Cargando…
Functional interplay between antagonistic bacteria and Rhizoctonia solani in the tomato plant rhizosphere
Microbial interactions with plant roots play an imperial role in tomato plant growth and defense against the Rhizoctonia solani. This study performed a field experiment with two antagonistic bacteria (Pseudomonas and Bacillus) inoculated in healthy and Rhizoctonia solani treated soil in tomato rhizo...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548980/ https://www.ncbi.nlm.nih.gov/pubmed/36225362 http://dx.doi.org/10.3389/fmicb.2022.990850 |
_version_ | 1784805561581174784 |
---|---|
author | Solanki, Manoj Kumar Solanki, Anjali Chandrol Rai, Shalini Srivastava, Supriya Kashyap, Brijendra Kumar Divvela, Praveen Kumar Kumar, Sudheer Yandigeri, Mahesh S. Kashyap, Prem Lal Shrivastava, Alok Kumar Ali, Baber Khan, Shahid Jaremko, Mariusz Qureshi, Kamal Ahmad |
author_facet | Solanki, Manoj Kumar Solanki, Anjali Chandrol Rai, Shalini Srivastava, Supriya Kashyap, Brijendra Kumar Divvela, Praveen Kumar Kumar, Sudheer Yandigeri, Mahesh S. Kashyap, Prem Lal Shrivastava, Alok Kumar Ali, Baber Khan, Shahid Jaremko, Mariusz Qureshi, Kamal Ahmad |
author_sort | Solanki, Manoj Kumar |
collection | PubMed |
description | Microbial interactions with plant roots play an imperial role in tomato plant growth and defense against the Rhizoctonia solani. This study performed a field experiment with two antagonistic bacteria (Pseudomonas and Bacillus) inoculated in healthy and Rhizoctonia solani treated soil in tomato rhizosphere to understand the metabolic pattern and microbial function during plant disease suppression. In the present study, we assessed soil and microbial enzymes, bacterial and fungal cell forming unit (CFU), and carbon utilization profiling through Bio-Eco plates of rhizoplane samples. Antagonist bacteria and pathogen interaction significantly (p < 0.05) influenced the bacterial count, soil enzymes (chitinase and glucanase), and bacterial function (siderophore and chitinase production). These results indicated that these variables had an imperial role in disease suppression during plant development. Furthermore, the metabolic profiling showed that carbon source utilization enhanced under fruit development and ripening stages. These results suggested that carbon sources were essential in plant/pathogen/antagonist interaction. Substrates like β-methyl-D-glucoside, D-mannitol, D-galacturonic acid, N-acetyl-D-glucosamine, and phenylethylamine strongly connect with the suppuration of root rot disease. These carbon sources may help to propagate a healthy microbial community to reduce the pathogen invasion in the plant root system, and these carbon sources can be stimulators of antagonists against pathogens in the future. |
format | Online Article Text |
id | pubmed-9548980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95489802022-10-11 Functional interplay between antagonistic bacteria and Rhizoctonia solani in the tomato plant rhizosphere Solanki, Manoj Kumar Solanki, Anjali Chandrol Rai, Shalini Srivastava, Supriya Kashyap, Brijendra Kumar Divvela, Praveen Kumar Kumar, Sudheer Yandigeri, Mahesh S. Kashyap, Prem Lal Shrivastava, Alok Kumar Ali, Baber Khan, Shahid Jaremko, Mariusz Qureshi, Kamal Ahmad Front Microbiol Microbiology Microbial interactions with plant roots play an imperial role in tomato plant growth and defense against the Rhizoctonia solani. This study performed a field experiment with two antagonistic bacteria (Pseudomonas and Bacillus) inoculated in healthy and Rhizoctonia solani treated soil in tomato rhizosphere to understand the metabolic pattern and microbial function during plant disease suppression. In the present study, we assessed soil and microbial enzymes, bacterial and fungal cell forming unit (CFU), and carbon utilization profiling through Bio-Eco plates of rhizoplane samples. Antagonist bacteria and pathogen interaction significantly (p < 0.05) influenced the bacterial count, soil enzymes (chitinase and glucanase), and bacterial function (siderophore and chitinase production). These results indicated that these variables had an imperial role in disease suppression during plant development. Furthermore, the metabolic profiling showed that carbon source utilization enhanced under fruit development and ripening stages. These results suggested that carbon sources were essential in plant/pathogen/antagonist interaction. Substrates like β-methyl-D-glucoside, D-mannitol, D-galacturonic acid, N-acetyl-D-glucosamine, and phenylethylamine strongly connect with the suppuration of root rot disease. These carbon sources may help to propagate a healthy microbial community to reduce the pathogen invasion in the plant root system, and these carbon sources can be stimulators of antagonists against pathogens in the future. Frontiers Media S.A. 2022-09-26 /pmc/articles/PMC9548980/ /pubmed/36225362 http://dx.doi.org/10.3389/fmicb.2022.990850 Text en Copyright © 2022 Solanki, Solanki, Rai, Srivastava, Kashyap, Divvela, Kumar, Yandigeri, Kashyap, Shrivastava, Ali, Khan, Jaremko and Qureshi. https://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 | Microbiology Solanki, Manoj Kumar Solanki, Anjali Chandrol Rai, Shalini Srivastava, Supriya Kashyap, Brijendra Kumar Divvela, Praveen Kumar Kumar, Sudheer Yandigeri, Mahesh S. Kashyap, Prem Lal Shrivastava, Alok Kumar Ali, Baber Khan, Shahid Jaremko, Mariusz Qureshi, Kamal Ahmad Functional interplay between antagonistic bacteria and Rhizoctonia solani in the tomato plant rhizosphere |
title | Functional interplay between antagonistic bacteria and Rhizoctonia solani in the tomato plant rhizosphere |
title_full | Functional interplay between antagonistic bacteria and Rhizoctonia solani in the tomato plant rhizosphere |
title_fullStr | Functional interplay between antagonistic bacteria and Rhizoctonia solani in the tomato plant rhizosphere |
title_full_unstemmed | Functional interplay between antagonistic bacteria and Rhizoctonia solani in the tomato plant rhizosphere |
title_short | Functional interplay between antagonistic bacteria and Rhizoctonia solani in the tomato plant rhizosphere |
title_sort | functional interplay between antagonistic bacteria and rhizoctonia solani in the tomato plant rhizosphere |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548980/ https://www.ncbi.nlm.nih.gov/pubmed/36225362 http://dx.doi.org/10.3389/fmicb.2022.990850 |
work_keys_str_mv | AT solankimanojkumar functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT solankianjalichandrol functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT raishalini functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT srivastavasupriya functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT kashyapbrijendrakumar functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT divvelapraveenkumar functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT kumarsudheer functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT yandigerimaheshs functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT kashyappremlal functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT shrivastavaalokkumar functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT alibaber functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT khanshahid functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT jaremkomariusz functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere AT qureshikamalahmad functionalinterplaybetweenantagonisticbacteriaandrhizoctoniasolaniinthetomatoplantrhizosphere |