Arbuscular mycorrhizal dialogues: Do you speak 'plantish' or 'fungish'?

Trends in Plant Science

Volumn 20, Issue 3, 2015, Pages 150-154

  Bonfante, Paola ^a   Genre, Andrea ^a  

^a UNIVERSITY OF TURIN   (Italy)

Author keywords

Arbuscular mycorrhizal fungi; Chitin; Cutin monomers; Receptors; Signal molecules; Strigolactones

Indexed keywords

FUNGI; GLOMEROMYCOTA;

GLOMEROMYCOTA; GROWTH, DEVELOPMENT AND AGING; MICROBIOLOGY; MYCORRHIZA; PHYSIOLOGY; PLANT; PLANT DEVELOPMENT; SIGNAL TRANSDUCTION; SYMBIOSIS;

GLOMEROMYCOTA; MYCORRHIZAE; PLANT DEVELOPMENT; PLANTS; SIGNAL TRANSDUCTION; SYMBIOSIS;

EID: 84924071707     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2014.12.002     Document Type: Review

References (48)

1. Oldroyd G.E., et al. The rules of engagement in the legume-rhizobial symbiosis. Annu. Rev. Genet. 2011, 45:119-144.
2. Rogers C., Oldroyd G.E. Synthetic biology approaches to engineering the nitrogen symbiosis in cereals. J. Exp. Bot. 2014, 65:1939-1946.
3. Liang Y., et al. Non legumes respond to rhizobial Nod factors by suppressing the innate immune response. Science 2013, 341:1384-1387.
4. Lace B., et al. Gate crashing arbuscular mycorrhizas: in vivo imaging shows the extensive colonization of both symbionts by Trichoderma atroviride. Environ. Microbiol. Rep. 2014, Published online October 23, 2014. 10.1111/1758-2229.12221.
5. Bulgarelli D., et al. Structure and functions of the bacterial microbiota of plants. Annu. Rev. Plant Biol. 2013, 64:807-838.
6. Hayashi M., Parniske M. Symbiosis and pathogenesis: what determines the difference?. Curr. Opin. Plant Biol. 2014, 20:v-vi.
7. Nadal M., Paszkowski U. Polyphony in the rhizosphere: presymbiotic communication in arbuscular mycorrhizal symbiosis. Curr. Opin. Plant Biol. 2013, 16:473-479.
8. Bonfante P., Genre A. Plants and arbuscular mycorrhizal fungi: an evolutionary-developmental perspective. Trends Plant Sci. 2008, 13:492-498.
9. Matusova R., et al. The strigolactone germination stimulants of the plant-parasitic Striga and Orobanche spp. are derived from the carotenoid pathway. Plant Physiol. 2005, 139:920-934.
10. Akiyama K., et al. Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi. Nature 2005, 435:824-827.
11. Besserer A., et al. Strigolactones stimulate arbuscular mycorrhizal fungi by activating mitochondria. PLoS Biol. 2006, 4. Published online June 27, 2006. 10.1371/journal.pbio.0040226.
12. Brewer P.B., et al. Diverse roles of strigolactones in plant development. Mol. Plant 2013, 6:18-28.
13. Koltai H. Receptors, repressors, PINs: a playground for strigolactone signaling. Trends Plant Sci. 2014, 19:727-733.
14. Delaux P.M., et al. Origin of strigolactones in the green lineage. New Phytol. 2012, 195:857-871.
15. Kretzschmar T., et al. A petunia ABC protein controls strigolactone-dependent symbiotic signalling and branching. Nature 2012, 483:3-8.
16. Besserer A., et al. GR24, a synthetic analogue of strigolactones, stimulates the mitosis and growth of the arbuscular mycorrhizal fungus Gigaspora rosea by boosting its energy metabolism. Plant Physiol. 2008, 148:402-413.
17. Anca I.A., et al. The ftsZ gene of the endocellular bacterium 'Candidatus Glomeribacter gigasporarum' is preferentially expressed during the symbiotic phases of its host mycorrhizal fungus. Mol. Plant Microbe Interact. 2009, 22:302-310.
18. Moscatiello R., et al. The intracellular delivery of TAT-aequorin reveals calcium mediated sensing of environmental and symbiotic signals by the arbuscular mycorrhizal fungus Gigaspora margarita. New Phytol. 2014, 203:1012-1020.
19. 2+ spiking in Medicago truncatula roots and their production is enhanced by strigolactone. New Phytol. 2013, 198:190-202.
20. Tisserant E., et al. Genome of an arbuscular mycorrhizal fungus provides insight into the oldest plant symbiosis. Proc. Natl. Acad. Sci. U.S.A. 2013, 110:20117-20122.
21. Lin K., et al. Single nucleus genome sequencing reveals high similarity among nuclei of an endomycorrhizal fungus. PLoS Genet. 2014, 10. Published online January 9, 2014. 10.1371/journal.pgen.1004078.
22. Wang E., et al. A common signaling process that promotes mycorrhizal and oomycete colonization of plants. Curr. Biol. 2012, 4:2242-2246.
