Literature DB >> 27040117

Resistance against Echinostoma caproni (Trematoda) secondary infections in mice is not dependent on the ileal protein production.

Alba Cortés1, Javier Sotillo2, Carla Muñoz-Antolí3, Carla Martín-Grau3, J Guillermo Esteban3, Rafael Toledo3.   

Abstract

UNLABELLED: Echinostoma caproni (Trematoda: Echinostomatidae) is an intestinal trematode, which has been widely employed to investigate the factors determining the rejection of intestinal helminths. Protein production patterns of intestinal epithelial cells are related to the infection-induced changes that determine the course of E. caproni infections. Herein, we compare the protein production profiles in the ileum of four experimental groups of mice: control; infected; dewormed and reinfected. Worm burdens were significantly lower in secondary infections, confirming the generation of partial resistance to homologous secondary infections in mice. However, quantitative comparison by 2D-DIGE showed that the protein production profile is similar in control and dewormed mice, and after primary and secondary E. caproni infections. These results showed that, unexpectedly, protein production changes in E. caproni infections are not responsible of resistance development. Fifty-one protein spots were differentially produced between control/treated and infected/reinfected mice and 37 of them were identified by mass spectrometry. The analysis of differentially abundant proteins indicate that cell metabolism and the regulation of proliferation and cell death are the most affected processes after primary and secondary E. caproni infections. These results provide new insights into the proteins involved in the regulation of tissue homeostasis after intestinal infection. SIGNIFICANCE: Intestinal helminthiases are highly prevalent parasitic infections with about 1 billion people infected worldwide. In this scenario, better understanding of host-parasite relationships is needed to elucidate the factors that determine intestinal helminth rejection. The intestinal trematode Echinostoma caproni has been broadly employed in this field, with resistance against secondary homologous infections reported in mice. In this paper, new insights are provided in the regulation of tissue homeostasis after intestinal infection. The unexpected lack of an altered pattern of ileal protein production associated to resistance development suggests that this resistance depends on rapid changes, affecting the early establishment of worms, rather than the activation of later effector mechanisms. These results may contribute to the development of new control tools for the management of these parasitic infections.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  2D-DIGE; Echinostoma caproni; Infection resistance; Mouse intestine; Praziquantel

Mesh:

Year:  2016        PMID: 27040117     DOI: 10.1016/j.jprot.2016.03.034

Source DB:  PubMed          Journal:  J Proteomics        ISSN: 1874-3919            Impact factor:   4.044


  4 in total

1.  Adaptation of the secretome of Echinostoma caproni may contribute to parasite survival in a Th1 milieu.

Authors:  Alba Cortés; Carla Muñoz-Antolí; María Álvarez-Izquierdo; Javier Sotillo; J Guillermo Esteban; Rafael Toledo
Journal:  Parasitol Res       Date:  2018-02-12       Impact factor: 2.289

2.  Ileal proteomic changes associated with IL-25-mediated resistance against intestinal trematode infections.

Authors:  María Álvarez-Izquierdo; J Guillermo Esteban; Carla Muñoz-Antoli; Rafael Toledo
Journal:  Parasit Vectors       Date:  2020-07-02       Impact factor: 3.876

3.  Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses.

Authors:  María Álvarez-Izquierdo; Miguel Pérez-Crespo; J Guillermo Esteban; Carla Muñoz-Antoli; Rafael Toledo
Journal:  Parasit Vectors       Date:  2020-12-04       Impact factor: 3.876

4.  Interleukin-25 Induces Resistance Against Intestinal Trematodes.

Authors:  Carla Muñoz-Antoli; Alba Cortés; Rebeca Santano; Javier Sotillo; J Guillermo Esteban; Rafael Toledo
Journal:  Sci Rep       Date:  2016-09-23       Impact factor: 4.379

  4 in total

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