Low Temperature Synthesis of Superparamagnetic Iron Oxide (Fe3O4) Nanoparticles and Their ROS Mediated Inhibition of Biofilm Formed by Food-Associated Bacteria.

In the present study, a facile environmentally friendly approach was described to prepare monodisperse iron oxide (Fe3O4) nanoparticles (IONPs) by low temperature solution route. The synthesized nanoparticles were characterized using x-ray diffraction spectroscopy (XRD), Raman spectroscopy, field emission scanning electron microscopy (FESEM) measurements, Fourier-Transform Infrared Spectroscopy (FTIR), and Thermogravimetric analysis (TGA) analyses. XRD patterns revealed high crystalline quality of the nanoparticles. SEM micrographs showed the monodispersed IONPs with size ranging from 6 to 9 nm. Synthesized nanoparticles demonstrated MICs of 32, 64, and 128 μg/ml against Gram negative bacteria i.e., Serratia marcescens, Escherichia coli, and Pseudomonas aeruginosa, respectively, and 32 μg/ml against Gram positive bacteria Listeria monocytogenes. IOPNs at its respective sub-MICs demonstrated significant reduction of alginate and exopolysaccharide production and subsequently demonstrated broad-spectrum inhibition of biofilm ranging from 16 to 88% in the test bacteria. Biofilm reduction was also examined using SEM and Confocal Laser Scanning Microscopy (CLSM). Interaction of IONPs with bacterial cells generated ROS contributing to reduced biofilm formation. The present study for the first time report that these IONPs were effective in obliterating pre-formed biofilms. Thus, it is envisaged that these nanoparticles with broad-spectrum biofilm inhibitory property could be exploited in the food industry as well as in medical settings to curtail biofilm based infections and losses.

Introduction

Bacteria grow not only in planktonic form but also in sessile form attached to a surface called biofilm. Environmental factors such as reduced nutrient availability or harsh conditions, trigger the formation of biofilm that starts with the attachment of free motile cells to a surface and culminates with the dispersal of biofilm cells. After the attachment and before the dispersal, maturation phase occurs, where the attached cells secrete a matrix of extracellular polymeric substances (EPS) (O’Toole et al., 2000). Biofilms are resistant to antibiotics, disinfectants and dynamic or hostile environmental conditions and are thus, difficult to eliminate (Garrett et al., 2008).

Since biofilms provide suitable conditions to the bacteria for survival, bacteria in biofilm mode pose a serious threat to the food industry. Biofilms formed on food-contact surfaces can lead to contamination of food during processing and post processing (Srey et al., 2013; Espina et al., 2017). Thus, pathogens like Escherichia coli, Listeria monocytogenes, Staphylococcus aureus, and Serratia marcescens that form strong biofilms and are responsible for foodborne outbreaks should be given special attention in the food industry. To combat the threat of biofilm formation in food industry, efficient cleaning and disinfection procedures should be followed. These procedures are quite effective as they efficiently remove food debris and inactivate biofilm cells and hence prevent contamination of food (Chmielewski and Frank, 2003; Srey et al., 2013). Disinfectants such as quaternary ammonium compounds, acids, peroxides and chlorine are used in food industries but currently, their use is being restricted due to the toxicity and environmental concerns associated with them (Da Costa et al., 2014; Yang et al., 2014; Pechacek et al., 2015; Lavorgna et al., 2016). Moreover, these biocides corrode the surfaces and development of resistance against them make them unsuitable for use (Neyret et al., 2014; Akbas, 2015). Owing to the above issues as a part of the regulatory changes, some of the disinfectant have been deemed dangerous and are banned for future use (European Parliament, 2006). Consequently, the scientific community is searching for safe and eco-friendly alternatives to biocides.

