Trans-Cinnamaldehyde, Eugenol and Carvacrol Reduce Campylobacter jejuni Biofilms and Modulate Expression of Select Genes and Proteins

Campylobacter jejuni is the leading cause of human foodborne illness globally, and is strongly linked with the consumption of contaminated poultry products. Several studies have shown that C. jejuni can form sanitizer tolerant biofilm leading to product contamination, however, limited research has been conducted to develop effective control strategies against C. jejuni biofilms. This study investigated the efficacy of three generally recognized as safe status phytochemicals namely, trans-cinnamaldehyde (TC), eugenol (EG), or carvacrol (CR) in inhibiting C. jejuni biofilm formation and inactivating mature biofilm on common food contact surfaces at 20 and 37°C. In addition, the effect of phytochemicals on biofilm architecture and expression of genes and proteins essential for biofilm formation was evaluated. For the inhibition study, C. jejuni was allowed to form biofilms either in the presence or absence of sub-inhibitory concentrations of TC (0.75 mM), EG (0.61 mM), or CR (0.13 mM) for 48 h and the biofilm formation was quantified at 24-h interval. For the inactivation study, C. jejuni biofilms developed at 20 or 37°C for 48 h were exposed to the phytochemicals for 1, 5, or 10 min and surviving C. jejuni in the biofilm were enumerated. All phytochemicals reduced C. jejuni biofilm formation as well as inactivated mature biofilm on polystyrene and steel surface at both temperatures (P < 0.05). The highest dose of TC (75.64 mM), EG (60.9 mM) and CR (66.56 mM) inactivated (>7 log reduction) biofilm developed on steel (20°C) within 5 min. The genes encoding for motility systems (flaA, flaB, and flgA) were downregulated by all phytochemicals (P < 0.05). The expression of stress response (cosR, ahpC) and cell surface modifying genes (waaF) was reduced by EG. LC-MS/MS based proteomic analysis revealed that TC, EG, and CR significantly downregulated the expression of NapA protein required for oxidative stress response. The expression of chaperone protein DnaK and bacterioferritin required for biofilm formation was reduced by TC and CR. Scanning electron microscopy revealed disruption of biofilm architecture and loss of extracellular polymeric substances after treatment. Results suggest that TC, EG, and CR could be used as a natural disinfectant for controlling C. jejuni biofilms in processing areas.

Campylobacter jejuni is the leading cause of human foodborne illness globally, and is strongly linked with the consumption of contaminated poultry products. Several studies have shown that C. jejuni can form sanitizer tolerant biofilm leading to product contamination, however, limited research has been conducted to develop effective control strategies against C. jejuni biofilms. This study investigated the efficacy of three generally recognized as safe status phytochemicals namely, trans-cinnamaldehyde (TC), eugenol (EG), or carvacrol (CR) in inhibiting C. jejuni biofilm formation and inactivating mature biofilm on common food contact surfaces at 20 and 37 • C. In addition, the effect of phytochemicals on biofilm architecture and expression of genes and proteins essential for biofilm formation was evaluated. For the inhibition study, C. jejuni was allowed to form biofilms either in the presence or absence of sub-inhibitory concentrations of TC (0.75 mM), EG (0.61 mM), or CR (0.13 mM) for 48 h and the biofilm formation was quantified at 24-h interval. For the inactivation study, C. jejuni biofilms developed at 20 or 37 • C for 48 h were exposed to the phytochemicals for 1, 5, or 10 min and surviving C. jejuni in the biofilm were enumerated. All phytochemicals reduced C. jejuni biofilm formation as well as inactivated mature biofilm on polystyrene and steel surface at both temperatures (P < 0.05). The highest dose of TC (75.64 mM), EG (60.9 mM) and CR (66.56 mM) inactivated (>7 log reduction) biofilm developed on steel (20 • C) within 5 min. The genes encoding for motility systems (flaA, flaB, and flgA) were downregulated by all phytochemicals (P < 0.05). The expression of stress response (cosR, ahpC) and cell surface modifying genes (waaF) was reduced by EG. LC-MS/MS based proteomic analysis revealed that TC, EG, and CR significantly downregulated the expression of NapA protein required for oxidative stress response. The expression of chaperone protein DnaK and bacterioferritin required for biofilm formation was reduced by TC

