Bacterial cultures and growth conditions

The Listeria species (Table 1) were grown at 37°C for 16–18 h in Tryptic soy broth (TSB; Becton Dickinson, Sparks, MD, USA) containing 0.6% yeast extract (TSB-YE; Acumedia, Lansing, MI, USA); Listeria enrichment broth (LEB, BD); or Fraser Broth (FB, BD). Other non-Listeria bacteria were grown in TSB-YE and lactic acid bacteria were grown in MRS broth (DeMan Rogosa Sharpe: BD) at 37°C for 16–18 h.

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Table 1. Bacterial strains used in this study.

https://doi.org/10.1371/journal.pone.0160544.t001

Protein identification by mass spectrometry

The p30 protein band was first localized in the Coomassie stained SDS-PAGE with the help of the Western blot (mAb-3F8) performed in parallel. The protein band was then excised from the gel and submitted for MALDI-TOF MS+MS/MS (matrix-assisted laser desorption ionization, time-of-flight mass spectrometry followed by tandem mass spectrometry) analysis by two laboratories: Applied Biomics (Hayward, CA, USA) and the Purdue University sequencing facility (West Lafayette, IN, USA). In both laboratories, the Voyager-DE Pro (Applied Biosystems) mass spectrometer was used, and sample treatment and experimental procedures were also the same. Briefly, the gel spots were reduced, alkylated, washed, and dehydrated prior to a trypsin digestion and peptide recovery. After MALDI-TOF, the most abundant peptides were submitted to MS/MS. The data from MALDI-TOF was analyzed by peptide mass fingerprint (PMF), while the data from MS/MS was analyzed by peptide fragmentation mapping. Results from both MS and MS/MS were combined, where tandem MS served as a validation step, and analyzed with MASCOT protein identification software (Matrix Science, London, UK) using three different databases (the NCBI/GenBank, and two of L. monocytogenes genomes [GenBank: AE017262.2, and FM242711.1]). The hits using the NCBI/GenBank entire database were filtered to those corresponding to Listeria proteins. For all three databases, the hits were filtered by including the best protein score of each protein and excluding hits with zero confidence interval (CI%) (S1 Table). The proteins with the highest scores (100 CI%) include, fructose 1,6-bisphosphate aldolase (FBA) class II; transcriptional repressor (CodY); elongation factor Tu (Tuf); and enolase (Eno). Thus, the full protein sequences were obtained from GenBank and analyzed their length/mass and predicted function. This way, it was possible to filter the initial candidates to two hits (fba and codY) which were further expressed in E. coli.

Cloning and expression of recombinant protein target

Specific primers (Eurofins MWG Operon, Germany) were designed to target fba and codY, (GenBank code: fba: ACK38405.11; codY: CAC99358.1) using Vector NTI 11.0 software (Invitrogen) in order to amplify the complete open reading frame (ORF) of both genes. To insert fba and codY ORFs into pAE expression vector, the restriction sites for BamHI and KpnI enzymes were incorporated into the forward and reverse primers (For-Fba: 5′-GCGGATCCATGCCTATCGTTAACA-3′; Rev-Fba: 5′-CGGGGTACCTTACGCTTTACCGTTA-3’; For-CodY: 5′-CGGGATCCATGACTTTATTAGAA-3′; Rev-CodY: 5′-CGGGGTACCTTAGTTATTTTTCAA-3’). The ORFs were amplified from the genomic DNA of L. monocytogenes ATCC 19114 by PCR using an Eppendorf thermocycler (Mastercycler EP gradient S) with the following standardized conditions: 94°C for 7 min, and then 35 cycles consisting of 94°C for 1 min, 50°C for 1 min, 72°C for 2 min, and a final extension of 72°C for 7 min. The amplicons were digested with BamHI and KpnI and ligated into pAE using T4 DNA Ligase (Fermentas, Thermo Fisher Scientific). The pAE-fba and pAE-codY constructs were inserted into E. coli TOP10 (Invitrogen) by electroporation, and clones were selected on LB-agar containing ampicillin (100 μg/mL). The recombinant plasmids were also transformed into E. coli BL21 (DE3) pLysS or E. coli BL21 (DE3) Star competent cells (Invitrogen). The cells were grown until log phase (OD₆₀₀ = 0.5–0.7), when 0.5 mM IPTG was added for 3 h at 37°C. The cultures were then harvested, suspended in lysis buffer (100 mM NaH₂PO₄, 10 mM Tris-HCl, and 20 mM imidazole; pH 8.0), and sonicated (5 cycles of 15 s). Then, protein extracts were separated by SDS-PAGE 12%, electrotransferred onto a Hybond-ECL nitrocellulose membrane (GE Healthcare) and immunoprobed with mAb-3F8 and anti-6xHis antibody (Sigma-Aldrich) [55].

