Aug 26, 2024

Public workspaceViral Enumeration of EPS Samples Using Wet Mount Epifluorescence Microscopy

This protocol is a draft, published without a DOI.
  • 1Department of Bioinformatics and Genomics, North Carolina Research Campus, The University of North Carolina at Charlotte, Kannapolis, North Carolina, USA;
  • 2Computational Intelligence to Predict Health and Environmental Risks (CIPHER), The University of North Carolina at Charlotte, Charlotte, North Carolina, USA;
  • 3Department of Marine Sciences and Geoscience, University of Connecticut, Storrs, Connecticut, USA
Madeline Bellanger
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External link: https://journals.asm.org/doi/full/10.1128/aem.01744-23
Protocol Citation: Madeline Bellanger, Pieter Visscher, Richard Allen White III 2024. Viral Enumeration of EPS Samples Using Wet Mount Epifluorescence Microscopy. Protocol exchange https://protocols.io/view/viral-enumeration-of-eps-samples-using-wet-mount-e-dj7m4rk6
Manuscript citation:
Bellanger M, Visscher P, White RA.2023.Viral enumeration using cost-effective wet-mount epifluorescence microscopy for aquatic ecosystems and modern microbialites. Appl Environ Microbiol89:e01744-23.https://doi.org/10.1128/aem.01744-23
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: August 26, 2024
Last Modified: August 26, 2024
Protocol Integer ID: 106445
Keywords: EFM, epifluorescence microscopy, viral enumeration, microbialite, enumeration, phage
Funders Acknowledgement:
NASA Astrobiology Institute
Grant ID: NNH22ZDA001N-EXO
Abstract
Epifluorescence microscopy (EFM) has been the gold standard method for environmental viral enumeration for over 25 years. Currently, standard EFM methods using the Anodisc filters are no longer cost-effective (>$15 per slide). We present a cost-effective method for environmental viral enumeration from aquatic samples, microbial mats, and exopolymeric substances (EPSs) within modern microbialites using EFM. Our integrated approach, which includes filtration, differential centrifugation, chloroform treatment, glutaraldehyde fixation, benzonase nuclease treatment, probe sonication (EPS and mat only), SYBR Gold staining, wet mounting, and imaging, provides a robust method for modern microbialites and aquatic samples. Our method provides a robust and cost-effective (~$0.75 per sample) viral enumeration within modern microbialites and aquatic ecosystems.
Guidelines
This method is used to enumerate viruses in EPS samples collected from the environment. See our protocols for water viral enumeration, microbial mat viral enumeration, and soil viral enumeration!
Materials
Consumables
  • Whatman grade 1 qualitative filter paper
  • 0.65 µm PVDF Durapore membrane filter (hydrophilic)
  • 0.45 µm PVDF Durapore membrane filter (hydrophilic)
  • 0.22 µm PVDF Durapore membrane filter (hydrophilic)
  • 30 kDa MWCO Millipore centrifuge filters (of desired size)
  • 1.5 mL low protein binding, nuclease free microcentrifuge tubes
  • P1000 pipette tips
  • P200 pipette tips
  • P10 pipette tips
  • 5 ml Eppendorf tubes
  • Microscope slides
  • Slide covers

Chemicals
  • 70% Ethanol
  • 25% EM grade glutaraldehyde
  • Chloroform
  • EDTA
  • Benzonase
  • SYBR Gold nucleic acid stain
  • Poly-L-Lysine 0.1% w/v
  • 1X PBS
  • Ascorbic acid
  • Microscope immersion oil

Equipment
  • P1000 pipette
  • P200 pipette
  • P10 pipette
  • Centrifuge capable of holding 50 ml conical tubes or wide neck bottles (62 mm diameter; 146 mm length, only if using Centricon-70 plus centrifuge filters)
  • Microcentrifuge
  • Vortexer
  • Probe sonicator
  • Heat block
  • Balance
  • Fluorescence microscope equipped with a 100x oil immersion lens and blue excitation light (495 nm)
Protocol materials
ReagentChloroform
Step 5
ReagentBenzonase® NucleaseMerck MilliporeSigma (Sigma-Aldrich)Catalog #E1014 SIGMA
Step 17
Safety warnings
  • Fixation with glutaraldehyde and chloroform treatment needs to be performed in a fume hood with a face shield and proper PPE.
  • Needles used to remove glutaraldehyde from serum vials need to be disposed of in a sharps container within the fume hood. Never replace the cap on a needle. Once the needle has been used, immediately deposit it into the sharps container.
Sample Collection and Cleaning
Sample Collection and Cleaning
Tare a 1.5 mL low protein binding nuclease free tube on a top loading balance.
Collect approximately Amount100 mg of mat using a scoopula or similar tool cleaned with 70% ethanol and transfer to the tube. Record the mass of the mat sample.
Add Amount900 µL ultrafiltrate from the same location to the tube.
Vortex at medium-high speed for Duration00:00:10 .
10s
Add Amount500 µL of ReagentChloroformContributed by users to the sample.
Safety information
A lab coat, face and eye protection, and double gloves should be worn whenever working with chloroform, in addition to being performed in a fume hood.

Note
A small glass pasteur pipette must be used when working with chloroform. The pasteur pipette’s full volume should be 500 μL.

Toxic
Centrifuge the samples at Centrifigation14.000 rpm, 00:05:00 (standard mini-fuge speed).

5m
Centrifigation
Carefully pipette Amount92 µL of the top layer of supernatant into a fresh 1.5 mL low protein binding nuclease free microcentrifuge tube, proceed to the next section: Fixation (Go togo to step #8 ).

