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Schistosoma mansoni Infection Is Impacted by Malnutrition

Schistosomiasis remains one of the most important neglected tropical diseases in the world. It mainly affects developing countries, where it often coexists with malnutrition. Despite this, few studies have investigated the relationship between schistosomiasis and malnutrition. Herein, we evaluate th...

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Autores principales: Maciel, Poliane Silva, Gonçalves, Ricardo, Antonelli, Lis Ribeiro do Valle, Fonseca, Cristina Toscano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017134/
https://www.ncbi.nlm.nih.gov/pubmed/33815321
http://dx.doi.org/10.3389/fmicb.2021.635843
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author Maciel, Poliane Silva
Gonçalves, Ricardo
Antonelli, Lis Ribeiro do Valle
Fonseca, Cristina Toscano
author_facet Maciel, Poliane Silva
Gonçalves, Ricardo
Antonelli, Lis Ribeiro do Valle
Fonseca, Cristina Toscano
author_sort Maciel, Poliane Silva
collection PubMed
description Schistosomiasis remains one of the most important neglected tropical diseases in the world. It mainly affects developing countries, where it often coexists with malnutrition. Despite this, few studies have investigated the relationship between schistosomiasis and malnutrition. Herein, we evaluate the impact of malnutrition on experimental S. mansoni infection. Mice were divided into 5 groups: Control (Ctrl) diet (14% protein and 10% lipids), low-protein 3% (LP 3%), low-protein 8% (LP 8%), low-fat 2.5% (LF 2.5%), and low-fat 5% (LF 5%). Mice were fed with their respective diets and were infected when a difference of approximately 20% in the body weight between mice from any experimental group and mice from the control group was achieved. Nutritional, parasitological, and immunological parameters were assessed either just before infection and/or approximately 50 days later before mice were perfused. Our results showed that the 3% low-protein diet was the only one capable of establishing malnutrition in mice. Mice fed with this diet showed: (i) significant reduction in body weight and serum albumin levels before infection, (ii) decreased levels of all biochemical parameters evaluated before perfusion, (iii) decreased numbers of schistosome eggs trapped in intestines and impaired parasite fecundity, (iv) a delay in the granuloma development with a smaller granuloma area, and (v) reduced levels of IL-4 and IFN-γ in the liver. Our findings demonstrate that low protein supply leads to malnutrition in mice and impacts the cytokine milieu in the liver and granuloma formation. Additionally, the establishment of our murine malnutrition model will enable future studies aiming to better understand the complex relationships between nutrition, immune responses, and infection outcome.
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spelling pubmed-80171342021-04-03 Schistosoma mansoni Infection Is Impacted by Malnutrition Maciel, Poliane Silva Gonçalves, Ricardo Antonelli, Lis Ribeiro do Valle Fonseca, Cristina Toscano Front Microbiol Microbiology Schistosomiasis remains one of the most important neglected tropical diseases in the world. It mainly affects developing countries, where it often coexists with malnutrition. Despite this, few studies have investigated the relationship between schistosomiasis and malnutrition. Herein, we evaluate the impact of malnutrition on experimental S. mansoni infection. Mice were divided into 5 groups: Control (Ctrl) diet (14% protein and 10% lipids), low-protein 3% (LP 3%), low-protein 8% (LP 8%), low-fat 2.5% (LF 2.5%), and low-fat 5% (LF 5%). Mice were fed with their respective diets and were infected when a difference of approximately 20% in the body weight between mice from any experimental group and mice from the control group was achieved. Nutritional, parasitological, and immunological parameters were assessed either just before infection and/or approximately 50 days later before mice were perfused. Our results showed that the 3% low-protein diet was the only one capable of establishing malnutrition in mice. Mice fed with this diet showed: (i) significant reduction in body weight and serum albumin levels before infection, (ii) decreased levels of all biochemical parameters evaluated before perfusion, (iii) decreased numbers of schistosome eggs trapped in intestines and impaired parasite fecundity, (iv) a delay in the granuloma development with a smaller granuloma area, and (v) reduced levels of IL-4 and IFN-γ in the liver. Our findings demonstrate that low protein supply leads to malnutrition in mice and impacts the cytokine milieu in the liver and granuloma formation. Additionally, the establishment of our murine malnutrition model will enable future studies aiming to better understand the complex relationships between nutrition, immune responses, and infection outcome. Frontiers Media S.A. 2021-03-19 /pmc/articles/PMC8017134/ /pubmed/33815321 http://dx.doi.org/10.3389/fmicb.2021.635843 Text en Copyright © 2021 Maciel, Gonçalves, Antonelli and Fonseca. 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 Microbiology
Maciel, Poliane Silva
Gonçalves, Ricardo
Antonelli, Lis Ribeiro do Valle
Fonseca, Cristina Toscano
Schistosoma mansoni Infection Is Impacted by Malnutrition
title Schistosoma mansoni Infection Is Impacted by Malnutrition
title_full Schistosoma mansoni Infection Is Impacted by Malnutrition
title_fullStr Schistosoma mansoni Infection Is Impacted by Malnutrition
title_full_unstemmed Schistosoma mansoni Infection Is Impacted by Malnutrition
title_short Schistosoma mansoni Infection Is Impacted by Malnutrition
title_sort schistosoma mansoni infection is impacted by malnutrition
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017134/
https://www.ncbi.nlm.nih.gov/pubmed/33815321
http://dx.doi.org/10.3389/fmicb.2021.635843
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