The study was conducted with 30 C. jejuni strains from the analysis of 280 cooled chicken carcasses ready for commercialization from September to November of 2015, from a Brazilian poultry exporting industry, with a complete production cycle.

Isolation was previously performed according to International Standards Organization (2006) and identification of the species was done by multiplex PCR according to Harmon et al. (1997). After confirmation, the strains were stored at −80°C in UHT skimmed milk.

To perform subcultures for reactivation, the strains were seeded for 48 h in Bolton broth (Oxoid) supplemented with 5% of defibrinated ram blood (Laborclin) at 37°C in microaerophilic conditions (Probac), followed by plaque peal in CCDA Agar (Campylobacter Blood-Free Selective Agar Base) (Oxoid) incubated under the same conditions (International Standards Organization, 2006).

In the adhesion and biofilm assays, the strains were cultured for 48 h under microaerophylia at 37°C in 20 mL of Mueller Hinton broth (MH) (Difco), using as inoculum the culture present in the plates of CCDA Agar. In parallel, these assays were performed using 20 mL of Mueller Hinton broth supplemented with 5% of chicken juice (Birk et al., 2004)—equivalent to the 100% concentration according to Brown et al. (2015)—to simulate the conditions of industry. After growing in both conditions, the suspensions were adjusted to an OD₆₀₀ = 0.22 to 0.28, corresponding to a count of 10⁴ CFU/mL. The cells were centrifuged (5,000 rpm, 10 min, 4°C) and washed twice (0.9% NaCl) before the beginning of cultures for adhesion and biofilm assays.

The scanning electron microscopy (SEM) analysis was performed for simple (only C. jejuni) and mixed biofilms (C. jejuni paired with Salmonella sp., Escherichia coli, Pseudomonas aeruginosa or Staphylococcus aureus). The inoculum preparation, growth conditions and incubation were the same as previously described for Campylobacter: microaerophilic atmosphere at 37°C for 48 h. Both, in the SEM and in the biofilm matrix composition assay, only three C. jejuni strains, phylogenetically distinct by PFGE and with different classifications of BFI (Biofilm Formation Index) were used.

In phylogenetic analysis by PFGE, the bacteria were cultured at 42°C overnight in a brain and heart infusion agar (BHI agar) with 5% of defibrinated sheep blood under microaerophilic conditions. The present culture on the agar was resuspended in saline (0.85% NaCl) until reaching OD₆₁₀ = 0.570–0.820 for carrying out the enzymatic digestion process.

Controls used in the study were C. jejuni strains (ATCC 33291, NCTC 11351, and IAL 2383) and C. coli (ATCC 43478). For mixed cultures, Escherichia coli strain (ATCC 25922), P. aeruginosa (PAO 1), Salmonella Enteritidis (ATCC 13076), and Staphylococcus aureus (ATCC 25923) were used.

The adhesion test was performed according to Sulaeman et al. (2009) with modifications. Briefly, 200 μl of the bacterial suspension containing 10⁴ cells prepared in MH broth and MH with 5% of chicken juice was added in 96-well plates. After incubation for 4 h at 37°C under microaerophylia, the adherent bacteria were washed twice with 0.9% NaCl solution and collected in wells filled with the same solution by scraping during 90 s. The obtained cell suspension was serially diluted and seeded in CCDA agar for enumeration in CFU. All strains were evaluated in triplicate and in three independent replicates.

Biofilms were formed as described by Kudirkiene et al. (2012), with modifications. Briefly, 200 μl of the bacterial suspension containing 10⁴ cells prepared in MH broth and MH with 5% of chicken juice was added in 96-well plates. For biomass formation, the plates were incubated for 48 h at 37°C in microaerophilic conditions.

After incubation, the media were removed, the wells were washed twice with 0.9% NaCl solution and dried for 30 min at 55°C. Total biomass was measured by fixation with 0.1% Crystal Violet (LaborClin) for 5 min, followed by elution with alcohol-acetone solution, containing 80% of ethanol and 20% of acetone (Synth®). The eluted dye was removed from each well and placed in a new 96-well microtiter plate for reading at OD₅₉₅ (BA–bacteria adhered). The assays were done with eight replicates for each strain in three replicates. For the determination of the Biofilm Formation Index, the following formula was used: BFI=BA−PCBS

Where BFI represents the final result regarding the Biofilm Formation Index, BA the optical density obtained in the mixture of bacteria adhered, PC the absorbance value in the control wells without microorganisms, BS the optical density (OD₆₀₀) of the suspended cultures in MH and MH with 5% of chicken juice (Naves et al., 2008). The final classification followed Table 1.

