Method Article

In Situ Characterization of Shewanella oneidensis MR1 Biofilms by SALVI and ToF-SIMS

DOI:

10.3791/55944

āø±

August 18th, 2017

In This Article

Summary

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

This article presents a method for growing a biofilm for in situ time-of-flight secondary ion mass spectrometry for chemical mapping in its hydrated state, enabled by a microfluidic reactor, System for Analysis at the liquid Vacuum Interface. The Shewanella oneidensis MR-1 with green fluorescence protein was used as a model.

Abstract

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Bacterial biofilms are surface-associated communities that are vastly studied to understand their self-produced extracellular polymeric substances (EPS) and their roles in environmental microbiology. This study outlines a method to cultivate biofilm attachment to the System for Analysis at the Liquid Vacuum Interface (SALVI) and achieve in situ chemical mapping of a living biofilm by time-of-flight secondary ion mass spectrometry (ToF-SIMS). This is done through the culturing of bacteria both outside and within the SALVI channel with our specialized setup, as well as through optical imaging techniques to detect the biofilm presence and thickness before ToF-SIMS analysis. Our results show the characteristic peaks of the Shewanella biofilm in its natural hydrated state, highlighting upon its localized water cluster environment, as well as EPS fragments, which are drastically different from the same biofilm's dehydrated state. These results demonstrate the breakthrough capability of SALVI that allows for in situ biofilm imaging with a vacuum-based chemical imaging instrument.

Introduction

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Bacterial biofilms are surface-associated communities which have evolved over time as a defense for bacteria to survive varying adverse physical and mechanical stimuli, wherein cells are able to attach and survive in many possible environments.1,2 Biofilms are vastly investigated and have applications in many fields such as biomedicine, biomedical engineering, agriculture, and industrial research and development.1,2 Understanding the chemical mapping of these complex microbial communities, including their self-produced extracellular polymeric substance....

Access restricted. Please log in or start a trial to view this content.

Protocol

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

1. Preparation of Materials

  1. Preparation of Medium Tubing
    1. Serum Bottles (one needed per biofilm culture and three needed per growth curve)
      Note: As mentioned in the introduction, any growth medium suitable to provide the nutrients needed for the strain of bacteria of interest can be utilized for this procedure; in this case, "nanowires" media and TSB without dextrose medium was used for the growth of S. oneidensis MR-1 GFP.13
      1. Deposit 20 mL of growth medium into one 70 mL serum bottle, cap the stopper and crimp the bottle. Cover the top with a piece of clean sterile a....

Access restricted. Please log in or start a trial to view this content.

Results

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

These representative results serve to show how the chemical profile of the attached biofilm can be identified and interpreted, as obtained through ToF-SIMS. After plotting mass spectra from ToF-SIMS data acquisition, highlighted briefly in the procedures section, peak identification should be conducted in order to assign identities to each respective m/z value. This can be done through extensive literature review on mass spectrometry on bacteria and specific chemical fragments that are ex.......

Access restricted. Please log in or start a trial to view this content.

Discussion

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

After inoculating at log-phase, it is important to test the number of days and temperature at which the biofilm should grow before it is healthy and thick enough for imaging, as described in step 3.1. This procedure specifically covers culturing a S. oneidensis MR1 biofilm at room temperature; however different room temperatures can influence the rate of growth. Therefore, it is critical to use optical imaging to understand whether the biofilm is ready before proceeding to ToF-SIMS analysis. Similarly, different strains .......

Access restricted. Please log in or start a trial to view this content.

Disclosures

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

The authors have nothing to disclose.

Acknowledgements

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

We are grateful to the Pacific Northwest National Laboratory (PNNL) Earth and Biological Sciences (EBD) mission seed Laboratory Directed Research and Development (LDRD) fund for support. Instrumental access was provided through a W. R. Wiley Environmental Molecular Sciences Laboratory (EMSL) General User Proposal. EMSL is a national scientific user facility sponsored by the Office of Biological and Environmental Research (BER) at PNNL. The authors thank Dr. Yuanzhao Ding for proof reading the manuscript and providing useful feedback. PNNL is operated by Battelle for the DOE under Contract DE-AC05-76RL01830.

