Antimicrobial Effect of Moringa oleifera Leaves Extract on Foodborne Pathogens in Ground Beef

Consumers nowadays are becoming more aware of the importance of using only meat products containing safe and natural additives. Hence, using natural food additives for extending the shelf life of meat along with delaying microbial growth has become an urgent issue. Given the increasingly popular view of Moringa oleifera leaves as a traditional remedy and also the scarcity of published data concerning its antimicrobial effect against foodborne pathogens in meat and meat products, we designed the present study to investigate the antimicrobial effect of Moringa oleifera leaves aqueous extract (0.5%, 1%, and 2%) on ground beef during refrigerated storage at 4 °C for 18 days. MLE revealed potent antimicrobial properties against spoilage bacteria, such as aerobic plate count and Enterobacteriaceae count. MLE 2% showed a significant (p < 0.01) reduction in the counts of E. coli O157:H7, Salmonella enterica serovar Typhimurium, and Staphylococcus aureus artificially inoculated to ground beef by 6.54, 5.35, and 5.40 log10 CFU/g, respectively, compared to control, by the 18th day of storage. Moringa leaves extract (MLE) had no adverse effect on the overall acceptability and other sensory attributes; moreover, it induced a slight improvement in the tenderness and juiciness of treated ground beef, compared to the control. Therefore, MLE can be used as a healthy, natural, and safe preservative to increase meat products’ safety, quality, and shelf stability during cold storage. A promising approach for using natural food additives rather than chemical preservatives could begin new frontiers in the food industry, as they are more safe and do not constitute health risks to consumers.


Introduction
Meat is a prime source of high-biological value protein, vitamins, and minerals. Despite being nutritious, its high moisture content, water activity, and suitable pH render meat an excellent medium for microbial growth and lipid oxidation, which induces shelflife quality deterioration [1]. The microbial contamination of meat occurs mainly during processing, by contact with dirty skin, intestinal contents, contaminated facility equipment, such as knives, saws, and grinders, contact with infected food handlers, or exposure to polluted air and water [2]. Proper handling and preservation could reduce the growth of most spoilage and pathogenic bacteria. Total aerobic plate count (APC) and Enterobacteriaceae foodborne pathogens (Escherichia coli O157:H7, Salmonella enterica serovar Typhimurium, and Staphylococcus aureus), along with the determination of the shelf life extension, through the enumeration of aerobic plate count and Enterobacteriaceae count, as well as sensory attributes of ground beef during cold-storage at 4 • C for 18 days.

Collection and Preparation of MLE
Fresh M. oleifera leaves were obtained from a local herbal store in Tanta city, El-Gharbia Governorate, Egypt. MLE was prepared according to the technique mentioned by Shah et al. [13]. The leaves were washed well with water to remove any adhering dirt, then dried in a hot air oven at 60 • C and ground into a fine powder in a heavy-duty grinder. The powder was passed through sieve No. 60 and extracted by soaking 400 g of dried powder in 2 L of boiled water at room temperature for 1 h, with frequent stirring with a glass rod. The obtained aqueous extract of M. oleifera leaves was filtered by Whatman No. 1 filter paper, and the residue was re-extracted again with 1 L distilled water. Both filtrates were mixed and freeze-dried. The resultant extract was kept in a sterile glass container and stored at 4 • C until use.

Ground Beef Treatment and Preparation for Shelf-Life Determination and Sensory Attributes
Twelve kilograms of fresh beef cuts were bought from a butcher shop in Tanta city, El-Gharbia Governorate, Egypt. Beef cuts were packed in sterile plastic bags, and transferred in an ice box to the Food Microbiology Laboratory, Department of Food Hygiene and Control, Faculty of Veterinary Medicine, Benha University. The fresh beef was cut by a sterile sharp knife and minced using a clean sterile 0.32 cm grinder plate and divided into 4 groups (3 kg each). Three groups were treated with different concentrations of M. oleifera leaves aqueous extracts (0.5%, 1%, and 2%) and the fourth group served as control (without any treatment). The treated groups with different concentrations of MLE were mixed thoroughly for five minutes by hand, to have a homogenous mixture. The meat of both control and treated groups was formed into meatballs (25 g each), packaged into sterile impermeable plastic pouches, and kept in the refrigerator at 4 • C for 18 days to examine its sensory attributes and microbial count (aerobic plate count and Enterobacteriaceae counts) to determine its the shelf-life.

