A shift in the virulence potential of Corynebacterium pseudotuberculosis biovar ovis after passage in a murine host demonstrated through comparative proteomics
© The Author(s). 2017
Received: 15 January 2016
Accepted: 4 January 2017
Published: 22 March 2017
Corynebacterium pseudotuberculosis biovar ovis, a facultative intracellular pathogen, is the etiologic agent of caseous lymphadenitis in small ruminants. During the infection process, C. pseudotuberculosis changes its gene expression to resist different types of stresses and to evade the immune system of the host. However, factors contributing to the infectious process of this pathogen are still poorly documented. To better understand the C. pseudotuberculosis infection process and to identify potential factors which could be involved in its virulence, experimental infection was carried out in a murine model using the strain 1002_ovis and followed by a comparative proteomic analysis of the strain before and after passage.
The experimental infection assays revealed that strain 1002_ovis exhibits low virulence potential. However, the strain recovered from the spleen of infected mice and used in a new infection challenge showed a dramatic change in its virulence potential. Label-free proteomic analysis of the culture supernatants of strain 1002_ovis before and after passage in mice revealed that 118 proteins were differentially expressed. The proteome exclusive to the recovered strain contained important virulence factors such as CP40 proteinase and phospholipase D exotoxin, the major virulence factor of C. pseudotuberculosis. Also, the proteome from recovered condition revealed different classes of proteins involved in detoxification processes, pathogenesis and export pathways, indicating the presence of distinct mechanisms that could contribute in the infectious process of this pathogen.
This study shows that C. pseudotuberculosis modifies its proteomic profile in the laboratory versus infection conditions and adapts to the host context during the infection process. The screening proteomic performed us enable identify known virulence factors, as well as potential proteins that could be related to virulence this pathogen. These results enhance our understanding of the factors that might influence in the virulence of C. pseudotuberculosis.
Corynebacterium pseudotuberculosis biovar ovis is a Gram-positive facultative intracellular pathogen. It is the etiologic agent of Caseous Lymphadenitis (CLA) in small ruminants, a disease characterized by abscess formation in lymph nodes and internal organs . Cases of human infection caused by C. pseudotuberculosis have been reported and are associated with occupational exposure . CLA is globally distributed and causes significant economic losses in goats, and sheep herds . The pathogenic process of C. pseudotuberculosis in the host comprises two phases: (i) initial colonization and replication in lymph nodes that drain the site of infection, which is associated with pyogranuloma formation, and (ii) a secondary cycle of replication and dissemination via the lymphatic or circulatory systems. This dissemination is promoted by the action of phospholipase D (PLD) exotoxin, the major virulence factor of C. pseudotuberculosis, which allows this pathogen to contaminate visceral organs and lymph nodes, where it ultimately induces lesion formation [3–5].
Exported proteins reportedly favor the infection process in pathogenic bacteria; this class of proteins is involved in adhesion and invasion of host cells, nutrient acquisition, toxicity, and in the evasion of the host immune system . Different strategies like the transposon mutagenesis have been adopted to identify C. pseudotuberculosis biovar ovis exported proteins . Additionally, comparative proteomics has been applied to characterize the extracellular proteome of C. pseudotuberculosis biovar ovis, as well as, the extracellular immunoproteome (strains C231_ovis and 1002_ovis) [8–11]. In these studies, some proteins of the strain 1002_ovis, suspected to be virulence factors, were not detected suggesting this strain presents a low virulence. The surface proteome of C. pseudotuberculosis biovar ovis was also characterized using bacterial strains isolated from the lymph nodes of naturally infected sheep. This proteomic analysis allowed the identification of proteins that could favor the survival of this pathogen during the chronic phase of CLA .
The experimental passage of bacterial pathogens through in vitro or in an in vivo model is a strategy that has been applied to evaluate the virulence potential of several pathogens. By generating a confrontation between the pathogen and the dynamic network of host factors, including the immune system components, it helps to identify bacterial factors involved in virulence [12–19]. In this study, the strain 1002_ovis was experimentally inoculated in mice [20, 21] to identify factors which could contribute to virulence in C. pseudotuberculosis biovar ovis. Comparative proteomics of the culture supernatant from this strain collected before and after the experimental passage in mice was carried out to identify factors that might contribute to virulence of 1002_ovis.
