This protocol illustrates the important consecutive steps required to assess the relevance of monitoring vitality parameter and DNA repair processes in reviving Bacillus subtilis spores after treatment with low pressure plasma by tracking fluorescence-labelled DNA repair proteins via time-resolved confocal microscopy and scanning electron microscopy.
Plasma sterilization is a promising alternative to conventional sterilization methods for industrial, clinical, and spaceflight purposes. Low pressure plasma (LPP) discharges contain a broad spectrum of active species, which lead to rapid microbial inactivation. To study the efficiency and mechanisms of sterilization by LPP, we use spores of the test organism Bacillus subtilis because of their extraordinary resistance against conventional sterilization procedures. We describe the production of B. subtilis spore monolayers, the sterilization process by low pressure plasma in a double inductively coupled plasma reactor, the characterization of spore morphology using scanning electron microscopy (SEM), and the analysis of germination and outgrowth of spores by live cell microscopy. A major target of plasma species is genomic material (DNA) and repair of plasma-induced DNA lesions upon spore revival is crucial for survival of the organism. Here, we study the germination capacity of spores and the role of DNA repair during spore germination and outgrowth after treatment with LPP by tracking fluorescently-labelled DNA repair proteins (RecA) with time-resolved confocal fluorescence microscopy. Treated and untreated spore monolayers are activated for germination and visualized with an inverted confocal live cell microscope over time to follow the reaction of individual spores. Our observations reveal that the fraction of germinating and outgrowing spores is dependent on the duration of LPP-treatment reaching a minimum after 120 s. RecA-YFP (yellow fluorescence protein) fluorescence was detected only in few spores and developed in all outgrowing cells with a slight elevation in LPP-treated spores. Moreover, some of the vegetative bacteria derived from LPP-treated spores showed an increase in cytoplasm and tended to lyse. The described methods for analysis of individual spores could be exemplary for the study of other aspects of spore germination and outgrowth.
A major goal of space exploration is the search for signatures of life forms and biomolecules on other planetary bodies and moons in our solar system. The transfer of microorganisms or biomolecules of terrestrial origin to critical areas of exploration is of particular risk to impact the development and integrity of life-detection missions on planetary bodies such as Mars and Europa1. The international guidelines of planetary protection, established by the Committee of Space Research (COSPAR) in 1967, impose strict regulations on manned and robotic missions to other planets, their moons, asteroids, and other celestial bodies and regulate the cleaning and sterilization of a spacecraft and critical hardware components prior to launch in order to eliminate contaminating terrestrial microorganisms and prevent cross contamination of celestial bodies2. Over the last decade, the application of non-thermal plasmas has gained wide attention in biomedical and nutritional research, as well as in spaceflight applications3,4,5. Plasma sterilization is a promising alternative to conventional sterilization methods as it offers rapid and efficient microbial inactivation6, while being gentle to sensitive and heat labile materials. Plasma discharges contain a mixture of reactive agents such as free radicals, charged particles, neutral/excited atoms, photons in the ultraviolet (UV), and vacuum ultraviolet (VUV) spectrum which lead to rapid microbial inactivation3. In this study, we use low-pressure plasma generated by double inductively coupled low-pressure plasma (DICP) source7,8 to inactivate Bacillus subtilis endospores distributed on glass test surface.
Gram-positive bacteria of the family Bacillaceae are widely distributed in natural habitats of soil, sediments, and air as well as in unusual environments such as clean room facilities and the International Space Station9,10,11. The most distinct feature of the genus Bacillus is the ability to form highly resistant dormant endospores (hereafter referred to as spores) to survive unfavorable conditions, such as nutrient depletion12. Spores are generally much more resistant than their vegetative cell counterparts to a variety of treatments and environmental stresses, including heat, UV, gamma irradiation, desiccation, mechanical disruption, and toxic chemicals, such as strong oxidizers or pH-changing agents (reviewed in references13,14) and are therefore ideal objects for testing the efficiency of microbial inactivation methods. Since genomic DNA is a major target of the plasma treatment of bacteria15,16, the repair of plasma-induced DNA lesions (e.g. DNA double strand breaks) upon spore revival is crucial for survival of bacteria13,17.