The number of sessile cells was determined by counting in CFU. After biofilm formation as described in the previous item, the wells were washed twice with a 0.9% NaCl solution, and the biomass was removed by scraping the wells for 90 s. The obtained cell suspension was serially diluted and plated on CCDA agar plates to obtain the number of CFU. All the assays were performed in triplicate, on three independent occasions.

The genomic DNA was extracted by the Wizard Genomic DNA Purification Kit (Promega), following the protocol provided by the manufacturer. Purified DNA (10 ng) was used as template for all PCR reactions. The PCR conditions and primers used in this study are described in Table 2.

The studied genes were flaA (motility), cadF (intracellular colonization), luxS (quorum-sensing mechanism), dnaJ (thermotolerance), htrA (aids in growth under stress), cbrA (resistance to osmotic shock), and sodB (tolerance to oxidative stress).

PCR reactions were performed using the GoTaq® Green Master Mix kit (Promega) according to the manufacturer's instructions. The amplified products were subjected to 1.5% agarose gel electrophoresis using the TBE 0.5x runner buffer (Invitrogen) and as a molecular weight standard of 100 pb marker (Invitrogen).

To examine the interaction between C. jejuni biofilms with biocides components and nanoparticles, the protocol described by Lu et al. (2012) was used. The chemical compounds tested were: Chlorhexidine 1% solution, Sodium Hypochlorite 1%, Peracetic Acid 0.8% and Zinc Oxide (ZnO) nanoparticles 6 mmol/L.

Ten colonies grown in CCDA plates were diluted in 10 mL of 0.9% NaCl solution, adjusted according Mc Farland scale 0.5. From this solution, a 100 μL aliquot (corresponding to 10⁷ cells), was inoculated onto a sterile cellulose membrane with 0.45 μm of porosity and 47 mm of diameter on a Brucella agar plate (Difco) enriched with 5% of defibrinated sheep blood. The plates were incubated at 37°C in microaerophilia and in every 24 h the membrane was transferred to a new plate, during 3 days.

Subsequently, the membrane was placed in a flask containing 20 mL of MH broth with respective concentrations of the chemical compounds. The flasks were incubated in microaerophylia at 37°C for 24 h. Subsequently, the membrane was washed three times with phosphate buffer (PBS), followed by treatment in 25 mL of 0.1% trypsin for 15 min at room temperature. Thereafter, the resulting solution of the incubation underwent serial dilutions for further counting.

The biofilm stability assay was performed according to the protocol described by Chaignon et al. (2007), with some modifications. Biofilms were formed into 96-well plates as described above. After 48 h of growth, the culture medium was removed, the wells were washed twice with sterile 0.9% NaCl solution and then filled with 200 μl of a proteinase K solution (Invitrogen, USA) on concentration of 1 mg/ml in 20 mM Tris (pH 7.5) and 100 mM NaCl or 200 μl of a 10 mM sodium metaperiodate solution (Sigma-Aldrich, USA) prepared in 50 mM acetate buffer (pH 4.5). The plates were incubated for 2 h at 37°C. After treatment, the biofilms were washed with 200 μL of sterile 0.9% NaCl and stained with 1% crystal violet. The absorbance was evaluated on a plate reader at 595 nm with an alcohol-ketone solution containing 80% of ethanol and 20% of acetone (Synth®), as white. The experiment was performed in biofilms of three C. jejuni strains formed with chicken juice. All assays were performed in eight wells, on three independent occasions.

The preparation of the material for analysis in SEM was done according to Brown et al. (2014) with modifications. Simple and mixed biofilms in the MH and chicken juice media were formed in glass beads with a diameter of 5 mm, respecting the growth conditions described for Campylobacter: microaerophilic atmosphere at 37°C for 48 h. After biomass formation, the samples were fixed with 2.5% glutaraldehyde and 2.5% paraformaldehyde in 0.1 M buffer PBS (pH 7.4) overnight at 4°C. The fixative was removed, and the samples washed three times with PBS buffer. The beads were post-fixed with 1% osmium tetroxide for 2 h and washed three times with PBS buffer. The beads were dehydrated in a series of ethanol solutions (30, 40, 50, 60, 70, 80, and 90% and then three times at 100%) for 20 min for each step.

