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This protocol aims to provide detailed procedures for collecting, fixing, and maintaining mycoheterotrophic plant samples, applying different microscopy techniques such as scanning and transmission electron microscopy, light, confocal, and fluorescence microscopy to study fungal colonization in plants tissues and seeds germinated with mycorrhizal fungi.
Structural botany is an indispensable perspective to fully understand the ecology, physiology, development, and evolution of plants. When researching mycoheterotrophic plants (i.e., plants that obtain carbon from fungi), remarkable aspects of their structural adaptations, the patterns of tissue colonization by fungi, and the morphoanatomy of subterranean organs can enlighten their developmental strategies and their relationships with hyphae, the source of nutrients. Another important role of symbiotic fungi is related to the germination of orchid seeds; all Orchidaceae species are mycoheterotrophic during germination and seedling stage (initial mycoheterotrophy), even the ones that photosynthesize in adult stages. Due to the lack of nutritional reserves in orchid seeds, fungal symbionts are essential to provide substrates and enable germination. Analyzing germination stages by structural perspectives can also answer important questions regarding the fungi interaction with the seeds. Different imaging techniques can be applied to unveil fungi endophytes in plant tissues, as are proposed in this article. Freehand and thin sections of plant organs can be stained and then observed using light microscopy. A fluorochrome conjugated to wheat germ agglutinin can be applied to the fungi and co-incubated with Calcofluor White to highlight plant cell walls in confocal microscopy. In addition, the methodologies of scanning and transmission electron microscopy are detailed for mycoheterotrophic orchids, and the possibilities of applying such protocols in related plants is explored. Symbiotic germination of orchid seeds (i.e., in the presence of mycorrhizal fungi) is described in the protocol in detail, along with possibilities of preparing the structures obtained from different stages of germination for analyses with light, confocal, and electron microscopy.
Structural research in botany, covering plant morphology and anatomy, is basic in understanding the whole organism1,2, and provides indispensable perspectives to integrate and contribute to knowledge regarding the ecology, physiology, development, and evolution of plants3. Methods in plant morphology and anatomy currently comprise protocols, equipment, and knowledge developed recently as well as more than a century ago2. The continuous execution and adaptation of classical methods (e.g., light microscopy) along with more recent techniques (e.g., confocal microsco....
1. Collecting, fixing, and maintaining samples
NOTE: Fully MH plants can usually be found in the dark forest understory12,13, mainly in humid and litter-abundant areas, whereas partially MH plants can be found in more open forests12,13. MH plants usually have well-developed subterranean organs in a variety of shapes and sizes.
Following the essential stages of fixing plant tissue yields cellular structures as similar as possible to the living state, considering the morphology, volume, and spatial organization of cellular components and tissues16. Observe such traits in the samples after chemical fixation (Figure 4). Figure 4C-F represents adequately fixed samples under light microscopy. Following the fixation procedures de.......
Image analyses in plant anatomy and morphology have an important potential to fulfil objectives and help understand the relationships between mycoheterotrophic plants and their indispensable fungal endophytes, as demonstrated by studies of subterranean organs6,40, structural analyses of symbiotic germination of seeds39, and aerial and reproductive structures41. Structural botany, despite having lost its prestige and.......
The authors have nothing to disclose.
The authors thank funding from FAEPEX and FAPESP (2015/26479-6). MPP thanks Capes for his master's degree scholarship (process 88887.600591/2021-00) and CNPq. JLSM thanks CNPq for productivity grants (303664/2020-7). The authors also thank the access to equipment and assistance provided by LME (Laboratory of Electron Microscopy - IB/Unicamp), INFABiC (National Institute of Science and Technology on Photonics Applied to Cell Biology - Unicamp), and LaBiVasc (Laboratory of Vascular Biology - DBEF/IB/Unicamp); LAMEB (UFSC) and Eliana de Medeiros Oliveira (UFSC) for contributions to cryoprotection protocol; LME for contributions to TEM protocol.
