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Temporal dynamics of bacterial and fungal communities during the infection of Brassica rapa roots by the protist Plasmodiophora brassicae : The impact of a pathogen on the plant root and rhizosphere microbiota
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1522-2624(200008)163:4<381::aid-jpln381>3.0.co;2-7openalex-snapshot
Qualitative and quantitative analysis of water-soluble root exudates in relation to plant species and development
inferredcites →https://doi.org/10.1007/s001220051557openalex-snapshot
Mapping of one major gene and of QTLs involved in resistance to clubroot in Brassica napus
inferredcites →https://doi.org/10.1007/s00248-012-0132-9openalex-snapshot
Changes in Root Bacterial Communities Associated to Two Different Development Stages of Canola (Brassica napus L. var oleifera) Evaluated through Next-Generation Sequencing Technology
inferredcites →https://doi.org/10.1007/s002480000087openalex-snapshot
The Diversity of Archaea and Bacteria in Association with the Roots of Zea mays L.
inferredcites →https://doi.org/10.1007/s00344-009-9101-zopenalex-snapshot
Life Cycle of Plasmodiophora brassicae
inferredcites →https://doi.org/10.1007/s11104-007-9514-zopenalex-snapshot
Lorenz Hiltner, a pioneer in rhizosphere microbial ecology and soil bacteriology research
inferredcites →https://doi.org/10.1007/s11104-008-9568-6openalex-snapshot
The rhizosphere: a playground and battlefield for soilborne pathogens and beneficial microorganisms
inferredcites →https://doi.org/10.1007/s11104-008-9814-yopenalex-snapshot
Plant-driven selection of microbes
inferredcites →https://doi.org/10.1016/j.chom.2015.01.011openalex-snapshot
Structure and Function of the Bacterial Root Microbiota in Wild and Domesticated Barley
inferredcites →https://doi.org/10.1016/j.mycres.2009.09.008openalex-snapshot
A comparison of Olpidium isolates from a range of host plants using internal transcribed spacer sequence analysis and host range studies
inferredcites →https://doi.org/10.1016/j.rhisph.2017.11.004openalex-snapshot
Bacterial community structure associated with the addition of nitrogen and the dynamics of soluble carbon in the rhizosphere of canola (Brassica napus) grown in a Podzol
inferredcites →https://doi.org/10.1016/j.soilbio.2017.11.012openalex-snapshot
Ralstonia solanacearum pathogen disrupts bacterial rhizosphere microbiome during an invasion
inferredcites →https://doi.org/10.1016/j.tplants.2012.04.001openalex-snapshot
The rhizosphere microbiome and plant health
inferredcites →https://doi.org/10.1016/s0929-1393(99)00028-1openalex-snapshot
Phylogenetic diversity of bacterial communities differing in degree of proximity of Lolium perenne and Trifolium repens roots
inferredcites →https://doi.org/10.1023/a:1003997421340openalex-snapshot
Evaluation of French Brassica oleracea landraces for resistance to Plasmodiophora brassicae
inferredcites →https://doi.org/10.1038/hdy.2014.91openalex-snapshot
Improving soil bacterial taxa–area relationships assessment using DNA meta-barcoding
inferredcites →https://doi.org/10.1038/ismej.2015.41openalex-snapshot
Stability and succession of the rhizosphere microbiota depends upon plant type and soil composition
inferredcites →https://doi.org/10.1038/ismej.2015.82openalex-snapshot
Fungal invasion of the rhizosphere microbiome
inferredcites →https://doi.org/10.1038/ismej.2016.109openalex-snapshot
Root microbiota dynamics of perennial Arabis alpina are dependent on soil residence time but independent of flowering time
inferredcites →https://doi.org/10.1038/nature11237openalex-snapshot
Defining the core Arabidopsis thaliana root microbiome
inferredcites →https://doi.org/10.1038/nature11336openalex-snapshot
Revealing structure and assembly cues for Arabidopsis root-inhabiting bacterial microbiota
inferredcites →https://doi.org/10.1038/ncomms11362openalex-snapshot
