{"id":10527,"date":"2020-07-16T13:02:45","date_gmt":"2020-07-16T13:02:45","guid":{"rendered":"https:\/\/mycor.iam.inrae.fr\/IAM\/?page_id=10527"},"modified":"2020-07-16T13:40:00","modified_gmt":"2020-07-16T13:40:00","slug":"metatranscriptomics-of-forest-soil-ecosystems","status":"publish","type":"page","link":"https:\/\/mycor.iam.inrae.fr\/IAM\/?page_id=10527","title":{"rendered":"Metatranscriptomics of Forest Soil Ecosystems"},"content":{"rendered":"<div>\n<img loading=\"lazy\" decoding=\"async\" title=\"IMG_2136\" src=\"https:\/\/mycor.iam.inrae.fr\/IAM\/wp-content\/uploads\/2020\/07\/IMG_21361-1024x380.jpg\" alt=\"\" width=\"524\" height=\"194\"><\/p>\n<p>Forest soils (including litter, humus and coarse woody debris) host  diverse microbial communities that impact tree health and productivity,  and which play pivotal roles in terrestrial carbon sequestration, and  biogeochemical cycles. Among these microbial communities, fungi are  undoubtly major players. Traditionally, they have been divided into  discrete ecological guilds, such as leaf litter-decomposers, humus  saprobes, white- and brown-rot wood decayers, parasites and mycorrhizal  symbionts. However, the actual functional properties of individual  species, and the synergistic effects among them, are often obscure.  Moreover, the basic biodiversity of the vast majority of soil systems  (e.g., boreal forests and subartic taiga) remains unexplored using  high-throughput DNA barcoding approaches.<\/p>\n<\/div>\n<p>We hypothesize that firm distinctions between fungi commonly labeled  mycorrhizal, wood decomposer, humus and litter saprobes are, in some  instances, unwarranted, and that crucial ecosystem processes, such as  carbon sequestration, wood and litter decay and trophic mutualism, can  only be understood in the context of interactions among multiple species  representing a functional continuum. The number of available fungal  genomes has expanded dramatically in recent months, and this provides  unprecedented opportunities to study the functional (and taxonomic)  diversity of soil communities.<\/p>\n<p>Within the framework of the <a href=\"http:\/\/www.jgi.doe.gov\/CSP\/index.html\" target=\"_blank\" rel=\"noopener noreferrer\">DOE Joint Genome Institute Community Sequencing Program<\/a>,  we have therefore embarked in a challenging large-scale  metatranscriptomics project to explore the interaction of forest trees  with communities of soil fungi, including ectomycorrhizal symbionts that  dramatically affect tree growth, and saprotrophic soil fungi impacting  carbon sequestration in forests. We are going to sequence the  metatranscriptome of soil fungi (i.e., wood decayers, litter and humus  saprotrophs, and ectomycorrhizal symbionts) in woody debris,  litter\/humus, rhizosphere and ectomycorrhizal roots of ecosystems  representative of major Earth biomes, the boreal, temperate and  mediterranean forests.<\/p>\n<p><em><img loading=\"lazy\" decoding=\"async\" class=\"alignleft\" title=\"IMG_2343\" src=\"https:\/\/mycor.iam.inrae.fr\/IAM\/wp-content\/uploads\/2020\/07\/IMG_2343-150x150.jpg\" alt=\"\" width=\"150\" height=\"150\">Metatranscriptome samples.<\/em> A range of forest ecosystems has been selected on the basis of their  ecological importance and the availability of metadata linked to these  forest sites. In contrast to agricultural soils, forest soils, in  particular those of boreal forests with low pH values, are characterised  by strong vertical stratification due to the resulting absence of fauna  causing mixing. This provides a spatial structure for evaluation of  hypotheses concerning functional attributes of taxa occupying spatially  distinct horizons.<\/p>\n<p>Sampling will be conducted on selected stands in long-term observatories (LTOs) or national survey sites:<\/p>\n<ul>\n<li>Boreal forests: <a href=\"http:\/\/www.lternet.edu\/sites\/bnz\/\" target=\"_blank\" rel=\"noopener noreferrer\">Bonanza Creek<\/a> (Alaska) and Siljansfors (Sweden).<\/li>\n<li>Temperate forests: <a href=\"http:\/\/www.biology.duke.edu\/fungi\/mycolab\/DFMO.html\" target=\"_blank\" rel=\"noopener noreferrer\">DOE long term studies at Duke Forest<\/a>, the post-fire stands at the <a href=\"http:\/\/www.fs.usda.gov\/wps\/portal\/fsinternet\/%21ut\/p\/c5\/04_SB8K8xLLM9MSSzPy8xBz9CP0os3gjAwhwtDDw9_AI8zPwhQoY6IeDdGCqCPOBqwDLG-AAjgb6fh75uan6BdnZaY6OiooA1tkqlQ%21%21\/dl3\/d3\/L2dJQSEvUUt3QS9ZQnZ3LzZfMjAwMDAwMDBBODBPSEhWTjBNMDAwMDAwMDA%21\/?ss=110103&amp;navtype=forestBean&amp;navid=091000000000000&amp;pnavid=null&amp;cid=null&amp;ttype=main&amp;pname=Bitterroot%20National%20Forest%20-%20Home\" target=\"_blank\" rel=\"noopener noreferrer\">Bitterroot National Forest<\/a> and Michigan maple N-deposition sites (USA), a  forest-woodland-grassland transect in Rollainville (France), and the  Breuil-Chenue plantation (France).