Aerobic Plate Counts and Enterobacteriaceae Counts for Shelf Life Determination
Aerobic plate counts and Enterobacteriaceae counts were tested from Day 0 and every 3 days thereafter for a period of 18 days. Ten grams of the control and treated groups were taken and homogenized with 90 mL of sterile 0.1% peptone water (CM0009; Oxoid Ltd., Basingstoke, UK) using a laboratory blender for 2 min. Ten-fold serial dilutions were prepared according to the technique recommended by ISO [14]. Appropriate dilutions were plated on Plate Count Agar (PCA, CM0325; Oxoid Ltd., Basingstoke, UK), and incubated at 30 • C for 48 h to enumerate aerobic plate counts (APC) [15]. Enterobacteriaceae counts (EBC) were enumerated by pouring 1 mL of the appropriate dilutions into a sterile Petri dish containing 15 mL of the violet red bile glucose (VRBGA, CM 0485; Oxoid Ltd., Basingstoke, UK), which had been previously prepared then cooled to 45 • C in a water bath and carefully mix the medium to cool. Once the agar was solidified, an additional 10 mL of medium was added onto the surface of the inoculated plate and incubated at 37 • C for 24 h [16]. The bacterial colonies in the different countable plates of APC and EBCs were counted per gram of all tested samples.

Bacterial Strains Used and Preparation of Inocula
Three different wild-type foodborne pathogens species previously isolated from meat products in our laboratory were used in this study: Escherichia coli O157:H7, Salmonella enterica serovar Typhimurium, and Staphylococcus aureus. The culture of each pathogen strain was grown in tryptone soy broth (CM0129; Oxoid Ltd., Basingstoke, UK) and incubated for 24 h at 37 • C. One mL of the original dilution of each fresh bacterial culture was transferred in a tube containing 9 mL of sterile 0.1% peptone water (CM0009; Oxoid Ltd., Basingstoke, UK) in a successive manner to make 10-fold dilution series to achieve the desired inoculation level of each pathogenic strain. The appropriate inoculum level of 10 8 CFU/mL prepared from each foodborne pathogen strain was streaked on the surface of Sorbitol MacConkey Agar supplemented with cefixime and potassium tellurite (CM0813, SR0172; Oxoid Ltd., Basingstoke, UK), Xylose-Lysine-Desoxycholate agar (XLD Agar, CM0469; Oxoid Ltd., Basingstoke, UK), and Baird-Parker selective agar with egg-yolk tellurite emulsion (CM275, S00R54; Oxoid Ltd., Basingstoke, UK) for the isolation of E. coli O157:H7, S. enterica serovar Typhimurium, and S. aureus, respectively. The plates inoculated with foodborne pathogen strains were incubated at 37 • C for 24 h, and specific colonies of the number of the different bacterial pathogens were calculated to detect the inoculation levels, which were found to equal 10.16 ± 0.47, 10.27 ± 0.41, 10.62 ± 0.52, and10.55 ± 0.34 log 10 CFU/mL for E. coli O157:H7, S. enterica serovar Typhimurium, and S. aureus, respectively.