Survival trade-offs in plant roots during colonization by closely related beneficial and pathogenic fungi
inferredcites →https://doi.org/10.1038/ncomms2431openalex-snapshot
Turnover of soil bacterial diversity driven by wide-scale environmental heterogeneity
inferredcites →https://doi.org/10.1038/nprot.2013.099openalex-snapshot
Count-based differential expression analysis of RNA sequencing data using R and Bioconductor
inferredcites →https://doi.org/10.1038/nrmicro2504openalex-snapshot
Microbial seed banks: the ecological and evolutionary implications of dormancy
inferredcites →https://doi.org/10.1038/nrmicro2910openalex-snapshot
Microbial life in the phyllosphere
inferredcites →https://doi.org/10.1038/s41396-018-0093-1openalex-snapshot
Disease-induced assemblage of a plant-beneficial bacterial consortium
inferredcites →https://doi.org/10.1038/srep28774openalex-snapshot
Unlocking the bacterial and fungal communities assemblages of sugarcane microbiome
inferredcites →https://doi.org/10.1046/j.1365-3059.1996.d01-155.xopenalex-snapshot
Variation for virulence on Brassica napus L. amongst Plasmodiophora brassicae collections from France and derived single‐spore isolates
inferredcites →https://doi.org/10.1046/j.1439-0434.2003.00744.xopenalex-snapshot
Pathotype Separation of Plasmodiophora brassicae by the Host Plant
inferredcites →https://doi.org/10.1073/pnas.1321597111openalex-snapshot
Quantitative divergence of the bacterial root microbiota in Arabidopsis thaliana relatives
inferredcites →https://doi.org/10.1073/pnas.1414592112openalex-snapshot
Structure, variation, and assembly of the root-associated microbiomes of rice
inferredcites →https://doi.org/10.1073/pnas.1616148114openalex-snapshot
Simplified and representative bacterial community of maize roots
inferredcites →https://doi.org/10.1073/pnas.92.10.4197openalex-snapshot
Molecular mechanisms of defense by rhizobacteria against root disease.
inferredcites →https://doi.org/10.1093/bioinformatics/btp616openalex-snapshot
edgeR : a Bioconductor package for differential expression analysis of digital gene expression data
inferredcites →https://doi.org/10.1093/jxb/erv466openalex-snapshot
The plant microbiome explored: implications for experimental botany
inferredcites →https://doi.org/10.1093/nar/gkn879openalex-snapshot
The Ribosomal Database Project: improved alignments and new tools for rRNA analysis
inferredcites →https://doi.org/10.1093/nar/gks1219openalex-snapshot
The SILVA ribosomal RNA gene database project: improved data processing and web-based tools
inferredcites →https://doi.org/10.1093/pcp/pcv127openalex-snapshot
Both the Jasmonic Acid and the Salicylic Acid Pathways Contribute to Resistance to the Biotrophic Clubroot AgentPlasmodiophora brassicaein Arabidopsis
inferredcites →https://doi.org/10.1094/mpmi-01-15-0016-ropenalex-snapshot
Linking Jasmonic Acid Signaling, Root Exudates, and Rhizosphere Microbiomes
inferredcites →https://doi.org/10.1111/1574-6976.12028openalex-snapshot
The rhizosphere microbiome: significance of plant beneficial, plant pathogenic, and human pathogenic microorganisms
inferredcites →https://doi.org/10.1111/j.1364-3703.2011.00729.xopenalex-snapshot
Plasmodiophora brassicae : a review of an emerging pathogen of the Canadian canola ( Brassica napus ) crop
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01650.xopenalex-snapshot
Dynamic of the genetic structure of bacterial and fungal communities at different developmental stages of Medicago truncatula Gaertn. cv. Jemalong line J5
inferredcites →https://doi.org/10.1111/j.1751-7915.2011.00307.xopenalex-snapshot
Molecular biomass and MetaTaxogenomic assessment of soil microbial communities as influenced by soil DNA extraction procedure
inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1111/jam.12946openalex-snapshot
A review: what is the spermosphere and how can it be studied?
