Pyroptosis and adaptive immunity mechanisms are promptly engendered in mesenteric lymph-nodes during pig infections with Salmonella enterica serovar Typhimurium
© Martins et al.; licensee BioMed Central Ltd. 2013
Received: 30 January 2013
Accepted: 25 November 2013
Published: 5 December 2013
In this study, we explored the transcriptional response and the morphological changes occurring in porcine mesenteric lymph-nodes (MLN) along a time course of 1, 2 and 6 days post infection (dpi) with Salmonella Typhimurium. Additionally, we analysed the expression of some Salmonella effectors in tissue to complete our view of the processes triggered in these organs upon infection. The results indicate that besides dampening apoptosis, swine take advantage of the flagellin and prgJ expression by Salmonella Typhimuriun to induce pyroptosis in MLN, preventing bacterial dissemination. Furthermore, cross-presentation of Salmonella antigens was inferred as a mechanism that results in a rapid clearance of pathogen by cytotoxic T cells. In summary, although the Salmonella Typhimurium strain employed in this study was able to express some of its major virulence effectors in porcine MLN, a combination of early innate and adaptive immunity mechanisms might overcome virulence strategies employed by the pathogen, enabling the host to protect itself against bacterial spread beyond gut-associated lymph-nodes. Interestingly, we deduced that clathrin-mediated endocytosis could contribute to mechanisms of pathogen virulence and/or host defence in MLN of Salmonella infected swine. Taken together, our results are useful for a better understanding of the critical protective mechanisms against Salmonella that occur in porcine MLN to prevent the spread of infection beyond the intestine.
Infections by Salmonella are a major health problem in the developing and developed world. In the European Union, despite the current decreasing trend of human cases, Salmonella persists as the main cause of food-borne outbreaks . Pork is considered to be a significant source of Salmonella to humans next to eggs and poultry meat . Indeed, according to the European food safety authority (EFSA), Salmonella enterica serovar Typhimurium (herein Salmonella Typhimurium) is the second serovar most frequently reported in human salmonellosis and infection by this pathogen is mostly associated with the consumption of contaminated pork .
Since the food industry and direct contact with infected animals represent the main sources of non-typhoid Salmonella, prevention of human salmonellosis depends significantly on decreasing the prevalence of infection in livestock hosts . Salmonella Typhimurium infected pigs generally carry this serotype asymptomatically in the tonsils, intestines and gut-associated lymphoid tissue, posing an important threat to animal and human health . Epidemiological studies assert that Salmonella prevalence in slaughter swine lymph nodes varies widely at the country level, ranging from0 to 29% . Although salmonellosis in pigs has been the subject of intensive research , a thorough knowledge of the pathogenesis of porcine infections with broadhost range Salmonella serotypes is still necessary. A combination of system-wide approaches and in vivo infection models is expected to generate precise and novel data to analyze the response to Salmonella infections in pigs . Thus, whole-genome expression analysis has been used to explore gene expression changes during infection of pigs by Salmonella, contributing to identify molecules and pathways associated with the host response to infection [7, 8]. More recently, proteomic techniques have also been employed as a step towards a detailed understanding of the disease mechanisms [9, 10]. However, despite this, there is a need to deepen understanding of the biological processes that control host-pathogen interaction and Salmonella persistence in porcine lymphatic tissue, which could provide new targets for treatment and control of salmonellosis in this species. Therefore, the objective of the current study was to explore the early transcriptional response of porcine mesenteric lymph-nodes (MLN) to Salmonella Typhimurim using a time-course analysis of an in vivo infection. In addition, the expression of some pathogen virulence effectors, as well as the morphological alterations associated with the presence of the bacteria in the tissue were also evaluated.
Materials and methods
Experimental infection and tissue sampling
Sixteen crossbred weaned piglets of approximately four weeks of age, serologically and fecal-negative for Salmonella were used in an experimental infection described elsewhere . Briefly, twelve piglets were orally infected with 108 cfu of a Salmonella Typhimurium phagetype DT104 strain isolated from a naturally infected pig , whereas the control group (4 animals) received sterile medium. Non-infected control pigs were necropsied prior to the experimental infection (0 day post-infection – dpi) and four randomly chosen infected piglets were necropsied at 1, 2 or 6 dpi. Samples of MLN were collected from all experimental animals and immediately frozen in liquid nitrogen for RNA and protein isolation or fixed in 10% neutral buffered formalin for histological processing. All procedures involving animals were performed in accordance with the European regulations regarding the protection of animals used for experimental and other scientific purposes. Piglets were housed in experimental isolation facilities of the University of Leon (Spain). Animal care and procedures were in accordance with the guidelines of the Good Experimental Practices (GEP), under the supervision of the Ethical and Animal Welfare Committee of the University of Leon (Spain).
