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Distinct signaling routes mediate intercellular and intracellular rhizobial infection in Lotus japonicus
Rhizobial infection of legume roots during the development of nitrogen-fixing root nodules can occur intracellularly, through plant-derived infection threads traversing cells, or intercellularly, via bacterial entry between epidermal plant cells. Although it is estimated that around 25% of all legum...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133683/ https://www.ncbi.nlm.nih.gov/pubmed/33793909 http://dx.doi.org/10.1093/plphys/kiaa049 |
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author | Montiel, Jesús Reid, Dugald Grønbæk, Thomas H Benfeldt, Caroline M James, Euan K Ott, Thomas Ditengou, Franck A Nadzieja, Marcin Kelly, Simon Stougaard, Jens |
author_facet | Montiel, Jesús Reid, Dugald Grønbæk, Thomas H Benfeldt, Caroline M James, Euan K Ott, Thomas Ditengou, Franck A Nadzieja, Marcin Kelly, Simon Stougaard, Jens |
author_sort | Montiel, Jesús |
collection | PubMed |
description | Rhizobial infection of legume roots during the development of nitrogen-fixing root nodules can occur intracellularly, through plant-derived infection threads traversing cells, or intercellularly, via bacterial entry between epidermal plant cells. Although it is estimated that around 25% of all legume genera are intercellularly infected, the pathways and mechanisms supporting this process have remained virtually unexplored due to a lack of genetically amenable legumes that exhibit this form of infection. In this study, we report that the model legume Lotus japonicus is infected intercellularly by the IRBG74 strain, recently proposed to belong to the Agrobacterium clade of the Rhizobiaceae. We demonstrate that the resources available for L. japonicus enable insight into the genetic requirements and fine-tuning of the pathway governing intercellular infection in this species. Inoculation of L. japonicus mutants shows that Ethylene-responsive factor required for nodulation 1 (Ern1) and Leu-rich Repeat Receptor-Like Kinase (RinRK1) are dispensable for intercellular infection in contrast to intracellular infection. Other symbiotic genes, including nod factor receptor 5 (NFR5), symbiosis receptor-like kinase (SymRK), Ca(2+/)calmodulin dependent kinase (CCaMK), exopolysaccharide receptor 3 (Epr3), Cyclops, nodule inception (Nin), nodulation signaling pathway 1 (Nsp1), nodulation signaling pathway 2 (Nsp2), cystathionine-β-synthase (Cbs), and Vapyrin are equally important for both entry modes. Comparative RNAseq analysis of roots inoculated with IRBG74 revealed a distinctive transcriptome response compared with intracellular colonization. In particular, several cytokinin-related genes were differentially regulated. Corroborating this observation, cyp735A and ipt4 cytokinin biosynthesis mutants were significantly affected in their nodulation with IRBG74, whereas lhk1 cytokinin receptor mutants formed no nodules. These results indicate a differential requirement for cytokinin signaling during intercellular rhizobial entry and highlight distinct modalities of inter- and intracellular infection mechanisms in L. japonicus. |
format | Online Article Text |
id | pubmed-8133683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81336832021-05-25 Distinct signaling routes mediate intercellular and intracellular rhizobial infection in Lotus japonicus Montiel, Jesús Reid, Dugald Grønbæk, Thomas H Benfeldt, Caroline M James, Euan K Ott, Thomas Ditengou, Franck A Nadzieja, Marcin Kelly, Simon Stougaard, Jens Plant Physiol Regular Issue Rhizobial infection of legume roots during the development of nitrogen-fixing root nodules can occur intracellularly, through plant-derived infection threads traversing cells, or intercellularly, via bacterial entry between epidermal plant cells. Although it is estimated that around 25% of all legume genera are intercellularly infected, the pathways and mechanisms supporting this process have remained virtually unexplored due to a lack of genetically amenable legumes that exhibit this form of infection. In this study, we report that the model legume Lotus japonicus is infected intercellularly by the IRBG74 strain, recently proposed to belong to the Agrobacterium clade of the Rhizobiaceae. We demonstrate that the resources available for L. japonicus enable insight into the genetic requirements and fine-tuning of the pathway governing intercellular infection in this species. Inoculation of L. japonicus mutants shows that Ethylene-responsive factor required for nodulation 1 (Ern1) and Leu-rich Repeat Receptor-Like Kinase (RinRK1) are dispensable for intercellular infection in contrast to intracellular infection. Other symbiotic genes, including nod factor receptor 5 (NFR5), symbiosis receptor-like kinase (SymRK), Ca(2+/)calmodulin dependent kinase (CCaMK), exopolysaccharide receptor 3 (Epr3), Cyclops, nodule inception (Nin), nodulation signaling pathway 1 (Nsp1), nodulation signaling pathway 2 (Nsp2), cystathionine-β-synthase (Cbs), and Vapyrin are equally important for both entry modes. Comparative RNAseq analysis of roots inoculated with IRBG74 revealed a distinctive transcriptome response compared with intracellular colonization. In particular, several cytokinin-related genes were differentially regulated. Corroborating this observation, cyp735A and ipt4 cytokinin biosynthesis mutants were significantly affected in their nodulation with IRBG74, whereas lhk1 cytokinin receptor mutants formed no nodules. These results indicate a differential requirement for cytokinin signaling during intercellular rhizobial entry and highlight distinct modalities of inter- and intracellular infection mechanisms in L. japonicus. Oxford University Press 2020-12-04 /pmc/articles/PMC8133683/ /pubmed/33793909 http://dx.doi.org/10.1093/plphys/kiaa049 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Regular Issue Montiel, Jesús Reid, Dugald Grønbæk, Thomas H Benfeldt, Caroline M James, Euan K Ott, Thomas Ditengou, Franck A Nadzieja, Marcin Kelly, Simon Stougaard, Jens Distinct signaling routes mediate intercellular and intracellular rhizobial infection in Lotus japonicus |
title | Distinct signaling routes mediate intercellular and intracellular rhizobial infection in Lotus japonicus |
title_full | Distinct signaling routes mediate intercellular and intracellular rhizobial infection in Lotus japonicus |
title_fullStr | Distinct signaling routes mediate intercellular and intracellular rhizobial infection in Lotus japonicus |
title_full_unstemmed | Distinct signaling routes mediate intercellular and intracellular rhizobial infection in Lotus japonicus |
title_short | Distinct signaling routes mediate intercellular and intracellular rhizobial infection in Lotus japonicus |
title_sort | distinct signaling routes mediate intercellular and intracellular rhizobial infection in lotus japonicus |
topic | Regular Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133683/ https://www.ncbi.nlm.nih.gov/pubmed/33793909 http://dx.doi.org/10.1093/plphys/kiaa049 |
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