Bioactivity of Essential Oils for Mitigation of Listeria monocytogenes Isolated from Fresh Retail Chicken Meat

Listeria monocytogenes is one of the most severe foodborne pathogens found in several habitats. Therefore, this study aims to investigate the antilisterial activity of different essential oils (EOs) against multidrug-resistant (MDR) L. monocytogenes strains isolated from fresh chicken meat. Our results showed that the prevalence of L. monocytogenes in the examined samples was 48%. Seventy-eight isolates were identified as L. monocytogenes. Out of these, 64.1% were categorized as MDR and were categorized in 18 patterns with 50 MDR isolates. One isolate was selected randomly from each pattern to investigate their biofilm-forming ability, resistance, and virulence genes incidence. Out of 18 MDR isolates, 88.9% showed biofilm-forming ability. Moreover, the most prevalent resistance genes were ermB (72%), aadA (67%), penA (61%), and floR genes (61%). However, the most prevalent virulence genes were inlA (94.4%), prfA (88.9%), plcB (83.3%), and actaA (83.3%). The antilisterial activity of EOs showed that cinnamon bark oil (CBO) was the most effective antilisterial agent. CBO activity could be attributed to the bioactivity of cinnamaldehyde which effects cell viability by increasing the bacterial cell electrical conductivity, ion leakage, and salt tolerance capacity loss. Therefore, CBO could be an effective alternative natural agent for food safety applications.


Introduction
Despite modern advances in food processing and preservation techniques, food protection is a growing public health concern [1]. In particular, the survival of microorganisms in foods is a critical concern, as it can cause food spoilage, infection, and illness [2]. Listeria monocytogenes is considered one of the primary foodborne pathogens because of its widespread prevalence and high tolerance against severe environmental conditions such as salt, temperature, and pH, among all known Listeria spp. [3]. L. monocytogenes is a foodborne pathogen that can be found in various food products and is considered a significant concern for foodborne bacterial pathogens [4]. Clinical disease caused by L. monocytogenes infections varies from gastroenteritis with fever to invasive infections that require hospitalization and may result in death [1].
L. monocytogenes, the main cause of listeriosis, is an intracellular bacterium that can invade several cell types. In addition, L. monocytogenes can cross the intestinal and cross barriers between the blood vessels of the brain and placenta in the case of pregnancy and 1.
Investigate the prevalence of L. monocytogenes in fresh retail chicken meat; 2.
Detect the antibiogram profile of the isolated L. monocytogenes; 3.
Investigate the activity of different EOs as antimicrobial agents against multidrugresistant L. monocytogenes; 5.
Study the effect of EOs on bacterial cell viability and integrity loss, as indicated by increased electrical conductivity, ion leakage, and salt tolerance capacity loss.
The results obtained in this study are expected to reveal valuable details about the bioactivity of EOs as antilisterial agents and expand our understanding of the antibacterial mechanism. Thus, this study could contribute to food preservative and pharmaceutical industries applications.

Sampling
As illustrated in the experimental setup, Figure 1, seventy-five fresh retail chicken meat samples, including breasts, thighs, and livers, were used in this study and randomly collected from 12 different supermarkets and four different brands in ElSharkia, Egypt, from April to November 2020. Afterward, to avoid cross-contamination, each sample was labeled and delivered in a sterile plastic storing bag and transferred in a cooling icebox (4 • C) immediately to the hygienic food laboratory, Faculty of Veterinary Medicine, ElSharkia University, within three hours after sampling and immediately analyzed.

Isolation of L. monocytogenes
All collected samples were examined for L. monocytogenes incidence based on the International Standards Organization guidelines [20]. As shown in Figure 1, the primary enrichment and secondary enrichment were performed for chicken meat samples. Afterward, for the bacterial isolation, a loopful of enrichment cultures was streaked on Listeria Selective Agar (Oxoid Hampshire, UK) supplemented with SR0140E (Oxford formulation) and CHROMagarTM Listeria (CHROMagar, Paris, France).
On CHROMagar TM , blue colonies surrounded by a white halo were isolated, while on Oxford agar, brown colonies surrounded by a black halo were isolated. To purify the colonies, they were streaked on the surface of trypticase soy agar supplemented with 0.6% yeast extract (TSAYE) and incubated for 24 h at 37 °C. Gram staining, oxidase, catalase, motility, spore formation, acid production from mannitol, D-Xylose, and L-Rhamnose tests were used to confirm the colonies from TSAYE as L. monocytogenes. Additionally, βhemolytic activity and Christine-Atkins-Munch-Petersen (CAMP) were performed based on Bergey's Manual of Systematic Bacteriology [21]. A stock culture of L. monocytogenes serotype 1/2b and Staphylococcus aureus ATCC 25923 were obtained from the Food Control Department, Zagazig University [22] and used as reference strains for biochemical tests and the CAMP test, respectively.

