Literature DB >> 18604649

Testate amoebae (Arcellinida and Euglyphida) vs. Ericoid mycorrhizal and DSE fungi: a possible novel interaction in the mycorrhizosphere of ericaceous plants?

M Vohník1, Z Burdíková, J Albrechtová, M Vosátka.   

Abstract

Common occurrence of testate amoebae (TA) in the rhizosphere of mycorrhizal plants indicates existence of yet undocumented ecological interactions, involving three distinct groups of organisms: soil protists, mycorrhizal fungi, and their host plants. This tripartite relationship was to date investigated only to a limited extent, despite its probable importance for processes taking place in the mycorrhizosphere. In this study, we (1) explored spectra of different TA genera naturally associated with the rhizoplane of three autochthonous European Rhododendron species, (2) screened natural fungal colonization of the TA shells occupying the rhizoplane of selected rhododendrons, and (3) carried out two in vitro experiments addressing the question whether TA shells may serve as a nutrient source for ericoid mycorrhizal fungi (ErMF) and dark septate endophytes (DSE). Our field observations indicated that TA regularly associated with the rhizoplane of all screened rhododendrons and that ErMF and/or DSE associated with their roots possibly exploited the TA shells as a nutrient source. We were unable to detect any major differences among the TA spectra from the rhizoplanes with respect to the three Rhododendron species. The spectra were dominated by Diplochlamys, Centropyxis, Cyclopyxis, Euglypha, Trinema, and Assulina. Positive, neutral, and negative associations were found for various TA genera x Rhododendron species combinations. The highest fungal colonization was observed in Centropyxidae and Trigonopyxidae, reaching up to 45% of the shells in the case of Trigonopyxis. In the in vitro experiments, both ErMF Rhizoscyphus ericae and DSE Phialocephala fortinii regularly colonized TA shells, utilizing them as a source of nutrients. We hypothesize a complex relationship between ErMF-DSE and TA. If corroborated, it would represent an interesting nutrient loop in the mycorrhizosphere of ericaceous plants.

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Year:  2008        PMID: 18604649     DOI: 10.1007/s00248-008-9402-y

Source DB:  PubMed          Journal:  Microb Ecol        ISSN: 0095-3628            Impact factor:   4.552


  6 in total

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Authors: 
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4.  Inhibition of seedling survival under Rhododendron maximum (Ericaceae): could allelopathy be a cause?

Authors:  E T Nilsen; J F Walker; O K Miller; S W Semones; T T Lei; B D Clinton
Journal:  Am J Bot       Date:  1999-11       Impact factor: 3.844

5.  Evidence for subdivision of the root-endophyte Phialocephala fortinii into cryptic species and recombination within species.

Authors:  Christoph R Grünig; Bruce A McDonald; Thomas N Sieber; Scott O Rogers; Ottmar Holdenrieder
Journal:  Fungal Genet Biol       Date:  2004-07       Impact factor: 3.495

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Authors:  M Vohník; M Fendrych; J Albrechtová; M Vosátka
Journal:  Folia Microbiol (Praha)       Date:  2007       Impact factor: 2.629

  6 in total
  7 in total

1.  Ecology of testate amoebae in the Komořany ponds in the Vltava Basin.

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Journal:  Microb Ecol       Date:  2012-07       Impact factor: 4.552

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Authors:  Martin Vohník; Zuzana Burdíková; Aleš Vyhnal; Ondřej Koukol
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Authors:  Martin Vohník; Jesse J Sadowsky; Petr Kohout; Zuzana Lhotáková; Rolf Nestby; Miroslav Kolařík
Journal:  PLoS One       Date:  2012-06-25       Impact factor: 3.240

6.  Improved endoglucanase production and mycelial biomass of some ericoid fungi.

Authors:  O R Adeoyo; B I Pletschke; J F Dames
Journal:  AMB Express       Date:  2017-01-03       Impact factor: 3.298

7.  Statistical analysis of co-occurrence patterns in microbial presence-absence datasets.

Authors:  Kumar P Mainali; Sharon Bewick; Peter Thielen; Thomas Mehoke; Florian P Breitwieser; Shishir Paudel; Arjun Adhikari; Joshua Wolfe; Eric V Slud; David Karig; William F Fagan
Journal:  PLoS One       Date:  2017-11-16       Impact factor: 3.240

  7 in total

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