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A subcompatible rhizobium strain reveals infection duality in Lotus

Lotus species develop infection threads to guide rhizobia into nodule cells. However, there is evidence that some species have a genetic repertoire to allow other modes of infection. By conducting confocal and electron microscopy, quantification of marker gene expression, and phenotypic analysis of...

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Autores principales: Liang, Juan, Klingl, Andreas, Lin, Yen-Yu, Boul, Emily, Thomas-Oates, Jane, Marín, Macarena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436148/
https://www.ncbi.nlm.nih.gov/pubmed/30775775
http://dx.doi.org/10.1093/jxb/erz057
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author Liang, Juan
Klingl, Andreas
Lin, Yen-Yu
Boul, Emily
Thomas-Oates, Jane
Marín, Macarena
author_facet Liang, Juan
Klingl, Andreas
Lin, Yen-Yu
Boul, Emily
Thomas-Oates, Jane
Marín, Macarena
author_sort Liang, Juan
collection PubMed
description Lotus species develop infection threads to guide rhizobia into nodule cells. However, there is evidence that some species have a genetic repertoire to allow other modes of infection. By conducting confocal and electron microscopy, quantification of marker gene expression, and phenotypic analysis of transgenic roots infected with mutant rhizobia, we elucidated the infection mechanism used by Rhizobium leguminosarum Norway to colonize Lotus burttii. Rhizobium leguminosarum Norway induces a distinct host transcriptional response compared with Mesorhizobium loti. It infects L. burttii utilizing an epidermal and transcellular infection thread-independent mechanism at high frequency. The entry into plant cells occurs directly from the apoplast and is primarily mediated by ‘peg’-like structures, the formation of which is dependent on the production of Nod factor by the rhizobia. These results demonstrate that Lotus species can exhibit duality in their infection mechanisms depending on the rhizobial strain that they encounter. This is especially relevant in the context of interactions in the rhizosphere where legumes do not encounter single strains, but complex rhizobial communities. Additionally, our findings support a perception mechanism at the nodule cell entry interface, reinforcing the idea that there are successive checkpoints during rhizobial infection.
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spelling pubmed-64361482019-04-01 A subcompatible rhizobium strain reveals infection duality in Lotus Liang, Juan Klingl, Andreas Lin, Yen-Yu Boul, Emily Thomas-Oates, Jane Marín, Macarena J Exp Bot Research Papers Lotus species develop infection threads to guide rhizobia into nodule cells. However, there is evidence that some species have a genetic repertoire to allow other modes of infection. By conducting confocal and electron microscopy, quantification of marker gene expression, and phenotypic analysis of transgenic roots infected with mutant rhizobia, we elucidated the infection mechanism used by Rhizobium leguminosarum Norway to colonize Lotus burttii. Rhizobium leguminosarum Norway induces a distinct host transcriptional response compared with Mesorhizobium loti. It infects L. burttii utilizing an epidermal and transcellular infection thread-independent mechanism at high frequency. The entry into plant cells occurs directly from the apoplast and is primarily mediated by ‘peg’-like structures, the formation of which is dependent on the production of Nod factor by the rhizobia. These results demonstrate that Lotus species can exhibit duality in their infection mechanisms depending on the rhizobial strain that they encounter. This is especially relevant in the context of interactions in the rhizosphere where legumes do not encounter single strains, but complex rhizobial communities. Additionally, our findings support a perception mechanism at the nodule cell entry interface, reinforcing the idea that there are successive checkpoints during rhizobial infection. Oxford University Press 2019-03-01 2019-02-18 /pmc/articles/PMC6436148/ /pubmed/30775775 http://dx.doi.org/10.1093/jxb/erz057 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://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/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Liang, Juan
Klingl, Andreas
Lin, Yen-Yu
Boul, Emily
Thomas-Oates, Jane
Marín, Macarena
A subcompatible rhizobium strain reveals infection duality in Lotus
title A subcompatible rhizobium strain reveals infection duality in Lotus
title_full A subcompatible rhizobium strain reveals infection duality in Lotus
title_fullStr A subcompatible rhizobium strain reveals infection duality in Lotus
title_full_unstemmed A subcompatible rhizobium strain reveals infection duality in Lotus
title_short A subcompatible rhizobium strain reveals infection duality in Lotus
title_sort subcompatible rhizobium strain reveals infection duality in lotus
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436148/
https://www.ncbi.nlm.nih.gov/pubmed/30775775
http://dx.doi.org/10.1093/jxb/erz057
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