Cargando…

Pathogen Infection and Host-Resistance Interactively Affect Root-Associated Fungal Communities in Watermelon

Interactions of pathogen infection, host plant resistance, and fungal communities are poorly understood. Although the use of resistant watermelon cultivars is an effective control measure of watermelon wilt disease, fungal communities may also have significant effects on the development of the soil-...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Lihui, Nicolaisen, Mogens, Larsen, John, Zeng, Rong, Gao, Shigang, Dai, Fuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793699/
https://www.ncbi.nlm.nih.gov/pubmed/33424807
http://dx.doi.org/10.3389/fmicb.2020.605622
_version_ 1783634044372647936
author Xu, Lihui
Nicolaisen, Mogens
Larsen, John
Zeng, Rong
Gao, Shigang
Dai, Fuming
author_facet Xu, Lihui
Nicolaisen, Mogens
Larsen, John
Zeng, Rong
Gao, Shigang
Dai, Fuming
author_sort Xu, Lihui
collection PubMed
description Interactions of pathogen infection, host plant resistance, and fungal communities are poorly understood. Although the use of resistant watermelon cultivars is an effective control measure of watermelon wilt disease, fungal communities may also have significant effects on the development of the soil-borne pathogen complexes. We characterized the root and rhizosphere fungal communities associated with healthy and diseased watermelons of three different cultivars with different susceptibilities toward wilt disease by paired-end Illumina MiSeq sequencing. Thirty watermelon plants including highly wilt-resistant, moderately resistant, and susceptible cultivars were collected from a greenhouse, half of which showing clear wilt symptoms and the other half with no symptoms. Patterns of watermelon wilt disease and the response of the fungal communities varied among the three cultivars. The amount of the pathogen Fusarium oxysporum f. sp. niveum was higher in diseased root and rhizosphere samples, particularly in the susceptible cultivar, and was significantly positively correlated with the disease index of Fusarium wilt. Plant health had significant effects on root-associated fungal communities, whereas only the highly resistant cultivar had significant effects only on the rhizosphere fungal communities. Co-occurrence networks revealed a higher complexity of fungal communities in the symptom-free roots compared to diseased roots. In addition, networks from roots of the highly resistant plants showing symptoms had a higher complexity compared to the susceptible cultivars. Keystone species were identified for the plants with different symptom severity and the different cultivars in the root and rhizosphere, such as Fusarium oxysporum, Monosporascus cannonballus, and Mortierella alpina. Overall, the most important factor determining fungal communities in the roots was plant symptom severity, whereas in the rhizosphere, plant genotype was the most important factor determining fungal communities.
format Online
Article
Text
id pubmed-7793699
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-77936992021-01-09 Pathogen Infection and Host-Resistance Interactively Affect Root-Associated Fungal Communities in Watermelon Xu, Lihui Nicolaisen, Mogens Larsen, John Zeng, Rong Gao, Shigang Dai, Fuming Front Microbiol Microbiology Interactions of pathogen infection, host plant resistance, and fungal communities are poorly understood. Although the use of resistant watermelon cultivars is an effective control measure of watermelon wilt disease, fungal communities may also have significant effects on the development of the soil-borne pathogen complexes. We characterized the root and rhizosphere fungal communities associated with healthy and diseased watermelons of three different cultivars with different susceptibilities toward wilt disease by paired-end Illumina MiSeq sequencing. Thirty watermelon plants including highly wilt-resistant, moderately resistant, and susceptible cultivars were collected from a greenhouse, half of which showing clear wilt symptoms and the other half with no symptoms. Patterns of watermelon wilt disease and the response of the fungal communities varied among the three cultivars. The amount of the pathogen Fusarium oxysporum f. sp. niveum was higher in diseased root and rhizosphere samples, particularly in the susceptible cultivar, and was significantly positively correlated with the disease index of Fusarium wilt. Plant health had significant effects on root-associated fungal communities, whereas only the highly resistant cultivar had significant effects only on the rhizosphere fungal communities. Co-occurrence networks revealed a higher complexity of fungal communities in the symptom-free roots compared to diseased roots. In addition, networks from roots of the highly resistant plants showing symptoms had a higher complexity compared to the susceptible cultivars. Keystone species were identified for the plants with different symptom severity and the different cultivars in the root and rhizosphere, such as Fusarium oxysporum, Monosporascus cannonballus, and Mortierella alpina. Overall, the most important factor determining fungal communities in the roots was plant symptom severity, whereas in the rhizosphere, plant genotype was the most important factor determining fungal communities. Frontiers Media S.A. 2020-12-17 /pmc/articles/PMC7793699/ /pubmed/33424807 http://dx.doi.org/10.3389/fmicb.2020.605622 Text en Copyright © 2020 Xu, Nicolaisen, Larsen, Zeng, Gao and Dai. 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 Microbiology
Xu, Lihui
Nicolaisen, Mogens
Larsen, John
Zeng, Rong
Gao, Shigang
Dai, Fuming
Pathogen Infection and Host-Resistance Interactively Affect Root-Associated Fungal Communities in Watermelon
title Pathogen Infection and Host-Resistance Interactively Affect Root-Associated Fungal Communities in Watermelon
title_full Pathogen Infection and Host-Resistance Interactively Affect Root-Associated Fungal Communities in Watermelon
title_fullStr Pathogen Infection and Host-Resistance Interactively Affect Root-Associated Fungal Communities in Watermelon
title_full_unstemmed Pathogen Infection and Host-Resistance Interactively Affect Root-Associated Fungal Communities in Watermelon
title_short Pathogen Infection and Host-Resistance Interactively Affect Root-Associated Fungal Communities in Watermelon
title_sort pathogen infection and host-resistance interactively affect root-associated fungal communities in watermelon
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793699/
https://www.ncbi.nlm.nih.gov/pubmed/33424807
http://dx.doi.org/10.3389/fmicb.2020.605622
work_keys_str_mv AT xulihui pathogeninfectionandhostresistanceinteractivelyaffectrootassociatedfungalcommunitiesinwatermelon
AT nicolaisenmogens pathogeninfectionandhostresistanceinteractivelyaffectrootassociatedfungalcommunitiesinwatermelon
AT larsenjohn pathogeninfectionandhostresistanceinteractivelyaffectrootassociatedfungalcommunitiesinwatermelon
AT zengrong pathogeninfectionandhostresistanceinteractivelyaffectrootassociatedfungalcommunitiesinwatermelon
AT gaoshigang pathogeninfectionandhostresistanceinteractivelyaffectrootassociatedfungalcommunitiesinwatermelon
AT daifuming pathogeninfectionandhostresistanceinteractivelyaffectrootassociatedfungalcommunitiesinwatermelon