INTRODUCTION
Campylobacter is one of the major foodborne pathogens that causes gastroenteritis in humans worldwide (Marder et al., 2017). Recent reports have shown that the incidence of Campylobacter infections has increased by 10% in 2017 compared to 2014-2016 with an annual incidence of 17.83 per 100,000 people in the United States (Marder et al., 2017). Among the major Campylobacter species, Campylobacter jejuni is responsible for approximately 90% of the reported campylobacteriosis cases in humans (Cody et al., 2013). In addition, C. jejuni infections have been associated with the occurrence of Guillain-Barré syndrome and reactive arthritis causing significant economic losses and disease burden globally (Spiller, 2007;Gradel et al., 2009;Hoffmann et al., 2012).
The primary source of human C. jejuni infections is the handling and/or consumption of contaminated poultry products (Rosner et al., 2017). The survival of C. jejuni in the environment such as water and feed plays a critical role in C. jejuni colonization in the birds and subsequent contamination of poultry products during carcass processing (Annan-Prah and Janc, 1988;Dhillon et al., 2006;Boysen et al., 2016). Several studies have shown that the biofilm-forming capacity in bacteria facilitates increased tolerance to sanitizers (Somers et al., 1994;Melo et al., 2017). Therefore, there is a high possibility that product contamination in processing environment could be due to the presence of biofilms. A biofilm is an assemblage of surfaceassociated microbial communities embedded within the matrix of extracellular polymeric substances (Donlan, 2002;Donlan and Costerton, 2002). The ability of C. jejuni to form biofilm has been demonstrated on different surfaces, including plastic, glass and steel under different oxygen concentrations Reuter et al., 2010;Bronowski et al., 2014;Brown et al., 2014;Bronnec et al., 2016). Moreover, studies have demonstrated that C. jejuni biofilm formation can be enhanced by atmospheric oxygen and in the presence of chicken meat juice (Reuter et al., 2010;Brown et al., 2014). Thus, C. jejuni biofilms constitute a significant food safety hazard.
The formation of bacterial biofilm begins with initial attachment of bacteria to a surface. The surface attachment strengthens, and the bacterial community becomes irreversibly attached to the target surface. This is followed by maturation of the biofilm and dispersion of bacteria to new location (Donlan and Costerton, 2002). A number of genes that contribute to biofilm formation have been characterized in C. jejuni (Bronowski et al., 2014). Several genes coding for motility (Joshua et al., 2006;Kalmokoff et al., 2006;Kim et al., 2015) are essential for biofilm formation. These include flaA, flaB, flaC, flaG, fliA, fliS, flgA, and flhA. In addition, genes encoding stress response (spoT, csrA, ahpC, cosR, and cprS) (Fields and Thompson, 2008;McLennan et al., 2008;Svensson et al., 2009;Oh and Jeon, 2014;Turonova et al., 2015), bacterial cell surface modifications (peb4, waaF) (Asakura et al., 2007;Naito et al., 2010) and quorum sensing (luxS) (Reeser et al., 2007) are also critical for biofilm formation and maturation in C. jejuni. One of the critical components of bacterial biofilm is the exopolysaccharide layer (EPS), which protects underlying bacterial population from harsh environmental conditions. The impermeability of EPS along with the slower growth rates and metabolism of bacteria in the biofilms makes them resistant to disinfectants, antimicrobials and antibiotics (Reuter et al., 2010;Borges et al., 2016). In a recent study, C. jejuni population in biofilms was found to exhibit up to 32-fold higher resistance to gentamicin than in the corresponding planktonic forms (Malik et al., 2017). In addition, biofilm facilitates C. jejuni to survive for a longer period of time (up to 24 days) as compared to planktonic cells under aerobic conditions or in water (Joshua et al., 2006;Lehtola et al., 2006). Thus, developing appropriate processing plant hygiene and sanitation are critical for controlling C. jejuni biofilms.
Current intervention approaches for controlling C. jejuni biofilms include use of chemicals (Somers et al., 1994;Melo et al., 2017), biofilm-degrading enzymes (Brown et al., 2015;Kim et al., 2017) and application of bacteriophages (Siringan et al., 2011). Chemical disinfectants such as chlorine, trisodium phosphate and quaternary ammonium compounds have been extensively investigated for their antibiofilm efficacy against C. jejuni, however, these compounds have limited effectiveness in controlling C. jejuni biofilm, especially in the presence of organic matter (Northcutt et al., 2005;Oyarzabal, 2005). Moreover, production of mutagens is of concern (Dore, 2015). The use of biofilm-degrading enzymes for controlling biofilms has been reported in various bacteria, including C. jejuni (Brown et al., 2015;Kim et al., 2017). However, the efficacy of biofilm-degrading enzyme could be reduced with the production of high quantities of EPS and proteolytic activity of exoenzymes produced by the mature biofilms (Whitchurch et al., 2002). Similarly, treatment of C. jejuni biofilms with bacteriophages has limited application due to the chance of emergence of resistance strains (Siringan et al., 2011). Therefore, there is a need for a novel strategy to control C. jejuni biofilms.
Phytochemicals have been used as natural antimicrobials for treating human infections since ancient time. The majority of phytochemicals are secondary metabolites produced as a defense mechanism to protect plants from pathogenic microorganisms (Borges et al., 2016). A variety of phytochemicals have been evaluated for their antibacterial effect against foodborne pathogens and several active components have been identified (Burt, 2004;Holley and Patel, 2005). However, very few studies have investigated the potential of phytochemicals for controlling C. jejuni biofilms. Trans-cinnamaldehyde (TC) is an aldehyde extracted from the bark of cinnamon (Cinnamomum zeylandicum), whereas eugenol (EG) and carvacrol (CR) are the active components of clove oil (Eugenia caryophyllus) and oregano oil (Origanum glandulosum), respectively. All the aforementioned phytochemicals are classified as generally recognized as safe by the United States Food and Drug Administration (21 Code of Federal Regulation part 172.515) (Adams et al., 2004(Adams et al., , 2005Knowles et al., 2005). Previous studies have demonstrated the antibiofilm effect of TC, EG and CR in various bacteria such as Salmonella Typhimurium (Trevisan et al., 2018), S. Enteritidis (Čabarkapa et al., 2019, Listeria monocytogenes (Upadhyay et al., 2013) and Pseudomonas aeruginosa (Letsididi et al., 2018;Lou et al., 2019). However, their antibiofilm effect in C. jejuni has not been determined.
In this study, we investigated the antibiofilm efficacy of TC, EG, and CR against C. jejuni at two temperatures (20 and 37 • C) and on two surfaces (polystyrene and stainlesssteel) that are commonly encountered in processing plant environment. The effect of phytochemical treatments on C. jejuni biofilm architecture was visualized using scanning electron microscopy and confocal laser scanning microscopy. Moreover, the effects of TC, EG, and CR on the transcription of C. jejuni genes and proteins critical for biofilm formation were determined.

C. jejuni Strain and Culture Conditions
Campylobacter jejuni NCTC 11168 strain was cultured in 10 mL of Campylobacter enrichment broth (CEB; International Diagnostics Group, Bury, Lancashire, United Kingdom) and incubated under microaerophilic condition (5% O 2 , 10% CO 2 , and 85% N 2 ) at 42 • C for 48 h. Following growth, C. jejuni was centrifuged and washed twice with Butterfield's phosphate diluent (BPD, 0.625 mM potassium dihydrogen phosphate, pH 7.2) and resuspended in CEB to use as inoculum.