Bacterial strains and growth conditions
The C. pseudotuberculosis biovar ovis strain 1002 (1002_ovis) was isolated from a goat in Brazil; this strain was cultivated under standard conditions in brain–heart infusion broth (BHI-HiMedia Laboratories Pvt. Ltd., India) at 37 °C. When necessary, 1.5% of agar was added to the medium for a solid culture. For extracellular proteomic analyses, 1002_ovis was grown in a chemically defined medium (CDM) [(Na2HPO4_7H2O (12.93 g/L), KH2PO4 (2.55 g/L), NH4Cl (1 g/L), MgSO4_7H2O (0.20 g/L), CaCl2 (0.02 g/L) and 0.05% (v/v) Tween 80], 4% (v/v) MEM Vitamins Solution (Invitrogen, Gaithersburg, MD, USA), 1% (v/v) MEM Amino Acids Solution (Invitrogen), 1% (v/v) MEM Non-Essential Amino Acids Solution (Invitrogen), and 1.2% (w/v) glucose at 37 °C .
Experimental infection of strain 1002_ovis in a murine model (in vivo assay)
The standardization of the parameters for infection was performed according to Moraes et al.  and Ribeiro et al. . Female BALB/c mice between six and eight weeks old were used in all experiments. They were provided by the Animal Care Facility of the Biological Sciences Institute from the Federal University of Minas Gerais and were handled by the guidelines of the UFMG Ethics Committee on Animal Testing (Permit Number: CETEA 103/2011). For the bacterial passage assay using the murine model, two groups of three mice each was infected via intraperitoneal injection with 106 colony forming units (CFU) of strain 1002_ovis. Thirty-six hours after infection, all animals were sacrificed. Their spleens were aseptically removed to recover the bacterial strain, as described below: the spleen removed from each animal was then, individually macerated in sterile saline solution (0.9% NaCl2), seeded onto BHI agar plates and incubated for 48 h at 37 °C. Subsequently, one recovered bacterial colony was cultured in BHI broth. The recovered bacteria were then referred to as Recovered (Rc). For the bacterial virulence assay, we used the freshly recovered bacteria and bacteria that did not contact the murine host as a control, which is referred to as Control (Ct). Groups of five mice were infected with Rc and Ct, via intraperitoneal injection of a suspension containing 106 CFU or 105 CFU. The animals’ survival rates were calculated and represented in GraphPad Prism v.5.0 (GraphPad Software, San Diego, CA, USA) using the Kaplan-Meier survival function. The results of 1002_ovis CFU count in the organs were calculated using the two-way ANOVA test.
Preparation of proteins from culture filtrates for proteome analysis
For proteomic analysis, the Ct and Rc (three independently recovered colonies) that was obtained from infected mice spleens as described above were grown in CDM at OD600 = 0.8. The cultures were then centrifuged for 20 min at 2700 × g. The supernatants were then filtered using 0.22-μm filters, 30% (w/v) ammonium sulfate was added to the samples, and the pH of the mixtures was adjusted to 4.0. Next, 20 mL N-butanol was added to each sample. The samples were centrifuged for 10 min at 1350 xg and 4 °C. The interfacial precipitate was collected and resuspended in 1 mL of 20 mM Tris–HCl pH 7.2 . Finally the concentration protein was determined by Bradford method .