Dot and Western blot assays

Listeria spp. were grown in 50 mL of LEB or FB at 37°C for 18 h, centrifuged (7000 ×g, 5 min) and the cell pellets were suspended in the sample solvent (4.6% SDS, 10% β-mercaptoethanol, 0.124 M Tris, and 20% glycerol; pH 6.9). Cells were sonicated four times for 15 s each for total protein preparation. For cell fractionation, crude proteins were prepared from whole cell lysates, and from supernatant, cell wall and cytoplasm as described before [5]. For the Western blot assays, the proteins (~25 μg/well) were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE; 10%-acrylamide; Bio-Rad, Hercules, CA, USA) and blotted onto Immobilon-P membranes (Millipore Bedford, MA, USA). The membranes were blocked with 5% skimmed milk for 1 h at room temperature (RT), washed with PBST, and reacted with mAb-3F8 (0.6 mg/mL) and anti-InlA mAb-2D12 (1 mg/mL) diluted in 1:1000 in PBST for 1 h at RT. After washing, the membranes were incubated with an HRP-conjugated goat anti-mouse polyvalent antibody (Sigma, St Louis, MO, USA). Antibody-reactive bands were developed using a chemiluminescence ECL kit (Thermo Fisher Scientific, Rockford, IL, USA) or colorimetric substrate system (6 mg of DAB, 3.3-diaminobenzidine tetrahydrochloride; 10 μL of 30% H₂O₂; 9 mL of 50 mM Tris-HCl; pH 7.6; 1 mL of 0.3% nickel sulfate).

Dot blot assays were performed using five microliters of approximately 10⁸ cells/mL of live or heat-killed cell suspensions of Listeria spp., Salmonella enterica serovar Enteritidis, and Escherichia coli O157:H7, spotted onto nitrocellulose membranes (Bio-Rad). The membranes were allowed to air-dry for 15 min, and were then blocked with 5% skimmed milk in PBS for 30 min. Further steps were performed as described above for Western blot.

Inhibition analysis of L. monocytogenes adhesion to epithelial cells by mAb-3F8

Freshly grown washed cultures of L. monocytogenes were suspended in 1 mL of mammalian cell culture medium (DMEM-10F; Dulbecco’s Modified Eagles Medium containing 10% fetal calf serum) to obtain approximately 10⁶ cells/mL. Bacteria were treated with mAb (1 mg/mL) and incubated at 37°C for 20 min with gentle agitation, washed, and suspended in DMEM-10F and added to HCT-8 cell (ileocecal cells; CCL 244; ATCC) monolayer in 24-well plate at a multiplicity of infection (MOI) of 10:1 (bacteria: HCT-8 cell) as before [56]. Non-adherent bacterial cells were removed by washing and the cells were treated with 0.1% Triton X-100 to disrupt cell attachment and bacterial adhesions were quantified by plating serial dilutions onto BHI agar. All experiments were carried out using a positive control anti-InlA mAb-2D12 [42], and a negative anti-N-acetylmuramidase mAb-C11E9 [34].