Antibiotics Susceptibility Test
In order to detect MDR L. monocytogenes isolates, fresh bacterial colonies of L. monocytogenes isolates were separately grown at 37 °C in brain heart infusion broth (BHI; Merck, Darmstadt, Germany) for 24 h, and each inoculum was cultured on Mueller Hinton Agar (MHA) with 5% sheep blood (Merck, Darmstadt, Germany). Susceptibility to 14 different antibiotics (MAST, Merseyside, UK) is listed in Table 1. The antibiotic selection was performed based on its effectiveness against Gram-positive bacteria. The antibiotics susceptibility test (AST) was determined using the standard disk diffusion

Isolation of L. monocytogenes
All collected samples were examined for L. monocytogenes incidence based on the International Standards Organization guidelines [20]. As shown in Figure 1, the primary enrichment and secondary enrichment were performed for chicken meat samples. Afterward, for the bacterial isolation, a loopful of enrichment cultures was streaked on Listeria Selective Agar (Oxoid Hampshire, UK) supplemented with SR0140E (Oxford formulation) and CHROMagarTM Listeria (CHROMagar, Paris, France).
On CHROMagar TM , blue colonies surrounded by a white halo were isolated, while on Oxford agar, brown colonies surrounded by a black halo were isolated. To purify the colonies, they were streaked on the surface of trypticase soy agar supplemented with 0.6% yeast extract (TSAYE) and incubated for 24 h at 37 • C. Gram staining, oxidase, catalase, motility, spore formation, acid production from mannitol, D-Xylose, and L-Rhamnose tests were used to confirm the colonies from TSAYE as L. monocytogenes. Additionally, βhemolytic activity and Christine-Atkins-Munch-Petersen (CAMP) were performed based on Bergey's Manual of Systematic Bacteriology [21]. A stock culture of L. monocytogenes serotype 1/2b and Staphylococcus aureus ATCC 25923 were obtained from the Food Control Department, Zagazig University [22] and used as reference strains for biochemical tests and the CAMP test, respectively.

Antibiotics Susceptibility Test
In order to detect MDR L. monocytogenes isolates, fresh bacterial colonies of L. monocytogenes isolates were separately grown at 37 • C in brain heart infusion broth (BHI; Merck, Darmstadt, Germany) for 24 h, and each inoculum was cultured on Mueller Hinton Agar (MHA) with 5% sheep blood (Merck, Darmstadt, Germany). Susceptibility to 14 different antibiotics (MAST, Merseyside, UK) is listed in Table 1. The antibiotic selection was performed based on its effectiveness against Gram-positive bacteria. The antibiotics susceptibility test (AST) was determined using the standard disk diffusion Kirby-Bauer [23]. The inhibition zone diameters (IZD) were measured, including the disc diameter, the re-

Biofilm Quantification
The microtiter plate assay (MPA) was carried out according to Lee et al. [44] with minor modifications. In brief, selected overnight growing colonies were diluted to obtain an OD 600 of 0.1 in each growth medium. A volume of 200 µL of the bacterial solution was transferred to 96-well microplates in triplicate wells. As a negative control, a sterile medium was used. Microplates were incubated for 24 h in static conditions at 30 • C. Plates were placed upside down, and then planktonic cells and the media were removed by tapping gently. Wells were washed using sterile saline solution (300 µL; 8.5 g NaCl/L) to remove loosely attached bacteria. Afterward, biofilms were fixed with 300 µL of ethanol (96% v/v) for 20 min then dried at 25 • C after ethanol removal.
For bacterial staining, 220 µL/well of crystal violet (0.1% w/v; CV; Merck, Darmstadt, Germany) was added, and plates were incubated in static conditions for 30 min. The solution was then removed by sharply placing the plates upside down. Wells were washed three times with 300 µL of saline solution and dried at 25 • C, then filled with acetic acid (150 µL; 33% v/v). Plates were set on a plate shaker for 10 min with slight agitation, and the amount of destained CV was assessed by reading OD 600 using a microplate reader (BioTek EL800; Winooski, VT, USA). The experiment was performed in triplicates.