2D-PAGE electrophoresis and Mass Spectrometry
The 2-DE procedure and in-gel protein digestion were performed as described previously [9, 10]. Approximately 300 μg of the protein extract from of each condition was dissolved in rehydration buffer (Urea 7 M, thiourea 2 M, CHAPS 2%, Tris–HCl 40 mM, bromophenol blue 0.002%, DTT 75 mM, IPG Buffer 1%). Samples were applied to 18 cm pH 3–10 N.L strips (GE Healthcare, Pittsburgh, USA). Isoelectric focusing (IEF) was performed using the apparatus IPGphor 2 (GE Healthcare) under the following voltages: 100 V 1 h, 500 V 2 h, 1000 V 2 h, 10,000 V 3 h, 10,000 V 6 h, 500 V 4 h. The IPG strips were placed on 12% acrylamide/bis acrylamide gels in an Ettan DaltSix II system (GE Healthcare). The gels were stained with Coomassie Blue G-250 staining solution, and 2-DE gels were scanned using an Image Scanner (GE Healthcare). The Image Master 2D Platinum 7 (GE Healthcare) software was used to analyze the generated images and all spots were matched and analyzed by gel-to-gel comparison. The quantification of the spots was calculated according percentage volume (% Vol) and spots with reproducible changes in abundance were considered to be differentially expressed. Protein spots were excised from the gels, and in-gel digestion was carried out using trypsin enzyme (Promega, Sequencing Grade Modified Trypsin, Madison, WI, USA). The peptides were then desalted and concentrated using ZIP TIP C18 tips (Eppendorf).
The samples were subsequently analyzed for MS and MS/MS modes, using an MALDI-TOF/TOF mass spectrometer Autoflex IIITM (Bruker Daltonics, Billerica USA). The equipment was controlled in a positive/reflector way using the Flex-ControlTM software (Brucker Daltonics). External calibration was performed using peptide standards samples (angiotensin II, angiotensin I, substance P, bombesin, ACTH clip 1–17, ACTH clip 18–39, somatostatin 28, bradykinin Fragment 1–7, Renin Substrate tetra decapeptide porcine) (Bruker Daltonics). The peptides were added to the alpha-cyano-4-hydroxycinnamic acid matrix, applied on an Anchor-ChipTM 600 plate (Brucker Daltonics) and analyzed by Autoflex III. The search parameters were as follows: enzyme; trypsin; fixed modification, carbamidomethylation (Cys); variable modifications, oxidation (Met); mass values, monoisotopic; maximum missed cleavages, 1; and peptide mass tolerance of 0.005% Da (50 ppm). The results obtained by MS/MS were used to identify proteins utilizing the MASCOT_ (http://www.matrixscience.com) program and compared with the genomic data of the Actinobacteria class deposited in the NCBI nr database.
2D nanoUPLC-HDMSE data acquisition and Data Processing
The protein extracts from three biological replicates of each condition were concentrated using spin columns with a 10 kDa threshold (Millipore, Billerica, MA, USA) to perform the label-free proteomic analysis. The protein was denatured (0.1% RapiGEST SF at 60 °C for 15 min) (Waters, Milford, CA, USA), reduced (10 mM DTT), alkylated (10 mM iodoacetamide) and enzymatically digested with trypsin (Promega). The digestion process was stopped by adding 10 μL of 5% TFA (Fluka, Buchs, Germany), and glycogen phosphorylase (Sigma, Aldrich, P00489) was added to the digested samples after digest at 20 fmol.uL−1 as an internal standard for normalization. Each replicate was injected using a two-dimensional reversed phase (2D RPxRP) nanoUPLC-MS (Nano Ultra Performance Liquid Chromatography Mass Spectrometry) approach with 171 multiplexed high definition mass spectrometry (HDMSE) label-free quantitation . Qualitative and quantitative experiments were performed using both a 1 h reversed phase gradient from 7% to 40% (v/v) acetonitrile (0.1% v/v formic acid) at 500 nL.min−1 and a nanoACQUITY UPLC 2D RPxRP Technology system . A nanoACQUITY 174 UPLC HSS T3 1.8 μm, 75 μm × 15 cm column (pH 3) was used with an RP XBridge BEH130 C18 5 μm 300 μm x 50 mm nanoflow column (pH 10). Typical on-column sample loads were 250 ng of the total protein digests for each of the 5 fractions (250 ng/fraction/load). All analyses were performed using nano electrospray ionization in the positive ion mode nanoESI (+) and a NanoLockSpray (Waters, Manchester, UK) ionization source. The mass spectrometer was calibrated using an MS/MS spectrum of [Glu1]-Fibrinopeptide B human (Glu-Fib) solution (100 fmol.uL-1) delivered through the NanoLockSpray source reference sprayer. Multiplexed data-independent (DIA) scanning with additional specificity and selectivity for non-linear ‘T-wave’ ion mobility (HDMSE) experiments were performed using a Synapt G2-S HDMS mass spectrometer (Waters, Manchester, UK).