Immunoblotting to detect Listeria spp. in food samples

The mAb-3F8 and mAb-2D12 [42] were used to identify Listeria from food matrices by immunoblotting. Listeria monocytogenes ATCC 19114 and L. innocua (approximately 2 CFU/g) strains were aseptically inoculated into 10 g of Brazilian Minas Frescal cheese (a ready-to-eat soft cheese, Santa Clara brand, purchased from Nacional (Walmart) grocery store in Pelotas, Southern of Rio Grande do Sul state, Brazil). The cheese was then incubated for 15 min at 25°C to promote the interaction of bacteria with the cheese matrix. The samples were then placed in stomacher bags containing 90 mL of FB in each bag, mixed for 2 min using a stomacher (MK 1204, ITR Ltd., Brazil), and incubated at 37°C for 18 h. Cheese samples without inoculated bacteria served as negative controls. Thereafter, 10 mL of each cheese supernatant were collected carefully from the bags to avoid removing any large particles, transferred to 15 mL tubes, and centrifuged (1000 ×g for 10 min). Finally, the pellets were washed twice with PBS-T and suspended in 10 mL PBS. As positive controls, the same L. monocytogenes and L. innocua strains were grown in 10 mL of FB and processed as above.

To perform the SDS-PAGE and Western blot, the 10 mL of bacterial suspensions were centrifuged and suspended in 1 mL PBS and transferred to a 1.5 mL tube. After another round of centrifugation, the bacterial pellet was suspended in 100 μL of 2X sample solvent buffer (4.6% SDS, 10% β-mercaptoethanol, 0.124 M Tris, 20% glycerol, pH 6.9) and sonicated (3 times, 15 sec each) and heated for 10 min at 95°C. Samples were separated in SDS-PAGE (12%-acrylamide) and transferred onto PVDF membranes and probed with peroxidase conjugated mAb-3F8 (mAb-3F8-HRP) and mAb-2D12 (mAb-3F8-HRP) and then developed with DAB [42]. The Listeria counts from the inoculums and the enrichment broths were determined by plating the cultures on BHI and MOX agar and incubating at 37°C for 24–48 h.

Construction of an antigen library using ORFeome display technology

The genomic DNA of L. monocytogenes ATCC 7644 was amplified with illustra Ready-to-go GenomiPhi V3 DNA amplification kit (GE Healthcare, Freiburg, Germany) following the manufacturer’s instructions. The amplicon was sonicated with four pulsed cycles of 2 min one pulsed cycle of 1 min. After checking that DNA fragments had between 200 and 1,500 bp in an agarose gel, a DNA-end repair reaction was performed with Fast DNA End repair kit (Thermo Scientific, Langenselbold, Germany) as described by the manufacturer. Further, the resulting DNA and cloned into pHORF3 phagemid [57] digested with PmeI (New England Biolabs) and transformed into electrocompetent E. coli SS320 (Lucigen). Transformed cells were titrated and stored at -80°C after overnight growth in a 24.5 cm² dish at 37°C. Afterwards, 1 mL of the E. coli containing the library was inoculated in 400 mL of 2xYT-GA (2x yeast extract and tryptone medium, containing glucose 100 mM and ampicillin 100 μg/mL) and grown until OD₆₀₀ ≈ 0.5. Twenty-five mL of the culture was transferred to a 50-mL tube and 2.5 × 10¹¹ CFU of Hyperphage [58] was added. The tube was incubated 30 min at 37°C and 30 min at 37°C under 250 rpm, and then centrifuged (3,220 ×g for 10 min, RT). The pellet was suspended in 10 mL of 2xYT-AK (2xYT containing ampicillin 100 μg/mL and kanamycin 25 μg/mL), and transferred to additional 390 mL of this medium, which was then incubated at 30°C for 24 h. The culture was centrifuged (10,000 ×g, 10 min, 4°C) and the supernatant transferred to another tube in which 50 mL of PEG-NaCl solution (PEG 6,000 20% (w/v), NaCl 2.5 M) was added. The tube was incubated overnight at 4°C and centrifuged (10,000 ×g, 1 h, 4°C), then the pellet was suspended in 10 mL of pre-chilled PBS and centrifuged again (20,000 ×g, 10 min, 4°C). The supernatant was filtered with 0.45-μm membranes and 2.5 mL of PEG-NaCl solution was added. After 20 min on ice, it was centrifuged again (20,000 ×g, 30 min, 4°C), and the pellet suspended in 1 mL PBS. This final suspension containing phage was titrated and had some clones sequenced for library-quality checking.

