RNA Interference Restricts Rift Valley Fever Virus in Multiple Insect Systems

ABSTRACT The emerging bunyavirus Rift Valley fever virus (RVFV) is transmitted to humans and livestock by a large number of mosquito species. RNA interference (RNAi) has been characterized as an important innate immune defense mechanism used by mosquitoes to limit replication of positive-sense RNA f...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Isabelle Dietrich, Stephanie Jansen, Gamou Fall, Stephan Lorenzen, Martin Rudolf, Katrin Huber, Anna Heitmann, Sabine Schicht, El Hadji Ndiaye, Mick Watson, Ilaria Castelli, Benjamin Brennan, Richard M. Elliott, Mawlouth Diallo, Amadou A. Sall, Anna-Bella Failloux, Esther Schnettler, Alain Kohl, Stefanie C. Becker
Formato: article
Lenguaje:EN
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://doaj.org/article/fde5cdc0929746909c36eafb689b407d
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:fde5cdc0929746909c36eafb689b407d
record_format dspace
spelling oai:doaj.org-article:fde5cdc0929746909c36eafb689b407d2021-11-15T15:21:47ZRNA Interference Restricts Rift Valley Fever Virus in Multiple Insect Systems10.1128/mSphere.00090-172379-5042https://doaj.org/article/fde5cdc0929746909c36eafb689b407d2017-06-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00090-17https://doaj.org/toc/2379-5042ABSTRACT The emerging bunyavirus Rift Valley fever virus (RVFV) is transmitted to humans and livestock by a large number of mosquito species. RNA interference (RNAi) has been characterized as an important innate immune defense mechanism used by mosquitoes to limit replication of positive-sense RNA flaviviruses and togaviruses; however, little is known about its role against negative-strand RNA viruses such as RVFV. We show that virus-specific small RNAs are produced in infected mosquito cells, in Drosophila melanogaster cells, and, most importantly, also in RVFV vector mosquitoes. By addressing the production of small RNAs in adult Aedes sp. and Culex quinquefasciatus mosquitoes, we showed the presence of virus-derived Piwi-interacting RNAs (piRNAs) not only in Aedes sp. but also in C. quinquefasciatus mosquitoes, indicating that antiviral RNA interference in C. quinquefasciatus mosquitoes is similar to the described activities of RNAi in Aedes sp. mosquitoes. We also show that these have antiviral activity, since silencing of RNAi pathway effectors enhances viral replication. Moreover, our data suggest that RVFV does not encode a suppressor of RNAi. These findings point toward a significant role of RNAi in the control of RVFV in mosquitoes. IMPORTANCE Rift Valley fever virus (RVFV; Phlebovirus, Bunyaviridae) is an emerging zoonotic mosquito-borne pathogen of high relevance for human and animal health. Successful strategies of intervention in RVFV transmission by its mosquito vectors and the prevention of human and veterinary disease rely on a better understanding of the mechanisms that govern RVFV-vector interactions. Despite its medical importance, little is known about the factors that govern RVFV replication, dissemination, and transmission in the invertebrate host. Here we studied the role of the antiviral RNA interference immune pathways in the defense against RVFV in natural vector mosquitoes and mosquito cells and draw comparisons to the model insect Drosophila melanogaster. We found that RVFV infection induces both the exogenous small interfering RNA (siRNA) and piRNA pathways, which contribute to the control of viral replication in insects. Furthermore, we demonstrate the production of virus-derived piRNAs in Culex quinquefasciatus mosquitoes. Understanding these pathways and the targets within them offers the potential of the development of novel RVFV control measures in vector-based strategies.Isabelle DietrichStephanie JansenGamou FallStephan LorenzenMartin RudolfKatrin HuberAnna HeitmannSabine SchichtEl Hadji NdiayeMick WatsonIlaria CastelliBenjamin BrennanRichard M. ElliottMawlouth DialloAmadou A. SallAnna-Bella FaillouxEsther SchnettlerAlain KohlStefanie C. BeckerAmerican Society for MicrobiologyarticleDrosophila melanogasterRNA interferenceRift Valley fever virusantiviral immunitymosquitoMicrobiologyQR1-502ENmSphere, Vol 2, Iss 3 (2017)
institution DOAJ
collection DOAJ
language EN
topic Drosophila melanogaster
RNA interference
Rift Valley fever virus
antiviral immunity
mosquito
Microbiology
QR1-502
spellingShingle Drosophila melanogaster
RNA interference
Rift Valley fever virus
antiviral immunity
mosquito
Microbiology
QR1-502
Isabelle Dietrich
Stephanie Jansen
Gamou Fall
Stephan Lorenzen
Martin Rudolf
Katrin Huber
Anna Heitmann
Sabine Schicht
El Hadji Ndiaye
Mick Watson
Ilaria Castelli
Benjamin Brennan
Richard M. Elliott
Mawlouth Diallo
Amadou A. Sall
Anna-Bella Failloux
Esther Schnettler
Alain Kohl
Stefanie C. Becker
RNA Interference Restricts Rift Valley Fever Virus in Multiple Insect Systems
