Antagonistic Activity of Lactic Acid Bacteria and Rosa rugosa Thunb. Pseudo-Fruit Extracts against Staphylococcus spp. Strains

: Staphylococcus bacteria are ubiquitous microorganisms. They occur in practically all envi-ronments. They also show the ability to colonize the skin and mucous membranes of humans and animals. The current trend is to look for new natural factors (e.g., plant extracts rich in polyphenols) limiting the growth of undesirable bacteria in food and cosmetics or use as an adjunct in antibiotic therapy. The aim of this study was to evaluate the effect of extracts from Rosa rugosa Thunb. on the antagonistic properties of selected lactic acid bacteria strains in relation to Staphylococcus spp. isolates. The biological material consisted of seven strains of lactic acid bacteria (LAB) and seven strains of bacteria of the Staphylococcus genus. The anti-staphylococcal properties of the Rosa rugosa Thunb. DM/dm) were tested using the well method. The conducted research showed that the pomace extracts of the pseudo-fruit ( Rosa rugosa Thunb.) had the ability to inhibit the growth of Staphylococcus spp. bacteria. The minimum concentration of polyphenols inhibiting the growth of staphylococci was in the range of 0.156–0.625 mg/mL. The conducted research showed that combined lactic acid bacteria and extracts from the pomace from the pseudo-fruit Rosa rugosa Thunb. (LR systems) may be factors limiting the growth of Staphylococcus spp. bacteria. As a result of the research, two-component antagonist systems consisting of LAB cultures and extracts from Rosa rugosa Thunb. pomace were developed, which effectively limited the growth of the test strains of Staphylococcus spp. In 41% of all tested cases, the zone of inhibition of growth of bacteria of the genus Staphylococcus spp. after the use of two-component antagonist systems was higher than that as a result of the control culture (without the addition of extracts).


Introduction
Staphylococcus bacteria are ubiquitous microorganisms. They occur in practically all environments. They also show the ability to colonize the skin and mucous membranes of humans and animals. Often in the form of biofilm, they inhabit environmental, medical material and implant, and food production surfaces (polypropylene, polystyrene, and stainless steel) [1][2][3]. Staphylococcus spp. strains can be brought into food with raw materials and by humans participating in the production process. For example, enterotoxic strains of the genus Staphylococcus are often isolated from dairy products. Staphylococcus aureus is a widespread causative agent of mastitis in cattle [4]. In the process of obtaining milk from cows with staphylococcal mastitis, even with good filtration, the number of staphylococci

Research Material
The research material consisted of four extracts (two water-ethanol extracts-crude (EC) and purified (EP)-and two water-acetone extracts: crude (AC) and purified (AP)) made of frozen Rosa rugosa Thunb. pseudo-fruit pomace. The exact preparation of the extracts was described by Piekarska-Radzik et al. [39]. For the frozen pomace of Rosa rugosa Thunb. pseudo-fruit, two portions of 2 kg (after the production of rose juice produced on the same day) (Polska Róża, Falenty New) were subjected to 0.5 h of water extraction at a ratio of 1:2 (v/v). Next, the pomace was extracted twice statically for 24 h with a 60% percent acetone solution or 60% ethanol at a ratio of 1:3 (v/v). The received ethanol and acetone extracts were concentrated in a vacuum evaporator (Hei-VAP Precision, Heidolph, Schwabach, Germany). The concentrated acetone or ethanol extracts were then divided into two parts. One of them was purified by column chromatography on Amberlite XAD 1600 N (divinylbenzene copolymer) (30.0 × 3.7 cm). The concentrated crude extracts were applied to the column (flow rate: 3-5 mL/min). Then, the column was washed with water, and the adsorbed polyphenols were eluted with 10% and 68% ethanol. The alcohol fractions were combined and concentrated on a Heidolph 24/7 automatic evaporator. The crude and purified extracts were freeze-dried using a freeze dryer (Christ, Alpha 1-2 LD plus, Osterode am Harz, Germany). In the obtained freeze-dried extracts, the content of the selected groups of polyphenols was determined by using HPLC chromatographic methods. The concentrations of ellagitannins, ellagic acid, and flavonols were determined in the extracts by dissolving 100 mg in 80% methanol in 10-mL volumetric flask, diluted, and analyzed as described by Karlińska et al. [40,41] and Sójka et al. [42]. Procyanidins and free catechin were determined as described by Milala et al. [16].

Biological Material
The biological material consisted of six lactic acid bacteria strains deposited in the Pure Culture Collection of Industrial Microorganisms of the Institute of Fermentation Technology and Microbiology ŁOCK 105 (Łódź, Poland) and the Levilactobacillus brevis MG451814 strain, the nucleotide sequence which was deposited in the GenBank NCBI database. Due to the reclassification of the Lactobacillus genus carried out in 2020, the current and new taxonomic names of the strains used in the research are summarized in Table 1. All strains of lactic acid bacteria (stored in MAST CRYOBANK; Mast Group Ltd., Merseyside, UK) were activated by transfer to a fresh Broth MRS medium (Merck, Darmstadt, Germany) and cultured at 30 • C or 37 • C (depending on the strain) for 24 h.
Seven strains of bacteria of the genus Staphylococcus were used as test strains. The five strains are environmental isolates. The strains were obtained by surface swabbing from the skin of healthy volunteers aged 24 to 30 years (2 female and 1 male). No invasive or inconvenient methods were used to collect the samples. In non-invasive sampling, our research institution (Institute of Fermentation Technology and Microbiology, Lodz University of Technology) did not require the approval of the ethics committee to conduct research using this microorganism in in vitro tests. All donors were volunteers who were informed about the planned analytical procedures and agreed to publication of the obtained data. The species affiliation of the Staphylococcus isolates was confirmed by molecular methods based on sequence analysis of the 16S ribosomal RNA gene. The nucleotide sequences of the strains obtained from the wild were deposited in the GenBank database (The National Center for Biotechnology Information). The species affiliation and accession numbers of the tested strains are presented in Table 2. In contrast, two strains, S. aureus ATCC 25923 and S. epidermidis DSMZ 3270, were used as reference strains in the tests of antagonist activity.

The Minimum Concentration of Polyphenols (MIC) That Inhibits the Growth of Staphylococcus Bacteria
In order to determine the minimum concentration of polyphenols inhibiting the growth of bacteria of the genus Staphylococcus, a deep culture of the studied microorganisms was performed. For this purpose, 6 wells were cut (10 mm in diameter) into a plate from a 24-h culture of Staphylococcus bacteria (density 10 8 CFU/mL) with a sterile crank and removed with a sterile preparation needle. Added to the holes created in this way was 100 µL of appropriately diluted extracts from the pseudo-fruit pomace Rosa rugosa Thunb., with a content in the extracts in the range of 0.0006-2.5 mg/mL. The negative control was 5% DMSO. The plates were then placed in an incubator (37 • C) for 18-24 h. After this time, the zone of inhibition of growth of the bacteria of the Staphylococcus genus was measured. The results were given in mm ± standard deviation (SD). The lowest concentration of polyphenols at which growth inhibition of the test bacteria was still observed was assumed to be the MIC value (mg/mL).

