Temporal dynamics of bacterial and fungal communities during the infection of Brassica rapa roots by the protist Plasmodiophora brassicae.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 24 08 2018
accepted: 29 01 2019
entrez: 26 2 2019
pubmed: 26 2 2019
medline: 13 11 2019
Statut: epublish

Résumé

The temporal dynamics of rhizosphere and root microbiota composition was compared between healthy and infected Chinese cabbage plants by the pathogen Plasmodiophora brassicae. When inoculated with P. brassicae, disease was measured at five sampling dates from early root hair infection to late gall development. The first symptoms of clubroot disease appeared 14 days after inoculation (DAI) and increased drastically between 14 and 35 DAI. The structure of microbial communities associated to rhizosphere soil and root from healthy and inoculated plants was characterized through high-throughput DNA sequencing of bacterial (16S) and fungal (18S) molecular markers and compared at each sampling date. In healthy plants, Proteobacteria and Bacteroidetes bacterial phyla dominated the rhizosphere and root microbiota of Chinese cabbage. Rhizosphere bacterial communities contained higher abundances of Actinobacteria and Firmicutes compared to the roots. Moreover, a drastic shift of fungal communities of healthy plants occurred between the two last sampling dates, especially in plant roots, where most of Ascomycota fungi dominated until they were replaced by a fungus assigned to the Chytridiomycota phylum. Parasitic invasion by P. brassicae disrupted the rhizosphere and root-associated community assembly at a late step during the root secondary cortical infection stage of clubroot disease. At this stage, Flavisolibacter and Streptomyces in the rhizosphere, and Bacillus in the roots, were drastically less abundant upon parasite invasion. Rhizosphere of plants colonized by P. brassicae was significantly more invaded by the Chytridiomycota fungus, which could reflect a mutualistic relationship in this compartment between these two microorganisms.

Identifiants

pubmed: 30802246
doi: 10.1371/journal.pone.0204195
pii: PONE-D-18-24941
pmc: PMC6388920
doi:

Substances chimiques

RNA, Ribosomal, 16S 0
RNA, Ribosomal, 18S 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0204195

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Lionel Lebreton (L)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Anne-Yvonne Guillerm-Erckelboudt (AY)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Kévin Gazengel (K)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Juliette Linglin (J)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Morgane Ourry (M)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Pascal Glory (P)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Alain Sarniguet (A)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Stéphanie Daval (S)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Maria J Manzanares-Dauleux (MJ)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

Christophe Mougel (C)

IGEPP, INRA, AGROCAMPUS OUEST, Université Rennes, Le Rheu, France.

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