Nanomaterials have attracted a lot of interest from the researchers globally in the efficient control of microorganisms owing to their ability to cover larger surface to volume and distinct physical and chemical properties (Morones et al., 2005). Nanomaterials are being developed for a variety of functions related to food industry like food contact surfaces, food packaging, etc., (Handford et al., 2014; Al-Shabib et al., 2016). Small size of these particles (1–100 nm) and their large surface area to volume ratio make them possess altered physicochemical properties in comparison to large size particles (Bouwmeester et al., 2014). In recent years, use of metallic nanoparticles as antimicrobials has gained immense attention (Allaker, 2010). Metal oxide nanoparticles possess more potent antimicrobial activity in comparison to metallic nanoparticles due to high surface areas, unusual crystalline structure with more number of edges and corners and presence of other reactive sites (Sathyanaraynan et al., 2013). Iron-oxide nanoparticles are special class of metal oxide nanoparticles possessing magnetic properties and superior biocompatibility. Superparamagnetic iron oxide nanoparticles (IONPs) consist of maghemite, magnetite or hematite particles with core size ranging from 10 nm to 100 nm in diameter and are widely used in biomedical settings (Wahajuddin and Arora, 2012). Several reports describing the broad-spectrum antimicrobial properties of IONPs have emerged recently (Prabhu et al., 2015; Ismail et al., 2015; Ahmad et al., 2017). Moreover, iron oxide is already approved by food and drug administration (FDA) for medical and food applications, making IONPs good candidates to study their biofilm inhibitory properties. In comparison to the quantum of reports published on bactericidal action of IONPs, limited information is available on the possible biofilm inhibitory mechanism of these nanoparticles.

Therefore, in the present investigation superparamagnetic IONPs were synthesized, characterized using modern spectroscopy and electron microscopy techniques and examined for their biofilm inhibition activity against food-associated bacteria viz. Escherichia coli, Pseudomonas aeruginosa, Listeria monocytogenes, and Serratia marcescens. The other aim of this study was to decipher the plausible mechanism of action of the synthesized IONPs on the bacterial cells.

Materials and Methods

Bacterial Strains

Escherichia coli ATCC 25922, Pseudomonas aeruginosa PAO1, Serratia marcescens ATCC 13880, and Listeria monocytogenes (laboratory strain) were used in this study. All bacterial strains maintained as glycerol cultures at -80°C. For experiment purpose an aliquot from glycerol cultures were cultivated on Luria–Bertani (LB) medium (Oxoid) and maintained at 37°C.

Nanoparticle Synthesis

Firstly, 2 g ferric chloride and 2 g ferric sulfate (Sigma-Aldrich, United States) were mixed in 50 ml deionized water and stirred to maintain a homogenous solution. Then, 8 ml of 25% ammonia solution was added drop wise under vigorous stirring in which 8 ml Polyethylene glycol (PEG) (Sigma-Aldrich, United States) was also added quickly before heating the solution to 80°C for 1 h on a hot plate. After that, the solution was washed by centrifugation at 12000 g five times with deionized water and with ethyl alcohol diluted to 70% followed by drying the sample at 80°C in the oven overnight.

Characterization

The phase purity of the prepared samples was characterized by X-ray diffraction using Phillips X’pert (MPD-3040) X-ray diffractometer with Cu Kα radiations (λ = 1.5406 Å) operated at voltage of 40 kV and current of 30 mA. Fourier transmission infrared (FTIR) spectrum of the nanoparticles (as pellets in KBr) was recorded using a Fourier transmission infrared spectrometer (Nicolet Impact 410 DSP) in the range of 4000 to 400 cm−1 with a resolution of 1 cm−1. The surface morphology of the nanoparticles was studied using field emission scanning electron microscopy (FESEM) using a TESCAN; MIRA II LMH microscope. In order to get the phonon vibrational study of the IONPs, a micro-Raman spectrometer (NRS-3100) was used with a 532 nm solid state primary laser as an excitation source at room temperature. The thermal study of the synthesized product was carried out using thermo gravimetric analyzer (TGA-DTA; SCHIMADZU) up to 1000°C in air at the heating rate of 5°C/min, after purging nitrogen gas.

Determination of Minimum Inhibitory Concentration (MIC)

Minimum inhibitory concentrations (MICs) of IONPs were determined against four pathogenic bacteria using micro-broth dilution assay described by Andrews (2001). All test pathogens were subject to IONP concentrations ranging from 0.125–1024 μg/ml in a series of two fold dilutions. Lowest concentration at which no visible growth of the bacteria was observed was termed MIC.