Inoculation of Ground Beef Treated with MLE by Foodborne Pathogens
Another 3 kg of fresh beef collected from the same butcher shop were used to detect the antimicrobial effect of MLE on some foodborne pathogens, including E. coli O157:H7, S. enterica serovar Typhimurium, and S. aureus. The 3 kg of purchased ground beef were divided into four groups (750 g each), three of them were treated with different concentrations of MLE (0.5%, 1%, and 2%) and the fourth group served as control (without any treatment). Each of the four groups (three treatments and one control) were subdivided into three subgroups (250 g each) to be inoculated with either E. coli O157:H7, S. enterica serovar Typhimurium, or S. aureus. Each meat group (250 g each) was inoculated with 2.5 mL from each prepared pathogen inoculum (about 10 log 10 CFU/mL) and thoroughly mixed by hand for 3 min, under aseptic conditions, to gain a homogenous mixture containing about 8 log 10 CFU/g of each foodborne pathogen. The artificially-inoculated ground beef with the specific foodborne pathogens was formed into meatballs (25 g each), packaged in sterile plastic pouches, and kept in the refrigerator at 4 • C for 18 days. The artificially-inoculated ground beef was examined every 3 days during the storage period (18 days). The isolation and identification of the different foodborne pathogens were conducted according to techniques recommended by ISO [17][18][19] for E. coli O157:H7, S. enterica serovar Typhimurium, and S. aureus, respectively. The counts of samples tested were expressed as CFU/g.

Sensory Evaluation
The sensory assessment of untreated beef meatballs (control group) and treated groups with different concentrations of MLE was conducted on Day 0 (the day of meatballs preparation) and every 3 days thereafter for a period of 18 days. Beef meatballs (25 g each) were put individually in a clean aluminum foil and cooked in an electrical cooking oven at 180 • C for 20 min. The cooked beef meatballs were blind-coded with random numbers and presented to 15 trained panelists from the staff members of the Food Hygiene and Control Department, Faculty of Veterinary Medicine, Benha University, Egypt. An eight-point hedonic scoring scale was used to judge Moringa flavor intensity, characteristic flavor for beef meatballs, tenderness, and juiciness (https://www.depts.ttu.edu/meatscience/docs/ TTUBeefSensoryForm.pdf) (accessed on 30 June 2022), whereas a nine-point hedonic scale was used to determine the overall acceptability of beef meatballs tested [20].

Statistical Analyses
Triplicate measurement was applied for all samples. The obtained results were analyzed using SPSS software (SPSS Inc., ver. 21, Chicago, IL, USA). The difference between the means of counts of the different microbial categories between various treatments was assessed by one-way analysis of variance. Sensory attribute results were determined us-ing the general linear model (GLM). Results were considered statistically significant at p-values < 0.05.

Results and Discussion
The APC of beef meatballs tested on Day 0 ranged from 3.68 to 3.72 log 10 CFU/g with no significant difference between the control and treated beef meatballs with 0.5%, 1%, and 2% MLE ( Figure 1). However, on Day 3, beef meatballs treated with 0.5%, 1%, and 2% MLE displayed a significant (p < 0.05) decrease in APC by 1.16, 1.42, and 1.54 log 10 CFU/g, respectively, when compared with the control sample. Likewise, on Day 6, treated beef meatballs with 0.5%, 1%, and 2% MLE showed a significant decrease in APC by 1.57, 2.13, and 2.34 log 10 CFU/g, respectively, compared to the control (4.70, 4.14, and 3.93, respectively vs. 6.27 log 10 CFU/g) ( Figure 1). On Days 9, 12, and 15, treated beef meatballs with 2% MLE revealed a significant (p < 0.01) reduction rate of APC by 2.89, 2.92, and 3.27 log 10 CFU/g, respectively when compared to the control sample ( Figure 1). The APC of both control and MLE-treated samples increased with time. Such an increase showed significant differences by Day 3, 9, 12, and 18, and thereafter throughout the storage period for control, 0.5%, 1.0%, and 2% of MLE-treated samples, respectively, when compared with their corresponding initial counts on Day 0. Throughout the storage period (18 days), the APC of all treated beef meatballs with 0.5%, 1%, and 2% MLE remained below 7 log 10 CFU/g (Figure 1), which is the maximal permissible limit (MPL) for APC in ground beef according to ICMSF [21]. This limit was exceeded in control meatballs on Days 12, 15, and 18 of storage ( Figure 1).

