Fungal community on decomposing leaf litter undergoes rapid successional changes

. 2013 Mar ; 7 (3) : 477-86. [epub] 20121011

Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid23051693

Fungi are considered the primary decomposers of dead plant biomass in terrestrial ecosystems. However, current knowledge regarding the successive changes in fungal communities during litter decomposition is limited. Here we explored the development of the fungal community over 24 months of litter decomposition in a temperate forest with dominant Quercus petraea using 454-pyrosequencing of the fungal internal transcribed spacer (ITS) region and cellobiohydrolase I (cbhI) genes, which encode exocellulases, to specifically address cellulose decomposers. To quantify the involvement of phyllosphere fungi in litter decomposition, the fungal communities in live leaves and leaves immediately before abscission were also analysed. The results showed rapid succession of fungi with dramatic changes in the composition of the fungal community. Furthermore, most of the abundant taxa only temporarily dominated in the substrate. Fungal diversity was lowest at leaf senescence, increased until month 4 and did not significantly change during subsequent decomposition. Highly diverse community of phyllosphere fungi inhabits live oak leaves 2 months before abscission, and these phyllosphere taxa comprise a significant share of the fungal community during early decomposition up to the fourth month. Sequences assigned to the Ascomycota showed highest relative abundances in live leaves and during the early stages of decomposition. In contrast, the relative abundance of sequences assigned to the Basidiomycota phylum, particularly basidiomycetous yeasts, increased with time. Although cellulose was available in the litter during all stages of decomposition, the community of cellulolytic fungi changed substantially over time. The results indicate that litter decomposition is a highly complex process mediated by various fungal taxa.

Zobrazit více v PubMed

Amann R, Ludwig W, Schleifer K. Phylogenetic identification and in situ detection of individual microbial cells without cultivation. Microbiol Rev. 1995;59:143–169. PubMed PMC

Amend AS, Seifert KA, Bruns TD. Quantifying microbial communities with 454 pyrosequencing: does read abundance count. Mol Ecol. 2010;19:5555–5565. PubMed

Aneja MK, Sharma S, Fleischmann F, Stich S, Heller W, Bahnweg G, et al. Microbial colonization of beech and spruce litter - influence of decomposition site and plant litter species on the diversity of microbial community. Microb Ecol. 2006;52:127–135. PubMed

Baldrian P.2008Enzymes of saprotrophic basidiomycetesIn: Boddy L, Frankland J, van West P (eds).Ecology of Saprotrophic Basidiomycetes Academic Press: New York; 19–41.

Baldrian P, Valášková V. Degradation of cellulose by basidiomycetous fungi. FEMS Microbiol Rev. 2008;32:501–521. PubMed

Baldrian P, Voříšková J, Dobiášová P, Merhautová V, Lisá L, Valášková V. Production of extracellular enzymes and degradation of biopolymers by saprotrophic microfungi from the upper layers of forest soil. Plant Soil. 2011;338:111–125.

Baldrian P, Kolařík M, Štursová M, Kopecký J, Valášková V, Větrovský T, et al. Active and total microbial communities in forest soil are largely different and highly stratified during decomposition. ISME J. 2012;6:248–258. PubMed PMC

Baldrian P, Šnajdr J, Merhautová V, Dobiášová P, Cajthaml T, Valášková V.(in press). Responses of the extracellular enzyme activities in hardwood forest to soil temperature and seasonality and the potential effects of climate change Soil Biol Biochemdoi:10.1016/j.soilbio.2012.01.020 DOI

Berg B, McClaugherty C, Santo AVD, Johnson D. Humus buildup in boreal forests: effects of litter fall and its N concentration. Can J Forest Res. 2001;31:988–998.

Boberg JB, Ihrmark K, Lindahl BD. Decomposing capacity of fungi commonly detected in Pinus sylvestris needle litter. Fungal Ecol. 2011;4:110–114.

