Skip to main content


Front. Microbiol., 05 December 2019
Sec. Infectious Agents and Disease
Volume 10 - 2019 |

The Transcription Factor ArcA Modulates Salmonella’s Metabolism in Response to Neutrophil Hypochlorous Acid-Mediated Stress

  • 1Laboratorio de Microbiología Molecular, Departamento de Ciencias Biológicas, Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago, Chile
  • 2Centro de Bioinformática y Biología Integrativa, Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago, Chile
  • 3Laboratorio de Patogenesis Bacteriana, Facultad de Medicina, Universidad Andres Bello, Santiago, Chile
  • 4Centro de Biotecnología Vegetal, Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago, Chile
  • 5FONDAP Center for Genome Regulation, Universidad Andres Bello, Santiago, Chile
  • 6Wellcome-Wolfson Institute for Experimental Medicine, Queen’s University Belfast, Belfast, United Kingdom
  • 7Millennium Institute on Immunology and Immunotherapy, Departamento de Ciencias Biológicas, Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago, Chile

Salmonella Typhimurium, a bacterial pathogen with high metabolic plasticity, can adapt to different environmental conditions; these traits enhance its virulence by enabling bacterial survival. Neutrophils play important roles in the innate immune response, including the production of microbicidal reactive oxygen species (ROS). In addition, the myeloperoxidase in neutrophils catalyzes the formation of hypochlorous acid (HOCl), a highly toxic molecule that reacts with essential biomolecules, causing oxidative damage including lipid peroxidation and protein carbonylation. The bacterial response regulator ArcA regulates adaptive responses to oxygen levels and influences the survival of Salmonella inside phagocytic cells. Here, we demonstrate by whole transcriptomic analyses that ArcA regulates genes related to various metabolic pathways, enabling bacterial survival during HOCl-stress in vitro. Also, inside neutrophils, ArcA controls the transcription of several metabolic pathways by downregulating the expression of genes related to fatty acid degradation, lysine degradation, and arginine, proline, pyruvate, and propanoate metabolism. ArcA also upregulates genes encoding components of the oxidative pathway. These results underscore the importance of ArcA in ATP generation inside the neutrophil phagosome and its participation in bacterial metabolic adaptations during HOCl stress.


The pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) can adapt to different environments by rapidly modulating gene expression (Hébrard et al., 2011). Critically to its infection cycle, this bacterium can survive the microbicidal action of immune cells, including neutrophils (Ibarra and Steele-Mortimer, 2009; Ruby et al., 2012; Behnsen et al., 2015).

Salmonella promotes its own internalization to the host via several effector proteins associated with Salmonella Pathogenicity Island 1 (SPI-1), namely: SipA, SipC, and SptP (LaRock et al., 2015). Once engulfed, the bacterium encounters the oxidative burst, a process in which oxygen is reduced to form superoxide radicals and other toxic reactive oxygen species (ROS). Neutrophils possess two enzymes at play: NADPH oxidase, which initiates the production of O2, and myeloperoxidase (MPO), which produces hypochlorous acid (HOCl) (Winterbourn and Kettle, 2013).

Hypochlorous acid is a highly toxic compound that rapidly reacts with functional groups in cysteine, methionine, lysine, histidine, and tyrosine residues, forming mono- and dichloro-amines (Hawkins and Davies, 2002; Beavers and Skaar, 2016). It also targets DNA and lipids, leading to genome-wide mutations, protein inactivation, and membrane perturbations (Pattison and Davies, 2001). Major changes in the bacterial metabolite profile occur as early as after 5 min of HOCl-induced stress, including major shifts in fatty acids, amino acids, and other organic acids such as acetic and formic acid (Drazic et al., 2015).

Metabolic adjustments are essential for bacterial survival. S. Typhimurium can adapt in vivo according to the infected cell type or in vitro to the components of the culture medium (Eriksson et al., 2003; Wang et al., 2010; Hébrard et al., 2011; Srikumar et al., 2015). For instance, the bacterium does not require a complete TCA cycle for efficient replication in epithelial cells and macrophages (Garcia-Gutierrez et al., 2016), and the bacterial cell activates the use of lipid metabolism as an energy source (Diacovich et al., 2017). Biosynthesis of aromatic amino acids, purine, LPS core, O-antigen, and enzymes involved in glycolysis and the TCA cycle, mannose utilization and oxidative phosphorylation are relevant pathways for efficient infection (Chaudhuri et al., 2009), and the most up-regulated functional categories of S. Typhimurium genes within macrophages are involved in carbohydrate and amino acid metabolism (Srikumar et al., 2015).

