Skip to main content
Log in

An in vivo whole-plant experimental system for the analysis of gene expression in extraradical mycorrhizal mycelium

  • Original Article
  • Published:
Mycorrhiza Aims and scope Submit manuscript

Abstract

Arbuscular mycorrhizal fungi (AMF) establish beneficial mutualistic symbioses with land plants, receiving carbon in exchange for mineral nutrients absorbed by the extraradical mycelium (ERM). With the aim of obtaining in vivo produced ERM for gene expression analyses, a whole-plant bi-dimensional experimental system was devised and tested with three host plants and three fungal symbionts. In such a system, Funneliformis mosseae in symbiosis with Cichorium intybus var. foliosum, Lactuca sativa, and Medicago sativa produced ERM whose lengths ranged from 9.8 ± 0.8 to 20.8 ± 1.2 m per plant. Since ERM produced in symbiosis with C. intybus showed the highest values for the different structural parameters assessed, this host was used to test the whole-plant system with F. mosseae, Rhizoglomus irregulare, and Funneliformis coronatus. The whole-plant system yielded 1–7 mg of ERM fresh biomass per plant per harvest, and continued producing new ERM for 6 months. Variable amounts of high-quality and intact total RNA, ranging from 15 to 65 μg RNA/mg ERM fresh weight, were extracted from the ERM of the three AMF isolates. Ammonium transporter gene expression was successfully determined in the cDNAs obtained from ERM of the three fungal symbionts by RT-qPCR using gene-specific primers designed on available (R. irregulare) and new (F. mosseae and F. coronatus) ammonium transporter gene sequences. The whole-plant experimental system represents a useful research tool for large production and easy collection of ERM for morphological, physiological, and biochemical analyses, suitable for a wide variety of AMF species, for a virtually limitless range of host plants and for studies involving diverse symbiotic interactions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References

  • Allen JW, Shachar-Hill Y (2009) Sulfur transfer through an arbuscular mycorrhiza. Plant Physiol 149:549–560

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Aono T, Maldonado-Mendoza IE, Dewbre GR, Harrison MJ, Saito M (2004) Expression of alkaline phosphatase genes in arbuscular mycorrhizas. New Phytol 162:525–534

    Article  CAS  Google Scholar 

  • Aroca R, Bago A, Sutka M, Paz JA, Cano C, Amodeo G, Ruiz-Lozano JM (2009) Expression analysis of the first arbuscular mycorrhizal fungi aquaporin described reveals concerted gene expression between salt-stressed and nonstressed mycelium. Molecular Plant-microbe Interact 22:1169–1178

    Article  CAS  Google Scholar 

  • Bago B, Cano C (2005) Breaking myths on arbuscular mycorrhizas in vitro biology. In: Declerck S, Strullu DG, Fortin A (eds) In vitro culture of mycorrhizas. Soil biology series, vol. 4. Springer, Berlin, Heidelberg, New York, pp 111–138

  • Bago A, Cano C, Toussaint JP, Smith S, Dickson S (2006) Interactions between the arbuscular mycorrhizal (AM) fungus Glomus intraradices and nontransformed tomato roots of either wild-type or AM-defective phenotypes in monoxenic cultures. Mycorrhiza 16:429–436

  • Battini F, Cristani C, Giovannetti M, Agnolucci M (2016) Multifunctionality and diversity of culturable bacterial communities strictly associated with spores of the plant beneficial symbiont Rhizophagus intraradices. Microbiol Res 183:68–79

    Article  CAS  PubMed  Google Scholar 

  • Becard G, Fortin J (1988) Early events of vesicular-arbuscular mycorrhiza formation on Ri T-DNA transformed roots. New Phytol 108:211–218

  • Belmondo S, Fiorilli V, Pérez-Tienda J, Ferrol N, Marmeisse R, Lanfranco L (2014) A dipeptide transporter from the arbuscular mycorrhizal fungus Rhizophagus irregularis is upregulated in the intraradical phase. Frontiers Plant Sci 5:436

