Lactobacillus reuteri and Enterococcus faecium from Poultry Gut Reduce Mucin Adhesion and Biofilm Formation of Cephalosporin and Fluoroquinolone-Resistant Salmonella enterica

Simple Summary Enteric infections, such as Salmonella spp., are common in the poultry sector. Even though the European Union has banned the use of growth-promoting antibiotics; many countries continue to use these synthetic medications, leading to the emergence of antibiotic resistance (especially cephalosporin and fluoroquinolones) in non-typhoidal Salmonella, limiting treatment options. Probiotics are beneficial bacteria that reside in the intestine and help improve the host’s health; they are also one of the most popular antibiotic alternatives. As a result, we set out to collect lactic acid bacteria from the poultry gut that had never been fed a medicated diet and conduct in vitro probiotic studies. L. reuteri PFS4, E. faecium PFS13, and E. faecium PFS14 were screened as potential probiotic candidates. The obtained strains show good aggregation, mucin adherence, antibiofilm, and anti-salmonella activities. More research is now being conducted to determine the strain’s efficacy in commercial poultry. Abstract Non-typhoidal Salmonella (NTS) can cause infection in poultry, livestock, and humans. Although the use of antimicrobials as feed additives is prohibited, the previous indiscriminate use and poor regulatory oversight in some parts of the world have resulted in increased bacterial resistance to antimicrobials, including cephalosporins and fluoroquinolones, which are among the limited treatment options available against NTS. This study aimed to isolate potential probiotic lactic acid bacteria (LAB) strains from the poultry gut to inhibit fluoroquinolone and cephalosporin resistant MDR Salmonella Typhimurium and S. Enteritidis. The safety profile of the LAB isolates was evaluated for the hemolytic activity, DNase activity, and antibiotic resistance. Based on the safety results, three possible probiotic LAB candidates for in vitro Salmonella control were chosen. Candidate LAB isolates were identified by 16S rDNA sequencing as Lactobacillus reuteri PFS4, Enterococcus faecium PFS13, and Enterococcus faecium PFS14. These strains demonstrated a good tolerance to gastrointestinal-related stresses, including gastric acid, bile, lysozyme, and phenol. In addition, the isolates that were able to auto aggregate had the ability to co-aggregate with MDR S. Typhimurium and S. Enteritidis. Furthermore, LAB strains competitively reduced the adhesion of pathogens to porcine mucin Type III in co-culture studies. The probiotic combination of the selected LAB isolates inhibited the biofilm formation of S. Typhimurium FML15 and S. Enteritidis FML18 by 90% and 92%, respectively. In addition, the cell-free supernatant (CFS) of the LAB culture significantly reduced the growth of Salmonella in vitro. Thus, L. reuteri PFS4, E. faecium PFS13, and E. faecium PFS 14 are potential probiotics that could be used to control MDR S. Typhimurium and S. Enteritidis in poultry. Future investigations are required to elucidate the in vivo potential of these probiotic candidates as Salmonella control agents in poultry and animal feed.

The in vitro characterization of potential probiotics is considered as a practical approach to evaluate isolates against multidrug-resistant (MDR) pathogens [26][27][28]. Competitive inhibition, growth kinetics, and co-aggregation are some of the most used methods to investigate the potential of probiotics for pathogen control. Several in vitro and in vivo studies have provided evidence that probiotic bacteria can help control Salmonella in food animals [29,30]. As part of the one health concept, controlling Salmonella in food producing animals and food production systems using probiotics could ultimately reduce pathogen spread to humans. Probiotic-mediated control of cephalosporin-and quinolone-resistant NTS could help contain the spread of antimicrobial resistance to other pathogens, further benefiting animals and humans.
Although routinely used as human probiotics, lactic acid bacteria (LAB) isolated from the poultry gut have not been extensively studied as potential probiotics for use in the poultry industry. To the best of our knowledge, very little information on the potential antagonistic activity of LAB against third generation cephalosporin and quinolone resistant NTS is available. The current study aims to screen probiotic LAB isolated from poultry gut for their potential inhibitory effect against MDR S. Typhimurium and S. Enteritidis of a poultry origin.

Isolation of Lactic Acid Bacteria
Cloacal swab samples were collected from broilers (n = 10) in three local poultry farms located in the Islamabad capital territory. The birds' health was certified by the resident veterinarian before sampling. The birds were reared on an antibiotic-free diet. Samples were immediately stored at 4 • C and were processed within 6 h. The fecal samples were processed as previously described [31]. Three to five suspected lactic acid bacteria colonies were characterized by Gram-staining and catalase testing, followed by microscopic examination. Only Gram-positive, catalase-negative isolates with a rod or coccus shape were selected for further studies.

