Improve Research Reproducibility A Bio-protocol resource
Peer-reviewed
tooltip

Histochemical Preparations to Depict the Structure of Cauliflower Leaf Hydathodes

用于研究花椰菜叶泌水孔结构的组织化学制备

AC Aude Cerutti
MA Marie-Christine Auriac
LN Laurent D. Noël
Alain Jauneau Alain Jauneau

发布: 2017年10月20日第7卷第20期 DOI: 10.21769/BioProtoc.2452 浏览次数: 8451

评审: Hiroyuki HiraiYunbing MaAnonymous reviewer(s)

download pdf PDF PDF
ask Q&A
引用
收藏
Cited by

参见作者原研究论文

The authors used this protocol in:

Cover of Plant Physiology, featuring study using the protocol.

Jun 2017

Advertisement

Submit your protocol to the Special Issue on Technologies for RNA Detection
Presubmission Inquiry

实验方案合集

专注于特定技术或应用的、详细的、经过同行评审的实验方案合集

Cancer Research
Immunology
Developmental Biology
Microbiology
Neuroscience
Cell Imaging - A Special Collection for Cell Bio 2023
查看更多 more

相关实验方案

活体叶片切片成像观察细胞内叶绿体运动及细胞间相互作用

活体叶片切片成像观察细胞内叶绿体运动及细胞间相互作用

Yuta Kato [...] Mitsutaka Taniguchi

2025年08月05日 2177 阅读

耐盐耐旱细菌分离株中生长素、铁载体和氰化氢产量的定量评估及其对黄瓜生长的作用

耐盐耐旱细菌分离株中生长素、铁载体和氰化氢产量的定量评估及其对黄瓜生长的作用

Zeinab Fotoohiyan and Ali Salehi Sardoei

2025年10月05日 1271 阅读

活细胞监测叶绿体片段自噬过程

活细胞监测叶绿体片段自噬过程

Masanori Izumi [...] Shinya Hagihara

2025年11月05日 1595 阅读

Abstract

Hydathodes are plant organs present on leaf margins of a wide range of vascular plants and are the sites of guttation. Both anatomy and physiology of hydathodes are poorly documented. We have recently reported on the anatomy of cauliflower and Arabidopsis thaliana hydathodes and on their infection by the vascular pathogenic bacterium Xanthomonas campestris pv. campestris (Xcc) (Cerutti et al., 2017). Because hydathodes are natural infection routes for several pathogens, it is necessary to have a deep knowledge of their anatomy to further better interpret images of infected hydathodes. Here, we described different detailed protocols for gaining information on hydathode anatomy which are applicable to a wide range of plants (including monocots like barley and rice). Nomarsky and confocal microscopy were used to observe clarified thick samples. Optical microscopy in transmitted light and transmission electron microscopy were used to observed thin and ultrathin sections.

Keywords: Cauliflower (花椰菜) search Hydathode (泌水孔) search Xanthomonas (黄单胞菌) search

Background

In literature, different techniques were used to study hydathodes (Perrin, 1972; Chen and Chen, 2007; Wang et al., 2011; Singh, 2014). From light microscopy (on entire tissues or on section of resin-embedded samples) to scanning or transmission electron microscopy, a large panel of protocols and techniques was available. To our knowledge, these techniques were not used in combination and laser confocal microscopy was never used to depict hydathode structures. Moreover, we noticed variations from protocols to protocols. We presented here different techniques used in combination. They are well-adapted to cauliflower and Arabidopsis thaliana. They have been successfully applied to other plants like monocotyledons (barley and rice) and should be likely used to a larger variety of plant species. We encourage the users to apply these protocols to gain complementary information on the hydathode at different scales during infection.

