A pyruvate transporter in the apicoplast of apicomplexan parasites

Author:

Chen Pu12ORCID,Chen Yukun12,Xia Ningbo1ORCID,Fan Bolin1,Niu Zhipeng1,He Zhengming1,Wang Xu3,Yuan Jing3ORCID,Gupta Nishith45ORCID,Shen Bang12678ORCID

Affiliation:

1. National Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, Hubei Province, People’s Republic of China

2. Hubei Hongshan Laboratory, Wuhan 430070, Hubei Province, People’s Republic of China

3. State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signal Network, School of Life Sciences, Xiamen University, Xiamen 361005, Fujian Province, People’s Republic of China

4. Intracellular Parasite Education and Research Labs, Department of Biological Sciences, Birla Institute of Technology and Science, Pilani 500078, Hyderabad, India

5. Department of Molecular Parasitology, Faculty of Life Sciences, Humboldt University, Berlin 10115, Germany

6. Shenzhen Institute of Nutrition and Health, Huazhong Agricultural University, Shenzhen 518000, Guangdong Province, People’s Republic of China

7. Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518000, Guangdong Province, People’s Republic of China

8. Frontiers Science Center for Animal Breeding and Sustainable Production, Wuhan 430070, Hubei Province, People’s Republic of China

Abstract

Pyruvate lies at a pivotal node of carbon metabolism in eukaryotes. It is involved in diverse metabolic pathways in multiple organelles, and its interorganelle shuttling is crucial for cell fitness. Many apicomplexan parasites harbor a unique organelle called the apicoplast that houses metabolic pathways like fatty acid and isoprenoid precursor biosyntheses, requiring pyruvate as a substrate. However, how pyruvate is supplied in the apicoplast remains enigmatic. Here, deploying the zoonotic parasite Toxoplasma gondii as a model apicomplexan, we identified two proteins residing in the apicoplast membranes that together constitute a functional apicoplast pyruvate carrier (APC) to mediate the import of cytosolic pyruvate. Depletion of APC results in reduced activities of metabolic pathways in the apicoplast and impaired integrity of this organelle, leading to parasite growth arrest. APC is a pyruvate transporter in diverse apicomplexan parasites, suggesting a common strategy for pyruvate acquisition by the apicoplast in these clinically relevant intracellular pathogens.

Funder

MOST | National Key Research and Development Program of China

MOST | National Natural Science Foundation of China

Sino-German Science Center

HZAU-AGIS Cooperation Fund

DST-SERB

German Research Foundation

Wellcome Trust DBT India Alliance

Fundamental Research Fundi for Central Universities in China

Publisher

Proceedings of the National Academy of Sciences

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