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Salmonella enterica, a common food-borne bacterial pathogen, is believed to change its protein expression profile in the presence of different environmental stress such as that caused by the exposure to hydrogen peroxide (H2O2), which can be generated by phagocytes during infection and represents an important antibacterial mechanism of host cells. Among Salmonella proteins, the effectors of Salmonella pathogenicity island 1 and 2 (SPI-1 and SPI-2) are of particular interest since they are expressed during host infection in vivo and are important for invasion of epithelial cells and for replication in organs during systemic infection, respectively. However, the expression profiles of these proteins upon exposure to H2O2 or to host cells in vivo during the established phase of systemic infection have not been extensively studied.
Using stable isotope labeling coupled with mass spectrometry, we performed quantitative proteomic analysis of Salmonella enterica serovar Enteritidis and identified 76 proteins whose expression is modulated upon exposure to H2O2. SPI-1 effector SipC was expressed about 3-fold higher and SopB was expressed approximately 2-fold lower in the presence of H2O2, while no significant change in the expression of another SPI-1 protein SipA was observed. The relative abundance of SipA, SipC, and SopB was confirmed by Western analyses, validating the accuracy and reproducibility of our approach for quantitative analysis of protein expression. Furthermore, immuno-detection showed substantial expression of SipA and SipC but not SopB in the late phase of infection in macrophages and in the spleen of infected mice.
We have identified Salmonella proteins whose expression is modulated in the presence of H2O2. Our results also provide the first direct evidence that SipC is highly expressed in the spleen at late stage of salmonellosis in vivo. These results suggest a possible role of SipC and other regulated proteins in supporting survival and replication of Salmonella under oxidative stress and during its systemic infection in vivo.
Salmonella enterica is one of the leading causes of food-borne illnesses around the world [1,2]. There are two major serotypes of Salmonella enterica, namely Salmonella enterica serovar Enteritidis (S. Enteritidis) and Typhimurium (S. Typhimurium). In recent years, S. Enteritidis represents one of the most commonly reported serotypes associated with food poisoning illness in the United States . Two hallmarks of Salmonella pathogenesis are the invasion of non-phagocytic cells such as the epithelial cells of the intestinal mucosa, and the survival inside macrophages during systemic infection. The mechanisms of both processes are linked to the functions of two type III secretion systems (T3SS) of Salmonella that are encoded and regulated by a cluster of genes at the Salmonella Pathogenicity Island 1 and 2 (SPI-1 and SPI-2), respectively. It is believed that SPI-1 T3SS is responsible for invasion of non-phagocytic cells, while SPI-2 T3SS is essential for intracellular replication and systemic infection [4,5].
In order to survive and replicate in an aerobic environment, organisms including Salmonella must cope with reactive oxygen species such as hydrogen peroxide (H2O2), which are formed in respiring cells as incomplete reduction products of molecular oxygen, and which can cause damage to DNA, RNA, protein, and lipids [6-8]. To respond to oxidative stress, bacteria activate a set of globally regulated genes, including two known stimulons: peroxide stimulons and superoxide stimulons [7,9-12].
The response of Salmonella to oxidative stress represents a key component of its pathogenesis [7,9]. Reactive oxygen species generated by the NADPH phagocytic oxidase system in phagocytes play an important role in controlling Salmonella replication in macrophages and systemic infection in the spleen [13,14]. To combat the damaging effects of this oxidative stress and survive in macrophages during systemic infection such as in the spleen, it is believed that Salmonella uses unique strategies and expresses specific proteins to carry out defense and repair functions [7,9]. While little is known about the expression of SPI-1 factors upon oxidative stress, several SPI-1 factors SipA, SopA, SopB, SopD, and SopE2 of S. Typhimurium were found to be expressed in the spleen of infected animals at the late stages of infection when Salmonella is believed to replicate in splenic macrophages [15,16]. These results suggest that in addition to their generally recognized roles in invasion, the SPI-1 factors may also play an important role post-invasion, including a possible role in resistance to the oxidative stress generated by tissue macrophages. An understanding of the expression profiles of Salmonella SPI-1 factors and other proteins in the presence of reactive oxygen species such as H2O2 should provide insight into the identification of virulent determinants important for Salmonella to survive in macrophages and cause systemic infection in the spleen in vivo.