Test Pathogens
S. Typhimurium FML15 and S. Enteritidis FML18, previously isolated from poultry feces, were selected as the test pathogens. Both serovars were multi-drug resistant (MDR), and resistance was observed against third generation cephalosporin and quinolone, as characterized in our previous study [32].

Safety Assessments 2.3.1. Hemolytic Activity
The hemolytic activity was determined as described previously [25]. Overnightgrown bacterial cultures were streaked on Blood agar (Oxoid, Hampshire, UK). Agar plates were incubated at 37 • C for 48-72 h and were observed for the formation of any clean (α-hemolysis), greenish (β-hemolysis) hemolytic zones or no zone (γ-hemolysis) around the LAB colonies [33]. Staphylococcus aureus was used as a positive control.

DNase Activity
For the DNA degradation activity, bacterial colonies were streaked on DNase agar (Oxoid, Hampshire, UK). The plates were incubated for 48-72 h at 37 • C and were observed for the clear zone of the DNase activity [34]. DNase activity was considered positive in the clear or pinkish zones surrounding the colonies [35]. S. aureus was used as a positive control.

Identification of the Lactic Acid Bacterial Isolates
The selected lactic acid bacteria were identified by partial sequencing of the 16S rDNA genes. The genomic DNA was extracted using the phenol-chloroform extraction method, as described previously [38]. The DNA was quantified using a nanodrop spectrophotometer (Thermo Scientific) as per the user manual. The extracted DNA was used as a template in PCR targeted at the 16S rRNA gene using primers 9F (GAGTTTGATCCTGGCTCAG) and 1510R (GGCTACCTTGTTACGA), with the following PCR conditions: 1 cycle of 94 • C for 5 min followed by 35 cycles of 94 • C for 30 s, 54 • C for 45 s, and 72 • C for 30 s, and finally 1 cycle of 7 min at 72 • C [39]. The purified PCR products of the selected LAB isolates were sequenced [40]. The strains were identified by comparing the sequences with the GenBank database using the Basic Local Alignment Search Tool [41].

Acid Tolerance
The resistance to a low pH was assessed in vitro to determine the isolates' ability to withstand passage through the gastric cavity, as described previously [39]. LAB isolates were grown for 24 h at 37 • C in MRS and M17 broth. In addition, 30 µL overnight-grown LAB isolates were suspended in 150 µL of MRS broth and M17 broth adjusted to pH 2.0 by 1M HCl. The cell suspensions were incubated anaerobically at 37 • C for 4 h. After incubation, bacterial growth was monitored by measuring the absorbance at 600 nm. All experiments were performed in triplicate.

Bile Tolerance
Bile tolerance tests for LAB isolates were performed as described [39]. First, 30 µL of overnight grown LAB isolates were suspended in 150 µL of MRS, and M17 broth with 0.3% bile salt (Oxoid, Hampshire, UK) was added to each well, while mixtures without bile salt were used as a control. The cell suspensions were incubated anaerobically at 37 • C for 4 h. Optical density (OD) at 600 nm was measured for monitoring the growth kinetics on a microtiter plate reader (Bio-Rad Laboratories, CA, USA). All of the experiments were performed in triplicate.

Lysozyme Tolerance
The lysozyme tolerance test was performed as described previously [39]. The overnightgrown cultures were harvested by centrifugation at 3500× g for 5 min. The bacterial cells were washed with phosphate buffer saline (PBS) and were re-suspended in a sterile PBS solution. The cell suspension (10 µL) was then inoculated into a PBS solution containing lysozyme (100 mg/L). Isolates inoculated in PBS without lysozyme were used as a control. LAB isolates were incubated at 37 • C. OD was measured at 600 nm after 30 and 90 min.

