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Unique bacterial assembly, composition, and interactions in a parasitic plant and its host
How plant-associated microbiota are shaped by, and potentially contribute to, the unique ecology and heterotrophic life history of parasitic plants is relatively unknown. Here, we investigate the leaf and root bacterial communities of the root holoparasite Orobanche hederae and its host Hedera spp....
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/PMC7094075/ https://www.ncbi.nlm.nih.gov/pubmed/31912143 http://dx.doi.org/10.1093/jxb/erz572 |
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author | Fitzpatrick, Connor R Schneider, Adam C |
author_facet | Fitzpatrick, Connor R Schneider, Adam C |
author_sort | Fitzpatrick, Connor R |
collection | PubMed |
description | How plant-associated microbiota are shaped by, and potentially contribute to, the unique ecology and heterotrophic life history of parasitic plants is relatively unknown. Here, we investigate the leaf and root bacterial communities of the root holoparasite Orobanche hederae and its host Hedera spp. from natural populations. Root bacteria inhabiting Orobanche were less diverse, had fewer co-associations, and displayed increased compositional similarity to leaf bacteria relative to Hedera. Overall, Orobanche bacteria exhibited significant congruency with Hedera root bacteria across sites, but not the surrounding soil. Infection had localized and systemic effects on Hedera bacteria, which included effects on the abundance of individual taxa and root network properties. Collectively, our results indicate that the parasitic plant microbiome is derived but distinct from the host plant microbiota, exhibits increased homogenization between shoot and root tissues, and displays far fewer co-associations among individual bacterial members. Host plant infection is accompanied by modest changes of associated microbiota at both local and systemic scales compared with uninfected individuals. Our results are a first step towards extending the growing insight into the assembly and function of the plant microbiome to include the ecologically unique but often overlooked guild of heterotrophic plants. |
format | Online Article Text |
id | pubmed-7094075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70940752020-03-30 Unique bacterial assembly, composition, and interactions in a parasitic plant and its host Fitzpatrick, Connor R Schneider, Adam C J Exp Bot Research Papers How plant-associated microbiota are shaped by, and potentially contribute to, the unique ecology and heterotrophic life history of parasitic plants is relatively unknown. Here, we investigate the leaf and root bacterial communities of the root holoparasite Orobanche hederae and its host Hedera spp. from natural populations. Root bacteria inhabiting Orobanche were less diverse, had fewer co-associations, and displayed increased compositional similarity to leaf bacteria relative to Hedera. Overall, Orobanche bacteria exhibited significant congruency with Hedera root bacteria across sites, but not the surrounding soil. Infection had localized and systemic effects on Hedera bacteria, which included effects on the abundance of individual taxa and root network properties. Collectively, our results indicate that the parasitic plant microbiome is derived but distinct from the host plant microbiota, exhibits increased homogenization between shoot and root tissues, and displays far fewer co-associations among individual bacterial members. Host plant infection is accompanied by modest changes of associated microbiota at both local and systemic scales compared with uninfected individuals. Our results are a first step towards extending the growing insight into the assembly and function of the plant microbiome to include the ecologically unique but often overlooked guild of heterotrophic plants. Oxford University Press 2020-03-25 2020-01-06 /pmc/articles/PMC7094075/ /pubmed/31912143 http://dx.doi.org/10.1093/jxb/erz572 Text en © The Author(s) 2020. 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 Fitzpatrick, Connor R Schneider, Adam C Unique bacterial assembly, composition, and interactions in a parasitic plant and its host |
title | Unique bacterial assembly, composition, and interactions in a parasitic plant and its host |
title_full | Unique bacterial assembly, composition, and interactions in a parasitic plant and its host |
title_fullStr | Unique bacterial assembly, composition, and interactions in a parasitic plant and its host |
title_full_unstemmed | Unique bacterial assembly, composition, and interactions in a parasitic plant and its host |
title_short | Unique bacterial assembly, composition, and interactions in a parasitic plant and its host |
title_sort | unique bacterial assembly, composition, and interactions in a parasitic plant and its host |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094075/ https://www.ncbi.nlm.nih.gov/pubmed/31912143 http://dx.doi.org/10.1093/jxb/erz572 |
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