In Situ Detection of Bacteria in Mouse Gingival Tissue Sections

Abstract

Source: Choi, Y. S., et al. In Situ Detection of Bacteria within Paraffin-embedded Tissues Using a Digoxin-labeled DNA Probe Targeting 16S rRNA. J. Vis. Exp. (2015).

This video demonstrates the in situ detection of bacteria in mouse gingival tissue sections using digoxin-labeled DNA probes targeting bacterial DNA. The section is incubated with the probe. Alkaline phosphatase-conjugated antibodies specific to digoxin are added. Endogenous phosphatases are inactivated, and a colored precipitate is obtained by substrate addition. The section is counterstained, dehydrated, cleared in xylene, and mounted before microscopic visualization of bacteria.

Protocol

All procedures involving animal samples have been reviewed and approved by the appropriate animal ethical review committee.

1. Probe Preparation

1. PCR amplification of the probe
   1. For the Porphyromonas gingivalis–specific probe, amplify a 343-bp DNA fragment of P. gingivalis 16S rRNA by PCR using the genomic DNA of P. gingivalis and the following primers: 5'- TGC AAC TTG CCT TAC AGA GG-3' and 5'- ACT CGT ATC GCC CGT TAT TC-3'. Perform amplifications with the following cycle conditions: 35 cycles at 95 °C for 30 s, 60 °C for 30 s, and 72 °C for 1 min 20 s, followed by a 5 min extension at 72 °C.
   2. Amplify the eubacterial probe using a 70-bp DNA fragment (5'-CAGGTGCTGCATGGCTGTCGTCAGCTCGTGTTGTGAAATGTTGGGTTAAGTCCCGCAACGAGCGCAACCC-3') synthesized as an oligonucleotide and the following primers: 5'-CAG GTR CTG CMT GGY-3' and 5'-AGG GTT GCG CTC GTT-3'. Perform amplifications with the following cycle conditions: 40 cycles at 94°C for 30 s, 60 °C for 30 s, and 72 °C for 1 min 20 s, followed by a 5 min extension at 72 °C.
   3. Precipitate the PCR products (≥500 µl) by adding 3 M sodium acetate (pH 5.2) and 100% ethanol (at a 10:1:2 ratio) and incubating at -20 °C for 2 hr.
   4. Centrifuge the mixture at 14,000 x g for 15 min, resuspend the pellet in 100 µl of Tris-ethylenediaminetetraacetic acid (EDTA) or TE buffer, and measure the DNA concentration by optical density at 260 nm.
2. Digoxigenin (DIG)-labeling using a DIG DNA labeling and detection kit
   1. Mix 3 µg of the probe with water to a final volume of 15 µl.
   2. Denature the DNA at 95 °C for 10 min and quickly chill on ice.
   3. Add 2 µl of 10x hexanucleotide mix, 2 µl of deoxynucleoside triphosphate (dNTP)-labeling mix, and 1 µl of Klenow enzyme to 15 µl of the denatured DNA.
   4. Mix and incubate at 37 °C for 24 h to 48 h, and stop the reaction by heating at 65 °C.
3. Check the sensitivity of the DIG-labeled probe using a DIG DNA labeling and detection kit
   1. Manually load 1 µl of serial dilutions of the positive control probe provided in the kit and 1 ng of the DIG-labeled probe on the nylon membrane and dry for 5 min at room temperature (RT).
   2. Briefly soak the membrane in 2x saline-sodium citrate (SSC) buffer (0.3 M sodium chloride or NaCl, 30 mM sodium citrate, pH 7.0) and incubate the membrane at 80 °C for 1 hr to immobilize the DNA.
   3. Briefly soak the membrane in maleic acid buffer (MAB, 0.1 M maleic acid, 0.15 M NaCl, pH 7.5) and incubate with anti-DIG alkaline phosphatase (AP)-conjugated antibody diluted (1:5,000) in 6 ml of blocking solution provided in the kit at RT for 30 min.
   4. Wash the membrane with MABT (MAB containing 1% Tween 20) and apply 40 µl of the nitro-blue tetrazolium/5-bromo-4-chloro-3'-indolyl phosphate (NBT/BCIP) solution mixed with 2 ml detection buffer (0.1 M tris(hydroxymethyl)aminomethane hydrochloride or Tris-HCl, 0.1 M NaCl, 0.05 M magnesium chloride or MgCl₂, pH 9.5) onto the membrane for 1 min. If the sensitivity of the labeled probe is not satisfactory, repeat steps from 1.1.3 to 1.3.4.
   5. Measure the DNA concentration of the labeled probe (OD₂₆₀) and adjust the concentration to 100 ng µl-1.
4. Check the specificity of the DIG-labeled probe
   1. Denature genomic DNA samples (25 ng 3 µl-1 per sample) from various bacterial species, including the bacterium targeted by the specific probe, at 95 °C for 10 min and quickly chill on ice.
   2. Manually load the denatured DNA on the nylon membrane and dry for 20 min at RT.
   3. Briefly soak the membrane in 2x SSC buffer and incubate the membrane at 80 °C for 2 hr to immobilize the DNA.
   4. Block the membrane with a blocking solution at RT for 1 hr.
   5. Dilute the probe at 1 ng µl-1 in hybridization buffer, denature the diluted probes, and apply them onto the membrane.
   6. Incubate the membrane at 45 °C for 1 hr.
   7. Wash the membrane three times with 2x SSC buffer.
   8. Briefly soak the membrane in MAB.
   9. Incubate with anti-DIG AP-conjugated antibody diluted (1:2,000) in 6 ml of blocking solution at RT for 1 hr.
   10. Wash the membrane with MABT and apply 40 µl of the NBT/BCIP solution mixed with 2 ml detection buffer.
   11. When the probe does not achieve the expected specificity, increase the hybridization temperature until the specificity is observed.