Antagonistic Activity of Lactic Acid Bacteria
The antagonistic properties of lactic acid bacteria were investigated using the bar method [43,44]. The method is based on the observation of parallel growth of the strains (the indicator and the antagonistic ones). For this purpose, 1 mL was taken from a 24-h LAB culture with a density of 10 9 CFU/mL and plunged into a sterile Petri dish (by pouring over cooled MRS Agar, pouring it to the upper limit of the plate height). Next, from solidified MRS medium overgrown with LAB, 10-mm (diameter) bars were cut out and put on the prepared agar (nutrient agar, Merck) containing test microorganisms (Staphylococcus strain) (10 5 -10 6 CFU/mL). The dishes were incubated at 37 • C for 24 h. Following incubation, the diameter of the test strain growth inhibition zone was measured. The results were given in mm as the mean value of three repetitions ± standard deviation. In this way, a control culture was obtained.
On the other hand, the two-component antagonist (LR) system was obtained by LAB culture with Rosa rugosa Thunb. pseudo-fruit pomace extracts. MRS Agar with the addition of Rosa rugosa Thunb. pseudo-fruit pomace extracts with a final polyphenol concentration of 0.156 mg/mL (the concentration did not inhibit LAB growth, as shown in the publication by Piekarska-Radzik et al. [39]). The plates prepared in this way were incubated for 24 h at the temperature optimal for the growth of each of the tested lactic acid bacteria strains. After incubation with a sterile cork, bars were cut from the plates and placed on the culture plates of the test Staphylococcus spp. isolates. Cultures of the test strains were prepared identically to those in Section 2.3. After the plates were incubated with the antagonist test, the zones of inhibition of growth of Staphylococcus spp. around the bars were measured. The results were given in mm as the mean value of three repetitions ± standard deviation.

The Acidity of Lactic Acid Bacteria
The effect of Rosa rugosa Thunb. pseudo-fruit pomace extracts on the acidic activity of the LAB was assessed by measuring the pH. The extracts were added to the stock culture in the Broth MRS medium bed so that the final concentration of polyphenols in each of the samples was 0.156 mg/mL. After inoculation by 1% (v/v) LAB inoculum (density of inoculum: 10 8 -10 9 CFU/mL), the samples were cultivated for 48 h at the temperature optimal for LAB growth. After 24 and 48 h of culturing, the pH of the culture was tested (ELMETRON pH-meter, Poland, with a glass electrode (ELMETRON CP-411, Warsaw, Poland)).

Statistical Analysis
All experiments were performed in at least three independent replicates, and the result was reported as the mean value. For the obtained results, the value of the standard deviation was also calculated.
The obtained data were statistically analyzed using STATISTICA 12 software (StatStoft, San Francisco, CA, USA) using the one-way ANOVA and Tukey's post hoc test with a confidence interval of p ≤ 0.05.

The Minimum Concentration of Polyphenols That Inhibit the Growth of Staphylococcus Bacteria
The effect of Rosa rugosa Thunb. pseudo-fruit pomace extracts on the growth of bacteria of the genus Staphylococcus is presented in Table 3. Both the water-ethanol and water-acetone extracts showed a high antagonistic potential. The minimum concentration of polyphenols (MIC) inhibiting the growth of bacteria of the genus Staphylococcus was in the range of 0.156-0.625 mg/mL for most of the tested strains. In the case of the Staphylococcus epidermidis R1A strain, the MIC value of the water-ethanol extracts was above 2.5 mg/mL. The sensitivity of the studied Staphylococcus spp. strains to the presence of polyphenols contained in the extracts of Rosa rugosa Thunb. pseudo-fruit pomace in the environment of their growth is an individual (strain) feature. Nevertheless, it should be noted that the type of extraction influences the antagonistic potential of the obtained extracts. The extracts obtained with the use of acetone showed a slightly higher antagonistic activity than the water-ethanol extracts. Purifying the extracts (regardless of the solvent used) also influenced the antagonistic activity of the obtained extracts.

Antagonistic Activity of Lactic Acid Bacteria
Table A1 (in Appendix A) and Figure 1 show the antagonistic activity of lactic acid bacteria against Staphylococcus spp. strains. The tested LAB showed a high antagonistic potential against the test bacteria of the Staphylococcus genus.
Both the S. aureus ATCC 25923 and S. epidermidis DSMZ 3270 reference strains were sensitive to the metabolites of the LABs used. The growth inhibition zone for the ATCC 25923 strain was from 14.33 ± 0.58 mm to 21.00 ± 0.00 mm, while for the DSMZ 3270 strain, the values ranged from 17.22 ± 0.58 mm to 20.33 ± 0.58 mm. When analyzing the sensitivity of the environmental test strains of Staphylococcus spp. to the metabolites of the LAB tested, it was noted that the R1A strain showed resistance to the metabolites of two lactic acid bacteria strains: Lacticaseibacillus rhamnosus ŁOCK 0943 and Levilactobacillus brevis MG451814. In the case of the Levilactobacillus brevis MG451814 strain, its antagonistic potential was also limited in relation to the Staphylococcus spp. strains designated as S. haemolyticus R2A and S. aureus S2A. However, in the case of the test strain S. saprophyticus S1A, the strain MG451814 was characterized by the highest antagonistic activity (the zone of growth inhibition was 50.00 ± 0.00 mm). Moreover, it was found that the S1A strain was characterized by a higher sensitivity to the metabolites of the LAB bacteria studied (mean value of the growth inhibition, statistically significant) compared with the remaining Staphylococcus spp. potential was also limited in relation to the Staphylococcus spp. strains designated as S. haemolyticus R2A and S. aureus S2A. However, in the case of the test strain S. saprophyticus S1A, the strain MG451814 was characterized by the highest antagonistic activity (the zone of growth inhibition was 50.00 ± 0.00 mm). Moreover, it was found that the S1A strain was characterized by a higher sensitivity to the metabolites of the LAB bacteria studied (mean value of the growth inhibition, statistically significant) compared with the remaining Staphylococcus spp.