Following the identification of proteins, the quantitative data were packaged using dedicated algorithms  and searching against a database with default parameters to account for ions . The databases used were reversed on-the-fly during the database queries and appended to the original database to assess the false positive rate during identification. For proper spectra processing and database searching conditions, the ProteinLynxGlobalServer v.2.5.2 (PLGS) with IdentityE and ExpressionE informatics v.2.5.2 (Waters, Manchester, UK) was used. UniProtKB (release 2013_01) with manually reviewed annotations was used, and the search conditions were based on taxonomy (Corynebacterium pseudotuberculosis). One missed cleavage by trypsin was allowed be up to 1 and various modifications as carbamidomethyl (C), Acetyl N terminal, phosphoryl (STY) and oxidation (M) were allowed . The proteins collected were organized by the PLGS ExpressionE tool algorithm into a statistically significant list that corresponded to higher or lower regulation ratios between the different groups. For protein quantitation, we used the PLGS v2.5.2 software with the IdentifyE algorithm using the Hi3 methodology. The search threshold to accept each spectrum was the default value for a false discovery rate 4%. The quantitation values were averaged over all samples, and the standard deviations of p < 0.05, which were determined using the ExpressionE software, refer to the differences between biological replicates.
The proteins identified in 1002_ovis under both conditions were analyzed using the following prediction tools: SecretomeP 2.0 server, to predict proteins exported from non-classical systems (positive prediction score greater than to 0.5)  and PIPs software, to predict proteins in the pathogenicity islands . Gene ontology (GO) functional annotations were generated using the Blast2GO tool .
List of proteins identified in 1002_ovis control and recovered by 2D-PAGE-MS/MS
5, 6, 7
Trypsin-like serine protease
Serine-type endopeptidase activity
Cytochrome c oxidase sub II
Cytochrome-c oxidase activity
Calcium ion binding
Sphingomyelin phosphodiesterase D activity
Phosphopyruvate hydratase activity
Trehalose corynomycolyl transferase B
Transferase activity, transferring acyl groups other than
Proteins differentially produced among the recovered and control condition
Fold Change_Log(2) a
Periplasmic binding protein LacI
Oligopeptide binding protein oppAb
ABC transporter domain containing ATP
Oligopeptide binding protein oppAb
Oligopeptide binding protein oppAb
ABC type metal ion transport system permease
Glutamate binding protein GluB
Iron(3+)-hydroxamate-binding protein fhuD
Septum formation initiator protein
DNA synthesis and repair
GTP binding protein YchF
Chromosome partitioning protein ParBb
DNA polymerase III subunit beta
Nucleoid associated proteinc
DNA directed RNA polymerase subunit
tRNA rRNA methyltransferase
DNA directed RNA polymerase subunit omega
DNA directed RNA polymerase subunit beta
RNA polymerase-binding protein RbpA
30S ribosomal protein S6
Elongation factor Gb
Peptidyl prolyl cis trans isomeraseb
Phenylalanine tRNA ligase beta subunit
50S ribosomal protein L13
50S ribosomal protein L5b
Proline tRNA ligaseb
50S ribosomal protein L10b
50S ribosomal protein L23b
50S ribosomal protein L24
30S ribosomal protein S8c,b
30S ribosomal protein S10b
50S ribosomal protein L29
50S ribosomal protein L27b
50S ribosomal protein L25
50S ribosomal protein L18
50S ribosomal protein L1
ATP dependent chaperone protein ClpB
Aspartate tRNA ligase
Arginine tRNA ligase
Metallopeptidase family M24
Penicillin binding protein transpeptidaseb