Thus, we study the germination capacity of spores and the role of DNA repair during spore germination and outgrowth after treating the spores with low pressure argon plasma by following individual spores and their expression of fluorescence-labelled DNA repair protein RecA with time-resolved confocal fluorescence microscopy. We give a step by step instruction of the preparation of B. subtilis spores in monolayers for achieving reproducible test results, the treatment of spore monolayers with low pressure plasma for sterilization, the preparation of plasma treated spores for ultrastructural evaluation using scanning electron microscopy (SEM), and live cell microscopy analysis at the level of individual spores in concert with monitoring the active DNA repair processes occurring within the cell in response to plasma treatment.
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1. Bacillus subtilis Spore Production and Purification
- For spore production, transfer a 5 mL overnight culture of the respective B. subtilis strain, supplemented with appropriate antibiotics, to 200 mL double-strength liquid Schaeffer sporulation medium (per liter 16 g nutrient broth, KCl 2 g, 0.5 g MgSO4*7 H2O, 2 mL 1 M Ca(NO3)2, 2 mL 0.1 M MnCl2 *• 4 H2O, 2 mL 1 mM FeSO4, 2 mL 50% (w/v) glucose18) and cultivate it with vigorous aeration at 37 °C for 72 h or until > 95% of the culture has sporulated. The spores of following strains are used: B. subtilis PY79 (wild type) B. subtilis PY79ΔrecA::neo (deficient of DNA repair protein RecA) B. subtilis PY79 recA-yfp::cat (RecA fused with yellow fluorescent protein [YFP]19).
- Harvest spores by centrifugation for 15 min at 3,000 x g in 50 mL tubes and purify the samples by repeated washing steps (up to 15 times) using sterile distilled H2O and check for purity and germination status by phase-contrast microscopy. Ensure that spore suspensions consist out of phase-bright spores (> 99%) and are free of vegetative cells (rods), germinated spores (black/ grey appearance) and cell debris, otherwise further microscopy experiments can be disturbed. Wash the sample until desired purity is reached.
- Determinate the spore titer by plating out 50 µL of 10-fold serial dilutions on LB-agar (i.e.: Use 30 µL sample + 270 µL sterile water for a 1:10 dilution. Take 30 µL from the particular dilution to 270 µL H2O for a 1:100 dilution and so forth) to calculate the CFU (colony forming units) and incubate the plates at 37 °C overnight. After CFU determination, adjust the sample to 109 spores per mL by concentrating or diluting with sterile water.
2. Sample Preparation of Aerosol-deposited Bacillus subtilis Spores
NOTE: Accumulation and overlapping of spores might lead to shadowing effects during the treatment, ultimately resulting in falsified inactivation kinetics. To minimize this problem, prepare spore samples by an aerosol-deposition technique20. Briefly, control the high-precision two-substance nozzle with an electric timer that regulates the liquid throughput in concert with the flow of pressurized carrier gas (here N2). Disperse the injected liquid sample through the nozzle outlet using the nitrogen gas flow.
- Place a sample carrier in form of sterilized microscopic slides (for survival kinetics) or round 25 mm coverslips (for fluorescent tracking of DNA repair processes/cLSM; confocal laser scanning microscopy) inside the electrically operated aerosol spraying unit in alignment with the nozzle. The used spore concentration needs to correspond to a hundredfold of the desired final concentration.
- Transfer 1 mL of the spore culture to the nozzle fluid inlet and initiate the spraying process of 0.1 s at a pressure of 1.3 bar. The sprayed spore suspension (1 x 107) forms a thin film on the microscopic slide that dries rapidly within seconds to form a uniformly distributed spore monolayer. Store the treated sample carriers in a sterile container at room temperature.