....

Access restricted. Please log in or start a trial to view this content.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
ToF-SIMSIONTOFTOF.SIMS 5Resolution:>10,000 m/Δm for mass resolution;>4,000 m/Δm for high spatial resolution
System for Analysis at the Liquid Vacuum Interface (SALVI)Pacific Northwest National LaboratoryN/ASALVI is a unique, self-contained, portable analytical tool that, for the first time, enables vacuum based scientific instruments such as time-of-flight secondary ion mass spectrometry (ToF-SIMS) to analyze liquid surfaces in their natural state at the molecular level.
-80°C FreezerNew Brunswick ScientificN/AU410 Premium Energy Efficient Ultra-Low Temperature Freezer
4°C RefrigeratorBioCold ScientificN/ACOLDBOX1
Orbital ShakerNew Brunswick ScientificN/AInnova 4900 Multi-Tier Environmental Shaker, set at 30 degrees Celsius for serum bottle and flask culturing, set at 150rpm.
Syringe PumpCole-ParmerEW-74905-02Cole-Parmer Syringe Pump, Infusion Only, Touchscreen Control 74905-02, used for injecting liquid into the tubing system and SALVI at a constant flowrate.
IncubatorBarnstead InternationalLT1465X3Lab-Line incubator, set at 30 degrees Celsius for plate culturing.
AutoclaveGetinge533LSUsed to sterilize PEEK fittings, tubing systems, serum vials, and medium. Model 533LS Vacuum Steam Sterilizer
SpectrophotometerThermo Fisher Scientific4001-000GENESYS 20 spectrophotometer for OD600 readings of cuvettes for growth curves.
Biological Safety CabinetThermo Fisher Scientific13851300 Series AZ Biological Safety Cabinet
Fluorescence MicroscopeNikonN/ANikon OPTIPHOT-2 fluorescence microscope with camera and super high pressure mercury lamp power supply.
pH MeterMettler Toledo51302803Used to test the pH of the ā€œnanowiresā€ medium after finished and before autoclaving.
PEEK UnionValcoZU1TPKFor connecting the inlet and outlet of SALVI, the syringe to the tubing system, and the inlet of the SALVI to the drip chamber of the tubing system.
5 Axes Sample StageIONTOFN/AStage is self-made for mounting SALVI in ToF-SIMS.
Barnstead Nanopure Water Purification SystemThermo Fisher ScientificD11921ROpure LP Reverse Osmosis filtration module (D2716)
PipetteThermo Fisher Scientific21-377-821Range: 100 to 1,000 µL.
Pipette TipNeptune2112.96.BS1,000 µL pipette tips
Razor Blade HandleStanleyN/AStanley Bostitch Razor Blade Scraper with 5 Single-Edge Blades, used for cutting PTFE tubing
SyringeBD3096591 mL
SyringeBD3096573 mL
SyringeBD3096465 mL; Used for making the drip chamber
SyringeBD30960410 mL
SyringeBD30283020 mL
Disposable PipetteThermo Fisher Scientific13-678-1125 mL Fisherbrandā„¢ Sterile Polystyrene Disposable Serological Pipets with Magnifier Stripe, for filling serum bottles.
Electric Pipette FillerPipet-aidP-57260Vacuum pressure electric serological pipette filler
Serum BottleSigma33109-UHolds approximately 69 mL of liquid for culture growth, optimum for use of 20mL culture per bottle.
Anaerobic Culture TubeVWR89167-178Anaerobic Tubes, 18 x 150 mm, Supplied with 20 mm Blue Butyl Rubber Stopper and Aluminum Seal.
Rubber StopperSigma27235-USilicone stopper, used for sealing serum bottles and for creating the tubing system/drip chamber.
Aluminum Crimp Seal (without septum)Sigma27227-UAluminum seal for top of serum bottle for use with serum bottle crimper.
Serum Bottle Aluminum Seal CrimperWheaton22430730 mm crimper with standard seal.
PTFE TubingSupelco58697-U1.58 mm OD x 0.5 mm ID 50 ft. PTFE Teflon tubing, used for creating the tubing system.
Disposable CuvettesGMBH759085D1.5 Ml for use with spectrophotometer.
NeedleBD30301522G; used for serum bottle injection.
NeedleBD30512023G; used for punching-through rubber stopper to create drip tubing system.
Shewanella oneidensis MR-1 with GFPN/AN/AMatthysse AG, Stretton S, Dandie C, McClure NC, & Goodman AE (1996) Construction of GFP vectors for use in Gram-negative bacteria other than Escherichia coli. FEMS Microbiol Lett 145(1):87-94.Ā 
