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Host biotin is required for liver stage development in malaria parasites.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2018 Mar 13; Vol. 115 (11), pp. E2604-E2613. Date of Electronic Publication: 2018 Feb 26. - Publication Year :
- 2018
-
Abstract
- Acetyl-CoA carboxylase (ACC) is a biotin-dependent enzyme that is the target of several classes of herbicides. Malaria parasites contain a plant-like ACC, and this is the only protein predicted to be biotinylated in the parasite. We found that ACC is expressed in the apicoplast organelle in liver- and blood-stage malaria parasites; however, it is activated through biotinylation only in the liver stages. Consistent with this observation, deletion of the biotin ligase responsible for ACC biotinylation does not impede blood-stage growth, but results in late liver-stage developmental defects. Biotin depletion increases the severity of the developmental defects, demonstrating that parasite and host biotin metabolism are required for normal liver-stage progression. This finding may link the development of liver-stage malaria parasites to the nutritional status of the host, as neither the parasite nor the human host can synthesize biotin.<br />Competing Interests: The authors declare no conflict of interest.<br /> (Copyright © 2018 the Author(s). Published by PNAS.)
- Subjects :
- Acetyl-CoA Carboxylase metabolism
Animals
Apicoplasts metabolism
Carbon-Nitrogen Ligases metabolism
Hep G2 Cells
Humans
Liver metabolism
Malaria parasitology
Mice
Protozoan Proteins metabolism
Biotin metabolism
Host-Parasite Interactions physiology
Liver parasitology
Malaria metabolism
Plasmodium metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 115
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 29483266
- Full Text :
- https://doi.org/10.1073/pnas.1800717115