3. Low Pressure Plasma Treatment
- Prepare the plasma system for treatment of biological samples and operate the system at 5 Pa with argon plasma at 500 W for 5 min. By this, all surfaces in the system are cleaned and warmed up. This reduces sticking of molecules from ambient air, namely nitrogen, oxygen, and water, while venting the system. After the pretreatment of the system, vent the chamber and place the samples carefully in the center of the reactor vessel with the help of glass racks.
- Use at least three biological replicates. Close the chamber and evacuate below 2 Pa. Afterwards, fill the process gas into the chamber. Regulate the pressure in the system to 5 Pa.
- After the defined process time, turn off the power and gas supply, and carefully vent the system to prevent blowing the samples from the sample holder. After ventilation, remove the samples and place the samples for the next parameter in the system. For non-plasma-treated controls expose samples to vacuum only (5 Pa) in presence of the process gas equivalent to the longest applied plasma time.
4. Recovery and Evaluation of Spore Survival
- Prepare a solution of autoclaved 10% polyvinyl acetate (PVA) and cover the sample carrier carefully with approximately 500 µL and let them air-dry for 4 h. Strip off the dried PVA layer (now containing the spore sample) using sterile forceps and transfer it to a 2 mL reaction tube. Add 1 mL of sterile water to the tube and dissolve the PVA layer via vortexing. This procedure leads to >95% recovery of spores and does not affect their germination capability21.
- Serially dilute the sample at 1:10 in sterile water in a 96-well plate (i.e. 270 µL sterile H2O + 30 µL sample/former dilution). Plate out 50 µL of each dilution on Lysogeny broth nutrient agar (LB), incubate the plates at 37 °C overnight and enumerate the number of grown colonies (CFU).
5. Live Cell Microscopy and Tracking of DNA Repair Processes in Germinating Spores
- For germination experiments, prepare a 1 mm thick 1.5% LB-agar pad, by boiling 700 µL medium and pipet it into a sterile microscopy petri dish. After 10 min, cut out an 8 mm x 8 mm x 1 mm LB-agar pad with a sterile scalpel and transfer the agar carefully on top of the spore monolayers which are resting on 25 mm glass coverslips.
NOTE: This step is crucial for visualization of individual spores and allow following their reaction, towards the activation of germination induced by the nutrient agar. Thus, the LB-agar serves two purposes, (1) to fix the spores at the surface, which avoids relocalization along the surface and out of optical focus, and (2) to activate the spore for germination.
- After covering the sample with agar, transfer the glass coverslip quickly into an imaging chamber and microscope the samples with an automated confocal laser-scanning microscope with inverted optics using a 63X/1.3 plane apochromatic oil immersion objective.
- Perform imaging of fluorescence (YFP) with an excitation wavelength of 514 nm and emission can be detected between 520 and 560 nm.
- Record bright-field images in scanning mode using one of the photo multipliers (transmitted-light path).
- Record time-lapse series with a laser power of 2.6%, and set the confocal aperture to 5 airy units and at a sample frequency of 1 frame per 30 s from 0 h to 5 h, depending on the experiment. It is of particular note that high doses of monochromatic laser illumination at 514 nm completely inhibit germination (Figure 1A, B).
- Keep the samples at 37 °C (ambient air humidity) in a heating stage during the entire imaging process. Use at least three biological replicates for each condition. In case of spore aggregation, multilayered spore distribution or contamination by dust particles, blocking of the plasma treatment ("shadowing") might occur and enable germination of shadowed spores (Figure 1C, D).
