Cargando…

Rhizosphere Microbiomes from Root Knot Nematode Non-infested Plants Suppress Nematode Infection

Root knot nematodes (RKN, Meloidogyne spp.) are serious pathogens of numerous crops worldwide. Understanding the roles plant rhizosphere soil microbiome play during RKN infection is very important. The current study aims at investigating the impacts of soil microbiome on the activity of RKN. In this...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Dongmei, Feng, Hui, Schuelke, Taruna, De Santiago, Alejandro, Zhang, Qimeng, Zhang, Jinfeng, Luo, Chuping, Wei, Lihui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657434/
https://www.ncbi.nlm.nih.gov/pubmed/30666369
http://dx.doi.org/10.1007/s00248-019-01319-5
_version_ 1783438795891277824
author Zhou, Dongmei
Feng, Hui
Schuelke, Taruna
De Santiago, Alejandro
Zhang, Qimeng
Zhang, Jinfeng
Luo, Chuping
Wei, Lihui
author_facet Zhou, Dongmei
Feng, Hui
Schuelke, Taruna
De Santiago, Alejandro
Zhang, Qimeng
Zhang, Jinfeng
Luo, Chuping
Wei, Lihui
author_sort Zhou, Dongmei
collection PubMed
description Root knot nematodes (RKN, Meloidogyne spp.) are serious pathogens of numerous crops worldwide. Understanding the roles plant rhizosphere soil microbiome play during RKN infection is very important. The current study aims at investigating the impacts of soil microbiome on the activity of RKN. In this study, the 16S rRNA genes of the bacterial communities from nematode-infested and non-infested rhizosphere soils from four different plants were sequenced on the Illumina Hi-Seq platform. The soil microbiome effects on RKN infection were tested in a greenhouse assay. The non-infested soils had more microbial diversity than the infested soils from all plant rhizospheres, and both soil types had exclusive microbial communities. The inoculation of the microbiomes from eggplant and cucumber non-infested soils to tomato plants significantly alleviated the RKN infection, while the microbiome from infested soil showed increased the RKN infection. Furthermore, bacteria Pseudomonas sp. and Bacillus sp. were screened out from non-infested eggplant soil and exhibited biocontrol activity to RKN on tomato. Our findings suggest that microbes may regulate RKN infection in plants and are involved in biocontrol of RKN. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00248-019-01319-5) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6657434
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-66574342019-08-09 Rhizosphere Microbiomes from Root Knot Nematode Non-infested Plants Suppress Nematode Infection Zhou, Dongmei Feng, Hui Schuelke, Taruna De Santiago, Alejandro Zhang, Qimeng Zhang, Jinfeng Luo, Chuping Wei, Lihui Microb Ecol Plant Microbe Interactions Root knot nematodes (RKN, Meloidogyne spp.) are serious pathogens of numerous crops worldwide. Understanding the roles plant rhizosphere soil microbiome play during RKN infection is very important. The current study aims at investigating the impacts of soil microbiome on the activity of RKN. In this study, the 16S rRNA genes of the bacterial communities from nematode-infested and non-infested rhizosphere soils from four different plants were sequenced on the Illumina Hi-Seq platform. The soil microbiome effects on RKN infection were tested in a greenhouse assay. The non-infested soils had more microbial diversity than the infested soils from all plant rhizospheres, and both soil types had exclusive microbial communities. The inoculation of the microbiomes from eggplant and cucumber non-infested soils to tomato plants significantly alleviated the RKN infection, while the microbiome from infested soil showed increased the RKN infection. Furthermore, bacteria Pseudomonas sp. and Bacillus sp. were screened out from non-infested eggplant soil and exhibited biocontrol activity to RKN on tomato. Our findings suggest that microbes may regulate RKN infection in plants and are involved in biocontrol of RKN. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00248-019-01319-5) contains supplementary material, which is available to authorized users. Springer US 2019-01-21 2019 /pmc/articles/PMC6657434/ /pubmed/30666369 http://dx.doi.org/10.1007/s00248-019-01319-5 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Plant Microbe Interactions
Zhou, Dongmei
Feng, Hui
Schuelke, Taruna
De Santiago, Alejandro
Zhang, Qimeng
Zhang, Jinfeng
Luo, Chuping
Wei, Lihui
Rhizosphere Microbiomes from Root Knot Nematode Non-infested Plants Suppress Nematode Infection
title Rhizosphere Microbiomes from Root Knot Nematode Non-infested Plants Suppress Nematode Infection
title_full Rhizosphere Microbiomes from Root Knot Nematode Non-infested Plants Suppress Nematode Infection
title_fullStr Rhizosphere Microbiomes from Root Knot Nematode Non-infested Plants Suppress Nematode Infection
title_full_unstemmed Rhizosphere Microbiomes from Root Knot Nematode Non-infested Plants Suppress Nematode Infection
title_short Rhizosphere Microbiomes from Root Knot Nematode Non-infested Plants Suppress Nematode Infection
title_sort rhizosphere microbiomes from root knot nematode non-infested plants suppress nematode infection
topic Plant Microbe Interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657434/
https://www.ncbi.nlm.nih.gov/pubmed/30666369
http://dx.doi.org/10.1007/s00248-019-01319-5
work_keys_str_mv AT zhoudongmei rhizospheremicrobiomesfromrootknotnematodenoninfestedplantssuppressnematodeinfection
AT fenghui rhizospheremicrobiomesfromrootknotnematodenoninfestedplantssuppressnematodeinfection
AT schuelketaruna rhizospheremicrobiomesfromrootknotnematodenoninfestedplantssuppressnematodeinfection
AT desantiagoalejandro rhizospheremicrobiomesfromrootknotnematodenoninfestedplantssuppressnematodeinfection
AT zhangqimeng rhizospheremicrobiomesfromrootknotnematodenoninfestedplantssuppressnematodeinfection
AT zhangjinfeng rhizospheremicrobiomesfromrootknotnematodenoninfestedplantssuppressnematodeinfection
AT luochuping rhizospheremicrobiomesfromrootknotnematodenoninfestedplantssuppressnematodeinfection
AT weilihui rhizospheremicrobiomesfromrootknotnematodenoninfestedplantssuppressnematodeinfection