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Article

The Antimicrobial Activities of Silver Nanoparticles from Aqueous Extract of Grape Seeds against Pathogenic Bacteria and Fungi

by
Fatimah Al-Otibi
*,
Shahad K. Alkhudhair
,
Raedah I. Alharbi
,
Abdulaziz A. Al-Askar
,
Reem M. Aljowaie
and
Sameha Al-Shehri
Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 22452, Riyadh 11495, Saudi Arabia
*
Author to whom correspondence should be addressed.
Molecules 2021, 26(19), 6081; https://0-doi-org.brum.beds.ac.uk/10.3390/molecules26196081
Submission received: 11 September 2021 / Revised: 4 October 2021 / Accepted: 5 October 2021 / Published: 8 October 2021
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Abstract

:
Grape seed extract (GSE) is a natural source of polyphenolic compounds and secondary metabolites, which have been tested for their possible antimicrobial activities. In the current study, we tested the antibacterial and antifungal activities of aqueous GSE and the biosynthesized silver nanoparticles loaded with GSE (GSE-AgNPs) against different pathogens. The biosynthesized GSE-AgNPs were assessed by UV spectroscopy, dynamic light scattering (DLS), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), and gas chromatography/mass spectrometry (GC/MS). The antimicrobial activities were assessed against different bacterial and fungal species. DLS analysis showed that GSE-AgNPs had a Z-Average of 91.89 nm while UV spectroscopy showed that GSE-AgNPs had the highest absorbance at a wavelength of ~415 nm. FTIR analysis revealed that both of GSE and GSE-AgNPs consisted of different functional groups, such as hydroxyl, alkenes, alkyne, and aromatic rings. Both FE-SEM and TEM showed that GSE-AgNPs had larger sizes and rough surfaces than GSE and AgNO3. The results showed significant antimicrobial activities of GSE-AgNPs against all tested species, unlike GSE, which had weaker and limited effects. More studies are needed to investigate the other antimicrobial activities of GSE.

1. Introduction

The use of natural organic materials in the food industry (e.g., plant extracts to replace chemical or synthetic antimicrobials and antioxidants in the treatment of various foodborne pathogens) is trending worldwide [1]. Furthermore, drug resistance and decreased biosafety levels have prompted researchers and microbiologists to seek natural alternatives of known and confirmed antimicrobial characteristics [2]. The usage of plant extracts in folk medicine and pharmaceutics is because they are rich in polyphenols, quinones, flavonoids, alkaloids, and lectins [3].
Grape seed extract (GSE) is rich in polyphenolic compounds and secondary metabolites, which have significant antimicrobial activities against different pathogens, such as Gram-negative and Gram-positive bacteria [4]. The effectiveness of GSE inhibition depends on the concentration of the extract, percentage of phenols, and the type of bacterium [5]. Furthermore, GSE was tested for its possible anti-inflammatory, cardioprotective, chemopreventive, anticarcinogenic, and antioxidant activities, which might be of pharmacological and medical importance [6]. Similar to most natural products, GSE is almost safe, with an intended uptake for up to 11 months in human studies without any significant side effects. Moreover, the food and drug administration (FDA) has generally recognized it as safe (GRAS notice (GRN) no. 658) [7]. This shows that GSE is a promising antimicrobial agent in medical and non-medical studies and applications.
The pH and solubility levels are key regulators of the antimicrobial effects of different plant extracts, which can further affect the sensibility of some microbes to the inhibitory effects [8]. The unique, superior, and indispensable properties of nanomaterials have resulted in emerging innovative nanotechnology being explored in various biological and medical studies [9]. The eco-friendly synthesis of monodispersed nanoparticles using plant extracts (i.e., against various microbial and chronic diseases) has created remarkable advantages in the pharmacological industry [10].
This current study evaluates the inhibitory effects of aqueous GSE against some pathogenic bacteria and fungi, and assesses the antimicrobial activities of GSE green nanoparticles.

