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‘Candidatus Phytoplasma solani’ interferes with the distribution and uptake of iron in tomato

BACKGROUND: ‘Candidatus Phytoplasma solani’ is endemic in Europe and infects a wide range of weeds and cultivated plants. Phytoplasmas are prokaryotic plant pathogens that colonize the sieve elements of their host plant, causing severe alterations in phloem function and impairment of assimilate tran...

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Autores principales: Buoso, Sara, Pagliari, Laura, Musetti, Rita, Martini, Marta, Marroni, Fabio, Schmidt, Wolfgang, Santi, Simonetta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734453/
https://www.ncbi.nlm.nih.gov/pubmed/31500568
http://dx.doi.org/10.1186/s12864-019-6062-x
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author Buoso, Sara
Pagliari, Laura
Musetti, Rita
Martini, Marta
Marroni, Fabio
Schmidt, Wolfgang
Santi, Simonetta
author_facet Buoso, Sara
Pagliari, Laura
Musetti, Rita
Martini, Marta
Marroni, Fabio
Schmidt, Wolfgang
Santi, Simonetta
author_sort Buoso, Sara
collection PubMed
description BACKGROUND: ‘Candidatus Phytoplasma solani’ is endemic in Europe and infects a wide range of weeds and cultivated plants. Phytoplasmas are prokaryotic plant pathogens that colonize the sieve elements of their host plant, causing severe alterations in phloem function and impairment of assimilate translocation. Typical symptoms of infected plants include yellowing of leaves or shoots, leaf curling, and general stunting, but the molecular mechanisms underlying most of the reported changes remain largely enigmatic. To infer a possible involvement of Fe in the host-phytoplasma interaction, we investigated the effects of ‘Candidatus Phytoplasma solani’ infection on tomato plants (Solanum lycopersicum cv. Micro-Tom) grown under different Fe regimes. RESULTS: Both phytoplasma infection and Fe starvation led to the development of chlorotic leaves and altered thylakoid organization. In infected plants, Fe accumulated in phloem tissue, altering the local distribution of Fe. In infected plants, Fe starvation had additive effects on chlorophyll content and leaf chlorosis, suggesting that the two conditions affected the phenotypic readout via separate routes. To gain insights into the transcriptional response to phytoplasma infection, or Fe deficiency, transcriptome profiling was performed on midrib-enriched leaves. RNA-seq analysis revealed that both stress conditions altered the expression of a large (> 800) subset of common genes involved in photosynthetic light reactions, porphyrin / chlorophyll metabolism, and in flowering control. In Fe-deficient plants, phytoplasma infection perturbed the Fe deficiency response in roots, possibly by interference with the synthesis or transport of a promotive signal transmitted from the leaves to the roots. CONCLUSIONS: ‘Candidatus Phytoplasma solani’ infection changes the Fe distribution in tomato leaves, affects the photosynthetic machinery and perturbs the orchestration of root-mediated transport processes by compromising shoot-to-root communication. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-6062-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-67344532019-09-12 ‘Candidatus Phytoplasma solani’ interferes with the distribution and uptake of iron in tomato Buoso, Sara Pagliari, Laura Musetti, Rita Martini, Marta Marroni, Fabio Schmidt, Wolfgang Santi, Simonetta BMC Genomics Research Article BACKGROUND: ‘Candidatus Phytoplasma solani’ is endemic in Europe and infects a wide range of weeds and cultivated plants. Phytoplasmas are prokaryotic plant pathogens that colonize the sieve elements of their host plant, causing severe alterations in phloem function and impairment of assimilate translocation. Typical symptoms of infected plants include yellowing of leaves or shoots, leaf curling, and general stunting, but the molecular mechanisms underlying most of the reported changes remain largely enigmatic. To infer a possible involvement of Fe in the host-phytoplasma interaction, we investigated the effects of ‘Candidatus Phytoplasma solani’ infection on tomato plants (Solanum lycopersicum cv. Micro-Tom) grown under different Fe regimes. RESULTS: Both phytoplasma infection and Fe starvation led to the development of chlorotic leaves and altered thylakoid organization. In infected plants, Fe accumulated in phloem tissue, altering the local distribution of Fe. In infected plants, Fe starvation had additive effects on chlorophyll content and leaf chlorosis, suggesting that the two conditions affected the phenotypic readout via separate routes. To gain insights into the transcriptional response to phytoplasma infection, or Fe deficiency, transcriptome profiling was performed on midrib-enriched leaves. RNA-seq analysis revealed that both stress conditions altered the expression of a large (> 800) subset of common genes involved in photosynthetic light reactions, porphyrin / chlorophyll metabolism, and in flowering control. In Fe-deficient plants, phytoplasma infection perturbed the Fe deficiency response in roots, possibly by interference with the synthesis or transport of a promotive signal transmitted from the leaves to the roots. CONCLUSIONS: ‘Candidatus Phytoplasma solani’ infection changes the Fe distribution in tomato leaves, affects the photosynthetic machinery and perturbs the orchestration of root-mediated transport processes by compromising shoot-to-root communication. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-6062-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-09-10 /pmc/articles/PMC6734453/ /pubmed/31500568 http://dx.doi.org/10.1186/s12864-019-6062-x Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Buoso, Sara
Pagliari, Laura
Musetti, Rita
Martini, Marta
Marroni, Fabio
Schmidt, Wolfgang
Santi, Simonetta
‘Candidatus Phytoplasma solani’ interferes with the distribution and uptake of iron in tomato
title ‘Candidatus Phytoplasma solani’ interferes with the distribution and uptake of iron in tomato
title_full ‘Candidatus Phytoplasma solani’ interferes with the distribution and uptake of iron in tomato
title_fullStr ‘Candidatus Phytoplasma solani’ interferes with the distribution and uptake of iron in tomato
title_full_unstemmed ‘Candidatus Phytoplasma solani’ interferes with the distribution and uptake of iron in tomato
title_short ‘Candidatus Phytoplasma solani’ interferes with the distribution and uptake of iron in tomato
title_sort ‘candidatus phytoplasma solani’ interferes with the distribution and uptake of iron in tomato
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734453/
https://www.ncbi.nlm.nih.gov/pubmed/31500568
http://dx.doi.org/10.1186/s12864-019-6062-x
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