After treatment with RNAlater-ICE (Ambion, Inc, Austin, TX, USA), MLN samples were soaked in RLT buffer (Qiagen, Valencia, CA, USA) and disrupted in a rotor-stator homogenizer. RNA was isolated using the AllPrep DNA/RNA/Protein Mini Kit (Qiagen), digested with the RNase-Free DNase Set (Qiagen) according to the manufacturer’s instructions and routinely precipitated with ethanol. RNA integrity was evaluated using the Experion RNA automated electrophoresis system (Bio-Rad, Hercules, CA, USA) before being quantified using a ND-1000 spectrophotometer (Nanodrop Technologies, Wilminton, USA).
Gene expression analysis was carried out using the GeneChip Porcine Genome Array of the Affymetrix platform (Affymetrix Inc., Santa Clara, CA, USA) at the Genomics Unit of CABIMER (Andalusian Center for Molecular Biology and Regenerative Medicine, Seville, Spain). This chip contains 23 937 probe sets to interrogate 23 256 transcripts in the pig, which represents 20 201 genes. The One-Cycle Eukaryotic Target Labeling Assay was used to obtain biotinylated cRNA to be used in the subsequent chip hybridization according to the manufacturer’s instructions (Expression Analysis Technical Manual, Affymetrix). The biotinylated cRNA targets were then cleaned up, fragmented, and hybridized with the GeneChip Porcine Genome Array following Affymetrix recommended protocols. Chips were washed, stained with a GeneChip Fluidics Station 450 (Affymetrix) using the standard fluidics protocol and scanned with an Affymetrix GeneChip Scanner 3000 (Affymetrix). Probe signal intensities were captured and processed with the GeneChip Operating Software 1.4.0.036 (Affymetrix) and the resulting CEL files were reprocessed using robust multi-array average normalization (RMA) . Because the aim of analysis was to detect changes in gene expression along a time-course of infection, differentially expressed (DE) genes were accessed by the BATS (Bayesian Analysis of Time Series) software package , using default settings. A Bayes Factor (BF) value of 0.05 was used as cutoff to rank significantly regulated transcripts. Since the Affymetrix Porcine GeneChip is not fully annotated in all the features, it was re-annotated with Blast2GO  with a minimum E-value of 10-10 and a minimum similarity of 50%.
Systems biology analysis
The list of genes that showed significant changes in expression was uploaded into Ingenuity Pathway Analysis (IPA, Ingenuity Systems Inc, Redwood City, CA, USA)  for bioinformatics analysis. Additionally, the DAVID Bioinformatic Database  was used applying the default settings to refine some data from IPA analysis. Gene interaction networks were automatically generated, ranked by score and depicted on IPA as follows: each node in the network diagram represented a gene and its relationship with other molecules was represented by a line (solid and dotted lines represent direct and indirect association respectively). Nodes with a red background were input genes detected in this study while grey nodes were molecules inserted by IPA based upon the Ingenuity Knowledge Base to produce a highly connected network. The score estimated the probability that a collection of genes equal to or greater than the number in a network could be achieved by chance alone. Scores of 3 or higher were considered to have a 99.9% confidence of not being generated by random chance alone. For statistical analysis of enriched functions/pathways, an IPA Knowledge Base was used as a reference set and the Fisher’s exact test was employed to estimate the significance of association. P-values below 0.05 were considered statistically significant. For graphical representation of the canonical pathways, the ratio indicates the percentage of genes taking part in a pathway that could be found in an uploaded data set and –log(p-value) means the level of confidence of association. The threshold line represented a p-value of 0.05.
Relative gene expression analysis by qPCR
Microarray data validation by qPCR.