2. Results and Discussion

2.1. The Morphological Characteristics the Biosynthesized GSE-AgNPs

One of the most widely-used techniques for the green synthesis of silver nanoparticles is the method described by Xu et al. 2015. The production of AgNPs in a colloidal form depends on the physical reduction of an aqueous solution of silver nitrate (AgNO3) [11]. This method has the advantage of a higher purity of synthesized particles due to the absence of a chemical solvent [12]. The usage of a ceramic heater will concentrate the solution by evaporation and induce vibrational motion on the surface plasmon, which will further reduce the silver ions (Ag+) (yellowish) and form spherical NPs (brownish) without agglomeration [13]. In the current study, GSE was mixed with an aqueous solution of AgNO3 that turned from light yellow to brown (Figure 1), which indicates the formation of GSE-AgNPs. It was reported that GSE contains a great variety of polyphenolic antioxidants, such as proanthocyanidins, which consist of dimers, trimers, tetramers, and oligomers of monomeric catechins [14], which might explain the ability of GSE to induce an efficient reduction of Ag+ ions to obtain stable GSE-AgNPs for long-term techniques.
To study the characterization of GSE and the formed nanoparticles, several experiments were performed to investigate the different chemical and morphological changes. The optical properties of GSE-AgNPs are a reflection of their morphological characteristics, such as size, shape, and concentration [15]. A previous study stated that the UV-excitation of colloidal structures of silver nanoparticles can induce a surface plasmon resonance (SPR) with maximum absorbance of 400–500 nm [16]. In the current study, the UV spectroscopy showed that GSE-AgNPs had the highest absorbance broad peak (~1.3 cm−1) at the wavelength of ~415 nm (Figure 2A), which reflects the surface plasmon resonance of the synthesized nanoparticles. In accordance with our findings, a previous study showed that the AgNPs of grapefruit (Vitis vinifera) extract showed a spectral band at 450 nm, where that higher OD reflected the reduction of the Ag+ ions to form the metallic (Ag0) [17]. Another study showed that pH induced a shift of the absorbance peaks of AgNPs of different extracts of grape stalk waste from 307 nm in the acidic medium (pH 2), 450 nm at the neutral pH 7 with the Milli-Q water as a solvent, and 470 higher pH, which indicated the stability of aqueous GSE-AgNPs [18]. Another study used two different nanoparticles of silver and iron of the proanthocyanidin compound isolated from grape seeds and showed that the silver nanoparticles had higher absorbance (530 nm) compared to iron (380 nm) [19]. All of these studies suggest that silver nanoparticles could be reduced successfully with GSE aqueous extract using the green physical biosynthesis and that the resulting GSE-AgNPs will have higher stability compared to other solvents, nanoparticles, or chemical synthesis techniques.
The results of the dynamic light scattering (DLS) analysis showed that GSE-AgNPs had the Z-Average of 91.89 nm with a polydispersity index (PDI) value of 0.189 and intercept of 0.943. As shown in Figure 2B, DLS analysis produced the highest peak at 114.7 ± 50.08 nm with 98.7% intensity. In contrast, a previous study showed that the DLS results of synthesized silver nanoparticles of grapefruit extract had a smaller diameter size of 19 nm [17]. Another study showed that the solid lipid nanoparticles loaded with grapeseed or grape skin extracts had mean diameter sizes of 189 ± 2 and 188 ± 18, respectively, compared to the unloaded SLN with 142 ± 10 nm, and that were used in the treatment of human brain-like endothelial cells [20]. Another study showed that SLN particles loaded with grape seed-derived proanthocyanidins had an average diameter size of 243 ± 24 nm with PDI of 0.41–0.51, which successfully increased the ROS production in airway epithelial cells [21]. All of these studies showed that, despite the different sizes of different nanoparticles of grape extracts, all of them were efficient delivery systems. To confirm the morphological characteristics of the biosynthesized nanoparticles, field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) were used. Estimations of different particle sizes were measured by ImageJ version 1.51j8 (National Institutes of Health (NIH), Bethesda, MD, USA) https://imagej.nih.gov/ij/ (accessed on 1 May 2021).
The FE-SEM results showed that the GSE-AgNPs had less-smooth surfaces with an average diameter size of 103–119 nm compared to the unloaded nanoparticles of 77.7 nm (Figure 3). However, the results of TEM showed that GSE, AgNO3, and GSE-AgNPs had diameter sizes of 13–23 nm, 12–18 nm, and 44–49 nm, respectively, which appeared as spherical dense crystals (Figure 4). These differences in size might be due to the technical differences between the two techniques, where the higher magnification power of TEM (100,000×) recognizes the smaller particles, while the too-low magnification power of SEM (50,000×) will show the particles with wider diameters. Furthermore, SEM is based on using the reflected or knock-off electron beams, which might show wider sizes due to the variable morphologies of the particles where TEM is based on, using the transmitted electrons, which penetrate through the particles to create more accurate images of the scanned particles [22].
Different studies used these two imaging techniques to evaluate the morphological characteristics of GSE nanoparticles. In agreement with our findings, a previous study reported that TEM analysis of AgNPs of grape stalk waste extract had a diameter of 54.3 ± 0.1 nm at pH 6, which decreased with acidic pH 4 to 27.7 ± 0.6 nm [18]. Similarly, another study showed that TEM images of AgNPs loaded with grapefruit extracts had a size diameter of 18–20 nm where the particles appeared as crystalline spheres [17]. In contrast, another study showed that TEM imaging resulted in an average size of 187–191 nm for SLN nanoparticles of grape extracts [20]. Despite different sizes obtained by these techniques, all of them confirmed the synthesis of GSE-AgNPs.