2. In Situ Hybridization

Note: To avoid drying of the specimens and reagents, perform all incubations in a humidified chamber lined with wet paper towels.

1. De-paraffinization and rehydration of tissue sections
   1. Prepare 4 µm-thick tissue sections from paraffin-embedded blocks. Formalin, paraformaldehyde, and zinc-based fixative are compatible with this protocol.
   2. Prepare all reagents using diethyl pyrocarbonate (DEPC)-treated water.
   3. Heat slides in a dry oven at 60 °C for 30 min and incubate slides at RT for 30 min.
   4. Immerse slides in 100% xylene for 5 min three times; use fresh xylene each time.
      Note: Do this de-waxing procedure in a chemical fume hood.
   5. Immerse slides in 100% ethanol for 5 min twice, using fresh ethanol each time, and rehydrate specimens in serial 90%, 80%, and 70% ethanol solutions for 5 min each.
   6. Immerse slides in DEPC-treated water for 1 min and wash slides in DEPC-treated phosphate-buffered saline or PBS (pH 7.4) for 6 min.
2. Pretreatments of tissue sections
   1. Immerse slides in 0.1 N hydrochloric acid for 20 min and wash slides in DEPC-treated water for 30 s.
   2. Draw a hydrophobic barrier surrounding specimens using a wax pen.
      Note: The size of the hydrophobic barrier depends on the size of specimens. Therefore, the volumes of reagents used in the following steps vary depending on the size of specimens but have to fill the hydrophobic barrier (50 µl for small specimens and 400 µl for large specimens).
   3. Treat specimens with 50 to 400 µl of proteinase K (1 to 10 µg ml^-1 in DEPC-treated PBS) in a dry oven at 37 °C for 30 min and wash slides in DEPC-treated 1x PBS for 1 min.
   4. Soak slides in 4% paraformaldehyde in DEPC-treated PBS for 10 min, then wash slides in DEPC-treated PBS for 1 min.
   5. Soak slides in 0.1 M triethanolamine-HCl (pH 8.0) containing 0.5% acetic anhydride for 20 min and wash slides in DEPC-treated water for 30 s.
3. Hybridization with the probe and washing
   1. Immerse slides in 2x SSC buffer for 20 min.
   2. Dilute the probe at 1 ng µl^-1 in hybridization buffer (4x SSC, 50% [vol/vol] formamide, 1x Denhardt’s solution, 10% [wt/vol] dextran sulfate, 0.1% [wt/vol] sodium dodecyl sulfate, 0.4 mg ml-1 salmon sperm DNA). For negative controls, mix the labeled probe with a 10-fold excess amount of non-labeled probe.
   3. Denature the diluted probes and apply 50 to 400 µl onto tissue sections. Place a cover slip on the slide and seal it with nail polish.
   4. Heat slides in the PCR machine at 90 °C for 10 min and incubate slides in a humidified chamber overnight (O/N) at 45 °C or optimal temperature determined at step 1.4.11.
   5. Cool the slides at 4 °C for 30 min, remove cover slips, and immerse slides in a serial SSC buffer as follows: 4x SSC for 10 min, pre-warmed (45 °C) 2x SSC for 20 min, 2x SSC for 10 min, and 0.2x SSC for 10 min.
4. Detection with anti-DIG AP-conjugated antibody
   1. Wash slides in MABT for 5 min.
   2. Block with 50 to 400 µl of blocking solution with 1% Tween 20 for 20 min.
   3. Add 50 to 400 µl of anti-DIG-AP antibody diluted in blocking solution (1:1,000) and incubate at 37 °C for 90 min.
   4. Wash slides in MABT for 10 min.
   5. Immerse slides in detection buffer containing 1% Tween 20 for 5 min.
   6. Treat with 50 to 400 µl of 1 mM levamisole (in detection buffer containing 1% Tween 20) for 5 min to inactivate endogenous alkaline phosphatase.
   7. Distribute 50 to 400 µl of the premixed NBT/BCIP solution (diluted in detection buffer at 1:100) onto each specimen and incubate slides in a humidified chamber at RT for 2 to 3 hr until the developed signal is satisfactory.
   8. Rinse slides with de-ionized water to stop visualization and apply 50 to 400 µl of 0.05% [wt/vol] methyl green as a counterstain at 37 °C for 10 min.
   9. Rinse slides with de-ionized water, dehydrate in 100% ethanol, and immerse in xylene.
   10. Apply 80 µl of mounting solution onto each slide and cover with cover slips.

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Acetic anhydride	Sigma	6404
50% Dextran sulfate solution	Millipore	S4030
50X Denhardt’s solution	Sigma	D2532
Diethyl pyrocarbonate (DEPC)	Sigma	P159220
Digoxigenin (DIG) DNA labeling and detection kit	Roche	11 093 657 910
Formamide	Sigma	F9037
ImmEdge™ Pen	Dako	H-400
Levamisole	Vector	SP-5000
Magnesium chloride	Sigma	246964
Maleic acid	Sigma	M0375
Methyl green	Sigma	M6776
Paraformaldehyde	Sigma	P1648
Permount	Fisher	SP15-500
Salmon sperm DNA solution	Invitrogen	#15632-011
Sodium chloride	Sigma	S9625
Sodium citrate	Duksan	D1420
Sodium dodecyl sulfate	Amresco	227
Triethanolamine-HCl	Sigma	90279
Tris-HCl	Research organics	3098T