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The effector candidate repertoire of the arbuscular mycorrhizal fungus Rhizophagus clarus

BACKGROUND: Arbuscular mycorrhizal fungi (AMF) form an ecologically important symbiosis with more than two thirds of studied land plants. Recent studies of plant-pathogen interactions showed that effector proteins play a key role in host colonization by controlling the plant immune system. We hypoth...

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Autores principales: Sędzielewska Toro, Kinga, Brachmann, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746824/
https://www.ncbi.nlm.nih.gov/pubmed/26861502
http://dx.doi.org/10.1186/s12864-016-2422-y
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author Sędzielewska Toro, Kinga
Brachmann, Andreas
author_facet Sędzielewska Toro, Kinga
Brachmann, Andreas
author_sort Sędzielewska Toro, Kinga
collection PubMed
description BACKGROUND: Arbuscular mycorrhizal fungi (AMF) form an ecologically important symbiosis with more than two thirds of studied land plants. Recent studies of plant-pathogen interactions showed that effector proteins play a key role in host colonization by controlling the plant immune system. We hypothesise that also for symbiotic-plant interactions the secreted effectome of the fungus is a major component of communication and the conservation level of effector proteins between AMF species may be indicative whether they play a fundamental role. RESULTS: In this study, we used a bioinformatics pipeline to predict and compare the effector candidate repertoire of the two AMF species, Rhizophagus irregularis and Rhizophagus clarus. Our in silico pipeline revealed a list of 220 R. irregularis candidate effector genes that create a valuable information source to elucidate the mechanism of plant infection and colonization by fungi during AMF symbiotic interaction. While most of the candidate effectors show no homologies to known domains or proteins, the candidates with homologies point to potential roles in signal transduction, cell wall modification or transcription regulation. A remarkable aspect of our work is presence of a large portion of the effector proteins involved in symbiosis, which are not unique to each fungi or plant species, but shared along the Glomeromycota phylum. For 95 % of R. irregularis candidates we found homologs in a R. clarus genome draft generated by Illumina high-throughput sequencing. Interestingly, 9 % of the predicted effectors are at least as conserved between the two Rhizophagus species as proteins with housekeeping functions (similarity > 90 %). Therefore, we state that this group of highly conserved effector proteins between AMF species may play a fundamental role during fungus-plant interaction. CONCLUSIONS: We hypothesise that in symbiotic interactions the secreted effectome of the fungus might be an important component of communication. Identification and functional characterization of the primary AMF effectors that regulate symbiotic development will help in understanding the mechanisms of fungus-plant interaction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2422-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-47468242016-02-10 The effector candidate repertoire of the arbuscular mycorrhizal fungus Rhizophagus clarus Sędzielewska Toro, Kinga Brachmann, Andreas BMC Genomics Research Article BACKGROUND: Arbuscular mycorrhizal fungi (AMF) form an ecologically important symbiosis with more than two thirds of studied land plants. Recent studies of plant-pathogen interactions showed that effector proteins play a key role in host colonization by controlling the plant immune system. We hypothesise that also for symbiotic-plant interactions the secreted effectome of the fungus is a major component of communication and the conservation level of effector proteins between AMF species may be indicative whether they play a fundamental role. RESULTS: In this study, we used a bioinformatics pipeline to predict and compare the effector candidate repertoire of the two AMF species, Rhizophagus irregularis and Rhizophagus clarus. Our in silico pipeline revealed a list of 220 R. irregularis candidate effector genes that create a valuable information source to elucidate the mechanism of plant infection and colonization by fungi during AMF symbiotic interaction. While most of the candidate effectors show no homologies to known domains or proteins, the candidates with homologies point to potential roles in signal transduction, cell wall modification or transcription regulation. A remarkable aspect of our work is presence of a large portion of the effector proteins involved in symbiosis, which are not unique to each fungi or plant species, but shared along the Glomeromycota phylum. For 95 % of R. irregularis candidates we found homologs in a R. clarus genome draft generated by Illumina high-throughput sequencing. Interestingly, 9 % of the predicted effectors are at least as conserved between the two Rhizophagus species as proteins with housekeeping functions (similarity > 90 %). Therefore, we state that this group of highly conserved effector proteins between AMF species may play a fundamental role during fungus-plant interaction. CONCLUSIONS: We hypothesise that in symbiotic interactions the secreted effectome of the fungus might be an important component of communication. Identification and functional characterization of the primary AMF effectors that regulate symbiotic development will help in understanding the mechanisms of fungus-plant interaction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2422-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-09 /pmc/articles/PMC4746824/ /pubmed/26861502 http://dx.doi.org/10.1186/s12864-016-2422-y Text en © Sędzielewska Toro and Brachmann. 2016 Open AccessThis 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
Sędzielewska Toro, Kinga
Brachmann, Andreas
The effector candidate repertoire of the arbuscular mycorrhizal fungus Rhizophagus clarus
title The effector candidate repertoire of the arbuscular mycorrhizal fungus Rhizophagus clarus
title_full The effector candidate repertoire of the arbuscular mycorrhizal fungus Rhizophagus clarus
title_fullStr The effector candidate repertoire of the arbuscular mycorrhizal fungus Rhizophagus clarus
title_full_unstemmed The effector candidate repertoire of the arbuscular mycorrhizal fungus Rhizophagus clarus
title_short The effector candidate repertoire of the arbuscular mycorrhizal fungus Rhizophagus clarus
title_sort effector candidate repertoire of the arbuscular mycorrhizal fungus rhizophagus clarus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746824/
https://www.ncbi.nlm.nih.gov/pubmed/26861502
http://dx.doi.org/10.1186/s12864-016-2422-y
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