R3A
(g) (h) S1A   Figure 1). Each of the 28 LR systems was effective in inhibiting the growth of Staphylococcus bacteria. The anti-staphylococcal potential of the 28 LR systems (expressed in terms of growth inhibition zones) was in the range of 12-28 mm. Interestingly, each of the 28 systems inhibited the growth of the environmental isolates tested. This was especially important in relation to the control sample, in which in four cases saw the tested lactic acid bacteria not showing anti-staphylococcal properties. It should be noted that in these cases, the addition of extracts may positively affect the antistaphylococcal properties of lactic acid bacteria.
In the case of the S. epidermidis R1A strain, the highest anti-staphylococcal activity was observed in the system consisting of the Lacticaseibacillus rhamnosus ŁOCK 0943 strain with the addition of purified acetone extract and Levilactobacillus brevis ŁOCK 0992 with the addition of purified ethanol extract (Figure 1a,b). Both zones of growth inhibition were close to 40 mm. On the other hand, the weakest effect limiting the growth of staphylococci was observed for systems based on the culture of Levilactobacillus brevis ŁOCK 0980 (regardless of the addition of the extract). The greatest antimicrobial potential was observed in LR systems based on the culture of Levilactobacillus brevis ŁOCK 0992 with crude extracts and Lacticaseibacillus rhamnosus ŁOCK 0943 with purified extracts. Due to the addition of acetone and ethanol extracts, the systems constructed on the basis of Lacticaseibacilluss brevis ŁOCK 0943 and Levilactobacillus brevis MG451814 cultures showed anti-staphylococcal potential (zone of growth inhibition in the range of 20-40 mm), despite the fact that the basic culture did not show anti-staphylococcal properties in this strain. Moreover, in most cases (20/28), the two-component LR systems showed a statistically significant higher antimicrobial potential than the stock culture ( Figure 2 and Table A2, Appendix A). It should also be noted that neither of the systems exhibited a statistically significantly lower antimicrobial potential than the stock culture.
In the case of the S. haemolyticus R2A strain, it was not possible to clearly define which two-component LR system had the highest and lowest anti-staphylococcal potentials (Figure 1c,d). The highest anti-staphylococcal potential (33-38-mm growth inhibition   Table A2 (Appendix A) shows the antagonistic properties of the two-component LR systems. By combining 7 different LABs with four Rosa rugosa Thunb pseudo-fruit pomace extracts, 28 2-component LR systems were obtained, for which the anti-staphylococcal potential was tested ( Figure 1). Each of the 28 LR systems was effective in inhibiting the growth of Staphylococcus bacteria. The anti-staphylococcal potential of the 28 LR systems (expressed in terms of growth inhibition zones) was in the range of 12-28 mm. Interestingly, each of the 28 systems inhibited the growth of the environmental isolates tested. This was especially important in relation to the control sample, in which in four cases saw the tested lactic acid bacteria not showing anti-staphylococcal properties. It should be noted that in these cases, the addition of extracts may positively affect the antistaphylococcal properties of lactic acid bacteria.
In the case of the S. epidermidis R1A strain, the highest anti-staphylococcal activity was observed in the system consisting of the Lacticaseibacillus rhamnosus ŁOCK 0943 strain with the addition of purified acetone extract and Levilactobacillus brevis ŁOCK 0992 with the addition of purified ethanol extract (Figure 1a,b). Both zones of growth inhibition were close to 40 mm. On the other hand, the weakest effect limiting the growth of staphylococci was observed for systems based on the culture of Levilactobacillus brevis ŁOCK 0980 (regardless of the addition of the extract). The greatest antimicrobial potential was observed in LR systems based on the culture of Levilactobacillus brevis ŁOCK 0992 with crude extracts and Lacticaseibacillus rhamnosus ŁOCK 0943 with purified extracts. Due to the addition of acetone and ethanol extracts, the systems constructed on the basis of Lacticaseibacilluss brevis ŁOCK 0943 and Levilactobacillus brevis MG451814 cultures showed anti-staphylococcal potential (zone of growth inhibition in the range of 20-40 mm), despite the fact that the basic culture did not show anti-staphylococcal properties in this strain. Moreover, in most cases (20/28), the two-component LR systems showed a statistically significant higher antimicrobial potential than the stock culture ( Figure 2 and Table A2, Appendix A). It should also be noted that neither of the systems exhibited a statistically significantly lower antimicrobial potential than the stock culture.
In the case of the S. haemolyticus R2A strain, it was not possible to clearly define which two-component LR system had the highest and lowest anti-staphylococcal potentials (Figure 1c,d). The highest anti-staphylococcal potential (33-38-mm growth inhibition  In the case of t two-component LR (Figure 1c,d). The  Table A2 (Appendix A) shows the antagonistic properties of the two-component LR systems. By combining 7 different LABs with four Rosa rugosa Thunb pseudo-fruit pomace extracts, 28 2-component LR systems were obtained, for which the anti-staphylococcal potential was tested ( Figure 1). Each of the 28 LR systems was effective in inhibiting the growth of Staphylococcus bacteria. The anti-staphylococcal potential of the 28 LR systems (expressed in terms of growth inhibition zones) was in the range of 12-28 mm. Interestingly, each of the 28 systems inhibited the growth of the environmental isolates tested. This was especially important in relation to the control sample, in which in four cases saw the tested lactic acid bacteria not showing anti-staphylococcal properties. It should be noted that in these cases, the addition of extracts may positively affect the antistaphylococcal properties of lactic acid bacteria.
In the case of the S. epidermidis R1A strain, the highest anti-staphylococcal activity was observed in the system consisting of the Lacticaseibacillus rhamnosus ŁOCK 0943 strain with the addition of purified acetone extract and Levilactobacillus brevis ŁOCK 0992 with the addition of purified ethanol extract (Figure 1a,b). Both zones of growth inhibition were close to 40 mm. On the other hand, the weakest effect limiting the growth of staphylococci was observed for systems based on the culture of Levilactobacillus brevis ŁOCK 0980 (regardless of the addition of the extract). The greatest antimicrobial potential was observed in LR systems based on the culture of Levilactobacillus brevis ŁOCK 0992 with crude extracts and Lacticaseibacillus rhamnosus ŁOCK 0943 with purified extracts. Due to the addition of acetone and ethanol extracts, the systems constructed on the basis of Lacticaseibacilluss brevis ŁOCK 0943 and Levilactobacillus brevis MG451814 cultures showed anti-staphylococcal potential (zone of growth inhibition in the range of 20-40 mm), despite the fact that the basic culture did not show anti-staphylococcal properties in this strain. Moreover, in most cases (20/28), the two-component LR systems showed a statistically significant higher antimicrobial potential than the stock culture ( Figure 2 and Table A2, Appendix A). It should also be noted that neither of the systems exhibited a statistically significantly lower antimicrobial potential than the stock culture.
In the case of the S. haemolyticus R2A strain, it was not possible to clearly define which two-component LR system had the highest and lowest anti-staphylococcal potentials (Figure 1c,d). The highest anti-staphylococcal potential (33-38-mm growth inhibition  Table A2 (Appendix A) shows the antagonistic properties of the two-component LR systems. By combining 7 different LABs with four Rosa rugosa Thunb pseudo-fruit pomace extracts, 28 2-component LR systems were obtained, for which the anti-staphylococcal potential was tested ( Figure 1). Each of the 28 LR systems was effective in inhibiting the growth of Staphylococcus bacteria. The anti-staphylococcal potential of the 28 LR systems (expressed in terms of growth inhibition zones) was in the range of 12-28 mm. Interestingly, each of the 28 systems inhibited the growth of the environmental isolates tested. This was especially important in relation to the control sample, in which in four cases saw the tested lactic acid bacteria not showing anti-staphylococcal properties. It should be noted that in these cases, the addition of extracts may positively affect the anti-staphylococcal properties of lactic acid bacteria.
In the case of the S. epidermidis R1A strain, the highest anti-staphylococcal activity was observed in the system consisting of the Lacticaseibacillus rhamnosus ŁOCK 0943 strain with the addition of purified acetone extract and Levilactobacillus brevis ŁOCK 0992 with the addition of purified ethanol extract (Figure 1a,b). Both zones of growth inhibition were close to 40 mm. On the other hand, the weakest effect limiting the growth of staphylococci was observed for systems based on the culture of Levilactobacillus brevis ŁOCK 0980 (regardless of the addition of the extract). The greatest antimicrobial potential was observed in LR systems based on the culture of Levilactobacillus brevis ŁOCK 0992 with crude extracts and Lacticaseibacillus rhamnosus ŁOCK 0943 with purified extracts. Due to the addition of acetone and ethanol extracts, the systems constructed on the basis of Lacticaseibacilluss brevis ŁOCK 0943 and Levilactobacillus brevis MG451814 cultures showed anti-staphylococcal potential (zone of growth inhibition in the range of 20-40 mm), despite the fact that the basic culture did not show anti-staphylococcal properties in this strain. Moreover, in most cases (20/28), the two-component LR systems showed a statistically significant higher antimicrobial potential than the stock culture ( Figure 2 and Table A2, Appendix A). It should also be noted that neither of the systems exhibited a statistically significantly lower antimicrobial potential than the stock culture. control sample. It is worth noting, however, that in the case of the LR systems, in each of the studied cases, the anti-staphylococcal properties of the systems were observed (while not all LAB strains showed anti-staphylococcal activity). Only in 2% of the cases did the addition of polyphenols to LAB cultures not change their anti-staphylococcal potentials. It should be noted that in the LR systems, a concentration of polyphenols equal to 0.156 mg/mL was used, which for 14 out of 20 cases permitted the use of a concentration lower than the MIC value for the Staphylococcus spp. strains tested.  and S. saprophyticus S1A, S. aureus S2A. The selected symbols show the difference in the size of the zone: "↓" = growth inhibition zone after using the LR system, lower than in the case of control culture; "↑" = growth inhibition zone after the application of the environmental LR system, higher than in the case of the control culture; and "=" = the zone of inhibition of growth after the application of the LR system, the same as in the case of control culture. Statistically significant changes are marked by different colors: = statistically significant reduction in the size of the growth inhibition zone in the LR systems; = statistically significant increase in the size of the zones of growth inhibition in the LR systems; = no statistically significant differences in the size of the growth inhibition zones.