2.2. The Chemical Composition Analysis of the Studied Materials

In addition to the morphological characteristics, it was mandatory to analyze the chemical composition of the studied materials to investigate more about their functional groups. To achieve that purpose, the Fourier-transform infrared spectroscopy (FTIR) and gas chromatography/mass spectrometry technique (GC/MS) were used to analyze the different functional groups or the phenolic constituents of studied materials. FTIR analysis of GSE showed seven distinct functional groups of single bonds (alcohol and aliphatic alkene) and double bonds (olefinic alkene and aromatic rings (polysaccharides). On the other hand, FTIR analysis of GSE-AgNPs resulted in eight functional groups with single bonds (alcohols), double bonds (olefinic alkene, aromatic rings, and nitrogen compounds), and triple bonds (alkynes) (Figure 5, Table 1). The reduction in the number of the functional alcoholic groups from two in GSE to only one in GSE-AgNPs can be explained by the higher boiling point of -OH groups [23]. This increases the ability and suitability of nanoparticles to hydrogen bonding and other chemical reactions, where the biosynthesized GSE-AgNPs are more stable against these reactions [23]. The stronger triple bonds (alkyne groups) in GSE-AgNPs might refer to their higher stability, as well, compared to GSE. Both materials had multiple aromatic compounds, which might be due to the higher polysaccharide content of the seeds. Furthermore, some nitrogen compounds were detected in FTIR analysis of GSE-AgNPs, which might be explained by the reaction of the free NO3− ions with other products of the grapeseed extract (Table 1). In agreement with our findings, several studies showed that the FTIR analysis of GSE (water extract) had cis double bond =CH, methylene -CH2, aromatic C-C-valence, CH3, and CH2 aliphatic functional group [19,24].
The GC/MS analysis of GSE showed the presence of five phenolic compounds; 3-hydroxyflavone, anthocyanins, gallic acid, cianidanol, and epicatechin gallate (Table 2). According to the Retention Index (RI) threshold calculations, GSE contained 3-Hydroxyflavone, which was reported to have stronger antimicrobial activity against different bacterial and fungal strains [25]. Moreover, 47.83% RI revealed the presence of anthocyanins, which is a sensitive antimicrobial agent against Candida albicans, Staphylococcus aureus, Escherichia coli, Enterococcus faecalis, and Streptococcus pyogenes [26,27]. The flavone compounds of gallic acid, cianidanol, and epicatechin gallate had adequate antibacterial activities against E. coli, Pseudomonas aeruginosa, S. aureus, and Bacillus subtilis, as well [28].
Several studies reported similar findings for GC/MS analysis of GSE. In the study conducted by Gorodyska et al. 2018, the isopropanol extract of red grape seeds (Vitis vinifera L.) contained several phenolic compounds, such as gallic acid, ellagic acid, epicatechin, kaempferol, and myricetin [29]. Another study detected cyanidin, catechin, chlorogenic acid, gallic acid, ellagic acid, epicatechin gallate, and proanthocyanidin B in the methanolic extract of grapeseed [30,31]. All of these characteristics show the importance of GSE as a possible antimicrobial agent.

2.3. Antibacterial Activity of GSE and the Biosynthesis of GSE-AgNPs

In the current study, we tested the inhibitory effect of the aqueous GSE and the biosynthesized nanoparticles on the bacterial growth of two Gram-positive strains (S. aureus and B. subtilis) and two Gram-negative strains (E. coli and P. aeruginosa), as shown in Figure 6. The treatment with either 50 or 100% of aqueous GSE solution resulted in strong inhibition of B. subtilis and S. aureus, unlike the other bacterial species, which had not been affected.
On the other hand, the treatment with GSE-AgNPs resulted in stronger inhibition of all species; moreover, it inhibited the bacterial growth of B. subtilis and S. aureus more than the inhibition induced by GSE alone. Neither water nor AgNO3 showed any inhibitory effect on the studied species, which confirms the quality of the experiments. The statistical analysis by one-way ANOVA (Table 3) revealed that treatments with 50% and 100% doses of GSE, and GSE-AgNPs induced inhibition zone diameters of 10.5 ± 0.61, 11 ± 0.44, and 13.5 ± 1 mm, respectively, in the plates of B. subtilis, which was significant compared to untreated plates, p < 0.001. Similarly, in S. aureus plates, the treatments with 50% and 100% doses of GSE, and GSE-AgNPs induced inhibition zone diameters of 13.5 ± 1.61, 15 ± 2, and 15 ± 2 mm, respectively, which was also significant compared to the control, p < 0.001. GSE did not induce any significant inhibition of either E. coli or P. aeruginosa species, while GSE-AgNPs induced significant inhibition compared to the untreated control p < 0.001. In all species, treatment with GSE-AgNPs induced stronger inhibition than GSE alone, at all doses.
Several studies reported the strong antibacterial properties of grape products. A previous study showed that GSE induced a growth inhibition of 5–7 log CFU/mL and 2.2–2.6 log CFU/mL against Campylobacter jejuni [32] and Alicyclobacillus acidoterrestris [33], respectively. In agreement with our findings, a previous study showed that the aqueous extract of Vitis vinifera L. seeds induced significant growth inhibition of B. subtilis and S. aureus but not for P. aeruginosa [34]. In contrast, another study showed that only the petroleum ether extract of grape seeds at 20% were effective against B. subtilis, E. coli, S. aureus, and P. aeruginosa, while the lower concentrations did not induce any significant growth inhibition [35]. This effect might be explained because the petroleum ether will remove fatty material and resale the active materials in the grape seeds, which will induce a more inhibitory effect. Few studies have shown the significant antibacterial activity of GSE-AgNPs against B. subtilis [36,37,38], E. coli [36,38], P, aeruginosa [38], and S. aureus [36,39]. It is known that silver ions can stimulate the production of reactive oxygen species (ROS), which increase the oxidative stress and DNA fragmentation in cells [40]. However, lower concentrations of AgNO3 (<5 mM) were found to induce no DNA fragmentation [41], which explains its null effect in the current study as we used only 0.2 mM. Our results, in combination with the previous studies, suggested GSE-AgNPs as a possible bactericidal agent against both Gram-positive and Gram-negative species.