EthanolThermo Fisher ScientificĀ S25310A95% Denatured
TSABD212305Tryptic soy agar for culturing the model organism (S. oneidensis) used in this protocol
PIPES BufferSigmaP-1851Used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Sodium HydroxideSigmaS-5881Used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Ammonium ChlorideSigmaA-5666Used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Potassium ChlorideSigmaP-4504Used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Sodium Phosphate MonobasicSigmaS-9638Used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Sodium ChlorideThermo Fisher ScientificS271-3Used for ā€œnanowiresā€ medium, and used to make mineral solution used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Sodium lactateSigmaL-137560%(w/w) syrup @ 98% pure, d=1.3 g/mL, 7M, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Sodium BicarbonateSigmaS-5761Used to make ferric NTA solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Nitrilotriacetic Acid Trisodium SaltSigmaN-0253Used to make ferric NTA solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Iron (III) ChlorideSigma451649Used to make ferric NTA solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Magnesium SulfateSigma208094Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Manganese (II) Sulfate MonohydrateSigmaM-7634Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Iron(II) Sulfate HeptahydrateSigma215422Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Calcium Chloride DihydrateSigma223506Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Cobalt(II) ChlorideSigma60818Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Zinc ChlorideSigma229997Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Copper(II) Sulfate PentahydrateSigmaC-8027Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Aluminum Potassium Sulfate DodecahydrateSigma237086Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Boric AcidSigmaB-6768Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Sodium Molybdate DihydrateSigma331058Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Nickel(II) ChlorideSigma339350Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Sodium Tungstate DihydrateSigma14304Used to make minerals solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
D-BiotinSigma47868Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Folic AcidSigmaF-7876Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Pyridoxine HydrochlorideSigmaP-9755Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Riboflavin (B2)Sigma47861Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Thiamine HydrochlorideSigmaT-4625Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Nicotinic AcidSigmaN4126Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
D-Pantothenic Acid Hemicalcium SaltSigma21210Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Vitamin B12SigmaV-2876Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
4-Aminobenzoic AcidSigmaA-9878Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}
Thioctic AcidSigmaT-1395Used to make vitamin solution, used for ā€œnanowiresā€ medium {Hill, E.A. 2007}

References

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,
  1. Renner, L. D., Weibel, D. B. Physicochemical regulation of biofilm formation. MRS Bull. 36 (5), 347-355 (2011).
  2. Flemming, H. C., Wingender, J. The biofilm matrix. Nat Rev Microbiol. 8 (9), 623-633 (2010).
  3. Aldeek, F., et al.

Access restricted. Please log in or start a trial to view this content.

Reprints and Permissions

Request permission to reuse the text or figures of this JoVE article

Request Permission

Tags

Biofilm ImagingMicrofluidic ChannelTime of Flight Secondary Ion Mass SpectrometrySystem for Analysis at Liquid Vacuum InterfaceIn Situ Chemical MappingExtracellular Polymeric SubstancesBacterial Biofilm Cultivation

Related Articles