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Lipids in Entamoeba histolytica: Host-Dependence and Virulence Factors
Lipids are essential players in parasites pathogenesis. In particular, the highly phagocytic trophozoites of Entamoeba histolytica, the causative agent of amoebiasis, exhibit a dynamic membrane fusion and fission, in which lipids strongly participate; particularly during the overstated motility of t...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075943/ https://www.ncbi.nlm.nih.gov/pubmed/32211340 http://dx.doi.org/10.3389/fcimb.2020.00075 |
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author | Castellanos-Castro, Silvia Bolaños, Jeni Orozco, Esther |
author_facet | Castellanos-Castro, Silvia Bolaños, Jeni Orozco, Esther |
author_sort | Castellanos-Castro, Silvia |
collection | PubMed |
description | Lipids are essential players in parasites pathogenesis. In particular, the highly phagocytic trophozoites of Entamoeba histolytica, the causative agent of amoebiasis, exhibit a dynamic membrane fusion and fission, in which lipids strongly participate; particularly during the overstated motility of the parasite to reach and attack the epithelia and ingest target cells. Synthesis and metabolism of lipids in this protozoan present remarkable difference with those performed by other eukaryotes. Here, we reviewed the current knowledge on lipids in E. histolytica. Trophozoites synthesize phosphatidylcholine and phosphatidylethanolamine by the Kennedy pathway; and sphingolipids, phosphatidylserine, and phosphatidylinositol, by processes similar to those used by other eukaryotes. However, trophozoites lack enzymes for cholesterol and fatty acids synthesis, which are scavenged from the host or culture medium by specific mechanisms. Cholesterol, a fundamental molecule for the expression of virulence, is transported from the medium into the trophozoites by EhNPC1 and EhNPC2 proteins. Inside cells, lipids are distributed by different pathways, including by the participation of the endosomal sorting complex required for transport (ESCRT), involved in vesicle fusion and fission. Cholesterol interacts with the phospholipid lysobisphosphatidic acid (LBPA) and EhADH, an ALIX family protein, also involved in phagocytosis. In this review, we summarize the known information on phospholipids synthesis and cholesterol transport as well as their metabolic pathways in E. histolytica; highlighting the mechanisms used by trophozoites to dispose lipids involved in the virulence processes. |
format | Online Article Text |
id | pubmed-7075943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70759432020-03-24 Lipids in Entamoeba histolytica: Host-Dependence and Virulence Factors Castellanos-Castro, Silvia Bolaños, Jeni Orozco, Esther Front Cell Infect Microbiol Cellular and Infection Microbiology Lipids are essential players in parasites pathogenesis. In particular, the highly phagocytic trophozoites of Entamoeba histolytica, the causative agent of amoebiasis, exhibit a dynamic membrane fusion and fission, in which lipids strongly participate; particularly during the overstated motility of the parasite to reach and attack the epithelia and ingest target cells. Synthesis and metabolism of lipids in this protozoan present remarkable difference with those performed by other eukaryotes. Here, we reviewed the current knowledge on lipids in E. histolytica. Trophozoites synthesize phosphatidylcholine and phosphatidylethanolamine by the Kennedy pathway; and sphingolipids, phosphatidylserine, and phosphatidylinositol, by processes similar to those used by other eukaryotes. However, trophozoites lack enzymes for cholesterol and fatty acids synthesis, which are scavenged from the host or culture medium by specific mechanisms. Cholesterol, a fundamental molecule for the expression of virulence, is transported from the medium into the trophozoites by EhNPC1 and EhNPC2 proteins. Inside cells, lipids are distributed by different pathways, including by the participation of the endosomal sorting complex required for transport (ESCRT), involved in vesicle fusion and fission. Cholesterol interacts with the phospholipid lysobisphosphatidic acid (LBPA) and EhADH, an ALIX family protein, also involved in phagocytosis. In this review, we summarize the known information on phospholipids synthesis and cholesterol transport as well as their metabolic pathways in E. histolytica; highlighting the mechanisms used by trophozoites to dispose lipids involved in the virulence processes. Frontiers Media S.A. 2020-03-10 /pmc/articles/PMC7075943/ /pubmed/32211340 http://dx.doi.org/10.3389/fcimb.2020.00075 Text en Copyright © 2020 Castellanos-Castro, Bolaños and Orozco. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Castellanos-Castro, Silvia Bolaños, Jeni Orozco, Esther Lipids in Entamoeba histolytica: Host-Dependence and Virulence Factors |
title | Lipids in Entamoeba histolytica: Host-Dependence and Virulence Factors |
title_full | Lipids in Entamoeba histolytica: Host-Dependence and Virulence Factors |
title_fullStr | Lipids in Entamoeba histolytica: Host-Dependence and Virulence Factors |
title_full_unstemmed | Lipids in Entamoeba histolytica: Host-Dependence and Virulence Factors |
title_short | Lipids in Entamoeba histolytica: Host-Dependence and Virulence Factors |
title_sort | lipids in entamoeba histolytica: host-dependence and virulence factors |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075943/ https://www.ncbi.nlm.nih.gov/pubmed/32211340 http://dx.doi.org/10.3389/fcimb.2020.00075 |
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