Extracellular amastigotes of T rypanosoma cruzi are potent inducers of phagocytosis in mammalian cells

Summary The protozoan parasite T rypanosoma cruzi , the aetiological agent of C hagas' disease, has two infective life cycle stages, trypomastigotes and amastigotes. While trypomastigotes actively enter mammalian cells, highly infective extracellular amastigotes (type I   T . cruzi ) rely on actin‐mediated uptake, which is generally inefficient in non‐professional phagocytes. We found that extracellular amastigotes ( EAs ) of T . cruzi   G strain (type I ), but not Y strain (type II ), were taken up 100‐fold more efficiently than inert particles. Mammalian cell lines showed levels of parasite uptake comparable to macrophages, and extensive actin recruitment and polymerization was observed at the site of entry. EA uptake was not dependent on parasite‐secreted molecules and required the same molecular machinery utilized by professional phagocytes during large particle phagocytosis. Transcriptional silencing of synaptotagmin VII and CD 63 significantly inhibited EA internalization, demonstrating that delivery of supplemental lysosomal membrane to form the phagosome is involved in parasite uptake. Importantly, time‐lapse live imaging using fluorescent reporters revealed phagosome‐associated modulation of phosphoinositide metabolism during EA uptake that closely resembles what occurs during phagocytosis by macrophages. Collectively, our results demonstrate that T . cruzi   EAs are potent inducers of phagocytosis in non‐professional phagocytes, a process that may facilitate parasite persistence in infected hosts.