Materials and Reagents

  1. Microscope glass slides (Thermo Fisher Scientific, Superfrost, catalog number: 10143560WCUT )
  2. Cover slip 24 x 60 mm (Thermo Fisher Scientific, catalog number: 15747592 )
  3. Razor blades
  4. Cauliflower (Brassica oleracea var. botrytis, cultivar Clovis)
    Notes:
    1. Cauliflower plants were grown in a controlled greenhouse.
    2. All the experiments used the second true leaf from four-weeks-old plants.
  5. Chloral hydrate (Sigma-Aldrich, catalog number: 23100 )
  6. Glycerol (C3H8O3) (VWR, catalog number: 24387.326 )
  7. Calcofluor (Fluorescent Brightener 28) (Sigma-Aldrich, catalog number: F3543 )
  8. Triton X-100 (Sigma-Aldrich, catalog number: T8787 )
  9. Sodium cacodylate (Sigma-Aldrich, catalog number: C4945 )
  10. Glutaraldehyde EM grade (Electron Microscopy Sciences, catalog number: 16214 )
  11. Osmium tetroxide (OsO4) (Electron Microscopy Sciences, catalog number: 19150 )
  12. Ethanol (C2H5OH) (Sigma-Aldrich, catalog number: 32221 )
  13. Epon (Electron Microscopy Sciences, catalog number: 14120 )
    Note: Composition of the resin: Embed-812 (45 g), DDSA (36 g), NMA (18 g) and BDMA (1.35 ml). Embedding kit in which accelerator DMP30 is replaced by BDMA (Electron Microscopy Sciences, catalog number: 11400 ).
  14. Borax (Sigma-Aldrich, catalog number: B3545 )
  15. Toluidine blue (RAL Diagnostics, catalog number: 361590 )
  16. Methylene blue (Merck, catalog number: 159270 )
  17. Basic fuchsin (Sigma-Aldrich, catalog number: 857343 )
  18. Periodic acid (VWR, Prolabo, catalog number: 20.593.151 )
  19. Acetic acid (CH3COOH) (CARLO ERBA Reagents, catalog number: 302016 )
  20. Thiocarbohydrazide (Sigma-Aldrich, catalog number: 223220 )
  21. Silver proteinate (Roques for histology) (Sigma-Aldrich, catalog number: 05495 )
  22. Aceton (CH3COCH3) (Fisher Scientific, catalog number: 10395640 )
  23. Clarification solution (see Recipes)
  24. Fixation solution (see Recipes)
  25. Sodium cacodylate buffer (see Recipes)
  26. Borax solution with toluidine blue and methylene blue (see Recipes)
  27. Basic fuchsin solution (see Recipes)
  28. Periodic acid solution (see Recipes)
  29. Silver proteinate solution (see Recipes)

Equipment

  1. Hollow punch (Harris, Uni-Core) (Electron Microscopy Sciences, catalog number: 69039-70 )
  2. Ultra-microtome (Leica Microsystems, Reichert-Jung, model: UltraCut E )
  3. Optical microscope equipped for Nomarski (Leica Microsystems, model: DM IRB-E )
  4. Confocal microscope (Leica Microsystems, model: Leica TCS SP2 ) equipped with a diode laser at 405 nm
  5. Diaphragm pump vacuum or other vacuum sources
  6. Stirrer hotplate (IKA)
  7. Microwave apparatus (Leica Microsystems, model: EM AMW )
  8. Flat bottom embedding capsule (Electron Microscopy Sciences, catalog number: 70021 )
  9. Oven (Memmert, model: UFE500BO )
  10. Histo diamond knife (Diatome Histo) for semi-thin sections (0.5 µm) to optical observations
  11. Ultra diamond knife (Diatome Ultra 45) for ultra-thin sections (70-80 nm) to transmission electron microscopy
  12. Hot plate (slides warmer) (C & A Scientific, Premiere, model: XH-2002 )
  13. Optical microscope (ZEISS, model: Axioplan 2 )
  14. CCD camera (ZEISS, model: AxioCam MRc )
  15. Transmission electron microscope (Hitachi, model: HT7700 )
  16. Gold grid (Electron Microscopy Sciences, catalog number: FCF200-Au )

Software

  1. Pro Plus 4.0 Imaging software (Media Cybernetics, Silver Spring, MD, USA)

Procedure

English
中文翻译

文章信息

版权信息

© 2017 The Authors; exclusive licensee Bio-protocol LLC.

如何引用

Readers should cite both the Bio-protocol article and the original research article where this protocol was used:

  1. Cerutti, A., Auriac, M., Noël, L. D. and Jauneau, A. (2017). Histochemical Preparations to Depict the Structure of Cauliflower Leaf Hydathodes. Bio-protocol 7(20): e2452. DOI: 10.21769/BioProtoc.2452.
  2. Cerutti, A., Jauneau, A., Auriac, M. C., Lauber, E., Martinez, Y., Chiarenza, S., Leonhardt, N., Berthomé, R. and Noël, L. D. (2017). Immunity at cauliflower hydathodes controls systemic infection by Xanthomonas campestris pv campestris. Plant Physiol 174(2): 700-716.

    3. ris ris Download Citation in RIS Format

分类

植物科学 > 植物免疫 > 宿主-细菌相互作用

植物科学 > 植物细胞生物学 > 细胞成像

细胞生物学 > 细胞成像 > 固定组织成像

您对这篇实验方法有问题吗？

在此处发布您的问题，我们将邀请本文作者来回答。同时，我们会将您的问题发布到Bio-protocol Exchange，以便寻求社区成员的帮助。

post 发布问题
0 Q&A
pen 提交稿件