Disease-induced assemblage of a plant-beneficial bacterial consortium

TY - JOUR

T1 - Disease-induced assemblage of a plant-beneficial bacterial consortium

AU - Berendsen, Roeland L.

AU - Vismans, Gilles

AU - Yu, Ke

AU - Song, Yang

AU - de Jonge, Ronnie

AU - Burgman, Wilco P

AU - Burmølle, Mette

AU - Herschend, Jakob

AU - Bakker, Peter A. H. M.

AU - Pieterse, Corné M. J.

PY - 2018/6/1

Y1 - 2018/6/1

N2 - Disease suppressive soils typically develop after a disease outbreak due to the subsequent assembly of protective microbiota in the rhizosphere. The role of the plant immune system in the assemblage of a protective rhizosphere microbiome is largely unknown. In this study, we demonstrate that Arabidopsis thaliana specifically promotes three bacterial species in the rhizosphere upon foliar defense activation by the downy mildew pathogen Hyaloperonospora arabidopsidis. The promoted bacteria were isolated and found to interact synergistically in biofilm formation in vitro. Although separately these bacteria did not affect the plant significantly, together they induced systemic resistance against downy mildew and promoted growth of the plant. Moreover, we show that the soil-mediated legacy of a primary population of downy mildew infected plants confers enhanced protection against this pathogen in a second population of plants growing in the same soil. Together our results indicate that plants can adjust their root microbiome upon pathogen infection and specifically recruit a group of disease resistance-inducing and growth-promoting beneficial microbes, therewith potentially maximizing the chance of survival of their offspring that will grow in the same soil.

AB - Disease suppressive soils typically develop after a disease outbreak due to the subsequent assembly of protective microbiota in the rhizosphere. The role of the plant immune system in the assemblage of a protective rhizosphere microbiome is largely unknown. In this study, we demonstrate that Arabidopsis thaliana specifically promotes three bacterial species in the rhizosphere upon foliar defense activation by the downy mildew pathogen Hyaloperonospora arabidopsidis. The promoted bacteria were isolated and found to interact synergistically in biofilm formation in vitro. Although separately these bacteria did not affect the plant significantly, together they induced systemic resistance against downy mildew and promoted growth of the plant. Moreover, we show that the soil-mediated legacy of a primary population of downy mildew infected plants confers enhanced protection against this pathogen in a second population of plants growing in the same soil. Together our results indicate that plants can adjust their root microbiome upon pathogen infection and specifically recruit a group of disease resistance-inducing and growth-promoting beneficial microbes, therewith potentially maximizing the chance of survival of their offspring that will grow in the same soil.

U2 - 10.1038/s41396-018-0093-1

DO - 10.1038/s41396-018-0093-1

M3 - Journal article

C2 - 29520025

SN - 1751-7362

VL - 12

SP - 1496

EP - 1507

JO - I S M E Journal

JF - I S M E Journal

ER -