Article: Mycorrhiza

Reconstructing the evolutionary history of gypsy retrotransposons in the Périgord black truffle (Tuber melanosporum Vittad.) T Payen, C Murat, F Martin. Mycorrhiza, 1-11

Abstract

Truffles are ascomycete fungi belonging to genus Tuber, and they form ectomycorrhizal associations with trees and shrubs. Transposable elements constitute more than 50 % of the black Périgord truffle (Tuber melanosporum) genome, which are mainly class 1 gypsy retrotransposons, but their impact on its genome is unknown. The aims of this study are to investigate the diversity of gypsy retrotransposons in this species and their evolutionary history by analysing the reference genome and six resequenced genomes of different geographic accessions. Using the reverse transcriptase sequences, six different gypsy retrotransposon clades were identified. Tmt1 and Tmt6are the most abundant transposable elements, representing 14 and 13 % of the T. melanosporumgenome, respectively. Tmt6 showed a major burst of proliferation between 1 and 4 million years ago, but evidence of more recent transposition was observed. Except for Tmt2, the other clades tend to aggregate, and their mode of transposition excluded the master copy model. This suggests that each new copy has the same probability of transposing as other copies. This study provides a better view of the diversity and dynamic nature of gypsy retrotransposons in T. melanosporum. Even if the major gypsy retrotransposon bursts are old, some elements seem to have transposed recently, suggesting that they may continue to model the truffle genomes.

Seminar: Leticia Pérez Izquierdo

The next seminar will be given by Leticia Pérez Izquierdo. Her talk will be given in the seminar room of LGEF building at 1.30pm Friday the 25th. Leticia will talk about:
 
 “Factors structuring fungal communities in Mediterranean forest ecosystems »

Article: Tree Genetics and Genomes

Genetic diversity and genetic structure of black alder (Alnus glutinosa [L.] Gaertn) in the Belgium-Luxembourg-France cross-border area

Dominique Mingeot Claude HussonPatrick MertensBernard WatillonPierre BertinPhilippe Druart. Tree Genomics and Genomes

 

Abstract

Due to its beneficial effects on river ecosystems, black alder (Alnus glutinosa) is one of the tree species selected for planting on riverbanks in the cross-border area encompassing Wallonia in Belgium, Lorraine in France, and Luxembourg. The preservation of this species, however, is threatened by an invasive pathogen that particularly targets and kills young alder individuals. The objectives of this study were to characterize the genetic diversity and the genetic structure of A. glutinosa at this local level with the aim of assisting the conservation and replanting strategies and to determine if a germplasm collection comprising individuals from the same cross-border area captures the diversity present in the region. Nuclear simple sequence repeat (SSR) and chloroplastic DNA (cpDNA) markers were used to analyze four local wild populations and the germplasm collection which is representative of two river catchments and six legal provenance regions. Three populations distant from the studied area were also included. A panel of 14 nuclear SSR loci revealed high allelic diversity and very low differentiation among wild populations (mean FST = 0.014). The germplasm collection displayed a range of alleles that were representative of the different populations, and no significant differentiation between the germplasm collection and the local wild populations was observed, making this collection, as far as allelic diversity is concerned, suitable for providing trees for riverbank replanting programs. Using SSR markers, various statistical approaches consistently indicated the lack of a significant geographical structure at the level of the river catchments or provenance regions. In contrast, two cpDNA haplotypes were detected and displayed a cross-border geographically structured distribution that could be taken into account in defining new cross-border provenance regions.