Gas Chromatography/Mass Spectrometry (GC/MS) Analysis of EOs
Seven EOs, namely, cinnamon bark oil (CBO), thyme (wild) oil (TWO), thyme (red) oil (TRO), thyme (geraniol) oil (TGO), coriander oil (CRO), lavender (true) oil (LTO), and rosemary oil (RO), were purchased from National Research Center (NRC Cairo, Egypt) based on their antilisterial activity in a literature survey and their use in traditional medicine [7][8][9][10][11][12]15] to evaluate their antilisterial activity against MDR L. monocytogenes. EOs were stored at 4 • C for further experiments. EOs chemical composition analysis was assessed using the Agilent 6890 N gas chromatograph (Agilent Technologies; Palo Alto, CA, USA) equipped with an HP-5MS capillary column (30 m × 0.25 mm × 0.25 µm). The oven temperature was adjusted to increase from 60 to 250 • C at a rate of 4 • C per min for 15 min. Transfer line temperature was 250 • C. Helium was used as the carrier gas with a flow rate of 1 mL/min. The EO sample was diluted in pentane, and the injection volume was 1 µL, while the split/splitless injector temperature was set at 280 • C. The EO sample was injected in the split mode with a split ratio of 40.8/1. However, a quadrupole mass spectrometer was scanned over the 35-

Antilisterial Activity of EOs
EOs were diluted using Tween 20 (0.5%, v/v) [45] at the following concentrations 0.5, 0.25, 0.15, and 0.1% (v/v) and filtered using sterilized nylon syringe filters (0.22 µm). The antimicrobial activity was assessed by a standard disc diffusion assay [46]. Briefly, MHA plates were inoculated using 200 µL of bacterial suspension (10 6 CFU/mL) on the agar surface. Afterward, the paper disk (6 mm; Biomérieux, Lyon, France) was impregnated with 20 µL of each concentration and placed on MHA plates surface (Oxoid, Badhoevedorp, Netherlands). As a control, Tween 20 was used. The prepared plates were then incubated for 24 h at 37 • C. Ampicillin (10 µg/disk) was used as reference controls. The antibacterial activity was assessed by measuring the mean of inhibitory zones diameters. The experiment was performed in triplicates.
An EO that exhibited efficient antibacterial activity was selected to detect the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) by the broth dilution technique. Briefly, one colony of each bacterial strain was sampled and inoculated in 25 mL brain heart infusion broth and incubated at 37 • C for 24 h to obtain a bacterial suspension of 10 9 CFU/mL, then diluted with buffered peptone water to achieve 10 5 CFU/mL bacterial suspensions. Serial dilutions of EOs with a concentration ranging from 0.125-2.5% v/v were prepared with brain heart infusion broth and mixed with bacterial suspensions to give a volume of 4 mL and a final concentration of bacteria of approximately 5 × 10 4 CFU/mL and incubated at 37 • C for 24 h. The MIC was considered as the lowest concentration that inhibits visible growth. The MBC 90 was determined by subculturing 100 µL from each negative test tube onto plate count agar plates. MBC 90 was defined as the lowest concentration of the antimicrobial agent that inhibits ≥ 90% of bacterial isolates. The effect of EOs on L. monocytogenes viability was investigated using a time-kill assay, according to Li et al. [47]. Briefly, a bacterial culture treated with EOs at the MIC was taken as the treatment sample, and dimethyl sulfoxide (5%, DMSO) was used as a control. The prepared cultures were incubated for 8 h at 37 • C. The samples were collected every 2 h and diluted in phosphate-buffer (pH 7.4), then inoculated over the nutrient agar and incubated for 24 h at 37 • C. Bacterial colonies in the treatment and control plates were counted and presented in Log10 (CFU/mL).