The expression of Salmonella genes (including those encoding SPI-1 factors) in vitro under various conditions has been extensively studied [17-21]. However, most of these studies were performed by examining the transcription levels of Salmonella genes either using microarray or a reporter system [17,19-23]. Recently, proteomic analysis of Salmonella protein expression in the spleen of infected animals has been reported . Furthermore, Smith and co-workers have reported global protein profiles of Salmonella enterica serovars Typhimurium and Typhi cultured at the stationary phase, logarithmic (log) phase, or phagosome-mimicking culture conditions, and the expression profiles of proteins in infected macrophages [25-28]. However, to our knowledge, global expression profiling of Salmonella proteins upon exposure to reactive oxygen species such as H2O2 has not been reported, and efforts to identify proteins whose expression levels are affected by oxidative stress have been limited mostly to a few proteins at a time [9,29,30]. In addition, expression of Salmonella proteins including those of SPI-1 in vivo during the established phase of infection has not been extensively studied.
In this study, we have modified the procedure of Stable Isotope Labeling by Amino acids in Cell culture (SILAC) [31,32] to develop a mass spectrometry (MS)-based approach to carry out quantitative proteomic analysis of Salmonella. Using this procedure, we have identified 76 proteins from a strain of Salmonella enterica serovar Enteritidis that are differentially regulated upon exposure to H2O2. The results on selected SPI-1 proteins were confirmed by Western blot analyses, validating the accuracy and reproducibility of our approach for quantitative analyses of protein expression. The expression of several SPI-1 proteins was further analyzed in infected macrophages and in the spleen of infected mice. These results suggest a possible role for SPI-1 proteins in Salmonella infection in the presence of oxidative stress and in systemic infection in an animal host.
We used a virulent clinical isolate of Salmonella enterica serovar Enteritidis SE2472 for this analysis. Our previous studies have shown that almost all clinical strains analyzed, including SE2472, exhibited similar levels of resistance to H2O2 . We chose this strain to examine the expression profiles of Salmonella proteins upon exposure to H2O2, a stress condition relevant to what Salmonella may encounter in macrophages and in the spleen during bacterial infection in vivo. To determine protein levels in two or more different biological states (e.g. in the absence and presence of H2O2), we modified the SILAC procedure (Figure (Figure1)1) in which the introduction of a stable isotope 15N into the protein mixture provides a means to quantitatively analyze two sets of protein mixtures simultaneously [31,32]. Stable isotope-based quantification relies on the premise that the relative signal intensity of two analytes that are chemically identical but different in stable isotope compositions can be resolved in a mass spectrometer, thus giving a true measure of the relative abundance of the analytes [31,32,34,35]. To determine the efficiency of the labeling and incorporation of the heavy isotope, SE2472 was grown in 15N-containing LB broth-like media. SE2472 appeared to grow in the normal (14N) and 15N-containing LB broth-like media as well as in the LB broth as they reach similar titers in these media (data not shown). Bacteria were harvested at different time points and the extent of 15N-labeling of Salmonella proteins was examined by MS analysis in comparison to the control 14N labeled bacteria. Growth in 15N-labeled media for 6 hours or more was sufficient to label the entire Salmonella proteome with 15N (data not shown). The proteins examined and all the peptides of each protein appeared to have identical incorporation rate. Accordingly, all labeling experiments were carried out for at least 6 hours in this study.
One of our main objectives in the study was to use the expression of the labeled proteins to monitor Salmonella protein levels when Salmonella is exposed to oxidative stress. Thus, it is necessary to determine whether 15N-labeled Salmonella retain the growth and oxidative stress-resistant properties of the unlabeled SE2472 in vitro. 15N-labeled Salmonella appeared to grow as well as the unlabeled bacteria in LB broth (Figure (Figure2A).2A). No detectable difference in the colony size and morphology was observed between these two cultures. Furthermore, no difference was detected between the survival of the N14- and N15-labeled bacteria in either the LB broth-like labeling media or the LB broth in the presence of 5 mM H2O2, a concentration well below the minimal inhibition concentration (MIC) of SE2472 (20 mM) but substantially above the natural extracellular environment (Figure (Figure2B2B).
To investigate the expression profiles of Salmonella upon exposure to oxidative stress, single colonies of SE2472 were grown in 14N- or 15N-containing LB broth-like media and only the 15N culture was treated with 5 mM H2O2 for 2 hours to simulate the oxidative stress condition (Figure (Figure1).1). Total proteins from the 14N- and 15N- samples were extracted and quantified. A 1:1 (by weight) mixture of two samples was prepared and 200 μg of total proteins were separated by two-dimensional (2-D) gel electrophoresis. Visualization by silver staining revealed approximately 200 protein spots across the pI and molecular weight range of the gel, which were further investigated using quantitative proteomics (Figure (Figure33).