The samples were dried in CPD (Critical Drying Point) (CPD 030, Baltec, Germany) using liquid carbon dioxide as the transition fluid. The samples were coated with a 20 nm thick layer of gold (SCD 050, Baltec, Germany) and visualized on MEV VP Zeiss Supra 55 SEM FEG operating at 5 kV.

The isolates were typed by PFGE according to the protocol described in the Center Disease and Control (2013). Digestion of the intact genomic DNA was done with 30 U of the enzyme Sma I (Invitrogen) for 2 h at 25°C. The DNA fragments were separated on 1% agarose gel (SeaKem Gold) in 0.5X TBE buffer in the CHEF DRIII (Bio-Rad) apparatus, for a period of 18 h, with the following parameters, 200 v, 120° angle, Gradient of 6 v/cm and buffer temperature of 14°C.

The gels were stained with ethidium bromide and photographed under UV light. The analysis for dendrogram formation was performed using GelCompare II software. The comparison of the band patterns was performed by the UPGMA analysis method, using the Dice similarity coefficient.

The obtained results were analyzed using GraphPad Prism, version 6.0. Qualitative and quantitative biofilm formation tests were evaluated using simple variance analysis (ANOVA). For the biofilm inhibition test, ANOVA was used to compare the results of the control with the resistant strains in the test groups, and to analyze the counts between the control strains and tests separately. For the simple comparisons of two variables, in the biofilm stability test, Student's t-test was used. All tests were performed at a confidence level of 95%.

The adhesion assays were conducted in Mueller Hinton and Muller Hinton supplemented with chicken juice media with an initial bacterial concentration of approximately 10³ CFU/well. The indices found showed that the ability to adhere to the polystyrene varied according to the strain.

The results showed that all tested strains had adhesion capacity when inoculated in Muller Hinton (MH) and MH + 5% of chicken juice, but there was a reduction in counts (p < 0.05) compared to the initial inoculum when the strains were held at Mueller Hinton.

In Mueller Hinton, 46.7% (14/30) of the strains showed medium adhesion pattern, with a count above the average in all the tests, and 53.3% (16/30) of the strains showed weak adhesion by presenting lower values than those obtained in the general mean of the initial inoculum (p < 0.05), as shown in Figure 1.

The values were significantly higher (p < 0.05) when the strains were inoculated in the chicken juice, with all 30 (100%) strains classified as strongly adherent, because they had higher counts than the initial inoculum.

The ability of these strains to adhere strongly in conditions similar to those present in the avian industry (chicken juice) helps to explain their survival and persistence in the slaughterhouse. The 4-h incubation period was sufficient for the initial establishment of the biofilm structure, and thus could act as a constant source of contamination in the industry.

The nutritive particles available in chicken juice can form a thin layer above the surface of the polystyrene wells and on glass surfaces that facilitate this bacterial adhesion (Li, 2016).

All of C. jejuni strains (100%) were capable of forming strong biofilms when supplemented with chicken juice by the crystal violet test (Table 3). The same did not occur when in the presence of Mueller Hinton, where none of the strains presented a strong producer profile under this condition. The inclusion of chicken juice promoted a significant increase in bacterial biomass, increasing in average 1.70 the Biofilm Formation Index (BFI) when compared to the value found in non-supplemented samples.

In the condition not supplemented with chicken juice, 10/30 (33.3%) strains did not form biofilms, 13/30 (43.3%) were classified as weak producer and 7/30 (23.3%) as medium producer, according to Table 1.

These data shows that surfaces in contact with organic matter inside the industry may harbor these biofilms, since there is a constant presence of chicken juice during the processing of chicken carcasses. If hygiene measures are not frequent and sufficiently conducted, the exudate present in the chicken carcass guarantees conditions for C. jejuni maintenance.

The data obtained in the biofilm counts proved the differences obtained in the tests with crystal violet. Starting from a constant initial inoculum (p > 0.05) in all assays, it was observed that in both, the adhesion and biofilm formation, had a significant increase in the counts and in bacterial multiplication in the presence of chicken juice when compared to the counts in Mueller Hinton (Table 4).