Metallo beta lactamase superfamily proteinc
Trypsin like serine protease
ATP dependent Clp protease proteolyticb
Penicillin binding proteinb
Succinate dehydrogenase flavoprotein
Phosphoenolpyruvate carboxykinase GTPb
ATP synthase subunit alpha
Glycerophosphoryl diester phosphodiestec
Methylmalonyl CoA carboxyltransferase 1b
Amino acid metabolism
Succinyl CoA Coenzyme A transferase
Mycothione glutathione reductase
Glyoxalase Bleomycin resistance proteinc
Universal stress protein Ab
Ferredoxin ferredoxin NADP reductaseb
Stress related proteinb
Thiol disulfide isomerase thioredoxin
Metabolism of nucleotides and nucleic acids
Deoxycytidine triphosphate deaminase
D methionine binding lipoprotein metQ
UDP glucose 4 epimeraseb
Ribose-5-phosphate isomerase B
Cytochrome c nitrate reductase small
Maltotriose binding protein
D methionine binding lipoprotein metQ
LSR2 like protein
Serine aspartate repeat containing protein
DoxX family protein
List of proteins identified in the exclusive proteome of recovered-condition
Cation transport protein
Uncharacterized iron regulated membranea
Amino acid metabolism
LytR family transcriptional regulatora
ABC transporter substrate binding lipoprotein
Manganese ABC transporter substrate bindinga
Phosphate ABC transporter phosphate bindinga
D alanyl D alanine carboxypeptidase OS
Cell wall organization
Gamma type carbonic anhydratase
Urease accessory protein UreD
Copper resistance protein CopC
Glutaredoxin like protein nrdH
ATP dependent RNA helicase rhlE
Cell wall channel
Important factors directly linked to C. pseudotuberculosis virulence, like the PLD phospholipase, as well as, the CP40 protease were detected only in the proteome of recovered 1002_ovis (Tables 1 and 3). Also, components of several secretion systems were also activated in the bacteria recovered. These include proteins related to hemin uptake, ATP-binding cassette (ABC) transporters and the Opp transporter, like OppA, OppC, and OppD. Proteins related to detoxification process were also specifically identified in the Rc supernatant: e.g. the glutaredoxin-like protein NrdH, which belongs to the NrdH-redoxins, a family of small protein disulfide oxidoreductases , mycothiol glutathione reductase present in Actinobacteria  and copper resistance protein CopC (Tables 2 and 3). In addition, we have identified 31 proteins in the recovered condition that also were detected in a strain of C. pseudotuberculosis isolated directly from ovine lymph nodes  (Tables 2 and 3). Proteins involved in the resistance to antimicrobial agents, such as penicillin-binding proteins, metallo-beta-lactamase, and penicillin-binding protein transpeptidase and proteases like Clp protease involved in the expression of cytotoxins in Staphylococcus aureus and Listeria monocytogenes [36, 37] were found induced in Rc supernatant.
To investigate the protein factors that could influence the adaptive processes of C. pseudotuberculosis biovar ovis during the infection process, we combined a unique bacterial passage experiment in mice with proteomic analyses of 1002_ovis culture supernatants, collected before and after passage. In the first analysis, we observed that strain 1002_ovis (isolated from caprine) exhibited a low virulence potential, which is consistent with previous reports indicating the low virulence potential of this strain [38, 39]. Although a recent in silico analysis of the 1002_ovis genome predicted various genes involved in virulence , studies examining the exoproteome of this strain under laboratory growth conditions failed to detect many of these virulence proteins (e.g., PLD exotoxin or proteins involved in the pathway of cell invasion, detoxification) [8–10].
