Abstract

Photosynthetic orchids associate with mycorrhizal fungi that can be mostly ascribed to the “rhizoctonia” species complex. Rhizoctonias’ phylogenetic diversity covers a variety of ecological/nutritional strategies that include, beside the symbiosis establishment with host plants, endophytic and pathogenic associations with non-orchid plants or saprotrophic soil colonization. In addition, orchid mycorrhizal fungi (OMF) that establish a symbiotic relationship with an orchid host can later proliferate in browning and rotting orchid tissues. Environmental triggers and molecular mechanisms governing the switch leading to either a saprotrophic or a mycorrhizal behavior in OMF remain unclear. As the sequenced OMF genomes feature a wide range of genes putatively involved in the degradation of plant cell wall (PCW) components, we tested if these transitions may be correlated with a change in the expression of some PCW degrading enzymes. Regulation of several genes encoding PCW degrading enzymes was evaluated during saprotrophic growth of the OMF Tulasnella calospora on different substrates and under successful and unsuccessful mycorrhizal symbioses. Fungal gene expression in planta was investigated in two orchid species, the terrestrial Mediterranean Serapias vomeracea and the epiphytic tropical Cattleya purpurata. Although we only tested a subset of the CAZyme genes identified in the T. calospora genome, and we cannot exclude therefore a role for different CAZyme families or members inside a family, the results showed that the degradative potential of T. calospora is finely regulated during saprotrophic growth and in symbiosis, often with a different regulation in the two orchid species. These data pose novel questions about the role of fungal PCW degrading enzymes in the development of unsuccessful and successful interactions.

Highlights

  • Orchids associate with a diverse range of mycorrhizal fungi whose taxonomic position mainly correlates with the plant habitat and photosynthetic ability [1,2]

  • A±lt4h.o0ugSDh t)h. eAplethrcoeungthagtehoef apseyrmcebniotatgicealolyf gaseyrmmibniaotteicdaslleyedgserwmaisnhaitgedhesrefeodrsbwotahsSh. ivgohmeerrafocerabaontdh fSo.rvCo.mpeurrapcuearaatan,dthfeorraCte. pouf roprucrhaitda,ptrhoetorcaotremosf dorecvheildoppinrogtobceoyromnds dtheevePl3opstianggebweaysonhdightheer, Pin3bsottahgeorwchaisdhsipgehceier,s,infolbloowthinogrcshyimd bsipoetciciegse, rfmolilnoawtiionng. symbHioetaiclthgeyrmpriontaotcioonrm. s of C. purpurata developed into seedlings containing typical hyphal coils withiHneraolotht ycepllrso.toMcoyrcmorsrhoifzCal. rpouortpucroaltoandizeavteiolonpwedasinctoonfiseremdelidngbsycsotnaitnaiinnigngwtityhpitchael FhIyTpCh-aWl choeialst GweitrhminArgogoltutcienlilns.(MWyGcAor)rchoinzajulgraotoet, schoolowniinzgattihoenpwreassenccoenofifrmcheidtinbiyn sthtaeinfuinnggawl ictehlltwheallF(IFTiCg-uWrehSe1a)t

  • An intriguing question is whether the several genes coding for plant cell wall (PCW) degrading enzymes found in orchid mycorrhizal fungi (OMF) are needed mainly for saprotrophic growth or whether they play important functions in symbiosis

Read more

Summary

Introduction

Orchids associate with a diverse range of mycorrhizal fungi whose taxonomic position mainly correlates with the plant habitat and photosynthetic ability [1,2]. The environmental and/or molecular clues leading to the different outcomes of plant-fungus interactions are currently unknown It is unclear whether the occasional rotting protocorms are the results of the OMF killing the orchid host as a necrotroph, or whether the fungus overgrows dead plant tissues as a saprotroph. The T. calospora (isolate AL13/4D) genome contains about one hundred CAZymes-coding genes, more than its saprotrophic sister taxon Botryobasidium botryosum [17] Among these genes, several encode CAZymes and AAs involved in the degradation of plant cell wall (PCW) polysaccharides, including seven GH6 and twenty-seven GH7 (i.e., cellobiohydrolases with a role in the extensive saccharification of cellulose) in addition to thirty-three lytic polysaccharide monooxygenases (LPMOs) of the AA9 family [18]. A role of CAZymes during the development of the ectomycorrhizal (ECM) symbiosis has been suggested [19,20], and CAZymes may be needed to degrade the plant cell wall and to form intracellular fungal structures in endomycorrhizal associations [21]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call