MINI REVIEW article

Front. Cell. Infect. Microbiol.

Sec. Virus and Host

Volume 15 - 2025 | doi: 10.3389/fcimb.2025.1613923

Pathogens that infect mammalian cells via sulfonated glycosaminoglycans

Provisionally accepted
  • Mater Research Institute – The University of Queensland, Brisbane, Australia

The final, formatted version of the article will be published soon.

Sulfonated glycosaminoglycans, such as heparan sulfate and dermatan sulfate, form major components of the cell surface and extracellular matrix, and display vital roles in mammalian physiology, including growth and development. The identification of specific binding to different glycosaminoglycans by a variety of pathogens has led to increased interest in this mechanism for understanding infection. Over the past four decades there have been more than 300 studies on various pathogens that utilize glycosaminoglycans in their infection process. Currently, no articles have collated all known pathogens that use this process. So it is timely that this article provides an overview of all known pathogens that use glycosaminoglycans to enhance their binding and/or infection in human cells. This was done by using the search terms "sulfate/sulphate" "pathogen", "virus", "bacteria", "parasite", "infection" and "glycosaminoglycans" to curate peer reviewed and relevant original research articles from PubMed. This search found that glycosaminoglycans are used in the infection process for 59 viruses, 28 bacteria, and 8 other pathogens (i.e. parasitic protozoa, prions). These findings highlight the conserved and widespread use of glycosaminoglycans for enhancing pathogen infection. In addition, the curated list of pathogens in this study provides a resource for future studies to consider potential therapeutic approaches for targeted disruption of the interaction between pathogens and glycosaminoglycans.

Keywords: sulfate, virus, Bacteria, parasite, Infection, glycosaminoglycan, proteoglycan

Received: 18 Apr 2025; Accepted: 22 May 2025.

Copyright: © 2025 Morris and Dawson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Paul Anthony Dawson, Mater Research Institute – The University of Queensland, Brisbane, Australia

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