One explanation for this relies on the fact that after being first isolated, strains 1002_ovis have been maintained, in vitro, under laboratory conditions with extensive passages on the culture medium, which may alter the gene expression profile of the strain, especially for effectors related to bacterial virulence. This phenomenon has also been reported in other pathogens such as Mycobacterium bovis, Helicobacter pylori, S. aureus, and L. monocytogenes. In vitro passages of these bacteria on culture medium altered both bacterial physiology and virulence profile [41–44]. However, we showed that the bacterial passage process in a murine model changed the virulence potential of strain 1002_ovis. Previous reports on experimental serial passages showed that pathogens such as H. pylori, Escherichia coli, Xenorhabdus nematophila, Arcobacter butzleri, and Salmonella enterica also exhibited altered virulence profiles after in vivo passage in a host, which helped identifying factors that contribute to infectious process [14–19]. Thus, as observed in these pathogens, the recovered condition also showed increased capacity to persist into host, when compared with control condition. The altered physiology and virulence status observed in 1002_ovis is supported by our proteomic analyses, where several proteins involved in processes favoring infection and host adaptation were differentially expressed after passage in mice.
Although our study focused on the C. pseudotuberculosis extracellular proteins, cytoplasmic proteins were also detected in the proteomic analyses. The presence of cytoplasmic proteins in the extracellular fraction is reported in several other proteomic studies [8–10, 12, 45]. It may be partially due to cell lysis and thus, be considered artifacts. However, cytoplasmic proteins in the culture supernatant may act as moonlighting proteins and be exported via a non-classical secretion pathway [30, 46]. The moonlighting proteins are described both Gram-positive and Gram-negative bacteria, and can be detected in different subcellular locations (cytoplasm, membrane, cell surface, and extracellular environment) and exhibit distinct functional behavior depending on the host cell type [46, 47]. Interestingly, some proteins, such as Chromosome partitioning protein ParB, Phosphoenolpyruvate carboxykinase GTP, Methylmalonyl CoA carboxyltransferase 12S subunit, Acetate kinase, and Enolase, induced in the Rc supernatants were identified only in the membrane shaving of C. pseudotuberculosis harvested directly from ovine lymph nodes .
The passage process in mice was also able to induce other proteins identified in Rc supernatants, and which contribute to the adhesion process. Proteins with an LPTXG domain, which characterizes the cell-wall anchored proteins, were identified and included monomers of membrane pilus. This latter class of proteins is described in pathogenic Corynebacterium species and may contribute especially in the process of cellular adhesion . In Campylobacter jejuni, serial passages in mice induce the expression of invasiveness and increase the capacity of cell invasion . Components of the Opp system were induced by the passage process, too. The Opp system facilitates the uptake of extracellular peptides, which are further used as carbon and nitrogen sources for bacterial nutrition . Proteins that comprise the Opp system also were induced in a field isolated of C. pseudotuberculosis biovar ovis, when compared with the strain C231_ovis a laboratory reference strain [12, 50]. In the pathogen Mycobacterium avium the OppA gene was highly expressed during the infection in a mouse model . We have identified known secreted virulence factors as CP40 serine protease, which previously shown to be necessary for C. pseudotuberculosis virulence potential and to induce an immune response [52, 53].
An important factor that precedes the chronic stage of infection by C. pseudotuberculosis is the capacity of this pathogen to disseminate within the host, which consequently favors the establishment of the disease . In C. pseudotuberculosis, this process is mediated by the action of PLD exotoxin, a major virulence factor of this pathogen [54, 55] that catalyzes the dissociation of sphingomyelin and increases vascular permeability, which contributes to the dissemination process of C. pseudotuberculosis in the host. Here, PLD was only detected in the proteome of the Rc condition. This result is noteworthy because, a previous proteomic study performed by our research group, PLD was not identified in the extracellular proteome of 1002_ovis [8–10]. McKean et al.  showed that pld expression is expressed by different environmental factors, thus during the infection and recuperation process 1002_ovis was exposed to different environmental and stimulus, which may have affected the pld expression. A study showed that a pld mutant strain is indeed unable to disseminate and yields reduced virulence . Here, we observed the presence of caseous lesions in different organs only at the end of experimental infection, only in the group of mice infected with the Rc condition. Altogether, the observations suggest that the expression of PLD can be modified by the passage in the host and can thus change the virulence potential of 1002_ovis.