Western blot analysis
For protein extractions, MLN samples from all experimental animals were separately homogenized on ice with lysis buffer (7 M urea, 2 M thiourea, 4% w/v CHAPS, 0.5 mM PMSF) using a glass tissue-lyser and protein lysate concentration was determined using a Bradford Protein Assay (Bio-Rad). Subsequently, protein from individual replicates belonging to the same group was pooled (30 ug total), electrophoretically fractionated in 12% (w/v) SDS-PAGE gels and transferred onto a PVDF membrane (Millipore, Bedford, MA, USA). Western blot assays were carried out as described by Martins et al.  employing the following primary antibodies: 4B7/8 for swine histocompatibility class I antigen (SLAI) detection , 1 F12 for swine histocompatibility class II antigen (SLAII) detection , anti-CTLA4 (Epitomics, Burlingame, CA, USA) and anti-Clathrin light chain (ab24579, Abcam, Cambridge, UK). To confirm equal sample loading, membranes were reblotted with anti-GAPDH monoclonal antibody (GenScript, Picastaway, NJ, USA) and no statistical differences for GAPDH abundance were observed between groups in all assays. Membranes were scanned in an FLA-5100 imager (Fujifilm, Tokyo, Japan) and signal intensity was determined using Multigauge software (Fujifilm, Tokyo, Japan) as previously described .
Histopathology, immunohistochemistry and confocal microscopy analysis
Paraffin sections (5 μm) of formalin fixed samples were routinely processed and stained with hematoxylin and eosin (H&E) to evaluate tissue morphology. For immunohistochemistry assays, a standard avidin-biotin peroxidase method was performed as described elsewhere  employing 1 F12 monoclonal antibody and a biotinylated anti-mouse Ig (Dako, Barcelona, Spain) as a secondary antibody. Immunofluorescence using confocal microscopy was performed employing the anti-SLAII 1 F12 monoclonal antibody, a rabbit polyclonal antibody against the Salmonella somatic (O4, 5, 12) antigen  and a rabbit polyclonal antibody anti-Salmonella Typhimurium flagellin . Fluorescein isothiocyanate (FITC)-conjugated goat anti-rabbit IgG (Sigma-Aldrich, St. Louis, MO, USA) and Alexa Fluor 594 anti-mouse IgG (Life Technologies, Carlsbad, CA, USA) were used as secondary antibodies. Immunostaining was performed as described by Robertson et al. . Briefly, deparaffinized sections of formalin fixed MLN were blocked for 30 min with 1% bovine serum albumin and 2% foetal calf serum in PBS. Then, sections were incubated overnight at 4 °C with primary antibodies, washed three times with PBS for 5 min and incubated for 1 h at 37 °C with fluorescent secondary antibodies. For negative controls, primary antibody was omitted. Finally, sections were washed three times for 5 min in PBS containing 1.43 μM 4′,6-diamidino-2-phenylindole (DAPI, Life Technologies). Samples were subsequently evaluated and imaged using an LSM 5 Exciter confocal microscope (Carl Zeiss, Jena, Germany).
Cell death analysis
Formalin fixed MLN samples were evaluated for cell death by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), employing the TUNEL Apoptosis Detection Kit for Paraffin-embedded Tissue Sections (GenScript, Picastaway, NJ, USA) according to the manufacturer’s instructions. Briefly, proteinase K treated samples were permeabilized with 0.1% Triton X-100 and 0.1% sodium citrate for 10 min and incubated with Blocking Solution II (GenScript) for 30 min. Subsequently, tissues were covered with 50 μL of TUNEL Reaction Mixture (GenScript), incubated at 37 °C for 1 h in a dark humidified chamber and washed in PBS. Sections were examined in an LSM 5 Exciter confocal microscope (Carl Zeiss MicroImaging GmbH, Jena, Germany) using excitation wave 450–500 nm and emission wave 515–565 nm (green). Fluorescence intensity was quantified with the ImageJ software 1.46r  and data were analyzed by ANOVA (p-value cutoff of 0.05) using SPSS 15.0 for Windows (SPSS Inc).