Antigen panning for target confirmation

mAb-3F8 was diluted in panning solution (BSA 1% (w/v), dried skim milk 1% (w/v), PBS) and coated on two wells (1.5 μg/well) of a Costar ELISA plate (Corning, Wiesbaden, Germany). Two additional wells were coated with panning solution only; the plate was incubated overnight at 4°C. The L. monocytogenes ATCC 7644 library (≈1 × 10¹⁰ CFU/mL) was diluted in panning solution and added to the panning solution well for pre-incubation for 30 min at RT, while the wells containing mAb-3F8 were blocked with the same solution. The library was further transferred to the wells containing the antibody and incubated 1.5 h at RT. Then, the wells were washed and eluted with 10 μg/mL of trypsin diluted in PBS. The eluted phages were used to infect E. coli TG1 (OD₆₀₀ ≈ 0.5), which was further infected with helperphage M13K07 (MOI 1:20). Infected E. coli TG1 cells were grown overnight at 30°C, 500 rpm. On the next day, the cultures were centrifuged (3,220 ×g, 10 min, RT) and the supernatant containing phage used instead of the library. In total, three panning rounds were done, and the phage eluted after the 2^nd and 3^rd rounds were used to infect E. coli XL1-Blue MRF’, which were diluted, plated on 2xYT-GA agar plates, and grown overnight at 37°C.

Phage production and ELISA for screening of mAb-3F8 target

The resulting plates from the 2^nd and 3^rd panning rounds were used to acquire 46 colonies from each, which were transferred to a 96-well culture plate containing 2xYT-GA. The plate was grown overnight at 34°C and then 20 μL was used to inoculate another plate with 180 μL/well of the same medium, which was incubated 2 h at 37°C. Then, clones in each well were infected with Hyperphage (MOI 1:20), centrifuged (3,220 ×g, RT, 10 min), and the medium was changed to 2xYT-AK; the plate was then incubated overnight at 30°C, 800 rpm. On the next day, the plate was centrifuged again and 150 μL of the supernatant transferred to another plate, in which 40 μL/well of PEG solution was added and incubated 1 h at 4°C. The plate was centrifuged (1 h, 3,220 ×g, 4°C), the pellet suspended in 150 μL of PBS and centrifuged again (10 min, 3,220 ×g, 4°C). Finally, 50 μL of each supernatant was added to 50 μL of PBS in a Costar ELISA plate (Corning, Wiesbaden, Germany), which was incubated overnight at 4°C for coating. Afterwards, the plate was blocked with 2% MPBS-T (PBS-T with 2% (w/v) of skimmed milk powder) for 30 min at RT, and further incubated with 3F8 antibody (1 μg/mL) for 1 h at RT. Then, goat anti-mouse IgA, M, G HRP-conjugated antibody (AntibodiesOnline, Prod. ABIN376851, 1:4,000) was incubated 1 h at RT. A well with anti-M13 (pVIII) HRP-conjugated (1:40,000) served as positive control for phage production. The reactions were developed with TMB solution for 15 min and read at 450 nm. Reactive clones had their phagemids extracted and sent for sequencing.

Peptide membrane for the epitope mapping of mAb-3F8

Based on the sequencing results of the screening, a 25-amino acid peptide was identified as the potential mAb-3F8 epitope. To narrow down the amino acids that were important for the interaction, a PepSpots membrane (JPT Peptide Technologies GmbH, Berlin, Germany) was ordered containing 16 peptides with 9 amino-acids each, covering 24 of the 25 amino acids previously identified. The immunoblot was carried out following the manufacturer’s instructions. Briefly, the membrane was activated with methanol, washed with TBS-T, and blocked with 2% MTBS-T overnight at 4°C. Then, mAb-3F8 (1 μg/mL) was added and incubated 3 h at RT, followed by the addition of goat anti-mouse IgA, M, G HRP-conjugated antibody (AntibodiesOnline, 1:4,000), which was incubated 2 h at RT. The membrane was then washed with TBS-T for 1 h at RT prior to the addition of substrate solution (SuperSignal West Pico, Thermo Scientific, Langenselbold, Germany). The images were captured using ChemiDoc XRS equipment (Bio-Rad, München, Germany).