Another attribute of PLD is its capacity to alter the viability of macrophage cells during the infection . However, before promoting macrophages lysis, C. pseudotuberculosis has to be able to resist the hostile environment inside macrophages mainly against reactive oxygen species (ROS) and reactive nitrogen species (RNS). Thus, the induction of proteins involved in detoxification processes in Rc could be contributed for its resistance against ROS and RNS. The inductions of proteins related to oxidative stress also were observed in Shigella flexneri, after recuperation process in an in vivo infection model. We detected the mycothione glutathione reductase, a component of the mycothiol system, which is present in Mycobacterium and Rhodococcus genera. This system is used as an alternative mechanism of disulphide reduction and contributes to the cytosolic redox homeostasis and the resistance to ROS . Glutaredoxin-like protein, NrdH, which plays an important role in the resistance to ROS, and is present in C. glutamicum  and M. tuberculosis  was also detected.
On the other hand, some proteins like dihydroxybiphenyl dioxygenase, Metallo beta lactamase superfamily protein, Formamidopyrimidine DNA glycosylase, MerR family transcriptional regulator, which were induced by 1002_ovis during the exposition to nitric oxide [57, 58] were also found induced in this study in the recovered condition. These proteins are related to different processes of resistance to nitrosative stress, DNA repair, antibiotic resistance, and transcription, these results show a set of proteins involved in the adaptation process of 1002_ovis to nitric oxide, which could contribute to the pathogenic process of this pathogen. Another type of defense of the host immune system against bacterial infection is the utilization of copper . Here, CopC, a protein related to copper resistance, was detected in recovered 1002_ovis. In M. tuberculosis, proteins involved in copper resistance are essential to virulence [60, 61]. Thus, the association of this factor related to an antioxidant system with PLD could promote an effective pathway of defense against the action of the innate immune system and consequently contributes to virulence process of C. pseudotuberculosis.
In conclusion, the virulence potential and proteomic profiles of strain 1002_ovis undergo dramatic changes after recovery from experimentally infected mice. The proteomic screening outlined, after the serial passage in murine model showed a set of proteins that were induced in the recovered condition. Into this group were detected known secreted virulence factors, as well as some proteins which could contribute in its virulence. Therefore, more study is necessary to show the true role of these proteins in the virulence of C. pseudotuberculosis. Altogether, our results demonstrate that in vitro passages alter the expression of C. pseudotuberculosis exoproteome leading to a reduced virulence and that a single passage in vivo, in a murine model, can induce significant changes in the C. pseudotuberculosis extracellular proteome, contributing to the increase in virulence of this pathogen.
The authors would like to thank to Pará State Genomics and Proteomics Network and Waters Corporation, Brazil.
The work was supported by the Brazilian Federal Agency for the Support and Evaluation of Graduate Education (CAPES), Pará Research Foundation (FAPESPA), Minas Gerais Research Foundation (FAPEMIG) and the National Council for Scientific and Technological Development (CNPq). Yves Le Loir is the recipient of a PVE grant (71/2013) from Programa Ciências sem Fronteiras.
Availability of data and materials
The datasets supporting the results of this article were then concatenated into a *xlsx file at peptide and protein level to fulfill the requirements and is available at supplemental material including sequence coverage and a number of identified peptides for each protein sequence identified. It also includes the native peptide information. In addition other data are included within the article.
VA, WMS, and FAD designed the experiments. WMS and FAD performed in vivo experiments. WMS, TLPC, and NS performed microbiological analyses and sample preparation for proteomic analysis. GHMFS and WMS conducted the proteomic analysis. WMS and SCS performed bioinformatics analysis of the data. YLL, AM, and HF contributed substantially to data interpretation and revisions. VA, AS, and YLL participated in all steps of the project as coordinators, and critically reviewed the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
All animals used in this study were provided by the Animal Care Facility of the Biological Sciences Institute from the Federal University of Minas Gerais and were handled by the guidelines of the UFMG Ethics Committee on Animal Testing (Permit Number: CETEA 103/2011).
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