Selective capture of transcribed sequences (SCOTS)
Selective capture of Salmonella transcripts from MLN of pigs at 2 dpi was performed by the SCOTS method , following the procedure described by Sheikh et al. . Briefly, 5 μg of total RNA from infected MLN samples was converted into first strand cDNA by using random priming and Superscript III reverse transcription (Life Technologies). Subsequently second strand cDNA was produced employing DNA polymerase I (Klenow fragment, Life Technologies). To create a corresponding in vitro Salmonella Typhimurium cDNA sample for comparison, the same bacterial isolate employed in the experimental infection was grown to early-log growth phase (OD600 = 0.3) and late-log growth phase (OD600 = 0.8) in Luria Bertani (LB) broth. Afterwards, Salmonella Typhimurium transcripts were selectively captured from in vivo and in vitro double stranded cDNA by hybridization to sonicated biotinylated genomic Salmonella DNA, which was previously blocked with Salmonella ribosomal DNA fragments. Microbial cDNA-genomic DNA hybrids were then captured by binding to streptavidin-coated beads (Dynabeads M-280 streptavidin, Invitrogen) and bacterial transcripts were eluted by alkaline denaturation. Eluted bacterial cDNA was then PCR-amplified with conserved primers and finally purified using Qiagen PCR column purification kit (Qiagen). After that, one round captured and purified cDNA from both in vitro and in vivo conditions were quantified by spectrophotometry and used as template (10 ng) for qPCR assays as described above. Primer pairs used for amplifications can be found as supporting information (see Additional file 2). Gene expression levels were estimated employing gyrA as the reference gene. Since tissue from uninfected pigs was negative for Salmonella, those samples could not be used as reference for fold change calculations of pathogen gene expresion. In addition, most screened genes showed Cq values inferior to those observed for gyrA in infected MLN. For these reasons, gene expression levels were alternatively estimated as follows: gyrA Cq – target gene Cq. Higher values meant higher expression levels and vice-versa.
Transcriptional changes in porcine MLN upon salmonella Typhimurium infection and data validation
Microarray technology coupled to a Bayesian analysis was employed to explore the transcriptional response of porcine MLN to Salmonella Typhimurium along a time course of 1, 2 and 6 dpi. BATS, a method specifically designed for the analysis of time series microarray data , revealed significant changes in expression (BF < 0.05) for 290 transcripts, representing 285 unique genes, as a result of the bacterial challenge (see Additional file 3). Then, to validate data, qPCR assays were performed on a panel of fourteen genes identified by BATS analysis. As expected, all of them were confirmed to be significantly regulated (p < 0.05) after infection (Table 1). Furthermore, an identical expression trend was observed for most screened genes by qPCR and microarray analysis.
Biological interpretation of microarray data
Top five biological functions enriched in MLN of pigs infected with Salmonella Typhimurium .
Input genes (n)
4.64E-05 – 2.65E-02
6.52E-05 – 1.86E-02
1.8E-04 – 1.68E-02
1.8E-04 – 2.67E-02
Cell-to-cell signaling and interaction
1.8E-04 – 2.67E-02
Modulation of immune response mechanisms
Tissue morphology and cell death
Salmonella Typhimurium localization and gene expression in vivo
Gut-associated lymphoid tissues have been proved to be an important niche for Salmonella during pig infections. Previous reports stated that Salmonella Typhimurium can be found in MLN of infected pigs from 2 h  up to 6 weeks after oral inoculation  and sustain these organs as immune inductive sites during pig salmonellosis [6, 7, 10, 26, 27]. For this reason, in this work we aimed at dissecting host response mechanisms occurring in porcine MLN upon interaction with Salmonella Typhimurium. Additionally, expression of some Salmonella virulence effectors was also analyzed in infected tissues attempting to integrate information from both the host and pathogen.
The systems biology analysis reported in this study demonstrates the involvement of MHC molecules in several mechanisms triggered in swine MLN after bacterial challenge. Intriguingly, both MHCI and MHCII encoding genes were found to be down-regulated all along the studied time course, in spite of the increased levels observed for these receptors at 1 dpi by Western blot and microscopic analysis. We envisage that initially, antigen presenting cells bearing high levels of MHC migrate to MLN leading to an increase of these receptors in tissue, as suggested by the detection of Salmonella antigens in cells showing high levels of MHCII. Subsequently, processes carried out in MLN might reduce MHC mRNA and protein expression levels at later times of infection. Previous studies demonstrate that Salmonella interferes with antigen presentation by reducing MHCII surface expression via a mechanism dependent on the Salmonella pathogenicity island (SPI)- 2 encoded effector SifA [28–30]. It is noteworthy that in this study we show that sifA is expressed by Salmonella Typhimurium in porcine MLN. Besides, it has been previously observed by us  and others  that pig infections with Salmonella Typhimurium do not produce an up-regulation of cytokines involved in T helper 1 (Th1) response in MLN, on the contrary to previous reports in mice . These findings could be related to the ability of pathogens to limit antigen presentation to CD4 restricted T cells by reducing MHCII levels in infected cells. Salmonella removes mature MHCII complexes from the cell surface by enhancing their ubiquitination in a clathrin and AP2-dependent way . Curiously, we identified the “Protein ubiquitination pathway” and “Clathrin-mediated endocytosis signaling” as the most significantly affected canonical pathways upon infection. In spite of the reported use of clathrin-mediated endocytosis in bacterial-induced internalization, Salmonella is not able to employ this machinery to invade . So, instead of promoting direct entry of the pathogen to host cells, enrichment of clathrin-mediated endocytosis could be related to the modulation of MHCII expression by Salmonella found in tissue. Therefore, this evidence as a whole could suggest a hampering of processes mediated by MHCII in swine MLN following Salmonella infection.
