Leishmania promastigotes require lipophosphoglycan to actively modulate the fusion properties of phagosomes at an early step of phagocytosis

The lipophosphoglycan (LPG) of Leishmania promastigotes plays key roles in parasite survival in both insect and mammalian hosts. Evidence suggests that LPG decreases phagosome fusion properties at the onset of infection in macrophages. The mechanisms of action of this molecule are, however, poorly understood. In the present study, we used a panoply of Leishmania mutants displaying modified LPG structures to determine more precisely how LPG modulates phagosome–endosome fusion. Using an in vivo fusion assay measuring, at the electron microscope, the transfer of solute materials from endosomes to phagosomes, we provided further evidence that the repeating Gal(β1,4)Man(α1‐PO 4 ) units of LPG are responsible for the alteration in phagosome fusion. The inhibitory effect of LPG on phagosome fusion was shown to be more potent towards late endocytic organelles and lysosomes than early endosomes, explaining how Leishmania promastigotes can avoid degradation in hydrolase‐enriched compartments. The involvement of other repeating unit‐containing molecules, including the secreted acid phosphatase, in the inhibition process was ruled out, as an LPG‐defective mutant ( lpg1 − ) which secretes repeating unit‐containing glycoconjugates was present in highly fusogenic phagosomes. In L. major , oligosaccharide side‐chains of LPG did not contribute to the inhibition process, as Spock, an L. major mutant lacking LPG side‐chains, blocked fusion to the same extent as wild‐type parasites. Finally, dead parasites internalized from the culture medium were not as efficient as live parasites in altering phagosome–endosome fusion, despite the presence of LPG. However, the killing of parasites with vital dyes after their sequestration in phagosomes had no effect on the fusion properties of this organelle. Collectively, these results suggest that living promastigotes displaying full‐length cell surface LPG can actively influence macrophages at an early stage of phagocytosis to generate phagosomes with poor fusogenic properties.