Figure 1: Potential problems observed during confocal live cell fluorescence microscopy of plasma treated spores. (A, B) Inhibition of spore germination by high doses of monochromatic (514 nm) laser illumination. (A) Overview (3 x 3 stitched frames) of B. subtilis (LAS72, RecA-YFP) spores 180 min after initiation of germination. The frame in the middle was exposed at 30 s intervals to high doses of laser light (514 nm, 70% laser power), whereas the surrounding regions (= frames) were not illuminated (merged image of bright-field channel and RecA-YFP fluorescence; ordered structures were caused by using 35 mm imaging dishes with an imprinted 500 µm grid). (B) demonstrates a 4X magnified view of the border between illuminated and non-illuminated region showing that spores, which were exposed to high doses of monochromatic laser illumination did not germinate and grow out, whereas spores in non-illuminated regions fully recover to vegetative bacteria expressing bright RecA-YFP fluorescence (green signal). (C, D) Spores covered by contaminating particles or multiple layers of spore (arrows) seems to protect underlying spores from inactivation by plasma treatment and allow their germination and outgrowth ("shadowing effect"). (C) Spores were plasma-treated for 60 s and imaged 180 min after initiation of germination or in (D) for 120 s and imaged after 240 min. Please click here to view a larger version of this figure.
6. Scanning Electron Microscopy (SEM)
- Use scanning electron microscopy to provide ultrastructural information about the surface morphology of plasma treated spores in comparison to untreated controls. Coat dried spore monolayers on coverslips with gold-palladium (3 nm) by using a sputter-coater. Use a field-emission scanning electron microscope for imaging the samples, operated at 5 kV acceleration voltage including an in-lens secondary electron detector to reveal topography contrast.
7. Data Analysis
- Determine the spore survival from the quotient N/N0, where N is the average CFU of treated samples and N0 is the average CFU of untreated vacuum controls. Plot spore inactivation by argon plasma treatment as a function of time (in seconds). Express all data as averages and standard deviations (n = 3).
- Analyze images obtained by live cell imaging using the imaging software. Quantify the proportion of spore germination and outgrowing after plasma treatment, count spores in representative frames at the beginning of the experiment as well as after 4 h. For significance determination in spore survival assays, use one-way ANOVA-tests (analysis of variance) with statistical software). P values <0.05 are considered as statistically significant.
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Survival of plasma-treated B. subtilis spores
Plasma treatment of the B. subtilis spores used in this study show a decrease in survival with increasing duration of the plasma treatment (Figure 2). Spores of the strain expressing the recA-gene fused to YFP showed survival curves similar to spores of the wild type strain, indicating that the genetic modification has no significant effect on the bacterial vitality. Spores of the RecA-deficient strain exhibit a higher sensitivity towards plasma treatment compared to spores of the wild type strain, demonstrating that the presence of the RecA gene is reducing plasma-induced loss of vitality. Especially short plasma treatment of 15 s (P <0.003) and 30 s (P <0.004) cause a significant decrease of the vitality in RecA-deficient strains in comparison to wild type and RecA-YFP strains. After 90 s of plasma treatment, the vitality of all strains is reduced by approximately three orders of magnitude.
Figure 2: Survival of B. subtilis spores from different strains after treatment with low-pressure argon plasma. Survival (mean CFU of plasma treated spores/mean CFU of vacuum treated spores; error bars represent standard deviation) is plotted against duration of plasma treatment. PY79 (wild type; closed circles), LAS72 (RecA-YFP; gray circles) and LAS24 (ΔrecA; open circles). Statistical analysis showed no significant differences in spore survivability between PY79 (unmodified RecA) and LAS72 (RecA-YFP-fusion).
Ultrastructural analysis of plasma-treated spores by SEM
To get an idea of the morphological impact of the plasma treatment on the spores, scanning electron microscopy (SEM) was used to analyze the surface morphology of plasma treated spores in comparison to vacuum-treated spores (control). The outer surface of B. subtilis spores reveal characteristic longitudinal ridge-like structures which are constantly visible in all treated and untreated spores (Figure 3). Plasma treatment up to 30 s induces no significant changes of the spore surface morphology in comparison to control (Figure 3A-C). Increasing duration of plasma treatment (60 - 240 s) leads to a more granular spore surface (Figure 3D-F) and small cracks and fissures can be observed in spores treated for 120 or 240 s. Moreover, small globules arise on spore surfaces (120 s and 240 s treatments, Figure 3E, F), which is caused by released material from the coat, cortex or from the inner core22. These globules cover the whole spore and can be found on the vein-shaped structures as well as on intermediate surfaces.