Analysis with matrix-assisted laser desorption/ionisation-time of flight (MALDI-ToF) mass spectrometry was performed to map tryptic fragments from the mixture of the 14N- and 15N-(unexposed and H2O2-exposed) samples, where two sets of peptide fingerprints appear on the same spectrum (Figure (Figure4,4, Table Table1).1). We distinguished the two sets of peaks by initially using the 14N peaks to identify the protein and amino acid contents of each peak (Figure (Figure44 and Table Table1),1), then using peak information to deduce the location of the 15N peaks. The ratio of the peak heights (15N/14N) was then used for relative quantification (Figures (Figures11 and and4).4). Figure Figure44 shows an example taken from a protein sample, a tryptic peptide fragment FTGWYDVDLSEK (MW 1459.81) from S. Enteritidis phosphoglyceromutase. A peak at m/z 1473 represents the 15N-labeled population (Figure (Figure4,4, upper spectrum), which does not appear in the unlabeled population. The ratio of two peak intensities (27 and 17, respectively) represents a relative protein expression level of 0.6, or a 40% downregulation. To further increase the accuracy of our results, each set of experiments was repeated three times. Only those proteins that were detected and identified with high confidence in all three independent experiments are listed in Table Table22.
Predicting the location of 15N peaks for any given peptide was a two-step process. First, the protein was identified and the amino acid contents of each peak were searched using the MASCOT software. Based on the number of nitrogen atoms in the peptide, a prediction was then made as to the molecular weight of the 15N peaks. To facilitate this process, we developed a custom VBScript for Microsoft Excel that automatically predicts 15N peak locations with a simple copy and paste feature. Using this script, many sets of peak data can be processed within minutes, virtually eliminating the need to manually inspect each peak for the number of nitrogen atoms.
Using the developed program, we generated a list of 103 SE2472 proteins and their expression profiles upon exposure to H2O2 (Table (Table11 and and2).2). All these proteins were detected and identified with high confidence in all three independent experiments. We should note that the absence of a protein in our results does not necessarily mean it was not expressed and/or induced; instead its expression status is yet to be determined. The majority of protein expression was up-regulated, albeit at different levels. We further categorized proteins into different groups based on their functions, as shown in Table Table3.3. Interestingly, SipC and SopB, which are the SPI-1 translocase and effector, were differentially expressed in the presence of H2O2. SipC was about 3-fold higher and SopB was 2-fold lower in the exposed samples, while no significant change in the expression of another SPI-1 protein SipA was observed (Table (Table22 and and33).
To demonstrate the validity of our proteomic results, we examined the relative abundance of SipA, SipC, and SopB by Western blot analysis. Salmonella strains SipA(HF), SipC(HF) and SopB(HF) were derived from SE2472 and contained a FLAG epitope tag sequence at the carboxyl terminus of sipA, sipC and sopB, respectively . The tagged strains grew in LB broth as well as the parental strain SE2472, indicating that the insertion of the tag sequence did not significantly affect bacterial growth in vitro (data not shown). To study the pathogenesis of the tagged strains in oral and systemic infection, we infected BALB/c mice intragastrically and intraperitoneally with the tagged Salmonella strains and compared infected mice to those infected with the wild type SE2472. The survival of infected mice and the colonization of spleen, liver, and ileum of the infected mice by Salmonella were determined at different time points post infection. For BALB/c mice infected intragastrically with 1 × 106 CFU of the tagged or the wild type strains, all infected mice died within 7 days post infection and no significant difference was observed among the wild type and the tagged strains (Figure (Figure5A).5A). No significant difference in the colonization of the internal organs such as spleen, liver, and ileum, was observed between the parental (wild type) SE2472 strain and the tagged strains regardless of the route of inoculation (Table (Table4).4). These results suggest that tagging of the target ORF does not impair the invasiveness, growth, and virulence of the bacteria, and that the tagged strains can be used as model strains to study infection of Salmonella in vitro and in vivo, including the expression of the SPI-1 proteins.
To determine the effect of H2O2 on the expression of the tagged ORFs, bacterial strains were grown in LB broth in the absence and presence of H2O2. Western blot analyses were used to determine the expression of the tagged proteins with an anti-FLAG antibody (Figure (Figure5B,5B, top panel). The expression of bacterial FliC protein, which was not significantly altered in the presence of 5 mM H2O2 (Table (Table2),2), was used as the internal control (Figure (Figure5B,5B, lower panel). Normalization of samples was also carried out by loading total proteins extracted from the same CFU (e.g. 5 × 107 CFU) of bacteria in each lane. Consistent with the results from our proteomic analyses (Table (Table22 and and3),3), the levels of SipC and SopB were about 3-fold higher and 2-fold lower in the presence of H2O2, respectively, while no change in the expression of SipA was detected (Figure 5B-C).