Effect on Growth

Growth kinetics of the tested bacteria was examined in the presence and absence of sub-inhibitory concentrations (sub-MICs) of IONPs. Overnight grown cultures of Escherichia coli, Pseudomonas aeruginosa, Serratia marcescens, and Listeria monocytogenes were inoculated to obtain a final concentration of 1.6 × 106 CFU/ml followed by treatment with respective sub-MICs of IONPs. The treated and untreated bacteria were incubated on shaking incubator (100 rpm) at 37°C and growth was measured spectrophotometrically at 600 nm for 24 h.

Effect on Alginate Production

Overnight culture of Pseudomonas aeruginosa (1%) was added to LB broth medium supplemented with or without IONPs (8–64 μg/ml) and incubated overnight at 37°C under shaking (100 rpm). After incubation alginate production was estimated as described by Gopu et al. (2015). Briefly, 70 μl of test sample and 600 μl of boric acid-sulphuric acid solution (4:1) was mixed in an ice bath. After vortexing for 10 s, the mixture was again subjected to ice bath. 20 μl of 0.2% carbazole dissolved in ethanol was added to the above mixture and vortexed for 10 s. The mixture was incubated for 30 min at 55°C and quantification was done at 530 nm using a microplate reader.

Effect on Exopolysaccharides Production

The test bacteria were grown in the presence and absence of respective sub-MICs of IONPs at 37°C. Successively, the grown cultures were centrifuged (20000 g, 20 min) and supernatant was filtered through 0.22 μm syringe filter (CAT: SFNY04R, Axiva, India). Exopolysaccharides was precipitated by adding three volumes of chilled ethanol (100%) to the resultant supernatant and incubating overnight at 4°C (Huston et al., 2004). Exopolysaccharides was then quantified by measuring sugars following the method of Dubois et al. (1956).

Effect on Biofilm Formation

Crystal violet assay for biofilm quantification was adopted and the assay was carried in 96-well microtiter (P5366 Sigma, Sigma-Aldrich, United States) plates as described by (O’Toole and Kolter, 1998). Briefly, overnight cultures of test bacteria were re-suspended in fresh LB medium in the presence and the absence of respective sub-MICs of IONPs and incubated statically at 37°C for 24 h. After the incubation, the wells of microtiter plate were washed thrice with phosphate buffer (pH 7.2). The biofilms in the microtiter plates stained with a 0.1% crystal violet solution for 5 min. After removing the excessive dye biofilm was quantified by solubilizing the dye in ethanol (90% v/v) and measuring the absorbance at OD470.

Visualization of Biofilm Architecture

Scanning Electron Microscopy (SEM)

Sub-MICs of IONPs were used to treat bacterial cells (P. aeruginosa and L. monocytogenes). Glass coverslips placed in wells of the microtitre plate were inoculated with overnight grown test pathogens and incubated for 24 h at 30°C. IONP treated and untreated coverslips were washed with sterile PBS to remove unadhered cells. All samples were fixed with 2% formaldehyde and 2.5% glutaraldehyde. Fixed coverslips were washed thrice with PBS and subjected to ethanol drying. Completely dried coverslips were gold coated and visualized under scanning electron microscope (SEM, JEOL-JSM 6510 LV, Japan).

Confocal Laser Scanning Microscopy (CLSM)

For CLSM, biofilms on coverslips were grown as described above. All coverslips were stained with 0.1% w/v acridine orange for 15 min in darkness. Stained samples were washed with PBS to remove excess stain and observed for biofilm inhibition at 40 × magnification and excitation filter 515–560 nm (Zeiss Spinning disk confocal microscope, Zeiss Germany).

Effect of IONPS on Bacterial Cell Morphology

Interaction of the test bacteria with IONPs was examined by SEM. Overnight grown cultures treated and untreated with respective sub-MICs of IONPs were analyzed using SEM (JEOL, Japan). Particle elemental identity was determined using EDAX technique as mentioned earlier (Ahmed et al., 2018).