Figure 3: SEM of B. subtilis (LAS72, RecA-YFP) spores sprayed on glass coverslips after low-pressure plasma treatment. Spores exposed to vacuum only and not to plasma (control) are shown in (A). (B-F) Spores which were plasma-treated with increasing duration (15, 30, 60, 120 and 240 s). Spores which were plasma-treated 60 s or longer appear more granular at their surface than control spores or spores which were plasma-treated for 15 and 30 s. Cracks and fissures (white arrows) are visible at the surface of spores plasma-treated for 120 or 240 s. Please click here to view a larger version of this figure.
Live cell microscopy of plasma-treated B. subtilis spores
Live cell microscopy of reviving spores from B. subtilis strains expressing the fluorescence-labelled repair protein RecA (RecA-YFP) is performed in order to analyze the germination capacity and the expression of RecA-YFP of individual spores in response to plasma treatment. Here, we use time-resolved confocal laser-scanning microscopy to follow germination, outgrowth, and progression into vegetative state of plasma-treated spores (Figure 4) with respect to potentially known issues e.g. shadowing effects or the inhibition of germination by high doses of monochromatic laser illumination (Figure 1). Spores exposed to vacuum only (control, Figure 4A-C), exhibit few fluorescent signals during early states of spore revival (0 - 65 min, not shown). An increase in fluorescence intensity, most probably due to accumulation of RecA-YFP, is observed at ≥ 65 min when vegetative cells are formed and first cells start to divide. All of these cells harbor a fluorescence signal accumulated in at least one position inside of each cell. Almost all spores (98 ± 2%; 589 ± 14, n = 4) treated with vacuum as a control germinate and develop a rod-shaped cell morphology with a rather uniform length of individual cells (Figure 4B-C). In contrast to spores in vacuum controls, spores treated for 15 s with plasma already show a reduced germination capacity of less than 75 ± 4% (197 ± 8 spores, n = 3, Figure 4D-F), indicating that plasma treatment induces damage in dormant spores, which prevents germination. In addition, the morphology of outgrowing cells is different from the morphology of cells in controls. Cells grow either into extensively long rods (longer than compared to control) or remain small and stick in the spore coat (Figure 4G-I). Moreover, most elongated cells lyse with increasing cell size (white arrow heads, Figure 4F). Fluorescence signals of RecA-YFP within the cells seem to be slightly increased in comparison to the signals in control cells (Figure 4C, F), but no significant differences can be observed (not shown). Spores which were plasma treated for 30 s germinate up to 25 ± 6% (99 ± 4 spores, n = 3) and vegetative cells are notably delayed in growth in comparison to control spores and spores after 15 s of plasma-treatment. Vegetative cells are rather small and rod-shaped but vary in length (Figure 4G-I). However, cells of all sizes may lyse during longer incubation times as seen for samples after 15 s of plasma-treatment. After 60 s of plasma-treatment less than 2 ± 2% (8 ± 8 spores, n = 3) spores are able to form vegetative cells (Figure 4J-L). Spores which are plasma-treated for 90, 120 or 240 s can be analyzed, but they show no outgrowth or any change in fluorescence levels of RecA-YFP (not shown).
Figure 4: Confocal laser-scanning live cell microscopy of B. subtilis spores from a strain expressing RecA-YFP after plasma treatment and initiation of germination. Spores were followed over time (one image per 30 s) and images for time-points 0, 2 and 4 h are shown. (A-C) Spores treated with vacuum only and not with plasma (control) germinate and grow out to vegetative cells (B) and enter exponential growth phase (C). (D-L) Spores treated for different duration with the low-pressure argon plasma show significant differences in their outgrowth in comparison to spores of the control (see text for details). (D-F) 15 s treatment (white arrow heads represent vegetative cells, which recently lysed), (G-I) 30 s treatment (black arrow heads visualize vegetative cells, which were small and stick in the spore coat) and (J-L) 60 s treatment after 0 h, 2 h and 4 h spore recovery time. Please click here to view a larger version of this figure.