Immunodetection of the SPI-1 proteins in cultured media in the absence and presence of H2O2 validated the proteomic observations. To evaluate the presence of these proteins in an environment more relevant to infection, the tagged Salmonella strains were used to infect macrophages and mice, and the expression of the tagged proteins was determined by immunodetection at different time points following infection. The expression of the tagged proteins in the bacterial strains isolated from the macrophages and the spleen of infected mice was detected using Western blot analysis with an anti-FLAG antibody and normalized using the expression of bacterial protein DnaK as the internal control (Figure 6A-B). Normalization of protein samples was also carried out by loading total proteins extracted from the same CFU (e.g. 5 × 107 CFU) of bacteria in each lane. The protein level of DnaK did not appear to be significantly different in bacteria recovered from macrophages , and from the spleen of infected animals as similar amount of the DnaK protein was detected from 5 × 107 CFU of each bacterial strain regardless of infection route (intraperitoneally or intragastrically) or time point postinfection (12-24 hours or 5-7 days)(data not shown).
In cultured macrophages, SipA, SipC, and SopB were all expressed at the early phase (e.g. 0.2 h) of infections. However, by 5 hr post infection, the levels of the three SPI-1 proteins diverged, with the SipC level increased, the SopB level decreased while SipA level remained unchanged (Figure (Figure6A6A and and6C).6C). To determine the relative abundance of these proteins in the spleen during systemic infection, BALB/c mice were infected intraperitoneally. Salmonella was recovered from the spleen at different time points postinfection, and the expression levels of the tagged proteins were determined. Similar to the results of macrophage infection, all three proteins were detected during the early stage of infection (i.e. 0.5 days). However, at a later stage of systemic infection (i.e. 5 days), the level of SipC increased and the level of SopB decreased while the level of SipA remained unchanged (Figure (Figure6B6B and and6D).6D). These results correlated with those observed in the proteomic analyses and in the macrophage experiments. Furthermore, these data strongly suggest that different SPI-1 factors are specifically expressed at late stage of Salmonella infection, and highlight a possible role of SipC in late phase of macrophage and in vivo infections of Salmonella.
In the postgenomic era, new methodologies are needed that can quantitatively, globally, and accurately measure protein expression in cells and tissues . In this study, we have modified the SILAC method to develop a stable isotope labeling procedure coupled with MS analysis to carry out quantitative proteomic analysis of Salmonella. As a "proof of principle" pilot study, a total of 103 SE2472 proteins were monitored for their expression profiles upon exposure to H2O2.
At least seventy six proteins have been found to be modulated in the presence of H2O2. For example, the expression of SPI-1 proteins SipC and SopB was found to be differentially regulated in the presence of H2O2, while the expression of SipA remained unchanged. The level of SipC increased with H2O2 exposure, and the level of SopB decreased. These results were confirmed using Western blot analyses of protein expressions from FLAG-tagged Salmonella strains incubated with H2O2, validating the accuracy and reproducibility of our system for quantitative analyses of protein expression.
Many Salmonella proteins we analyzed showed a moderate amount of up-regulation upon exposure to oxidative stress (Table (Table22 and and3),3), consistent with earlier studies involving E. coli's response to oxidative stress [9-11,38]. For example, RecA (DNA strand exchange and recombinant protein) has been shown to be induced along with members of heat shock proteins . The expression of superoxide dismutase SodB, which is a part of the SoxRS system [6,7,9], increased by 110%. When categorized by protein functions, we observed several patterns (Table (Table3).3). First, many enzymes involved in glycolysis and the TCA cycle were upregulated, showing up to a 330% increase. Consistent with the increase in general metabolism, amino acid biosynthesis was also affected in a positive fashion. Considering that intermediates from the glycolytic pathway are used in amino acid biosynthesis, the overall upregulation in downstream pathways is expected. This is consistent with our previous observations that amino acid supplementation increased the resistance of E. coli to H2O2 . Interestingly, the pentose phosphate pathway was relatively unaffected in the presence of H2O2. Since one of the primary functions of the pathway is to generate ribose-5-phosphate for the synthesis of nucleotides and nucleic acids, other enzymes involved in nucleotide biosynthesis should show little change either. As expected, three such enzymes detected in this study (i.e. amidophosphoribosyltransferase, thymidine phosphorylase, and uridine phosphorylase) showed a varied response, ranging from a minor upregulation to a downregulation (Table (Table3).3). Further investigation of additional enzymes involved in the process should reveal the nature of this response.
