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Alteration of Bacterial Wilt Resistance in Tomato Plant by Microbiota Transplant
Plant-associated microbiota plays an important role in plant disease resistance. Bacterial wilt resistance of tomato is a function of the quantitative trait of tomato plants; however, the mechanism underlying quantitative resistance is unexplored. In this study, we hypothesized that rhizosphere micr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427413/ https://www.ncbi.nlm.nih.gov/pubmed/32849735 http://dx.doi.org/10.3389/fpls.2020.01186 |
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author | Choi, Kihyuck Choi, Jinhee Lee, Pyeong An Roy, Nazish Khan, Raees Lee, Hyoung Ju Weon, Hang Yeon Kong, Hyun Gi Lee, Seon-Woo |
author_facet | Choi, Kihyuck Choi, Jinhee Lee, Pyeong An Roy, Nazish Khan, Raees Lee, Hyoung Ju Weon, Hang Yeon Kong, Hyun Gi Lee, Seon-Woo |
author_sort | Choi, Kihyuck |
collection | PubMed |
description | Plant-associated microbiota plays an important role in plant disease resistance. Bacterial wilt resistance of tomato is a function of the quantitative trait of tomato plants; however, the mechanism underlying quantitative resistance is unexplored. In this study, we hypothesized that rhizosphere microbiota affects the resistance of tomato plants against soil-borne bacterial wilt caused by Ralstonia solanacearum. This hypothesis was tested using a tomato cultivar grown in a defined soil with various microbiota transplants. The bacterial wilt-resistant Hawaii 7996 tomato cultivar exhibited marked suppression and induction of disease severity after treatment with upland soil-derived and forest soil-derived microbiotas, respectively, whereas the transplants did not affect the disease severity in the susceptible tomato cultivar Moneymaker. The differential resistance of Hawaii 7996 to bacterial wilt was abolished by diluted or heat-killed microbiota transplantation. Microbial community analysis revealed the transplant-specific distinct community structure in the tomato rhizosphere and the significant enrichment of specific microbial operational taxonomic units (OTUs) in the rhizosphere of the upland soil microbiota-treated Hawaii 7996. These results suggest that the specific transplanted microbiota alters the bacterial wilt resistance in the resistant cultivar potentially through a priority effect. |
format | Online Article Text |
id | pubmed-7427413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74274132020-08-25 Alteration of Bacterial Wilt Resistance in Tomato Plant by Microbiota Transplant Choi, Kihyuck Choi, Jinhee Lee, Pyeong An Roy, Nazish Khan, Raees Lee, Hyoung Ju Weon, Hang Yeon Kong, Hyun Gi Lee, Seon-Woo Front Plant Sci Plant Science Plant-associated microbiota plays an important role in plant disease resistance. Bacterial wilt resistance of tomato is a function of the quantitative trait of tomato plants; however, the mechanism underlying quantitative resistance is unexplored. In this study, we hypothesized that rhizosphere microbiota affects the resistance of tomato plants against soil-borne bacterial wilt caused by Ralstonia solanacearum. This hypothesis was tested using a tomato cultivar grown in a defined soil with various microbiota transplants. The bacterial wilt-resistant Hawaii 7996 tomato cultivar exhibited marked suppression and induction of disease severity after treatment with upland soil-derived and forest soil-derived microbiotas, respectively, whereas the transplants did not affect the disease severity in the susceptible tomato cultivar Moneymaker. The differential resistance of Hawaii 7996 to bacterial wilt was abolished by diluted or heat-killed microbiota transplantation. Microbial community analysis revealed the transplant-specific distinct community structure in the tomato rhizosphere and the significant enrichment of specific microbial operational taxonomic units (OTUs) in the rhizosphere of the upland soil microbiota-treated Hawaii 7996. These results suggest that the specific transplanted microbiota alters the bacterial wilt resistance in the resistant cultivar potentially through a priority effect. Frontiers Media S.A. 2020-08-07 /pmc/articles/PMC7427413/ /pubmed/32849735 http://dx.doi.org/10.3389/fpls.2020.01186 Text en Copyright © 2020 Choi, Choi, Lee, Roy, Khan, Lee, Weon, Kong and Lee http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Choi, Kihyuck Choi, Jinhee Lee, Pyeong An Roy, Nazish Khan, Raees Lee, Hyoung Ju Weon, Hang Yeon Kong, Hyun Gi Lee, Seon-Woo Alteration of Bacterial Wilt Resistance in Tomato Plant by Microbiota Transplant |
title | Alteration of Bacterial Wilt Resistance in Tomato Plant by Microbiota Transplant |
title_full | Alteration of Bacterial Wilt Resistance in Tomato Plant by Microbiota Transplant |
title_fullStr | Alteration of Bacterial Wilt Resistance in Tomato Plant by Microbiota Transplant |
title_full_unstemmed | Alteration of Bacterial Wilt Resistance in Tomato Plant by Microbiota Transplant |
title_short | Alteration of Bacterial Wilt Resistance in Tomato Plant by Microbiota Transplant |
title_sort | alteration of bacterial wilt resistance in tomato plant by microbiota transplant |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427413/ https://www.ncbi.nlm.nih.gov/pubmed/32849735 http://dx.doi.org/10.3389/fpls.2020.01186 |
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