Seminar: David Barker

We will receive the visit of David Barker from Plant Microorganism Interaction Lab in Toulouse next thursday and friday. D. Barker will give a talk the 11th  (Friday) at 1.30pm in the LGEF meeting room. His talk will be about:
“Cell signaling and remodeling during initial stages of root endosymbiotic colonization »

Article: PLoS ONE

Impact of Phanerochaete chrysosporium on the Functional Diversity of Bacterial Communities Associated with Decaying Wood Hervé Vincent, Ketter Elodie, Pierrat Jean-Claude, Gelhaye Eric, Frey-Klett Pascale. PLoS ONE 1 (11), e0147100

Abstract

Bacteria and fungi naturally coexist in various environments including forest ecosystems. While the role of saprotrophic basidiomycetes in wood decomposition is well established, the influence of these fungi on the functional diversity of the wood-associated bacterial communities has received much less attention. Based on a microcosm experiment, we tested the hypothesis that both the presence of the white-rot fungus Phanerochaete chrysosporium and the wood, as a growth substrate, impacted the functional diversity of these bacterial communities. Microcosms containing sterile sawdust were inoculated with a microbial inoculum extracted from a forest soil, in presence or in absence of Pchrysosporium and subsequently, three enrichment steps were performed. First, bacterial strains were isolated from different microcosms previously analyzed by 16S rRNA gene-based pyrosequencing. Strains isolated from Pchrysosporium mycosphere showed less antagonism against this fungus compared to the strains isolated from the initial forest soil inoculum, suggesting a selection by the fungus of less inhibitory bacterial communities. Moreover, the presence of the fungus in wood resulted in a selection of cellulolytic and xylanolytic bacterial strains, highlighting the role of mycospheric bacteria in wood decomposition. Additionally, the proportion of siderophore-producing bacteria increased along the enrichment steps, suggesting an important role of bacteria in iron mobilization in decaying-wood. Finally, taxonomic identification of 311 bacterial isolates revealed, at the family level, strong similarities with the high-throughput sequencing data as well as with other studies in terms of taxonomic composition of the wood-associated bacterial community, highlighting that the isolated strains are representative of the wood-associated bacterial communities.

Article: Frontiers in Plant Science

The poplar Rust-Induced Secreted Protein (RISP) inhibits the growth of the leaf rust pathogen Melampsora larici-populina and triggers cell culture alkalinisation B Petre, A Hecker, H Germain, P Tsan, J Sklenar, G Pelletier, A Séguin, … Frontiers in Plant Science 7, 97

Abstract

Plant cells secrete a wide range of proteins in extracellular spaces in response to pathogen attack. The poplar Rust-Induced Secreted Protein (RISP) is a small cationic protein of unknown function that was identified as the most induced gene in poplar leaves during immune responses to the leaf rust pathogen Melampsora larici-populina, an obligate biotrophic parasite. Here, we combined in planta and in vitro molecular biology approaches to tackle the function of RISP. Using a RISP-mCherry fusion transiently expressed in Nicotiana benthamiana leaves, we demonstrated that RISP is secreted into the apoplast. A recombinant RISP specifically binds to M. larici-populina urediniospores and inhibits their germination. It also arrests the growth of the fungus in vitro and on poplar leaves. Interestingly, RISP also triggers poplar cell culture alkalinisation and is cleaved at the C-terminus by a plant-encoded mechanism. Altogether our results indicate that RISP is an antifungal protein that has the ability to trigger cellular responses.

MetaMicrobial Environmental Genomics

A new book of the series:  “Methods in Molecular Biology ” (Volume 1399 2016) entitled “MetaMicrobial Environmental Genomics” has been edited by F. Martin and S. Uroz

One chapter entitled :”Identification and in situ Distribution of a Fungal Gene Marker: The Mating Type Genes of the Black Truffle” has been written by H. De la Varga and C. Murat

Article: Mycorrhiza

Temporal changes of bacterial communities in the Tuber melanosporum ectomycorrhizosphere during ascocarp development. A Deveau, S Antony-Babu, F Le Tacon, C Robin, P Frey-Klett, S Uroz. Mycorrhiza, 1-11

