Summary

An Easy and Flexible Inoculation Method for Accurately Assessing Powdery Mildew-Infection Phenotypes of Arabidopsis and Other Plants

Published: March 09, 2021
doi:

Summary

We present a protocol for constructing a simple spore-distribution system consisting of an inoculation box with a ~50 µm mesh and a transparent plastic chamber. This can be used to evenly inoculate plants with powdery mildew spores, thereby enabling accurate and reproducible assessment of disease phenotypes of plants under study.

Abstract

Reducing crop losses due to fungal diseases requires improved understanding of the mechanisms governing plant immunity and fungal pathogenesis, which in turn requires accurate determination of disease phenotypes of plants upon infection with a particular fungal pathogen. However, accurate disease phenotyping with unculturable biotrophic fungal pathogens such as powdery mildew is not easy to achieve and can be a rate-limiting step of a research project. Here, we have developed a safe, efficient, and easy-to-operate disease phenotyping system using the Arabidopsis-powdery mildew interaction as an example. This system mainly consists of three components: (i) a wooden inoculation box fitted with a removable lid mounted with a stainless steel or nylon mesh of ~50 µm pores for inoculating a flat of plants with fungal spores, (ii) a transparent plastic chamber with a small front opening for minimizing spore escape while conducting inoculation inside, and (iii) a spore-dislodging and distribution method for even and effective inoculation. The protocols described here include the steps and parameters for making the inoculation box and the plastic chamber at a low cost, and a video demonstration of how to use the system to enable even inoculation with powdery mildew spores, thereby improving accuracy and reproducibility of disease phenotyping.

Introduction

Powdery mildew is one of the most common and important diseases of numerous food crops and ornamental plants1. Studies of powdery mildew diseases have been very popular, as evidenced by over 10,500 publications as the search result with “powdery mildew” as key word at the Web of Science (as of November 2020). Indeed, powdery mildew (represented by Blumeria graminis) is considered to be one of the top 10 fungal pathogens by the journal of Molecular Plant Pathology2. Quantification of disease susceptibility is a necessary step in characterization of plant genes contributing to disease resistance or susceptibility, or functional identification of candidate effector genes in powdery mildew. However, reliable disease phenotyping is far more challenging with powdery mildew compared to that with most other fungal pathogens, partly because, unlike spores of the latter, spores of powdery mildew species (such as Golovinomyces cichoracearum UCSC1 based on our lab experience) show reduced viability after going through a water-suspension process3,4. Inadequate and/or uneven inoculation of test plants with a particular powdery mildew pathogen may lead to inaccurate phenotyping results.

A number of inoculation methods were reported for powdery mildew studies. These include (i) brushing spores directly from infected leaves to test plants5, (ii) spraying a spore suspension to test plants6, (iii) blowing spores using a vacuum-operated settling tower to plants at the bottom of the tower7, and (iv) spore delivery by the combinatorial use of a nylon mesh membrane and sound-based vibration8. The spore-brushing (or dusting) method is easy to perform but uneven in nature, thus it may not be accurate for quantitative assessment. Spore-spraying is convenient and even, but as stated above may result in poor spore germination4. The latter two (i.e., iii-iv) are much-improved methods capable of achieving even inoculation; however, both are not flexible in adjusting their inoculation capacity in terms of the number of plants to be inoculated in a single event, making either apparatus is not trivial, and their operation is restricted to lab areas where there is a vacuum and/or electricity source.

Our lab has been working with plant-powdery mildew interaction for over 20 years9,10. Over the past decade, we tested a number of inoculation methods and recently developed a simple and yet effective powdery mildew inoculation method. This mesh-based spore-brushing method can ensure even inoculation, and is simple and scalable, thus should be easily adopted by any laboratory working with powdery mildew.

Protocol

1. Making a standard inoculation box with a removable top lid mounted with a mesh Purchase a roll of 50 µm nylon membrane mesh or 48 µm stainless steel mesh (recommended) from stores. Make sure to order enough for cutting into multiple pieces of 14 in x 26 in for replacement of worn mesh. Purchase one 1/4 in x 2 ft x 4 ft medium density fiberboard or plywood, and cut two 24-1/2 in x 10 in pieces and two 12 in x 10 in pieces for making an inoculation box.Use 8 corner clamps for supporting t…

Representative Results

Here, we present a new powdery mildew spore inoculation method that is easy to prepare, operate and adjust. Figure 1 shows the assembly of the standard inoculation box with emphasis on the make of the removable lid mounted with a 50 µm membrane mesh. Figure 2 shows the assembly of the inoculation chamber. Figure 3 illustrates the key steps of the inoculation process using this system. Figure 4 show…

Discussion

Our meshed-box-based inoculation method has several advantages over other inoculation methods. First, it can achieve even distribution of spores if operated properly, as demonstrated in Figure 5. Second, the use of ~50 µm mesh, plus spore-dislodging by gentle shaking of infected leaves can reduce plant infection by thrips or other plant-infecting insects that are present in source plants. Third, the use of different-sized inoculation boxes for inoculating plants or detached leaves insid…

Offenlegungen

The authors have nothing to disclose.