The results obtained in the adhesion assays showed that in relation to the initial inoculum there was a significant reduction in the counts when the strains were inoculated in MH and a significant increase in the chicken juice (p < 0.05). This fact reveals the difficulty of maintaining and developing the initial structure of the biofilm in Mueller Hinton.

The values obtained in the adhesion (4 h) in chicken juice were similar to those found after 48 h (biofilm) in MH, indicating another evidence of the superiority of chicken juice in the establishment of the sessile form of C. jejuni. In addition, the high counts detected in chicken juice after biofilm formation, suggests that in this condition the biofilm may be well established.

Analysis of the seven genes potentially required for the formation of strong biofilms in C. jejuni showed that all strains (100%) have the potential to form strong biofilms, since all the genes evaluated were identified in the 30 strains.

These findings are consistent with the results obtained in the counts and the colorimetric test (crystal violet) of the biofilms of C. jejuni in the presence of chicken juice. This supplement probably allowed expression of genes associated with the transition to sessile form, including the studied genes.

The use of chemical agents had a high potential for elimination of viable cells from C. jejuni biofilms. For all the used products, was a significant reduction in the bacterial counts in relation to the untreated biofilm. In 17/30 (56.7%) of biofilms, total elimination of the microorganism was observed for all chemical agents tested.

Figure 2 shows the counts obtained in the untreated biofilms, which obtained a mean value of 6.41 Log CFU/mL (p > 0.05), and the resistant biofilms treated with the different products that showed growth after 24 h in contact.

The inclusion of sodium hypochlorite 1% allowed the survival of 6/30 (20.0%) of the strains, with a mean count of 1.30 log CFU/mL. This value did not differ between strains (p > 0.05), and demonstrated a reduction of about 5.11 log cycles relative to untreated biofilm.

There was also no difference in counts after the use of chlorhexidine 1% (p > 0.05) for 4/30 (13.3%) strains tolerant to this agent. The mean count of 1.33 log CFU/mL after treatment showed a mean decrease of 5.08 log cycles compared to the control.

For peracetic acid and ZnO nanoparticles (NPs), the reduction in the number of CFUs varied significantly (p < 0.05) among the tolerant strains, indicating that persistence in the presence of these agents may be a characteristic strain-dependent.

Seven of the 30 strains (23.3%) in the sessile form survived in the presence of peracetic acid with counts varying from 1.34 to 2.16 log of CFU/mL. Therefore, the reduction was from 4.25 to 5.07 log cycles compared to the control.

In the presence of ZnO NPs, it was observed that 13/30 (43.3%) strains were tolerant and presented the highest log of CFU/mL, alternating from 2.09 to 4.07. The decrease was from 2.34 to 4.32 log cycles in relation to the control.

In general, chlorhexidine 1%, sodium hypochlorite 1% and peracetic acid 0.8% presented equivalent efficiency in the control of C. jejuni biofilm (p > 0.05), due to the high number of biofilms removed and by the low counts obtained for the resistant strains. ZnO NPs presented the lowest treatment efficacy (p < 0.05).

Table 5 shows the resistance profiles of the agents obtained for the 13 strains that showed growth after the biofilm inhibition test.

The presence of biofilms resistant to disinfectant agents shows that there are probably intrinsic or extrinsic adaptive mechanisms that allow their survival. According to Table 5, two strains showed resistance profile VI (F206 and F246), that is, they are tolerant to all agents and may characterize a problem in the industry due to the difficulty of eliminating them and the risk of dissemination of this characteristic to other strains.

At the SEM assay we observed changes in biomass formed for the three types of biofilm patterns identified in the MH: F80 (unable to produce biofilm), F255 (weak producer) and F256 (medium producer). In addition, difference in yield was noted when the substrate for its growth was supplemented with chicken juice (Figure 3).

Figure 3A shows the presence of isolated bacteria, indicating the inability to form biofilm in this condition. In 4c and 4e the initial formation of biofilm is observed, with primary production of extracellular matrix. Already in 3b, 3d, and 3f (in chicken juice) there is formation of the mature biofilm, with a tridimensional structure of the evident matrix.

The composition assay performed with proteinase K and sodium metaperiodate promoted protein degradation and carbohydrate oxidation (Figure 4).