....Name | Company | Catalog Number | Comments |
Acetone | Sigma-Aldrich | 179124 | (for SEM stubs mounting) |
Agar-agar (AA) | Sigma-Aldrich | A1296 | (for seeds germination tests) |
Calcofluor White Stain | Sigma-Aldrich | 18909 | fluorescent dye (detects cellulose) |
Citrate Buffer Solution, 0.09M pH 4.8 | Sigma-Aldrich | C2488 | (for toluidine blue O staining) |
Conductive Double-Sided Carbon Tape | Fisher Scientific | 50-285-81 | (for SEM) |
Confocal Microscope | Zeiss | (any model) | |
Copper Grids | Sigma-Aldrich | G4776 | (for TEM) |
Critical-point dryer | Balzers | (any model) | |
Cryostat | Leica Biosystems | (any model) | |
Dissecting microscope | Leica Biosystems | (= stereomicroscope, any model) | |
Entellan | Sigma-Aldrich | 107960 | rapid mounting medium for microscopy |
Ethyl alcohol, pure (≥99.5%) | Sigma-Aldrich | 459836 | (= ethanol, for dehydration processes) |
Formaldehyde solution, 37% | Sigma-Aldrich | 252549 | (for NBF solution preparation) |
Formalin solution, neutral buffered, 10% | Sigma-Aldrich | HT501128 | histological tissue fixative |
Gelatin capsules for TEM | Fisher Scientific | 50-248-71 | (for resin polymerisation in TEM) |
Gelatin solution, 2% in H2O | Sigma-Aldrich | G1393 | (dilute for slides preparation - OCT adherence) |
Glutaraldehyde solution, 25% | Sigma-Aldrich | G6257 | (for Karnovsky’s solution preparation) |
HistoResin | Leica Biosystems | 14702231731 | glycol methacrylate (GMA) embedding kit |
Iodine | Sigma-Aldrich | 207772 | (for Lugol solution preparation) |
Lead(II) nitrate | Sigma-Aldrich | 228621 | Pb(NO3)2 (for TEM contrast staining) |
Light Microscope | Olympus | (any model) | |
LR White acrylic resin | Sigma-Aldrich | L9774 | hydrophilic acrylic resin for TEM |
Lugol solution | Sigma-Aldrich | 62650 | (for staining) |
Metal stubs for specimen mounts | Rave Scientific | (for SEM, different models) | |
Microtome | Leica Biosystems | manual rotary microtome or other model | |
Oatmeal agar (OMA) | Millipore | O3506 | (for seeds germination tests) |
OCT Compound, Tissue-Tek | Sakura Finetek USA | 4583 | embedding medium for frozen tissues |
Osmium tetroxide | Sigma-Aldrich | 201030 | OsO4 (for TEM postfixation) |
Parafilm M | Sigma-Aldrich | P7793 | sealing thermoplastic film |
Paraformaldehyde | Sigma-Aldrich | 158127 | (for Karnovsky’s solution preparation) |
Poly-L-lysine solution, 0.1% in H2O | Sigma-Aldrich | P8920 | (for slides preparation - OCT adherence) |
Poly-Prep Slides | Sigma-Aldrich | P0425 | poly-L-lysine coated glass slides |
Polyethylene Molding Cup Trays | Polysciences | 17177A-3 | (6x8x5 mm, for embbeding samples in GMA resin) |
Polyethylene Molding Cup Trays | Polysciences | 17177C-3 | (13x19x5 mm, for embbeding samples in GMA resin) |
Potassium iodide | Sigma-Aldrich | 221945 | (for Lugol solution preparation) |
Potato Dextrose Agar (PDA) | Millipore | 70139 | (for seeds germination tests) |
Scanning Electron Microscope | Jeol | (any model) | |
Silane [(3-Aminopropyl)triethoxysilane] | Sigma-Aldrich | A3648 | (for slides preparation - OCT adherence) |
Silane-Prep Slides | Sigma-Aldrich | S4651 | glass slides coated with silane |
Silica gel orange, granular | Supelco | 10087 | (for dessicating processes) |
Sodium cacodylate trihydrate | Sigma-Aldrich | C0250 | (for glutaraldehyde-sodium cacodylate buffer) |
Sodium hydroxide | Sigma-Aldrich | S5881 | NaOH (for Karnovsky’s solution preparation and TEM contrast staining) |
Sodium hypochlorite solution | Sigma-Aldrich | 425044 | NaClO (for seeds surface disinfection) |
Sodium phosphate dibasic, anhydrous | Sigma-Aldrich | 71640 | Na2HPO4 (for NBF solution and PB preparation) |
Sodium phosphate monobasic monohydrate | Sigma-Aldrich | S9638 | NaH2PO4·H2O (for NBF and PB) |
Sputter coater | Balzers | (any model) | |
Sucrose | Sigma-Aldrich | S0389 | C12H22O11 (for cryoprotection and germination test) |
Sudan III | Sigma-Aldrich | S4131 | (for staining) |
Sudan IV | Sigma-Aldrich | 198102 | (for staining) |
Sudan Black B | Sigma-Aldrich | 199664 | (for staining) |
Syringe | (3 mL, any brand, for TEM contrast staining) | ||
Syringe Filter Unit, Millex-GV 0.22 µm | Millipore | SLGV033R | PVDF, 33 mm, gamma sterilized (for TEM contrast staining) |
Tek Bond Super Glue 793 | Tek Bond Saint-Gobain | 78072720018 | liquid cyanoacrylate adhesive, medium viscosity |
Toluidine Blue O | Sigma-Aldrich | T3260 | (for staining) |
Transmission Electron Microscope | Jeol | (any model) | |
Triphenyltetrazolium chloride | Sigma-Aldrich | T8877 | (for the tetrazolium test in seeds germination) |
Trisodium citrate dihydrate | Sigma-Aldrich | S1804 | Na3(C6H5O7)·2H2O (for TEM contrast staining) |
Ultramicrotome | Leica Biosystems | (any model) | |
Uranyl acetate | Fisher Scientific | 18-607-645 | UO2(CH3COO)2 (for TEM contrast staining) |
Vacuum pump | (any model) | ||
Wheat Germ Agglutinin, Alexa Fluor 488 Conjugate | TermoFisher Scientific | W11261 | fluorescent dye-conjugated lectin (detects sialic acid and N-acetylglucosaminyl residues) |
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