Separation of Single-stranded DNA, Double-stranded DNA and RNA from an Environmental Viral Community Using Hydroxyapatite Chromatography

1. Preparation of Solutions

Before performing hydroxyapatite chromatography, phosphate buffers must be prepared and the hydroxyapatite must be properly hydrated.

1. 1M Phosphate Solution, pH 6.8: In a 1L flask dissolve 119.98g of sodium phosphate monobasic in 1L of sterile, DEPC-treated H₂O. Prepare a 1M sodium phosphate dibasic solution in a 1L flask by dissolving 141.96g of sodium phosphate dibasic in 1L of sterile, DEPC-treated H₂O. Combine the mono- and di- solutions at a ratio of 1:1. Place flask on a stir plate and mix using a magnetic stir bar. Adjust pH to 6.8 by adding sodium hydroxide (to increase pH) or phosphoric acid (to decrease pH).
2. 0.12M Phosphate Buffer: In a 500ml flask, combine 30ml of 1M Phosphate Solution, pH 6.8, 2.5ml of 10% sodium dodecyl sulphate (SDS), and 5ml of 0.5M EDTA. Add sterile, DEPC-treated H2O to a volume of 225ml. Adjust pH to 6.8. Add sterile, DEPC-treated H2O to 250ml. Autoclave.
3. 0.18M Phosphate Buffer: In a 500ml flask, combine 45ml of 1M Phosphate Solution, pH 6.8, 2.5ml of 10% sodium dodecyl sulphate (SDS), and 5ml of 0.5M EDTA. Add sterile, DEPC-treated H₂O to a volume of 225ml. Adjust pH to 6.8. Add sterile, DEPC-treated H₂O to 250ml. Autoclave.
4. 0.20M Phosphate Buffer: In a 500ml flask, combine 50ml of 1M Phosphate Solution, pH 6.8, 2.5ml of 10% sodium dodecyl sulphate (SDS), and 5ml of 0.5M EDTA. Add sterile, DEPC-treated H₂O to a volume of 225ml. Adjust pH to 6.8. Add sterile, DEPC-treated H₂O to 250ml. Autoclave.
5. 0.40 M Phosphate Buffer: in a 500ml flask, combine 100ml of 1M Phosphate Solution, pH 6.8, 2.5ml of 10% sodium dodecyl sulphate (SDS), and 5ml of 0.5M EDTA. Add sterile, DEPC-treated H₂O to a volume of 225ml. Adjust pH to 6.8. Add sterile, DEPC-treated H₂O to 250ml. Autoclave.
6. “1.00M Phosphate Buffer” (actual concentration of phosphate in this solution is .91M): In a 500ml flask, combine 30ml of 1M Phosphate Solution, pH6.8, 2.5ml of 10% sodium dodecyl sulphate (SDS), and 5ml of 0.5M EDTA. Add sterile, DEPC-treated H2O to a volume of 225ml. Adjust pH to 6.8. Add sterile, DEPC-treated H₂O to 250ml. Autoclave.
7. Hydroxyapatite hydration: Weight out 1g of hydroxyapatite and add to a 50ml tube. Add 6ml of 0.12M phosphate buffer to the hydroxyapatite and invert to mix. Prior to use bring temperature to 60°C and mix thoroughly. Store for extended periods of time at 4°C.
8. Prior to use, equilibrate all phosphate buffers and hydrated hydroxyapatite at 60°C.

2. Preparation of Econo-Column

1. Close stopcock. Rinse column several times with deionized H₂O by repeatedly inverting the column and decanting.
2. Remove the stopcock from the Econo-column and autoclave the column to sterilize.
3. Replace and close stopcock. Add 1ml of Sigmacote to the sterile Econo-column and coat all glass surfaces. Open the stopcock and decant.
4. Attach column to a circulating water bath and set temperature to 60°C. To einsure the least amount of heat loss across the column wrapping the column in an insulating agent such as aluminum foil or foam pipe insulation is recommended.
5. Rinse the Econo-column twice with sterile, RNase-free H₂O then twice with sterile, RNase-free 0.12M Phosphate Buffer.

3. Hydroxypaptite Chromotography

1. Making sure the stopcock is closed, slowly add 2ml of pre-prepared, resuspended hydroxyapatite to the bottom of the Econo-column using a sterile 2ml serological pipette.
2. Allow the hydroxyapatite to settle under the force of gravity for 30 minutes.
3. Drain buffer from column and close stopcock. Combine nucleic acids with 0.12M phosphate buffer in a final volume of 500 μl and incubate at 60°C for 10 minutes in a heat block or water bath.
4. Quickly apply nucleic acids prepared in 0.12M phosphate buffer to the hydroxyapatite using a 2ml serological pipette making sure not to disturb the column.
5. Allow the nucleic acids to bind to the hydroxyapatite for 30 minutes.
6. Place a 15ml tube under the column, open the stopcock and collect the initial sample containing ssDNA. Close stopcock.
7. Add 6ml of 0.12M phosphate buffer to the hydroxyapatite making sure not to disturb the column, open the stopcock, and collect single-stranded DNA in the 15ml tube from the previous step. Close stopcock.
8. Add 1 volume of a phenol:chloroform:isoamyl alcohol (25:25:1 v/v/v) solution to the tube, mix vigorously and centrifuge at 3500 x g for 15 minutes. Transfer supernatant containing ssDNA to a new 15ml tube.
9. Repeat 3.76 and 3.87 using 6ml of 0.20M phosphate buffer to elute and purify RNA from the column making sure to use a new 15ml tube for collection.
10. Repeat 3.76 and 3.87 using 6ml of 0.40M phosphate buffer to elute and purify dsDNA from the column making sure to use a new 15ml tube for collection.
11. Repeat 3.76 and 3.87 using 6ml of 1.00M phosphate buffer to strip the column of any residual dsDNA making sure to use a new 15ml tube for collection.