Sequence and structure analysis of FBA

To access the location of the identified epitope of mAb-3F8, the structure of FBA was predicted using RaptorX online software [59] using standard settings. COTH online software was used to calculate the dimer interfaces for FBA [60]. All structure manipulation and image acquirement were done with PyMol v1.3 software [61]. Multiple sequence alignment of full proteins was done using ClustalOmega tool [55], while alignment of short sequences was done with T-Coffee tool [62]. Phylogenetic analysis were done using ClustalPhylogeny [63]. The identities and similarities were calculated with EMBOSS Needle [64].

mAb-3F8-reactive protein is FBA class II

Following the MALDI-TOF mass spectrometry analysis, four proteins—fructose 1,6-bisphosphate aldolase (FBA) class II, transcriptional repressor CodY, elongation factor Tu (Tuf), and enolase (Eno)–received the highest scores with 100 CI %, and thus were further analyzed using Swiss-Prot and NCBI databases. FBA is a 284-amino-acid (aa)-long protein with a calculated MW of 29,936 Da, and is close to our SDS-PAGE-estimated molecular mass (30-kDa) (Fig 1). Thus, mAb-3F8-reactive 30-kDa protein was presumably considered the FBA class II (lmo2556). CodY (lmo1280) is a 259-aa-long intracellular GTP binding protein with an approximate MW of 28,614 Da [65] and is primarily located in the intracellular compartment, and mAb-3F8 reacts with whole cells, thus CodY was less likely to be the target, but it was cloned to validate our results. Tuf is a 395-aa-long protein with estimated mass of 43 kDa [66], which is much higher than the expected 30 kDa. Likewise, Eno is a 430-aa-long protein with estimated mass of 46 kDa [67] and this size is well above 30 kDa. Hence, these last two proteins were excluded from being a potential target of mAb-3F8.

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Fig 1. Western blot assay with recombinant rCodY and rFBA proteins to determine the target of mAb-3F8.

(A) Western blot using mAb-3F8 as primary antibody shows that this mAb reacts with purified rFBA, as well as protein extract of L. monocytogenes, but not with rCodY. (B) The reaction using Anti-His primary antibody as control shows that both rFBA and rCodY were present in detectable amounts on the membrane.

https://doi.org/10.1371/journal.pone.0160544.g001

Next, we cloned both fba (encoding FBA) and codY (encoding CodY) into E. coli expression vectors to produce rFBA and rCodY proteins and to confirm their reactivity with the mAb-3F8. Both recombinant proteins were affinity purified and after immunoblotting, only rFBA showed strong reactions with mAb-3F8 while rCodY did not (Fig 1A). Anti-6xHis antibody was used as a positive control to the assay (Fig 1B). This confirms that the antigen for mAb-3F8 is FBA class II protein.

FBA is detectable only in Listeria species

In our previous work, we have shown the specific reaction of mAb-3F8 with a single protein band of about 30 kDa present in the eight Listeria species tested and the 13 serotypes of L. monocytogenes [42]. In the current work, we showed again that the mAb-3F8 had no cross-reaction with additional Gram-positive or Gram-negative bacteria tested in Western blot (Staphylococcus aureus, Bacillus subtilis, B. cereus, B. thuringiensis, Salmonella enterica ser. Typhimurium, S. enterica ser. Enteritidis, E. coli O157:H7, Lactococcus lactis, Enterococcus aerogenes, Lactobacillus paracasei, Klebsiella pneumonia, and Enterococcus faecalis) (Fig 2A). It is also shown that the target is recognized specifically in Listeria species both in Western blot (Fig 2B), and dot blot using both live and heat-killed cells (Fig 2C). Since it is a non-described target for Listeria spp., we also tested its expression pattern in the two most common selective media (LEB, FB) used to isolate the pathogen. After a Western blot with whole cell lysates of the 3 most frequent serotypes of L. monocytogenes (4b, 1/2a, and 1/2b), it is clear that FBA is expressed regardless the medium used (Fig 2D).