Aerobic respiration control (ArcA) is one of the main transcriptional regulators of the metabolic shift from anaerobic to aerobic conditions and the control of enzymatic defenses against ROS (Evans et al., 2011). ArcA regulates key genes for Salmonella survival in response to anaerobiosis, aerobiosis, low oxygen, hydrogen peroxide, and life within phagocytic cells (Shalel-Levanon et al., 2005; Evans et al., 2011; Morales et al., 2013; Park et al., 2013; Jiang et al., 2017; Pardo-Esté et al., 2018; Wang et al., 2018). ArcA also regulates membrane permeability in response to ROS generated by H2O2 and HOCl, specifically by repressing the expression of multiple porin genes such as bhsA, ompD, ompC, ompS2, ompF, and ompW (Calderon et al., 2011; Gebendorfer et al., 2012; Morales et al., 2012; Ipinza et al., 2014). Inside macrophages and neutrophils, ArcA modulates the expression of ompW, ompD, and ompF (Pardo-Esté et al., 2018).

In this study, we determined the role of ArcA in Salmonella Typhimurium under HOCl stress. Whole transcriptome analyses revealed a direct relation between ArcA and metabolism modulation under 1 mM NaOCl treatment. Additionally, as neutrophils are phagocytes that use HOCl as their main ROS-related microbicide, we determined gene expression levels in key participants of biosynthetic pathways and found that ArcA is also involved in the bacterial transcriptional response to the environment encountered inside these cells. We demonstrated that transcription level values present mostly a positive correlation in each condition evaluated, underlining the role played by ArcA during the transcriptional response to HOCl in general. ArcA also reduces the magnitude of bacterial oxidative damage inside neutrophils, suggesting an important role for ArcA in the ability of S. Typhimurium to survive HOCl stress during its infective cycle.

Materials and Methods

Ethics Statement

Animals were treated following the recommendations in the Guide for the Care and Use of Laboratory Animals of the US National Institutes of Health, and the protocol was approved by the Bioethics Committee of Universidad Andrés Bello, Protocol 06/2016 within the framework of FONDECYT Grant #1160315.

Bacterial Strains and Growth Conditions

The Typhimurium 14028s parental strain and ΔarcA were maintained on LB agar plates in aerobiosis unless otherwise indicated. Cells were grown aerobically with shaking in LB medium at 37°C until reaching an OD600 of 0.4. S. enterica serovar Typhimurium 14028s ΔarcA:aph strain was obtained previously (Calderon et al., 2011).

Mouse Bone-Marrow-Derived Neutrophils

C57BL/6 female mice (7–8 weeks old) were used to obtain bone-marrow-derived neutrophils (BMDNs). Mice were kept in plastic cages in a temperature-controlled environment (22–24°C). To prepare mouse neutrophils, bone marrow was extracted as previously described (Swamydas and Lionakis, 2013) and neutrophils were obtained using the mouse Neutrophil Isolation Kit (Milenybiotec) according to the manufacturer’s instructions. This resulted in the isolation of an average of 800,000 neutrophils/ml with around 85% viability; these were positive for CD11b and Ly6G, as determined by flow cytometry. The viability of neutrophils was also monitored throughout the experiments by trypan blue staining.

