Literature DB >> 19539057

Use and endocytosis of iron-containing proteins by Entamoeba histolytica trophozoites.

Fernando López-Soto1, Nidia León-Sicairos, Magda Reyes-López, Jesús Serrano-Luna, Cynthia Ordaz-Pichardo, Carolina Piña-Vázquez, Guillermo Ortiz-Estrada, Mireya de la Garza.   

Abstract

Iron is essential for nearly all organisms; in mammals, it is part of proteins such as haemoglobin, and it is captured by transferrin and lactoferrin. Transferrin is present in serum, and lactoferrin is secreted by the mucosa and by neutrophils at infection sites, as a host iron-withholding response, sequestering iron away from invading microorganisms. Additionally, all cells contain ferritin, which sequesters iron when its intracellular levels are increased, detoxifying and preventing damage. Liver ferritin contains 50% of iron corporal reserves. During evolution, pathogens have evolved diverse strategies to obtain iron from their hosts in order to survive. The protozoan Entamoeba histolytica invades the intestinal mucosa, causing dysentery, and the trophozoites often travel to the liver producing hepatic abscesses; thus, intestine and liver proteins could be important iron supplies for E. histolytica. We found that E. histolytica trophozoites can grow in both ferrous and ferric iron, and that they can use haemoglobin, holo-transferrin, holo-lactoferrin, and ferritin as in vitro iron sources. These proteins supported the amoeba growth throughout consecutive passages, similarly to ferric citrate. By confocal microscopy and immunoblotting, iron-binding proteins were observed specifically bound to the amoeba surface, and they were endocytosed, trafficked through the endosomal/lysosomal route, and degraded by neutral and acidic cysteine-proteases. Transferrin and ferritin were mainly internalized through clathrin-coated vesicles, and holo-lactoferrin was mainly internalized by caveola-like structures. In contrast, apo-lactoferrin bound to membrane lipids and cholesterol, inducing cell death. The results suggest that in vivo trophozoites secrete products that can destroy enterocytes, erythrocytes, and hepatocytes, releasing transferrin, haemoglobin, ferritin, and other iron-containing proteins, which, together with lactoferrin derived from neutrophils and acinar cells, could be used as abundant iron supplies by amoebas.

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Year:  2009        PMID: 19539057     DOI: 10.1016/j.meegid.2009.05.018

Source DB:  PubMed          Journal:  Infect Genet Evol        ISSN: 1567-1348            Impact factor:   3.342


  10 in total

1.  Transferrin regulates mRNA levels of a gene involved in iron utilization in Entamoeba histolytica.

Authors:  Cristhian Sánchez-Cruz; Mavil López-Casamichana; Areli Cruz-Castañeda; José de Jesús Olivares-Trejo
Journal:  Mol Biol Rep       Date:  2011-09-27       Impact factor: 2.316

2.  Evidence for a novel Entamoeba histolytica lectin activity that recognises carbohydrates present on ovalbumin.

Authors:  Bradley T Heron; Adam Sateriale; Jose E Teixeira; Christopher D Huston
Journal:  Int J Parasitol       Date:  2010-08-31       Impact factor: 3.981

3.  The complete genome sequence of 'Candidatus Liberibacter solanacearum', the bacterium associated with potato zebra chip disease.

Authors:  Hong Lin; Binghai Lou; Jonathan M Glynn; Harshavardhan Doddapaneni; Edwin L Civerolo; Chuanwu Chen; Yongping Duan; Lijuan Zhou; Cheryl M Vahling
Journal:  PLoS One       Date:  2011-04-28       Impact factor: 3.240

4.  Iron-Binding Protein Degradation by Cysteine Proteases of Naegleria fowleri.

Authors:  Moisés Martínez-Castillo; Gerardo Ramírez-Rico; Jesús Serrano-Luna; Mineko Shibayama
Journal:  Biomed Res Int       Date:  2015-05-18       Impact factor: 3.411

5.  Gene expression profiling in Entamoeba histolytica identifies key components in iron uptake and metabolism.

Authors:  Nora Adriana Hernández-Cuevas; Christian Weber; Chung-Chau Hon; Nancy Guillen
Journal:  PLoS One       Date:  2014-09-11       Impact factor: 3.240

6.  The genome of the myxosporean Thelohanellus kitauei shows adaptations to nutrient acquisition within its fish host.

Authors:  Yalin Yang; Jie Xiong; Zhigang Zhou; Fengmin Huo; Wei Miao; Chao Ran; Yuchun Liu; Jinyong Zhang; Jinmei Feng; Meng Wang; Min Wang; Lei Wang; Bin Yao
Journal:  Genome Biol Evol       Date:  2014-11-08       Impact factor: 3.416

7.  Synthetic bovine lactoferrin peptide Lfampin kills Entamoeba histolytica trophozoites by necrosis and resolves amoebic intracecal infection in mice.

Authors:  César Díaz-Godínez; Ximena González-Galindo; Thuluz Meza-Menchaca; Raúl J Bobes; Mireya de la Garza; Nidia León-Sicairos; Juan P Laclette; Julio C Carrero
Journal:  Biosci Rep       Date:  2019-01-08       Impact factor: 3.840

8.  PTEN differentially regulates endocytosis, migration, and proliferation in the enteric protozoan parasite Entamoeba histolytica.

Authors:  Samia Kadri; Kumiko Nakada-Tsukui; Natsuki Watanabe; Ghulam Jeelani; Tomoyoshi Nozaki
Journal:  PLoS Pathog       Date:  2022-05-02       Impact factor: 7.464

9.  Proteases from Entamoeba spp. and Pathogenic Free-Living Amoebae as Virulence Factors.

Authors:  Jesús Serrano-Luna; Carolina Piña-Vázquez; Magda Reyes-López; Guillermo Ortiz-Estrada; Mireya de la Garza
Journal:  J Trop Med       Date:  2013-02-07

10.  Cytosolic peroxidases protect the lysosome of bloodstream African trypanosomes from iron-mediated membrane damage.

Authors:  Corinna Hiller; Amrei Nissen; Diego Benítez; Marcelo A Comini; R Luise Krauth-Siegel
Journal:  PLoS Pathog       Date:  2014-04-10       Impact factor: 6.823

  10 in total

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