2.4. Antifungal Activity of GSE and the Biosynthesis of GSE-AgNPs

The effect of aqueous GSE on the mycelial growth of were Fusarium solani, Fusarium oxysporum, Helminthosporium rostratum, and Alternaria alternata. The strains were tested by the agar well diffusion method (Figure 7). The results showed that GSE had significant reduction in the growth of all species, except for A. alternata, while the slowest growth was for H. rostratum by 22.75 ± 0.2 mm compared to the control 87.19 ± 0.07 mm, p < 0.001. Similarly, treatment with GSE-AgNPs induced stronger mycelial growth inhibition of all spices than GSE and AgNO3. The maximum inhibitory effect was for H. rostratum by 9.11 ± 0.03 mm compared to control at 87.19 ± 0.07 mm, p < 0.001 (Table 4).
Several studies had evaluated the antifungal activity of GSE, particularly against Candida spp. In the study conducted by Eslami et al. 2017, the minimum inhibitory concentration (MIC) of GSE against Candida glabrata and Candida krusei was 50 µg/mL, which showed significant inhibition compared to the control [42]. Another study showed that GSE at doses of 6–20 mg/L had antifungal activity against C. albicans, as well [43]. In accordance with our findings, a previous study showed that the ethanolic extract of grapefruit tendrils had a significant fungicidal effect against different Fusarium species such as F. oxysporum, F. culmorum, F. solani, F. coeruleum, F. sporotrichioides, F. verticillioides, and F. tabacinum, while another species, Rhizoctonia solani, showed significant resistance [44]. Another study showed that polymeric proanthocyanidins isolated from grape seeds by ethanolic extraction had significant antifungal activity against Botrytis cinerea by inhibiting the spore germination [45]. Another study showed that the lonely application of GSE did not induce any inhibition of the mycelial growth of A. alternata [46]. To our knowledge, this is the first study that reported the antifungal activity of aqueous GSE against H. rostratum fungus.
As shown in Figure 7 and Table 4, the biosynthesized nanoparticles almost did not allow the mycelial growth of H. rostratum (<10%) while F. solani and A. alternata had minimum and limited growths of about 20% and 17% compared to the untreated plates. The minimal fungicidal effects of either GSE or GSE-AgNPs were for F. oxysporum that grow up to 25% of the untreated fungus. Noticeably, even with limited effect, the growth of F. oxysporum was not semi-circular as in the case of the untreated control, but it looks more like a condensed amoeboid-shape, which might suggest weak resistance of the fungal species to GSE-AgNPs. Despite limited studies that demonstrated the antifungal activity of GSE-AgNPs, some studies showed similar effects of other nanoparticles. In the study conducted by Sagana et al. 2020, the zinc oxide nanoparticles of aqueous GSE induced a growth inhibition to 16 mm of C. albicans 24 h post-treatment [47]. Similarly, another study showed that titanium oxide nanoparticles of aqueous GSE reduced the growth of C. albicans to 12 mm compared to the control [48]. All of these studies, in addition to our findings, highlight the antimicrobial activities of GSE against different pathogenic bacteria and fungi.

3. Materials and Methods

3.1. Chemicals and Reagents

Silver nitrate (AgNO3) and all other chemicals for nanoparticle preparation were purchased from Sigma-Aldrich (Sigma-Aldrich Chemie GmbH, Taufkirchen, Germany). The materials for bacterial and fungal cultures were purchased from Thermo Fisher Scientific (Thermo Fisher Scientific, Waltham, MA, USA).

3.2. Preparation of Aqueous GSE

The red grape was purchased from a local market in Saudi Arabia and classified at the department of Botany and Microbiology, Faculty of Science, King Saud University, Riyadh, Saudi Arabia. The fruit diameter was about 6 mm, reddish with pale wax bloom. It was classification as Vitis vinifera L., a member of the Vitaceae or Grape family. The seeds were collected, gently washed, air dried, ground by an electric miller, and stored at room temperature (25 °C) until use. An amount of 20 g of the powder was dissolved into 200 mL of ultrapure water, vortexed, and boiled for 15 min. After cooling, the extract was filtered, centrifuged, and the supernatant was collected. The supernatant was yellowish-brown and stored at 4 °C for future use.

3.3. Microorganisms

Both of the previously identified bacterial and fungal strains were obtained from the department of Plant Protection, College of Food and Agricultural Sciences, King Saud University. Four bacterial strains were used for the preliminary studies, S. aureus, E. coli, B. subtilis, and P. aeruginosa. The fungal strains were F. solani, F. oxysporum, H. rostratum, and A. alternata.

