Effects of Sphagnum Leachate on Competitive Sphagnum Microbiome Depend on Species and Time

TitleEffects of Sphagnum Leachate on Competitive Sphagnum Microbiome Depend on Species and Time
Publication TypeJournal Article
Year of Publication2019
AuthorsHamard S., Robroek B.JM, Allard P.M, Signarbieux C., Zhou S.Z, Saesong T., de Baaker F., Buttler A., Chiapusio G., Wolfender J.L, Bragazza L., Jassey V.EJ
JournalFrontiers in MicrobiologyFrontiers in MicrobiologyFrontiers in Microbiology
Date PublishedSep
Type of ArticleArticle
ISBN Number1664-302X
Accession NumberWOS:000484516700001
Keywordsacid, allelopathy and allelochemicals, carbon, communities, dynamics, mass-spectrometry, metabolomics, microbial networks, Microbial respiration and biomass, Microbiology, peatland, plant competition, plant-exudates, secondary compounds, soil, soil food-web, testate amebas, vertical microdistribution

Plant specialized metabolites play an important role in soil carbon (C) and nutrient fluxes. Through anti-microbial effects, they can modulate microbial assemblages and associated microbial-driven processes, such as nutrient cycling, so to positively or negatively cascade on plant fitness. As such, plant specialized metabolites can be used as a tool to supplant competitors. These compounds are little studied in bryophytes. This is especially notable in peatlands where Sphagnum mosses can dominate the vegetation and show strong interspecific competition. Sphagnum mosses form carpets where diverse microbial communities live and play a crucial role in Sphagnum fitness by regulating C and nutrient cycling. Here, by means of a microcosm experiment, we assessed to what extent moss metabolites of two Sphagnum species (S. fallax and S. divinum) modulate the competitive Sphagnum microbiome, with particular focus on microbial respiration. Using a reciprocal leachate experiment, we found that interactions between Sphagnum leachates and microbiome are species-specific. We show that both Sphagnum leachates differed in compound richness and compound relative abundance, especially sphagnum acid derivates, and that they include microbial-related metabolites. The addition of S. divinum leachate on the S. fallax microbiome immediately reduced microbial respiration (-95%). Prolonged exposition of S. fallax microbiome to S. divinum leachate destabilized the food web structure due to a modulation of microbial abundance. In particular, leachate addition decreased the biomass of testate amoebae and rotifers but increased that of ciliates. These changes did not influence microbial CO2 respiration, suggesting that the structural plasticity of the food web leads to its functional resistance through the replacement of species that are functionally redundant. In contrast, S. fallax leachate neither affected S. divinum microbial respiration, nor microbial biomass. We, however, found that S. fallax leachate addition stabilized the food web structure associated to S. divinum by changing trophic interactions among species. The differences in allelopathic effects between both Sphagnum leachates might impact their competitiveness and affect species distribution at local scale. Our study further paves the way to better understand the role of moss and microbial specialized metabolites in peatland C dynamics.

Short TitleFront. Microbiol.Front. Microbiol.
Alternate JournalFront. Microbiol.