In both MH and chicken juice biofilms, the proteinase treatment almost completely removed the biomass formed by the three strains tested. However, the carbohydrate oxidant showed little or no effect (F255 in MH) on the biofilm produced by these strains.

For the mixed biofilm assays of C. jejuni with Escherichia coli, P. aeruginosa, Salmonella Enteritidis and Staphylococcus aureus the SEM demonstrated competitive disadvantage of the three strains of C. jejuni tested. The predominance of the other species was clear as shown in Figure 5, indicating the selection pressure exerted by the other species on C. jejuni.

In Figure 6 was possible to verify the alteration in the biomass formed by the crystal violet method compared to the control group composed of simple biofilm of only C. jejuni.

In practically all the tests, there was a higher production of biomass in relation to the control. The exception is in the mixed biofilms with P. aeruginosa that exhibited a different behavior from that found for the other species. In the presence of MH, the biofilm production was exacerbated (p < 0.001), but in chicken juice the biomass was significantly lower, showing that some factor present in chicken juice could inhibit the transition to sessile form in this specie.

This fact was also observed in SEM, by the formation of a denser biomass in MH when compared to chicken juice (Figures 5E,F).

The assays concerning to the composition of the matrix for mixed cultures are probably more related to the other species and not, in fact, to C. jejuni. For all mixed biofilms the composition was predominantly proteic, except for mixed biofilms with P. aeruginosa whose presence of carbohydrates was more evident (data not shown).

Twenty three pulsotypes (A-V) were identified by PFGE, being 17 of them characterized as distinct profiles (Figure 7).

Five profiles (A, I, K, M, and U) were classified as clusters with homology higher than 80%, composed of strains with the same genotype. The M-type pulse was designated as a clone because it showed 100% of similarity.

The K, M, and U pulsotypes, grouped isolated strains on the same date, indicating possible cross-contamination among the samples. However, the A and I pulses presented isolated strains at different dates suggesting the persistence of this genotype in the industry, probably due to the biofilm formation.

During the last decade, C. jejuni has been regularly presented as the leading cause of bacterial foodborne infections in Europe and the USA. Given the importance to public health of this zoonosis, it is relevant to understand the survival mechanisms adopted by this pathogen.

One of the mysteries of the genus Campylobacter is that it is a pathogenic microorganism that survives successfully in the host and industrial environment under stressful conditions, and paradoxically is a mandatory microaerophilic that survives poorly under controlled laboratory conditions. In addition, in comparison to other agents causing foodborne disease, such as E. coli and Salmonella spp., C. jejuni needs a low infective dose (500–800 CFU) to cause disease in the host (Black et al., 1988). Although this may contribute to infection, it is still unclear what allows the bacteria to survive during transmission under adverse conditions.

Survival in a biofilm would be an explanation to protect bacteria from various environmental stresses, antimicrobial agents and/or disinfectants and the immune response of the host.

In this study we found that these structures represent a reservoir of cells and that the level of biofilm formation by C. jejuni is clearly increased under conditions similar to those found in the industry with the presence of chicken juice.

The detection of viable cells in significant quantities in biofilms formed in chicken juice corroborates the idea that survival and persistence in the production chain may represent the main problem of contamination in final product. Despite the use of microaerophylia for this study, it is known that the mature biofilm can provide an adequate environment for microaerophilic growth allowing the ideal conditions for maintenance and dissemination of this pathogen (Reuter et al., 2010).

The biofilm formation involves the succession of several steps, starting with initial adhesion. For this reason, C. jejuni's ability to adhere to a inert surface was investigated, in order to subsequently assess their ability to initiate and develop the biofilm. The adhesion capacity was variable and lower in the 30 strains tested in MH. The delayed adhesion profile may indicate less ability to acquire the sessile form, but may also be related to the need for a prolonged period of contact with the surface to lead to a stronger future adhesion (Turonova et al., 2015). In contrast, in chicken juice the counts showed high adhesion capacity for all strains. The medium supplemented with chicken juice allowed a better condition for adhesion to the inert surface (Li, 2016).

The results obtained in both colorimetric and quantitative tests revealed the superiority of chicken juice in relation to MH.