3.4. Bio Synthesis of Silver Nanoparticles of GSE

The preparation of AgNO3 loaded with aqueous GSE (GSE-AgNPs) was described by Xu et al. 2015 [11]. Briefly, 20 mL of 1 mM aqueous solution of AgNO3 were mixed with 1 mL (200 mg/mL) of GSE extract and boiled at 95 °C for 10 min. The new solution of synthesized GSE-AgNPs turned into lighter brown as compared to the light-yellow un-boiled solution of GSE.

3.5. Characterization of Synthesized GSE-AgNPs

3.5.1. UV Spectroscopy

UV-visible spectrophotometer (Shimadzu, Tokyo, Japan) was used for the characterization of GSE-AgNPs. The reduction of pure Ag+ ions was checked at 200–800 nm by UV-2450 double-beam according to the manufacturer’s instructions, as described previously [49]. The experiment was performed in triplicates.

3.5.2. Dynamic Light Scattering (DLS) Analysis

To measure the stability of the colloidal nanoparticles, it is important to measure their effective surface charge or zeta potential, which reflects their surface energy [50]. To detect the particle size distribution, it is important to use the DLS technique, which will calculate the PDI and Z-Average, which refers to the width of the overall distribution and the size distribution by intensity of the specific particle, respectively [51]. In the current study, DLS was used to measure the PDI and Z-Average by the Zetasizer (Malvern Panalytical, Malvern, UK), according to the manufacturer’s instructions.

3.5.3. Field Emission Scanning Electron Microscopy (FE-SEM)

The FE-SEM technique by JEOL JEM-2100 microscope (JEOL, Peabody, MA, USA) was used to investigate the external morphology and physical characteristics of the synthesized nanoparticles, as described previously [52]. Briefly, a drop of nanoparticle suspensions with a volume of 8 μL was placed onto 200 mesh grids with a carbon support film (Agar Scientific, London, UK), rinsed with ethanol and air-dried. Then, the sample was fixed on an appropriate SEM holder and the images were taken at an accelerating voltage of 15 kV using JEM-2100 optic system (JEOL, Peabody, MA, USA). The experiment was performed in triplicates.

3.5.4. Transmission Electron Microscopy (TEM)

The TEM technique by JEM-1011 transmission electron microscope (JEOL Ltd. Inc., Tokyo, Japan) was used to confirm the crystalline structure of the synthesized nanoparticles. The preparation and processing of slides were according to the manufacturer’s instructions, as described previously [53].

3.5.5. Fourier-Transform Infrared Spectroscopy (FTIR)

FTIR analysis is a powerful analytical technique that is used for the identification (or confirmation) of any unknown material. It works through the radiation of the sample by an infrared radiation of 10,000 to 100 cm−1, which causes vibration (or rotation) that can be further detected on a pyroelectric detector at the range of 400–4000/cm. The resulting spectrum is unique to each material and is represented as a number of particular descending peaks of a particular wavenumber, which represent specific functional groups [54]. In the current study, FTIR spectroscopy was used to analyze the components of the newly synthetized GSE-AgNPs to confirm its composition. A dedicated FTIR spectrometer (Nicolet 6700 FTIR Spectrometer, Waltham, MA, USA) at the range of 500–4000/cm was used. The experiment was performed in triplicates.

3.5.6. Gas Chromatography/Mass Spectrometry Technique (GC/MS)

The GC/MS analysis was performed by using a dedicated thermo-gas chromatograph/mass spectrometer (model Shimadzu 2010) equipped with Rtx-5MS capillary column (30 m long, 0.25 mm in diameter, film thickness of 0.25 μm). The carrier gas was helium and the maximum usable temperature was 280 °C. The data were analyzed using the libraries of National Institute of Standards and Technology (NIST) database https://www.nist.gov/ (accessed on 20 May 2021) and Wiley Registry of Mass Spectral Data https://0-sciencesolutions-wiley-com.brum.beds.ac.uk/solutions/technique/gc-ms/wiley-registry-of-mass-spectral-data-12th-edition/ (accessed on 20 May 2021). The experiment was performed in triplicates.