Phenol Tolerance
Gut microbes can break down aromatic amino acids, which result in the formation of phenol, which can inhibit the growth of LAB. Therefore, resistance to phenol tolerance by LAB is vital for their survival in GIT. Overnight-grown bacterial cultures were inoculated in respective broths supplemented with 0.4% phenol. OD was measured at 600 nm [39].
2.6. Cell Surface Properties 2.6.1. Auto Aggregation and Co-Aggregation Assay The aggregation ability of LAB strains was studied as described previously [42]. The overnight grown culture was harvested by centrifugation at 5000× g for 20 min at 4 • C, and was washed and then suspended in PBS. Optical densities were adjusted at 0.25 ± 0.05 OD to maintain the number of bacterial cells (10 7 -10 8 CFU/mL). For auto-aggregation, the OD of the LAB strains was recorded at 0 h and 24 h at 37 • C. The aggregation percentage was expressed as [1 − (A Time /A 0 ) × 100], where A Time represents the absorbance of the mixture at 24 h and A 0 represents the absorbance at 0 h (21). The criteria for the auto-aggregation ability determination were (low, 16-35%; medium, 35-50%; and high, 50% and above) [43].
For the co-aggregation assay, bacterial suspensions of LAB strains, as described above, were mixed with an equal volume (4 mL) of the overnight grown cultures of Salmonella in a sterile falcon tube; the mixtures were incubated at 37 • C. After 24 h, the OD 620 nm was measured, and the percent co-aggregation was calculated as follows: [(A pathog + A LAB )/2 − (A mix )/(A pathog C A LAB )/2] × 100, where A pathog and A LAB represent the absorbance in the tubes containing only the pathogen and LAB strain, respectively, and A mix represents the absorbance of the mixture at 24 h [42].

Microbial Adhesion to Hydrocarbon Test (MATH)
A bacterial cell surface hydrophobicity assay was performed with some modifications [44]. LAB isolates cultivated in MRS and M17 broth at 37 • C for 24 h were harvested by centrifugation at 8000× g for 10 min, and the cell pellet was washed thrice with sterile PBS and was re-suspended in the same media. The optical densities were maintained 1 ± 0.05 at 600 nm. Initially, 3 mL of the bacterial cell suspension was transferred to a sterile falcon tube, followed by the addition of 1 mL of hydrocarbons. Three hydrocarbons were tested in this study, namely: toluene (apolar, aromatic), xylene (apolar, aromatic), and chloroform (polar, aliphatic). The tubes were incubated at 37 • C for 10 min for temperature equilibrium, followed by 15 s vortexing, and were then set at 37 • C for 20 min for the phase separation. The lower aqueous phase was carefully collected in a separate glass tube, and OD 600 nm was recorded.
OD i is the initial OD of the cell suspension, and OD t is OD of the aqueous phase recorded at 600 nm after 20 min.

Mucin Adhesion Assay
The previously reported method was used to determine the in vitro mucin adhesion assay [45]. Flat-bottom 96 well microtiter plates were coated with 300 µL porcine mucin type III (10 mg/mL (Sigma-Aldrich, Inc. St. Louis, MO, USA) suspended in sterile PBS kept overnight at 4 • C. Plates were washed thrice with sterile PBS to remove unbound mucin from the wells. For competitive mucin adhesion, 100 µL of LAB culture with absorbance adjusted to 0.25 ± 0.05 and 100 µL of each of the Salmonella serovars were added to the mucin-coated wells simultaneously and were co-incubated for 90 min. After incubation, the wells were washed five times with PBS. Adhered bacterial cells were then treated with 300 µL Triton X in a sterile phosphate buffer solution to the separate bacterial cells. The viable cell count was measured by enumerating the LAB strains and Salmonella serovars on MRS agar, M17 agar, and SS agar. The % relative adhesion was calculated by (CFU/mL after adhesion/CFU/mL before adhesion) × 100.

Biofilm Formation Potential of Lactic Acid Bacteria
The quantification of the biofilm formation by lactic acid bacteria was determined as described previously [21]. Briefly, 150 µL of MRS and M17 broth were added to each well of 96 flat-bottom microtiter plates along with 50 µL of an overnight culture of L. reuteri and E. faecium. The 96 well microtiter plates were incubated at 37 • C for 48 h. To quantify the biofilm formation, the wells were gently washed thrice with PBS. Biofilms were then fixed with 2 mL methanol for 15 min, and the microplates were dried at room temperature. Then 2 mL of the 2% v/v crystal violet solution was added to each well and was incubated at room temperature for 5 min. The excess stain was removed by washing with sterilized water. The adherent cells were removed with 2 mL of 33% v/v glacial acetic acid. Each well's optical density (OD) was measured at 600 nm using a plate reader (Bio-Rad, Hercules, CA, USA). The experiment was performed in triplicate. The cut-off (OD C ) was defined as the mean OD value of the negative control. On the basis of OD, isolates were classified as follows: (4 × OD C ) < OD = strongly adherent, (2 × OD C ) < OD ≤ (4 × OD C ) = moderately adherent, OD C < OD ≤ (2 × OD C ) = weakly adherent, and OD ≤ OD C = non-adherent [46].