Bodeker ITM, Nygren CMR, Taylor AFS, Olson A, Lindahl BD. ClassII peroxidase-encoding genes are present in a phylogenetically wide range of ectomycorrhizal fungi. ISME J. 2009;3:1387–1395. PubMed

Carrino-Kyker SR, Swanson AK. Temporal and spatial patterns of eukaryotic and bacterial communities found in vernal pools. Appl Environ Microbiol. 2008;74:2554–2557. PubMed PMC

de Boer W, Folman LB, Summerbell RC, Boddy L. Living in a fungal world: impact of fungi on soil bacterial niche development. FEMS Microbiol Rev. 2005;29:795–811. PubMed

Di Marino E, Scattolin L, Bodensteiner P, Agerer R. Sistotrema is a genus with ectomycorrhizal species - confirmation of what sequence studies already suggested. Mycol Prog. 2008;7:169–176.

Dickie IA, Fukami T, Wilkie JP, Allen RB, Buchanan PK. Do assembly history effects attenuate from species to ecosystem properties? A field test with wood-inhabiting fungi. Ecol Lett. 2012;15:133–141. PubMed

Dilly O, Bartsch S, Rosenbrock P, Buscot F, Munch JC. Shifts in physiological capabilities of the microbiota during the decomposition of leaf litter in a black alder (Alnus glutinosa (Gaertn.) L.) forest. Soil Biol Biochem. 2001;33:921–930.

Duong LM, McKenzie EHC, Lumyong S, Hyde KD. Fungal succession on senescent leaves of Castanopsis diversifolia in Doi Suthep-Pui National Park, Thailand. Fungal Divers. 2008;30:23–36.

Edgar RC. Search and clustering orders of magnitude faster than BLAST. Bioinformatics. 2010;26:2460–2461. PubMed

Edwards IP, Upchurch RA, Zak DR. Isolation of fungal cellobiohydrolase I genes from sporocarps and forest soils by PCR. Appl Environ Microbiol. 2008;74:3481–3489. PubMed PMC

Frankland JC. Fungal succession - unravelling the unpredictable. Mycol Res. 1998;102:1–15.

Hering TF. Fungal decomposition of oak leaf litter. Trans Brit Mycol Soc. 1967;50:267–273.

Jumpponen A, Jones KL. Seasonally dynamic fungal communities in the Quercus macrocarpa phyllosphere differ between urban and nonurban environments. New Phytol. 2009a;186:496–513. PubMed

Jumpponen A, Jones KL. Massively parallel 454 sequencing indicates hyperdiverse fungal communities in temperate Quercus macrocarpa phyllosphere. New Phytol. 2009b;184:438–448. PubMed

Kjoller A, Struwe S. Microfungi in ecosystems: fungal occurrence and activity in litter and soil. Oikos. 1982;39:289–422.

Koide K, Osono T, Takeda H. Colonization and lignin decomposition of Camellia japonica leaf litter by endophytic fungi. Mycoscience. 2005;46:280–286.

Korkama-Rajala T, Mueller MM, Pennanen T. Decomposition and fungi of needle litter from slow- and fast-growing norway spruce (Picea abies) clones. Microb Ecol. 2008;56:76–89. PubMed

Kubartova A, Ranger J, Berthelin J, Beguiristain T. Diversity and decomposing ability of Saprophytic fungi from temperate forest litter. Microb Ecol. 2009;58:98–107. PubMed

Li W, Godzik A. Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences. Bioinformatics. 2006;22:1658–1659. PubMed

Lindahl BD, Finlay RD. Activities of chitinolytic enzymes during primary and secondary colonization of wood by basidiomycetous fungi. New Phytol. 2006;169:389–397. PubMed

Melillo J, Aber J, Linkins A, Ricca A, Fry B, Nadelhoffer K. Carbon and nitrogen dynamics along the decay continuum: plant litter to soil organic matter. Plant Soil. 1989;115:189–198.

O‘Brien HE, Parrent JL, Jackson JA, Moncalvo JM, Vilgalys R. Fungal community analysis by large-scale sequencing of environmental samples. Appl Environ Microbiol. 2005;71:5544–5550. PubMed PMC

Osono T, Takeda H. Organic chemical and nutrient dynamics in decomposing beech leaf litter in relation to fungal ingrowth and succession during 3-year decomposition processes in a cool temperate deciduous forest in Japan. Ecol Res. 2001;16:649–670.