Chicken carcass exudates contain a complex mixture of carbohydrates, proteins, lipids, and sugars (Chmielewski and Frank, 2007), providing an ideal medium for the proliferation and survival of bacteria. The accumulation of these organic materials allows the formation of micro-layers on the surfaces that aid in bacterial fixation, together with greater availability of nutrients (Hwang et al., 2012).

Thus, in the industrial environment, the presence of meat-based exudates may exacerbate the problem of contamination by C. jejuni. Our results add and are consistent with the findings of Brown et al. (2015) who also detected the efficiency of chicken juice at different concentrations in the biofilm production for five Campylobacter strains.

Once the phenotypic characterization was performed concerning the sessile kind of living, analysis of the specific genes revealed that all strains possess the genes required to develop a biofilm.

Thus, gene identification in the strains of C. jejuni did not explain the differences in the classification of the biofilms formed in MH. In contrast, the identification of all the genes surveyed in all strains is consistent with the strong producer character obtained in chicken juice. Therefore, chicken juice is likely to provide all the necessary conditions for expression of the genetic potential recorded by the presence of flaA, cadF, luxS, dnaJ, htrA, cbrA, and sodB genes and this same ability is not detected in MH.

The genes linked to quorum-sensing, adhesion, adverse conditions and motility were all previously described as important for the acquisition of the sessile form (Kalmokoff et al., 2006; Svensson et al., 2009; Howlett et al., 2012; Sulaeman et al., 2012; Avila-Ramirez et al., 2013; van Alphen et al., 2014).

There are reports that flagellar expression is required for the formation of biofilms by C. jejuni (Lehtola et al., 2006; Reeser et al., 2007), including flaA and flaB genes (Reuter et al., 2010). However, the absence of these characteristics does not completely prevent the acquisition of the sessile form. The advantage in the expression of this characteristic is due to the initial fixation, biofilm structuring, orientation to a pre-existing biofilm in addition to the correlation with other non-flagellar extracellular proteins that contribute indirectly to the sessile lifestyle (Howard et al., 2009; Kim et al., 2015).

Numerous genes in Campylobacter were previously described as mediators of adhesion in vitro. Among them, the cadF gene that encodes the binding proteins CadF fibronectin (Konkel et al., 2010).

Several enzymes and proteins are already described by the involvement in bacterial protection against oxidative stress, whose action is related to peroxide or superoxide detoxification. Among them, the enzyme superoxide dismutase (SodB) appears as a major regulator in C. jejuni (Flint et al., 2014; Kim et al., 2015).

Some quorum-sensing systems have already been detected in Campylobacter. The production of AI-1 (acyl-homoserine autoinducer) represents one of these mechanisms, which accumulates in the extracellular environment and diffuses freely in the bacterial cytoplasm, which at high levels binds to a cellular transcription enhancer (luxS) that encodes the luciferase, a metabolic key enzyme in the SAM recycling pathway (S-adenosylmethionine). This metabolite is essential in the performance of important biosynthetic reactions, such as the methylation of bacterial DNA, the synthesis of polyamines and bacterial vitamins. The most important performance of the luxS gene is associated with the synthesis of a new AI called autoinducer-2 (AI-2). Increased bacterial population growth also promotes elevation of AI-2 concentrations in the environment. The luxS gene acts in the formation of several molecular compounds, which together are called AI-2 variants. These molecules have potential for recognition and inclusion of mixed populations and of the same species in biofilms (Xavier and Bassler, 2005).

Much of C. jejuni has functional LuxS enzymes and is capable of producing AI-2. However, the presence of nutrients is necessary for the production of AI-2, and these are found in foods, such as milk and chicken juice, even when the microorganisms are kept under adverse conditions, such as in oxidative stress and in low temperatures (Ligowska et al., 2011; Parveen and Cornell, 2011; Tazumi et al., 2011; Plummer, 2012).

In the poultry industry investigated, the chemical agents: peracetic acid 0.8%, sodium hypochlorite 1% and chlorhexidine 1%; are used by the quality control team. On the other hand, ZnO NPs, represent a potential sanitizing agent for experimental use, with no usual application in hygiene in the food producing industries.

The results showed that the three agents used in the industry routine were more effective in elimination, although 9/30 (30.0%) of the strains were identified to be tolerant to at least one of them. In contrast, ZnO NPs showed less efficacy with 13/30 (43.3%) resistant strains and with counts higher than the other agents.