Effect of MLE on Enterobacteriaceae Counts (EBCs)
Enterobacteriaceae are a family of facultatively anaerobic Gram-negative bacteria within the Enterobacterales order that contains many important foodborne pathogens, such as Salmonella, Shigella, Escherichia coli, Proteus, Klebsiella, and Yersinia [25]. The presence of Enterobacteriaceae in meat might be due to poor hygienic conditions during the handling and processing of meat and meat products.
The present study exhibited no significant difference in the initial EBCs (Day 0) between control and treated beef meatballs ( Figure 2). However, on Day 3, beef meatballs treated with 0.5%, 1%, and 2% MLE displayed a significant (p < 0.05) decrease in EBCs when compared to the control sample by 1.01, 1.23, and 1.47 log10 CFU/g, respectively. Similarly, on Day 6, treated beef meatballs with 0.5%, 1%, and 2% MLE showed a signifi- At the end of the storage period (Day 18), control meatballs exhibited high APC of 8.15 log 10 CFU/g, whereas treated beef meatballs with 0.5%, 1%, and 2% MLE showed a significant (p < 0.01) decrease in APC when compared to the control sample by 1.60, 2.60, and 3.19 log 10 CFU/g, respectively ( Figure 1). Similarly, Hazra et al. [22] showed that the total plate counts (TPCs) in ground buffalo meat were significantly (p < 0.05) decreased after adding MLE at 1.5% and 2%. The same authors mentioned that fresh leaf juice could prevent the growth of microorganisms. Additionally, chicken sausages treated with 0.5%, 0.75% and 1% MLE exhibited significantly (p < 0.05) low TPC values throughout the storage period (5 weeks), when compared with chicken sausages treated with 0.25% MLE and control sample [23]. The addition of 1 g/kg Moringa leaf extract (ethanolic-aqueous) to ground beef samples kept for 6 days at 4 • C lowered total viable counts (p < 0.05) than that in the control and butylated hydroxytoluene (BHT) treated samples by Day 3 of storage [24]. These results indicate that MLE can be used as a natural antimicrobial agent in meat products.