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Sterilization of surfaces using low-temperature, low-pressure plasma is a promising alternative to rather conventional sterilization procedures such as treatment with ionizing radiation, chemicals (e.g. gases like H2O2 or ethylene oxide) or dry and moist heat23. Ordinary sterilization methods mostly provide an effective sterilization, but they are known to influence the treated material and represent a potential risk for the operator. Low-pressure plasma offers a rapid and homogeneous biological inactivation using the composition of several components such as UV photons, free electrons, ions and exited atoms or molecules (e.g. ROS). Therefore, LPP can be applied to heat- and corrosion sensitive materials, such as thermoplastic polymers for implants, electronic instruments or complex 3D-structures. In the present paper we demonstrate the application of such a test system, in which monolayers of sprayed B. subtilis spores20 are treated in a particular low-pressure plasma reactor which was described recently in detail7. Microscopic bright-field examination of plasma-treated spores may be sufficient for obtaining an overall estimate of the sterilization efficiency. However, we are interested in targeting the underlying mechanisms of low pressure plasma and its influence on spore inactivation on a molecular level. In combination with fluoresce-tracking microscopy it enables us to shed light on the details of this particular molecular response in plasma-treated spores and potentially give us insights into the fundamental inactivation mechanism of low pressure plasma.
Here, we focus on the analysis of the plasma-treatment efficiency and effects by using live cell microscopy, which allows following individual spores after initiation of germination. Remarkably, this particular approach reveals a couple of new results which cannot be provided by measuring revitalization of the entire spore population using determination of cell number or CFU. First of all, plasma-treatment of spores not only affects the capacity of outgrowth in a dose-dependent manner, as expected from the measurement of survival by determination of CFUs, but also the morphology of vegetative cells, which often develop large rods unable to form septa according to proper cell division along with small cells sticking in the spore (15 s of plasma-treatment) or cells at a reduced length (30 s of plasma-treatment). Observations of cells with reduced length showed no recovery to normal cell length at later time points. Moreover, live cell imaging reveals that most of the morphologically altered cells lyse at later stages of observation. This means that damage acquired by the spores during plasma-treatment is only effective at later stages of spore revitalization, presumably due to DNA damage and that the machinery used for germination and outgrowth is more robust towards plasma sterilization than the machinery needed for vegetative growth. Remarkably, expression of the DNA-repairing RecA protein seems to be low and almost absent in spores and develops during outgrowth and vegetative phase as indicated by an increase in RecA-YFP fluorescence17. However, even a slightly increased RecA expression in outgrowing plasma-treated spores, in comparison to control spores, does not help to rescue cell vitality quantitatively, because most cells lyse or burst after outgrowth, especially after more than 3 h of incubation. This effect can be visualized using live cell movies from time lapse images of germinated spores. We cannot exclude that this effect is overemphasized by the particular cultivation condition where the cells are forced in a monolayer using a thin overlay of agar.
Another outcome of the analysis by live cell microscopy is that particulate contaminations (e.g. dust particles, other spores) on the spore monolayer surface can shield the underlying spores from the damaging effects of the plasma. In such cases even longer plasma-treatment seems to be inefficient. Since such contaminations are difficult to avoid completely, alternative plasma-treatment strategies should be tested, such as using planetary rotation during plasma treatment in conjunction with extended duration of the treatment. The analysis by SEM indicates that the spore coat is perforated with increased duration of plasma-treatment which is in line with the theory of plasma-mediated effects on matter22,24. A prolonged exposure time (>240 s) to plasma might even perforate the contaminating particles and thus may damage and inactivate the underlying spores.
