Nailma S A Dos Santos
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.
Authors
Carlos F. Estevez-Castro
Juan P. Macedo
Daniela F. Chame
Thiago Castro-Gomes
Mariana Santos-Cardoso
Gabriela A. Burle-Caldas
Courtney Nicole Covington courtney.n.covington@durham.ac.uk
PGR Student Doctor of Philosophy
Professor Patrick Steel p.g.steel@durham.ac.uk
Professor
Terry K. Smith
Professor Paul Denny p.w.denny@durham.ac.uk
Professor
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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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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