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The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales
Mucormycosis is a lethal disease caused by Mucorales, which are emerging as human causes that explain the high mortality for this disease. Consequently, the research community is searching for virulence determinants that could be repurposed as targets to develop new treatments against mucormycosis....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956310/ https://www.ncbi.nlm.nih.gov/pubmed/33668930 http://dx.doi.org/10.3390/ijms22052282 |
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author | Pérez-Arques, Carlos Navarro-Mendoza, María Isabel Murcia, Laura Navarro, Eusebio Garre, Victoriano Nicolás, Francisco Esteban |
author_facet | Pérez-Arques, Carlos Navarro-Mendoza, María Isabel Murcia, Laura Navarro, Eusebio Garre, Victoriano Nicolás, Francisco Esteban |
author_sort | Pérez-Arques, Carlos |
collection | PubMed |
description | Mucormycosis is a lethal disease caused by Mucorales, which are emerging as human causes that explain the high mortality for this disease. Consequently, the research community is searching for virulence determinants that could be repurposed as targets to develop new treatments against mucormycosis. Our work explores an RNA interference (RNAi)-based approach to find targets involved in the virulence of Mucorales. A transcriptomewide analysis compared sRNAs and their target mRNAs in two Mucor lusitanicus different pathotypes, virulent and avirulent, generating a list of 75 loci selected by their differential sRNA accumulation in these strains. As a proof of concept and validity, an experimental approach characterized two loci showing opposite behavior, confirming that RNAi activity causes their differential expression in the two pathotypes. We generated deletion mutants for two loci and a knockin-strain overexpressing for one of these loci. Their functional analysis in murine virulence assays identified the gene wex1, a putative DEDDy exonuclease with RNase domains, as an essential factor for virulence. The identification of wex1 showed the potential of our approach to discover virulence factors not only in Mucorales but also in any other fungal model with an active RNAi machinery. More importantly, it adds a new layer to the biological processes controlled by RNAi in M. lusitanicus, confirming that the Dicer-dependent RNAi pathway can silence gene expression to promote virulence. |
format | Online Article Text |
id | pubmed-7956310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79563102021-03-15 The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales Pérez-Arques, Carlos Navarro-Mendoza, María Isabel Murcia, Laura Navarro, Eusebio Garre, Victoriano Nicolás, Francisco Esteban Int J Mol Sci Article Mucormycosis is a lethal disease caused by Mucorales, which are emerging as human causes that explain the high mortality for this disease. Consequently, the research community is searching for virulence determinants that could be repurposed as targets to develop new treatments against mucormycosis. Our work explores an RNA interference (RNAi)-based approach to find targets involved in the virulence of Mucorales. A transcriptomewide analysis compared sRNAs and their target mRNAs in two Mucor lusitanicus different pathotypes, virulent and avirulent, generating a list of 75 loci selected by their differential sRNA accumulation in these strains. As a proof of concept and validity, an experimental approach characterized two loci showing opposite behavior, confirming that RNAi activity causes their differential expression in the two pathotypes. We generated deletion mutants for two loci and a knockin-strain overexpressing for one of these loci. Their functional analysis in murine virulence assays identified the gene wex1, a putative DEDDy exonuclease with RNase domains, as an essential factor for virulence. The identification of wex1 showed the potential of our approach to discover virulence factors not only in Mucorales but also in any other fungal model with an active RNAi machinery. More importantly, it adds a new layer to the biological processes controlled by RNAi in M. lusitanicus, confirming that the Dicer-dependent RNAi pathway can silence gene expression to promote virulence. MDPI 2021-02-25 /pmc/articles/PMC7956310/ /pubmed/33668930 http://dx.doi.org/10.3390/ijms22052282 Text en © 2021 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 Pérez-Arques, Carlos Navarro-Mendoza, María Isabel Murcia, Laura Navarro, Eusebio Garre, Victoriano Nicolás, Francisco Esteban The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales |
title | The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales |
title_full | The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales |
title_fullStr | The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales |
title_full_unstemmed | The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales |
title_short | The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales |
title_sort | rnai mechanism regulates a new exonuclease gene involved in the virulence of mucorales |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956310/ https://www.ncbi.nlm.nih.gov/pubmed/33668930 http://dx.doi.org/10.3390/ijms22052282 |
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