Reactive Oxygen Species (ROS Studies)

Detection of ROS Production

2,7-dichlorofluorescein diacetate (DCFH-DA) (Sigma-Aldrich, United States) dye was used for the detection of ROS produced. The number of bacterial cells was adjusted to 108 CFU/ml and DCFH-DA was mixed with the bacteria in 1:2000 ratio. The mixture was shaken (100 rpm) for 30 min duration at 37°C. Post incubation the bacterial cells were pelleted out and washed thrice in PBS to remove DCFH outside the cells. The washed cells were exposed to respective 1/2 × MIC of IONPs. Fluorescence spectrophotometer was used to determine fluorescence intensity of DCFH at excitation wavelength of 488 nm and emission wavelength of 535 nm. (Qayyum et al., 2017).

Plasmid DNA Cleavage

The mechanistic experiment for the nuclease activity of IONPs (10 μM) with pBR322 DNA (100 ng) in 5 mM Tris–HCl/50 mM NaCl buffer at pH = 7.4 was studied by using various radical scavengers viz, dimethyl sulfoxide (DMSO, 1 mM), hydrogen peroxide (H2O2, 1 mM), superoxide dismutase (SOD, 10 units), t-butyl alcohol (t-BuOH, 1 mM), sodium azide (NaN3, 1 mM), Deuterium oxide (D2O, 1 mM) using gel electrophoresis. Reaction mixtures were incubated at 37°C for 1h. Following the incubation, the reaction mixtures were mixed with loading buffer (25% bromophenol blue, 30% glycerol, and 0.25% xylene cyanol) and loaded on 1% agarose gel (0.5 g of Agarose in 50 ml 1X TBE buffer). The electrophoresis was carried out for 2 h at 40 V in TAE buffer (pH7.4) using horizontal electrophoresis system (CAT-H815184, Genetix, India) followed by ethidium bromide (1.0 μg/ml) staining. DNA bands were visualized with Bio-Rad Gel DocTMXR. Standard protocol was used for these experiments with slight modifications (Tabassum et al., 2013; Khan et al., 2014; Tabassum et al., 2015).

Effect of IONPs on Dispersal of Preformed Biofilms

The effect of sub-MICs (1/16 × MIC-1/2 × MIC) of IOPNs on the dispersal of preformed biofilms of the test bacteria was determined by method described by Wu et al. (2013). Biofilms of the test bacteria were allowed to develop in 96 well microtiter plates for 24 h at 37°C. After incubation, planktonic cells were removed gently with a pipette and 100 μl of IONPs were added to each well along with 100 μl of sterile LB broth. In control wells only broth was added. Plate was incubated at 37°C for 24 h and formed biofilms were quantified as previously described.

Results and Discussion

Synthesis and Characterization of IONPs

The structural and crystalline nature of the IONPs was studied through X-ray diffraction analysis. XRD pattern of Fe3O4 is presented in Figure 1A. In the XRD pattern of Fe3O4, the peak position and relative intensity of the reflection peaks of the samples confirm crystalline cubic spinel structure of the magnetite which is well matched with the JCPDS card No. 86-1359 (Luo et al., 2016). From this study, considering the peak at degrees, average particle size has been estimated by using the Scherer formula:

FIGURE 1

Characterization of Iron oxide nanoparticle (A) XRD patterns (B) Raman spectra (C) FTIR spectra (D) Thermogravimetric analysis.

Where λ is wave length of X-ray (0.1541 nm), β is FWHM (full width at half), 𝜃 is the diffraction angle, and D is particle diameter size. The average grain size of the IONPs nanoparticles was calculated to be ∼8 nm using Debye–Scherer’s equation.

Figure 1B shows the Raman spectrum of IONPs. It is clear that the Raman bands at 220.2 and 491.2 cm−1 could be assigned to the scattering of A1g mode of Fe3O4, while the bands at 284, 398 and 601 cm−1 were attributed to the scattering of Eg mode of Fe3O4.