We have noted that different proteins within the same operon may exhibit different expression levels in our results. Differential expression of proteins within the same operon has been reported  and may represent a regulatory mechanism for the expression of functional protein complexes. We have also noted that in some instances one protein was detected while another within the same operon was not. For example, redundant hydrogen peroxide scavenger systems have been reported to be present in Salmonella . In our results, AhpC was not regulated while the other scavengers (KatE, KatG, KatN and TsaA) were not detected. One of the reasons for the divergence from expected protein level could be the limitation of the methodology we used in the study.
We used two-dimensional (2-D) gel electrohphoresis coupled with peptide fingerprinting by mass spectrometry which allowed us to perform global protein profiling quantitatively. However, our methodology is limited to proteins that can be detected by 2-D gel electrophoresis and identified by peptide fingerprinting. Proteins with low abundance or could not be identified by peptide fingerprinting for various reasons (e. g. post-translational modifications, resistance to trypsin digestion, or poor ionization of peptides) were not included in our analysis. Thus, our study by no means encompasses all the possible proteins expressed by SE2472 and we are presenting only the proteins we were able to successfully identify by peptide fingerprinting with high confidence in all three independent experiments. The absence of a protein in our results does not necessarily mean it was not expressed and/or induced; instead its expression status is yet to be determined. Our results are consistent with the notion that current proteomic approaches, including liquid chromatography mass spectrometry (LC-MS) and MALDI-ToF procedures, do not have the capacity to detect the entire proteomes of Salmonella [25-28]. Each approach has been shown to detect a distinct set of Salmonella proteins that exhibited limited overlap of protein coverage, and these complementary approaches should be carried out independently to generate a complete and full coverage of bacterial proteomes.
Our proteomic results on SPI-1 proteins SipA, SipC, and SopB suggest that the expression of these proteins may be differentially modulated during infection under biologically relevant environments that resemble the oxidative stress condition. Efficient expression of SipA at late stage of infection in macrophages and in the spleen, as shown in our results, has been observed in Salmonella enterica serovar Typhimurium [15,16]. This is consistent with its functions in modulating actin dynamics and bacterial localization in infected macrophages [42-44] and in inducing inflammatory response for supporting Salmonella infection [45,46].
Our results of SopB protein expression are consistent with recent proteomic analysis results that Salmonella enterica serovar Typhimurium (strain 14028) reduced SopB protein expression by more than 2-fold within 4 hours of infection of RAW264.7-like macrophages . SopB encodes a phosphoinositide phosphatase and is a multifunctional protein important for bacterial infection . It facilitates bacterial invasion by inducing membrane ruffling and modulating actin polymerization [49-51], and stimulates inducible nitric oxide synthase (iNOS) production long after invasion and participates in the formation of the Salmonella-containing vacuole in macrophages [52-54]. Recently, SopB has been shown to carry out its diverse functions by localizing to different cellular compartments in a ubiquitin-dependent manner . The reduced expression of SopB in the presence of H2O2 and at later time points of infection in macrophages and in the spleen in our study is consistent with the notion that SopB negatively regulates expression of sorting nexin 6 (SNX6), a protein involved in intracellular transport .
Our results also provide the first direct evidence that SipC is expressed in the spleen at late stages of Salmonella enterica serovar Enteritidis infection in mice. SipC is a Salmonella invasion protein (Sip) that is central for the initiation of the bacterial entry process. SipC and SipB form an extracellular complex following their secretion through the SPI-1 T3SS, and they are thought to assemble into a plasma membrane-integral structure (translocon) that mediates effector delivery [55-57]. Furthermore, SipC has been reported to promote actin nucleation and contribute to Salmonella-induced inflammation . While the expression of SipC has been studied in vitro, its expression in the spleen has not been extensively investigated. The induced expression of SipC in Salmonella in the presence of oxidative stress and at late stages of infection in macrophages and in the spleen suggests that the level of this protein is highly regulated in vivo and that appropriate level of expression may contribute to the pathogenesis of Salmonella. This is consistent with recent observations that the translocase activity of SipC is important for the delivery of effector proteins and attachment of Salmonella to non-phagocytic cells; however, in the context of systemic infection, its actin-binding activity may facilitate bacterial infection of phagocytes [5,58,59]. Thus, examination of the expression of SipC and other SPI-1 factors both in vitro and in vivo in the context of infection, as reported in our study, is crucial to ultimately understand the actual functions and actions of these factors.