The presence of tolerant strains to different sanitizers suggests that the use of these agents in the routine of the industrial environment in an inadequate way can result in the sublethal exposure to these biocides, representing a real risk for the adaptation of these bacteria, besides positively influencing the production of biofilms (Keeratipibul and Techaruwichit, 2012; Techaruvichit et al., 2016).

As for ZnO NPs it is possible that tolerant bacteria have already acquired characteristics that confer this resistance, such as the presence of efflux pumps, ZnO resistance genes and the ability to maintain intact the integrity of membrane. This characteristic has already been identified in Escherichia coli and Enterococcus faecium (Mileyeva-Biebesheimer, 2011).

Although the use of chemical compounds provides benefits in disinfection, they have the limitation of not destroying the residual structures of the biofilm matrix that may facilitate their resurgence or maintenance (Ohsumi et al., 2015). Thus, special efforts are required for the complete removal of highly adherent biofilms adapted to C. jejuni biocides (Techaruvichit et al., 2016).

Probably, the effectiveness in the control is possible by the association of hygiene plans with different agents, respecting the periods between cleaning, besides strategies, like the periodical rotation of biocides.

For the three C. jejuni strains under sessile form in the glass beads, with MH substrate plus chicken juice, it was observed in SEM that the structure of the biofilm was quite similar, with a more expanded and stable architecture, besides the presence of irregular coverage along the surface of the sphere, consistent with the presence of several macrocolonies. Differently, in MH, this pattern varied according to the strain, so that the most developed structure observed was the presence of microcolonies that indicate the immature stage of the biofilm.

A study by Bronnec et al. (2016) compared the ultrastructure of two strains of C. jejuni in biofilm under microaerophilic and aerobiose conditions. The authors concluded that the differences revealed the formation of mature and immature biofilm, being a strain-dependent characteristic.

The variations in the architecture of the formed biofilms can have relation not only with the nutrient available to the bacterium, but also because it is a strain-dependent character. Turonova et al. (2015) showed that C. jejuni NCTC 11168 produces biofilm with multilayer type structure, while C. jejuni 81–176 was able to form finger-like biofilm with an open ultrastructure.

The capacity to form biofilm with open ultrastructure composed of wells and channels was identified in the three strains of C. jejuni tested in the presence of chicken juice. This type of heterogeneous structure gives the characteristic of a mature biofilm, which allows the formation of interconnected fluxes that aid in the access to nutrients for the cellular aggregates and in the drainage of the metabolic residues (Donlan and Costerton, 2002).

The composition assays allowed to identify that all strains reduced biomass with treatment with sodium metaperiodate and proteinase K, the last one being more significant. Thus, the treatment of biomass with products of proteolytic action can be considered an effective mechanism for partial degradation, allowing a better penetration of antimicrobial agents into the matrix. Although the use of proteinase K is expensive in the poultry industry, the effectiveness of the tests opens the prospects for the chemical industry to the development of other similar proteolytics and of lower cost, since they will probably not require the necessary purity to be used in molecular techniques.

Considering the proteic nature of biofilms, it is possible that the association of potent proteolytics in association with sanitizers is an adequate strategy in the prevention of C. jejuni biofilms.

The centesimal composition of MH and chicken juice was compared and it was found that the analysis of 100 mL of chicken juice has 2.79% of protein and 0.06% of carbohydrates. MH contains 1.85% protein and 0.2% of carbohydrate. Even with only 5% of chicken juice in the trials, the presence of a higher protein build-up added to the existence of blood and other unassessed components may have provided C. jejuni not only with the microaerophilic condition required for this microorganism, as well as a greater presence of iron, important conditions for its metabolism and consequent survival and multiplication, which may have had a positive influence on biofilm formation.

For the mixed biofilms it was observed that there was an increase in the formed biomass. This increase was significant depending on the microorganism to which the interaction occurred and the medium used. In addition, there was variability in the composition of the formed biofilm.

The competitive disadvantage of C. jejuni visualized in the SEM indicates that probably the identified variations in biomass and in the constitution may be more related to the characteristics of the other species than to the interaction itself.

SEM images demonstrated that the configuration of mixed biofilms presented the same pattern found in the monospecific biofilm of C. jejuni, in both MH and chicken juice. The exception was restrict to the interaction with P. aeruginosa that presented in addition a more compact and flat conformation with the presence of well delimited pores, and it was also identified a higher biomass in MH in comparison with chicken juice, that presented a significant difference (p < 0.001) in the colorimetric assay.