Inhibition of Pathogenic Biofilm Formation
The effect of cell-free supernatant (CFS) of the LAB strains on the biofilm formation of S. Typhimurium and S. Enteritidis was evaluated as previously described [47]. The modified crystal violet assay was performed in 96-well microtiter plates for the biofilm quantification. First, 100 µL overnight-grown Salmonella strains were added in a well in the presence of 100 µL of pH neutralized CFS of the LAB isolates. The cultures were incubated at 37 • C for 48 h. The Salmonella test pathogens without CFS were used as a positive control. After incubation, the developed biofilm was washed three times with 200 µL of distilled water and was air dried. Then, 100 µL of 0.2% crystal violet (Merck KGaA, Gernsheim, Germany) was added to each well, and the plate was incubated for 20 min to allow for biofilm staining. Subsequently, the wells were washed three times with distilled water, and were air-dried and treated with 200 µL of 95% ethanol (Sigma-Aldrich, Inc. St. Louis MO USA) to dissolve the crystal violet crystals. The plate was incubated for 30 min, and the intensity of the crystal violet was measured at 600 nm using a microplate reader (Bio-Rad, Hercules, CA, USA). The ability of CFS to affect biofilm formation was calculated by comparing the absorbance values of the CFS treated wells versus the untreated control wells. The experiments were performed in triplicate. To estimate the reduction percent of CFS, the following formula was used: Percentage inhibition = 100 − [(OD 600 of wells in the presence of CFS × 100)/OD 600 of wells in the presence of MRS]

Scanning Electron Microscopy
Scanning electron microscopy (SEM) was used to identify any changes or ruptures in the cell morphology of the Salmonella due to the effect of the CFS of the LAB strains, as described previously [48]. The overnight-grown culture of both Salmonella serovars were treated with CFS of L. reuteri PFS4, E. faecium PFS13, and E. faecium PFS14, alone and in combination, in a sterile 24-well microtiter plate (Corning, Corning, NY, USA) with a 12-mm round cover glass and were incubated for 48 h at 37 • C. The overnight-grown culture of both Salmonella enterica serovars in a tryptic soy broth (TSB) media with 12-mm round cover glass was used as the control. After incubation, the microtiter plate was gently washed to remove the non-adherent cells before fixation with 2.5% glutaraldehyde in a potassium phosphate buffer (50 mM, pH 7). The cover glass was dehydrated by chilled ethanol in a series (v/v) ranging from 30, 50, 70, 90, and 100%. For SEM, the specimens were dried to the critical point, coated with gold, and photographed with a scanning electron microscope (JSM-IT500HR, JEOL, Akishima, Japan).

Determination of the Antimicrobial Activity of the LAB Isolates
Aa time kill assay was performed as described previously [22]. Salmonella test pathogens were grown in a Luria broth (LB) media for 24 h at 37 • C. One hundred microliters of overnight-grown S. enterica serovars and pH neutralized CFS of LAB strains were co-cultured in a 96-well sterile microtiter plate and incubated at 37 • C. The number of viable bacteria was counted on an SS agar plate 0, 4, 8, 12, 24, and 48 h after incubation. Salmonella enterica strains without the cell-free supernatant of the LAB strains were taken as the positive control. The experiment was performed in triplicate.

Statistical Analysis
All of the experiments were carried out in triplicate. The standard deviations were determined with Microsoft Excel (Microsoft Corp., Albuquerque, NM, USA). A t-test was performed at the 95% confidence interval with SPSS20 (IBM Co., New York, NY, USA) to determine the statistical significance of the data.

Bacterial Isolates
A total of 17 potential LAB strains were selected from the gut of broiler chickens. Among the 17 isolates, nine were chosen from MRS agar plates and eight were chosen from M17 agar plates. The isolates were identified as LAB based on the following characteristics: Gram-positive, catalase negative, non-motile, and cocci-or rod-shaped.

Safety Assessment
Hemolytic, DNase, and Antibiotic Susceptibility Assay All 17 isolates showed negative results for hemolytic (γ-hemolysis) and DNase activity. However, a high resistance to most of the tested antibiotics, e.g., ciprofloxacin, chloramphenicol, third and fourth generation cephalosporin, amikacin, gentamicin, and vancomycin, was observed in the study ( Table 1). Most of the strains were sensitive to rifampin, imipenem, meropenem, linezolid, and nalidixic acid. The criteria for selecting potential probiotics were as follows: isolates must be susceptible to clinically significant antibiotics, i.e., quinolones, ampicillin, amoxicillin-clavulanic acid, and cephalosporin [49]. Only three isolates, PFS4, PFS13, and PFS14, were chosen for further investigation based on the selection criteria.