The chemical structure and functional groups of the as-prepared IONPs were studied through FTIR analysis. The FTIR spectra of the IONPs is shown in Figure 1C. The strong spectroscopic band at 558 cm−1, as illustrated in FTIR spectrum of IONPs, corresponding to the symmetric Fe-O (oxy-metallic) stretching vibration indicates the formation of IONPs. No other intense peaks observed in the IONPs confirm the high purity of the nanoparticles.

Thermal properties of IONPs were determined by analytical techniques of TG-DTA as shown in Figure 1D. All the measurements were conducted under nitrogen atmosphere at a heating rate of 5°C min−1 up to 600°C. The IONPs have the initial weight loss of 2.5% in the temperature range of 30–230°C. This first stage may be the release of adsorbed of water or OH groups adsorbed on the surface of the IONPs. In the second stage of curves, the sharp weight loss of 6.5% corresponds to oxidation products of Fe3O4 that are easily oxidized to give γ-Fe2O3 particles.

Morphological analysis for IONPs was studied by electron microscopic images. In the FESEM images of IONPs as shown in Figure 2A, it can be seen clearly that the Fe3O4 particles are uniformly aggregated, spherical shaped with size ranging from 6 to 9 nm, which is in good agreement with the XRD analysis. The EDX spectrum shows (Figure 2B) the IONPs combined pure O and Fe elements and no other impurities were detected, thus, the synthesized sample shows high purity.

FIGURE 2

(A) Field emission scanning electron microscopic (FESEM) images, and (B) EDX of IONPs.

Minimum Inhibitory Concentration

Minimum inhibitory concentrations (MIC) of IONPs was determined for all tested bacteria. MIC for E. coli was found to be 64 μg/ml, while for P. aeruginosa it was 128 μg/ml. For S. marcescens and L. monocytogenes 32 μg/ml was recorded as the MIC. Concentrations below MIC i.e., sub-MICs were considered for all assays and the respective MICs and sub-MICs for each tested bacteria is presented in Supplementary Table S1. The effect of sub-MICs of IONPs on the growth of the test bacteria was studied and no significant change in the pattern of growth of untreated control and treated bacteria was observed (Supplementary Figure S1). Thus, the growth kinetics study clearly shows that the IONPs did not inhibit growth of the pathogen at sub-MICs.

Inhibition of Alginate Production in P. aeruginosa PAO1

Alginate is a key component of the EPS of P. aeruginosa biofilm (Hay et al., 2009), the effect of sub-MICs of IONPs was studied for its efficacy to reduce the production of alginate. The obtained results showed that the alginate production was reduced in a dose dependent manner. At concentrations ranging from 08 to 64 μg/ml, IONPs inhibited alginate production by 28–79% in PAO1 (Figure 3A). Since alginate is responsible for conferring resistance to the pathogens against antimicrobials this is a crucial finding. Reduction in alginate production would decrease the level of resistance among bacteria and make them susceptible to the drugs. This is probably the first report on the inhibition of alginate by IONPs.

FIGURE 3

(A) Effect of sub-MICs of IONPs on alginate production in P. aeruginosa PAO1. (B) Effect of sub-MICs of IONPs on EPS production in tested bacteria. Means denoted by the different letter within parameter are significantly different at p > 0.05, using DMRT.

Inhibition of Exopolysaccharides

Exopolysaccharides maintain the biofilm architecture and act as a protective barrier. Additionally, they are responsible for conferring resistance to biofilm-enclosed microorganisms by preventing the entry of antimicrobials inside the microbial cells and changing the overall biofilm architecture (Fux et al., 2005). Hence, inhibition of EPS production will expose the cells growing in biofilm mode and thus, help in eliminating biofilm (Yildiz and Schoolnik, 1999). Considering the positive correlation between biofilm formation and exopolysaccharides production, an attempt was made to assess the effect of IONPs on exopolysaccharides production by tested bacteria. Exopolysaccharides extracted from IONPs treated and untreated cultures of tested bacteria were spectrometrically analyzed. Exopolysaccharides production in all pathogens decreased with increasing concentration of IONPs (Figure 3B). P. aeruginosa, E. coli, and S. marcescens demonstrated 19–73%, 15–80%, and 21–69% inhibition of exopolysaccharides in presence sub-MICs of IONPs, respectively, whereas, Gram positive L. monocytogenes exhibited 28–77% reduction in exopolysaccharides production at concentrations ranging from 2 to 16 μg/ml (Figure 3B.). The finding is in agreement with observations made with zinc oxide nanoparticles that showed 81, 69, 67, 59, and 68% decrease in exopolysaccharides production in P. aeruginosa PAO1, E. coli, L. monocytogenes, K. pneumoniae, and S. marcescens, respectively (Al-Shabib et al., 2018).

