ArticlePloS one2012
Mycorrhiza reduces adverse effects of dark septate endophytes (DSE) on growth of conifers.
Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.
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Who cites it
25 citing papers in PubMed.
- Effects of dark septate endophytic fungi on the performance of non-mycorrhizal cabbage plants under normal and low water conditions.Frontiers in microbiology · 2025Article
- Mycorrhizal and endophytic fungi structure forest below-ground symbiosis through contrasting but interdependent assembly processes.Environmental microbiome · 2024Article
- Novel epiphytic root-fungus symbiosis in the Indo-Pacific seagrass Thalassodendron ciliatum from the Red Sea.Mycorrhiza · 2024Article
- Mycorrhizal symbiosis and the nitrogen nutrition of forest trees.Applied microbiology and biotechnology · 2024Review
- Importance of Dark Septate Endophytes in Agriculture in the Face of Climate Change.Journal of fungi (Basel, Switzerland) · 2024Review
- Effects of root-colonizing fungi on pioneer Pinus thunbergii seedlings in primary successional volcanic mudflow on Kuchinoerabu Island, Japan.Mycorrhiza · 2024Article
- Effects of nursery production methods on fungal community diversity within soil and roots of Abies alba Mill.Scientific reports · 2023Article
- Morphogenesis and metabolomics reveal the compatible relationship amongMicrobiology spectrum · 2023Article
- Co-Inoculation with Arbuscular Mycorrhizal Fungi and Dark Septate Endophytes under Drought Stress: Synergistic or Competitive Effects on Maize Growth, Photosynthesis, Root Hydraulic Properties and Aquaporins?Plants (Basel, Switzerland) · 2023Article
- Contribution of Arbuscular Mycorrhizal and Endophytic Fungi to Drought Tolerance inPlants (Basel, Switzerland) · 2023Article
- Advances in the Role of Dark Septate Endophytes in the Plant Resistance to Abiotic and Biotic Stresses.Journal of fungi (Basel, Switzerland) · 2021Review
- Comparative genomics reveals dynamic genome evolution in host specialist ectomycorrhizal fungi.The New phytologist · 2021Article
- Article
- A shift from arbuscular mycorrhizal to dark septate endophytic colonization in Deschampsia flexuosa roots occurs along primary successional gradient.Mycorrhiza · 2017Article
- Article
- Tuber indicum shapes the microbial communities of ectomycorhizosphere soil and ectomycorrhizae of an indigenous tree (Pinus armandii).PloS one · 2017Article
- Globally distributed root endophyte Phialocephala subalpina links pathogenic and saprophytic lifestyles.BMC genomics · 2016Article
- Article
- Analysis of the Phialocephala subalpina Transcriptome during Colonization of Its Host Plant Picea abies.PloS one · 2016Article
- Composition of fungal soil communities varies with plant abundance and geographic origin.AoB PLANTS · 2015Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mycorrhizal roots are frequently colonized by fungi of the Phialocephala fortinii s.l.-Acephala applanata species complex (PAC). These ascomycetes are common and widespread colonizers of tree roots. Some PAC strains reduce growth increments of their hosts but are beneficial in protecting roots against pathogens. Nothing is known about the effects of PAC on mycorrhizal fungi and the PAC-mycorrhiza association on plant growth, even though these two fungal groups occur closely together in natural habitats. We expect reduced colonization rates and reduced negative effects of PAC on host plants if roots are co-colonized by an ectomycorrhizal fungus (ECM). Depending on the temperature regime interactions among the partners in this tripartite ECM-PAC-plant system might also change. To test our hypotheses, effects of four PAC genotypes (two pathogenic and two non-pathogenic on the Norway spruce), mycorrhization by Laccaria bicolor (strain S238N) and two temperature regimes (19°C and 25°C) on the biomass of the Douglas-fir (Pseudotsuga menziesii) and Norway spruce (Picea abies) seedlings were studied. Mycorrhization compensated the adverse effects of PAC on the growth of the Norway spruce at both temperatures. The growth of the Douglas-fir was not influenced either by PAC or mycorrhization at 19°C, but at 25°C mycorrhization had a similar protective effect as in the Norway spruce. The compensatory effects probably rely on the reduction of the PAC-colonization density by mycorrhizae. Temperature and the PAC strain only had a differential effect on the biomass of the Norway spruce but not on the Douglas-fir. Higher temperature reduced mycorrhization of both hosts. We conclude that ectomycorrhizae form physical and/or physiological barriers against PAC leading to reduced PAC-colonization of the roots. Additionally, our results indicate that global warming could cause a general decrease of mycorrhization making primary roots more accessible to other symbionts and pathogens.
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