Evaluation of Probiotic Properties
Tolerance to GIT Related Stresses The survival of isolates in the GIT is an essential feature of probiotics. All 17 isolates showed tolerance to GIT related stresses as shown in ( Figure S1). After selection of three LAB isolates on the basis of their safety profile, the tolerance to GIT-related stresses of selected LAB strains was shown in (Figure 1A-D). Acid tolerance is a vital characteristic for all probiotics. Bile salt tends to damage the cell membrane structure, so tolerance to bile salt is an essential characteristic of probiotics. All LAB isolates survived to exposure of pH 2 and 0.3% bile for 4 h (Figure 1A,B). The results indicate that all of the tested strains showed a high resistance to acid and bile. These isolates were subsequently evaluated for phenol resistance, where these showed increased tolerance to 0.4% phenol with OD values >1.000 after 24 h of incubation ( Figure 1C). All of the tested LAB isolates showed significant resistance to lysozyme (100 mg/L) after 90 min ( Figure 1D).

Molecular Identification of LAB Strains
The 16S rRNA sequences obtained were compared using the public database of NCBI. As a result, the LAB isolates were identified as L. reuteri PFS4, E. faecium PFS13, and E. faecium PFS14. A phylogenetic tree of bacterial isolates was created based on the minimum evolutionary distance to obtain a well-resolved tree. It was found that isolate PFS4 was under the group of Lactobacillus spp. and was closely related to identified organism L. reutei strain 1663 with a strong similarity of a 97% branch value. Isolates PFS13 and PFS14 was under the group of Enterococcus spp. and were closely related to the identified organism Enterococcus faecium strain BALG3 and Enterococcus faecium strain IMAU98437, with a strong similarity of 95% and 96% branch value, respectively ( Figure 2).

Auto-Aggregation and Co-Aggregation Assay
Auto-aggregation helps with adherence to epithelial cells in the intestine, and thus provides competitive adhesion against gut pathogens. All of the strains tested in this study exhibited some degree of auto-aggregation, ranging from 71.2% to 80.1%. The results indicate that each strain showed a good auto-aggregation ability according to the criteria described by [43]. Among these probiotic strains, L. reuteri PFS4 isolates showed the highest auto-aggregation capacity (80.1 ± 3.1%) at 24 h.
The co-aggregation ability of selected LAB isolates with Salmonella depends on the serovars ( Table 2). E. faecium PFS13 showed the maximum co-aggregation ability (66 ± 1.1% and 71 ± 1.5%) with S. Typhimurium and S. Enteritidis, respectively, while L. reuteri PFS4 and E. faecium PFS14 exhibited moderate co-aggregation with both Salmonella serovars. A combination of LAB isolates showed a high co-aggregation percentage (52.2% and 68.6%) with S. Typhimurium FML15 and S. Enteritidis FML18, respectively. Table 2. Auto and co-aggregation of potential LAB strains isolated from poultry.

In Vitro Mucin Adhesion Assay
All probiotic strains and Salmonella strains demonstrated a good mucin adhesion profile in the monoculture. The adhesion to porcine mucin films was >80% for all of the probiotic and Salmonella strains. The results revealed that L. reuteri PFS4 exhibited the highest percentage adhesion (92.6%), followed by E. faecium PFS13 (86.3%) and E. faecium PFS14 (84%) (Figure 4). However, the adhesion of Salmonella strains was significantly reduced in the presence of LAB isolates. The adhesion percentage of pathogenic strains, S. Typhimurium PF40 and S. Enteritidis PF76, was low (55.3% to 70.6%, and 51.6% to 65.3%, respectively) in the presence of LAB isolates compared with the untreated wells.

Biofilm Formation Assay
The biofilm formation by the probiotics is helpful in the competitive exclusion of gut pathogens in the intestine. Hence, the potential of probiotic candidates to form biofilms was evaluated in an in vitro assay. All of the probiotic candidate strains were capable of developing a moderate to strong biofilm ( Figure 5). Both E. faecium strains exhibited a strong biofilm formation (OD > 2.0) potential, whereas L. reuteri PFS4 showed a moderate biofilm formation (OD < 2.0).

Effect of CFS on Biofilm Formation Ability of Salmonella enterica
The ability of probiotics to reduce Salmonella biofilms is an important characteristic for therapeutic probiotics post Salmonella infection. Therefore, the Salmonella biofilms were treated with pH neutralized probiotic CFS to assess the biofilm inhibition potential. Maximum inhibition was observed in the case of probiotic combination (90 and 92%) followed by L. reuteri PFS4 (87 and 89%), E. faecium PFS13 (80 and 87%), and E. faecium PFS14 (79 and 83%) for both S. Typhimurium and S. Enteritidis, respectively. The Salmonella biofilm was significantly inhibited (p ≤ 0.05) by the CFS of the three probiotics strains, alone or combined ( Figure 6). However, the combination of CFS from all strains was better than the single strain CFS.