Preparation of Chicken Meat Juice
A previously published method was used for the preparation of chicken meat juice (Birk et al., 2004). Briefly, frozen whole chickens were obtained from the University of Arkansas poultry pilot processing plant (Fayetteville, AR, United States) and thawed overnight at 4 • C. The meat juice was collected and centrifuged at 4,000 rpm for 20 min to remove debris followed by filter sterilization (0.2 µm cellulose acetate membrane; VWR International, United States). Based on published literature (Brown et al., 2014) and growth curve analysis, chicken meat juice was added to CEB at 5% level and used for biofilm experiments.

Determination of C. jejuni Biofilm Formation on Polystyrene Plates and Stainless-Steel Coupons
The biofilm formation of C. jejuni on polystyrene plates and steel coupons was determined according to a previously published method with slight modifications (Brown et al., 2014). Briefly, 200 µL of CEB broth containing C. jejuni (∼6.0 Log CFU) was added to 96-well polystyrene plates or on steel coupons kept in 24-well polystyrene plates and incubated for 48 h at 20 or 37 • C under aerobic condition to facilitate biofilm formation. The biofilm formation was determined by 2, 3, 5-Triphenyltetrazolium chloride (TTC) staining at 24 h intervals. After staining, TTC solution was removed followed by air-drying and bound TTC dye was dissolved in 20% acetone in ethanol, and the A 500 value of the solution was measured. A similar procedure was used to determine C. jejuni biofilm formation in broth containing 5% chicken meat juice.

Determination of Sub-Inhibitory Concentrations and Minimum Bactericidal Concentrations of Phytochemicals
The sub-inhibitory concentration (SIC) and minimum bactericidal concentration (MBC) of each phytochemical against C. jejuni was determined according to a previously described method Wagle et al., 2017a,b). All three phytochemicals were purchased from Sigma-Aldrich (St. Louis, MO, United States). In brief, twofold dilutions of TC, EG, or CR in CEB (100 µL/well) were made in sterile 96-well polystyrene plates (Costar, Corning Incorporated, Corning, NY, United States) followed by inoculation with equal volume of C. jejuni (10 6 CFU/mL) and incubated at 37 • C for 24 h under microaerophilic conditions. The growth of C. jejuni was determined by plating on Campylobacter Line Agar (CLA) plates (Line, 2001). The highest concentration of phytochemicals that did not inhibit bacterial growth was selected as the SIC for the study, whereas the lowest concentration of phytochemicals that reduced C. jejuni counts significantly (>2 Log 10 CFU/mL) was taken as MBC.

Biofilm Inhibition and Inactivation Assays on Polystyrene Plates
The ability of TC, EG, and CR in inhibiting C. jejuni biofilm formation on polystyrene plates was determined according to a previously published method (Reeser et al., 2007;Lu et al., 2012). Two hundred microliters of culture (∼6.0 Log CFU) was added to each well of a sterile 96-well polystyrene plate, followed by addition of SICs of TC, EG, or CR. The plates were incubated at 20 or 37 • C for 48 h. A similar procedure was followed to test the antibiofilm efficacy of phytochemicals in the presence of 5% chicken meat juice. The biofilm formation was determined at 24 h intervals. At each time point, the spent medium was removed and the well was gently washed three times with BPD. The bacteria in the biofilms were removed using cell scrapper and plated on CLA plates. The biofilm associated C. jejuni were enumerated after incubation at 42 • C for 48 h.
The inactivation of mature C. jejuni biofilms by TC, EG and CR was determined as described previously (Kim et al., 2017). Briefly, C. jejuni (∼6.0 Log CFU, 200 µL) was allowed to form biofilm in 96-well polystyrene plate at 20 or 37 • C for 48 h. After mature biofilm was formed, the inactivation was carried out with 200 µL of TC (18.91, 37.82, or 75.64 mM), EG (15.22,30.45,or 60.90 mM) or CR (16.64,33.28,or 66.56 mM) in BPD for 1, 5, or 10 min. The treatment solution was discarded and 200 µL of Dey-Engley neutralizing broth (Difco Laboratories, Sparks, MD, United States) was added. The number of surviving C. jejuni in the biofilm was determined as described above. The study was repeated in the presence of 5% chicken meat juice.

Preparation of Stainless-Steel Coupons
A previously described method (Jeong and Frank, 1994) was used for the preparation of stainless-steel coupons (Type 304; diameter 5/8 inch; no. 4 finish). Briefly, steel coupons were cleaned with acetone followed by washing in distilled water and soaking in 100% ethanol. Finally, steel coupons were rinsed with distilled water, subjected to air dry and autoclaved at 121 • C for 15 min.

Biofilm Inhibition and Inactivation Assays on Stainless-Steel Coupons
To determine the effect of TC, EG, and CR in inhibiting biofilm formation and inactivating mature biofilm on stainlesssteel, a published method was used with slight modifications . For the inhibition study, steel coupons were incubated with 1 mL of C. jejuni (∼6.0 Log CFU) in 24well polystyrene plates containing SICs of phytochemicals at 20 or 37 • C for 48 h. C. jejuni counts in the biofilms on steel coupons were determined after washing three times with BPD at 24 h intervals.
For the inactivation of mature biofilm on steel coupons, mature biofilm was developed on steel coupons placed in 24well polystyrene plates containing C. jejuni (∼6.0 Log CFU) at 20 or 37 • C for 48 h. After biofilm formation, steel coupons were rinsed three times with BPD and transferred to new polystyrene plates and exposed to various doses of TC (18.91, 37.82, or 75.64 mM), EG (15.22,30.45,or 60.90 mM), or CR (16.64, 33.28, or 66.56 mM) for 1, 5, or 10 min. Following rinsing with BPD, the steel coupons were placed in 50 mL centrifuged tubes containing 3 × g sterile glass beads (diameter 2 mm; Thermo Fisher Scientific, Carlsbad, CA, United States) and 10 mL of Dey-Engley neutralizing broth, and vortexed for 1 min. The solution was serially diluted and plated on CLA. C. jejuni counts were enumerated after incubation of plates at 42 • C for 48 h. Similar inhibition and inactivation studies were conducted in the presence of 5% chicken meat juice in broth medium.