Cytoplasmic Membrane Permeability
L. monocytogenes cytoplasmic membrane permeability of the selected strains after the treatment using EOs was assessed according to Ye et al. [48] by evaluating the released ions into the bacterial solution supernatant, which increased the relative conductivity. This increase was assessed using a conductivity meter (Shanghai Precision Instruments Co., Ltd., Shanghai, China). The permeability of the cytoplasmic membrane was assessed based on the following equation: where RC 0 was the electrical conductivity of dead bacterial cells in glucose (5%) after treatment for 5 min in boiling water; RC 1 expresses the electrical conductivity of EO at the MIC mixed with glucose (5%); and RC 2 expresses the electrical conductivity of the treated bacterial culture with EO in the course of 12 h of incubation.

Potassium Ion Leakage Assay
The amount of leaked free potassium ions (K + ) from the tested L. monocytogenes strains was evaluated as reported by Bajpai et al. [49]. After the treatment of L. monocytogenes cells with EOs at MIC mixed with 0.1% peptone water and incubated at 37 • C for 8 h, the concentration of extracellular free ions (K + concentration) was tested every 2 h with a Kalium Potassium kit (Quantofix, Macherey-Nagel GmbH & Co. KG, Duren, Germany). L. monocytogenes ATCC 19115 was obtained from Food Control Department, Zagazig University, then treated with 5% DMSO and used as a control.

Cell Membrane Integrity Assay
The cell membrane integrity of the selected L. monocytogenes strains due to the action of EOs was evaluated as described by Carson et al. [50]. Bacterial samples were treated with the MIC of the most effective EO for each strain, while the control sample was treated with 5% DMSO. All samples were incubated at 37 • C. Samples were obtained every 30 min then centrifuged at 1000× g for 10 min. The supernatant absorbance (OD 260 nm) was measured using a spectrophotometer (SP-3000 plus, Optima, Tokyo, Japan). The absorbance corrections for the treated and control samples were performed by detecting the EOs values without bacteria in sterile peptone water.

Loss of Salt Tolerance Capacity Assay
As a result of EOs treatment, L. monocytogenes salt tolerance capacity loss was evaluated as described by Miksusanti et al. [51]. In brief, the treated bacterial culture using EOs at MIC was grown on nutrient agar plates containing various concentrations of NaCl (0, 2.5, 5.0, and 10.0%). Plates treated with 5% DMSO were used as a control. The prepared plates were incubated for 24 h at 37 • C. Bacterial colonies were counted in samples and control plates and presented in Log10 (CFU/mL).

Statistical Analysis
The data obtained were expressed as the means ± standard deviation. One-way analysis of variance was used to detect the significant differences at p < 0.05 using GraphPad Prism version 8. Heatmap representations with cluster analysis were performed using NCSS 2021 Statistical Software (NCSS, LLC. Kaysville, UT, USA, ncss.com/software/ncss). Our results were in agreement with Elmali et al. [52], who found a 37.5% prevalence of L. monocytogenes in 120 retail poultry meat samples. Additionally, Ceylan et al. [53] reported similar results and found that 32.76% prevalence of L. monocytogenes was found in 38 of 116 analyzed samples. Escudero-Gilete et al. [54] reported 26% prevalence in the retailed chicken meat samples. However, Goh et al. [55] found that L. monocytogenes was detected in 20% of the collected samples, and the prevalence of L. monocytogenes was relatively high in the breast meat samples (42.03%) followed by drumstick (11.27%) and thigh meat samples (7.14%). As a result, the high prevalence of L. monocytogenes in fresh retail chicken meat, possibly due to poor sanitary quality control, may cause a risk to human health.