Effect of MLE on Enterobacteriaceae Counts (EBCs)
Enterobacteriaceae are a family of facultatively anaerobic Gram-negative bacteria within the Enterobacterales order that contains many important foodborne pathogens, such as Salmonella, Shigella, Escherichia coli, Proteus, Klebsiella, and Yersinia [25]. The presence of Enterobacteriaceae in meat might be due to poor hygienic conditions during the handling and processing of meat and meat products.
The present study exhibited no significant difference in the initial EBCs (Day 0) between control and treated beef meatballs ( Figure 2). However, on Day 3, beef meatballs treated with 0.5%, 1%, and 2% MLE displayed a significant (p < 0.05) decrease in EBCs when compared to the control sample by 1.01, 1.23, and 1.47 log 10 CFU/g, respectively. Similarly, on Day 6, treated beef meatballs with 0.5%, 1%, and 2% MLE showed a significant reduction in EBCs when compared to the control sample by 1.11, 1.36, and 1.54 log 10 CFU/g, respectively (3.86, 3.61, and 3.43, respectively vs. 4.97 log 10 CFU/g) ( Figure 2). On Days 9, 12, and 15, beef meatballs treated with 2% MLE revealed a significant (p < 0.01) reduction rate of EBCs by 1.61, 2.09, and 2.12 log 10 CFU/g, respectively, when compared with the control sample ( Figure 2). The EBC of both control and MLE-treated samples increased with time. Such an increase showed significant differences by Day 3, 12, and 15 and thereafter throughout the storage period for control, 0.5%, and 1.0% of MLE-treated samples, respectively, when compared with their corresponding initial counts on Day 0. Interestingly, the EBCs did not show any significant increase throughout the storage period in 2% MLE-treated samples. Control meatballs showed high EBCs of 6.17 log10 CFU/g on Day 18 (the last day of the storage period), whereas treated beef meatballs with 0.5%, 1%, and 2% MLE exhibited a significant (p < 0.05) decrease in EBCs when compared with the control sample by 1.19, 1.76, and 2.17 log10 CFU/g, respectively (Figure 2). Similarly, a previous study by Rahman et al. [26] revealed that total coliform count was decreased significantly (p < 0.05) amongst Control meatballs showed high EBCs of 6.17 log 10 CFU/g on Day 18 (the last day of the storage period), whereas treated beef meatballs with 0.5%, 1%, and 2% MLE exhibited a significant (p < 0.05) decrease in EBCs when compared with the control sample by 1.19, 1.76, and 2.17 log 10 CFU/g, respectively (Figure 2). Similarly, a previous study by Rahman et al. [26] revealed that total coliform count was decreased significantly (p < 0.05) amongst goat meat nuggets treated with 0.1%, 0.2%, and 0.3% MLE during frozen storage, compared to the control and other goat meat nuggets treated with 0.1% butylated hydroxyanisole (BHA). Likewise, Mashau et al. [27] observed that at the end of the storage period (Day 15), control mutton patties revealed a high coliform count of 6.20 log 10 CFU/g, meanwhile, mutton patties treated with 1%, 2%, 3%, and 4% of MLE showed a significant low coliform count of 5.77, 4.88, 3.06, and 2.02 log 10 CFU/g, respectively, and the same authors found a significant increase in coliform counts in all treated samples, throughout the storage period (15 days).

Antimicrobial Effect of MLE against Foodborne Pathogens
Studies concerning the antimicrobial effect of MLE against foodborne pathogens are scarce and mostly focused on its in vitro effect against some foodborne pathogens. This study, is therefore, very crucial to elucidate the antibacterial effect of MLE against three of the most important foodborne pathogens in meat products.
By Day 15 of storage, beef meatballs treated with 0.5%, 1%, and 2% MLE revealed a significant (p < 0.01) decline in E. coli O157:H7 counts by 3.26, 4.27, and 5.39 log 10 CFU/g, respectively, in comparison with the control (Table 1). On Day 18, control meatballs showed a high count of inoculated E. coli O157:H7 of 8.54 log 10 CFU/g, whereas treated beef meatballs with 0.5%, 1%, and 2% MLE exhibited a significant (p < 0.01) reduction in E. coli O157:H7 counts by 3.70, 4.93, and 6.54 log 10 CFU/g, respectively, in comparison with the control (Table 1). Interestingly, our study revealed a potent antimicrobial effect of MLE against E. coli O157:H7 artificially inoculated to beef meatballs. In this context, Moyo et al. [28] found that the M. oleifera acetone extract at a concentration of 5 mg/mL had a potent bactericidal effect against multi-drug resistant E. coli isolates. The in vitro activity of M. oleifera leaf extracts showed that MLE had potent antimicrobial activity against Gram-negative bacteria, and the greatest inhibitory effect of the extracts was found towards E. coli [24]. The low-weight proteins and peptides may be responsible for the antimicrobial activity of M. oleifera leaves. Furthermore, E. coli was absent in chicken sausages treated with 0.25%, 0.5%, 0.75%, and 1% M. oleifera leaves [23]. Additionally, E. coli was highest in refrigerated chicken patties without M. oleifera leaf powder (MLP) compared to chicken patties treated with MLP [29]. Thus, MLE could be used as a potent antimicrobial agent to inhibit E. coli growth in meat products.

