Journal Article

An Endoplasmic Reticulum CREC Family Protein Regulates the Egress Proteolytic Cascade in Malaria Parasites

Asady, Beejan, Cobb, David W., Villegas, Alejandra, Brooks, Carrie F., Muralidharan, Vasant, Fierro, Manuel A., Moreno, Silvia N. J.

2020

Overview

The divergent eukaryotic parasites that cause malaria grow and divide within a vacuole inside a host cell, which they have to break open once they finish cell division. The egress of daughter parasites requires the activation of a proteolytic cascade, and a subtilisin-like protease initiates a proteolytic cascade to break down the membranes blocking egress. It is assumed that the parasite endoplasmic reticulum plays a role in this process, but the proteins in this organelle required for egress remain unknown. We have identified an early ER-resident regulator essential for the maturation of the recently discovered aspartic protease in the egress proteolytic cascade, plasmepsin X, which is required for maturation of the subtilisin-like protease. Conditional loss of PfERC results in the formation of immature and inactive egress proteases that are unable to breakdown the vacuolar membrane barring release of daughter parasites. The endoplasmic reticulum (ER) is thought to play an essential role during egress of malaria parasites because the ER is assumed to be required for biogenesis and secretion of egress-related organelles. However, no proteins localized to the parasite ER have been shown to play a role in egress of malaria parasites. In this study, we generated conditional mutants of the Plasmodium falciparum e ndoplasmic r eticulum-resident c alcium-binding protein (PfERC), a member of the CREC family. Knockdown of the PfERC gene showed that this gene is essential for asexual growth of P. falciparum . Analysis of the intraerythrocytic life cycle revealed that PfERC is essential for parasite egress but is not required for protein trafficking or calcium storage. We found that PfERC knockdown prevents the rupture of the parasitophorous vacuole membrane. This is because PfERC knockdown inhibited the proteolytic maturation of the subtilisin-like serine protease SUB1. Using double mutant parasites, we showed that PfERC is required for the proteolytic maturation of the essential aspartic protease plasmepsin X, which is required for SUB1 cleavage. Further, we showed that processing of substrates downstream of the proteolytic cascade is inhibited by PfERC knockdown. Thus, these data establish that the ER-resident CREC family protein PfERC is a key early regulator of the egress proteolytic cascade of malaria parasites. IMPORTANCE The divergent eukaryotic parasites that cause malaria grow and divide within a vacuole inside a host cell, which they have to break open once they finish cell division. The egress of daughter parasites requires the activation of a proteolytic cascade, and a subtilisin-like protease initiates a proteolytic cascade to break down the membranes blocking egress. It is assumed that the parasite endoplasmic reticulum plays a role in this process, but the proteins in this organelle required for egress remain unknown. We have identified an early ER-resident regulator essential for the maturation of the recently discovered aspartic protease in the egress proteolytic cascade, plasmepsin X, which is required for maturation of the subtilisin-like protease. Conditional loss of PfERC results in the formation of immature and inactive egress proteases that are unable to breakdown the vacuolar membrane barring release of daughter parasites.

• Publisher: American Society for Microbiology
• Subject: Aspartic endopeptidase / Blood parasites / Calcium (reticular) / Calcium-binding protein / Calcium-Binding Proteins - genetics / Calcium-Binding Proteins - metabolism / Cell division / Cloning / Conditional mutant / CRISPR / egress / Endoplasmic reticulum / Endoplasmic Reticulum - metabolism / Gene Knockout Techniques / Genome editing / Hands / Host-Microbe Biology / Humans / Kinases / Malaria / Malaria - parasitology / Malaria, Falciparum - parasitology / Maturation / Organelles / Parasites / Parasitophorous vacuole / Peptide Hydrolases - metabolism / Peptides / Plasmodium / Plasmodium falciparum - genetics / Plasmodium falciparum - growth & development / Plasmodium falciparum - metabolism / Proteases / Protein transport / Proteins / Proteolysis / Protozoan Proteins - genetics / Protozoan Proteins - metabolism / Retention / Serine proteinase / Subtilisin / Vacuoles - metabolism