Microscopic Examination of C. jejuni Biofilms
Environmental scanning electron microscopy (ESEM) and confocal laser scanning microscopy (CLSM) were used to visualize the effect of TC, EG, and CR on biofilm architecture and the viability of C. jejuni in biofilms. C. jejuni (6 Log CFU) was inoculated on stainless-steel coupons and Lab-Tek twochamber (no. 1) borosilicate coverglass system (Nunc, Rochester, NY, United States) for ESEM and CLSM, respectively to develop biofilms at 37 • C for 2 days, and were exposed to TC (18.91 mM), EG (15.22 mM), or CR (16.64 mM) for 10 min. All the samples were rinsed with BPD before further processing. For ESEM, samples were fixed with 2.5% glutaraldehyde in 0.1 M PIPES buffer for 1 h, as described previously (Brown et al., 2014). After fixation, samples were rinsed three times with PIPES buffer and dehydrated in a series of ethanol solutions (at 30, 40, 50, 60, 70, 80, 90, and three times at 100%) for at least 10 min for each step. The biofilms were dried and coated with gold using Emitech SC7620 sputter coater (Quorum Technologies, Ltd., East Sussex, United Kingdom) for 135 s. The coated biofilm samples were visualized using SE detectors at 10 kV beam (Philips XL30 ESEM, FEI Company, Hillsboro, OR, United States). For the CLSM, the viability of C. jejuni in the biofilms were determined using FilmTracer TM Live/Dead Biofilm Viability Kit (Molecular probes, Eugene, OR, United States) according to a published method (Asakura et al., 2007). SYTO-9 and propidium iodide stains were used for the differential staining of live and dead cells. After staining for 20 min, biofilms were visualized in each chamber using a hybrid detector at 63 × objective in the Leica SP5 Confocal microscope (Leica Microsystems Inc., Buffalo Grove, IL, United States).

Gene Expression Analysis of C. jejuni Exposed to Phytochemical Treatments
The effect of TC, EG, and CR on the transcription of C. jejuni genes essential for biofilm formation was determined using real-time quantitative PCR (RT-qPCR) Wagle et al., 2017a,b). Briefly, C. jejuni (∼6.0 Log CFU/mL) was incubated in the presence or absence of SICs of TC, EG or CR at 37 • C for 12 h. The total RNA was extracted using RNA mini kit (Invitrogen, Carlsbad, CA, United States) and complementary DNAs were prepared using iScript cDNA synthesis kit (Bio-Rad Laboratories, Inc., CA, United States). The primers were designed using Primer 3 Software (National Center for Biotechnology Information, Bethesda, MD, United States) and obtained from Integrated DNA Technologies, Inc. (Coralville, IA, United States) ( Table 1). The specificity of primer was tested using NCBI-Primer BLAST, melt curve analysis and in silico PCR (Bikandi et al., 2004). The amplified products were detected by using SYBR Green reagents (Bio-Rad Laboratories, Inc.). The 16s rRNA gene was used as the endogenous control and comparative critical threshold ( Ct) method was employed to analyze relative expressions of candidate genes on Quant Studio 3 real-time PCR system (Applied Biosystems, Thermo Fisher Scientific).
Proteomic Analysis of C. jejuni in Biofilms Exposed to Phytochemical Treatments The effect of TC, EG, and CR on the proteome of C. jejuni in the biofilms was determined using liquid chromatography with tandem mass spectrometry (LC-MS/MS) as described Gene with Accession no.

Primer
Sequence (5 -3 ) 16S-rRNA (NC_002163.1) previously (Miyamoto et al., 2015). Briefly, C. jejuni (∼6.0 Log CFU/mL) was incubated in the presence or absence of SICs of phytochemicals and allowed to develop biofilms at 37 • C for 48 h. Following washing with BPD buffer, proteins were extracted using B-Per R bacterial protein extraction reagent (Thermo Fisher Scientific) and subjected to SDS-PAGE (4-12% Bis-Tris protein gel, Thermo Fisher Scientific). Each lane of gel was excised and destained with 50% acetonitrile in ammonium bicarbonate (Thermo Fisher Scientific) for 45 min and vacuum dried for 10 min. The protein extracts were treated with dithiothreitol (1.5 mg/mL in 25 mM ammonium bicarbonate; Bio-Rad) and reduced with iodoacetamide (37 mg/mL in ammonium bicarbonate; Bio-Rad) for 1 h. Following removal of iodoacetamide, the proteins were digested with trypsin (20 ng per µL in 25 mM ammonium bicarbonate) and incubated overnight at 37 • C. The resultant peptides were analyzed by LC-MS/MS technique using Agilent 1200 series microflow HPLC coupled to a Bruker AmaZon-SL quadrupole ion trap mass spectrometer (Bruker Daltonics Inc., Billerica, MA, United States) with a captive spray ionization source. The proteins were identified by matching MS/MS spectra to protein sequences of C. jejuni available at the uniprot.org using in house MASCOT software (Matrix Science Inc., Boston, MA, United States) (Perkins et al., 1999). The proteins were identified based on <5% false discovery rate using at least 2 unique peptides from a protein.

Statistical Analyses
A completely randomized design was used in the study with duplicate samples and the study was repeated three times. The data for each treatment and control were pooled from three independent trials within the same study before analysis. Bacterial counts were logarithmic transferred to maintain the homogeneity of variance (Byrd et al., 2001). The data of inhibition and inactivation assays were analyzed by using PROC MIXED procedure in the SAS version 9.3 software (SAS Institute Inc., Cary, NC, United States) and the treatment means were separated by least-square means analysis at P < 0.05 for statistical difference. The gene expression data were analyzed by using PROC MIXED procedure in the SAS and Student's t-test was used for comparisons between treatment and controls. For the proteomic analysis, Scaffold Proteome Software version 4.8 (Proteome Software Inc., Portland, OR, United States) was used to analyze MASCOT files and differentially expressed proteins between treated and un-treated biofilms were determined using Student's t-test.

