Chikungunya Virus Strains from Each Genetic Clade Bind Sulfated Glycosaminoglycans as Attachment Factors

Author:

McAllister Nicole12,Liu Yan3,Silva Lisete M.34,Lentscher Anthony J.12,Chai Wengang3,Wu Nian35,Griswold Kira A.12,Raghunathan Krishnan26,Vang Lo7,Alexander Jeff7,Warfield Kelly L.7,Diamond Michael S.8910,Feizi Ten3,Silva Laurie A.26ORCID,Dermody Terence S.126ORCID

Affiliation:

1. Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA

2. Center for Microbial Pathogenesis, UPMC Children’s Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA

3. Glycosciences Laboratory, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom

4. LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, Aveiro, Portugal

5. Division of Histology and Embryology, Medical College, Jinan University, Guangzhou, China

6. Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA

7. Emergent Travel Health, Emergent BioSolutions Inc., San Diego, California, USA

8. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA

9. Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA

10. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA

Abstract

Alphavirus infections are a global health threat, contributing to outbreaks of disease in many parts of the world. Recent epidemics caused by CHIKV, an arthritogenic alphavirus, resulted in more than 8.5 million cases as the virus has spread into new geographic regions, including the Western Hemisphere. CHIKV causes disease in the majority of people infected, leading to severe and debilitating arthritis. Despite the severity of CHIKV disease, there are no licensed therapeutics. Since attachment factors and receptors are determinants of viral tropism and pathogenesis, understanding these virus-host interactions can enhance our knowledge of CHIKV infection. We analyzed over 670 glycans and identified GAGs as the main glycan bound by CHIKV. We defined specific GAG components required for CHIKV binding and assessed strain-specific differences in GAG binding capacity. These studies provide insight about cell surface molecules that CHIKV binds, which could facilitate the development of antiviral therapeutics targeting the CHIKV attachment step.

Funder

UPMC Children's Hospital of Pittsburgh

HHS | NIH | National Institute of Allergy and Infectious Diseases

Wellcome

March of Dimes | March of Dimes Prematurity Research Center Ohio Collaborative

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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