The predominance of the other species in detriment of C. jejuni, in mixed biofilms, may be related to the biofilm formation time, since C. jejuni is a fastidious and demanding specie. In addition, the prevalence of other species in mixed biofilms has also been described previously and may indicate the existence of selection pressure exerted under C. jejuni in the first days.

According to Culotti and Packman (2015) only after 3 days of formation of the mixed biofilm of C. jejuni and P. aeruginosa was it possible to observe the presence of dispersed and discrete colonies of C. jejuni, which were present only on the surface of the biofilm formed by P. aeruginosa. In addition, the authors also detected that there was a predominance of P. aeruginosa biofilm morphology that remained unchanged in the C. jejuni presence and exhibited the same typical characteristics of the simple P. aeruginosa biofilm.

Several authors have already stated that both, co-inoculation and the inclusion of C. jejuni in pre-established biofilms facilitates subsequent growth of the sessile form of this agent (Zhang et al., 2013; Culotti and Packman, 2014, 2015).

Aswathanarayan and Vittal (2013) have suggested that different bacterial species secrete enzymes that modify the composition of extracellular polymeric substance (EPS) of biofilms in response to external stresses, resulting in changes in the biofilm architecture in a specific environment. In this way, the inclusion of different species in two substrates (MH and chicken juice) promoted these modifications.

The exception found in mixed biofilms with P. aeruginosa in chicken juice may represent a specific characteristic of this specie. Many animal macromolecules have been reported with the ability to form an adherent film, but not always capable of improving biofilm formation. For example, bovine serum albumin reduces formation of biofilms in S. aureus (Xu et al., 2008) and Burkholderia cepacia (Hwang et al., 2012). On the other hand, it is important for adhesion in Cronobacter (Healy et al., 2010). These differences also correlate with changes in the ability to express absorption proteins, leading to a variability in time to biofilm formation (Brown et al., 2015). In addition, the composition of the P. aeruginosa biofilm matrix is predominantly of polysaccharides, mainly alginate (Mann and Wozniak, 2012), which confers a differentiated structure, which can be detected in SEM and may represent another explanation for difficulty in adherence in the presence of chicken juice.

The high heterogeneity found in C. jejuni strains is due to the fact that most of them are naturally competent to take the DNA present in the environment and promote recombination in their genome, that is, they execute the transformation mechanism effectively, due to production of extracellular DNAse (Clark et al., 2014).

The presence of strains with high percentage of phylogenetic similarity in different flocks and in the same one, was also reported by other authors who stated that slaughter conditions may be the main responsible for the presence of strains with a high degree of homology in samples from the same flock, such as the equipment used in animal processing and cross-contamination (Petersen and Wedderkopp, 2001; Workman et al., 2008).

Our approach has shown that the ability of C. jejuni in developing a structured biofilm is highly variable depending on the strain when maintained in MH. However, when there is supplementation with chicken juice, all strains present a strong biofilm producer pattern. The chicken juice allows a greater fixation of C. jejuni as it assigns a surface more conditioned to bacterial adhesion.

Genome analysis revealed the high potential of strains in the acquisition of sessile lifestyle, phenotypically proven in chicken juice. Its variable behavior in MH and chicken juice, apparently results from modifications in the expression of genes involved in stress response, adhesion and biofilm formation.

The existence of tolerant strains to the tested biocides and most used in the poultry industry suggests the existence of exposure to sublethal concentrations, representing a real risk for the development of adaptation mechanisms.

The ultrastructure of simple and mixed biofilms showed the early maturity range when in chicken juice compared to MH. However, in biofilms with P. aeruginosa this pattern is inverted, probably due to the particular characteristics of this species.

Identification of the predominantly protein composition of C. jejuni biomass and also in mixed biofilms may aid in the future development of agents of action with proteolytic approach as a prevention and strategy of control. However, it is noteworthy that in mixed culture with P. aeruginosa there is predominance of a polysaccharide matrix.

Phylogenetic diversity was evidenced by the presence of 23 pulsotypes, which confirms the intrinsic characteristic of C. jejuni to easily recombine its genome by gene transformation.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.