Abstract

Ectomycorrhizae create a multitrophic ecosystem formed by the association between tree roots, mycelium of the ectomycorrhizal fungus, and a complex microbiome. Despite their importance in the host tree’s physiology and in the functioning of the ectomycorrhizal symbiosis, detailed studies on ectomycorrhiza-associated bacterial community composition and their temporal dynamics are rare. Our objective was to investigate the composition and dynamics of Tuber melanosporumectomycorrhiza-associated bacterial communities from summer to winter seasons in a Corylus avellana tree plantation. We used 16S ribosomal RNA (rRNA)-based pyrosequencing to compare the bacterial community structure and the richness in T. melanosporum’s ectomycorrhizae with those of the bulk soil. The T. melanosporum ectomycorrhizae harbored distinct bacterial communities from those of the bulk soil, with an enrichment in Alpha- and Gamma-proteobacteria. In contrast to the bacterial communities of truffle ascocarps that vastly varies in composition and richness during the maturation of the fruiting body and to those from the bulk soil, T. melanosporum ectomycorrhiza-associated bacterial community composition stayed rather stable from September to January. Our results fit with a recent finding from the same experimental site at the same period that a continuous supply of carbohydrates and nitrogen occurs from ectomycorrhizae to the fruiting bodies during the maturation of the ascocarps. We propose that this creates a stable niche in the ectomycorrhizosphere although the phenology of the tree changes.

Article: Plant, Cell & Environnement

The redox control of photorespiration: from biochemical and physiological aspects to biotechnological considerations. O Keech, P Gardeström, LA Kleczkowski, N Rouhier. Plant, Cell & Environment

 Abstract

Photorespiration is a complex and tightly regulated process occurring in photosynthetic organisms. This process can alter the cellular redox balance, notably via the production and consumption of both reducing and oxidizing equivalents. Under certain circumstances, these equivalents, as well as reactive oxygen or nitrogen species, can become prominent in subcellular compartments involved in the photorespiratory process, eventually promoting oxidative post-translational modifications of proteins. Keeping these changes under tight control should therefore be of primary importance. In order to review the current state of knowledge about the redox control of photorespiration, we primarily performed a careful description of the known and potential redox-regulated or oxidation sensitive photorespiratory proteins, and examined in more details two interesting cases: the glycerate kinase and the glycine cleavage system. When possible, the potential impact and subsequent physiological regulations associated with these changes have been discussed. In a second part, we reviewed the extent to which photorespiration contributes to cellular redox homeostasis considering, in particular, the set of peripheral enzymes associated with the canonical photorespiratory pathway. Finally, some recent biotechnological strategies to circumvent photorespiration for future growth improvements are discussed in the light of these redox regulations.

AAP: Australie

Programme de Mobilité Scientifique de l’Ambassade de France en Australie

En 2016, l’Ambassade de France en Australie propose un programme d’aide à la mobilité des chercheurs entre la France et l’Australie. Ce programme a pour objectif de faciliter la naissance ou le développement de collaborations de recherche d’excellence entre les deux pays. Ouvert aux chercheurs de toutes nationalités travaillant en France dans toutes les disciplines, il concerne uniquement la prise en charge des billets d’avion aller-retour en la France et l’Australie.

 Critères d’éligibilité

  1. L’appel à candidatures est ouvert en priorité aux jeunes chercheurs (Doctorants, Post-Doctorants, enseignants chercheurs) qui répondent obligatoirement à l’un de ces trois critères :

    Faire une thèse en France, idéalement en cotutelle OU,

    Effectuer un séjour postdoctoral en France OU,

    Occuper un poste d’enseignant-chercheur dans une université ou de chercheur dans un organisme de recherche en France.

  1. Mener un projet de recherche qui implique au minimum un partenaire scientifique ou technologique australien, ET

Participer à la définition, au développement ou au suivi d’une collaboration de recherche bilatérale.

  1. Mener une recherche d’excellence attestée à travers l’originalité du sujet de recherche, la qualité de l’équipe de recherche, les perspectives de valorisation et de transfert de technologies.

Pour candidater, il suffit de retourner un formulaire d’inscription et un justificatif de votre situation professionnelle actuelle. La date limite de dépôt de candidature est fixée au 24 Janvier 2016.

Rendez-vous sur le site de l’Ambassade pour candidater : http://www.ambafrance-au.org/Programme-mobilite-scientifique-2016

Pour toute demande d’information, merci de contacter Thomas Biedermann à l’Ambassade de France

thomas.biedermann@diplomatie.gouv.fr