Preparation of Actinoplanes missouriensis Zoospores and Assay for Their Adherence to Solid Surfaces

Materials and Reagents

1. Coverslips (18 x 18 mm, Matsunami Glass Industry, catalog number: C218181)
2. Glass dish (f 35 mm, AGC Techno Glass, catalog number: 3970-035)
3. Polystyrene dish (f 35 mm, AGC Techno Glass, catalog number: 1000-035)
4. Polystyrene dish (f 90 mm, Sansei Medical, catalog number: 01-013)
5. 1.5-ml centrifuge tube (Greiner Bio-One, catalog number: J618201)
6. 50-ml centrifuge tube (Corning, catalog number: 430829)
7. Shaking (Sakaguchi) flask (Sansyo, catalog number: 82-0317)
   
8. Double-sided tape (width 15 mm, thickness 0.086 mm, NICETACK, Nichiban)
9. Whatman^TM Filter paper (GE Healthcare Life Sciences, catalog number: 3030-917)
10. Toothpick
11. A. missouriensis 431^T (NBRC 102363^T)
12. Yeast extract (Becton, Dickinson and Company, catalog number: 212750)
13. Meat extract (Kyokuto, catalog number: 551-01240-8)
14. N-Z-Amine^® (FUJIFILM Wako Pure Chemical, catalog number: 146-08675)
15. D (+)-Maltose monohydrate (FUJIFILM Wako Pure Chemical, catalog number: 130-00615)
16. Agar powder (Kokusan Chemical, catalog number: 2111136)
17. Peptone (Becton, Dickinson and Company, catalog number: 211677)
18. Magnesium sulfate heptahydrate (MgSO₄·7H₂O) (Kokusan Chemical, catalog number: 2114992)
19. Saccharose (Kokusan Chemical, catalog number: 2111624)
20. Casamino acids, technical (Becton, Dickinson and Company, catalog number: 223120)
21. Dipotassium hydrogen phosphate (K₂HPO₄) (Kokusan Chemical, catalog number: 2115140)
22. Nitrohumic acid (Tokyo Chemical Industry, catalog number: H0161)
23. Sodium hydroxide (NaOH) (Kokusan Chemical, catalog number: 2112744)
24. Zinc chloride (ZnCl₂) (FUJIFILM Wako Pure Chemical, catalog number: 263-00271)
25. Iron (III) chloride hexahydrate (FeCl₃·6H₂O) (FUJIFILM Wako Pure Chemical, catalog number: 091-00872)
26. Cupric chloride, dihydrate (CuCl₂·2H₂O) (Kokusan Chemical, catalog number: 2150417)
27. Manganese (II) chloride tetrahydrate (MnCl₂·4H₂O) (FUJIFILM Wako Pure Chemical, catalog number: 139-00722)
28. Sodium tetraborate (Na₂B₄O₇·10H₂O) (Kokusan Chemical, catalog number: 2114089)
29. Ammonium molybdate ((NH₄)₆Mo₇O₂₄·4H₂O) (Kokusan Chemical, catalog number: 2152738)
30. Sodium chloride (NaCl) (Kokusan Chemical, catalog number: 2110733)
31. Bovine serum albumin (BSA) (Sigma-Aldrich, catalog number: A9647)
32. Ammonium hydrogencarbonate (NH₄HCO₃) (FUJIFILM Wako Pure Chemical, catalog number: 017-02875)
33. YBNM agar medium (see Recipes)
34. PYM broth (see Recipes)
35. HAT agar medium (see Recipes)
36. Nitrohumic acid solution (see Recipes)
37. Trace element solution (see Recipes)
    

Equipment

1. Mortar and pestle
2. Laminar flow cabinet
3. Flask shaker
4. Centrifuge (Kubota Corp., model: 5200)
5. Incubator (PHC Holdings, model: MIR-154)
6. Micropipette
7. Phase-contrast microscope (Olympus, model: IX73)
8. Objective lens (Olympus, model: UPLFLN20×PH)
9. Optical table (JVI, model: HAX-0605)
10. High speed recorder system (Digimo, model: LRH1540) with complementary metal-oxide semiconductor (CMOS) camera
    

Software

1. ImageJ (https://imagej.nih.gov/ij/)

Procedure

1. Preparation of A. missouriensis zoospores
   1. Inoculate A. missouriensis cells from a glycerol stock on YBNM agar medium and cultivate them at 30 °C in an incubator for 2 or 3 days (Figure 1).
      