Scanning Electron Microscopic Study
The biofilm produced by S. enterica serovars was confirmed by SEM. It was observed that the control sample (S. enterica serovars cultured into sterile TSB) showed a high cell density and aggregation ( Figure 7A,F). Compared with the control, the neutralizing CFS of the LAB strains reduced the adherence and aggregation of the tested Salmonella enterica strains after 48 h of incubation. These results agree with the findings of the crystal violet technique, which showed a significant reduction in bacterial adherence and biofilm formation ( Figure 6).

Effect of CFS on the Growth Kinetics of Salmonella enterica Serovars
The results of the time-kill assay indicated the ability of CFS to reduce the growth of Salmonella enterica serovars (Figure 8). The growth of S. Typhimurium FML15 and S. Enteritidis FML18 was significantly inhibited after culturing with CFS in all of the tested time points compared with the control cultures incubated without CFS (p ≤ 0.05). The inhibitory effect was more prominent on both serovars, as indicated by the lower CFU, particularly after 12 h of incubation. The CFS of the LAB combination significantly reduced the count of both Salmonella serovars by 2 log compared with the control Salmonella without any CFS after 12 h of incubation.

Discussion
The emergence of multi drug resistant (MDR) Salmonella enterica serovars Typhimurium and Enteritidis constitutes a significant health and economic threat for poultry and humans [8]. Therefore, the application of probiotics in the poultry industry as a suitable alternative to antibiotics in order to control enteric pathogens has received tremendous attention in recent years [50]. Thus, we investigated potential probiotics from the chicken gut to control clinically significant antibiotic-resistant Salmonella enterica.
Initially, 17 isolates from 10 poultry fecal samples were isolated based on their colony morphology, Gram staining, and biochemical characteristics. However, only three strains, L. reuteri PFS4, E. faecium PFS13, and E. faecium PFS14, were retained based on the selection criteria. The findings were consistent with previous studies, which found L. reuteri [51] and E. faecium [52] in the chicken gut. According to the previous study, L. reuteri is the most common Lactobacillus species in the chicken GIT, primarily found in the crop and cecum [53]. In addition, many previous studies have reported on the protective effect of L. reuteri [54,55] and E. faecium [56] against Salmonella serovars and other gut pathogens.
Potential probiotic LAB strains should withstand digestive system stress to benefit the health of their hosts. The ability to tolerate acid, bile salts, lysozyme, phenol, and the production of antimicrobial agents are all good indicators of a strain's survival in the GIT [57]. In this study, all 17 isolates tested for GIT-related stress tolerance exhibited a high potential to tolerate a low pH (2), 0.3% bile salt concentration, lysozyme (100 mg/mL), and 0.4 % phenol. The ability of LAB isolates to tolerate a low pH and bile is not a surprise, as one of LAB's natural habitat is the gastrointestinal tract of humans or animals [58]. Our results are in agreement with previous findings that reported on the survival of different LAB strains, including Enterococcus spp., L. salivarius, L. johnsonii, and L. reuteri, isolated from healthy chicken gut, being able to survive at pH 2 and 0.3% bile concentration [59][60][61]. Another study reported the resistance of LAB strains to lysozyme and 0.4% phenol isolated from poultry gut at varying degrees [51].
Lactobacilli is a probiotic genus widely employed in animal production [62]. Most Lactobacillus species (L. acidophilus, L. rhamnosus, and L. reuteri) strains demonstrate no pathogenicity or acute oral toxicity in animals [63]. Lactobacillus are considered GRAS "Generally Recognized as Safe" because of their long history of safe use in animal feed [64]. However, some researchers reported some enterococcal species as opportunistic pathogens that can cause infections in humans and animals. Thus, determining the safety of these strains is critical for selecting these strains for industrial purposes and, more importantly, as probiotics. However, in several investigations, E. faecium has also been used as a probiotic candidate in poultry birds [65,66].
All of the initially screened 17 isolates showed negative results for a hemolytic DNase activity and demonstrated variable antimicrobial resistance patterns towards the tested antibiotics ( Table 2). These results are following the previous study where E. faecium and L. reuteri showed a negative hemolytic and DNase activity [67]. The isolated LAB should be sensitive to antibiotics in order to avoid any potential transfer of undesirable antibiotic resistance to the intestinal microbiota [68][69][70]. Recently, many researchers have revealed that commensal microbes, including LAB isolates, contain antibiotic resistance genes similar to those found in pathogens [71]. Genes conferring resistance to tetracycline and cephalosporin detected and characterized in the Lactococcus spp. and Lactobacilli constitute a reservoir of resistance for potential food