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Heritability of tomato rhizobacteria resistant to Ralstonia solanacearum
BACKGROUND: Ralstonia solanacearum (Rs) is a soilborne phytopathogen that causes bacterial wilt and substantial yield losses in many plants, such as tomatoes. A resistant tomato cultivar can recruit a beneficial microbiome from soil to resist Rs. However, whether this recruitment is inheritable from...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753271/ https://www.ncbi.nlm.nih.gov/pubmed/36517876 http://dx.doi.org/10.1186/s40168-022-01413-w |
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author | Yin, Jiakang Zhang, Ziliang Zhu, Chengcheng Wang, Taotao Wang, Ruihong Ruan, Lifang |
author_facet | Yin, Jiakang Zhang, Ziliang Zhu, Chengcheng Wang, Taotao Wang, Ruihong Ruan, Lifang |
author_sort | Yin, Jiakang |
collection | PubMed |
description | BACKGROUND: Ralstonia solanacearum (Rs) is a soilborne phytopathogen that causes bacterial wilt and substantial yield losses in many plants, such as tomatoes. A resistant tomato cultivar can recruit a beneficial microbiome from soil to resist Rs. However, whether this recruitment is inheritable from resistant parent to progeny has not been determined. RESULTS: In the present study, we investigated the rhizosphere microbiomes of tomatoes with clear kinship and different resistance against Rs. Resistant tomatoes grown with the additions of natural soil or its extract showed lower disease indexes than those grown in the sterile soil, demonstrating the importance of soil microbiome in resisting Rs. The results of 16S ribosomal RNA gene amplicon sequencing revealed that the resistant cultivars had more robust rhizosphere microbiomes than the susceptible ones. Besides, the resistant progeny HF12 resembled its resistant parent HG64 in the rhizosphere microbiome. The rhizosphere microbiome had functional consistency between HF12 and HG64 as revealed by metagenomics. Based on multi-omics analysis and experimental validation, two rhizobacteria (Sphingomonas sp. Cra20 and Pseudomonas putida KT2440) were enriched in HF12 and HG64 with the ability to offer susceptible tomatoes considerable protection against Rs. Multiple aspects were involved in the protection, including reducing the virulence-related genes of Rs and reshaping the transcriptomes of the susceptible tomatoes. CONCLUSIONS: We found promising bacteria to suppress the tomato bacterial wilt in sustainable agriculture. And our research provides insights into the heritability of Rs-resistant tomato rhizobacteria, echoing the inheritance of tomato genetic material. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01413-w. |
format | Online Article Text |
id | pubmed-9753271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97532712022-12-16 Heritability of tomato rhizobacteria resistant to Ralstonia solanacearum Yin, Jiakang Zhang, Ziliang Zhu, Chengcheng Wang, Taotao Wang, Ruihong Ruan, Lifang Microbiome Research BACKGROUND: Ralstonia solanacearum (Rs) is a soilborne phytopathogen that causes bacterial wilt and substantial yield losses in many plants, such as tomatoes. A resistant tomato cultivar can recruit a beneficial microbiome from soil to resist Rs. However, whether this recruitment is inheritable from resistant parent to progeny has not been determined. RESULTS: In the present study, we investigated the rhizosphere microbiomes of tomatoes with clear kinship and different resistance against Rs. Resistant tomatoes grown with the additions of natural soil or its extract showed lower disease indexes than those grown in the sterile soil, demonstrating the importance of soil microbiome in resisting Rs. The results of 16S ribosomal RNA gene amplicon sequencing revealed that the resistant cultivars had more robust rhizosphere microbiomes than the susceptible ones. Besides, the resistant progeny HF12 resembled its resistant parent HG64 in the rhizosphere microbiome. The rhizosphere microbiome had functional consistency between HF12 and HG64 as revealed by metagenomics. Based on multi-omics analysis and experimental validation, two rhizobacteria (Sphingomonas sp. Cra20 and Pseudomonas putida KT2440) were enriched in HF12 and HG64 with the ability to offer susceptible tomatoes considerable protection against Rs. Multiple aspects were involved in the protection, including reducing the virulence-related genes of Rs and reshaping the transcriptomes of the susceptible tomatoes. CONCLUSIONS: We found promising bacteria to suppress the tomato bacterial wilt in sustainable agriculture. And our research provides insights into the heritability of Rs-resistant tomato rhizobacteria, echoing the inheritance of tomato genetic material. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01413-w. BioMed Central 2022-12-15 /pmc/articles/PMC9753271/ /pubmed/36517876 http://dx.doi.org/10.1186/s40168-022-01413-w Text en © The Author(s) 2022 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 Yin, Jiakang Zhang, Ziliang Zhu, Chengcheng Wang, Taotao Wang, Ruihong Ruan, Lifang Heritability of tomato rhizobacteria resistant to Ralstonia solanacearum |
title | Heritability of tomato rhizobacteria resistant to Ralstonia solanacearum |
title_full | Heritability of tomato rhizobacteria resistant to Ralstonia solanacearum |
title_fullStr | Heritability of tomato rhizobacteria resistant to Ralstonia solanacearum |
title_full_unstemmed | Heritability of tomato rhizobacteria resistant to Ralstonia solanacearum |
title_short | Heritability of tomato rhizobacteria resistant to Ralstonia solanacearum |
title_sort | heritability of tomato rhizobacteria resistant to ralstonia solanacearum |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753271/ https://www.ncbi.nlm.nih.gov/pubmed/36517876 http://dx.doi.org/10.1186/s40168-022-01413-w |
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