Change in the pH of the LAB Culture in the Presence of Rosa rugosa Thunb. Pseudo-Fruit Pomace Extracts
The changes in the pH value during the culture of seven LAB strains with the addition of polyphenols contained in Rosa rugosa Thunb. pseudo-fruit pomace extracts are presented in Table 4. The extracts in the concentration of 0.156 mg/mL (converted to the The changes in the zones of growth inhibition of Staphylococcus bacteria under the influence of polyphenols contained in the Rosa rugosa Thunb. pseudo-fruit pomace extracts. The control sample was the anti-staphylococcal properties of lactic acid bacteria without the addition of Rosa spp. extracts (AC = crude water-acetone extract, AP = purified water-acetone extract, EC = crude water-ethanol extract, and EP = purified water-ethanol extract). Strains: Lactobacillus acidophilus ŁOCK 0928, Lacticaseibacillus rhamnosus ŁOCK 0943, Levilactobacillus brevis ŁOCK 0944, Lacticaseibacillus casei ŁOCK 0979, Levilactobacillus brevis ŁOCK 0980, Levilactobacillus brevis ŁOCK 0992, Levilactobacillus brevis MG451814, S. epidermidis R1A, S. haemolyticus R2A, S. saprophyticus R3A, and S. saprophyticus S1A, S. aureus S2A. The selected symbols show the difference in the size of the zone: "↓" = growth inhibition zone after using the LR system, lower than in the case of control culture; "↑" = growth inhibition zone after the application of the environmental LR system, higher than in the case of the control culture; and "=" = the zone of inhibition of growth after the application of the LR system, the same as in the case of control culture. Statistically significant changes are marked by different colors: saprophyticus R3A, S. saprophyticus S1A, and S. aureus S2A), the use of LR systems resulted in a statistically significant reduction in the growth inhibition zones compared with the control sample. It is worth noting, however, that in the case of the LR systems, in each of the studied cases, the anti-staphylococcal properties of the systems were observed (while not all LAB strains showed anti-staphylococcal activity). Only in 2% of the cases did the addition of polyphenols to LAB cultures not change their anti-staphylococcal potentials. It should be noted that in the LR systems, a concentration of polyphenols equal to 0.156 mg/mL was used, which for 14 out of 20 cases permitted the use of a concentration lower than the MIC value for the Staphylococcus spp. strains tested.  and S. saprophyticus S1A, S. aureus S2A. The selected symbols show the difference in the size of the zone: "↓" = growth inhibition zone after using the LR system, lower than in the case of control culture; "↑" = growth inhibition zone after the application of the environmental LR system, higher than in the case of the control culture; and "=" = the zone of inhibition of growth after the application of the LR system, the same as in the case of control culture. Statistically significant changes are marked by different colors: = statistically significant reduction in the size of the growth inhibition zone in the LR systems; = statistically significant increase in the size of the zones of growth inhibition in the LR systems; = no statistically significant differences in the size of the growth inhibition zones.

Change in the pH of the LAB Culture in the Presence of Rosa rugosa Thunb. Pseudo-Fruit Pomace Extracts
The changes in the pH value during the culture of seven LAB strains with the addition of polyphenols contained in Rosa rugosa Thunb. pseudo-fruit pomace extracts are presented in Table 4. The extracts in the concentration of 0.156 mg/mL (converted to the = statistically significant reduction in the size of the growth inhibition zone in the LR systems; saprophyticus R3A, S. saprophyticus S1A, and S. aureus S2A), the use of LR systems resulted in a statistically significant reduction in the growth inhibition zones compared with the control sample. It is worth noting, however, that in the case of the LR systems, in each of the studied cases, the anti-staphylococcal properties of the systems were observed (while not all LAB strains showed anti-staphylococcal activity). Only in 2% of the cases did the addition of polyphenols to LAB cultures not change their anti-staphylococcal potentials. It should be noted that in the LR systems, a concentration of polyphenols equal to 0.156 mg/mL was used, which for 14 out of 20 cases permitted the use of a concentration lower than the MIC value for the Staphylococcus spp. strains tested.  and S. saprophyticus S1A, S. aureus S2A. The selected symbols show the difference in the size of the zone: "↓" = growth inhibition zone after using the LR system, lower than in the case of control culture; "↑" = growth inhibition zone after the application of the environmental LR system, higher than in the case of the control culture; and "=" = the zone of inhibition of growth after the application of the LR system, the same as in the case of control culture. Statistically significant changes are marked by different colors: = statistically significant reduction in the size of the growth inhibition zone in the LR systems; = statistically significant increase in the size of the zones of growth inhibition in the LR systems; = no statistically significant differences in the size of the growth inhibition zones.

Change in the pH of the LAB Culture in the Presence of Rosa rugosa Thunb. Pseudo-Fruit Pomace Extracts
The changes in the pH value during the culture of seven LAB strains with the addition of polyphenols contained in Rosa rugosa Thunb. pseudo-fruit pomace extracts are presented in Table 4. The extracts in the concentration of 0.156 mg/mL (converted to the = statistically significant increase in the size of the zones of growth inhibition in the LR systems; saprophyticus R3A, S. saprophyticus S1A, and S. aureus S2A), the use of LR systems resulted in a statistically significant reduction in the growth inhibition zones compared with the control sample. It is worth noting, however, that in the case of the LR systems, in each of the studied cases, the anti-staphylococcal properties of the systems were observed (while not all LAB strains showed anti-staphylococcal activity). Only in 2% of the cases did the addition of polyphenols to LAB cultures not change their anti-staphylococcal potentials. It should be noted that in the LR systems, a concentration of polyphenols equal to 0.156 mg/mL was used, which for 14 out of 20 cases permitted the use of a concentration lower than the MIC value for the Staphylococcus spp. strains tested.  and S. saprophyticus S1A, S. aureus S2A. The selected symbols show the difference in the size of the zone: "↓" = growth inhibition zone after using the LR system, lower than in the case of control culture; "↑" = growth inhibition zone after the application of the environmental LR system, higher than in the case of the control culture; and "=" = the zone of inhibition of growth after the application of the LR system, the same as in the case of control culture. Statistically significant changes are marked by different colors: = statistically significant reduction in the size of the growth inhibition zone in the LR systems; = statistically significant increase in the size of the zones of growth inhibition in the LR systems; = no statistically significant differences in the size of the growth inhibition zones.