Antimicrobial Effect of MLE against S. enterica serovar Typhimurium
There was no significant difference (p > 0.05) detected in the counts of inoculated S. enterica serovar Typhimurium amongst control and treated beef meatball samples with MLE on Day 0 and Day 3 of the storage period (Table 1). By Day 6, however, beef meatballs treated with 0.5%, 1%, and 2% MLE showed a significant (p < 0.05) reduction in S. enterica serovar Typhimurium counts in comparison with the control by 1.01, 1.20, and 2.02 log 10 CFU/g, respectively (Table 1). Treated beef meatballs with 0.5%, 1%, and 2% MLE exhibited a significant (p < 0.01) decrease of S. enterica serovar Typhimurium counts on Day 9 of storage in comparison with the control by 1.39, 1.85, and 2.73 log 10 CFU/g, respectively (Table 1). Likewise, on Day 12 of storage, treated meatballs with 0.5%, 1%, and 2% MLE revealed a significant (p < 0.01) reduction in S. enterica serovar Typhimurium count when compared with the control by 2.07, 2.46, and 3.58 log 10 CFU/g, respectively (Table 1). By Day 15 of storage, treated beef meatballs with 0.5%, 1%, and 2% MLE showed a significant (p < 0.01) reduction in S. enterica serovar Typhimurium counts by 2.67, 3.79, and 4.28 log 10 CFU/g, respectively, compared to the control (Table 1). On the last day of the storage period (Day 18), control meatballs showed a high count of inoculated S. enterica serovar Typhimurium of 8.05 log 10 CFU/g, whereas treated beef meatballs with 0.5%, 1%, and 2% MLE exhibited a significant (p < 0.01) reduction in S. enterica serovar Typhimurium counts by 3.10, 4.31, and 5.35 log 10 CFU/g, respectively, when compared with the control ( Table 1).
The antimicrobial activity of M. oleifera may be related to its content of phenolic and flavonoid compounds at concentrations greater than 1 g/kg; additionally, M. oleifera extract had a potent antimicrobial effect against many foodborne and human pathogens, such as Salmonella, Staphylococcus, and Escherichia coli [24]. Our findings were in line with a previous study conducted by Chakraborty et al. [30] that revealed that M. oleifera leaf extract is effective against S. typhimurium. Likewise, Adeyemi et al. [31] found that Salmonella was absent in all treated fish with M. oleifera. Additionally, Bukar et al. [32] declared the bioactivity of M. oleifera ethanol extract on pathogenic bacteria, for example, S. typhimurium, E. coli, and Enterobacter. Consequently, M. oleifera extracts could be used as promising food additives that possess antimicrobial properties against both spoilage and pathogenic microorganisms, which can enhance the storage life of meat and meat products and increase the profitability of the meat industry.
A previous study conducted by Moyo et al. [28] showed that MLE had antimicrobial properties by inhibiting the growth of S. aureus strains isolated from food and animal intestines. Jayawardana et al. [23] mentioned that M. oleifera leaves contain a chemical substance named pterygospermin that readily separates into two molecules of benzyl isothiocyanate, which is known to have antimicrobial properties. The same authors found that S. aureus was less than 10 2 CFU per gram in chicken sausages treated with 0.25%, 0.5%, 0.75%, and 1% M. oleifera leaves. Furthermore, Elhadi et al. [29] found that S. aureus counts were lower in refrigerated chicken patties treated with 100 g/kg MLP, than in chicken patties treated with 50 g/kg MLP and control patties (without treatment), throughout the storage periods (12 days). The same authors revealed that the antimicrobial properties of M. oleifera could be attributed to its contents of phytochemical compounds, for instance, polyphenols, flavonoids, other proteins, and peptides.

