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A Plasmodium homolog of ER tubule-forming proteins is required for parasite virulence.


ABSTRACT: Reticulon and REEP family of proteins stabilize the high curvature of endoplasmic reticulum (ER) tubules. Plasmodium berghei Yop1 (PbYop1) is a REEP5 homolog in Plasmodium. Here, we characterize its function using a gene-knockout (Pbyop1?). Pbyop1? asexual stage parasites display abnormal ER architecture and an enlarged digestive vacuole. The erythrocytic cycle of Pbyop1? parasites is severely attenuated and the incidence of experimental cerebral malaria is significantly decreased in Pbyop1?-infected mice. Pbyop1? sporozoites have reduced speed, are slower to invade host cells but give rise to equal numbers of infected HepG2 cells, as WT sporozoites. We propose that PbYOP1's disruption may lead to defects in trafficking and secretion of a subset of proteins required for parasite development and invasion of erythrocytes. Furthermore, the maintenance of ER morphology in different parasite stages is likely to depend on different proteins.

SUBMITTER: Shi X 

PROVIDER: S-EPMC7594924 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

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A Plasmodium homolog of ER tubule-forming proteins is required for parasite virulence.

Shi Xiaoyu X   Hai Lei L   Govindasamy Kavitha K   Gao Jian J   Coppens Isabelle I   Hu Junjie J   Wang Qian Q   Bhanot Purnima P  

Molecular microbiology 20200619 3


Reticulon and REEP family of proteins stabilize the high curvature of endoplasmic reticulum (ER) tubules. Plasmodium berghei Yop1 (PbYop1) is a REEP5 homolog in Plasmodium. Here, we characterize its function using a gene-knockout (Pbyop1∆). Pbyop1∆ asexual stage parasites display abnormal ER architecture and an enlarged digestive vacuole. The erythrocytic cycle of Pbyop1∆ parasites is severely attenuated and the incidence of experimental cerebral malaria is significantly decreased in Pbyop1∆-inf  ...[more]

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