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A parasitic fungus employs mutated eIF4A to survive on rocaglate-synthesizing Aglaia plants
Plants often generate secondary metabolites as defense mechanisms against parasites. Although some fungi may potentially overcome the barrier presented by antimicrobial compounds, only a limited number of examples and molecular mechanisms of resistance have been reported. Here, we found an Aglaia pl...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977294/ https://www.ncbi.nlm.nih.gov/pubmed/36852480 http://dx.doi.org/10.7554/eLife.81302 |
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author | Chen, Mingming Kumakura, Naoyoshi Saito, Hironori Muller, Ryan Nishimoto, Madoka Mito, Mari Gan, Pamela Ingolia, Nicholas T Shirasu, Ken Ito, Takuhiro Shichino, Yuichi Iwasaki, Shintaro |
author_facet | Chen, Mingming Kumakura, Naoyoshi Saito, Hironori Muller, Ryan Nishimoto, Madoka Mito, Mari Gan, Pamela Ingolia, Nicholas T Shirasu, Ken Ito, Takuhiro Shichino, Yuichi Iwasaki, Shintaro |
author_sort | Chen, Mingming |
collection | PubMed |
description | Plants often generate secondary metabolites as defense mechanisms against parasites. Although some fungi may potentially overcome the barrier presented by antimicrobial compounds, only a limited number of examples and molecular mechanisms of resistance have been reported. Here, we found an Aglaia plant-parasitizing fungus that overcomes the toxicity of rocaglates, which are translation inhibitors synthesized by the plant, through an amino acid substitution in a eukaryotic translation initiation factor (eIF). De novo transcriptome assembly revealed that the fungus belongs to the Ophiocordyceps genus and that its eIF4A, a molecular target of rocaglates, harbors an amino acid substitution critical for rocaglate binding. Ribosome profiling harnessing a cucumber-infecting fungus, Colletotrichum orbiculare, demonstrated that the translational inhibitory effects of rocaglates were largely attenuated by the mutation found in the Aglaia parasite. The engineered C. orbiculare showed a survival advantage on cucumber plants with rocaglates. Our study exemplifies a plant–fungus tug-of-war centered on secondary metabolites produced by host plants. |
format | Online Article Text |
id | pubmed-9977294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-99772942023-03-02 A parasitic fungus employs mutated eIF4A to survive on rocaglate-synthesizing Aglaia plants Chen, Mingming Kumakura, Naoyoshi Saito, Hironori Muller, Ryan Nishimoto, Madoka Mito, Mari Gan, Pamela Ingolia, Nicholas T Shirasu, Ken Ito, Takuhiro Shichino, Yuichi Iwasaki, Shintaro eLife Biochemistry and Chemical Biology Plants often generate secondary metabolites as defense mechanisms against parasites. Although some fungi may potentially overcome the barrier presented by antimicrobial compounds, only a limited number of examples and molecular mechanisms of resistance have been reported. Here, we found an Aglaia plant-parasitizing fungus that overcomes the toxicity of rocaglates, which are translation inhibitors synthesized by the plant, through an amino acid substitution in a eukaryotic translation initiation factor (eIF). De novo transcriptome assembly revealed that the fungus belongs to the Ophiocordyceps genus and that its eIF4A, a molecular target of rocaglates, harbors an amino acid substitution critical for rocaglate binding. Ribosome profiling harnessing a cucumber-infecting fungus, Colletotrichum orbiculare, demonstrated that the translational inhibitory effects of rocaglates were largely attenuated by the mutation found in the Aglaia parasite. The engineered C. orbiculare showed a survival advantage on cucumber plants with rocaglates. Our study exemplifies a plant–fungus tug-of-war centered on secondary metabolites produced by host plants. eLife Sciences Publications, Ltd 2023-02-28 /pmc/articles/PMC9977294/ /pubmed/36852480 http://dx.doi.org/10.7554/eLife.81302 Text en © 2023, Chen, Kumakura et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Chen, Mingming Kumakura, Naoyoshi Saito, Hironori Muller, Ryan Nishimoto, Madoka Mito, Mari Gan, Pamela Ingolia, Nicholas T Shirasu, Ken Ito, Takuhiro Shichino, Yuichi Iwasaki, Shintaro A parasitic fungus employs mutated eIF4A to survive on rocaglate-synthesizing Aglaia plants |
title | A parasitic fungus employs mutated eIF4A to survive on rocaglate-synthesizing Aglaia plants |
title_full | A parasitic fungus employs mutated eIF4A to survive on rocaglate-synthesizing Aglaia plants |
title_fullStr | A parasitic fungus employs mutated eIF4A to survive on rocaglate-synthesizing Aglaia plants |
title_full_unstemmed | A parasitic fungus employs mutated eIF4A to survive on rocaglate-synthesizing Aglaia plants |
title_short | A parasitic fungus employs mutated eIF4A to survive on rocaglate-synthesizing Aglaia plants |
title_sort | parasitic fungus employs mutated eif4a to survive on rocaglate-synthesizing aglaia plants |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977294/ https://www.ncbi.nlm.nih.gov/pubmed/36852480 http://dx.doi.org/10.7554/eLife.81302 |
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