receptor usage in different cell types.
Main Results:
- Sialic acid acts as an attachment factor and uncoating trigger for older EV-D68 strains.
- ICAM-5 is a neuron-specific receptor explaining neurotropism in AFM.
- MFSD6 is identified as a crucial entry receptor for diverse EV-D68 strains in respiratory and neuronal cells.
Conclusions:
- EV-D68 exhibits remarkable receptor plasticity, utilizing sialic acid, ICAM-5, and MFSD6.
- This adaptability influences tissue tropism, viral evolution, and disease manifestation.
- Understanding receptor-virus interactions, especially the MFSD6 interface, is crucial for developing novel EV-D68 therapeutics.
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