Sub-Inhibitory Concentrations and
Minimum Bactericidal Concentrations of TC, EG, and CR Against C. jejuni The SICs of phytochemicals were determined based on growth curve analysis (data not shown). We observed that 0.75 mM (0.01% v/v) of TC, 0.61 mM (0.01% v/v) of EG and 0.13 mM (0.002% v/v) of CR were the highest concentration of phytochemicals that did not reduce the growth of C. jejuni and were selected as the respective SIC for the study. Similarly, the lowest concentrations that reduced C. jejuni counts significantly were 2.27 mM (0.03%) for TC, 1.83 mM (0.03%) for EG and 0.26 mM (0.004%) for CR and these doses were taken as MBC.
Effect of Chicken Juice on C. jejuni Biofilm Formation on Polystyrene Plates and Stainless-Steel Coupons Figure 1 shows the C. jejuni biofilm formation on polystyrene plates and stainless-steel coupons in the presence or absence of 5% chicken meat juice. The presence of chicken juice significantly enhanced C. jejuni biofilm formation by ∼ twofold at both temperatures on both surfaces. In addition, the absorbance (indicator of adhered and metabolically active C. jejuni) was significantly higher in the 48 h biofilms developed at 37 • C than at 20 • C.
Effect of Sub-Inhibitory Concentrations of TC, EG, and CR on C. jejuni Biofilm Formation on Polystyrene Plates and Stainless-Steel Coupons  37 • C, the reduction was ∼0.56 Log CFU/mL at both time points (P < 0.05). Similar results were observed in the presence of chicken meat juice at both temperatures (Figures 2C,D) where the three phytochemicals exerted an inhibitory effect and reduced C. jejuni biofilm formation by ∼0.5 Log CFU/mL. Carvacrol was the most effective treatment and reduced C. jejuni in the biofilm by ∼1.5 and ∼0.75 Log CFU/mL, respectively, at 20 • C and 37 • C at the end of 48 h as compared to respective controls (Figures 2C,D).
The effect of TC, EG, and CR in inhibiting C. jejuni biofilm formation on stainless-steel coupons is shown in Figure 3. All phytochemicals reduced C. jejuni in the biofilm by ∼0.6 and ∼0.45 Log CFU/mL, respectively, at 20 ( Figure 3A) and 37 • C ( Figure 3B) at both time points (P < 0.05). Similar reductions were observed when biofilm was developed in the presence of 5% chicken meat juice on steel coupons (Figures 3C,D). Although phytochemicals were effective in reducing C. jejuni counts as compared to respective controls at 24 and 48 h, the phytochemicals did not inhibit the growth of C. jejuni biofilm at 48 h as compared to 24 h except at 37 • C in CEB ( Figure 3B).

Effect of TC, EG, and CR on Mature C. jejuni Biofilms Developed on Polystyrene Plates and Stainless-Steel Coupons
The efficacy of TC, EG and CR in inactivating mature C. jejuni biofilms on polystyrene plates and steel coupons is shown in Tables 2, 3, respectively. The number of C. jejuni recovered from control (biofilms not subjected to treatments) on polystyrene plates was ∼7.8 and ∼8.4 Log CFU/mL, respectively, at 20 and 37 • C in the broth medium ( Table 2). Similar counts were observed in the presence of 5% chicken meat juice on polystyrene plates (P > 0.05). At 20 • C on polystyrene, highest doses of TC (75.64 mM; 1%), EG (60.90 mM; 1%), and CR (66.56 mM; 1%) reduced the counts of C. jejuni to below detection limit (reductions > 7.0 Log CFU/mL) in the broth medium within 1 min of exposure time. Lower doses of TC (18.91 and 37.82 mM, corresponds to 0.25 and 0.5%, respectively), EG (15.22 and 30.45 mM; 0.25 and 0.5%), and CR (16.64 and 33.28 mM; 0.25 and 0.5%) reduced C. jejuni in the biofilms in a range from 3.2 to 3.8 Log CFU/mL in 10 min. The phytochemicals were effective in inactivating C. jejuni biofilms in the presence of chicken juice as well. For example, in the presence of chicken juice at 20 • C, 66.56 mM CR reduced C. jejuni counts by 6.69 Log CFU/mL (most effective treatment) followed by 33.28 mM CR or 60.90 mM EG (reductions ∼3.8 Log CFU/mL) in 10 min exposure time ( Table 2). At 37 • C in the broth medium, 60.90 mM EG or 66.56 mM CR was the most effective in reducing C. jejuni counts by ∼3.84 Log CFU/mL at the end of 10 min. The reductions were similar in the presence of chicken juice where TC (75.64 mM), EG (60.90 mM), and CR (66.56 mM) reduced the counts by 1.64, 4.11, and 4.88 Log CFU/mL, respectively, in 10 min ( Table 2).
On stainless-steel coupons, C. jejuni counts in the control biofilms developed at 20 • C were ∼6.3 Log CFU/mL ( Table 3). The biofilms developed at 37 • C had ∼7.8 Log CFU/mL of C. jejuni present. In the biofilms developed at 20 • C in the broth medium, EG (30.45, 60.90 mM) or CR (16.64, 33.28, and 66.56 mM) reduced the counts of C. jejuni to below detection limit as early as 1 min of treatment time. TC (37.82, 75.64 mM) treatments reduced the counts to below detection limit within 5 min of treatment. The lowest dose (15.22 mM) of EG also reduced the counts below detection within 5 min (reductions > 6.25 Log CFU/mL) whereas 18.91 mM TC significantly reduced the counts by ∼4.5 Log CFU/mL in 10 min exposure time. In the presence of 5% chicken meat juice, The biofilms were exposed to phytochemical treatment for 1, 5, or 10 min. Values (Log CFU/mL) presented as mean ± standard error of the mean. * The different superscripts within columns differ significantly at P < 0.05. ND: not detectable below 1 Log CFU/mL. Control 6.38 ± 0.11 a * 6.24 ± 0.09 a 6.35 ± 0.05 a 6.08 ± 0.07 a 6.00 ± 0.04 a 6.05 ± 0.03 a 7.91 ± 0.10 a 7.84 ± 0.03 a 7.88 ± 0.05 a 7.79 ± 0.08 a 7.89 ± 0.09 a 7.75 ± 0.07 a TC (mM) 18.91 3.62 ± 0.08 b 3.34 ± 0.06 b 1.85 ± 0.08 b 4.80 ± 0.07 b 4.23 ± 0.04 b 3.65 ± 0.06 b 6.11 ± 0.08 b 5.70 ± 0.10 b 5.05 ± 0.08 b 6.43 ± 0.04 b 6.12 ± 0.05 b 5.80 ± 0.07 b The biofilms were exposed to phytochemical treatments for 1, 5, or 10 min. Values (Log CFU/mL) presented as mean ± standard error of the mean. * The different superscripts within columns differ significantly at P < 0.05. ND: not detectable below 1 Log CFU/mL. At 37 • C in the broth medium, 33.28 or 66.56 mM CR or 60.90 mM EG was the most effective and reduced the counts below detection limit in 1 min. In addition, TC at 18.91, 37.82, and 75.64 mM reduced C. jejuni counts by 2.8, 3.7, and 4 Log CFU/mL, respectively, in 10 min exposure time. Similar results were observed in the presence of chicken juice where 33.28 or 66.56 mM of CR and 60.90 mM EG were the most effective treatments and reduced C. jejuni counts by ∼7.7 Log CFU/mL. In addition, the antibacterial activities of the TC, EG, and CR were significantly increased with an increase in exposure time on steel coupons (P < 0.05). For example, at 37 • C in the presence of chicken juice, 16.64 mM CR had significantly a higher reduction in 10 min than in 1 min exposure time (reductions ∼5.5 vs. 3 Log CFU/mL).

