Abstract

Entamoeba histolytica is the cause of amebic colitis and liver abscess. This parasite induces apoptosis in host cells and utilizes exposed ligands such as phosphatidylserine to ingest the apoptotic corpses and invade deeper into host tissue. The purpose of this work was to identify amebic proteins involved in the recognition and ingestion of dead cells. A member of the transmembrane kinase family, phagosome-associated TMK96 (PATMK), was identified in a proteomic screen for early phagosomal proteins. Anti-peptide affinity-purified antibody produced against PATMK demonstrated that it was a type I integral membrane protein that was expressed on the trophozoite surface, and that co-localized with human erythrocytes at the site of contact. The role of PATMK in erythrophagocytosis in vitro was demonstrated by: (i) incubation of ameba with anti-PATMK antibodies; (ii) PATMK mRNA knock-down using a novel shRNA expression system; and (iii) expression of a carboxy-truncation of PATMK (PATMKΔ932). Expression of the carboxy-truncation of PATMKΔ932 also caused a specific reduction in the ability of E. histolytica to establish infection in the intestinal model of amebiasis, however these amebae retained the ability to cause hepatic abscesses when directly injected in the liver. In conclusion, PATMK was identified as a member of the TMK family that participates in erythrophagocytosis and is uniquely required for intestinal infection.

Highlights

  • Entamoeba histolytica, the causative agent of amebiasis, is estimated to be the second leading cause of morbidity and mortality among protozoan parasites worldwide [1]

  • There is a highly ordered process by which the parasite Entamoeba histolytica interacts with human cells

  • Adherence via a parasite lectin is followed in seconds by killing, with only the corpse and not a living cell ingested by the ameba

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Summary

Introduction

The causative agent of amebiasis, is estimated to be the second leading cause of morbidity and mortality among protozoan parasites worldwide [1]. Little is known concerning why host cells are ingested and/or what affect this has on the course of disease. Invasive infection by E. histolytica leads to dramatic tissue destruction [3,4,5,6], including hallmarks of both apoptotic and necrotic host cell death [7,8,9]. Use of pancaspase inhibitors to interfere with apoptotic induction in vivo has reduced infection by this parasite [16]. Given these results we hypothesized that the identification of proteins which participate in the ingestion of the apoptotic corpse would be key to understanding virulence

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