Affiliation:
1. Department of Biochemistry, Virginia Tech, Blacksburg, Virginia, USA
Abstract
Nearly half a million deaths were attributed to malaria in 2017. Protozoan parasites of the genus
Plasmodium
cause disease in humans while replicating asexually within the host’s erythrocytes, with
P. falciparum
responsible for most of the mortality. Understanding how
Plasmodium
spp. have adapted to their unique host erythrocyte environment is important for developing malaria control strategies. Here, we demonstrate that
P. falciparum
coopts a host erythrocyte serine hydrolase termed acylpeptide hydrolase. By showing that the parasite requires acylpeptide hydrolase activity for replication, we expand our knowledge of host cell factors that contribute to robust parasite growth.
Funder
HHS | NIH | National Institute of Allergy and Infectious Diseases
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
7 articles.
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