and gut pathogens, thus presenting safety issues [72,73]. These results are in agreement with previous findings [74][75][76], which reported the safety and sensitivity of L. reuteri and Enterococcus strains isolated from poultry gut towards common antibiotics. The high intrinsic resistance and susceptibility of probiotic microorganisms to a variety of antibiotics are quite significant. Some LAB species, including L. reuteri, L. fermentum, L. rhamnosus, E. faecium, E. faecalis, and L. acidophilus, have intrinsic resistance to vancomycin, sulfamethoxazole/trimethoprim, and nalidixic acid [77]. LAB with acquired/transferable drug resistance genes are not GRAS (generally recognized as safe) and should not be added to probiotic foods or animal feed. Conjugative plasmids typically carry antibiotic resistance genes that can be passed on to other bacteria, leading to antibiotic-resistant enteropathogenic bacteria [78]. Therefore, due to safety issues, the antimicrobial resistance pattern of the bacterial species is an essential criterion for their selection as probiotic candidates.
Bacterial adhesion to intestinal surfaces could be initiated by non-specific physical interactions such as hydrophobic interactions, followed by adhesion by specific cell wall components at a second level [79]. Microbial cell surface hydrophobicity (MATH) is the most commonly used in vitro method to assess cell surface hydrophobicity in lactic acid bacteria [80]. Some researchers have reported a correlation between hydrophobicity and adhesion [81]. The hydrophobicity test can be considered as a pre-test for probiotic bacteria's ability to adhere to epithelial cells, preventing pathogens' colonization (Falah et al., 2019). Hydrophobicity is an important property for enhancing the first contact between the bacteria and host cells. The hydrophobicity of the cell surface of L. reuteri and E. faecium is determined in order to know the cell surface properties responsible for aggregation and adhesion. In our study, LAB isolates showed variable hydrophobicity with different hydrocarbons (53-89%). Low to high hydrophobicity abilities were observed in L. reuteri LR11, LR19, and LR26 (30-71.10%) isolated from the poultry gut [60]. In addition, [82] obtained a high hydrophobicity (>80%) among Enterococcus spp. isolated from poultry. Some authors have considered that L. reuteri and E. faecium, with a high hydrophobicity, have a better ability to bind to epithelial cells [83]. Aggregation helps probiotic strains colonize in the intestine and significantly attaches intestinal epithelial cells, preventing Salmonella adhesion. This test is essential for the selection of probable probiotic bacteria from the gut [84].
Auto-aggregation allows microorganisms of the same species to form self-forming communities, and this process is most commonly associated with microorganisms adhering to the intestinal mucosa [85]. Our data revealed that LAB isolates showed a high autoaggregation ability ranging from 71-80%. Similar findings were observed in previous studies, where L. reuteri, E. faecium, and other Lactobacillus spp. showed high auto-aggregation (70-90%) abilities [86,87]. In addition, some in vivo studies reported that the ability of high auto-aggregation of L. reuteri and E. faecium was strongly associated with adhesion [88,89].
Co-aggregation is the intercellular adhesion of different strains that are linked to the ability to associate with pathogens. The co-aggregation potential of gut probiotics enables the host to limit enteric pathogens like S. Typhimurium and S. Enteritidis [90]. In our study, E. faecium PFS13 had the most remarkable ability to co-aggregate with Salmonella Typhimurium FML15 and Salmonella Enteritidis FML18 (66.1% and 71.5%, respectively). Therefore, all three LAB strains in our study, with moderate to high co aggregation abilities, are potential probiotic candidates. The results obtained in our study correspond with previous findings, where L. reuteri, Enterococcus spp., and L. acidophilus showed a moderate to high co-aggregation (40-60%) ability with enteric pathogens, including S. enterica [42,91]. Many of the guidelines for probiotics' health benefits regard their ability to stay viable and conform to the host's intestine as a critical factor. Adherence allows probiotics to live longer in the GI tract and improves bacterial-host interactions, but it also aids in reducing gastric motility. As a result, probiotics' ability to adhere to mucosal surfaces and epithelial cells is essential [92].
Bacterial adhesion to the host mucin is thought to be critical in helping probiotic species colonize in any setting, the ability to exclude food-borne pathogens competitively, and to improve their ability to stimulate the immune system. The mucus layer not only serves as the first physical barrier to bacterial invasion of the gut epithelium, but it also serves as the first point of contact for gut bacteria with host cells. For many pathogens like Salmonella, mucin adhesion is an important element in virulence in the host. [93]. The mucus of the small and large intestines may contain many receptors that mediate the adherence of beneficial or harmful microorganisms [94]. All LAB isolates in this study showed good adhesion (84-92.6%) to porcine mucin Type III. In a previous study, L. reuteri showed a better adhesion (74%) ability than other LAB strains to the intestinal mucin [95].