    Article  Google Scholar 

  • Benabdellah K, Merlos MÁ, Azcón-Aguilar C, Ferrol N (2009) GintGRX1, the first characterized glomeromycotan glutaredoxin, is a multifunctional enzyme that responds to oxidative stress. Fungal Genet Biol 46:94–103

    Article  CAS  PubMed  Google Scholar 

  • Benedetto A, Magurno F, Bonfante P, Lanfranco L (2005) Expression profiles of a phosphate transporter gene (GmosPT) from the endomycorrhizal fungus Glomus mosseae. Mycorrhiza 15:620–627

    Article  CAS  PubMed  Google Scholar 

  • Bidondo LF, Pergola M, Silvani M, Colombo R, Bompadre J, Godeas A (2012) Continuous and long-term monoxenic culture of the arbuscular mycorrhizal fungus Gigaspora decipiens in root organ culture. Fungal Biol 116:729–735

  • Breuninger M, Trujillo CG, Serrano E, Fischer R, Requena N (2004) Different nitrogen sources modulate activity but not expression of glutamine synthetase in arbuscular mycorrhizal fungi. Fungal Genet Biol 41:542–552

    Article  CAS  PubMed  Google Scholar 

  • Bütehorn B, Gianinazzi-Pearson V, Franken P (1999) Quantification of β-tubulin RNA expression during asymbiotic and symbiotic development of the arbuscular mycorrhizal fungus Glomus mosseae. Mycol Res 103:360–364

    Article  Google Scholar 

  • Calabrese S, Pérez-Tienda J, Ellerbeck M, Arnould C, Chatagnier O, Boller T, Schüßler A, Brachmann A, Wipf D, Ferrol N, Courty P-E (2016) GintAMT3—a low-affinity ammonium transporter of the arbuscular mycorrhizal Rhizophagus irregularis. Front Plant Sci 7:679

    Article  PubMed  PubMed Central  Google Scholar 

  • Cappellazzo G, Lanfranco L, Bonfante P (2007) A limiting source of organic nitrogen induces specific transcriptional responses in the extraradical structures of the endomycorrhizal fungus Glomus intraradices. Curr Genet 51:59–70

    Article  CAS  PubMed  Google Scholar 

  • Cappellazzo G, Lanfranco L, Fitz M, Wipf D, Bonfante P (2008) Characterization of an amino acid permease from the endomycorrhizal fungus Glomus mosseae. Plant Physiol 147:429–437

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Casieri L, Ait Lahmidi N, Doidy J, Veneault-Fourrey C, Migeon A, Bonneau L, Courty PE, Garcia K, Charbonnier M, Delteil A, Brun A, Zimmermann S, Plassard C, Wipf D (2013) Biotrophic transportome in mutualistic plant-fungal interactions. Mycorrhiza 23:597–625

    Article  CAS  PubMed  Google Scholar 

  • Cruz C, Egsgaard H, Trujillo C, Ambus P, Requena N, Martins-Loucao MA, Jakobsen I (2007) Enzymatic evidence for the key role of arginine in nitrogen translocation by arbuscular mycorrhizal fungi. Plant Physiol 144:782–792

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • de Souza FA, Declerck S (2017) Mycelium development and architecture, and spore production of in monoxenic culture with Ri T-DNA transformed carrot roots. Mycologia 95:1004–1012

  • Délano-Frier JP, Tejeda-Sartorius M (2008) Unraveling the network: novel developments in the understanding of signaling and nutrient exchange mechanisms in the arbuscular mycorrhizal symbiosis. Plant Signal Behav 3:936–944

    Article  PubMed  PubMed Central  Google Scholar 

  • Delp G, Timonen S, Rosewarne GM, Barker SJ, Smith S (2003) Differential expression of Glomus intraradices genes in external mycelium and mycorrhizal roots of tomato and barley. Mycol Res 107:1083–1093

    Article  CAS  PubMed  Google Scholar 

  • Fellbaum CR, Gachomo EW, Beesetty Y, Choudhari S, Strahan GD, Pfeffer PE, Kiers ET, Bücking H (2012) Carbon availability triggers fungal nitrogen uptake and transport in arbuscular mycorrhizal symbiosis. Proc Natl Acad Sci 109:2666–2671