Osono T. Phyllosphere fungi on leaf litter of Fagus crenata: occurrence, colonization, and succession. Can J Bot. 2002;80:460–469.

Osono T. Colonization and succession of fungi during decomposition of Swida controversa leaf litter. Mycologia. 2005;97:589–597. PubMed

Osono T. Role of phyllosphere fungi of forest trees in the development of decomposer fungal communities and decomposition processes of leaf litter. Can J Microbiol. 2006;52:701–716. PubMed

Osono T. Ecology of ligninolytic fungi associated with leaf litter decomposition. Ecol Res. 2007;22:955–974.

Osono T, Hirose D, Fujimaki R. Fungal colonization as affected by litter depth and decomposition stage of needle litter. Soil Biol Biochem. 2006;38:2743–2752.

Osono T, Ishii Y, Takeda H, Seramethakun T, Khamyong S, To-Anun C, et al. Fungal succession and lignin decomposition on Shorea obutsa leaves in a tropical seasonal forest in northern Thailand. Fungal Divers. 2009;36:101–119.

Promputtha I, Lumyong S, Dhanasekaran V, McKenzie E, Hyde K, Jeewon R. A phylogenetic evaluation of whether endophytes become saprotrophs at host senescence. Microb Ecol. 2007;53:579–590. PubMed

Rajala T, Peltoniemi M, Hantula J, Mäkipää R, Pennanen T. RNA reveals a succession of active fungi during the decay of Norway spruce logs. Fungal Ecol. 2011;4:437–448.

Reeder J, Knight R. Rapidly denoising pyrosequencing amplicon reads by exploiting rank-abundance distributions. Nat Methods. 2010;7:668–669. PubMed PMC

Sadaka N, Ponge JF. Fungal colonization of phyllosphere and litter of Quercus rotundifolia Lam. in a holm oak forest (High Atlas, Morocco) Biol Fertil Soils. 2003;39:30–36.

Santamaría J, Bayman P. Fungal epiphytes and endophytes of coffee leaves (Coffea arabica) Microb Ecol. 2005;50:1–8. PubMed

Schneider T, Keiblinger KM, Schmid E, Sterflinger-Gleixner K, Ellersdorfer G, Roschitzki B, et al. Who is who in litter decomposition? Metaproteomics reveals major microbial players and their biogeochemical functions. ISME J. 2012;6:1749–1762. PubMed PMC

Slavikova E, Vadkertiova R, Vranova D. Yeasts colonizing the leaf surfaces. J Basic Microbiol. 2007;47:344–350. PubMed

Stone JK. Initiation and development of latent infections by Rhabdocline parkeri on Douglas-fir. Can J Bot. 1987;65:2614–2621.

Suto Y. Mycosphaerella chaenomelis sp. nov.: the teleomorph of Cercosporella sp., the causal fungus of frosty mildew in Chaenomeles sinensis, and its role as the primary infection source. Mycoscience. 1999;40:509–516.

Šnajdr J, Valášková V, Merhautová V, Herinková J, Cajthaml T, Baldrian P. Spatial variability of enzyme activities and microbial biomass in the upper layers of Quercus petraea forest soil. Soil Biol Biochem. 2008;40:2068–2075.

Šnajdr J, Cajthaml T, Valášková V, Merhautová V, Petránková M, Spetz P, et al. Transformation of Quercus petraea litter: successive changes in litter chemistry are reflected in differential enzyme activity and changes in the microbial community composition. FEMS Microbiol Ecol. 2011;75:291–303. PubMed

Štursová M, Žifčáková L, Leigh MB, Burgess R, Baldrian P. Cellulose utilisation in forest litter and soil: identification of bacterial and fungal decomposers. FEMS Microbiol Ecol. 2012;80:735–746. PubMed

Tang AMC, Jeewon R, Hyde KD. Succession of microfungal communities on decaying leaves of Castanopsis fissa. Can J Microbiol. 2005;51:967–974. PubMed

