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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
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