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Differential Pathogenic Gene Expression of E. histolytica in Patients with Different Clinical Forms of Amoebiasis

The etiological agent of human amoebiasis is the protozoan parasite E. histolytica; the disease is still an endemic infection in some countries and the outcome of infection in the host infection can range from asymptomatic intestinal infection to intestinal or liver invasive forms of the disease. Th...

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Autores principales: González-Rivas, Enrique, Nieves-Ramírez, Miriam, Magaña, Ulises, Morán, Patricia, Rojas-Velázquez, Liliana, Hernández, Eric, Serrano-Vázquez, Angélica, Partida, Oswaldo, Pérez-Juárez, Horacio, Ximénez, Cecilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650713/
https://www.ncbi.nlm.nih.gov/pubmed/33050280
http://dx.doi.org/10.3390/microorganisms8101556
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author González-Rivas, Enrique
Nieves-Ramírez, Miriam
Magaña, Ulises
Morán, Patricia
Rojas-Velázquez, Liliana
Hernández, Eric
Serrano-Vázquez, Angélica
Partida, Oswaldo
Pérez-Juárez, Horacio
Ximénez, Cecilia
author_facet González-Rivas, Enrique
Nieves-Ramírez, Miriam
Magaña, Ulises
Morán, Patricia
Rojas-Velázquez, Liliana
Hernández, Eric
Serrano-Vázquez, Angélica
Partida, Oswaldo
Pérez-Juárez, Horacio
Ximénez, Cecilia
author_sort González-Rivas, Enrique
collection PubMed
description The etiological agent of human amoebiasis is the protozoan parasite E. histolytica; the disease is still an endemic infection in some countries and the outcome of infection in the host infection can range from asymptomatic intestinal infection to intestinal or liver invasive forms of the disease. The invasive character of this parasite is multifactorial and mainly due to the differential expression of multiple pathogenic genes. The aim of the present work was to measure the differential expression of some genes in different specimens of patients with amoebic liver abscess (ALA) and specimens of genital amoebiasis (AG) by RT-qPCR. Results show that the expression of genes is different in both types of samples. Almost all studied genes were over expressed in both sets of patients; however, superoxide dismutase (Ehsod), serine threonine isoleucine rich protein (Ehstirp), peroxiredoxin (Ehprd) and heat shock protein 70 and 90 (Ehhsp-70, EHhsp-90) were higher in AG biopsies tissue. Furthermore, cysteine proteinases 5 and 2 (Ehcp5, Ehcp2), lectin (Ehgal/galnaclectin) and calreticulin (Ehcrt) genes directly associate with pathogenic mechanisms of E. histolytica had similar over expression in both AG and ALA samples. In summary the results obtained show that trophozoites can regulate the expression of their genes depending on stimuli or environmental conditions, in order to regulate their pathogenicity and ensure their survival in the host.
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spelling pubmed-76507132020-11-10 Differential Pathogenic Gene Expression of E. histolytica in Patients with Different Clinical Forms of Amoebiasis González-Rivas, Enrique Nieves-Ramírez, Miriam Magaña, Ulises Morán, Patricia Rojas-Velázquez, Liliana Hernández, Eric Serrano-Vázquez, Angélica Partida, Oswaldo Pérez-Juárez, Horacio Ximénez, Cecilia Microorganisms Article The etiological agent of human amoebiasis is the protozoan parasite E. histolytica; the disease is still an endemic infection in some countries and the outcome of infection in the host infection can range from asymptomatic intestinal infection to intestinal or liver invasive forms of the disease. The invasive character of this parasite is multifactorial and mainly due to the differential expression of multiple pathogenic genes. The aim of the present work was to measure the differential expression of some genes in different specimens of patients with amoebic liver abscess (ALA) and specimens of genital amoebiasis (AG) by RT-qPCR. Results show that the expression of genes is different in both types of samples. Almost all studied genes were over expressed in both sets of patients; however, superoxide dismutase (Ehsod), serine threonine isoleucine rich protein (Ehstirp), peroxiredoxin (Ehprd) and heat shock protein 70 and 90 (Ehhsp-70, EHhsp-90) were higher in AG biopsies tissue. Furthermore, cysteine proteinases 5 and 2 (Ehcp5, Ehcp2), lectin (Ehgal/galnaclectin) and calreticulin (Ehcrt) genes directly associate with pathogenic mechanisms of E. histolytica had similar over expression in both AG and ALA samples. In summary the results obtained show that trophozoites can regulate the expression of their genes depending on stimuli or environmental conditions, in order to regulate their pathogenicity and ensure their survival in the host. MDPI 2020-10-09 /pmc/articles/PMC7650713/ /pubmed/33050280 http://dx.doi.org/10.3390/microorganisms8101556 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
González-Rivas, Enrique
Nieves-Ramírez, Miriam
Magaña, Ulises
Morán, Patricia
Rojas-Velázquez, Liliana
Hernández, Eric
Serrano-Vázquez, Angélica
Partida, Oswaldo
Pérez-Juárez, Horacio
Ximénez, Cecilia
Differential Pathogenic Gene Expression of E. histolytica in Patients with Different Clinical Forms of Amoebiasis
title Differential Pathogenic Gene Expression of E. histolytica in Patients with Different Clinical Forms of Amoebiasis
title_full Differential Pathogenic Gene Expression of E. histolytica in Patients with Different Clinical Forms of Amoebiasis
title_fullStr Differential Pathogenic Gene Expression of E. histolytica in Patients with Different Clinical Forms of Amoebiasis
title_full_unstemmed Differential Pathogenic Gene Expression of E. histolytica in Patients with Different Clinical Forms of Amoebiasis
title_short Differential Pathogenic Gene Expression of E. histolytica in Patients with Different Clinical Forms of Amoebiasis
title_sort differential pathogenic gene expression of e. histolytica in patients with different clinical forms of amoebiasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650713/
https://www.ncbi.nlm.nih.gov/pubmed/33050280
http://dx.doi.org/10.3390/microorganisms8101556
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