Using a different quantitative proteomic analysis approach without stable isotope labeling, Smith and co-workers have recently reported the protein expression of Salmonella enterica serovars Typhimurium and Typhi that grew in different culture conditions (e.g. stationary, log, and phagosome-mimicking conditions) and in macrophages [25-28]. Proteomic analysis of Salmonella protein expression in the spleen of infected animals has also been reported . In these studies, the protein expression of the S. Typhimurium homologs of many of the oxidative stress-responsive proteins identified in our study were found to be modulated under phagosome-mimicking conditions and in macrophages, further validating our analysis as an accurate and reproducible approach for quantitative proteomic analysis. Some of our protein expression results may not be consistent with those of messenger RNA expression that have been recently published [19-23] as the expression of many Salmonella genes is tightly controlled both transcriptionally and post-transcriptionally [18,60]. Our results of protein expression in vivo may not necessarily correlate with the previous observations in vitro because of the different environments Salmonella was exposed to. The difference between our results and previously published reports may also be due to the difference in the serovars and strains used for the studies, and the coverage of the proteins due to different methodologies used for the studies [25-28,33]. None of these previous studies has reported the differential expression of SipA, SipC, and SopB in hydrogen peroxide-treated Salmonella, as described in our study. Our results complemented and further extended previous proteomic analysis of Salmonella, and furthermore, demonstrated the importance of examining the expression of Salmonella proteins, including SPI-1 proteins, in vitro using different quantitative proteomic analyses and in vivo in the context of infection.
Each of the currently-available proteomic approaches, including LC-MS and MALDI-ToF procedures, can only detect a subset of Salmonella proteins and may exhibit limited overlap of protein coverage with other methods [25-28]. It is suggested that these complementary approaches should be carried out independently to generate a comprehensive coverage of bacterial proteomes. Further investigation with our quantitative proteomic approach, in combination with examination and confirmation of the expression of these proteins in vivo, should provide significant insights into the role of these proteins in pathogenesis during Salmonella infection.
We have employed stable isotope labeling coupled with mass spectrometry to carry out a quantitative proteomic analysis of Salmonella enterica serovar Enteritidis. Seventy-six proteins whose expression is differentially modulated upon exposure to H2O2 have been identified. SPI-1 effector SipC was expressed approximately 3-fold higher and SopB was expressed approximately 2-fold lower in the presence of H2O2, while no significant change in the expression of another SPI-1 protein SipA was observed. The expression of these SPI-1 factors was confirmed by Western blot analyses, validating the accuracy and reproducibility of our approach for quantitative analyses of protein expression. Furthermore, substantial expression of SipA and SipC but not SopB was found in the late phase of infection in macrophages and in the spleen of infected mice. This study provides the first direct evidence that SipC is highly expressed in the spleen at late stage of salmonellosis in vivo. Our results also suggest a possible role of the identified proteins, including SipC, in supporting the survival and replication of Salmonella under oxidative stress and during its systemic infection in vivo.
All reagents were obtained from Sigma-Aldrich unless otherwise specified. Salmonella enterica serovar Enteritidis (clinical isolate SE2472)  was cultured in LB broth-like normal (14N) and 15N-labeled media (Silantes GmbH, München, Germany), which are identical in chemical composition. The percentage of 15N in the labeled media is more than 98% (Silantes GmbH, München, Germany). The cultures were inoculated with a starter culture grown in normal (14N) or 15N-labeled media until mid-log phase. Two hundred fifty milliliter culture medium was inoculated with each starter culture and grown at 37°C with shaking at 225 rpm for 4 h. 15N-labeled culture was treated with 5 mM H2O2, which is well below the minimal inhibition concentration (MIC) of SE2472 (20 mM), and both cultures were grown for 2 h following the addition of H2O2. Protein extraction was performed with B-PER® bacterial protein extraction reagent (Thermo Fisher Scientific, Rockford, IL) and quantified with Dc Protein Assay Kit (Bio-Rad, Hercules, CA), which has an error rate of 2.5% in our experiments. We took this error rate into consideration by classifying any protein that had a 5% change or less as unchanged (having a 0% change).
Protein samples were further solubilized in rehydration buffer (8 M urea, 2% CHAPS, 50 mM DTT, 0.2% Bio-Lyte® 3/10 ampholytes [Bio-Rad, Hercules, CA] and trace amount of Bromophenol Blue). ReadyStrip™ IPG strips (Bio-Rad, Hercules, CA) were loaded with 200 μg of protein samples (either normal or 1:1 mixture of normal and 15N-labeled samples) for preparative 2 D gels, and allowed to rehydrate for 18-22 h. Isoelectric focusing (IEF) was performed at 20°C using PROTEAN® IEF cell (Bio-Rad, Hercules, CA). A 3-step protocol (250 V-20 min/8,000 V-2.5 h/8,000 V-10,000 V.h) was used for the IEF procedure following manufacturer's recommendations (Bio-Rad, Hercules, CA).