Acknowledgements

The work was supported by the National Science Foundation (IOS-1901566) to S. Xiao. The authors would like to thank F. Coker and C. Hooks for the maintenance of the plant growth facility, and Jorge Zamora for technical help associated with fabrication of the inoculation box and chamber.

Materials

 48 µm stainless steel grid mesh screen; Size: 24" X 48"  Amazon NA For making the lid of an inoculation box
#6-32 x ¾" machine screws, flat washers and nuts  Home Depot NA For making an inoculation chamber
#6-32 zinc plated nylon lock nut (4-Pack) Home Depot NA For making an inoculation chamber
#6-32×3/8” Phillips flat head machine screws, flat washers and nuts  Home Depot NA For securing  magnet door catch plates
#8-32×1/2" machine screws, flat washers and nuts Home Depot NA For securing corner braces and door hinge
0.250 thick clear extruded acrylic film-masked sheet;  Size: 17 ½" X 20" Professional Plastics SACR.250CEF For making an inoculation chamber
0.250 thick clear extruded acrylic film-masked sheet; Size: 18" X 20"   Professional Plastics  SACR.250CEF For making an inoculation chamber
0.250 thick clear extruded acrylic film-masked sheet; Size: 18" X 30"  Professional Plastics SACR.250CEF For making an inoculation chamber
0.250 thick clear extruded acrylic film-masked sheet; Size: 20" X 29 ½ " Professional Plastics SACR.250CEF For making an inoculation chamber
1-5/8" cabinet door magnetic catch white Home Depot Model #P110-W For making an inoculation chamber
2" steel zinc-plated corner brace (8-Pack)  Home Depot  Model #13611  For making an inoculation box & chamber
3" Corner Clamp Harbor Freight Tools SKU 63653, 1852, 60589 For making inoculation chamber
3/4"  steel zinc plated corner brace (4-Pack) Home Depot Model #13542 For making an inoculation box & chamber
4-7/8" zinc-plated light duty door pull handles Home Depot Model #15184 For making an inoculation box
Fine fan-blender brushes Michaels Store M10472846  For inoculation
Kelleher 3/4" x 3/4" x 36" wood square dowel  Home Depot NA For making the lid of an inoculation box
Medium density fiberboard (1/4" x 2' x 4');  Home Depot Model# 1508104 For making an inoculation box
Round glass coverslips with a 500 µm grid ibidi USA Inc. 10816 For determining  spore density

Referenzen

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  2. Dean, R., et al. The top 10 fungal pathogens in molecular plant pathology. Molecular Plant Pathology. 13 (4), 414-430 (2012).
  3. Sakurai, H., Hirata, K. Some observations on the relation between the penetration hypha and haustorium of barley powdery mildew and host cell. V. Influence of water spray on the pathogen and host tissue. Annual Phytopathology Society of Japan. 24, 239-245 (1959).
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  7. Reifschneider, F. J. B., Boiteux, L. S. A vacuum-operated settling tower for inoculation of powdery mildew fungi. Phytopathology. 78 (11), 1463-1465 (1988).
  8. Chowdhury, A., Bremer, G. B., Salt, D. W., Miller, P., Ford, M. G. A novel method of delivering Blumeria graminis f. sp hordei spores for laboratory experiments. Crop Protection. 22 (7), 917-922 (2003).
  9. Xiao, S., et al. Broad-spectrum mildew resistance in Arabidopsis thaliana mediated by RPW8. Science. 291 (5501), 118-120 (2001).
  10. Xiao, S., Ellwood, S., Findlay, K., Oliver, R. P., Turner, J. G. Characterization of three loci controlling resistance of Arabidopsis thaliana accession Ms-0 to two powdery mildew diseases. The Plant Journal. 12 (4), 757-768 (1997).
  11. Reuber, T. L., et al. Correlation of defense gene induction defects with powdery mildew susceptibility in Arabidopsis enhanced disease susceptibility mutants. The Plant Journal. 16 (4), 473-485 (1998).
  12. Xiao, S., et al. The atypical resistance gene, RPW8, recruits components of basal defence for powdery mildew resistance in Arabidopsis. The Plant Journal. 42 (1), 95-110 (2005).
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Wu, Y., Diaz, D., Yin, J., Bloodgood, D., Sexton, W., Wei, C., Xiao, S. An Easy and Flexible Inoculation Method for Accurately Assessing Powdery Mildew-Infection Phenotypes of Arabidopsis and Other Plants. J. Vis. Exp. (169), e62287, doi:10.3791/62287 (2021).

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