On the contrary, network analysis also associated “Clathrin-mediated endocytosis signaling” to “CTLA4 signaling in cytotoxic T lymphocytes’ pathway”, bringing to light a possible role of the former process in adaptive immunity triggering. CTLA4, an important negative regulator of the T cell immune response , is endocytosed via a clathrin and dynamin-dependent route in activated T-cells . According to Johanns et al. , up-regulation of CTLA4 in regulatory T cells restrains effector T cell activation at early infection time points and allows the increase of bacterial burden during murine salmonellosis. Similarly, Inoue et al.  state that CTLA4-mediated Treg immunosuppression is critical in preventing the host from eliminating invasive pathogens. Given that, CTLA4 down-regulation, concurrent with clathrin up-regulation after the bacterial challenge, could indicate the repression of a mechanism of T cell inhibition in porcine MLN upon Salmonella Typhimurium infection. However, since clathrin could be involved in the establishment of both host immunity mechanisms and virulence strategies evolved by the pathogen, a deeper investigation of processes mediated by this molecule during infection is necessary and could provide relevant knowledge on the pathogenesis of porcine salmonellosis.
Current results also pointed to the generation of adaptive immunity mechanisms in infected tissue at a short time after infection. High MHCI levels observed by Western blot at 1 dpi reinforce our previous evidence that Salmonella antigens are cross-presented in swine MLN at initial stages of infection . Cross-presentation is a mechanism that enables antigen presenting cells to prime CD8+ T cells via their own MHCI molecules . Interestingly, it has been reported that differently from MHCII, Salmonella is not able to reduce MHCI surface expression of infected cells and consequently avoid early host cytotoxic response [28–30]. Therefore, cross-presentation might lead to an early Salmonella Typhimurium clearance by cytotoxic T cells during porcine infections, in agreement with the stimulation of Salmonella-specific CD8 T cells readily observed after mice and human infections . Additionally, CD180, an inducer of B cell proliferation, activation and differentiation , was uncovered to be up-regulated all along infection. Taken together, our results indicate that both cellular and humoral immunity mechanisms are effectively engendered in porcine MLN at a short time after infection with Salmonella Typhimurium. Thus, the dynamics of this protective response could be decisive in the course of infection by this pathogen in pigs.
Evidence of pyroptosis induction and apoptosis dampening in infected MLN were disclosed in the current study, supporting our previous reports . Thus, microarray data mining detected an enrichment of processes such as “Negative regulation of apoptosis” and “Antiapoptosis” after the bacterial challenge, in addition to up-regulation of genes encoding for an inhibitor of apoptosis proteins (IAP) like XIAP and PDCL3. Induction of apoptosis has been asserted as a strategy that facilitates Salmonella cell-to-cell spread during systemic infection . Nevertheless, it has also been reported that AvrA, a Salmonella effector protein, prevents the apoptotic elimination of host cell niche as a pathogen evasion mechanism . Intriguingly, we observed in vivo expression of spvB and sseL, both major Salmonella Typhimurium apoptosis inducers, and the apoptosis inhibitor avrA, indicating that Salmonella appeared to execute virulence mechanisms to modulate apoptosis in porcine MLN in its favor.
As in apoptosis, pyroptotic cells show DNA fragmentation, nuclear condensation and positive TUNEL staining [41, 42]. However, pyroptosis inherently results in inflammation due to caspase-1-mediated maturation of pro-IL-1β and pro-IL-18 and release of the cytoplasmic content, whereas the apoptotic cell is considered to be immunologically silent . In the current study, increase of TUNEL positive labeling was observed in the tissue at 1 dpi, as well as infiltration of inflammatory cells and IL1β up-regulation. Therefore, we propose that once apoptosis is dampened, the infected cell undergoes pyroptosis in swine MLN, producing pathogen discharge to the extracellular milieu and clearance of bacteria by innate mechanisms. In support of this, we previously reported an increase of phagocyte counts and mRNA levels of pro-inflammatory genes upon infection with Salmonella Typhimurium and a significant reduction of the pathogen burden at 6 dpi .
