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Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host
Ongoing host–pathogen interactions can trigger a coevolutionary arms race, while genetic diversity within the host can facilitate its adaptation to pathogens. Here, we used the diamondback moth (Plutella xylostella) and its pathogen Bacillus thuringiensis (Bt) as a model for exploring an adaptive ev...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083559/ https://www.ncbi.nlm.nih.gov/pubmed/36996102 http://dx.doi.org/10.1073/pnas.2300439120 |
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author | Guo, Zhaojiang Guo, Le Bai, Yang Kang, Shi Sun, Dan Qin, Jianying Ye, Fan Wang, Shaoli Wu, Qingjun Xie, Wen Yang, Xin Crickmore, Neil Zhou, Xuguo Zhang, Youjun |
author_facet | Guo, Zhaojiang Guo, Le Bai, Yang Kang, Shi Sun, Dan Qin, Jianying Ye, Fan Wang, Shaoli Wu, Qingjun Xie, Wen Yang, Xin Crickmore, Neil Zhou, Xuguo Zhang, Youjun |
author_sort | Guo, Zhaojiang |
collection | PubMed |
description | Ongoing host–pathogen interactions can trigger a coevolutionary arms race, while genetic diversity within the host can facilitate its adaptation to pathogens. Here, we used the diamondback moth (Plutella xylostella) and its pathogen Bacillus thuringiensis (Bt) as a model for exploring an adaptive evolutionary mechanism. We found that insect host adaptation to the primary Bt virulence factors was tightly associated with a short interspersed nuclear element (SINE - named SE2) insertion into the promoter of the transcriptionally activated MAP4K4 gene. This retrotransposon insertion coopts and potentiates the effect of the transcription factor forkhead box O (FOXO) in inducing a hormone-modulated Mitogen-activated protein kinase (MAPK) signaling cascade, leading to an enhancement of a host defense mechanism against the pathogen. This work demonstrates that reconstructing a cis–trans interaction can escalate a host response mechanism into a more stringent resistance phenotype to resist pathogen infection, providing a new insight into the coevolutionary mechanism of host organisms and their microbial pathogens. |
format | Online Article Text |
id | pubmed-10083559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-100835592023-09-30 Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host Guo, Zhaojiang Guo, Le Bai, Yang Kang, Shi Sun, Dan Qin, Jianying Ye, Fan Wang, Shaoli Wu, Qingjun Xie, Wen Yang, Xin Crickmore, Neil Zhou, Xuguo Zhang, Youjun Proc Natl Acad Sci U S A Biological Sciences Ongoing host–pathogen interactions can trigger a coevolutionary arms race, while genetic diversity within the host can facilitate its adaptation to pathogens. Here, we used the diamondback moth (Plutella xylostella) and its pathogen Bacillus thuringiensis (Bt) as a model for exploring an adaptive evolutionary mechanism. We found that insect host adaptation to the primary Bt virulence factors was tightly associated with a short interspersed nuclear element (SINE - named SE2) insertion into the promoter of the transcriptionally activated MAP4K4 gene. This retrotransposon insertion coopts and potentiates the effect of the transcription factor forkhead box O (FOXO) in inducing a hormone-modulated Mitogen-activated protein kinase (MAPK) signaling cascade, leading to an enhancement of a host defense mechanism against the pathogen. This work demonstrates that reconstructing a cis–trans interaction can escalate a host response mechanism into a more stringent resistance phenotype to resist pathogen infection, providing a new insight into the coevolutionary mechanism of host organisms and their microbial pathogens. National Academy of Sciences 2023-03-30 2023-04-04 /pmc/articles/PMC10083559/ /pubmed/36996102 http://dx.doi.org/10.1073/pnas.2300439120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Guo, Zhaojiang Guo, Le Bai, Yang Kang, Shi Sun, Dan Qin, Jianying Ye, Fan Wang, Shaoli Wu, Qingjun Xie, Wen Yang, Xin Crickmore, Neil Zhou, Xuguo Zhang, Youjun Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host |
title | Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host |
title_full | Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host |
title_fullStr | Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host |
title_full_unstemmed | Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host |
title_short | Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host |
title_sort | retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083559/ https://www.ncbi.nlm.nih.gov/pubmed/36996102 http://dx.doi.org/10.1073/pnas.2300439120 |
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