After the IEF procedure, the IPG strips were reduced in Equilibration Buffer I (6 M urea, 2% SDS, 0.375 M Tris-HCl [pH 8.8], 20% glycerol, 2% DTT) and alkylated in Equilibration Buffer II (6 M urea, 2% SDS, 0.375 M Tris-HCl [pH 8.8], 20% glycerol, 0.25% iodoacetamide). Strips were loaded onto 8-16% Criterion™ Tris-HCl SDS gel (Bio-Rad, Hercules, CA) and electrophoresed at 200 V for 65 min. Gels were visualized using Coomassie Brilliant Blue R-250 or silver staining (Invitrogen, Carlsbad, CA).
Gels were scanned and protein spots of interest were excised using the Xcise automated gel processor (Proteome Systems, North Ryde, Australia). Gel spots were destained and washed, followed by in-gel tryptic digestion using proteomic grade trypsin (Sigma-Aldrich, St. Louis, MO). Peptide fragments were collected and purified using ZipTip™ C18 reverse-phase prepacked resin (Millipore, Billerica, MA) and mixed with an equal volume of 10 mg/ml α-cyano-4-hydroxy-trans-cinnamic acid (Sigma-Aldrich, St. Louis, MO) in 0.1% trifluoroacetic acid (TFA)/50% acetonitrile solution and directly spotted onto a stainless steel target plate for mass analysis. Axima-CFR™ Plus (Shimadzu Biotech, Columbia, MD) was used for MALDI-ToF MS analysis, and 50-100 profiles were obtained for each sample, ensuring sufficient peak data for database interrogation. Probability-based scoring method with MASCOT database search engine (Matrix Science, Boston, MA) was used to identify each protein, based on the likelihood of search results being a random match. We used the following parameters for our protein identification: Database: NCBINR, MASCOT value cut off: greater than 62 (p < 0.05), Taxonomy: Salmonella, Missed cleavage: 1, Peptide Tolerance: +/- 0.75 Da, Variable modification: none, Fixed modification: none, Enzyme: Trypsin, Mass Values: Monoisotopic.
Tryptic peak data from MASCOT database searches was tabulated and elemental composition of each peptide fragment was determined using an in-house data analysis software. The process was further automated using a custom VBScript written for Microsoft Excel, which was designed to calculate predicted 15N peak location based on the primary amino acid sequence of tryptic peptide fragments. 14N/15N mixture MS spectrum was used to obtain peak intensity ratio between labeled (15N) and unlabeled (14N) samples to give relative quantification data. An average of 10 peaks was used to calculate the mean intensity ratios and the error percentage of each protein spot. Significant outliers were manually removed from the data set to prevent them from affecting the results (less than 2%). To further increase the accuracy of our results, experiments were preformed three times, and the results were the average from the triplicate experiments. Only those proteins that were detected and identified with high confidence in all three independent experiments are listed in Table Table11 and Table Table22.
Strains SipA(HF), SipC(HF) and SopB(HF) are derivatives of the wild type Salmonella enterica serovar Enteritidis strain SE2472 with a FLAG tag inserted in-frame at the C-terminus of each corresponding protein and have been described previously . Growth analysis of bacteria in LB or LB-like broth was carried out by first inoculating a single colony in 2 ml of either normal (14N) or 15N-labeled media and culturing at 37°C with shaking at 225 RPM overnight (about 16 hours) . Thirty microliters of the overnight culture were then inoculated into 3 ml fresh normal or 15N-labeled media or LB broth and cultured at 37°C with shaking at 225 RPM. At 0, 2, 4, and 6 hours after inoculation, 100 μl of bacterial culture were collected to determine their colony forming unit (CFU)/ml by plating. Salmonella grew in normal (14N) or 15N-labeled media as well as in LB broth (data not shown). To study the survival of Salmonella after exposure to H2O2, 20 μl of the overnight culture grown in normal (14N) or 15N-labeled media, or LB broth were added to 2 ml of fresh normal (14N) or 15N-labeled media, or LB broth containing 5 mM H2O2. At different time points of incubation, 100 μl of bacterial culture were collected, diluted, and plated onto LB agar plates to determine their CFU/ml [16,36]. Each sample was analyzed in triplicates and the analysis was repeated at least three times.
Colonies of tagged strains were inoculated in 1 ml of LB broth and cultured at 37°C with shaking at 225 RPM for 16 hours. To study the effect of H2O2 on the protein expression in vitro, 20 μl of overnight bacterial cultures were inoculated into 1 ml of antibiotic-free LB and shaken at 225 RPM at 37°C for 4 hours. The bacterial cultures were centrifuged at 5,000 × g for 5 minutes. The pelleted bacteria were re-suspended in 1 ml of fresh LB broth (control) or 1 ml of LB broth with 5 mM H2O2 and shaken at 225 RPM at 37°C for an additional 2 hours, and then collected.