Effect of Phytochemicals on Mature Biofilms Architecture and Viability of C. jejuni in the Biofilms
The effect of TC, EG, and CR on the biofilm architecture and viability of C. jejuni in the biofilms was visualized using ESEM and CLSM (Figure 4). The biofilm structure was intact and covered with EPS in control C. jejuni biofilm not exposed to phytochemicals (Figure 4A), whereas the exposure to TC (18.91 mM), EG (15.22 mM), and CR (16.64 mM) for 10 min removed a majority of the biofilm structure as depicted by loss of EPS and scattering of C. jejuni cells (Figures 4B-D, respectively). In addition, confocal microscopy revealed that the majority of C. jejuni were live (stained green) in the control biofilms, and dead (stained red) after treatments with TC, EG, and CR for 10 min (Figures 4a-d).
Effect of Phytochemicals on the Expression of C. jejuni Genes Coding for Biofilm Formation Figure 5 shows the effect of TC, EG, and CR on the expression of C. jejuni genes critical for biofilm formation. Phytochemicals at SICs level significantly modulated the expression of genes encoding for motility, cell surface modifications, stress response and quorum sensing. The SIC of TC significantly downregulated bacterial cell mobility genes flaA, flaB, and flgA by ∼11.7, 9, and 4.3-fold, respectively ( Figure 5A). However, quorum sensing gene (luxS) responsible for cell to cell communication during biofilm formation was upregulated by ∼ sixfold (P < 0.05). The expression of stress response genes (cosR, ahpC) was not affected by TC treatment (P > 0.05). Similar to TC, CR also downregulated motility genes flaA, flaB, flgA and upregulated luxS (Figure 5B). The phytochemical EG downregulated (fold change > 2) majority of the tested genes (flaA, flaB, flaG, flgA, waaF, cosR, and ahpC) critical for C. jejuni biofilm formation ( Figure 5C).

Effect of Phytochemicals on C. jejuni Biofilm Proteome
Overall, 76 proteins were identified in the proteome of C. jejuni present in the biofilms. Table 4 shows the differential protein expression of C. jejuni in biofilms subjected to phytochemicals treatment as compared to control biofilms. The presence of SIC of TC significantly upregulated three proteins and downregulated three proteins critical for biofilm formation (P < 0.05). The upregulated proteins were flagellar protein (FliL), cytochrome c553 (Cyf) and putative peptidyl-prolyl cisisomerase (Cbf2), whereas periplasmic nitrate reductase (NapA), chaperone (DnaK), and bacterioferritin were downregulated. Similar results were observed with EG, which upregulated cytochrome c553 (Cyf) and downregulated NapA (P < 0.05). The SIC of CR significantly upregulated NapB and FliL proteins and downregulated NapA and DnaK proteins. However, other identified proteins were not affected by the presence of phytochemicals (P > 0.05).