Change in the pH of the LAB Culture in the Presence of Rosa rugosa Thunb. Pseudo-Fruit Pomace Extracts
The changes in the pH value during the culture of seven LAB strains with the addition of polyphenols contained in Rosa rugosa Thunb. pseudo-fruit pomace extracts are presented in Table 4. The extracts in the concentration of 0.156 mg/mL (converted to the = no statistically significant differences in the size of the growth inhibition zones. In the case of the S. haemolyticus R2A strain, it was not possible to clearly define which two-component LR system had the highest and lowest anti-staphylococcal potentials (Figure 1c,d). The highest anti-staphylococcal potential (33-38-mm growth inhibition zone) was demonstrated by the systems consisting of all tested extracts (both crude and purified) with the culture of Levilactobacillus brevis ŁOCK 0992, a combination of crude extracts (both ethanol and acetone) with the culture of Levilactobacillus brevis ŁOCK0944. The same anti-staphyloccal potential was observed in the culture of Levilactobacillus brevis ŁOCK0980 bacteria with the addition of purified acetone extract and the culture of Lacticaseibacillus rhamnosus ŁOCK 0943 bacteria with crude ethanol extract. On the other hand, the lowest antimicrobial potential in relation to the S. haemolyticus R2A strain (growth inhibition zone: 21-28 mm) was observed in the systems consisting of Levilactobacillus brevis MG451814 bacterial cultures with the addition of acetone extracts (crude and purified) and purified ethanol extract, as well as in combining the culture of Levilactobacillus brevis ŁOCK0980 with crude extracts (acetone and ethanol) and the culture of Lactobacillus acidophilus ŁOCK 0928 with purified acetone extract and crude ethanol extract. All tested extracts used to create the LR systems based on the Levilactobacillus brevis MG451814 bacterial culture showed antagonistic activity (21-28-mm growth inhibition zone), although the stock culture did not show anti-staphylococcal properties. Moreover, in the vast majority of cases (24/28), the addition of extracts resulted in a statistically significant increase in the anti-staphylococcal properties compared with the anti-staphylococcal properties of the stock culture ( Figure 2 and Table A2, Appendix A). On the other hand, a statistically significant reduction in the antagonistic properties was observed only in the case of combining ethanol extracts with the Lactobacillus acidophilus ŁOCK0928 culture.
The studies of the antagonistic properties of the LR systems in the case of the S. saprophyticus R3A strain showed that the systems consisting of the Lactobacillus acidophilus ŁOCK 0928 strain (26-29-mm growth inhibition zone) and the systems constructed on the basis of the Levilactobacillus brevis ŁOCK 0992 strain (inhibition zone: 27-29 mm) were characterized by the highest antagonistic activity (Figure 1e,f). The lowest antagonistic activity (zone of growth inhibition in the range of 16-20 mm) was recorded for the system consisting of the Levilactobacillus brevis MG451814 culture and polyphenols contained in extracts from the Rosa rugosa Thunb. pseudo-fruit pomace. Low antimicrobial potential (growth inhibition zone: 17-19 mm) was also observed in the systems consisting of Levilactobacillus brevis ŁOCK 0980 cultures and cleaned crude ethanolic and acetone extracts, as well as for the system based on the culture of the Lacticaseibacillus casei ŁOCK 0979 strain and purified acetone extract (growth inhibition zone equal to 19.67 mm). It is worth mentioning that the addition of extracts to the culture of lactic acid bacteria would significantly affect their anti-staphylococcal properties in relation to the S. saprophyticus R3A strain (in 18/28 cases, the 2-component LR system showed statistically significantly lower anti-staphylococcal properties than the basic culture) ( Figure 2 and Table A2, Appendix A).
In the case of the S. saprophyticus S1A strain, the highest antagonistic activity was recorded in the LR system consisting of Levilactobacillus brevis ŁOCK 0992 and polyphenols contained in the crude acetone extract (zone of growth inhibition equal to 36 mm) (Figure 1g). On the other hand, the system consisting of purified ethanol extract and the Levilactobacillus brevis MG4511814 strain was characterized by the lowest anti-staphylococcal activity (Figure 1h). In the case of the purified acetone extracts, it was not possible to clearly indicate which environmental system showed the greatest antimicrobial potential in relation to the S. saprophyticus S1A strain (combination of purified acetone extract with the Levilactobacillus brevis ŁOCK 0992 strain, with a growth inhibition zone equal to 27.67 mm, and the combination of purified acetone extract and the Lactobacillus acidophilus ŁOCK 0928 strain, with a growth inhibition zone equal to 28.33 mm). In the case of ethanol extracts, the highest anti-staphylococcal activity was obtained by combining them with the Levilactobacillus brevis ŁOCK 0992 strain (zone of growth inhibition equal to 30.33 mm). The system based on the culture of Lactobacillus acidophilus ŁOCK 0928 bacteria and crude ethanol extract (zone of growth inhibition equal to 27.33 mm) also showed a high antimicrobial potential. The weakest anti-staphylococcal properties in relation to S. saprophyticus S1A were demonstrated by the combination of acetone extracts with the Levilactobacillus brevis ŁOCK 0980 strain and ethanol extracts with the Levilactobacillus brevis MG451814 strain (zones of growth inhibition equal to 15-17 mm). It should be noted that the antimicrobial activity of the 28 LR systems against the S. saprophyticus S1A strain was largely due to the antagonistic activity of the LAB strains used to create the system. In all cases (28/28), the addition of the extract resulted in a statistically significant reduction in anti-staphylococcal properties compared with the stock culture ( Figure 2). The S. aureus S2A strain, compared with the other environmental isolates, was the most resistant to the effects of the two-component LR systems (Figure 1i,j). This was evidenced by the fact that the highest zone of inhibition of growth (not exceeding 20 mm) was comparable to the value of the minimum zones of inhibition of growth of other staphylococci. In the case of the S. aureus S2A strain, an anti-staphylococcal potential was observed in the systems consisting of the culture of Levilactobacillius brevis ŁOCK 0992 with acetone extracts (zone of growth inhibition of about 19 mm) and the culture of Levilactobacillus brevis MG451814 with the addition of ethanol extracts (zone of growth inhibition in the interval 17-20 mm). A moderate anti-staphylococcal potential in relation to the S. aureus S2A strain (growth inhibition zone in the range of 17-19 mm) was also noted in the case of the Lactobacillus acidophilus ŁOCK 0928 bacteria cultures with crude extracts (ethanol and acetone) and in the system consisting of Levilactobacillus brevis ŁOCK0944 cultures with the addition of purified ethanol extract. The lowest antimicrobial potential in relation to the S. aureus S2A strain was demonstrated by the two-component LR systems consisting of Levilactobacillus brevis ŁOCK 0992 cultures in combination with ethanol extracts (crude and purified) and the combination of purified ethanol extract with the Levilactobacillus brevis ŁOCK 0980 culture. A low anti-staphylococcal potential was also characterized by systems consisting of the Levilactobacillus brevis MG451814 and Levilactobacillus brevis ŁOCK 0980 cultures in combination with acetone extracts (growth inhibition zone equal to 13.33 mm), as well as a combination of purified acetone extract with Lacticaseibacillus casei ŁOCK 0979 and Lactobacillus acid ŁOCK 0928 (growth inhibition zone in the range of 13-15 mm). It is worth noting that although 28 2-component LR systems were obtained to inhibit the growth of S. aureus S2A bacteria, the overall antagonistic activity of the LR systems toward this strain should be assessed as low. Four systems based on the Levilactobacillus brevis MG451814 strain showed anti-staphylococcal activity, although it was not observed in the control sample.
Out of all 28 LR systems tested, the strongest antagonistic activity was observed in relation to the S. epidermidis R1A strain using a system consisting of purified acetone extract and the Lacticaseibacillus rhamnosus ŁOCK 0943 strain. On the other hand, the weakest antagonistic properties of the LR systems were observed in the case of S. aureus S2A (a combination of both ethanol extracts with the Levilactobacillus brevis ŁOCK 0992 strain and a combination of purified ethanol extract with the Levilactobacillus brevis ŁOCK 0980 strain). Of all the environmental isolates tested, S. epidermidis R1A and S. haemolyticus R2A turned out to be the most sensitive strains to the effects of environmental systems consisting of polyphenols and LAB cultures. It is worth emphasizing that in the case of the antagonistic properties of the two-component LR systems, the antimicrobial activity against the S. epidermidis R1A and S. haemolyticus R2A strains was largely due to the addition of extracts. On the other hand, the S. aureus S2A strain was most resistant to the antagonistic effects of co-cultures of LABs and polyphenols. Figure 2 shows the differences in the size of the zones of inhibition of the growth of bacteria of the genus Staphylococcus caused by the action of LR systems in relation to the antagonistic properties of basic lactic acid bacteria cultures. The combination of lactic acid bacteria and polyphenols contained in the Rosa rugosa Thunb. pseudo-fruit pomace in a common culture system had a positive or negative effect, depending on the tested strain of the genus Staphylococcus. It is interesting that the lack of statistically significant differences in the operation of the LR system accounted for only 15% of all examined cases. Among the results with a statistically significant difference, nearly 41% showed a favorable effect from polyphenols on the LAB antagonistic properties (increase in the zone of growth inhibition). LR systems consisting of LAB and rose extracts significantly influenced the growth of the isolates S. epidermidis R1A and S. haemolyticus R2A. Both strains were more sensitive to the effects of LAB systems in combination with ethanol and acetone extracts than in the case of stock cultures. In the case of the remaining isolates (S. saprophyticus R3A, S. saprophyticus S1A, and S. aureus S2A), the use of LR systems resulted in a statistically significant reduction in the growth inhibition zones compared with the control sample. It is worth noting, however, that in the case of the LR systems, in each of the studied cases, the anti-staphylococcal properties of the systems were observed (while not all LAB strains showed anti-staphylococcal activity). Only in 2% of the cases did the addition of polyphenols to LAB cultures not change their anti-staphylococcal potentials. It should be noted that in the LR systems, a concentration of polyphenols equal to 0.156 mg/mL was used, which for 14 out of 20 cases permitted the use of a concentration lower than the MIC value for the Staphylococcus spp. strains tested.