      
      Figure 1. A YBNM agar plate (diameter, 9 cm) on which A. missouriensis mycelia are grown for 4 days at 30 °C
      
      
   2. Using a sterilized toothpick, cut the agar medium to prepare an agar piece (approximately 1 cm square), on the surface of which A. missouriensis mycelium has proliferated (Figure 2). Put the agar piece into PYM broth (100 ml) in a shaking flask to inoculate the mycelium, and cultivate the A. missouriensis cells by shaking at 120 rpm at 30 °C for 2 days (Figure 3).
      
      
      Figure 2. Preparation of an agar piece for the inoculation of A. missouriensis
      
      
      Figure 3. Liquid culture of A. missouriensis in a shaking flask (at 30 °C for 2 days)
      
      
   3. Collect the cells by centrifugation at 2,330 x g for 10 min at RT.
   4. Suspend the cells in 0.75% NaCl solution (50 ml) and centrifuge them at 2,330 x g for 10 min at RT.
   5. Resuspend the cells in 0.75% NaCl solution (10 ml; Figure 4) and inoculate a portion (0.1 ml) of the cell suspension on one HAT agar plate.
      
      
      Figure 4. A. missouriensis mycelia suspended in 0.75% NaCl solution
      
      
   6. Spread the cell suspension and completely dry the surface of the HAT agar medium.
   7. Incubate the plate at 30 °C for at least 7 days (Figure 5).
      
      
      Figure 5. A HAT agar plate (diameter, 9 cm) on which A. missouriensis are grown for 7 days at 30 °C. Many sporangia are produced on substrate mycelium.
      
      
   8. Pour 25 mM NH₄HCO₃ solution (10 ml) onto the HAT agar plate (Figure 6) and incubate it at 30 °C for 1 h.
      
      
      Figure 6. Pouring of NH₄HCO₃ solution onto HAT agar
      
      
   9. Collect the poured solution, which contains swimming zoospores (approximately 10⁴-10⁵ cells/μl; Figure 7). Keep the solution at RT until the use.
      
      
      Figure 7. A. missouriensis zoospore-containing solution
      
      
      
2. Zoospore adhesion test
   1. Attach a coverslip to a hydrophobic polystyrene dish or a hydrophilic glass dish by using two pieces of double-sided tape. Make a tunnel chamber by arranging the tape as parallel lines and making open slits on both sides of the coverslip (Figure 8). This arrangement enables a reproducible distance between the coverslip and dish, ensuring the fixed volume of the tunnel chamber, and also enables a replacement of the solution inside the chamber using a filter paper. The protocol using a similar tunnel chamber has already been published by Kasai and Miyata (2013).
      
      
      Figure 8. Illustration of a tunnel chamber
      
      
   2. (Optional; BSA-coating on the surface of a hydrophobic polystyrene dish) Using a micropipette, pour 1% BSA solution into the space between the dish and coverslip. Keep it at RT for 1 min. Absorb 1% BSA solution from a side of the chamber using a filter paper. By a similar procedure, wash the chamber with 25 mM NH₄HCO₃ solution. The BSA-coating treatment renders the dish surface hydrophilic. Through the treatment, the average proportion of the zoospores that adhered to the dish surface decreased from 41% (non-treated dish surface) to 0.2% (BSA-treated dish surface; Kimura et al., 2019).
   3. Using a micropipette, put the zoospore-containing solution (12 µl) carefully into the space between the dish and coverslip without introducing air bubbles. Incubate the chamber at RT for 10 min.
   4. Record the zoospores that adhered to the dish surface and the swimming zoospores in the tunnel by using a phase-contrast microscope equipped with a 20x objective lens. A lab recorder system and a CMOS camera enable the high-speed (200 frames per second) imaging. Scan the microscopic fields along the vertical direction for the analyzing region of the tunnel chamber in 3 s (600 images in total).
   5. Using a micropipette, put the 25 mM NH₄HCO₃ solution (150 μl) on one side of the tunnel and absorb the zoospore-containing solution from the other side using a filter paper to completely exchange the solution for 25 mM NH₄HCO₃ solution for the removal of the zoospores that did not adhere to the solid surface.
   6. Photograph the zoospores that adhered to the dish surface by using the microscope.
      