4. Desalting Nucleic Acid Samples

1. Transfer 4-5ml of sample to an Amicon Ultra-4 centrifugal filter device outfitted with a 30,000 molecular weight cut off Ultracel membrane.
2. Concentrate sample to < 500μl by spinning at 6,000 x g, 30°C, 5 minutes (or until concentrated volume is achieved) in a fixed angle rotor. Discard flow through.
3. Add the remainder of the sample(s) to the Amicon Ultra-4 centrifugal filter device and bring the volume up to 4-5ml with Rnase free 1X TE Buffer.
4. Concentrate sample to < 500μl by spinning at 6,000 x g, 30°C, 5 minutes (or until concentrated volume is achieved) in a fixed angle rotor. Discard flow through.
5. Add 4-5ml of Rnase free 1X TE Buffer to the Amicon Ultra-4 centrifugal filter device. Concentrate sample to < 500μl by centrifuging at 6,000 x g, 30°C, 5 minutes (or until concentrated volume is achieved) in a fixed angle rotor. Discard flow through.
6. Repeat step 4.5 an additional 5 times to completely desalt nucleic acid sample(s).
7. Transfer remaining sample(s) to a sterile 1.7ml eppendorf tube. Add 1/10th volume 3M sodium acetate, pH 7.0, two volumes of 100% ethanol, and 1μl of Glycoblue. Mix well by vortexing.
8. Centrifuge at 28,000 x g, 4°C, 60 minutes. Decant making sure not to disturb the pellet. Add 300μl of 70% ethanol. Spin at 28,000 x g, room temperature for 10 minutes. Decant, dry and resuspend each fraction in an appropriate volume of Rnase-free TE buffer.

5. Representative Results:

Figure 1 summarizes the methods presented for using hydroxyapatite chromatography to fractionate ssDNA, dsDNA and RNA nucleic acids from a mixed viral assemblage. This method exploits the charge interaction between the negatively charged phosphate backbone of the nucleic acids and the positively charged Ca²⁺ ions present in the hydroxyapatite and allows for the efficient fractionation of nucleic acid subtypes (ssDNA, dsDNA and RNA) with increasing phosphate buffer concentrations ¹².

The hydroxyapatite fractionation of an in vitro “community” of known ssDNA (M13mp18), dsDNA (lambda) and RNA (MS2 and phi6) viral genomes is illustrated in Figure 2. The nucleic acids were combined in equal concentrations, applied to the hydroxyapatite column and were eluted using an increasing concentration of phosphate buffer. Each nucleic acid subtype elutes independent of the others with less than 9% carry-over from one fraction to the next.

The application of this technique to nucleic acids isolated from a viral community collected from the Chesapeake Bay is shown in Figure 3. The total nucleic acid yield isolated from purified viruses was applied to the hydroxyapatite column. Genomic material consisting of ssDNA, RNA and dsDNA was independently eluted with 0.12M, 0.20M and 0.40M/1.00M concentrations of phosphate buffer respectively. Double-stranded DNA is eluted at phosphate concentrations of 0.40M and 1.00M and in this case, dominates this viral community compared to ssDNA and RNA genotypes. This observation is consistent with the expected viral community composition of marine and estuarine environments where the majority of recoverable nucleic acids are dsDNA ¹³.

Figure 1. Flow diagram of the hydroxyapatite chromatography method for the fractionation of nucleic acids. A mixture of ssDNA, dsDNA and RNA prepared in 0.12M phosphate buffer is heated to 60°C and applied to a hydroxyapatite column maintained at a constant 60°C using a circulating water bath. Nucleic acids (ssDNA, RNA and dsDNA) are eluted from the hydroxyapatite with increasing concentrations of a phosphate-containing buffer. This figure has been reproduced with permission from American Society of Microbiology and was originally featured in Andrews-Pfannkoch et al. 2010¹².

Figure 2. Separation of known viral nucleic acids using hydroxyapatite chromatography. Equal concentrations of M13mp18 ssDNA, MS2 ssRNA, phi6 dsRNA and lambda dsDNA (lanes 2-5, respectively) were combined (lane 6) and applied to a hydroxyapatite column. Single-stranded DNA (M13mp18), RNA (MS2/phi6) and dsDNA (lambda) were independently eluted from the hydroxyapatite column using 0.12M (lane 8), 0.18M (lane 9) and 0.40M/1.00M (lane 10). A 1kb ladder (lanes 1, 7) was used to confirm genome sizes. This figure has been reproduced with permission from American Society of Microbiology and was originally featured in Andrews-Pfannkoch et al. 2010¹².

Figure 3. Separation of viral nucleic acids isolated from a community within the Chesapeake Bay. Nucleic acids were isolated and applied to a hydroxyapatite column. ssDNA(lane 0.12M), RNA (lane 0.20M) and dsDNA(lanes 0.40M/1.0M) were independently eluted using phosphate buffer concentrations of 0.12M, 0.20M and 0.40M/1.00M, respectively. Hi Mass DNA Ladder (lane L1) and 1kb Ladder (lane L2) were used to visually confirm approximate molecular weight and mass of nucleic acids. This figure has been reproduced with permission from American Society of Microbiology and was originally featured in Andrews-Pfannkoch et al. 2010¹².