Change in the pH of the LAB Culture in the Presence of Rosa rugosa Thunb. Pseudo-Fruit Pomace Extracts
The changes in the pH value during the culture of seven LAB strains with the addition of polyphenols contained in Rosa rugosa Thunb. pseudo-fruit pomace extracts are presented in Table 4. The extracts in the concentration of 0.156 mg/mL (converted to the concentration of polyphenols) added to the initial culture (t = 0 h) did not significantly affect the pH value in any tested cases (no statistically significant differences). At the time of inoculation, the lowest pH was observed in the culture of Lactobacillus acidophilus ŁOCK 0928 (5.2-5.3). On the other hand, the starter culture of the Levilactobacillus brevis MG451814 strain was characterized by the highest pH value (5.7). The pH value at the time of inoculation in the case of the remaining cultures fluctuated in the range of 5.4-5.6. During the 48-h incubation (under optimal conditions for the growth of each of the microorganisms), the pH value of the culture gradually decreased. For all the tested strains, the highest decrease in the pH value was observed after the first day of culturing Lacticaseibacillus rhamnosus ŁOCK 0943 with the addition of crude ethanol extract (∆pH = 1.5 units). In turn, the lowest decrease in the pH value was recorded after a 24-h culture of Levilactobacillus brevis ŁOCK 0980 bacteria with the addition of crude ethanol extract (∆pH = 0.7 units). On the second day, the decrease in pH was much lower in all cases and did not exceed ∆ = 0.3 units. The highest decrease in pH value was observed in the culture of the Levilactobacillus brevis ŁOCK 0980 strain with the addition of crude ethanol extract (∆pH = 0.25 units). On the other hand, in the case of Levilactobacillus brevis ŁOCK 0944 with the addition of crude ethanol extract and the Lacticaseibacillus casei ŁOCK 0979 and Lactobacillus acidophilus ŁOCK 0928 cultures with the addition of purified acetone extract, the decrease in pH was practically imperceptible (∆pH = 0.02 units).
It should be noted, however, that extending the culture from 24 to 48 h for all 35 cultures resulted in a significant decrease in the pH value, and in 63% of cases, this value was statistically significant (in all cultures with the addition of purified ethanol extract and almost all control cultures, where the exception was Levilactobacillus brevis ŁOCK 0992).
After 48 h of incubation, the pH of the tested cultures was the highest for the Levilactobacillus brevis MG451814 strain in the culture with the addition of purified ethanol extract. It should be noted that the observed pH value (4.67) was statistically different from the pH value in the stock culture without the addition of extracts. However, there were no statistically significant differences with the pH value in the culture with crude acetone extract. On the other hand, the lowest pH value after 48 h of incubation was observed for the Lactobacillus acidophilus ŁOCK 0928 strain grown with the addition of crude extracts (3.97). However, this difference was not statistically significant compared with the cultures with purified extracts. A, B : Statistical differences (ANOVA, Tukey's post-hoc test (p ≤ 0.05)) between acetone (AC = crude, AP = purified) extracts and between ethanol (EC = crude, EP = purified) extracts (AC-AP, EC-EP) within the same LAB species. C, D : Statistical differences (ANOVA, Tukey's post-hoc test (p ≤ 0.05)) between the control sample (culture without extract) and samples with the addition of extracts (Control-AP, Control-AC, Control-EC, and Control-EP) within the same LAB species. a, b : Statistical differences (ANOVA, Tukey's post-hoc test (p ≤ 0.05)) between crude and purified extracts (AP-EP, AC-EC) within the same LAB species. *, # : Other statistical differences (ANOVA, Tukey's post-hoc test (p ≤ 0.05)) between extracts (AC-EP, AP-EC) within one LAB species. α, β, γ : Statistically significant differences in time (ANOVA, Tukey's post-hoc test (p ≤ 0.05)) between the same trials.