23. Murray J.D., et al. Signaling at the root surface: the role of cutin monomers in mycorrhization. Mol. Plant 2013, 6:1381-1383.
24. Kolattukudy P.E., et al. Surface signaling in pathogenesis. Proc. Natl. Acad. Sci. U.S.A. 1995, 92:4080-4087.
25. Sesma A., Osbourn A.E. The rice leaf blast pathogen undergoes developmental processes typical of root-infecting fungi. Nature 2004, 431:582-586.
26. Jeffree C.E. Structure and ontogeny of plant cuticles. Plant Cuticles: An Integrated Functional Approach 1996, 33-82. BIOS Scientific Publishers. G. Kerstiens (Ed.).
27. Dickman M.B., et al. A protein kinase from Colletotrichum trifolii is induced by plant cutin and is required for appressorium formation. Mol. Plant Microbe Interact. 2003, 16:411-421.
28. Navazio L., et al. A diffusible signal from arbuscular mycorrhizal fungi elicits a transient cytosolic calcium elevation in host plant cells. Plant Physiol. 2007, 144:673-681.
29. Calcagno C., et al. The exudate from an arbuscular mycorrhizal fungus induces nitric oxide accumulation in Medicago truncatula roots. Mycorrhiza 2012, 22:259-269.
30. 2+ spiking in the legume and nonlegume root epidermis. New Phytol. 2011, 189:347-355.
31. Kosuta S., et al. A diffusible factor from arbuscular mycorrhizal fungi induces symbiosis- specific MtENOD11 expression in roots of Medicago truncatula. Plant Physiol. 2003, 131:952-962.
32. Maillet F., et al. Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza. Nature 2011, 469:58-63.
33. Gutjahr C., et al. Presymbiotic factors released by the arbuscular mycorrhizal fungus Gigaspora margarita induce starch accumulation in Lotus japonicus roots. New Phytol. 2009, 183:53-61.
34. Czaja L.F., et al. Transcriptional responses towards diffusible signals from symbiotic microbes reveal MtNFP- and MtDMI3-dependent reprogramming of host gene expression by arbuscular mycorrhizal fungal lipochitooligosaccharides. Plant Physiol. 2012, 159:1671-1685.
35. Dénarié J., et al. Rhizobium lipo-chitooligosaccharide nodulation factors: signaling molecules mediating recognition and morphogenesis. Annu. Rev. Biochem. 1996, 65:503-535.
36. Liang Y., et al. Lipochitooligosaccharide recognition: an ancient story. New Phytol. 2014, 204:289-296.
37. Han Z., et al. Structural insight into the activation of plant receptor kinases. Curr. Opin. Plant Biol. 2014, 16:55-63.
38. Op den Camp R., et al. LysM-type mycorrhizal receptor recruited for Rhizobium symbiosis in the non-legume Parasponia. Science 2011, 331:909-912.
39. Tisserant E., et al. The transcriptome of the arbuscular mycorrhizal fungus Glomus intraradices (DAOM 197198) reveals functional tradeoffs in an obligate symbiont. New Phytol. 2011, 193:755-769.
40. Bonfante P., et al. Correlation between chitin distribution and cell wall morphology in the mycorrhizal fungus Glomus versiforme. Mycol. Res. 1990, 94:157-165.
41. Bonfante P. At the interface between mycorrhizal fungi and plants: the structural organization of cell walls, plasma membranes and cytoskeleton. The Mycota, IX: Fungal Associations 2001, 45-61. Springer. B. Hock (Ed.).
42. Miyata K., et al. The bifunctional plant receptor, OsCERK1, regulates both chitin-triggered immunity and arbuscular mycorrhizal symbiosis in rice. Plant Cell Physiol. 2014, 55:1864-1872.
43. Zamioudis C., Pieterse C.M.J. Modulation of host immunity by beneficial microbes. Mol. Plant Microbe Interact. 2012, 25:139-150.
44. Lohmann G.V., et al. Evolution and regulation of the Lotus japonicus LysM receptor gene family. Mol. Plant Microbe Interact. 2010, 23:510-521.
45. Nagahashi G., Douds D.D. The effects of hydroxy fatty acids on the hyphal branching of germinated spores of AM fungi. Fungal Biol. 2011, 115:351-358.
46. Feng F., et al. The crosstalk between chitin-induced defense and symbiosis. XVI International Congress on Molecular Plant-Microbe Interactions 2014.
47. Kloppholz S., et al. SA secreted fungal effector of Glomus intraradices promotes symbiotic biotrophy. Curr. Biol. 2011, 21:1204-1209.
48. Jones J.D.G., Dangl J.L. The plant immune system. Nature 2006, 444:323-329.