Tedersoo L, Nilsson RH, Abarenkov K, Jairus T, Sadam A, Saar I, et al. 454 Pyrosequencing and Sanger sequencing of tropical mycorrhizal fungi provide similar results but reveal substantial methodological biases. New Phytol. 2010;188:291–301. PubMed

Unterseher M, Schnittler M. Dilution-to-extinction cultivation of leaf-inhabiting endophytic fungi in beech (Fagus sylvatica L.) - different cultivation techniques influence fungal biodiversity assessment. Mycol Res. 2009;113:645–654. PubMed

Valášková V, Šnajdr J, Bittner B, Cajthaml T, Merhautová V, Hoffichter M, et al. Production of lignocellulose-degrading enzymes and degradation of leaf litter by saprotrophic basidiomycetes isolated from a Quercus petraea forest. Soil Biol Biochem. 2007;39:2651–2660.

Weber CF, Zak DR, Hungate BA, Jackson RB, Vilgalys R, Evans RD, et al. Responses of soil cellulolytic fungal communities to elevated atmospheric CO2 are complex and variable across five ecosystems. Environ Microbiol. 2011;13:2778–2793. PubMed

White TJ, Bruns TD, Lee SB, Taylor JW.1990Analysis of phylogenetic relationships by amplification and direct sequencing of ribosomal RNA genesIn: Innis MA, Gelfand DH, Sninsky JN, White TJ (eds).PCR Protocols: A Guide to Methods and Applications Academic Press: New York; 315–322.

Zhang P, Tian X, He X, Song F, Ren L, Jiang P. Effect of litter quality on its decomposition in broadleaf and coniferous forest. Eur J Soil Biol. 2008;44:392–399.

Žifčáková L, Dobiášová P, Kolářová Z, Koukol O, Baldrian P. Enzyme activities of fungi associated with Picea abies needles. Fungal Ecol. 2011;4:427–436.

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

Disruption of millipede-gut microbiota in E. pulchripes and G. connexa highlights the limited role of litter fermentation and the importance of litter-associated microbes for nutrition

. 2024 Sep 28 ; 7 (1) : 1204. [epub] 20240928

Functional similarity, despite taxonomical divergence in the millipede gut microbiota, points to a common trophic strategy

. 2024 Jan 29 ; 12 (1) : 16. [epub] 20240129

Plant community stability is associated with a decoupling of prokaryote and fungal soil networks

. 2023 Jun 22 ; 14 (1) : 3736. [epub] 20230622

Seasonal Shifts in Bacterial and Fungal Microbiomes of Leaves and Associated Leaf-Mining Larvae Reveal Persistence of Core Taxa Regardless of Diet

. 2023 Feb 14 ; 11 (1) : e0316022. [epub] 20230111

Amplified Drought Alters Leaf Litter Metabolome, Slows Down Litter Decomposition, and Modifies Home Field (Dis)Advantage in Three Mediterranean Forests

. 2022 Sep 30 ; 11 (19) : . [epub] 20220930

Fungi are more transient than bacteria in caterpillar gut microbiomes

. 2022 Sep 16 ; 12 (1) : 15552. [epub] 20220916

Fungal Community Development in Decomposing Fine Deadwood Is Largely Affected by Microclimate

. 2022 ; 13 () : 835274. [epub] 20220413

Forest Microhabitat Affects Succession of Fungal Communities on Decomposing Fine Tree Roots

. 2021 ; 12 () : 541583. [epub] 20210128

Root-Associated Fungal Communities From Two Phenologically Contrasting Silver Fir (Abies alba Mill.) Groups of Trees

. 2019 ; 10 () : 214. [epub] 20190305

Differences in the fungal communities nursed by two genetic groups of the alpine cushion plant, Silene acaulis

. 2018 Dec ; 8 (23) : 11568-11581. [epub] 20181121

Clearcutting alters decomposition processes and initiates complex restructuring of fungal communities in soil and tree roots

. 2018 Mar ; 12 (3) : 692-703. [epub] 20180115

Forest Soil Bacteria: Diversity, Involvement in Ecosystem Processes, and Response to Global Change

. 2017 Jun ; 81 (2) : . [epub] 20170412

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...