L. monocytogenes Drug Resistance and Their Drug Resistance Patterns
In our study, the susceptibility of 78 L. monocytogenes isolates to 14 antimicrobial agents is listed in Table 1. The resistance of L. monocytogenes isolates against ERY, GEN, and TET was 61.5, 73.1, and 61.5%, respectively. However, 66.7% of L. monocytogenes isolates showed susceptibility to AMP and VAN. Moreover, the susceptibility to RIF, CHL, and IPM was 64.1, 60.3, and 60.3%, respectively. The minimum effectiveness was revealed by CIP, CLI, LNZ, NAL, OXA, and TMP that presented susceptibility ranged from 30.8 to 56.4% of all L. monocytogenes strains.
The resistance profile of each L. monocytogenes isolate was presented in Supplementary Materials, Figure S1. The clustering analysis of these strains was carried out to select the MDR L. monocytogenes isolates. Fifty isolates (64.1%) were categorized as MDR L. monocytogenes, and their MAR indices ranged from 0.0 to 0.93, with an average of 0.43. The MAR index higher than 0.14 in our study referred to the tested L. monocytogenes strains originated from a high-risk source where antimicrobial agents are commonly used [56].
As shown in Table 2, drug resistance patterns (DRPs) obtained from the MDR strains were listed in 18 different DRPs. The most common DRPs were P1, P7, P5, and P5a, which included 18 isolates. However, P1a, P1b, P1c, and P3c included 12 isolates. These eight patterns included 60% (30/50) of all tested MDR strains. As a result, one MDR L. monocytogenes strain was chosen randomly from each DRP for further investigation.
Mpondo et al. [57] reported that Listeria spp. were found to have phenotypic resistance to erythromycin, sulfonamides, chloramphenicol, aminoglycosides, β-lactams, streptomycin, and tetracycline. As a result, antibiotic-resistant Listeria has emerged as a growing One Health concern, exacerbating the worldwide antibiotic resistance crisis and weakening gains in healthcare, food production, and life expectancy, while posing health concerns to the environment, humans, and animals. Olaimat et al. [58] stated that antibiotic resistance of L. monocytogenes isolated from food frequently utilized in the treatment of human listeriosis, such as gentamicin, ampicillin, and tetracycline, had been reported. According to Teuber [59], L. monocytogenes is susceptible to a wide variety of drugs with antibacterial effects against Gram-positive bacteria, such as ampicillin, gentamicin, erythromycin, and tetracyclines. However, most of the L. monocytogenes strains were resistant to cefepime, fosfomycin, cefotaxime, lincosamides, and oxacillin [60]. Additionally, our findings were similar to Bouymajane et al. [6], who found that most L. monocytogenes strains originating from different food samples were resistant to tetracycline (20.0%), ampicillin, and sulfamethoxazole/trimethoprim (33.0%), sulfamethoxazole (40.0%), erythromycin (60.0%), and amoxicillin/clavulanic acid (67.0%). They also found that MDR strains represented 66.7% of all isolated strains. Furthermore, vancomycin, rifampicin, and linezolid have been reported as effective agents in listerial infection disease [61]. Additionally, it has been proposed that rifampicin, considered effective against intracellular L. monocytogenes and may permeate the cerebrospinal fluid, could aid in the elimination of remaining bacteria [62]. Currently, antibiotic resistance has developed in L. monocytogenes isolated from the environment and foods, notably for antibiotics frequently used to treat listeriosis. As a result of the evolution of resistant strains, it is essential to monitor changes in the antibiotic resistance of L. monocytogenes. In this context, our results were different than those reported by Chen et al. [63], who found that none of the 72 L. monocytogenes strains isolated from the aquatic product was MDR strain. Therefore, we can conclude that the acquired resistance against antimicrobial agents varies based on the bacterial habitat and environment.

Drug Resistance Genes and Virulence Factors
The incidence of genes associated with the drug resistance described was investigated. As a result, the frequency of antibiotic resistance-encoding genes was detected ( Figure S2). Out of 18 MDR L. monocytogenes selected isolates, the incidence of ermB and aadA genes was 72% (13/18) and 67% (6/18), respectively. The incidence of penA and floR genes was 61% (11/18) for each gene. However, cmlA, ereA, and ereB express 44% (8/18) for each gene, and ampC, vanA, vanB, tetA, and tetB incidence was 33% (6/18), 33% (6/18), 39% (7/18), 28% (5/18), and 28% (5/18), respectively. Similar results were reported by Srinivasan et al. [64], who investigated the presence of resistance genes of L. monocytogenes isolated from the dairy farms and found a high presence of floR, penA, tetA, strA, and sulI. Additionally, resistance genes for different antibiotic classes are frequently found on the same plasmid. Moreover, as shown in Supplementary Materials, Figure S2 Van Stelten et al. [65] found that a large proportion of L. monocytogenes isolated from food production sources showed a low pathogenicity. However, our results showed that all tested L. monocytogenes strains harbor at least 63% of tested virulence genes, which reflect their high pathogenicity. Our results were in agreement with Rugna et al. [66], who found that all investigated L. monocytogenes strains had all tested virulence genes. Shen et al. [67] reported that the incidence of inlC and inlJ increases the pathogenicity of L. monocytogenes virulence factors. Therefore, our results suggest that L. monocytogenes strains originating from food are potentially virulent and could have an essential role in epidemics, regardless of their source.