3.6. Determination Antimicrobial Activity

3.6.1. Determination of Antibacterial Activity

The antibacterial activity was evaluated by measuring the zone of inhibition for each bacterial culture by the agar disk-diffusion method, as described previously [55]. Briefly, the bacterial strains were cultured on the Mueller–Hinton Agar (MHA) for 24 h at 37 °C, then two colonies of each plate were transferred to a tube of 10 mL distilled water and mixed thoroughly to maintain uniform distribution. Using sterile swabs, 0.2 mL of bacteria strain (2.5 × 105 CFU/mL) was swabbed uniformly onto individual MHA plate and allowed to dry for ten min. Four plates were prepared for each bacterium to test GSE, AgNO3, GSE-AgNPs, and one plate for distilled water to be used as negative control, separately.
The disk-diffusion method was applied by forming of adequately spaced wells (holes) of 4 mm diameter at the culture agar surface using a sterile metal cork borer. For control plates, a negative control was used. To test GSE, three wells were formed, supplied with 0.2 mL of three different concentration of the GSE extract (100%, 50%, & 10%). For AgNO3, GSE-AgNPs, and control plates, a single well/plate was formed and treated with 0.2 mL of either water, AgNO3, or GSE-AgNPs. All plates were kept under aseptic conditions, at room temperature, for one hour, to allow the agents to diffuse into agar medium. Subsequently, the plates were incubated for 24 h at 37 °C. At the end of the incubation period, the inhibition zones, the area surrounding the hole with no growth of inoculated microorganisms, were measured to the nearest millimeter, as described before [56]. The zone of inhibition was measured by ImageJ version 1.51j8 (National Institutes of Health (NIH), Bethesda, MD, USA) https://imagej.nih.gov/ij/ (accessed on 1 May 2021) at the scale of 2.61 pixels/mm. All experiments were performed in triplicates.

3.6.2. Determination of Antifungal Activity

The antifungal activity was assessed by the agar well diffusion method described by Daoud et al. 2019, with slight modification [57]. Briefly, potato dextrose agar (PDA) media (20 gm dextrose, 15 gm agar, 4 gm potato starch, 40 mg chlortetracycline, 25 mg chloramphenicol, and 1.4 gm tartaric acid) was prepared by boiling for 15 min at 121 °C in one liter of distilled water (pH 3.5 at 25 °C) with mixing to dissolve. The mixture was cooled to 55 to 60 °C followed by mixing with either GSE, AgNO3, GSE-AgNPs, or distilled water (negative control), then an appropriate amount from each PDA/antifungal agent was poured in a separate Petri dish and kept in sterile atmosphere until solidification. Later, a flint hole of 1 cm diameter was formed by a sterile metal cork borer at the center of the plate, then the fungus strains were added by direct plating. The mycelial growth inhibition was determined by measuring of the colony’s diameter after seven days. The mycelial growth was measured by ImageJ version 1.51j8 (National Institutes of Health (NIH), MD, United States) https://imagej.nih.gov/ij/ (accessed on 1 May 2021) at the scale of 2.61 pixels/mm. All experiments were performed in triplicates.

3.7. Statistical Analysis

The statistical analysis was performed by dedicated software (Minitab 2018, State College, PA, USA). Means and standard deviations were calculated for all quantitative data. One-way ANOVA was used to assess the significance levels of results at p < 0.05.

4. Conclusions

The current study showed the strong antimicrobial activities of aqueous GSE and the biosynthesized GSE-AgNPs against different Gram-positive, Gram-negative, and fungi species. The novelty of this work is that it is the first reporting/demonstration of antifungal activity of GSE-AgNPs and of the fungicidal activity of GSE or GSE-AgNPs against the red spot fungus H. rostratum. However, more studies are needed to investigate and demonstrate the antimicrobial activities of the most active constituents of grape seed and other grape-products.

Author Contributions

The study design, conception, and collection of samples were conducted by F.A.-O. and S.K.A. Experiments, data acquisition, and statistical analysis were conducted by R.I.A. and A.A.A.-A. Both R.M.A. and S.A.-S. conducted the literature search, writing, and preparation of the manuscript. F.A.-O., A.A.A.-A. and S.K.A. were responsible for final editing and reviewing of the manuscript. F.A.-O. was responsible for funding resources and acted as a guarantor and corresponding author. The final draft was reviewed and agreed upon by all authors. All authors have read and agreed to the published version of the manuscript.

Funding

This research project was supported by a grant from the Deanship of Scientific Research, King Saud University, who funded this work through research group no. (RG-1441-357).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data presented in this study are available within the current article. All statistical analysis results and raw data are available upon request from the corresponding author.

Acknowledgments

The authors extend their appreciation to the Deanship of Scientific Research at King Saud University for funding this work through research group no. “RG-1441-357”, King Saud University, Riyadh, Saudi Arabia.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of the GSE and GSE-AgNPs compounds are available from the authors.

