Glycan–glycan interactions determine Leishmania attachment to the midgut of permissive sand fly vectors

Hall, Amy R.; Blakeman, Jamie T.; Eissa, Ahmed M.; Chapman, Paul; Morales-García, Ana L.; Stennett, Laura; Martin, Oihane; Giraud, Emilie; Dockrell, David H.; Cameron, Neil R.; Wiese, Martin; Yakob, Laith; Rogers, Matthew E.; Geoghegan, Mark

Abstract

Direct glycan–glycan interactions are increasingly implicated in survival and pathogenicity of bacteria. Here, we show that they can be exploited by protozoan parasites in their insect hosts. Force spectroscopy revealed that Leishmania promastigotes display a high-affinity biomolecular interaction between their lipophosphoglycan glycocalyx and mimics of N-acetyl-D-galactosamine, commonly expressed on the midguts of a wide range of sand fly vector species. This enabled gut-adhesive nectomonad promastigotes of Leishmania mexicana to efficiently bind to membrane-bound mucin-like, O-linked glycoproteins of the sand fly Lutzomyia longipalpis, an event crucial for parasite survival, and accounts for a permissive mode of binding. Thus, direct interaction between parasite and sand fly midgut glycans are key to permitting vector competence for all forms of leishmaniasis worldwide. In addition, these studies demonstrate the feasibility of interfering with these interactions as transmission-blocking vaccine.

Citation

Hall, A. R., Blakeman, J. T., Eissa, A. M., Chapman, P., Morales-García, A. L., Stennett, L., Martin, O., Giraud, E., Dockrell, D. H., Cameron, N. R., Wiese, M., Yakob, L., Rogers, M. E., & Geoghegan, M. (2020). Glycan–glycan interactions determine Leishmania attachment to the midgut of permissive sand fly vectors. Chemical Science, 11(40), 10973-10983. https://doi.org/10.1039/d0sc03298k

• Journal Article Type: Article
• Acceptance Date: Sep 2, 2020
• Online Publication Date: Sep 3, 2020
• Publication Date: 2020-10
• Deposit Date: Nov 17, 2020
• Publicly Available Date: Nov 17, 2020
• Journal: Chemical Science
• Print ISSN: 2041-6520
• Electronic ISSN: 2041-6539
• Publisher: Royal Society of Chemistry
• Peer Reviewed: Peer Reviewed
• Volume: 11
• Issue: 40
• Pages: 10973-10983
• DOI: https://doi.org/10.1039/d0sc03298k
• Public URL: https://durham-repository.worktribe.com/output/1257068