Investigating pyroptosis as a mechanism of L. major cell‐to‐cell spread in the human BLaER1 infection model

Abstract

Leishmania is the causative agent of the tropical neglected disease leishmaniasis and infects macrophages as its definitive host cell. In order to sustain and propagate infections, Leishmania parasites have to complete cycles of exit and re‐infection. Yet, the mechanism driving the parasite spread to other cells remains unclear. Recent studies reported pro‐inflammatory monocytes as replicative niche of Leishmania major and showed prolonged expression of IL‐1β at the site of infection, indicating an activation of the NLRP3 inflammasome and pointing toward pyroptosis as a possible mechanism of parasite spread. To address the species‐specific inflammasome activation of human cells, we characterized the BLaER1 monocytes as a model for L. major infection. We found that BLaER1 monocytes support infection and activation by Leishmania parasites to the same extent as primary human macrophages. Harnessing the possibilities of this infection model, we first showed that BLaER1 GSDMD−/− cells, which carry a deletion of the pore‐forming protein gasdermin D, are more resistant to pyroptotic cell death and, concomitantly, display a strongly delayed release of intracellular parasite. Using that knockout in a co‐incubation assay in comparison with wild‐type BLaER1 cells, we demonstrate that impairment of the pyroptosis pathway leads to lower rates of parasite spread to new host cells, thus, implicating pyroptotic cell death as a possible exit mechanism of L. major in pro‐inflammatory microenvironments.

Mechanisms of host cell exit by intracellular pathogens

“…PCD encompasses apoptosis, necroptosis, and pyroptosis, but also includes autophagy, and accumulating evidence suggests that the manipulation of PCDinducing signal transduction pathways represents an exit strategy for a number of intracellular pathogens. In this context, two research articles and a review report on the role of PCD during host cell exit by pathogens like Coxiella (Schulze-Luehrmann et al, 2023), Leishmania (Volkmar et al, 2023) and Candida (Sonnberger et al, 2023).…”