<\/li>\n<li>Mediterranean forests at <a href=\"http:\/\/www.expeer.fr\/index.php?option=com_content&amp;view=article&amp;id=120&amp;Itemid=227\" target=\"_blank\" rel=\"noopener noreferrer\">Pu\u00e9chabon<\/a> near Montpellier (France) and at Aspurz south-western Pyrenees (Spain).<\/li>\n<\/ul>\n<p>For these soil samples, we will run: (1) Tag-encoded FLX-titanium  amplicon pyrosequencing (TEFAP) of the fungal rDNA ITS to survey the  existing communities and (2) RNA-Seq of soil samples. For this cDNA  profiling, we will sequence ~110Gbp per site for a total of 1 terabase  using Illumina HiSeq PE chemistry. Reads produced by RNA-Seq will be  used to reconstruct<em> de novo<\/em> the different fungal  metatranscriptomes (best case scenario). In addition, we will use  Illumina fragment recruitment, a process of aligning sequencing reads to  reference genomes. Metatranscriptomic reads will thus be aligned to the  &gt;100 genomes of soil fungi available in the<a href=\"http:\/\/genome.jgi-psf.org\/programs\/fungi\/index.jsf\" target=\"_blank\" rel=\"noopener noreferrer\"> JGI MycoCosm<\/a>.&nbsp;To  improve this crucial step, we also propose the gDNA sequencing and  RNA-Seq of the 25 most abundant fungal species harvested on the studied  sites to serve as the foundation for a reference database for  metagenomics of fungi and for a comprehensive survey of the potential  soil fungal metabolome. We will annotate the fungal  genomes\/transcriptomes and soil fungal metagenomes with all these  characteristics and will compare the different metagenomes in terms of  these characteristics.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignleft\" title=\"IMG_2321\" src=\"https:\/\/mycor.iam.inrae.fr\/IAM\/wp-content\/uploads\/2020\/07\/IMG_2321-150x150.jpg\" alt=\"\" width=\"150\" height=\"150\">These  experimental datasets will provide a mechanistic insight into the  fungal communities\u2019 structural organization and functioning in forests.  In addition, the present metagenomic data will give a comprehensive  picture of the organization of the tree-associated microbiome in terms  of metabolic pathways, subsystems, molecular functions and biological  processes.<\/p>\n<p>Sequencing of new fungal species will be performed in concert with  existing large-scale genome studies (e.g., the 1000 Fungal Genomes  project), so as to minimize unnecessary redundancies. As such we  recognize that this project represents a large effort and great  challenge in defining the microbiome of important forest ecosystems and a  group of micro-organisms, the soil fungi.<\/p>\n<p>The Consortium:&nbsp;Francis MARTIN,&nbsp;Scott BAKER, Dan CULLEN, Roger FINLAY, David HIBBETT,  Igor GRIGORIEV, Cheryl KUSKE, Roland MARMEISSE, Antonio  PISABARRO, Joey SPATAFORA, Jan STENLID &amp; Rytas VILGALYS<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Forest soils (including litter, humus and coarse woody debris) host diverse microbial communities that impact tree health and productivity, and which play pivotal roles in terrestrial carbon sequestration, and biogeochemical cycles. Among these microbial communities, fungi are undoubtly major players. &hellip; <a href=\"https:\/\/mycor.iam.inrae.fr\/IAM\/?page_id=10527\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":10523,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-10527","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/mycor.iam.inrae.fr\/IAM\/index.php?rest_route=\/wp\/v2\/pages\/10527","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/mycor.iam.inrae.fr\/IAM\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/mycor.iam.inrae.fr\/IAM\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/mycor.iam.inrae.fr\/IAM\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/mycor.iam.inrae.fr\/IAM\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=10527"}],"version-history":[{"count":0,"href":"https:\/\/mycor.iam.inrae.fr\/IAM\/index.php?rest_route=\/wp\/v2\/pages\/10527\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/mycor.iam.inrae.fr\/IAM\/index.php?rest_route=\/wp\/v2\/pages\/10523"}],"wp:attachment":[{"href":"https:\/\/mycor.iam.inrae.fr\/IAM\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=10527"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}