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Fellbaum CR, Mensah JA, Cloos AJ, Strahan GE, Pfeffer PE, Kiers ET, Bücking H (2014) Fungal nutrient allocation in common mycorrhizal networks is regulated by the carbon source strength of individual host plants. New Phytol 203:646–656

    Article  CAS  PubMed  Google Scholar 

  • Fiorilli V, Lanfranco L, Bonfante P (2013) The expression of GintPT, the phosphate transporter of Rhizophagus irregularis, depends on the symbiotic status and phosphate availability. Planta 237:1267–1277

    Article  CAS  PubMed  Google Scholar 

  • Fiorilli V, Belmondo S, Khouja HR, Abbà S, Faccio A, Daghino S, Lanfranco L (2016) RiPEIP1, a gene from the arbuscular mycorrhizal fungus Rhizophagus irregularis, is preferentially expressed in planta and may be involved in root colonization. Mycorrhiza 26:609–621

    Article  CAS  PubMed  Google Scholar 

  • Giovannetti M, Sbrana C, Avio L, Strani P (2004) Patterns of belowground plant interconnections established by means of arbuscular mycorrhizal mycorrhizal networks. New Phytol 164:175–181

    Article  Google Scholar 

  • Giovannetti M, Avio L, Sbrana C (2015) Functional significance of anastomosis in arbuscular mycorrhizal networks. In: Horton TR (ed) Mycorrhizal networks, ecological studies 224. Springer Science+Business Media, Dordrecht

    Google Scholar 

  • González-Chávez MDCA, del Pilar Ortega-Larrocea M, Carrillo-González R, Lopez-Meyer M, Xoconostle-Cázares B, Gomez SK, Harrison MJ, Maldonado-Mendoza IE (2011) Arsenate induces the expression of fungal genes involved in As transport in arbuscular mycorrhiza. Fungal Biol 115:1197–1209

    Article  Google Scholar 

  • González-Guerrero M, Azcón-Aguilar C, Mooney M, Valderas A, MacDiarmid CW, Eide DJ, Ferrol N (2005) Characterization of a Glomus intraradices gene encoding a putative Zn transporter of the cation diffusion facilitator family. Fungal Genet Biol 42:130–140

    Article  PubMed  Google Scholar 

  • González-Guerrero M, Cano C, Azcón-Aguilar C, Ferrol N (2007) GintMT1 encodes a functional metallothionein in Glomus intraradices that responds to oxidative stress. Mycorrhiza 17:327–335

    Article  PubMed  Google Scholar 

  • González-Guerrero M, Benabdellah K, Valderas A, Azcón-Aguilar C, Ferrol N (2010a) GintABC1 encodes a putative ABC transporter of the MRP subfamily induced by Cu, Cd, and oxidative stress in Glomus intraradices. Mycorrhiza 20:137–146

    Article  PubMed  Google Scholar 

  • González-Guerrero M, Oger E, Benabdellah K, Azcón-Aguilar C, Lanfranco L, Ferrol N (2010b) Characterization of a CuZn superoxide dismutase gene in the arbuscular mycorrhizal fungus Glomus intraradices. Current Genet 56:265–274

    Article  Google Scholar 

  • Helber N, Wippel K, Sauer N, Schaarschmidt S, Hause B, Requena N (2011) A versatile monosaccharide transporter that operates in the arbuscular mycorrhizal fungus Glomus sp. is crucial for the symbiotic relationship with plants. Plant Cell 23:3812–3823

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lanfranco L, Novero M, Bonfante P (2005) The mycorrhizal fungus Gigaspora margarita possesses a CuZn superoxide dismutase that is up-regulated during symbiosis with legume hosts. Plant Physiol 137:1319–1330

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Li T, Hu YJ, Hao ZP, Li H, Chen BD (2013) Aquaporin genes GintAQPF1 and GintAQPF2 from Glomus intraradices contribute to plant drought tolerance. Plant Signal Behav 8:e24030