DISCUSSION
Campylobacter contamination of poultry products represents a major risk factor for human campylobacteriosis. Despite being nutritionally fastidious, there is sufficient evidence that biofilm formation plays a critical role in the survival of C. jejuni in the processing environment (Murphy et al., 2006;García-Sánchez et al., 2017;Castro et al., 2018). The role of C. jejuni biofilm as a source of carcass contamination at the poultry processing facility is currently unknown especially since a comprehensive study determining C. jejuni biofilm at processing plant facility is lacking. Therefore, as a first step toward understanding the role of C. jejuni biofilms as a source of potential carcass contamination, we have developed C. jejuni biofilms on various surfaces commonly encountered in the processing plant and at conditions mimicking the processing plant environment. Furthermore, the efficacy of phytochemicals in killing C. jejuni biofilms was investigated.
The antibiofilm potential of phytochemicals was tested in the presence of 5% chicken meat juice to represent the meat environment as it has been shown previously that the presence of meat extracts modulates biofilm formation in C. jejuni (Brown et al., 2014). Brown et al. (2014) had also reported that chicken and pork meat juice (5-100%) enhanced C. jejuni biofilm formation by increasing attachment of C. jejuni to abiotic surfaces.
In order to effectively control C. jejuni biofilms in the processing plant, both prevention of biofilm formation and killing of pre-formed mature biofilms are important. Therefore, we tested the efficacy of phytochemicals in reducing biofilm formation as well as inactivating mature C. jejuni biofilms. We used the SIC of phytochemicals in the inhibition studies and hypothesized that the phytochemicals affect the critical genes and proteins required by planktonic cells for biofilm formation. The biofilms were developed for 48 h since our results (data not shown) and literature (Reeser et al., 2007) suggest that C. jejuni forms mature biofilm by 48 h. Carvacrol was most C. jejuni (6 Log CFU) was inoculated on stainless-steel coupons and Lab-Tek two-chamber (no. 1) borosilicate coverglass system for ESEM and CLSM, respectively, to develop biofilms at 37 • C for 2 days. The biofilms were exposed to phytochemicals for 10 min followed by gentle washing. For the ESEM (A-D), the treated biofilms were fixed with 2.5% glutaraldehyde and dehydrated in a series of ethanol concentration (30-100%). Dried biofilms were coated with gold using Emitech SC7620 sputter coater and visualized using 10 kV beam in ESEM. For the CLSM (a-d), the treated biofilms were stained with 0.01 mM SYTO (green dye) and 0.06 mM propidium iodide (red) for 20 min, and visualized at 63 × objective in Leica SP5 confocal microscope.
effective in inhibiting C. jejuni biofilms formation on polystyrene plates at 24 h (Figure 2), whereas these phytochemicals were not significantly different in their antibiofilm efficacy among on steel coupons (Figure 3) (P > 0.05). Similar results were reported with the SIC of TC, EG, and CR against L. monocytogenes (Upadhyay et al., 2013), where the authors observed significant reductions (∼1.5 Log CFU/mL) in counts in the biofilms developed for 48 h at 25 and 37 • C. Although the phytochemicals were effective in reducing C. jejuni biofilm formation compared to respective control (Figures 2, 3), they did not inhibit the growth of C. jejuni biofilm at 48 h as compared to 24 h except at 37 • C in CEB on steel coupons ( Figure 3B). This could potentially be due to degradation of phytochemicals leading to reduced efficacy or microbial metabolism of these compounds. However, the exact cause of this observation is not known.
Previous studies have shown that phytochemicals at SICs level significantly modulate the expression of genes critical for virulence of various pathogenic bacteria (Qiu et al., 2010;Maisuria et al., 2016), including C. jejuni (Castillo et al., 2014;Kovács et al., 2016;Upadhyay et al., 2017b;Wagle et al., 2017a,b). However, the potential mechanism of action of TC, EG and CR against C. jejuni genes critical for biofilm formation has not been studied. Therefore, a gene expression study was performed to study the change in gene expression profile of C. jejuni in response to TC, EG and CR. A variety of genes critical for C. jejuni biofilm formation has been previously characterized (Bronowski et al., 2014). Bacterial genes encoding flagellins (FlaA, FlaB, and FlaG) and flagellar biosynthesis protein (FlgA) are necessary at the initial stage of C. jejuni biofilm formation (Kalmokoff et al., 2006;Kim et al., 2015). Previously, proteomic analysis revealed that flagellins proteins (FlaA, FlaB) were expressed at higher levels in C. jejuni biofilms than in planktonic cells (Kalmokoff et al., 2006). Moreover, C. jejuni flgA mutants were non-motile leading to reduced biofilm formation on food contact surfaces (Kim et al., 2015). Similarly, cellbinding protein (Peb4) and inner core of lipooligosaccharides (WaaF) protect the bacterial cell during stress and contribute to survival by forming biofilm (Asakura et al., 2007;Naito et al., 2010). It was previously reported that CosR is an essential response regulator in C. jejuni, which regulates the transcription of oxidative stress genes (katA, ahpC) (Hwang et al., 2012;Turonova et al., 2015). In addition, CosR is the key protein in the maturation of biofilm and its overexpression was reported to enhance biofilm formation in C. jejuni (Oh and Jeon, 2014). Likewise, quorum sensing or cell-to-cell signaling has been reported to play an important role in the cell attachment to form biofilm. Biofilm formation was significantly reduced in C. jejuni luxS mutants compared to wild-type (Reeser et al., 2007). Therefore, we selected all the aforementioned genes critical for C. jejuni biofilm formation. We observed that TC, EG, and CR at SICs significantly downregulated the expression of select flagellar genes critical for initial attachment during biofilm formation (Figure 5). However, these phytochemicals differ from one another in reducing expression of quorum sensing and stress response genes. For example, EG significantly downregulated cosR and ahpC, however, these genes were not affected by TC and CR. Moreover, quorum sensing gene luxS was upregulated by TC and CR indicating that it could be a bacterial  compensatory mechanism against phytochemical treatments. These findings suggest that TC, EG, and CR may act through different mechanism(s).
