Cargando…
A parental transcriptional response to microsporidia infection induces inherited immunity in offspring
Parental infection can result in the production of offspring with enhanced immunity phenotypes. Critically, the mechanisms underlying inherited immunity are poorly understood. Here, we show that Caenorhabditis elegans infected with the intracellular microsporidian parasite N. parisii produce progeny...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099193/ https://www.ncbi.nlm.nih.gov/pubmed/33952520 http://dx.doi.org/10.1126/sciadv.abf3114 |
_version_ | 1783688555263950848 |
---|---|
author | Willis, Alexandra R. Zhao, Winnie Sukhdeo, Ronesh Wadi, Lina El Jarkass, Hala Tamim Claycomb, Julie M. Reinke, Aaron W. |
author_facet | Willis, Alexandra R. Zhao, Winnie Sukhdeo, Ronesh Wadi, Lina El Jarkass, Hala Tamim Claycomb, Julie M. Reinke, Aaron W. |
author_sort | Willis, Alexandra R. |
collection | PubMed |
description | Parental infection can result in the production of offspring with enhanced immunity phenotypes. Critically, the mechanisms underlying inherited immunity are poorly understood. Here, we show that Caenorhabditis elegans infected with the intracellular microsporidian parasite N. parisii produce progeny that are resistant to microsporidia infection. We determine the kinetics of the response and show that intergenerational immunity prevents host-cell invasion by Nematocida parisii and enhances survival to the bacterial pathogen Pseudomonas aeruginosa. We demonstrate that immunity is induced by the parental transcriptional response to infection, which can be mimicked through maternal somatic depletion of PALS-22 and the retinoblastoma protein ortholog, LIN-35. We find that other biotic and abiotic stresses (viral infection and cadmium exposure) that induce a similar transcriptional response as microsporidia also induce immunity in progeny. Together, our results reveal how a parental transcriptional signal can be induced by distinct stimuli and protect offspring against multiple classes of pathogens. |
format | Online Article Text |
id | pubmed-8099193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-80991932021-05-14 A parental transcriptional response to microsporidia infection induces inherited immunity in offspring Willis, Alexandra R. Zhao, Winnie Sukhdeo, Ronesh Wadi, Lina El Jarkass, Hala Tamim Claycomb, Julie M. Reinke, Aaron W. Sci Adv Research Articles Parental infection can result in the production of offspring with enhanced immunity phenotypes. Critically, the mechanisms underlying inherited immunity are poorly understood. Here, we show that Caenorhabditis elegans infected with the intracellular microsporidian parasite N. parisii produce progeny that are resistant to microsporidia infection. We determine the kinetics of the response and show that intergenerational immunity prevents host-cell invasion by Nematocida parisii and enhances survival to the bacterial pathogen Pseudomonas aeruginosa. We demonstrate that immunity is induced by the parental transcriptional response to infection, which can be mimicked through maternal somatic depletion of PALS-22 and the retinoblastoma protein ortholog, LIN-35. We find that other biotic and abiotic stresses (viral infection and cadmium exposure) that induce a similar transcriptional response as microsporidia also induce immunity in progeny. Together, our results reveal how a parental transcriptional signal can be induced by distinct stimuli and protect offspring against multiple classes of pathogens. American Association for the Advancement of Science 2021-05-05 /pmc/articles/PMC8099193/ /pubmed/33952520 http://dx.doi.org/10.1126/sciadv.abf3114 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Willis, Alexandra R. Zhao, Winnie Sukhdeo, Ronesh Wadi, Lina El Jarkass, Hala Tamim Claycomb, Julie M. Reinke, Aaron W. A parental transcriptional response to microsporidia infection induces inherited immunity in offspring |
title | A parental transcriptional response to microsporidia infection induces inherited immunity in offspring |
title_full | A parental transcriptional response to microsporidia infection induces inherited immunity in offspring |
title_fullStr | A parental transcriptional response to microsporidia infection induces inherited immunity in offspring |
title_full_unstemmed | A parental transcriptional response to microsporidia infection induces inherited immunity in offspring |
title_short | A parental transcriptional response to microsporidia infection induces inherited immunity in offspring |
title_sort | parental transcriptional response to microsporidia infection induces inherited immunity in offspring |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099193/ https://www.ncbi.nlm.nih.gov/pubmed/33952520 http://dx.doi.org/10.1126/sciadv.abf3114 |
work_keys_str_mv | AT willisalexandrar aparentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT zhaowinnie aparentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT sukhdeoronesh aparentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT wadilina aparentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT eljarkasshalatamim aparentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT claycombjuliem aparentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT reinkeaaronw aparentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT willisalexandrar parentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT zhaowinnie parentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT sukhdeoronesh parentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT wadilina parentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT eljarkasshalatamim parentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT claycombjuliem parentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring AT reinkeaaronw parentaltranscriptionalresponsetomicrosporidiainfectioninducesinheritedimmunityinoffspring |