    Article  PubMed  PubMed Central  Google Scholar 

  • Liu Q, Parsons AJ, Xue H, Jones CS, Rasmussen S (2013) Functional characterisation and transcript analysis of an alkaline phosphatase from the arbuscular mycorrhizal fungus Funneliformis mosseae. Fungal Genet Biol 54:52–59

    Article  CAS  PubMed  Google Scholar 

  • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 25:402–408

    Article  CAS  PubMed  Google Scholar 

  • López-Pedrosa A, Gonzalez-Guerrero M, Valderas A, Azcon-Aguilar C, Ferrol N (2006) GintAMT1 encodes a functional high-affinity ammonium transporter that is expressed in the extraradical mycelium of Glomus intraradices. Fungal Genet Biol 43:102–110

    Article  PubMed  Google Scholar 

  • Maldonado-Mendoza IE, Dewbre GR, Harrison MJ (2001) A phosphate transporter gene from the extra-radical mycelium of an arbuscular mycorrhizal fungus Glomus intraradices is regulated in response to phosphate in the environment. Mol Plant-Microbe Interact 14:1140–1148

    Article  CAS  PubMed  Google Scholar 

  • Mikkelsen BL, Rosendahl S, Jakobsen I (2008) Underground resource allocation between individual networks of mycorrhizal fungi. New Phytol 180:890–898

    Article  PubMed  Google Scholar 

  • Olsson PA, Burleigh SH, Van Aarle IM (2005) The influence of external nitrogen on carbon allocation to Glomus intraradices in monoxenic arbuscular mycorrhiza. New Phytol 168:677–686

    Article  CAS  PubMed  Google Scholar 

  • Olsson PA, Hansson MC, Burleigh SH (2006) Effect of P availability on temporal dynamics of carbon allocation and Glomus intraradices high-affinity P transporter gene induction in arbuscular mycorrhiza. Appl Environ Microbiol 72:4115–4120

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Pepe A, Giovannetti M, Sbrana C (2016) Different levels of hyphal self-incompatibility modulate interconnectedness of mycorrhizal networks in three arbuscular mycorrhizal fungi within the Glomeraceae. Mycorrhiza 26:325–332

    Article  CAS  PubMed  Google Scholar 

  • Pérez-Tienda J, Testillano PS, Balestrini R, Fiorilli V, Azcón-Aguilar C, Ferrol N (2011) GintAMT2, a new member of the ammonium transporter family in the arbuscular mycorrhizal fungus Glomus intraradices. Fungal Genet Biol 48:1044–1055

    Article  PubMed  Google Scholar 

  • Porcel R, Aroca R, Cano C, Bago A, Ruiz-Lozano JM (2006) Identification of a gene from the arbuscular mycorrhizal fungus Glomus intraradices encoding for a 14-3-3 protein that is up-regulated by drought stress during the AM symbiosis. Microb Ecol 52:575–582

    Article  PubMed  Google Scholar 

  • Requena N, Mann P, Franken P (2000) A homologue of the cell cycle check point TOR2 from Saccharomyces cerevisiae exists in the arbuscular mycorrrhizal fungus Glomus mosseae. Protoplasma 212:89–98

    Article  CAS  Google Scholar 

  • Requena N, Mann P, Hampp R, Franken P (2002) Early developmentally regulated genes in the arbuscular mycorrhizal fungus Glomus mosseae: identification of GmGIN1, a novel gene with homology to the C-terminus of metazoan hedgehog proteins. Plant Soil 244:129–139

    Article  CAS  Google Scholar 

  • Rosikiewicz P, Bonvin J, Sanders IR (2017) Cost-efficient production of in vitro Rhizophagus irregularis. Mycorrhiza. doi:10.1007/s00572-017-0763-2

  • Sawaki H, Saito M (2001) Expressed genes in the extraradical hyphae of an arbuscular mycorrhizal fungus, Glomus intraradices, in the symbiotic phase. FEMS Microbiol Lett 195:109–113

    Article  CAS  PubMed  Google Scholar 

  • Seddas PM, Arnould C, Tollot M, Arias CM, Gianinazzi-Pearson V (2008) Spatial monitoring of gene activity in extraradical and intraradical developmental stages of arbuscular mycorrhizal fungi by direct fluorescent in situ RT-PCR. Fungal Genet Biol 45:1155–1165