To determine the effect of TC, EG, and CR on proteome of C. jejuni present in the biofilms, LS-MS/MS based protein identification and quantification of phytochemical-treated and un-treated C. jejuni biofilms was conducted. Periplasmic nitrate reductase (NapABC enzyme) is an enzyme responsible for utilization of nitrate as an energy source for bacterial growth and also protects against oxidative stress (Pittman et al., 2007). Similarly, heat shock protein 70 kD (also known as chaperone DnaK) contributes to motility, stress responses, and pathogenesis in Escherichia coli (Arita-Morioka et al., 2015). A loss of this protein lead to reduction in biofilm formation in Staphylococcus aureus. Similar findings were observed with Streptococcus mutans where it regulates RpoS and CsgD proteins essential for curlidependent biofilm formation (Rockabrand et al., 1998;Arita-Morioka et al., 2015). In our proteomic analysis, NapA was significantly downregulated in TC, EG, and CR-treated biofilms as compared to un-treated C. jejuni biofilms ( Table 4). The SICs of TC and CR also reduced the expression of DnaK. In addition, we identified a few uncharacterized proteins and the specific roles of such proteins need to be explored in future studies. These results varied from the effect of EG on proteome of C. jejuni planktonic cells where proteins contributing to motility (MotA, MotB, FliA, FliD, FliF, FliL, and FliY) and energy taxis (IlvH, CetA, and CetB) were downregulated (Upadhyaya et al., 2017). In a separate study, TC significantly down-regulated the expression of several proteins (FrdA, AhpC, PstS, CeuE, HemC, and AspA) that contribute to cellular metabolism and stress tolerance on C. jejuni planktonic cells . This variation could be due to the differential protein expression between planktonic and biofilm states of C. jejuni as reported by Kalmokoff et al. (2006). In addition, the differential protein/gene expression between two states of C. jejuni could potentially contribute to the discrepancy in results between gene expression and proteomic analysis as the gene expression study was conducted on planktonic cells in the present study. These findings suggest that antibiofilm effect of TC, EG, and CR could potentially be mediated through modulation of these proteins critical for C. jejuni biofilm formation.
To inactivate mature C. jejuni biofilms, we used bactericidal concentrations of phytochemicals and hypothesized that phytochemicals kill biofilm associated C. jejuni by potentially disrupting their cell membrane thereby leading to membrane dysfunction, cellular damage and inactivation of biofilms from the surfaces. C. jejuni biofilms were developed for 48 h since our TTC staining results suggest that C. jejuni biofilm matures by 48 h (Figure 1). We found that TC, EG and CR were effective in killing C. jejuni in the mature biofilms on polystyrene ( Table 2) and steel surface ( Table 3) at both temperatures. Previously, Lu et al. (2012) had reported inactivation of C. jejuni biofilms after 24 h treatment time with 1 µM concentration of diallyl sulfide (an antimicrobial agent from Allum spp). Antibiofilm efficacy of TC, EG and CR has also been reported against L. monocytogenes (Upadhyay et al., 2013) and E. coli (Perez-Conesa et al., 2006) suggesting that the phytochemicals exert antibiofilm effect on several pathogens, however, commonalities in their mechanism of action against various pathogens or the presence of a single target across pathogens that the plant compounds affect has not been identified yet. Considering these results, the select phytochemicals could be effective in reducing C. jejuni biofilm formation either in monoculture or when present with other biofilm forming foodborne pathogens; however, further experiments are needed to validate the results on multispecies biofilm of C. jejuni.
In the inactivation studies, 66.56 mM CR was the most effective in killing C. jejuni biofilms formed in the presence of chicken meat juice on polystyrene surfaces at both temperatures (Table 2). Similarly, in the presence of chicken meat juice, CR was the most effective followed by EG and TC in inactivating C. jejuni biofilm on stainless-steel coupons at 37 • C in 1 min exposure time (Table 3). In general, we observed an increase in the antibiofilm effect of TC, EG and CR with an increase in their concentrations and more effective killing was found on biofilm developed at 20 • C than at 37 • C. The increased effectiveness of phytochemicals at 20 • C could be due to weak attachment of metabolically active C. jejuni to surfaces at 20 • C than at 37 • C after 48 h as reflected by the absorbance value in TTC staining (Figure 1). Similar results were reported by Reeser et al. (2007) where the absorbance was five times lower at 25 • C than at 37 • C in the C. jejuni biofilms developed for 48 h. In our study, phytochemicals were more effective in reducing biofilms developed on steel surfaces (Table 3) than on polystyrene plates (Table 2) owing to good hydrophobicity of plastic surfaces for interaction with bacteria leading to stronger biofilm formation. Previously, Reeser et al. (2007) had determined that the physiochemical properties of the abiotic surfaces affect the C. jejuni attachment on surfaces to form biofilm and reported a higher degree of C. jejuni biofilm on hydrophobic surfaces (polystyrene and polyvinyl chloride) than on hydrophilic surfaces (glass, copper, and steel).
To validate the inactivation results, we visualized the architecture of treated biofilms using ESEM and CLSM. We observed that EPS was detached from bacterial cell surface leading to scattering of C. jejuni cells after 10 min of exposure to TC (18.91 mM), EG (15.22 mM), or CR (16.64 mM) (Figures 4A-D). Since EPS is critical for C. jejuni biofilms, loss of EPS could be a potential antibiofilm mechanism of the tested phytochemicals. In addition, predominant C. jejuni in the control were live (green) whereas the majority of C. jejuni were dead (red) after treatments (Figures 4a-d). Similar results of confocal microscopy were reported previously with TC, EG and CR against L. monocytogenes biofilms (Upadhyay et al., 2013).
In conclusion, TC, EG, and CR were effective in reducing C. jejuni biofilm formation and inactivating mature biofilms on polystyrene plates and stainless-steel coupons at 20 and 37 • C. This reduction could potentially lead to reduced product contamination in processing plant. However, a correlation between a reduction in C. jejuni biofilm counts and corresponding reductions in pathogen load on carcass has not been conducted and could be a focus of future research. In addition, the effects of phytochemicals in monospecies biofilms of other C. jejuni strains as well as in multispecies C. jejuni biofilms should be evaluated in future studies. Proteomic analysis revealed select genes and proteins critical for biofilm formation were modulated by phytochemicals. However, further experiments are warranted to establish a correlation between changes in gene and corresponding protein expression in the biofilm.

DATA AVAILABILITY
The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.

AUTHOR CONTRIBUTIONS
BW and AU designed the study. BW, IU, SS, KA, RL, and AU conducted the experiments. BW wrote the manuscript. AU, KV, DD, and AD critically analyzed and revised the manuscript.