Fixation
Fixation
Add 8 μL of EM grade 25% glutaraldehyde to each of the 92 μL samples (final concentration of 2%). Pipette to mix.
Safety information
Fixation should be done in a fume hood as it requires working with glutaraldehyde Additionally, a lab coat, face and eye protection, and gloves should be worn whenever working with glutaraldehyde.

Allow samples to fix in the dark at Temperature4 °C for Duration00:30:00 .

30m
Incubation
OPTIONAL: Flash freeze samples using liquid nitrogen. If liquid nitrogen is not available, putting samples directly in a -80ºC freezer can be done. Samples can be stored in the -80ºC freezer until use.
Note
This is an optional stopping point. Freezing is not necessary and may cause a decrease in viral counts. If you do not have time to proceed to dyeing and imaging, freeze your samples until use.

Optional
Pause
Preparation for EFM and Imaging
Preparation for EFM and Imaging
Thaw fixed samples at room temperature (if applicable). During this time, start heating a heat block to Temperature37 °C . Start heating another heat block to Temperature80 °C .
Aliquot Amount20 µL of sample into a new 1.5 mL low protein binding nuclease free microcentrifuge tube.
Add Concentration0.1 millimolar (mM) EDTA to the sample with the tube on ice (Amount4 µL of Concentration0.5 millimolar (mM) EDTA).
Incubate the samples TemperatureOn ice for Duration00:15:00 in the dark.

15m
Incubation
Probe sonicate the samples in three Duration00:00:10 intervals with Duration00:00:10 between each interval at 50 Hz/40 amp while in an ice bath.
Note
  1. Use a foam tube rack to keep the mouth of the tube out of the water.
  2. Make sure to use a probe sonicator with a microtip to ensure the probe fits in the tube and makes contact with the sample for the duration of the 10 second interval.
  3. Clean the probe tip with 70% ethanol before and after each sample has been through the entire sonication cycle.

20s
Aliquot Amount19 µL of each sample into a new 1.5 mL low protein binding nuclease free microcentrifuge tube.

Add Amount1 µL of ReagentBenzonase® NucleaseMerck MilliporeSigma (Sigma-Aldrich)Catalog #E1014 SIGMA to each sample. Pipette to mix.
Incubate the samples in a heat block at Temperature37 °C for Duration00:30:00 .
30m
Incubation
Add Amount4 µL SYBR Gold working stock to the sample in the dark and pipette to mix.
Note
The stain is light sensitive so the following steps should be done in the dark. Before preparing working stock, be sure to check if there is already some prepared. Working stocks may be stored in the -20ºC freezer or one working stock at a time may be stored in the 4ºC fridge.
  1. Thaw commercial stock of ReagentSYBR Gold Nucleic Acid Gel StainContributed by usersCatalog # S-11494 at room temperature in the dark.
  2. Once the commercial stock is thawed, vortex for 10 seconds on medium-high speed, then centrifuge in a microcentrifuge for 5 minutes.
  3. Dilute the commercial stock 1:10 with autoclaved and filtered (0.22 μm PVDF membrane filters) molecular biology grade water in a fresh 5 mL Eppendorf tube.
  4. Filter the working stock through a 0.22 μm syringe filter into a fresh 5 mL Eppendorf tube.
  5. Aliquot 250 μL of the working stock into fresh black or darkened 1.5 mL low protein binding nuclease free microcentrifuge tubes.
  6. Store the working stocks at -20ºC.
  7. Working stock that is being used should be stored at 4ºC in the dark. It can work effectively for about a month, but will degrade over time (take note of when working stock is moved to 4ºC).
  8. Working stock at -20ºC can be stored indefinitely and transferred to 4ºC when ready to use. Avoid freezing and thawing multiple times.


Incubate the sample in a heat block covered in aluminum foil at Temperature80 °C for Duration00:15:00 .
15m
Incubation
While the sample is incubating, prepare a 10% ascorbic acid antifade solution.
Note
Ascorbic acid antifade needs to be prepared fresh each time, so only prepare a small amount as needed.
  1. Add 1 mL 1X PBS to a fresh 1.5 mL low protein binding nuclease free microcentrifuge tube.
  2. Add 0.1 g ascorbic acid to the tube.
  3. Mix thoroughly by vortexing until the ascorbic acid has dissolved completely.
  4. Filter the mixture twice through 0.22 μm syringe filters.

Remove the sample from the heat block and add Amount2 µL of ascorbic acid antifade solution. Pipette to mix.
Pipette Amount5 µL onto a clean, labeled, poly-L-lysine treated slide.
Note
  1. Thoroughly clean slides with 70% ethanol and allow slides to dry completely.
  2. Prepare a 10% polylysine solution by diluting Poly-L-Lysine 0.01% w/v 1:10 in autoclaved Nanopure water (18.2 MΩ) (using plastic pipette tips and a plastic container).
  3. Soak slides in the polylysine solution in a plastic container for 5 minutes (increasing time will not improve performance). Ensure there are no air bubbles on the slides.
  4. Dry slides in a drying oven at 60ºC for one hour or overnight at room temperature.
  5. Once dried, slides can be stored in a plastic slide box at room temperature until use.

Gently cover with a cover slide, avoiding creating air bubbles.
Image on a fluorescence microscope under FITC blue excitation light (495 nm) with a 100x oil stage.
Imaging
Protocol references
Bellanger M, Visscher P, White RA.2023.Viral enumeration using cost-effective wet-mount epifluorescence microscopy for aquatic ecosystems and modern microbialites. Appl Environ Microbiol 89:e01744-23. https://doi.org/10.1128/aem.01744-23