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Updated: May 28, 2026

Engineering Antiviral Agents via Surface Plasmon Resonance
Published on: June 14, 2022
Glycosphingolipids as receptors for non-enveloped viruses
Stefan Taube1, Mengxi Jiang1, Christiane E Wobus1
1Department of Microbiology and Immunology, University of Michigan Medical School, 5622 Medical Sciences Bldg. II, 1150 West Medical Center Dr., Ann Arbor, MI 48109, USA.
Glycosphingolipids act as receptors for various viruses, influencing infection and host susceptibility. This review details their role in viral entry for caliciviruses, rotaviruses, polyomaviruses, and parvoviruses.
Area of Science:
- Biochemistry
- Virology
- Cell Biology
Background:
- Glycosphingolipids are essential cell surface molecules involved in diverse biological processes.
- Microbial pathogens exploit cell surface glycosphingolipids for host cell attachment and infection.
- Specific carbohydrate structures on glycosphingolipids mediate interactions with microbes.
Purpose of the Study:
- To review the critical role of glycosphingolipids as receptors for non-enveloped viruses.
- To highlight how glycosphingolipid-virus interactions influence host susceptibility and viral entry pathways.
Main Methods:
- Literature review of studies investigating glycosphingolipids and viral interactions.
- Analysis of viral families including caliciviruses, rotaviruses, polyomaviruses, and parvoviruses.
- Focus on the molecular mechanisms of viral attachment and cell entry mediated by glycosphingolipids.
Main Results:
- Glycosphingolipids serve as specific attachment sites for multiple non-enveloped viruses.
- Binding to gangliosides, a type of glycosphingolipid, dictates viral internalization pathways for polyomaviruses.
- The interaction between viral components and host glycosphingolipids is a key factor in determining host susceptibility to infection.
Conclusions:
- Glycosphingolipids are crucial determinants of host-pathogen interactions, particularly in viral infections.
- Understanding these interactions is vital for deciphering viral pathogenesis and host range.
- Targeting glycosphingolipid-virus interactions may offer novel strategies for antiviral therapies.
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