L. monocytogenes Biofilm-Forming Ability
As shown in Supplementary Material, Figure S2 L. monocytogenes can form biofilms as a strategy to survive in food processing environments because cells in biofilms typically exhibit increased tolerance against antimicrobial agents in comparison with their planktonic counterparts [68]. The colonization of L. monocytogenes on the surfaces of food processing equipment is enabled by the attachment and production of biofilm [69]. However, the presence of different virulence factor genes such as prf A and hly is essential for effective biofilm formation by L. monocytogenes [70].
In our study, the presence of adhesion protein (lap) and internalin proteins (inlA, inlB, inlC, and inlJ) was observed in all strong biofilm-forming strains. Similarly, the occurrence of strong BFA in two isolates could be attributed to interruption or overexpression of biofilm-related genes [71].
In this study, among all tested MDR L. monocytogenes (18 isolates), five isolates had the maximum number of tested resistance and virulence genes. In addition to their ability to form biofilm was arranged into a cluster X, as shown in Figure 2. Identification and creation of a phylogenetic tree of the selected isolates were carried out using 16S rRNA gene sequencing (Figure 3

Essential Oil Antilisterial Activity
The chemical composition analysis of the tested EOs are listed in Table 3, showing the main constituent content obtained from a peak area relative to the total peak area in GC-MS analysis. GC-MS analysis showed a high percentage of cinnamaldehyde (63.4%), carvacrol (67.2%), γ-terpinene (22.8%), geranyl acetate (51.7%), linalool (62.2%), linalyl acetate (35.2%), and 1,8-cineole (28.5%) in CBO, TWO, TRO, TGO, CRO, LTO, and RO, respectively. * The main constituent content was detected from a peak area relative to the total peak area in GC-MS analysis. The main constituents content higher than 15% are listed.
The antibacterial activity of different EOs was investigated, as shown in Figure 4. Our results showed the efficiency of CBO, TWO, and TRO as antilisterial agents. However, CBO was the most effective antibacterial agent against all resistance and virulence genesproducing MDR L. monocytogenes. The concentration of 0.5 and 0.25% showed a significant (p < 0.05) inhibitory effect against the selected strains for all tested EOs than 0.15 and 0.1%. At 0.5%, the inhibition zone ranged from 39.2 mm in CBO against CML-61 to 10.2 mm in LTO and RO against CML-20 and CML-51, respectively. At 0.25%, the inhibition zone ranged from 32.7 mm in CBO against CML-61 to 9.1 mm in TGO against CML-61. However, at 0.15%, the inhibition zone ranged from 26.2 mm in CBO against CML-32 to 6.5 mm in RO against CML-51. At 0.1%, the inhibition zone ranged from 24.0 mm in CBO against CML-61 to 6.2 mm in RO against CML-51. Therefore, the CBO, MIC, and MBC90 values were detected, and our results showed that the MIC values varied from 0.25 to 0.5% (v/v) while MBC90 values ranged from 0.5 to 1.5% (v/v). Our findings were in agreement with Hoque et al. [72], who reported that CBO reduced L. monocytogenes in ground chicken meat by 2.0 Log CFU/g in one day. Additionally, Somrani et al. [15] showed that onion, garlic, and cinnamon essential oil were effective towards L. monocytogenes and are natural promising antimicrobial alternatives for food manufacture application. Additionally, Hussain et al. [16] stated that 0.025-0.05% of CBO addition was effective by stabilizing color and pH and retarding lipid Our findings were in agreement with Hoque et al. [72], who reported that CBO reduced L. monocytogenes in ground chicken meat by 2.0 Log CFU/g in one day. Additionally, Somrani et al. [15] showed that onion, garlic, and cinnamon essential oil were effective towards L. monocytogenes and are natural promising antimicrobial alternatives for food manufacture application. Additionally, Hussain et al. [16] stated that 0.025-0.05% of CBO addition was effective by stabilizing color and pH and retarding lipid oxidation through meat storage. The use of 0.5% of CBO leads to stability of color regardless of the bacteria growth reduction compared to other treatments. It can be suggested that adding 0.025% and 0.05% of CBO in meat can be considered as an option to sustain the quality of meat products.

