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Disruption of the inositol phosphorylceramide synthase gene affects Trypanosoma cruzi differentiation and infection capacity

Dos Santos, Nailma S A; Estevez-Castro, Carlos F.; Macedo, Juan P.; Chame, Daniela F.; Castro-Gomes, Thiago; Santos-Cardoso, Mariana; Burle-Caldas, Gabriela A.; Covington, Courtney N.; Steel, Patrick G.; Smith, Terry K.; Denny, Paul W.; Teixeira, Santuza M. R.

Disruption of the inositol phosphorylceramide synthase gene affects Trypanosoma cruzi differentiation and infection capacity Thumbnail


Authors

Nailma S A Dos Santos

Carlos F. Estevez-Castro

Juan P. Macedo

Daniela F. Chame

Thiago Castro-Gomes

Mariana Santos-Cardoso

Gabriela A. Burle-Caldas

Terry K. Smith

Santuza M. R. Teixeira



Contributors

Michael W. Gaunt
Editor

Abstract

Sphingolipids (SLs) are essential components of all eukaryotic cellular membranes. In fungi, plants and many protozoa, the primary SL is inositol-phosphorylceramide (IPC). Trypanosoma cruzi is a protozoan parasite that causes Chagas disease (CD), a chronic illness for which no vaccines or effective treatments are available. IPC synthase (IPCS) has been considered an ideal target enzyme for drug development because phosphoinositol-containing SL is absent in mammalian cells and the enzyme activity has been described in all parasite forms of T. cruzi. Furthermore, IPCS is an integral membrane protein conserved amongst other kinetoplastids, including Leishmania major, for which specific inhibitors have been identified. Using a CRISPR-Cas9 protocol, we generated T. cruzi knockout (KO) mutants in which both alleles of the IPCS gene were disrupted. We demonstrated that the lack of IPCS activity does not affect epimastigote proliferation or its susceptibility to compounds that have been identified as inhibitors of the L. major IPCS. However, disruption of the T. cruzi IPCS gene negatively affected epimastigote differentiation into metacyclic trypomastigotes as well as proliferation of intracellular amastigotes and differentiation of amastigotes into tissue culture-derived trypomastigotes. In accordance with previous studies suggesting that IPC is a membrane component essential for parasite survival in the mammalian host, we showed that T. cruzi IPCS null mutants are unable to establish an infection in vivo, even in immune deficient mice.

Citation

Dos Santos, N. S. A., Estevez-Castro, C. F., Macedo, J. P., Chame, D. F., Castro-Gomes, T., Santos-Cardoso, M., …Teixeira, S. M. R. (2023). Disruption of the inositol phosphorylceramide synthase gene affects Trypanosoma cruzi differentiation and infection capacity. PLoS Neglected Tropical Diseases, 17(9), Article e0011646. https://doi.org/10.1371/journal.pntd.0011646

Journal Article Type Article
Acceptance Date Sep 7, 2023
Online Publication Date Sep 20, 2023
Publication Date Sep 20, 2023
Deposit Date Nov 1, 2023
Publicly Available Date Nov 3, 2023
Journal PLOS Neglected Tropical Diseases
Print ISSN 1935-2727
Publisher Public Library of Science
Peer Reviewed Peer Reviewed
Volume 17
Issue 9
Article Number e0011646
DOI https://doi.org/10.1371/journal.pntd.0011646
Keywords Infectious Diseases; Public Health, Environmental and Occupational Health
Public URL https://durham-repository.worktribe.com/output/1874141

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Licence
http://creativecommons.org/licenses/by/4.0/

Copyright Statement
© 2023 Dos Santos et al. This is an
open access article distributed under the terms of
the Creative Commons Attribution License, which
permits unrestricted use, distribution, and
reproduction in any medium, provided the original
author and source are credited.





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