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Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus

Triatomine assassin bugs comprise hematophagous insect vectors of Trypanosoma cruzi, the causative agent of Chagas disease. Although the microbiome of these species has been investigated to some extent, only one virus infecting Triatoma infestans has been identified to date. Here, we describe for th...

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Autores principales: de Brito, Tarcísio Fontenele, Coelho, Vitor Lima, Cardoso, Maira Arruda, Brito, Ingrid Alexandre de Abreu, Berni, Mateus Antonio, Zenk, Fides Lea, Iovino, Nicola, Pane, Attilio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372912/
https://www.ncbi.nlm.nih.gov/pubmed/34407148
http://dx.doi.org/10.1371/journal.ppat.1009780
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author de Brito, Tarcísio Fontenele
Coelho, Vitor Lima
Cardoso, Maira Arruda
Brito, Ingrid Alexandre de Abreu
Berni, Mateus Antonio
Zenk, Fides Lea
Iovino, Nicola
Pane, Attilio
author_facet de Brito, Tarcísio Fontenele
Coelho, Vitor Lima
Cardoso, Maira Arruda
Brito, Ingrid Alexandre de Abreu
Berni, Mateus Antonio
Zenk, Fides Lea
Iovino, Nicola
Pane, Attilio
author_sort de Brito, Tarcísio Fontenele
collection PubMed
description Triatomine assassin bugs comprise hematophagous insect vectors of Trypanosoma cruzi, the causative agent of Chagas disease. Although the microbiome of these species has been investigated to some extent, only one virus infecting Triatoma infestans has been identified to date. Here, we describe for the first time seven (+) single-strand RNA viruses (RpV1-7) infecting Rhodnius prolixus, a primary vector of Chagas disease in Central and South America. We show that the RpVs belong to the Iflaviridae, Permutotetraviridae and Solemoviridae and are vertically transmitted from the mothers to the progeny via transovarial transmission. Consistent with this, all the RpVs, except RpV2 that is related to the entomopathogenic Slow bee paralysis virus, established persistent infections in our R. prolixus colony. Furthermore, we show that R. prolixus ovaries express 22-nucleotide viral siRNAs (vsiRNAs), but not viral piRNAs, that originate from the processing of dsRNA intermediates during viral replication of the RpVs. Interestingly, the permutotetraviruses and sobemoviruses display shared pools of vsiRNAs that might provide the basis for a cross-immunity system. The vsiRNAs are maternally deposited in the eggs, where they likely contribute to reduce the viral load and protect the developing embryos. Our results unveil for the first time a complex core virome in R. prolixus and begin to shed light on the RNAi-based antiviral defenses in triatomines.
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spelling pubmed-83729122021-08-19 Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus de Brito, Tarcísio Fontenele Coelho, Vitor Lima Cardoso, Maira Arruda Brito, Ingrid Alexandre de Abreu Berni, Mateus Antonio Zenk, Fides Lea Iovino, Nicola Pane, Attilio PLoS Pathog Research Article Triatomine assassin bugs comprise hematophagous insect vectors of Trypanosoma cruzi, the causative agent of Chagas disease. Although the microbiome of these species has been investigated to some extent, only one virus infecting Triatoma infestans has been identified to date. Here, we describe for the first time seven (+) single-strand RNA viruses (RpV1-7) infecting Rhodnius prolixus, a primary vector of Chagas disease in Central and South America. We show that the RpVs belong to the Iflaviridae, Permutotetraviridae and Solemoviridae and are vertically transmitted from the mothers to the progeny via transovarial transmission. Consistent with this, all the RpVs, except RpV2 that is related to the entomopathogenic Slow bee paralysis virus, established persistent infections in our R. prolixus colony. Furthermore, we show that R. prolixus ovaries express 22-nucleotide viral siRNAs (vsiRNAs), but not viral piRNAs, that originate from the processing of dsRNA intermediates during viral replication of the RpVs. Interestingly, the permutotetraviruses and sobemoviruses display shared pools of vsiRNAs that might provide the basis for a cross-immunity system. The vsiRNAs are maternally deposited in the eggs, where they likely contribute to reduce the viral load and protect the developing embryos. Our results unveil for the first time a complex core virome in R. prolixus and begin to shed light on the RNAi-based antiviral defenses in triatomines. Public Library of Science 2021-08-18 /pmc/articles/PMC8372912/ /pubmed/34407148 http://dx.doi.org/10.1371/journal.ppat.1009780 Text en © 2021 Brito et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
de Brito, Tarcísio Fontenele
Coelho, Vitor Lima
Cardoso, Maira Arruda
Brito, Ingrid Alexandre de Abreu
Berni, Mateus Antonio
Zenk, Fides Lea
Iovino, Nicola
Pane, Attilio
Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus
title Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus
title_full Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus
title_fullStr Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus
title_full_unstemmed Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus
title_short Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus
title_sort transovarial transmission of a core virome in the chagas disease vector rhodnius prolixus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372912/
https://www.ncbi.nlm.nih.gov/pubmed/34407148
http://dx.doi.org/10.1371/journal.ppat.1009780
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