Discussion
In recent years, a systematic increase in the number of microorganisms resistant to routinely used drugs has been observed. The spread of antibiotic resistance among staphylococci (including coagulase-negative strains) may pose a threat to human health. Many scientists believe that food may be the habitat of multi-drug resistant strains of the genus Staphylococcus and may be the transfer of antibiotic resistance between the environment and people [45]. The substrate for the development of antibiotic-resistant bacteria can be, among others, ready-to-eat, fermented milk products (for the preparation of which unpasteurized milk is used) [46]. Currently, it is methicillin resistance that is considered to be one of the most important problems in the control of staphylococci. Methicillin-resistant species are often phenotypically resistant to other β-lactam antibiotics used so far (including penicillin, oxacillin, nafcillin, or cephalosporins) [47]. According to the research conducted by Chajęcka-Wierzchowska et al. [47], more than 83% of methicillin-resistant Staphylococcus isolates (from ready-to-eat food) also showed resistance to tetracycline, rifampicin, and clindamycin. Moreover, the studies by Chajęcka-Wierzchowska et al. [47] showed that over 30% of food isolates are strains that have experienced multi-drug resistance (antibiotic resistance belonging to three or more classes). Hence, the aim of this study was to understand the anti-staphylococcal properties of four polyphenol-rich extracts from Rosa rugosa Thumb. pseudo-fruit pomace and seven strains of lactic acid bacteria.
The tested extracts from the pseudo-fruit pomace of Rosa rugosa Thunb. were characterized by a total content of polyphenols at the level of 8-33 mg per 100 g DM. The content of polyphenols in the extracts of rose pseudo-fruit depended primarily on the species of rose but also on the method of extraction. The extracts obtained from the pomace through the use of various solvents differed in the content of polyphenols. The content of polyphenols in the acetone extracts was higher than in the ethanolic extracts by 1.69 times (crude) and 1.14 times (purified). Ellagitannins and procyanidins dominated in all obtained extracts, and their shares were similar. According to research by Yi et al. [48], the methanol extracts of Rosa nutkana, Rosa pisocarpa, and Rosa woodsii contained 6-13 mg of polyphenols (GAE equivalent) per liter of extract. On the other hand, Nowak and Gawlik-Dziki [49] determined the content of polyphenols in 17 different species of roses (including Rosa canina, Rosa rugosa, Rosa villosa, and Rosa gallica). The total content of polyphenols in the extracts was in the range of 6-16% dry matter (which was 5-19 mg of flavonols per g of dry matter and 9-20 mg of ellagic acid per g of dry matter). The number of polyphenols (and their types) contained in rose extracts is primarily influenced by the part of the plant that was used to produce them. For example, the concentration of polyphenols in the extracts of the Rosa nutkana and Rosa woodsii rose hips obtained by Yi et al. [48] was higher than in the seed extracts.
Four extracts of pomace from Rosa rugosa Thunb. pseudo-fruit were used in the study, for which the antagonistic activity against Staphylococcus spp. was tested. The tested extracts, with a concentration of polyphenols ranging from 0.156 to 0.625 mg/mL, effectively inhibited the growth of the tested Staphylococcus bacteria. The research group of Yi et al. [48] investigated the antimicrobial potential of rose extracts (sourced from British Columbia (Canada)). The extracts inhibited the growth of gram-positive bacteria Enterococcus faecalis, Bacillus subtilis, S. aureus ATCC 25923, and methicillin-resistant clinical staphylococcal isolates. The studies of Yi et al. [48] showed that rose hip extracts demonstrate selective antimicrobial activity. The mean zone of inhibition of growth (including the diameter of the disc (6 mm)) of S. aureus ATCC 25923 bacteria was in the range of 9-15 mm in the case of whole extracts and in the range of 11-18 mm in the case of pericarp extracts (with the addition of 20 µL of extract per filter paper disc). Cendrowski et al. [21] studied the antibacterial properties of extracts made from the Rosa rugosa pseudo-fruit. For this purpose, they prepared various types of extracts (aqueous, ethanolic, supercritical, and enzymatic). The aqueous extracts showed antimicrobial activity against gram-positive bacteria such as Bacillus cereus or S. epidermidis and against gram-negative species (Escherichia coli). Interestingly, the minimum inhibitory concentration (MIC) of the tested aqueous extracts for S. aureus was over 128 mg/mL. Ethanol extracts strongly inhibited the growth of Bacillus subtilis bacteria, but only at a concentration of 32 mg/mL did they limit the growth of S. epidermidis (the MIC for the aqueous extracts was 16 mg/mL). Cendrowski et al. [21] did not determine the concentration of the Rosa rugosa ethanol extracts, which would have a bacteriostatic effect on staphylococci (the MBC exceeded the range of tested concentrations at 128 mg/mL). In contrast, the MIC of the enzymatic and supercritical extracts for S. aureus ATCC 25923 was 64 mg/mL. In the research conducted by the authors of the present work, two different solvents were used to extract polyphenols from rose pomace: ethanol and acetone. The highest concentration of polyphenols used was 2.5 mg/mL. Thus, it was the concentration in the case of ethanol extracts that turned out to be insufficient for limiting the growth of only one of the tested strains (S. epidermidis R1A). It should be noted, however, that the concentration of polyphenols of 2.5 mg/mL corresponded to the concentration of the ethanol extracts at the level of 8-30 mg/mL (depending on the degree of purification). Thus, the result obtained by the authors of the study is comparable to the anti-staphylococcal properties of rose extracts determined by Cendrowski et al. [21]. In the analyses by Adwan et al. [50], the effect of plant extracts on the growth of microorganisms was also investigated. One of the extracts was made from damask rose. The influence of the extract on the growth of the gram-positive bacteria S. aureus was analyzed. The ethanol extract of damask rose showed stronger bactericidal activity against staphylococci than the other extracts tested: lemon balm, mint, and marshmallow (MIC: 0.395-0.780 mg/mL). It should also be noted that rose extracts sometimes show stronger bactericidal properties compared with extracts prepared from other plants. The results obtained by Mishra et al. [51] showed that extracts (prepared with methanol and ethyl acetate) obtained from various parts of Rosa indica (leaves, stem, and flowers) also showed bactericidal activity against microorganisms considered pathogenic. All methanol extracts showed anti-staphylococcal properties against S. aureus. The greatest zone of inhibition of growth was recorded after the application of methanolic extract from flowers and stems (16-17 mm). The leaf extracts showed a lower antagonistic property: a growth inhibition diameter of 13 mm. Thus, the MIC of each of the Rosa indica extracts was 4.5 mg/mL. It is worth mentioning that the method of extracting polyphenols has a decisive influence on the antagonistic properties of Rosa spp. fruit extracts. Two solvents were used in this research: ethanol and acetone. The extracts were further purified by column chromatography on Amberlite XAD 1600 N. Stronger anti-staphylococcal activity was observed in the extracts obtained with the use of acetone and the purified extracts. Interestingly, according to the literature data, the ethanol extracts showed a higher antimicrobial potential. Halawani [52] not only investigated the antimicrobial properties of Rosa damascena extracts but also tried to determine the effect of the extraction solvent on the antimicrobial properties of the extracts (water, methanol, ethanol, and hexane). Their research showed that the highest anti-staphylococcal properties were obtained in the case of ethanol extracts (growth inhibition zone in the range of 27-30 mm; MIC: 62.5 µg/mL). A similar antimicrobial activity was observed in water (MIC: 62.5-125 µg/mL) and methanol (MIC: 62.5-250 µg/mL) extracts. The weakest antimicrobial property was observed in extracts prepared with the use of hexane. Shohayeb et al. [53] used many popular solvents to prepare Rosa damascena flower extracts (water, hexane, and ethanol and alcoholic extracts were suspended in chloroform, butanol, and ethyl acetate). Then, the bactericidal properties of the extracts against Streptococcus pyogenes, B. subtilis, and S. aureus were examined. The MIC value for the S. aureus strain ranged from 0.125 to 2.0 mg/mL. Nevertheless, the methanol and acetone extracts of Rosa damascena prepared by El-Shouny et al. [54] also demonstrated anti-staphylococcal properties. The antagonistic activity of the extracts at a concentration of 100 mg/mL resulted in the formation of zones of growth inhibition of S. aureus isolates at the level of 11-18 mm for the methanol extract and 14-18 mm for the acetone extract.