description ABSTRACT The emerging bunyavirus Rift Valley fever virus (RVFV) is transmitted to humans and livestock by a large number of mosquito species. RNA interference (RNAi) has been characterized as an important innate immune defense mechanism used by mosquitoes to limit replication of positive-sense RNA flaviviruses and togaviruses; however, little is known about its role against negative-strand RNA viruses such as RVFV. We show that virus-specific small RNAs are produced in infected mosquito cells, in Drosophila melanogaster cells, and, most importantly, also in RVFV vector mosquitoes. By addressing the production of small RNAs in adult Aedes sp. and Culex quinquefasciatus mosquitoes, we showed the presence of virus-derived Piwi-interacting RNAs (piRNAs) not only in Aedes sp. but also in C. quinquefasciatus mosquitoes, indicating that antiviral RNA interference in C. quinquefasciatus mosquitoes is similar to the described activities of RNAi in Aedes sp. mosquitoes. We also show that these have antiviral activity, since silencing of RNAi pathway effectors enhances viral replication. Moreover, our data suggest that RVFV does not encode a suppressor of RNAi. These findings point toward a significant role of RNAi in the control of RVFV in mosquitoes. IMPORTANCE Rift Valley fever virus (RVFV; Phlebovirus, Bunyaviridae) is an emerging zoonotic mosquito-borne pathogen of high relevance for human and animal health. Successful strategies of intervention in RVFV transmission by its mosquito vectors and the prevention of human and veterinary disease rely on a better understanding of the mechanisms that govern RVFV-vector interactions. Despite its medical importance, little is known about the factors that govern RVFV replication, dissemination, and transmission in the invertebrate host. Here we studied the role of the antiviral RNA interference immune pathways in the defense against RVFV in natural vector mosquitoes and mosquito cells and draw comparisons to the model insect Drosophila melanogaster. We found that RVFV infection induces both the exogenous small interfering RNA (siRNA) and piRNA pathways, which contribute to the control of viral replication in insects. Furthermore, we demonstrate the production of virus-derived piRNAs in Culex quinquefasciatus mosquitoes. Understanding these pathways and the targets within them offers the potential of the development of novel RVFV control measures in vector-based strategies.
format article
author Isabelle Dietrich
Stephanie Jansen
Gamou Fall
Stephan Lorenzen
Martin Rudolf
Katrin Huber
Anna Heitmann
Sabine Schicht
El Hadji Ndiaye
Mick Watson
Ilaria Castelli
Benjamin Brennan
Richard M. Elliott
Mawlouth Diallo
Amadou A. Sall
Anna-Bella Failloux
Esther Schnettler
Alain Kohl
Stefanie C. Becker
author_facet Isabelle Dietrich
Stephanie Jansen
Gamou Fall
Stephan Lorenzen
Martin Rudolf
Katrin Huber
Anna Heitmann
Sabine Schicht
El Hadji Ndiaye
Mick Watson
Ilaria Castelli
Benjamin Brennan
Richard M. Elliott
Mawlouth Diallo
Amadou A. Sall
Anna-Bella Failloux
Esther Schnettler
Alain Kohl
Stefanie C. Becker
author_sort Isabelle Dietrich
title RNA Interference Restricts Rift Valley Fever Virus in Multiple Insect Systems
title_short RNA Interference Restricts Rift Valley Fever Virus in Multiple Insect Systems
title_full RNA Interference Restricts Rift Valley Fever Virus in Multiple Insect Systems
title_fullStr RNA Interference Restricts Rift Valley Fever Virus in Multiple Insect Systems
title_full_unstemmed RNA Interference Restricts Rift Valley Fever Virus in Multiple Insect Systems
title_sort rna interference restricts rift valley fever virus in multiple insect systems
publisher American Society for Microbiology
publishDate 2017
url https://doaj.org/article/fde5cdc0929746909c36eafb689b407d
work_keys_str_mv AT isabelledietrich rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT stephaniejansen rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT gamoufall rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT stephanlorenzen rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT martinrudolf rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT katrinhuber rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT annaheitmann rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT sabineschicht rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT elhadjindiaye rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT mickwatson rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT ilariacastelli rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT benjaminbrennan rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT richardmelliott rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT mawlouthdiallo rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT amadouasall rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT annabellafailloux rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT estherschnettler rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT alainkohl rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
AT stefaniecbecker rnainterferencerestrictsriftvalleyfevervirusinmultipleinsectsystems
_version_ 1718428169808117760