      
      
3. Data analysis
   1. Convert the movie files recorded in Step B4 into AVI files. Convert the 8-bit images recorded in Step B6 into TIF files without compression using ImageJ, an image analysis software.
   2. Count the total number of swimming zoospores and those adhered to the dish surface in the analyzing region of the tunnel chamber by ImageJ using the microscopic images recorded in Step B4. The Color_FootPrint macro for ImageJ (http://www.jaist.ac.jp/ms/labs/hiratsuka/images/0/09/Color_FootPrint.txt) enables the visualization of the zoospore swimming trajectories (Hiratsuka et al., 2006).
      1. Open a movie file by using the command “File > Open”. Check off the boxes for “Use Virtual Stack” and “Convert to Grayscale”.
      2. Start the Color_FootPrint macro by using the command “Plugins > Macros > Color Footprint Rainbow”. The macro visualizes zoospore swimming trajectories (Figure 9B).
      3. Count the number of the stationary cells on the dish surface (Figure 9A) and the number of the colored trajectories, which represents the number of swimming zoospores, in the analyzing region of the tunnel chamber scanned in Step B4, by visual inspection.
         
         
         Figure 9. Counting the number of zoospores in the tunnel chamber by ImageJ. A. Input image; the first image of the total 600 scanning images is shown as a representative. B. Output image; colored trajectories are shown. Scale bar = 50 μm.
         
         
         
   3. Count the number of zoospores that adhered to the dish surface using the microscopic images recorded in Step B6 by ImageJ.
      1. Open an image by using the command “File > Open”.
      2. Select the analyzed region of the microscopic field scanned in Step B4 by using the “Rectangle” tool and clip the field by using the command “Image > Crop”.
      3. Set a threshold level by using the command “Image > Adjust > Threshold”.
      4. Count the number of zoospores by using the command “Analyze > Analyze Particles”. Set appropriate values of the parameters “Size” and “Circularity” (Figure 10).
         
         
         Figure 10. Counting the number of zoospores on the dish surface by ImageJ. A. Input image. Scale bar = 20 μm. B. Output image. A part of the original image is enlargedly shown.
         
         
   4. Calculate the adhesion ratio, i.e., the proportion of adhesive zoospores to whole zoospores: C3/C2. Correction values per unit area should be used for the calculation.

Notes

In the adhesion test, zoospores must be freshly prepared. Use zoospores within 1 h after collection. The collected zoospores should not be diluted because the dilution with a buffer may affect the motility of zoospores.

Recipes

1. YBNM agar medium
   0.1% yeast extract
   0.2% meat extract
   0.2% N-Z-Amine^®
   1% D (+)-maltose monohydrate
   Adjust pH to 7.0
   Add agar to 2% prior to autoclaving
2. PYM broth
   0.5% peptone
   0.3% yeast extract
   0.1% MgSO₄·7H₂O
   Adjust pH to 7.0
   Autoclave the broth
3. HAT agar medium
   0.1% saccharose
   0.01% casamino acids, technical
   0.05% K₂HPO₄
   2% nitrohumic acid solution
   1% trace element solution
   Adjust pH to 7.5
   Add agar to 2% prior to autoclaving
4. Nitrohumic acid solution
   
   1. Grind 10 g of nitrohumic acid with a mortar and pestle
   2. Add 100 ml of 0.8% NaOH solution little by little and suspend the nitrohumic acid powder
   3. Autoclave the suspension at 105 °C for 15 min
   4. Stir the suspension until cooling down to RT
   5. Autoclave again the suspension at 105 °C for 15 min
   6. Stir the suspension until cooling down to RT
   7. Centrifuge the suspension at 1,500 x g for 10 min at 4 °C
   8. Transfer the supernatant to a sterilized glass bottle and store at 4 °C
5. Trace element solution
   0.004% ZnCl₂
   0.02% FeCl₃·6H₂O
   0.001% CuCl₂·2H₂O
   0.001% MnCl₂·4H₂O
   0.001% Na₂B₄O₇·10H₂O
   0.001% (NH₄)₆Mo₇O₂₄·4H₂O
   Autoclave the solution
   

Acknowledgments

This protocol is adapted from Kimura et al. (2019). The above work was supported in part by Grants-in-Aid for Scientific Research no. 19H05685 (to Y.O.), 18H02122 (to Y.O.), 26252010 (to Y.O.), and 17K07711 (to T.T.), Grants-in-Aid for Young Scientists no. 16H06230 (to D.N.) and 15K18669 (to T.T.), and a Grant-in-Aid for JSPS Research Fellow no. 15J07768 (to T.K.) from the Japan Society for the Promotion of Science (JSPS) and the Ministry of Education, Culture, Sports, Science, and Technology of Japan (MEXT).

Competing interests

The authors declare no conflicts of interest associated with this manuscript.

References

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