Salinity and Drought Treatment Assays in Kenaf (Hibiscus cannabinus L.)    

Materials and Reagents

1. Sterile Petri dishes (JET, catalog number: TCD010090 )
   
2. Sterile filter paper (Sigma-Aldrich, catalog number: Z241091 )
   
3. Seeds: kenaf (cv Fuhong 992) [conserved in the Key Laboratory for Genetics, Breeding and Multiple Utilization of Crops of Fujian Agriculture and Forestry University (China)].
   
4. Sterile water (sterilized for 20 min at 121 °C/1 atm using an autoclave)
   
5. Sterile soil (Fafard^® growing mix 1-PV/C-1PV, Sun Gro Horticulture Canada Ltd.) (sterilized for 30 min at 121 °C/1 atm using an autoclave)
   
6. Sodium hypochlorite (NaClO) solution (15%) (Sinopharm Chemical Reagent, catalog number: 7681-52-9 )
   
7. Potassium nitrate (KNO₃) (Sinopharm Chemical Reagent, catalog number: 7757-79-1 )
   
8. Ammonium dihydric phosphate (NH₄H₂PO₄) (Sinopharm Chemical Reagent, catalog number: 7722-76-1 )
   
9. Ammonium nitrate (NH₄NO₃) (Sinopharm Chemical Reagent, catalog number: 6484-52-2 )
   
10. Calcium nitrate [Ca(NO₃)₂·4H₂O] (Sinopharm Chemical Reagent, catalog number: 13477-34-4 )
    
11. Magnesium sulphate (MgSO₄·7H₂O) (Sinopharm Chemical Reagent, catalog number: 10034-99-8 )
    
12. Ethylene diamine-N,N bis (2 hydroxyphenylacetic acid) Ferric sodium complex (Fe-EDDHA) (Sinopharm Chemical Reagent, catalog number: 16455-61-1 )
    
13. Boric acid (H₃BO₃) (Sinopharm Chemical Reagent, catalog number: 10043-35-3 )
    
14. Manganese chloride (MnCl₂·4H₂O) (Sinopharm Chemical Reagent, catalog number: 7773-01-5 )
    
15. Zinc sulphate (ZnSO₄·7H₂O) (Sinopharm Chemical Reagent, catalog number: 7446-20-0 )
    
16. Copper sulphate (CuSO₄·5H₂O) (Sinopharm Chemical Reagent, catalog number: 7758-98-7 )
    
17. Sodium molybdate (Na₂MoO₄·2H₂O) (Sinopharm Chemical Reagent, catalog number: 10102-40-6 )
    
18. Sodium chloride (NaCl) (Sinopharm Chemical Reagent, catalog number: 7647-14-5 )
    
19. PEG6000 (Sigma-Aldrich, catalog number: 81260 )
    
20. 5% (v/v) sodium hypochlorite(see Recipes)
    
21. Hoagland solution (see Recipes)
    
22. 200 mM sodium chloride (NaCl) solution (see Recipes)
    
23. 20% (w/v) PEG6000 solution (see Recipes)
    

Equipment

1. Plastic pots (10 cm diameter and 8 cm depth)
   
2. Clean bench (Suzhou AirTech , AirTech^®, model: SW-CJ-1FD )
   
3. Growth chamber (Yihengyiqi Shanghai, Blue pard^®, model: MGC-300A )
   
4. Autoclave (TOMY, model: SX-500 )
   
5. Precision balance (± 0.001)
   
6. Timer control
   

Procedure

1. Seed germination and culture
   1. Rinse the seeds under running water for 10 min, and then sterilize the seeds with 5% sodium hypochlorite for 10 min, and subsequently wash the seeds three times with sterile water (Figure 1A).
      
   2. Place the sterilized seeds in Petri dishes on filter paper saturated with sterile water, and maintain the seeds in complete darkness at 28 °C until germination (about 3 days) (Figure 1B and 1C).
      
   3. Transfer 3-5 days old seedlings to separate sterilized soil pots.
      
   4. Maintain the plants in growth chambers at 28 °C for 16 h with light and 26 °C for 8 h without light, 60% relative humidity, ~450 μmol m^-2 s^-1 light intensity, and supplement 100 ml 1/4 Hoagland solution to soil once a day (Figure 1D).
      
   5. Allow plants to grow up to 3-10 leaves stage (about 4 weeks) for salinity and drought treatments assays.
      
      
2. Salinity and drought treatments
   
   1. For salinity treatment, prepare 200 mM sodium chloride solution in Hoagland nutrient medium and supplement 100 ml of this solution to 10 pots individually once a day (Figure 1D).
      
   2. For drought treatment, prepare 20% (w/v) PEG6000 solution in Hoagland nutrient medium and supplement 100 ml of this solution to 10 pots individually once a day (Figure 1D).
      
   3. Harvest 3 treated leaves from each plant at different time points (e.g., 6, 12 and 24 h). Untreated samples were collected at the same interval as a control. Three biological replicates were obtained from each treatment (Figure 1E).
      
      
      Figure 1. Example of experimental procedure. A. Seeds rinsed under running water; B. Sterilized seeds on saturated filter paper in Petri dishes; C. Germinated seeds; D. Seedlings at cotyledon stage; E. Harvesting leaf samples (about 4 weeks) as pointed by red arrows after salinity and drought treatments.
      

Data analysis

RNA was isolated and used for selection reliable reference gene (such as ACT, 18S rRNA, EF1α) for Real-Time PCR (RT-qPCR) assay under salinity and drought stress, and this section was stated clearly in our paper (Niu et al., 2015).

Notes

1. Soil is sterilized for at least 30 min at 121 °C/1 atm using an autoclave.
   
2. Polyethylene glycol (PEG) is a flexible, water-soluble polymer, and it can be used to create high osmotic pressure. Therefore, it is used for applying osmotic pressure in plants to induce water deficit.
   
3. The same aged leaves should be taken from each sample type. Also use at least three individual lines from each treatment for analysis.
   
4. The volume of supplement is depended on the size of pots, watering frequency, and plant species. It is recommended that a series of assays should be done for a given plant species before stress treated.
   

Recipes

1. Hoagland solution
   Note: Hoagland solution is based on Hoagland No.2 solution (Hoagland et al., 1950) (Table 1).
   
   Table 1. Hoagland solution composition
   
   
   
2. 5% (v/v) sodium hypochlorite
   Add 33 ml 15% NaClO solution in the distilled water to get a final volume of 100 ml
   
3. 20% (w/v) PEG6000 solution
   Dissolve 20 g PEG6000 in distilled water
   Dilute with distilled water to get a final volume of 100 ml, and mix
   
4. 200 mM sodium chloride solution
   Dissolve 11.7 g NaCl in 1 L distilled water
   

Acknowledgments

This work was supported by grants from the 948 project of the Agricultural Department of China (2013-Z70), the National bast fiber germplasm resources project of China (K47NI201A) and National bast fiber research system of China (CARS-19-E06). This protocol was adapted from our recent publications (Niu et al., 2015).

References

1. Hoagland, D. R., Arnon, D. I. (1950). The water-culture method for growing plants without soil. California Agriculture Experiment Station 347: 34.
   
2. Niu, X., Qi, J., Chen, M., Zhang, G., Tao, A., Fang, P., Xu, J., Onyedinma, S. A. and Su, J. (2015). Reference genes selection for transcript normalization in kenaf (Hibiscus cannabinus L.) under salinity and drought stress. Peer J 3: e1347.