Biofilm Inhibition by IONPs

In the present study, sub-inhibitory concentrations (1/16 × MIC-1/2 × MIC) of IONPs were tested against biofilm formation of four bacterial species Pseudomonas, Escherichia, Listeria and Serratia. Figure 4 shows the representative bar graphs indicating IONPs inhibit biofilm formation in all the tested bacteria in a dose dependent manner. The data shows 16, 43, 71, and 82% biofilm reduction in P. aeruginosa PAO1; 28, 54, 70, and 77% in E. coli 25922; 22, 45, 61, and 88% in L. monocytogenes; 19, 39, 63, and 75% in S. marcescens 13880 as compared to untreated control (Figure 4).

FIGURE 4

Biofilm inhibition by sub-inhibitory concentrations of IOPNs. Means denoted by the different letter within parameter are significantly different at p > 0.05, using DMRT.

Formation of biofilm not only plays an important role in the pathogenesis, it is also responsible for food contamination, spoilage and transmission of diseases. Biofilm development is often regulated by signal-mediated quorum sensing phenomenon (Parsek and Greenberg, 2005). These results were further confirmed by visualizing the treated and untreated biofilm cells using SEM and CLSM. Significant reduction in the microcolony formation was observed and no clumping of the cells was seen upon their treatment with IONPs (Figure 5). Similar potent biofilm inhibitory effect was demonstrated with oleic acid coated IONPs against Gram negative (P. aeruginosa) and Gram positive bacteria (S. aureus) (Velusamy et al., 2016). The results are also in agreement with previously published report of Thukkaram et al. (2014), wherein, significant reduction in biofilm of E. coli and P. aeruginosa was recorded in presence of different concentrations (0.01–0.15 mg/mL) of IONPs. In another study, Agarwala et al. (2014) demonstrated similar biofilm inhibition in drug resistant pathogens (Staphylococcus aureus and Escherichia coli) after treatment with copper oxide and IONPs.

FIGURE 5

Visualization of biofilm inhibition. P. aeruginosa biofilm: (A,B) shows untreated controls and cells treated with 1/2 × MIC of IONPs as seen by the SEM (E,F) control and treated biofilms stained with acridine orange and visualized by CLSM. L. monocytogenes biofilm: (C,D) shows untreated controls and cells treated with 1/2 × MIC of IONPs as seen by the SEM (G,H) control and treated biofilms stained with acridine orange and visualized by CLSM.

Interaction of IONPs With Bacterial Cells

SEM images confirmed the interaction of IONPs with cells of L. monocytogenes. The elemental identity of the particle was confirmed by EDAX, and the results clearly demonstrated that these particles were of iron. The interaction of IONPs and bacteria is demonstrated in Figure 6. The Figure very clearly shows that there was little damage or physical damage of the bacterial cells as most cells were found to be intact. Thus, it is envisaged that the IONPs are not killing bacteria but are inhibiting biofilm by some other mechanism.

FIGURE 6

SEM images of L. monocytogenes cells treated with IONPs and their EDX spectra.

ROS Generation

ROS production upon addition of sub-MICs of IONPs was determined using DCFH-DA as a ROS indicator. The IONPs produced ROS when they were incubated with bacterial cells as shown in Figure 7A. In the presence of respective ½ × MIC of IONPs, ROS was found to be much greater than the untreated control and determined to be 280, 322, 252, and 181% in P. aeruginosa, E. coli, S. marcescens, and L. monocytogenes, respectively. The findings clearly point out that higher ROS was produced in Gram negative bacteria than the Gram positive L. monocytogenes. This can be attributed to the fact that cell wall of the Gram positive bacteria is thick and it restricts the entry of IONPs in comparison to Gram negative bacteria which subsequently leads to reduced ROS formation in Gram positive bacteria. ROS denature the proteins and damage other macromolecules as well as alter expression of bacterial virulence factors that includes biofilm inhibition (Su et al., 2009).