Sensory Evaluation
Moringa oleifera is a nutraceutical element rich in essential amino acids, minerals, and vitamins. M. oleifera leaves are considered a miracle food that could give enormous nutrition to people suffering from malnutrition and may be considered a protein and calcium supplement [33]. Moringa flavor intensity, characteristic flavor for beef meatballs, tenderness, juiciness, and the overall acceptability of treated and control beef meatball samples are shown in Table 2.
Moringa flavor intensity was significantly (p < 0.01) detected in treated beef meatballs with 0.5%, 1%, and 2% MLE throughout the storage periods (Table 2). M. oleifera leaves are rich in polyphenols, carotenoids, flavonoids, and other bioactive compounds, which give a favorable taste and aroma to foods [11]. Moreover, there was no significant difference detected in the characteristic flavor of beef meatballs, tenderness, juiciness, and overall acceptability between treated and control beef meatball samples; however, a slight improvement in both tenderness and juiciness was observed in treated meatball samples in comparison to the control ( Table 2). On the other hand, Rahman et al. [26] found a significant (p < 0.05) increase in the color, flavor, tenderness, juiciness, and overall acceptability of goat meat nuggets treated with 0.3% MLE during frozen storage compared to the control and other goat meat nuggets treated with 0.1% BHA. Furthermore, Evivie et al. [33] revealed that soy meatballs treated with 1%, 2%, 3%, and 4% M. oleifera leaves powder, as well as control samples, were generally accepted by panelists, although the addition of 2% or more of M. oleifera leaf powder to the meatballs decreased the panelists' acceptance, while 1% M. oleifera leaf powder had the same panelist acceptance rate as the control samples. Additionally, the addition of M. oleifera leaf powder to chicken patties up to concentrations of 50 g/kg did not affect the overall acceptability and other sensory parameters of chicken patties [29]. The shelf-life of meat products is greatly affected by microbiological, chemical, and sensory evaluations. In the present study, a high count of 10 7 CFU/g for APC and 10 4 CFU/g for EBC or more is usually associated with deteriorative changes that affect the sensory attributes and determine the product shelf life. Due to deteriorative changes noticed by changes in odor and color, sensory evaluation was not conducted from Day 9 and thereafter for control samples, from Day 12 and thereafter for beef meatballs treated with 0.5% MLE, and from Day 15 and afterward for beef meatballs treated with 1% MLE (Table 2). Moringa leaf extracts subjected to boiling for at least 15 min had higher antioxidant activity than raw leaves because boiling induced a significant increase in the proximate composition of leaves extract [34]. Moreover, MLE significantly increased the cooking yield and moisture and fat retention of treated mutton patties. Thus, the incorporation of MLE in meat products could help in the formation of a strong structure of meat products [27]. Therefore, MLE could be used as a valuable, natural, and safe preservative to improve the nutritional value, organoleptic properties, and shelf-stability of meat products. Similar to our findings, the M. oleifera flower increased the odor score, lipid stability, and shelf-life stability of chicken nuggets during cold storage for 20 days [35].

Conclusions
The present study indicates that adding Moringa oleifera leaves extract to ground beef has potent antimicrobial activity against food borne pathogens. Generally, M. oleifera leaves aqueous extracts 2% was the most effective treatment for controlling the growth of foodborne pathogens artificially inoculated to beef meatballs, including E. coli O157:H7, S. enterica serovar Typhimurium, and S. aureus, followed by 1% and 0.5% aqueous extracts of M. oleifera leaves. Fortunately, M. oleifera leaves aqueous extract did not affect the overall acceptability and the other sensory parameters of ground beef. Consequently, M. oleifera leaves extracts can be used as natural, safe, and cheap food additives to control the growth of foodborne pathogens and increase the shelf life of meat products. More research about the antimicrobial effect of M. oleifera leaves extract is required. Funding: This research paper is supported by the project "Increasing the impact of excellence research on the capacity for innovation and technology transfer within USAMVB Timis , oara" code 6PFE, submitted in the competition Program 1-Development of the national system of researchdevelopment, Subprogram 1.2-Institutional performance, Institutional development projects-Development projects of excellence in RDI.
Data Availability Statement: All data generated or analyzed during this study are included in the submitted version of the manuscript.

Conflicts of Interest:
The authors declare no conflict of interest.