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Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli
Trypanosomatid type I nitroreductases (NTRs), i.e., mitochondrial enzymes that metabolise nitroaromatic pro-drugs, are essential for parasite growth, infection, and survival. Here, a type I NTR of non-virulent protozoan Trypanosoma rangeli is described and compared to those of other trypanosomatids....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto Oswaldo Cruz, Ministério da Saúde
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452488/ https://www.ncbi.nlm.nih.gov/pubmed/28591312 http://dx.doi.org/10.1590/0074-02760160532 |
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author | Montenegro, Marjorie Cuervo, Claudia Cardenas, Constanza Duarte, Silvia Díaz, Jenny R Thomas, M Carmen Lopez, Manuel C Puerta, Concepcion J |
author_facet | Montenegro, Marjorie Cuervo, Claudia Cardenas, Constanza Duarte, Silvia Díaz, Jenny R Thomas, M Carmen Lopez, Manuel C Puerta, Concepcion J |
author_sort | Montenegro, Marjorie |
collection | PubMed |
description | Trypanosomatid type I nitroreductases (NTRs), i.e., mitochondrial enzymes that metabolise nitroaromatic pro-drugs, are essential for parasite growth, infection, and survival. Here, a type I NTR of non-virulent protozoan Trypanosoma rangeli is described and compared to those of other trypanosomatids. The NTR gene was isolated from KP1(+) and KP1(-) strains, and its corresponding transcript and 5’ untranslated region (5’UTR) were determined. Bioinformatics analyses and nitro-drug activation assays were also performed. The results indicated that the type I NTR gene is present in both KP1(-) and KP1(+) strains, with 98% identity. However, the predicted subcellular localisation of the protein differed among the strains (predicted as mitochondrial in the KP1(+) strain). Comparisons of the domains and 3D structures of the NTRs with those of orthologs demonstrated that the nitroreductase domain of T. rangeli NTR is conserved across all the strains, including the residues involved in the interaction with the FMN cofactor and in the tertiary structure characteristics of this oxidoreductase protein family. mRNA processing and expression were also observed. In addition, T. rangeli was shown to be sensitive to benznidazole and nifurtimox in a concentration-dependent manner. In summary, T. rangeli appears to have a newly discovered functional type I NTR. |
format | Online Article Text |
id | pubmed-5452488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Instituto Oswaldo Cruz, Ministério da Saúde |
record_format | MEDLINE/PubMed |
spelling | pubmed-54524882017-07-01 Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli Montenegro, Marjorie Cuervo, Claudia Cardenas, Constanza Duarte, Silvia Díaz, Jenny R Thomas, M Carmen Lopez, Manuel C Puerta, Concepcion J Mem Inst Oswaldo Cruz Short Communication Trypanosomatid type I nitroreductases (NTRs), i.e., mitochondrial enzymes that metabolise nitroaromatic pro-drugs, are essential for parasite growth, infection, and survival. Here, a type I NTR of non-virulent protozoan Trypanosoma rangeli is described and compared to those of other trypanosomatids. The NTR gene was isolated from KP1(+) and KP1(-) strains, and its corresponding transcript and 5’ untranslated region (5’UTR) were determined. Bioinformatics analyses and nitro-drug activation assays were also performed. The results indicated that the type I NTR gene is present in both KP1(-) and KP1(+) strains, with 98% identity. However, the predicted subcellular localisation of the protein differed among the strains (predicted as mitochondrial in the KP1(+) strain). Comparisons of the domains and 3D structures of the NTRs with those of orthologs demonstrated that the nitroreductase domain of T. rangeli NTR is conserved across all the strains, including the residues involved in the interaction with the FMN cofactor and in the tertiary structure characteristics of this oxidoreductase protein family. mRNA processing and expression were also observed. In addition, T. rangeli was shown to be sensitive to benznidazole and nifurtimox in a concentration-dependent manner. In summary, T. rangeli appears to have a newly discovered functional type I NTR. Instituto Oswaldo Cruz, Ministério da Saúde 2017-07 /pmc/articles/PMC5452488/ /pubmed/28591312 http://dx.doi.org/10.1590/0074-02760160532 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Montenegro, Marjorie Cuervo, Claudia Cardenas, Constanza Duarte, Silvia Díaz, Jenny R Thomas, M Carmen Lopez, Manuel C Puerta, Concepcion J Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli |
title | Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli
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title_full | Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli
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title_fullStr | Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli
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title_full_unstemmed | Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli
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title_short | Identification of a type I nitroreductase gene in non-virulent Trypanosoma rangeli
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title_sort | identification of a type i nitroreductase gene in non-virulent trypanosoma rangeli |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452488/ https://www.ncbi.nlm.nih.gov/pubmed/28591312 http://dx.doi.org/10.1590/0074-02760160532 |
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