inferredcites →https://doi.org/10.1111/nph.13312openalex-snapshot
The importance of the microbiome of the plant holobiont
inferredcites →https://doi.org/10.1126/science.aaa8764openalex-snapshot
Salicylic acid modulates colonization of the root microbiome by specific bacterial taxa
inferredcites →https://doi.org/10.1128/aem.01938-17openalex-snapshot
Identifying the Active Microbiome Associated with Roots and Rhizosphere Soil of Oilseed Rape
inferredcites →https://doi.org/10.1128/aem.03722-14openalex-snapshot
Emergence Shapes the Structure of the Seed Microbiota
inferredcites →https://doi.org/10.1128/aem.66.10.4356-4360.2000openalex-snapshot
PCR Primers That Amplify Fungal rRNA Genes from Environmental Samples
inferredcites →https://doi.org/10.1128/mmbr.00050-14openalex-snapshot
The Hidden World within Plants: Ecological and Evolutionary Considerations for Defining Functioning of Microbial Endophytes
inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120106openalex-snapshot
Structure and Functions of the Bacterial Microbiota of Plants
inferredcites →https://doi.org/10.1146/annurev-ecolsys-121415-032238openalex-snapshot
The Phyllosphere: Microbial Jungle at the Plant–Climate Interface
inferredcites →https://doi.org/10.1146/annurev.micro.62.081307.162918openalex-snapshot
Plant-Growth-Promoting Rhizobacteria
inferredcites →https://doi.org/10.1146/annurev.phyto.40.030402.110010openalex-snapshot
M ICROBIAL P OPULATIONS R ESPONSIBLE FOR S PECIFIC S OIL S UPPRESSIVENESS TO P LANT P ATHOGENS
inferredcites →https://doi.org/10.1186/gb-2010-11-3-r25openalex-snapshot
A scaling normalization method for differential expression analysis of RNA-seq data
inferredcites →https://doi.org/10.1371/journal.pone.0044279openalex-snapshot
Evaluation of the ISO Standard 11063 DNA Extraction Procedure for Assessing Soil Microbial Abundance and Community Structure
inferredcites →https://doi.org/10.1371/journal.pone.0056329openalex-snapshot
Bacterial Communities Associated with the Leaves and the Roots of Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0059859openalex-snapshot
Impact of Shortened Crop Rotation of Oilseed Rape on Soil and Rhizosphere Microbial Diversity in Relation to Yield Decline
inferredcites →https://doi.org/10.18637/jss.v069.i01openalex-snapshot
Least-Squares Means: The R Package lsmeans
inferredcites →https://doi.org/10.1890/0012-9658(2003)084[0511:caopca]2.0.co;2openalex-snapshot
CANONICAL ANALYSIS OF PRINCIPAL COORDINATES: A USEFUL METHOD OF CONSTRAINED ORDINATION FOR ECOLOGY
inferredcites →https://doi.org/10.3389/fevo.2018.00091openalex-snapshot
Influence of Belowground Herbivory on the Dynamics of Root and Rhizosphere Microbial Communities
inferredcites →https://doi.org/10.3389/fmicb.2014.00175openalex-snapshot
The impact of the pathogen Rhizoctonia solani and its beneficial counterpart Bacillus amyloliquefaciens on the indigenous lettuce microbiome
inferredcites →https://doi.org/10.3389/fmicb.2016.01314openalex-snapshot
Aboveground Whitefly Infestation-Mediated Reshaping of the Root Microbiota
inferredcites →https://doi.org/10.3389/fmicb.2017.01489openalex-snapshot
Crop Establishment Practices Are a Driver of the Plant Microbiota in Winter Oilseed Rape (Brassica napus)
inferredcites →https://doi.org/10.3389/fpls.2013.00165openalex-snapshot
The rhizosphere revisited: root microbiomics
inferredcites →https://doi.org/10.3389/fpls.2017.00132openalex-snapshot
Community Structure, Species Variation, and Potential Functions of Rhizosphere-Associated Bacteria of Different Winter Wheat (Triticum aestivum) Cultivars
inferredcites →https://doi.org/10.4014/jmb.1511.11058openalex-snapshot
Root Exudation by Aphid Leaf Infestation Recruits Root-Associated Paenibacillus spp. to Lead Plant Insect Susceptibility
inferredcites →https://doi.org/10.7717/peerj.3454openalex-snapshot
Ecophylogeny of the endospheric root fungal microbiome of co-occurring Agrostis stolonifera
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3390/microorganisms10040799openalex-snapshot
Three Preceding Crops Increased the Yield of and Inhibited Clubroot Disease in Continuously Monocropped Chinese Cabbage by Regulating the Soil Properties and Rhizosphere Microbial Community
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