Comparative Analysis of Two Neighboring Conducive and Suppressive Soils Toward Plant Parasitism Caused by Phelipanche ramosa on Brassica napus

被引:0
作者
Martinez, Lisa [1 ]
Pouvreau, Jean-Bernard [1 ]
Jestin, Christophe [2 ]
Montiel, Gregory [1 ]
Gravot, Antoine [3 ]
Berardocco, Solenne [3 ,4 ]
Marnet, Nathalie [4 ]
Bouchereau, Alain [3 ,4 ,5 ]
Delage, Erwan [6 ]
Simier, Philippe [1 ]
Poulin, Lucie [1 ]
机构
[1] Nantes Univ, CNRS, US2B, UMR 6286, F-44000 Nantes, France
[2] INRAE, Terres Inovia, F-35650 Le Rheu, France
[3] Univ Rennes, Inst Genet Environm & Plant Protect IGEPP, Natl Res Inst Agr Food & Environm INRAE, Inst Agro, F-35650 Le Rheu, France
[4] Natl Res Inst Agr Food & Environm INRAE, Biopolymers Interact Assemblies, Metab Profiling & Metabol Platform P2M2, F-35650 Le Rheu, France
[5] MetaboHUB, Natl Infrastructure Metabol & Flux, Toulouse, France
[6] Nantes Univ, IMT Atlantique, Ecole Cent Nantes, LS2N,UMR 6004,CNRS,INRIA, F-44000 Nantes, France
来源
PHYTOBIOMES JOURNAL | 2024年 / 8卷 / 04期
关键词
branched broomrape; metabolomics; metagenomics; parasitism suppression; rapeseed; soil microbiota; GERMINATION STIMULANTS; MICROBIAL-POPULATIONS; BROOMRAPE OROBANCHE; SEED-GERMINATION; L; POMEL; FUNGAL; STRIGOLACTONE; RHIZOSPHERE; INHIBITION; BIOCONTROL;
D O I
10.1094/PBIOMES-12-23-0140-R
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In Western France, rapeseed (Brassica napus) cultivation faces substantial yield losses due to the root holoparasitic plant Phelipanche ramosa. However, recent observations have shown a reduction in parasitism within previously heavily infested fields. This study investigates two neighboring rapeseed soils with distinct levels of parasitic infestation, considered suppressive and conducive. Using a cocultivation system of Brassica napus and P. ramosa, we comprehensively examined rhizosphere exudates, parasitic plant attachment, and rhizosphere soil microbiota. Our findings revealed that the suppressive soil effectively reduced parasitism by impeding broomrape attachment and development, as well as inducing necrosis of tubercles. This suppressive effect was specific to postattachment stages, leaving germination and haustoriogenesis preattachment stages unaffected. Analysis of microbial structures suggested that the suppression of parasitism is predominantly of fungal rather than bacterial origin. Correlation network analyses identified three groups of amplicon sequence variants (ASVs) associated with suppression. Notably, seven ASVs were inversely correlated with parasitic attachments, and only one ASV, identified as Berkeleyomyces, a necrotrophic fungus responsible for black root rot, was positively correlated with necrosis and was more abundant in the suppressive soil. This study demonstrates the contrasting parasitic plant development on two physicochemically similar soils, highlighting the central role of fungal dynamics in the rhizosphere. These results provide valuable insights into the mechanisms underlying soil-mediated suppression of P. ramosa, offering potential strategies for mitigating the impact of this root holoparasite on rapeseed yields in the region.
引用
收藏
页码:425 / 445
页数:21
相关论文
共 104 条
  • [51] The new nomenclature of Orobanche and Phelipanche
    Joel, D. M.
    [J]. WEED RESEARCH, 2009, 49 : 6 - 7
  • [52] A Novel Seimatosporium and Other Sporocadaceae Species Associated with Grapevine Trunk Diseases in Cyprus
    Kanetis, Loukas, I
    Taliadoros, Demetris
    Makris, Georgios
    Christoforou, Michalis
    [J]. PLANTS-BASEL, 2022, 11 (20):
  • [53] The soil microbiome modulates the sorghum root metabolome and cellular traits with a concomitant reduction of Striga infection
    Kawa, Dorota
    Thiombiano, Benjamin
    Shimels, Mahdere Z.
    Taylor, Tamera
    Walmsley, Aimee
    Vahldick, Hannah E.
    Rybka, Dominika
    Leite, Marcio F. A.
    Musa, Zayan
    Bucksch, Alexander
    Dini-Andreote, Francisco
    Schilder, Mario
    Chen, Alexander J.
    Daksa, Jiregna
    Etalo, Desalegn W.
    Tessema, Taye
    Kuramae, Eiko E.
    Raaijmakers, Jos M.
    Bouwmeester, Harro
    Brady, Siobhan M.
    [J]. CELL REPORTS, 2024, 43 (04):
  • [54] Incorporating 16S Gene Copy Number Information Improves Estimates of Microbial Diversity and Abundance
    Kembel, Steven W.
    Wu, Martin
    Eisen, Jonathan A.
    Green, Jessica L.
    [J]. PLOS COMPUTATIONAL BIOLOGY, 2012, 8 (10)
  • [55] Managing the plant microbiome for biocontrol fungi: examples from Hypocreales
    Kepler, Ryan M.
    Maul, Jude E.
    Rehner, Stephen A.
    [J]. CURRENT OPINION IN MICROBIOLOGY, 2017, 37 : 48 - 53
  • [56] Developing a thief: Haustoria formation in parasitic plants
    Kokla, Anna
    Melnyk, Charles W.
    [J]. DEVELOPMENTAL BIOLOGY, 2018, 442 (01) : 53 - 59
  • [57] Morphological Response of the Halophilic Fungal Genus Wallemia to High Salinity
    Kuncic, Marjetka Kralj
    Kogej, Tina
    Drobne, Damjana
    Gunde-Cimerman, Nina
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2010, 76 (01) : 329 - 337
  • [58] Revival of the genus Lentzea and proposal far Lechevalieria gen. nov.
    Labeda, DP
    Hatano, K
    Kroppenstedt, RM
    Tamura, T
    [J]. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY, 2001, 51 : 1045 - 1050
  • [59] Biological Control of Plant Pathogens: A Global Perspective
    Lahlali, Rachid
    Ezrari, Said
    Radouane, Nabil
    Kenfaoui, Jihane
    Esmaeel, Qassim
    El Hamss, Hajar
    Belabess, Zineb
    Barka, Essaid Ait
    [J]. MICROORGANISMS, 2022, 10 (03)
  • [60] WGCNA: an R package for weighted correlation network analysis
    Langfelder, Peter
    Horvath, Steve
    [J]. BMC BIOINFORMATICS, 2008, 9 (1)