Endophytic bacterial communities of oilseed rape associate with genotype-specific resistance against Verticillium longisporum.


Journal

FEMS microbiology ecology
ISSN: 1574-6941
Titre abrégé: FEMS Microbiol Ecol
Pays: England
ID NLM: 8901229

Informations de publication

Date de publication:
01 01 2020
Historique:
received: 09 09 2019
accepted: 25 11 2019
pubmed: 27 11 2019
medline: 21 8 2020
entrez: 27 11 2019
Statut: ppublish

Résumé

Associations of endophytic bacterial community composition of oilseed rape (Brassica napus L.) with quantitative resistance against the soil-borne fungal pathogen Verticillium longisporum was assessed by 16S rRNA gene amplicon sequencing in roots and hypocotyls of four plant lines with contrasting genetic composition in regard to quantitative resistance reactions. The plant compartment was found to be the dominating driving factor for the specificity of bacterial communities in healthy plants. Furthermore, V. longisporum infection triggered a stabilization of phylogenetic group abundance in replicated samples suggesting a host genotype-specific selection. Genotype-specific associations with bacterial phylogenetic group abundance were identified by comparison of plant genotype groups (resistant versus susceptible) and treatment groups (healthy versus V. longisporum-infected) allowing dissection into constitutive and induced directional association patterns. Relative abundance of Flavobacteria, Pseudomonas, Rhizobium and Cellvibrio was associated with resistance/susceptibility. Relative abundance of Flavobacteria and Cellvibrio was increased in resistant genotypes according to their known ecological functions. In contrast, a higher relative abundance of Pseudomonas and Rhizobium, which are known to harbor many species with antagonistic properties to fungal pathogens, was found to be associated with susceptibility, indicating that these groups do not play a major role in genetically controlled resistance of oilseed rape against V. longisporum.

Identifiants

pubmed: 31769797
pii: 5643882
doi: 10.1093/femsec/fiz188
pii:
doi:

Substances chimiques

RNA, Ribosomal, 16S 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© FEMS 2019.

Auteurs

Stefanie P Glaeser (SP)

Department of Applied Microbiology, Justus Liebig University, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany.

Iulian Gabur (I)

Department of Plant Breeding, Justus Liebig University, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany.

Hossein Haghighi (H)

Department of Applied Microbiology, Justus Liebig University, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany.
Department of Life Sciences, University of Modena and Reggio Emilia, Via Kenedy 17/I, 42124 Reggio Emilia, Italy.

Jens-Ole Bartz (JO)

Department of Applied Microbiology, Justus Liebig University, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany.

Peter Kämpfer (P)

Department of Applied Microbiology, Justus Liebig University, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany.

Rod Snowdon (R)

Department of Plant Breeding, Justus Liebig University, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany.

Christian Obermeier (C)

Department of Plant Breeding, Justus Liebig University, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing
Animals Hemiptera Insect Proteins Phylogeny Insecticides
Populus Soil Microbiology Soil Microbiota Fungi
Amaryllidaceae Alkaloids Lycoris NADPH-Ferrihemoprotein Reductase Gene Expression Regulation, Plant Plant Proteins

Classifications MeSH