In line with this, an elegant study by Miao et al.  stated that Salmonella Typhimurium is able to damper pyroptosis for its own advantage by avoiding flagellin expression during infection of mice. Interestingly, we found expression of Salmonella Typhimurium flagella component (FliC) and regulators (FliA and FljA) in infected MLN. Additionally, flagella expression by infecting bacteria found in tissue was also corroborated by labeling using a specific polyclonal antibody. Salmonella enterica alternately expresses two different flagellar filament proteins, FljB and FliC, in a process known as flagellar phase variation. In spite of the high homology level found between these proteins, their middle surface exposed sequences of amino acids are divergent, resulting in distinct antigenicities . It is noteworthy that our results demonstrate higher expression levels for fliC and its regulator fliA in vitro than in vivo. On the contrary, fljA, which is cotranscribed with fljB, was more expressed in Salmonella Typhimurium found in vivo. Moreover, this gene was notably less expressed than fliA and fliC in both early and late logarithmic phase cultures. Based on this, we deduced a skewing toward FliC flagellin expression by bacteria in vitro. Besides, we drew the inference that a more heterogeneous flagellin expression is found in Salmonella Typhimurium replicating in vivo and that induction of flagellar phase variation could be a strategy adopted by this pathogen to hinder pig immune response. Expression of prgJ was also uncovered in swine MLN. Curiously, repression of this effector has been reported as a mechanism of pyroptosis inhibition in vivo . Thus, it could be inferred that expression of flagellin and prgJ by Salmonella Typhimurium found in tissue might enable pigs to use pyroptosis to clear bacteria in gut associated lymph-nodes, protecting itself from pathogen dissemination. Nevertheless, an issue that should be addressed by our assumption is why pathogen burden in tissue peaks after pyroptosis triggering. Miao and Rajan  stated that in a single cell, pyroptosis only takes place at late times of infection, following bacteria replication. So, we inferred that increase of pathogen load at 2 dpi may be due to the release of replicated Salmonella from cells dead by pyroptosis.
Notably, the presence of TUNEL positive cells in MLN was significantly reduced at 2 and 6 dpi, suggesting a decrease of cell death by apoptosis or pyroptosis. As with any physiological process, excessive pyroptosis is detrimental to the host . So, modulation of this pathway by the host aiming to restore tissue integrity should be expected. Actually, we observed up-regulation of MAP3K7 and TRAF7, both involved in NF-kB and survival pathway activation, at 2 and 6 dpi. However, evidence indicates that inhibition of caspase-dependent apoptosis primes cells towards programmed necrosis . Since the mechanisms that dictate the cellular decision to survive by activating NF-kB or to die through apoptosis or necroptosis are still unclear  further research is necessary to clarify these results.
In conclusion, the results provided led us to infer that although the Salmonella Typhimurium strain employed in this study was able to express some of its major virulence effectors in porcine MLN, a combination of early host triggered innate and adaptive immunity mechanisms might overcome virulence strategies employed by pathogens. Besides preventing apoptosis, swine appear to take advantage of flagellin and prgJ expression by pathogens to induce pyroptosis in MLN. In this context, pyroptosis might consist in a host protective mechanism that prevents pathogen spread beyond gut-associated lymph-nodes. Furthermore, cross-presentation of Salmonella antigens in MLN might result in a rapid clearance of pathogens by cytotoxic T cells. Functional relevance was also shown by clathrin-mediated endocytosis that could contribute to mechanisms of pathogen virulence and/or host defence in MLN of Salmonella infected swine. Further analysis of examined mechanisms may support the discovery of novel strategies of host defense against Salmonella at the intestinal level.
We thank Erena Ruiz Mora, Juana Molina and Reyes Alvarez for skillful technical assistance, Esther Peralbo for technical support in confocal microscopy analysis (IMIBIC) and Eloisa Andújar and Mónica Pérez from the Genomic Unit of CABIMER for their excellent array technical assistance. This work was supported by the Junta de Andalucía (P07-AGR-02672), the Spanish Ministry of Science and Innovation (AGL2008-00400 and AGL2011-28904) and EU funds through the SABRE project and EADGENE network. RPM and CA are predoctoral researchers supported by the FPU Research Program of the Spanish Ministry of Education and Science.
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