To prepare protein samples from Salmonella, bacterial cultures (1 ml) were centrifuged at 5,000 × g and 4°C for 10 minutes. The pellets were re-suspended in 200 μl of bacterial lysis buffer (8 M urea, 2% CHAPS, and 10 mM Tris, pH8.0), sonicated for 15 seconds three times with an interval of 30 seconds, centrifuged at 5,000 × g and 4°C for 10 minutes, and then transferred into fresh tubes for Western blot analysis.
RAW264.7 macrophage-like cells (ATCC, Manassas, VA) were infected with stationary phase bacteria at a multiplicity of infection of 50. After incubation for 30 mins, infected cells were washed twice with phosphate-buffered saline (PBS) and incubated in DMEM medium supplemented with gentamicin (100 μg/ml) for 1 hour to eliminate extracellular bacteria. Then the cells were again washed twice with PBS, and incubated in DMEM supplemented with gentamicin (20 μg/ml). At various times postinfection, the cells were collected and resuspended in lysis buffer (120 mM NaCl, 4 mM MgCl2, 20 mM Tris-HCl [pH 7.5], 1%, Triton X-100) supplemented with protease inhibitors (complete EDTA-free cocktail, Roche Applied Science, Indianapolis, IN), incubated at 4°C for 1 hour, and centrifuged at 18,000 × g and 4°C for 10 minutes. The pellets that contained bacterial proteins were resuspended in PBS for Western blot analyses.
BALB/c mice (6-8 weeks old) were obtained from Jackson Laboratory (Bar Harbor, ME). Overnight bacterial cultures were serially diluted to suitable CFU/ml in PBS before infection. To assess the virulence of the tested strains, groups of five mice were either inoculated intragastrically with 1 × 106 CFU per mouse or intraperitoneally with 1 × 102 CFU per mouse. Mice were monitored during the course of infection, and those animals that exhibited extreme stress or became moribund were euthanized. For organ colonization experiments, groups of five mice were inoculated intraperitoneally with 1 × 104 or 1 × 106 CFU per BALB/c mouse of the bacterial strains, and were euthanized at 4 days or 12 hours after inoculation, respectively. Mice were also intragastrically infected with 1 × 106 CFU per BALB/c mouse of the bacterial strains, and were euthanized at 6 days after inoculation. Organs were collected and homogenized in PBS at 4°C. An aliquot of each homogenate was used to determine its CFU/ml by serial dilution with PBS and plating onto LB agar plates. Each sample was analyzed in triplicate and the analysis was repeated at least three times. The CFU of the sample was expressed as the average of the values obtained. The concentrations of bacteria were recorded as CFU/ml of organ homogenate. The limit of bacteria detection in the organ homogenates was 10 CFU/ml. To prepare protein extracts for Western blot analyses, the homogenates of the spleen samples were centrifuged and the pellets that contained the bacteria were resuspended in PBS, following the procedures described previously . All the experimental procedures with animals were in compliance with the guidelines and policies of the Animal Care and Use Committee (ACUC) of the University of California at Berkeley, and have been approved by the ACUC.
The denatured polypeptides from bacterial lysates were separated on SDS-containing 10-12% polyacrylamide gels cross-linked with N, N''-methylenebisacrylamide (0.05%), transferred electrically to nitrocellulose membranes (Bio-Rad, Hercules, CA), and reacted in an enzyme-linked immunoassay with a monoclonal anti-FLAG antibody (Sigma, St Louis, MO) and antibodies against Salmonella FliC (BioLegend, San Diego, CA) and DnaK (StressGen, Victoria, British Columbia, Canada), followed by an anti-mouse IgG conjugated with alkaline phosphatase [16,36]. The membranes were subsequently stained with a chemiluminescent substrate with the aid of a Western chemiluminescent substrate kit (Amersham Inc, GE Healthcare) and quantified with a STORM840 phosphorimager. Normalization of samples was also carried out by loading total proteins extracted from the same CFU (e.g. 5 × 107 CFU) of bacteria in each lane.
KK, EY, GV, HG, JS, FL, and SL conceived the study, performed the research, analyzed the results, and wrote the paper. All authors read and approved the final manuscript.
We thank Cindy Loui, Yong Bai, Hongwei Gu, and Huiyuan Jiang for suggestions and excellent technical assistance. K. K., G. V., and E. Y. were partially supported by a Block Grant Predoctoral Fellowship (UC-Berkeley). The research has been supported by grants from USDA (CALR-2005-01892) and NIH (RO1-AI041927 and RO1-AI014842).