FIGURE 7

(A) Reactive oxygen species (ROS) generation in the presence of IONPs using DCFH-DA as a ROS indicator. (B) The electrophoretic pattern is exhibiting nuclease activity of IONPs against pBR322 DNA for mechanistic pathways. [lane 1, DNA (100 ng) alone (control); lane 2, DNA (100 ng) + IONPs (10 μM), lane 3, DNA + IONPs (10 μM) + DMSO (1 mM); lane 4, DNA + IONPs + tBuOH (1 mM); lane 5, DNA + IONPs + NaN3 (1 mM); lane 6, DNA + IONPs + D2O (1 mM); lane 7, DNA + IONPs + SOD (10 units)].

Plasmid DNA Cleavage

The mechanistic pathway studied using electrophoretic pattern of the reaction of IONPs (10 μM) and pBR322 DNA (100 ng) in the presence of various radical scavengers is shown in Figure 7B. With the addition of DMSO, t-BuOH (hydroxyl radical scavengers) in the reaction mixture (IONPs + DNA) reduces the cleavage of the DNA, thus confirms the role of diffusible •OH radicals (lane 3,4). Moreover, when the NaN3 (singlet oxygen scavenger, 1O2) (lane 5) the cleavage was significantly inhibited and when D2O (increases the lifetime of O2) (Lane 6) and SOD (superoxide radical scavenger, O2•−) (lane 7) were added in the reaction mixture, the cleavage was significantly increased. Thus, the results indicate the generation of •OH, 1O2, and O2⋅ and freely diffusible radicals are responsible for the DNA cleavage. Therefore, it was speculated that biofilms integrity and the structure get disturbed by the ROS produced by IONPs, as the extracellular DNA plays a vital role in the biofilm formation at an early stage (Harmsen et al., 2010; Ibáñez de Aldecoa et al., 2017). Thus, the biofilm inhibition by the IONPs alludes to the ROS mediated pathway.

Dispersal of Preformed Biofilm by IONPs

Effect of sub-MICs of IONPs was observed on preformed biofilms of all the tested bacteria. At respective sub-MICs (1/16 × MIC-1/2 × MIC) significant reduction of 14–67%, 20–67%, 26–76%, and 15–71% in preformed biofilms of P. aeruginosa, E. coli, S. marcescens and L. monocytogenes was recorded, respectively (Figure 8). This is probably the first report demonstrating effective dispersal of pre-formed biofilms upon treatment with sub-MICs of IONPs.

FIGURE 8

Effect of IONPs on pre-formed biofilms of tested bacteria. Means denoted by the different letter within parameter are significantly different at p > 0.05, using DMRT.

Conclusion

The study describes an eco-friendly and facile method to synthesize monodisperse IONPs. The characterized nanoparticles reduced the biofilm formation significantly in all the test bacteria at sub-inhibitory concentrations. Generation of ROS due to the interaction between IONPs and bacterial cell could possibly be considered as underlying mechanism of action of the IONPs. These Superparamagnetic iron oxide (Fe3O4) nanoparticles also caused effective dispersal of pre-formed biofilms in all the bacteria. Thus, it is envisaged that these ROS generating IONPs can be exploited to combat the threat of biofilm formation in food industry and medical settings in the near future after careful investigation regarding their toxicity.

Author Contributions

NA-S, FH, FA, IA, and MZA conceived and designed the experiments. NA-S, FH, FA, RK, MZA, MSK, FAA, MoSK, MB, JK, SS, and AA performed the experiments. FH, FA, RK, MSK, FAA, MoSK, MB, JK, SS, MAA, AA, and IA analyzed the data. NA-S, FH, FA, IA, MZA, FA, RK, MoSK wrote the manuscript. MAA performed the experiments and analyzed the data. All authors reviewed and approved the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.