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Fig 2. Western and dot blots showing the presence of FBA in Listeria spp. only.

(A) SDS-PAGE 12% showing the protein preparations of two Listeria species and many related bacteria (upper part). In Western blot using mAb-3F8, only those extracts from Listeria showed a 30-kDa band corresponding to FBA. (B) Western blot using mAb-3F8 showing the presence of FBA in other Listeria species, but not in E. coli O157:H7 used as negative control. In this blot, mAb-2D12 (anti-InlA) was used together with mAb-3F8, showing an 88-kDa band corresponding to InlA, which is present only in L. monocytogenes. (C) The results found in the Western blot were same as the dot blot, in which only Listeria spp. (either live or heat-killed) could be detected when using mAb-3F8. (D) Western blot using both mAb-3F8 and -2D12 allows detection of three different serotypes of L. monocytogenes (4b, 1/2a, and 1/2b), no matter the medium used for their growth (LEB or FB).

https://doi.org/10.1371/journal.pone.0160544.g002

FBA is present in all cellular fractions and supernatant, but its secretion is not SecA2-dependent and it does not play role in adhesion

The analysis of Listeria spp. cellular fractions in Western blot revealed that FBA protein is present in all cellular fractions, i.e. cell wall, and intracellular (cytoplasm and membrane) (Fig 3A). Additionally, to the cell wall and intracellular fractions, Western blot with the secreted proteins from L. monocytogenes and L. marthii was made and showed that the protein is found in the culture supernatant (Fig 3B). Since translocation of many Listeria proteins to cell surface and the extracellular milieu (i.e., secretion) is aided by SecA2, an auxiliary secretion system, we examined the reaction of mAb-3F8 with protein preparations from cell wall and intracellular fractions of ΔsecA2 deletion mutant of L. monocytogenes and L. innocua strains [5]. However, there was no difference in reaction of mAb-3F8 to proteins from WT or ΔsecA2 deletion strains in neither fractions, suggesting that SecA2 pathway is not essential for the translocation of FBA protein to the cell wall or membrane (Fig 3C).

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Fig 3. Cell localization and adhesion experiments for FBA characterization.

(A) Western blot using mAb-3F8 show that FBA protein is present in the cell wall and intracellular (membrane and cytoplasm) of three different Listeria species tested. The top band shows reaction with anti-InlA mAb-2D12. (B) When using only mAb-3F8 in Western blot, it is possible to observe that FBA is also present in the culture supernatant of two different Listeria species. (C) Due to the presence of FBA in the cell wall, a L. monocytogenes mutant (ΔsecA2) was used to inquire the secretion pathway of FBA. However, no difference in band intensity was observed in the cell wall (CW) or intracellular (Intra) fractions between the wild type (WT) and mutant strains, indicating that the secretory pathway of FBA is not SecA2-dependent. (D) Adhesion experiments in vitro using HCT-8 cells show that mAb-3F8 has no inhibition activity, since it’s pre-incubation with L. monocytogenes cells shows similar levels of adhered bacteria as the negative controls with PBS and mAb-C11E9. The positive control mAb-2D12 (anti-InlA) was the only one to show significant reduction in adhesion.

https://doi.org/10.1371/journal.pone.0160544.g003

We also examined if FBA is involved in L. monocytogenes adhesion to mammalian cells. Adhesion experiment using the human ileocecal cell line, HCT-8, indicated that pretreatment of L. monocytogenes with mAb-3F8 did not block L. monocytogenes adherence, indicating that it is probably not involved in adhesion. In contrast, anti-InlA mAb-2D12 used as positive control significantly (P < 0.05) reduced adhesion of this bacterium (Fig 3D), since InlA is a well-known adhesion and invasion factor [68]. A negative control antibody, mAb-C11E9 that reacts with N-acetylmuramidase, had no effect on the adhesion of L. monocytogenes as expected [34,69]. These data indicate that FBA may not play a role in adhesion of L. monocytogenes on human intestine.