CBO Bioactivity as an Antilisterial Agent
Because of the notable inhibitory effect of CBO, the antilisterial mode of action of CBO against the selected L. monocytogenes strains was investigated using different techniques. As shown in Figure 5A, the viability of the bacterial cells decreased along with the incubation time compared to control. Our results also showed that the CML-61 strain was the most inhibited strain after 8 h of incubation due to the action of CBO followed by CML-20, CML-74, CML-32, and CML-51 with a bacterial count of 0.8 ± 0.1, 1.2 ± 0.1, 1.5 ± 0.2, and 2.6 ± 0.4 Log CFU/mL, respectively. oxidation through meat storage. The use of 0.5% of CBO leads to stability of color regardless of the bacteria growth reduction compared to other treatments. It can be suggested that adding 0.025% and 0.05% of CBO in meat can be considered as an option to sustain the quality of meat products.

CBO Bioactivity as an Antilisterial Agent
Because of the notable inhibitory effect of CBO, the antilisterial mode of action of CBO against the selected L. monocytogenes strains was investigated using different techniques. As shown in Figure 5A, the viability of the bacterial cells decreased along with the incubation time compared to control. Our results also showed that the CML-61 strain was the most inhibited strain after 8 h of incubation due to the action of CBO followed by CML-20, CML-74, CML-32, and CML-51 with a bacterial count of 0.8 ± 0.1, 1.2 ± 0.1, 1.5 ± 0.2, and 2.6 ± 0.4 Log CFU/mL, respectively. Moreover, the relative electrical conductivity showed a rapid increase for all tested bacterial strains treated with CBO, along with incubation time until the first 4 h. As shown in Figure 5B, CML-61 showed the highest susceptibility to CBO with an increase in the relative conductivity (14.6%) along with incubation time compared to control (0.85%), followed by CML-20 (12.6%), CML-74 (11.5%), CML-32 (11.1%), and CML-51 (10.1%).
Additionally, the loss of K + ions from MDR L. monocytogenes tested strains treated with CBO confirms the concept that EOs acts by rupture and disrupts the bacterial cell Moreover, the relative electrical conductivity showed a rapid increase for all tested bacterial strains treated with CBO, along with incubation time until the first 4 h. As shown in Figure 5B, CML-61 showed the highest susceptibility to CBO with an increase in the relative conductivity (14.6%) along with incubation time compared to control (0.85%), followed by CML-20 (12.6%), CML-74 (11.5%), CML-32 (11.1%), and CML-51 (10.1%).
Concerning cell membrane integrity assay, the concentration of 260 nm absorbing materials was evaluated, as shown in Figure 5D. For 120 min of incubation, the concentration of 260 nm absorbing compounds in culture filtrates treated with CBO at the MIC concentration gradually increased for all tested strains. CML-61 was the most susceptible strain to CBO and showed a significantly (p < 0.05) higher absorbance (OD 260 nm = 9.2) than control (OD 260 nm = 6.2) and other L. monocytogenes strains after 60 min. However, the other tested L. monocytogenes strains showed significant (p < 0.05) high absorbance than control, and insignificant variation was observed (p > 0.05).
Our study also revealed the effect of salt on L. monocytogenes cells treated with CBO at the MIC showed a gradual decline in viable cells number compared to the control sample. As shown in Figure 5E, there was insignificant variation (p > 0.05) in the bacterial count for CML-20, CML-32, CML-51, and CML-74 at different concentrations of NaCl and significant (p < 0.05) decrease in comparison with control. However, CML-61 showed significant decreases in comparison with other strains and control.
Due to the hydrophobic nature of cinnamaldehyde [13], it has the ability to penetrate the cytosol of treated bacterial cells easily because of the nature of Gram-positive bacterial membrane and leads to the rupture and damage of the cell membrane and consequently leads to cell lysis [73]. However, Cherrat et al. [14] investigated the effect of EOs on the viability of E. coli and Listeria innocua and reported that Gram-positive bacteria such as Listeria spp. are more susceptible to EOs than Gram-negative bacteria due to cell wall hydrophobic nature. Huang et al. [74] reported that CBO is an efficient agent towards foodborne pathogens by inhibiting microbes by various mechanisms such as rupture of the cell wall and the cytoplasmic membrane. Additionally, CBO causes leakage of cellular components, changes in fatty acid and phospholipid constituents, and inhibits protein translocation and genetic materials formation [75]. The significant leakage of cytosolic components was interpreted as an indicator of severe irreversible damage to the cell membrane [76]. Thus, ions and cell metabolites leakage from the CBO-treated bacterial cells could be effective as antilisterial activity. Patra and Baek [73] stated that the selectivity of the bacterial cell membrane plays a significant role in inhibiting the exiting of small ions such as Ca +2 , Na + , and K + . This control of membrane permeability is critical to several cellular activities as cell maintenance, transport, and energy transduction. It is thought that cinnamaldehyde could cause abnormalities in the cell membrane, leading to K + leakage and resulting in cellular damage and lysis ( Figure 6).
