Migration of Fasciola hepatica newly excysted juveniles is inhibited by high-mannose and oligomannose-type N-glycan-binding lectins

• Published in: Parasitology Vol. 144; no. 13; pp. 1708 - 1717
• Main Authors: GARCIA-CAMPOS, ANDRES, BAIRD, ALAN W., MULCAHY, GRACE
• Format: Journal Article
• Language: English
• Published: Cambridge, UK Cambridge University Press 01.11.2017
• Subjects: Animals; Antigens; Binding; Concanavalin A; Digestive system; Digestive tract; Economic impact; Entamoeba histolytica; Fasciola hepatica; Fasciola hepatica - physiology; Fascioliasis - parasitology; Giardia lamblia; Glycan; Host-Parasite Interactions; Immunology; Impact analysis; Infections; Ingestion; Intestine; Jejunum; Laboratories; Lectins; Lectins - metabolism; Livestock; Male; Mannose; Migration; N-glycans; Parasites; Parasitic diseases; Parasitology; Peritoneum; Polysaccharides; Polysaccharides - metabolism; Proteins; Proteomics; Rats, Wistar; Receptors; Sheets; Small intestine; Tegument; University colleges; Veterinary medicine; Fasciola hepatica; NEJ; glycans; GNL; lectins; mannose-type N-glycans; jejunum; migration inhibition; ConA
• ISSN: 0031-1820; 1469-8161
• DOI: 10.1017/S003118201700124X

Fasciola hepatica has both zoonotic importance and high economic impact in livestock worldwide. After ingestion by the definitive host, the Newly Excysted Juveniles (NEJ) penetrate the intestine before reaching the peritoneal cavity. The role of some NEJ-derived proteins in invasion has been documented, but the role of NEJ glycans or lectin-binding receptors during initial infection in the gut is still unknown. To address these questions, the migration of NEJ through rat intestine was recorded at 30 min intervals up to 150 min by two ex vivo methods. Firstly, jejunal sheets were challenged with NEJ incubated with biotinylated lectins. Secondly, untreated NEJ were incubated with distal jejunum pre-treated with lectins. Both Concanavalin A (ConA) and Galanthus nivalis (GNL), which recognize mannose-type N-glycans, significantly inhibited NEJ migration across the jejunum. Most of the lectins bound to the tegument and oral sucker of the NEJ, but only ConA and GNL maintained this interaction over 150 min. None of the lectins examined significantly reduced NEJ migration when pre-incubated with jejunal sheets, suggesting that host glycans might not be essential for initial binding/recognition of the gut by NEJ. Agents capable of blocking mannose-type N-glycans on the NEJ tegument may have potential for disrupting infection.