FBA allows the detection of L. monocytogenes from food

Western blot analysis of the cheese samples inoculated with L. monocytogenes allowed the detection of the two analyzed proteins: InlA (≈88 kDa), and FBA (≈30 kDa). Thus, it confirms the presence of L. monocytogenes in the sample. The cheese sample inoculated with L. innocua indicated the presence of a single band, corresponding to the 30-kDa FBA as expected. The bands in the protein extracts of the strains had the same size of purified proteins used as control in the assay (Fig 4). The cells isolated from the cheese were plated on MOX plates, indicating the presence of Listeria spp. in inoculated samples.

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Fig 4. SDS-PAGE and Western blot of bacteria from artificially contaminated cheese.

(A) SDS-PAGE (12%-acrylamide) showing the protein extracts from the bacteria after enrichment step using stomacher bags. Protein extracts from pure cultures were used as control. (B) Western blot using both mAb-3F8 and -2D12 on these protein extracts shows the expected detection bands: both InlA (88 kDa) and FBA (30 kDa) for the pathogenic strain; and only FBA (30 kDa) for the non-pathogenic. Purified rInlA and rFBA, and the pure cultures of L. monocytogenes and L. innocua were used as positive control for the antibodies.

https://doi.org/10.1371/journal.pone.0160544.g004

mAb-3F8 epitope allows distinguishing Listeria spp. in sequence level and is part of the catalytic site of FBA dimer

An antigen library of L. monocytogenes was built using ORFeome display technology. By employing this library against mAb-3F8, it was possible to detect a 25-aminoacid peptide from FBA that was possibly the epitope of the antibody. To narrow down the exact sequence involved in the recognition, a peptide membrane was used, in which it was possible to define a 14-amino acid region as the epitope (Fig 5A). We also noticed that a 9-amino acid sequence contributes mostly to the interaction with the antibody. When aligning FBA sequences from all organisms tested in Western blot, we observed that those from Listeria spp. are isolated in the cladogram, though it is closer to Bacillus species, and S. aureus (S1A Fig). An interesting finding is that the 14-amino acid peptide identified as mAb-3F8 epitope gives almost the same effect on the cladogram (S1B Fig). In fact, these findings are in accordance with the identity between the analyzed proteins, which show that only Bacillus spp. and S. aureus have >50% identity with Listeria spp. when considering the identified epitope (S2 Table).

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Fig 5. Epitope mapping of mAb-3F8 and position of the epitope in FBA structure.

(A) By using a peptide membrane, which was incubated with mAb-3F8 as primary antibody, it was possible to identify a 14-amino acid sequence as the epitope of mAb-3F8. In this sequence, it is also possible to observe that a 9-amino acid region (yellow) gives a higher reaction and, thus, is likely the most important recognition part of the epitope. Interestingly, Arg257 (orange), which may be part of the catalytic site of the dimeric form of FBA is present in the epitope. (B) The position of the epitope in FBA structure shows it is a loop-to-helix transition, which has many amino acid side chains exposed on the protein surface. (C) A closer look on the G3P site (part of the catalytic site) shows that Arg257 of Listeria spp. FBA (listFBA, left part) can play role on binding G3P, since binding pocket is similar to that from Giardia lamblia FBA (glFBA, right part). For graphical reasons, FBP molecule fitting in listFBA pocket has the same position of that one from glFBA, thus it may not represent the real fitting of this molecule in the structure. Asterisk (*) indicate that the amino acid is present in the partner subunit of the protein dimer.

https://doi.org/10.1371/journal.pone.0160544.g005

After predicting the structure of FBA with RaptorX software, it was possible to observe that the epitope sequence represents a transition from a loop to α-helix in FBA’s structure (Fig 5B). Since the prediction was made using FBA from Bacillus anthracis (PDB code: 3Q94) as template that has no publication describing the structure and no detailed information regarding this structure. However, when comparing the predicted structure with that from Giardia lamblia (glFBA, PDB code: 3GAY), it is likely that the epitope is part of the catalytic domain within the dimeric form of the protein. This part is called G3P site—referring that it can bind the G3P molecule—and is similar between the two proteins (Fig 5C). In this site, Arg257 (Arg280 in glFBA) of the partner subunit, which is present in the identified epitope, may play a role in the interaction with carbon 6 of FBP substrate.