Cargando…
The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses
The mosquito’s innate immune system defends against a variety of pathogens, and the conserved siRNA pathway plays a central role in the control of viral infections. Here, we show that transgenic overexpression of Dicer2 (Dcr2) or R2d2 resulted in an accumulation of 21-nucleotide viral sequences that...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182253/ https://www.ncbi.nlm.nih.gov/pubmed/35679279 http://dx.doi.org/10.1371/journal.pbio.3001668 |
_version_ | 1784723989486108672 |
---|---|
author | Dong, Yuemei Dong, Shengzhang Dizaji, Nahid Borhani Rutkowski, Natalie Pohlenz, Tyler Myles, Kevin Dimopoulos, George |
author_facet | Dong, Yuemei Dong, Shengzhang Dizaji, Nahid Borhani Rutkowski, Natalie Pohlenz, Tyler Myles, Kevin Dimopoulos, George |
author_sort | Dong, Yuemei |
collection | PubMed |
description | The mosquito’s innate immune system defends against a variety of pathogens, and the conserved siRNA pathway plays a central role in the control of viral infections. Here, we show that transgenic overexpression of Dicer2 (Dcr2) or R2d2 resulted in an accumulation of 21-nucleotide viral sequences that was accompanied by a significant suppression of dengue virus (DENV), Zika virus (ZIKV), and chikungunya virus (CHIKV) replication, thus indicating the broad-spectrum antiviral response mediated by the siRNA pathway that can be applied for the development of novel arbovirus control strategies. Interestingly, overexpression of Dcr2 or R2d2 regulated the mRNA abundance of a variety of antimicrobial immune genes, pointing to additional functions of DCR2 and R2D2 as well as cross-talk between the siRNA pathway and other immune pathways. Accordingly, transgenic overexpression of Dcr2 or R2d2 resulted in a lesser proliferation of the midgut microbiota and increased resistance to bacterial and fungal infections. |
format | Online Article Text |
id | pubmed-9182253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91822532022-06-10 The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses Dong, Yuemei Dong, Shengzhang Dizaji, Nahid Borhani Rutkowski, Natalie Pohlenz, Tyler Myles, Kevin Dimopoulos, George PLoS Biol Research Article The mosquito’s innate immune system defends against a variety of pathogens, and the conserved siRNA pathway plays a central role in the control of viral infections. Here, we show that transgenic overexpression of Dicer2 (Dcr2) or R2d2 resulted in an accumulation of 21-nucleotide viral sequences that was accompanied by a significant suppression of dengue virus (DENV), Zika virus (ZIKV), and chikungunya virus (CHIKV) replication, thus indicating the broad-spectrum antiviral response mediated by the siRNA pathway that can be applied for the development of novel arbovirus control strategies. Interestingly, overexpression of Dcr2 or R2d2 regulated the mRNA abundance of a variety of antimicrobial immune genes, pointing to additional functions of DCR2 and R2D2 as well as cross-talk between the siRNA pathway and other immune pathways. Accordingly, transgenic overexpression of Dcr2 or R2d2 resulted in a lesser proliferation of the midgut microbiota and increased resistance to bacterial and fungal infections. Public Library of Science 2022-06-09 /pmc/articles/PMC9182253/ /pubmed/35679279 http://dx.doi.org/10.1371/journal.pbio.3001668 Text en © 2022 Dong 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 Dong, Yuemei Dong, Shengzhang Dizaji, Nahid Borhani Rutkowski, Natalie Pohlenz, Tyler Myles, Kevin Dimopoulos, George The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses |
title | The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses |
title_full | The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses |
title_fullStr | The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses |
title_full_unstemmed | The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses |
title_short | The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses |
title_sort | aedes aegypti sirna pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182253/ https://www.ncbi.nlm.nih.gov/pubmed/35679279 http://dx.doi.org/10.1371/journal.pbio.3001668 |
work_keys_str_mv | AT dongyuemei theaedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT dongshengzhang theaedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT dizajinahidborhani theaedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT rutkowskinatalie theaedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT pohlenztyler theaedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT myleskevin theaedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT dimopoulosgeorge theaedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT dongyuemei aedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT dongshengzhang aedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT dizajinahidborhani aedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT rutkowskinatalie aedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT pohlenztyler aedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT myleskevin aedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses AT dimopoulosgeorge aedesaegyptisirnapathwaymediatesbroadspectrumdefenseagainsthumanpathogenicvirusesandmodulatesantibacterialandantifungaldefenses |