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Molecules 26 06081 g001 550
Figure 1. Physical biosynthesis of GSE-AgNPs. GSE-AgNPs were prepared by boiling with an aqueous solution of AgNO3 (1 mM), which turned it from light-yellow into brownish-yellow. (A) GSE, (B) GSE-AgNPs.
Figure 1. Physical biosynthesis of GSE-AgNPs. GSE-AgNPs were prepared by boiling with an aqueous solution of AgNO3 (1 mM), which turned it from light-yellow into brownish-yellow. (A) GSE, (B) GSE-AgNPs.
Molecules 26 06081 g001
Molecules 26 06081 g002 550
Figure 2. Analysis of the physical properties of GSE-AgNPs. The morphological analysis of the biosynthesised GSE-AgNPs showed their ability to induce higher SPR by UV excitation through either (A) UV spectroscopy, or (B) the size distribution curve by Zetasizer; three preparations of GSE-AgNPs, at the same concentrations, were used to confirm the results of DLS.
Figure 2. Analysis of the physical properties of GSE-AgNPs. The morphological analysis of the biosynthesised GSE-AgNPs showed their ability to induce higher SPR by UV excitation through either (A) UV spectroscopy, or (B) the size distribution curve by Zetasizer; three preparations of GSE-AgNPs, at the same concentrations, were used to confirm the results of DLS.
Molecules 26 06081 g002
Molecules 26 06081 g003 550
Figure 3. The FE-SEM imaging of GSE-AgNPs. A total of 8 μL were loaded on the 200 mesh grids with a carbon support film of JEOL JEM-2100 microscope. JEM-2100 optic system with 15 kV was used to capture the SEM images at the magnification powers of 20,000× (right) and 50,000× (left).
Figure 3. The FE-SEM imaging of GSE-AgNPs. A total of 8 μL were loaded on the 200 mesh grids with a carbon support film of JEOL JEM-2100 microscope. JEM-2100 optic system with 15 kV was used to capture the SEM images at the magnification powers of 20,000× (right) and 50,000× (left).
Molecules 26 06081 g003
Molecules 26 06081 g004 550
Figure 4. The TEM imaging of GSE-AgNPs. JEM-1011 transmission electron microscope was used to investigate the crystalline structure of (A) GSE, (B) GSE-AgNPs, and (C) AgNO3. The diameter sizes of the tested materials were measured by ImageJ software.
Figure 4. The TEM imaging of GSE-AgNPs. JEM-1011 transmission electron microscope was used to investigate the crystalline structure of (A) GSE, (B) GSE-AgNPs, and (C) AgNO3. The diameter sizes of the tested materials were measured by ImageJ software.
Molecules 26 06081 g004
Molecules 26 06081 g005 550
Figure 5. FTIR analysis. Nicolet 6700 FTIR Spectrometer was used to identify the functional groups in (A) GSE and (B) GSE-AgNPs at the range of 500–4000 cm−1.
Figure 5. FTIR analysis. Nicolet 6700 FTIR Spectrometer was used to identify the functional groups in (A) GSE and (B) GSE-AgNPs at the range of 500–4000 cm−1.
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Molecules 26 06081 g006 550
Figure 6. The antibacterial activity of aqueous GSE and the biosynthesized GSE-AgNPs. The bacterial growth was detected by measuring the inhibition zone using the agar disk-diffusion method by the Mueller–Hinton Agar. The plates were treated with (A) Milli-Q water as control, (B) GSE extract (100%, 50%, & 10%), (C) 0.2 mL AgNO3, or (D) 0.2 mL GSE-AgNPs. The zone of inhibition was measured after seven days ImageJ at the scale of 2.61 pixels/mm.
Figure 6. The antibacterial activity of aqueous GSE and the biosynthesized GSE-AgNPs. The bacterial growth was detected by measuring the inhibition zone using the agar disk-diffusion method by the Mueller–Hinton Agar. The plates were treated with (A) Milli-Q water as control, (B) GSE extract (100%, 50%, & 10%), (C) 0.2 mL AgNO3, or (D) 0.2 mL GSE-AgNPs. The zone of inhibition was measured after seven days ImageJ at the scale of 2.61 pixels/mm.
Molecules 26 06081 g006
Molecules 26 06081 g007 550
Figure 7. The antifungal activity of aqueous GSE and the biosynthesized GSE-AgNPs. The mycelial growth was measured by the agar well diffusion method using potato dextrose agar (PDA) media. The plates were treated with either (A) Milli-Q water as control, (B) GSE extract (100%), (C) 0.2 mL AgNO3, or (D) 0.2 mL GSE-AgNPs. The mycelial growth measuring of the colony diameter after seven days. The mycelial growth was measured by ImageJ at the scale of 2.61 pixels/mm.