Moreover, the loss of listerial cells' ability to maintain their growth at a higher salt concentration demonstrates that EOs effects on the bacterial cell membrane led to membrane rupture and decreased the ability of osmoregulation through high salt stress. This impaired ability could potentially impact the membrane's performance to appropriately regulate the cell under excessive salt concentrations, resulting in cell death [73]. Therefore, our results were in agreement with Zhang et al. [77], who revealed that cinnamon oil caused small electrolyte leakage, resulting in a significant increase in the electric conductivity. Furthermore, the concentration of proteins and nucleic acids in cell suspension was proportional related to cinnamon oil concentration. Additionally, they found that Gram-positive bacteria were more sensitive to cinnamon oil than Gram-negative bacteria. As well, Vasconcelos et al. [78] reported that cinnamon oils and their compounds had been reported to inhibit bacteria by damaging the cell membrane; altering the lipid profile, membrane porins, motility; inhibiting ATPases, cell division, and biofilm formation, and antiquorum sensing effects.
In particular, concerning the food safety applications, Chen et al. [79] reported that cinnamaldehyde is a hydrophobic aromatic aldehyde that has been approved by the FAO/WHO Expert Committee on Food Additives (JECFA) for use as a food flavoring agent. Moreover, Boughendjioua and Djeddi [80] reported that CBO physicochemical and organoleptic properties are very appreciated in perfumery and will be very coveted in the food, cosmetic, and pharmaceutical industry. Furthermore, Goñi et al. [81] and Ju et al. [12] found that CBO has an antimicrobial effect in baked foods without influencing the organoleptic properties. Chitosan films containing CBO has antimicrobial activity, keeping the natural organoleptic characteristics and extending the shelf life [82]. Generally, our results indicate the efficiency of the antilisterial activity of cinnamaldehyde toward resistance and virulence genes-producing MDR L. monocytogenes strains, maintaining good nutritional and organoleptic properties of food products. agent. Moreover, Boughendjioua and Djeddi [80] reported that CBO physicochemical and organoleptic properties are very appreciated in perfumery and will be very coveted in the food, cosmetic, and pharmaceutical industry. Furthermore, Goñi et al. [81] and Ju et al. [12] found that CBO has an antimicrobial effect in baked foods without influencing the organoleptic properties. Chitosan films containing CBO has antimicrobial activity, keeping the natural organoleptic characteristics and extending the shelf life [82]. Generally, our results indicate the efficiency of the antilisterial activity of cinnamaldehyde toward resistance and virulence genes-producing MDR L. monocytogenes strains, maintaining good nutritional and organoleptic properties of food products.

Conclusions
Listeria monocytogenes is one of the most severe foodborne pathogens. Our results revealed that the prevalence of L. monocytogenes in raw chicken meat in Zagazig city was 48%. Seventy-eight isolates were identified as L. monocytogenes. Of those, 64.1% of the identified isolates were multidrug resistance bacteria. Moreover, the study of resistance genes on the selected isolate showed that ermB, aadA, penA, and floR genes were the most

Conclusions
Listeria monocytogenes is one of the most severe foodborne pathogens. Our results revealed that the prevalence of L. monocytogenes in raw chicken meat in Zagazig city was 48%. Seventy-eight isolates were identified as L. monocytogenes. Of those, 64.1% of the identified isolates were multidrug resistance bacteria. Moreover, the study of resistance genes on the selected isolate showed that ermB, aadA, penA, and floR genes were the most prevalent genes. However, the most prevalent virulence genes were inlA, prf A, plcB, and actaA genes. On the other hand, the activity of seven different essential oils against MDR L. monocytogenes was investigated. Cinnamon bark oil showed high efficiency as an antilisterial agent against MDR L. monocytogenes isolated from retail chicken meat. Our results also interpret cinnamon bark oil bioactivity by disrupting the cell membrane