    Article  CAS  PubMed  Google Scholar 

  • Sieverding E, da Silva GA, Berndt R, Oehl F (2015) Rhizoglomus, a new genus of the Glomeraceae. Mycotaxon 129:373–386

    Article  Google Scholar 

  • Smith SE, Read DJ (2008) Mycorrhizal symbiosis, 3rd edn. Academic, San Diego

    Google Scholar 

  • Sokolski S, Dalpé Y, Séguin S, Khasa D, Lévesque CA, Piché Y (2010) Conspecificity of DAOM 197198, the model AM fungus, with Glomus irregulare: molecular evidence with three protein-encoding genes. Botany 88:829–838

    Article  CAS  Google Scholar 

  • Tamayo E, Gómez-Gallego T, Azcón-Aguilar C, Ferrol N (2014) Genome wide analysis of copper, iron and zinc transporters in the arbuscular mycorrhizal fungus Rhizophagus irregularis. Front Plant Sci 5:547. doi:10.3389/fpls.2014.00547

    Article  PubMed  PubMed Central  Google Scholar 

  • Tian CB, Kasiborski KR, Lammers PJ, Bucking H, Shachar-Hill Y (2010) Regulation of the nitrogen transfer pathway in the arbuscular mycorrhizal symbiosis: gene characterization and the coordination of expression with nitrogen flux. Plant Physiol 153:1175–1187

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tisserant E, Kohler A, Dozolme-Seddas P, Balestrini R, Benabdellah K, Colard A, Croll D, Da Silva C, Gomez SK, Koul R, Ferrol N, Fiorilli V, Formey D, Franken P, Helber N, Hijri M, Lanfranco L, Lindquist E, Liu Y, Malbreil M, Morin E, Poulain J, Shapiro H, van Tuinen D, Waschke A, Azcón-Aguilar C, Bécard G, Bonfante P, Harrison MJ, Küster H, Lammers P, Paszkowski U, Requena N, Rensing SA, Roux C, Sanders IR, Shachar-Hill Y, Tuskan G, Young JPW, Gianinazzi-Pearson V, Martin F (2012) The transcriptome of the arbuscular mycorrhizal fungus Glomus intraradices (DAOM 197198) reveals functional tradeoffs in an obligate symbiont. New Phytol 193:755–769

    Article  CAS  PubMed  Google Scholar 

  • Ubalijoro E, Hamel C, McClung CR, Smith DL (2001) Detection of chitin synthase class I and II type sequences in six different arbuscular mycorrhizal fungi and gene expression in Glomus intraradices. Mycol Res 105:470–476

    Article  CAS  Google Scholar 

  • Waschke A, Sieh D, Tamasloukht M, Fischer K, Mann P, Franken P (2006) Identification of heavy metal-induced genes encoding glutathione S-transferases in the arbuscular mycorrhizal fungus Glomus intraradices. Mycorrhiza 17:1–10

    Article  CAS  PubMed  Google Scholar 

  • Young JPW (2015) Genome diversity in arbuscular mycorrhizal fungi. Curr Opin Plant Biol 26:113–119

    Article  CAS  PubMed  Google Scholar 

  • Zhang L, Jiang C, Zhou J, Declerck S, Tian C, Feng G (2016) Increasing phosphorus concentration in the extraradical hyphae of Rhizophagus irregularis DAOM 197198 leads to a concomitant increase in metal minerals. Mycorrhiza 26:909–918

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

Financial support of University of Pisa and CNR is gratefully acknowledged. This paper was part of A. Pepe doctoral thesis work at the University of Pisa.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Manuela Giovannetti.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pepe, A., Sbrana, C., Ferrol, N. et al. An in vivo whole-plant experimental system for the analysis of gene expression in extraradical mycorrhizal mycelium. Mycorrhiza 27, 659–668 (2017). https://doi.org/10.1007/s00572-017-0779-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00572-017-0779-7

Keywords

Navigation