On the other hand, the adhesion of Salmonella serovars was significantly reduced when they co-cultured with LAB strains. The previous findings of an in vitro mucin adhesion assay revealed that L. reuteri, L. rhamnosus, and L. casei competitively excluded (13.26% to 25%) S. paratyphi A, S. Typhimurium SA2093, S. flexneri, and S. aureus TISTR from adhesion to porcine mucin. The inhibition of pathogen adhesion to the mucin is reported to prevent translocation and subsequently infection [96,97].
Pathogenic and non-pathogenic microorganisms form biofilms responsible for maintaining such microorganisms in healthy ecosystems in vivo [98]. The biofilm formation ability can be considered beneficial for probiotic strains, promoting colonization and longterm permanence on the host's mucosa [99]. Our data showed that all three LAB isolates are strong biofilm producers. Moderate to strong biofilm production by L. plantarum, L. reuteri, L. acidophilus, L. casei subsp. Pseudoplantarum. and E. faecium have been observed in previous studies [23,100]. Scanning electron microscope (SEM) images demonstrated a strong adherence and aggregation of S. Typhimurium and S. Enteritidis bacterial cells. Our SEM images also showed that the adherence of cells was minimized after CFS treatment. Similar findings were observed in a previous study where the CFS of different probiotic strains reduced biofilm formation [22]. The results of the in vitro mucin adhesion assay, aggregation abilities, cell surface hydrophobicity, and biofilm formation capability of our LAB isolates showed strong adhesion abilities. They can prevent NTS in poultry gut through a competitive adhesion mechanism. Some of the Lactobacillus spp. with a low adhesion and co-aggregation ability were excluded in a previous study, as they could not be selected as potential probiotic candidates [101]. Our findings provide the foundation for understanding L. reuteri and E. faecium adhesion mechanisms and for predicting adherence in various host models. The authors of [102] revealed that S. Enteritidis growth in poultry birds was considerably reduced by L. reuteri, with a good coaggregation ability and mucin adhesion profile.
Lactic acid bacteria produce various antimicrobial agents, including organic acids, ethanol, diacetyl, hydrogen peroxide, and antimicrobial peptides [103,104]. The inhibition of pathogenic bacterial biofilms through probiotics is an attractive target for therapeutic intervention [105]. Probiotics have received significant attention in recent years, leading to the discovery of biofilm inhibitors to counter foodborne pathogens, including S. Typhimurium and S. Enteritidis [42,106]. Our data suggest that pH neutralized CFS of selected LAB strains alone and in combination significantly reduced the biofilm formation (up to 84%) of Salmonella strains compared with the control. The anti-biofilm property of CFS of L. reuteri and E. faecium against Salmonella enterica has been reported in previous studies [23,42,106]. The antagonistic activity of certain microbes and their extracellular antibacterial compounds found in cell-free supernatants (CFSs) provides an excellent potential for controlling foodborne pathogens, including E. coli and Salmonella enterica [107]. The findings of the growth kinetic study revealed that all three LAB isolates, individually and in combination, significantly reduced the growth of Salmonella test pathogens for up to 12 h. These results of the antagonistic activity against Salmonella could be due to various antimicrobial substances produced by probiotic strains. L. reuteri and E. faecium produced various antimicrobial substances such as lactic acid, acetic acid, hydrogen peroxide, bacteriocins, and bacteriocins, like inhibitory substances. The authors of [108][109][110][111] studied the efficacy of CFS on MDR Salmonella and other Enterobacteracae species and revealed that CFS significantly inhibits the growth of pathogens.

Conclusions
Based on our findings, we may infer that the LAB strains isolated from poultry gut exhibit endurance to GIT related stress. L. reuteri and E. faecium strains demonstrated a co-aggregation potential and competitively reduced the mucin adhesion of S. Typhimurium and S. Enteritidis. This study provides evidence that isolated probiotic strains from poultry gut have an in vitro antagonistic activity towards extended spectrum cephalosporin and fluoroquinolone (key antibiotics for salmonellosis) resistant Salmonella serovars. Therefore, L. reuteri PFS4, E. faecium PFS13, and E. faecium PFS14 can be potential candidates to control extended spectrum cephalosporin and fluoroquinolones resistant Salmonella serovars after being subjected to in vivo studies. In vivo studies using these strains can be performed to elucidate their safety profile, growth, and disease prevention ability. As part of the One Health approach, resistant-specific pathogen control can help mitigate the resistant pathogen load in animals and it's spread to the associated food ecosystem.