There are also reports in the literature examining the antimicrobial potential of roses as a by-product in the food industry. An example of a product that is waste from the production of fruit juices is pomace. The work investigated extracts made of frozen Rosa rugosa Thunb. pseudo-fruit pomace resulting from the production of natural juices. Ren et al. [55] also used an extract from Rosa rugosa Thunb. var. plena Regal (by-product of production of rose tea or dried rose petals; Fragrant Rose Biological Technology Co., LTD in Pingyin) for testing antimicrobial properties. The total content of the compounds in the extract was divided into phenolics (0.31 mg/mL) and flavonoids (0.43 mg/mL). The three main components of the extract are hyperoside, kaempferol-3-O-rutoside, and rutin. Rosa rugosa Thunb. var. plena Regal extract showed antimicrobial properties against Cutibacterium acnes (called Propionibacterium acnes by Ren, et al. [55]) and S. aureus (MIC: 125 µg/mL). For the remaining bacteria (e.g., Listeria ivanovii, Salmonella Enteritidis, or E. coli) the MIC value of the tested extract exceeded 250 µg/mL.
Lactic acid produced as a result of fermentation makes LAB bacteria antagonistic to pathogenic microorganisms that pollute not only food but also other ecological niches [56].
The selection of an appropriate carbohydrate in the medium may increase the acidifying activity. Therefore, the addition of polyphenols from Rosa rugosa Thunb. pseudo-fruit pomace extracts in a concentration below 0.156 mg/mL does not affect the metabolic processes leading to acidification of the environment by the tested LAB bacteria. Yoon et al. [57] also proved that lowering the pH of LAB cultures is an obvious consequence of metabolic processes. The pH of Lactobacillus casei (Lacticaseibacillus casei) cultures decreased from 5 to 3.4, while in the case of Lactobacillus plantarum (Lactiplantibacillus plantarum) and Lactobacillus delbruecki subsp. delbruecki, the pH of the environment decreased from 5.8 to 3.6.
The tolerance of LAB to low pH levels is therefore a strain feature. It is worth noting that the intracellular pH of the LAB drops simultaneously with the decrease in the extracellular pH, which is an individual feature compared to other bacterial cells (e.g., pathogenic microorganisms) and may constitute the basis for their antimicrobial activity [58]. Measurement of the pH of LAB cultures is an indirect method for monitoring the acidity of the strains used for fermentation. Ren et al. [55] showed that the amount of acid (pH < 3.7) synthesized by two strains, T30 and S6, was higher than in the case of other LAB strains, for which the pH value was higher than 3.7 (the tested LAB strains belonged to the following species: Lactobacillus plantarum, Lactobacillus pentosus, and Lactobacillus paracasei (Lactiplantibacillus plantarum, Lactiplantibacillus pentosus, and Lacticaseibacillus paracaei)). The strains of lactic acid bacteria studied by the authors of the present study were characterized by a much higher antimicrobial potential compared with environmental isolates of the Staphylococcus genus and reference strains. The observed diameters of growth inhibition were in the range of 14-50 mm. It should be emphasized that not all lactic acid bacteria show anti-staphylococcal properties. The tested Levilactobacillus brevis MG 451,814 strain was not able to inhibit the growth of the following isolates: R1A, R2A, and S2A. However, in the case of the Lacticaseibacillus rhamnosus ŁOCK 0943 strain and the R1A isolate, the zones of growth inhibition were not determined either. Karska-Wysocki et al. [59], during their study of the antimicrobial potential of Lactobacillus acidophilus, Lactobacillus casei (Lactocaseibacillus casei), and Lactococcus cremoris in relation to 10 isolates of the genus Staphylococcus (methicillin-resistant strains) and the reference strain of S.aureus ATCC 43300, did not observe the anti-staphylococcal potential of Lactcoccus cremoris, whereas Mohamed et al. [60] did not demonstrate the anti-staphylococcal properties of Lactobacillus reuteri ATCC 55730 (Limosilactobacillus reuteri) (regardless of aerobic conditions).
During the present study, it was decided to create two-component antagonist environmental systems. The studies of Fang et al. [61] showed no effect of the base medium on the antagonistic activity of lactic acid bacteria. Therefore, a commercial MRS Agar (Merck, Germany) was used for the preparation of systems, which is optimal for the growth of lactic acid bacteria. LR systems were created by combining polyphenols contained in extracts of pseudo-fruit pomace Rosa rugosa Thunb. and selected strains of lactic acid bacteria. Earlier studies have shown that polyphenols at a concentration of 0.156 mg/mL have a prebiotic effect on the microorganisms used in the study [39]. It is worth noting that other scientists also looked for plant extracts that would inhibit the growth of pathogenic microflora while not limiting the growth of lactic acid bacteria. Chan et al. [62] investigated the potential of spice and herb extracts (e.g., Japanese knotweed, pomegranate peel, and cloves). The obtained extracts showed the ability to combat five species of pathogenic bacteria (B. cereus, E. coli, Salmonella enterica subsp. enterica, Shigella flexneri, and S. aureus). Thus, the extracts showed a prebiotic effect for four LAB species (the prebiotic effect was tested for the following strains of lactic acid bacteria: Lactobacillus acidophilus, Lactobacillus casei (Lacticaseibacillus casei), Lactobacillus plantarum (Lactiplantibacillus plantarum), and Lactobacillus rhamnosibus (Lacticaseibacillus rhamnosus)). In our work, we managed to compose antagonistic two-component antagonist systems based on the culture of selected LAB and pseudo-fruit pomace extracts from Rosa rugosa Thunb., which effectively limited the growth of both collection strains and environmental isolates belonging to the genus Staphylococcus spp.

Conclusions
Test extracts of pseudo-fruit pomace Rosa rugosa Thunb. constitute a valuable reservoir of compounds with anti-staphylococcal activity. The LR systems developed in the study showed a high antagonistic potential toward Staphylococcus spp. strains. Nevertheless, it should be noted that the effectiveness of the LR system depends on the LAB bacterial strain but above all on the sensitivity of the Staphylococcus spp. The extraction environment and the level of preparation purification are also important factors.
The creation of environmental two-component antagonist systems, in this case consisting of LAB and polyphenols from Rosa spp. (LR system), may therefore represent the beginning of the development of a new trend in the production of functional food or cosmetics or in the design of dietary supplements.

Data Availability Statement:
The data presented in this study are available on request from the corresponding author.

Conflicts of Interest:
The authors declare no conflict of interest. Table A1 shows the antagonistic activity of lactic acid bacteria against Staphylococcus spp. strains. The tested LABs showed high antagonistic potential against the test bacteria of the Staphylococcus genus. The mean values of the growth inhibition of Staphylococcus spp. showed no statistically significant differences. Nevertheless, it should be remembered that the antagonistic interactions between antagonistic LABs and the Staphylococcus spp. test strains were highly individual. Table A2 shows the antagonistic properties of the LR systems.