Figure 7. The antifungal activity of aqueous GSE and the biosynthesized GSE-AgNPs. The mycelial growth was measured by the agar well diffusion method using potato dextrose agar (PDA) media. The plates were treated with either (A) Milli-Q water as control, (B) GSE extract (100%), (C) 0.2 mL AgNO3, or (D) 0.2 mL GSE-AgNPs. The mycelial growth measuring of the colony diameter after seven days. The mycelial growth was measured by ImageJ at the scale of 2.61 pixels/mm.
Molecules 26 06081 g007
Table
Table 1. The FTIR analysis of the functional groups in the GSE and GSE-AgNPs.
Table 1. The FTIR analysis of the functional groups in the GSE and GSE-AgNPs.
Tested MaterialAbsorption (cm−1)AppearanceGroupCompound Class
GSE3754Medium, sharpO-H stretchingAlcohol
3446Strong, broadDimeric O-H stretch
2927Strong, broadMethylene C-H asymmetricAliphatic alkene
1624StrongSkeletal C-C vibrations (methyne)
775MediumAlkenyl C=C stretchOlefinic alkene
1458MediumC=C-C aromatic ring stretchAromatic ring
1058MediumAromatic C-H in-plane bend
GSE-AgNPs3276Strong, broadHydroxy group, H-bonded OH stretchAlcohol
2204Weak C≡C medial alkyne (disubstituted)Alkyne
2161Weak C≡C terminal alkyne (monosubstituted)
1992/1966Weak Aromatic combination bandsAromatic ring
2043/2022WeakTransition metal carbonyls, cyanide, thiocyanate, or isothiocyanate (-NCS)Carbonyl or inorganic
1634Medium Alkenyl C=C stretchOlefinic alkene
Table
Table 2. GC/MS analysis of GSE phenolic constituents.
Table 2. GC/MS analysis of GSE phenolic constituents.
Phenolic CompoundFormulaChemical StructureMolecular WeightMS Fragments (m/z)RI%
3-HydroxyflavoneC15H10O3 Molecules 26 06081 i001238.242 238.2574.80
AnthocyaninsC15H11O+ Molecules 26 06081 i002207.252207.0047.83
Gallic acidC7H6O5 Molecules 26 06081 i003170.12170.0029.81
CianidanolC15H14O6 Molecules 26 06081 i004290.271290.006.50
Epicatechin gallateC22H18O10 Molecules 26 06081 i005442.376442.001.12
RI: Retention index.
Table
Table 3. The antibacterial effect of GSE and biosynthesized nanoparticles by measuring the inhibition zone diameter (mm).
Table 3. The antibacterial effect of GSE and biosynthesized nanoparticles by measuring the inhibition zone diameter (mm).
StrainsControl10%GSE50%GSE100%GSEGSE-AgNPsAgNO3
B. subtilisMean ± SD0.07 ± 0.060.27 ± 0.2110.5 ± 0.6111 ± 0.4413.5 ± 10.5 ± 0.1
p-value10.6451.13 × 10−11 *7.02 × 10−12 *6.13 × 10−13 *0.327
E. coliMean ± SD0.07 ± 0.120.2 ± 0.10.3 ± 0.170.5 ± 0.112.5 ± 10.7 ± 0.1
p-value10.7060.5120.2331.35 × 10−13 *0.092
P. aeruginosaMean ± SD0.07 ± 0.060.07 ± 0.060.5 ± 0.10.7 ± 0.113.5 ± 10.1 ± 0.1
p-value110.2260.0874.37 × 10−14 *0.923
S. aureusMean ± SD0.03 ± 0.060.17 ± 0.1613.5 ± 1.6115 ± 215 ± 20.6 ± 0.1
p-value10.9043.37 × 10−8 *1.03 × 10−10 *1.03 × 10−10 *0.612
* p-value < 0.05 compared to control. SD: standard deviation.
Table
Table 4. GSE and biosynthesized nanoparticles affect the mycelial growth (mm) of the studied fungi.
Table 4. GSE and biosynthesized nanoparticles affect the mycelial growth (mm) of the studied fungi.
StrainsControlGSE
(100%)		GSE-AgNPs
(0.2 mL)		AgNO3
(0.2 mL)
F. solaniMean ± SD88.23 ± 0.0637.5 ± 0.2617.52 ± 0.0388.15 ± 0.1
p-value19.96 × 10−20 *1.21 × 10−37 *0.999
F. oxysporumMean ± SD88.39 ± 0.1567.5 ± 0.222.53 ± 0.1188.59 ± 0.11
p-value16.08 × 10−4 *1.08 × 10−32 *0.957
A. alternataMean ± SD88.51 ± 0.1184.91 ± 0.1814.49 ± 0.1588.43 ± 0.09
p-value10.4594.72 × 10−41 *0.997
H. rostratumMean ± SD88.19 ± 0.0722.75 ± 0.29.11 ± 0.0388.09 ± 0.13
p-value12.33 × 10−32 *6.39 × 10−47 *0.991
* p-value < 0.05. SD: Standard Deviation.
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Al-Otibi, F.; Alkhudhair, S.K.; Alharbi, R.I.; Al-Askar, A.A.; Aljowaie, R.M.; Al-Shehri, S. The Antimicrobial Activities of Silver Nanoparticles from Aqueous Extract of Grape Seeds against Pathogenic Bacteria and Fungi. Molecules 2021, 26, 6081. https://0-doi-org.brum.beds.ac.uk/10.3390/molecules26196081

AMA Style

Al-Otibi F, Alkhudhair SK, Alharbi RI, Al-Askar AA, Aljowaie RM, Al-Shehri S. The Antimicrobial Activities of Silver Nanoparticles from Aqueous Extract of Grape Seeds against Pathogenic Bacteria and Fungi. Molecules. 2021; 26(19):6081. https://0-doi-org.brum.beds.ac.uk/10.3390/molecules26196081

Chicago/Turabian Style

Al-Otibi, Fatimah, Shahad K. Alkhudhair, Raedah I. Alharbi, Abdulaziz A. Al-Askar, Reem M. Aljowaie, and Sameha Al-Shehri. 2021. "The Antimicrobial Activities of Silver Nanoparticles from Aqueous Extract of Grape Seeds against Pathogenic Bacteria and Fungi" Molecules 26, no. 19: 6081. https://0-doi-org.brum.beds.ac.uk/10.3390/molecules26196081

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