The presented protocol for live cell microscopy of spore germination and outgrowth can be suitable for other studies as well. Covering the spores with a thin layer of agar forces the spores in a distinct optical plane and restricts lateral movement. Both effects guarantee that spores and outgrowing cells stay within the selected imaging frame. Similar approaches have been described before25 but provide less flexibility than the method described here which allows choosing almost any sample carrier (e.g. a glass slide, coverslip or Petri dish). In our hands other vegetative bacteria could be analyzed by live cell microscopy using the agar-covering method). In any case, careful control experiments should be performed to evaluate possible effects of photo damage during live cell imaging, because we observed that high doses of monochromatic laser light completely inhibit spore germination. Apart from shortening the illumination time, i.e. by increasing the observation intervals, this phenomenon can be prevented by reducing the laser intensity and/or opening of the confocal aperture (pinhole).
In summary, among the techniques used for studying efficiency of plasma-treatment in the model of sprayed B. subtilis spore monolayers, live cell microscopy provides unique insights into cellular events during spore revival and offers the possibility to analyze the dynamics of fluorescence-labelled proteins. Moreover, the particular sample preparation, i.e. covering of spores with a thin layer of agar, could be paradigmatic for the imaging of other microorganisms by live cell microscopy.
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No conflicts of interest declared.
The authors thank Andrea Schröder for her excellent technical assistance during parts of this work and Nikea J. Ulrich for her assistance during the video shoot. We would also like to thank Lyle A. Simmons for his generous donation of the Bacillus subtilis strains: LAS72 and LAS24. This work was supported in parts by grants from the German Research Foundation (DFG) Paketantrag (PlasmaDecon PAK 728) to PA (AW 7/3-1) and RM (MO 2023/2-1) and the DLR grant DLR-FuW-Projekt ISS LIFE, Programm RF-FuW, Teilprogramm 475 (to F.M.F, M.R. and R.M.). F.M.F. was supported by a PhD scholarship of the Helmholtz Space Life Sciences Research School (SpaceLife) at the German Aerospace Center (DLR) in Cologne, Germany, which was funded by the Helmholtz Association (Helmholtz-Gemeinschaft) over a period of six years (Grant No. VH-KO-300) and received additional funds from the DLR, including the Aerospace Executive Board and the Institute of Aerospace Medicine. The results of this study will be included in the Ph.D. thesis of Felix M. Fuchs.
|Two substance nozzle (model 970-8)||Schlick||14,404||230 V, 50 Hz, D 4.484/8, 0.8 mm bore diameter|
|Luria Bertani Medium||Sigma Aldrich||70122-100G|
|Tube connectors||Festo||n/a||G 1/8|
|Magnetvalve DO35-3/2NC-G018-230AC||Bosch Rexroth||820005100|
|PLN Polyamid tube||Festo||558206||d = 6 mm|
|Electric Timer 550-2-C||Gefran||F000074||220 V|
|attofluor cell chamber||Menzel, Fisher Ref.||3406816||d=25 mm, round|
|MgSO4*7 H2O||Sigma Aldrich||13152|
|MnCl2 * 4 H2O||Sigma Aldrich||244589|
|FeSO4 * 7H2O||AppliChem||13446-34-9|
|Nutrient Broth (NB)||Merck||105443|
|Zeiss LSM 780, Axio Observer Z1||Carl Zeiss Microscopy GmbH||n/a|
|Leo 1530 Gemini||Carl Zeiss Microscopy GmbH||n/a|
|ZEN 2 and ZEN lite 2012 (Software)||Carl Zeiss Microscopy GmbH||n/a|
|SigmaPlot, version 13.0 (Statistic software)||Systat GmbH, Erkrath, Germany||n/a|
|Attofluor cell chamber||Invitrogen||A7816|
|µ-Dish 35 mm, high Grid-500 Glass Bottom||ibidi||81168|
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