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Trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato
BACKGROUND: The plant phyllosphere is a well-studied habitat characterized by low nutrient availability and high community dynamics. In contrast, plant trichomes, known for their production of a large number of metabolites, are a yet unexplored habitat for microbes. We analyzed the phyllosphere as w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067393/ https://www.ncbi.nlm.nih.gov/pubmed/33902724 http://dx.doi.org/10.1186/s40793-020-00364-9 |
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author | Kusstatscher, Peter Wicaksono, Wisnu Adi Bergna, Alessandro Cernava, Tomislav Bergau, Nick Tissier, Alain Hause, Bettina Berg, Gabriele |
author_facet | Kusstatscher, Peter Wicaksono, Wisnu Adi Bergna, Alessandro Cernava, Tomislav Bergau, Nick Tissier, Alain Hause, Bettina Berg, Gabriele |
author_sort | Kusstatscher, Peter |
collection | PubMed |
description | BACKGROUND: The plant phyllosphere is a well-studied habitat characterized by low nutrient availability and high community dynamics. In contrast, plant trichomes, known for their production of a large number of metabolites, are a yet unexplored habitat for microbes. We analyzed the phyllosphere as well as trichomes of two tomato genotypes (Solanum lycopersicum LA4024, S. habrochaites LA1777) by targeting bacterial 16S rRNA gene fragments. RESULTS: Leaves, leaves without trichomes, and trichomes alone harbored similar abundances of bacteria (10(8)–10(9) 16S rRNA gene copy numbers per gram of sample). In contrast, bacterial diversity was found significantly increased in trichome samples (Shannon index: 4.4 vs. 2.5). Moreover, the community composition was significantly different when assessed with beta diversity analysis and corresponding statistical tests. At the bacterial class level, Alphaproteobacteria (23.6%) were significantly increased, whereas Bacilli (8.6%) were decreased in trichomes. The bacterial family Sphingomonadacea (8.4%) was identified as the most prominent, trichome-specific feature; Burkholderiaceae and Actinobacteriaceae showed similar patterns. Moreover, Sphingomonas was identified as a central element in the core microbiome of trichome samples, while distinct low-abundant bacterial families including Hymenobacteraceae and Alicyclobacillaceae were exclusively found in trichome samples. Niche preferences were statistically significant for both genotypes and genotype-specific enrichments were further observed. CONCLUSION: Our results provide first evidence of a highly specific trichome microbiome in tomato and show the importance of micro-niches for the structure of bacterial communities on leaves. These findings provide further clues for breeding, plant pathology and protection as well as so far unexplored natural pathogen defense strategies. |
format | Online Article Text |
id | pubmed-8067393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80673932021-04-26 Trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato Kusstatscher, Peter Wicaksono, Wisnu Adi Bergna, Alessandro Cernava, Tomislav Bergau, Nick Tissier, Alain Hause, Bettina Berg, Gabriele Environ Microbiome Research Article BACKGROUND: The plant phyllosphere is a well-studied habitat characterized by low nutrient availability and high community dynamics. In contrast, plant trichomes, known for their production of a large number of metabolites, are a yet unexplored habitat for microbes. We analyzed the phyllosphere as well as trichomes of two tomato genotypes (Solanum lycopersicum LA4024, S. habrochaites LA1777) by targeting bacterial 16S rRNA gene fragments. RESULTS: Leaves, leaves without trichomes, and trichomes alone harbored similar abundances of bacteria (10(8)–10(9) 16S rRNA gene copy numbers per gram of sample). In contrast, bacterial diversity was found significantly increased in trichome samples (Shannon index: 4.4 vs. 2.5). Moreover, the community composition was significantly different when assessed with beta diversity analysis and corresponding statistical tests. At the bacterial class level, Alphaproteobacteria (23.6%) were significantly increased, whereas Bacilli (8.6%) were decreased in trichomes. The bacterial family Sphingomonadacea (8.4%) was identified as the most prominent, trichome-specific feature; Burkholderiaceae and Actinobacteriaceae showed similar patterns. Moreover, Sphingomonas was identified as a central element in the core microbiome of trichome samples, while distinct low-abundant bacterial families including Hymenobacteraceae and Alicyclobacillaceae were exclusively found in trichome samples. Niche preferences were statistically significant for both genotypes and genotype-specific enrichments were further observed. CONCLUSION: Our results provide first evidence of a highly specific trichome microbiome in tomato and show the importance of micro-niches for the structure of bacterial communities on leaves. These findings provide further clues for breeding, plant pathology and protection as well as so far unexplored natural pathogen defense strategies. BioMed Central 2020-09-17 /pmc/articles/PMC8067393/ /pubmed/33902724 http://dx.doi.org/10.1186/s40793-020-00364-9 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Kusstatscher, Peter Wicaksono, Wisnu Adi Bergna, Alessandro Cernava, Tomislav Bergau, Nick Tissier, Alain Hause, Bettina Berg, Gabriele Trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato |
title | Trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato |
title_full | Trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato |
title_fullStr | Trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato |
title_full_unstemmed | Trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato |
title_short | Trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato |
title_sort | trichomes form genotype-specific microbial hotspots in the phyllosphere of tomato |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067393/ https://www.ncbi.nlm.nih.gov/pubmed/33902724 http://dx.doi.org/10.1186/s40793-020-00364-9 |
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