Total RNA Extraction From NaOCl-Treated Bacteria and Infected BMDNs

For the total RNA extraction from in vitro NaOCl-treated bacteria, overnight cultures of S. Typhimurium 14028s and ΔarcA were diluted (1:100) and grown to OD600 ∼0.4, at which point they were exposed to 1 mM of NaOCl for 20 min before the extraction. Total RNA extraction from infected neutrophil-recovered bacteria was carried out as previously described (Pardo-Esté et al., 2018). Briefly, 107 bacteria/ml grown in microaerophilic conditions were incubated with BMDNs for 3 h. At 1 and 3 h post-infection (pi), cells were harvested, washed twice with PBS, and lysed with sodium deoxycholate (0.5% w/v in PBS), one sample was used as a bacterial viability control and was plated on LB plates. Bacteria were recovered after 1 mM of NaOCl treatment and BMDN infection. RNA extraction from bacteria in both experiments was carried out using the acid–phenol method (Koronakis and Hughes, 1988). RNA was suspended in 30 μl of nuclease-free water and stored at −80°C until used. The integrity of the RNA was assessed by 1.0% agarose gel electrophoresis, and its concentration and quality were verified spectrophotometrically by the OD260/280 ratio. The RNA was treated with 2 U of DNase I (Roche) for 1 h to remove contaminant DNA. To ensure no carry-over DNA in the samples, we routinely performed PCR amplifications using primers for bacterial 16s RNA and found no product using the RNA extract as a template.

RNA-Seq Analysis

Total RNA extracted from in vitro NaOCl-treated bacteria was depleted of rRNAs, used for cDNA library preparation, and sequenced by Macrogen Inc. (Seoul, South Korea). The TruSeq mRNA Library Prep Kit (Illumina, Inc.) was used, and cDNA was sequenced on an Illumina HiSeq 2500 platform. Two independent libraries (150 bp, single-end) were constructed for each sample (strain – treatment), corresponding to two biological replicates. An average of 9.5 million reads per sample were obtained, representing a depth of 315X. Quality control of raw data was carried out using FastQC v0.11.8 (Andrews, 2010) and filtering and trimming with PRINSEQ v0.20.4 (Schmieder and Edwards, 2011) with 100 bp, 0 N, and < Q20 thresholds. Gene expression levels were estimated by mapping reads against the S. enterica subsp. enterica serovar Typhimurium strain 14028s reference genome (GenBank: GCA_000022165.1) with Bowtie2 v2.3.5 (Langmead and Salzberg, 2012). The counts of reads that map against Salmonella ORFs were obtained using HTSeq v0.11.2 (Anders et al., 2015). The resulting matrix of counts was used to estimate differential gene expression using a normalization method implemented in the edgeR Bioconductor R Package (Robinson et al., 2010). First, we determined the response of each strain to NaOCl treatment by performing, separately, an analysis of differential gene expression in response to stress. From these data, we performed a second step, filtering both data sets-obtained previously with the genes that changed their expression in the mutant vs. the parental strain in control conditions. Third, we matched these data sets of genes to identify those that are only defendant of ArcA regulation under NaOCl stress. Expression values represent log2 after FC ± 2 and FDR ≤ 0.1 filters were applied. RNA-seq data is available in the NCBI SRA database under accession numbers SRR9188680 and SRR9188681 (Bioproject PRJNA357075). GO/KEGG enrichment analysis was carried out using the ClueGO plug-in (Bindea et al., 2009) via Cytoscape (Shannon et al., 2003).


RNA extracted from bacteria recovered from infected neutrophils was reverse transcribed into cDNA at 37°C for 1 h in 25 μl of a mixture containing 2.5 pmol of Random Primers (Invitrogen), 10 μl template RNA (5 mg), 0.2 mM dNTPs, 1 μl sterile water, 4 μl of 5 × buffer (250 mM Tris–HCl pH 8.3, 375 mM KCl, 15 mM MgCl2, and 10 mM DTT), and 200 U of reverse transcriptase (Invitrogen). The primers used for qRT-PCR are listed in Supplementary Table S1. The relative quantification of each transcript was performed using the Brilliant II SYBR Green QPCR Master Reagent and the Mx3000P detection system (Stratagene). The qRT-PCR mixture (20 μl) contained 1 μl of the cDNA template and 120 nM of each primer. The qRT- PCR was performed under the following conditions: 10 min at 95°C followed by 40 cycles of 30 s at 95°C, 45 s at 58°C, and 30 s at 72°C. Fold-change expression of target genes, normalized by the expression of a suitable gene selected in these experimental conditions were calculated as described (Pfaffl, 2011). talB gene expression was used for normalization, since we have validated this gene as showing stable expression under our experimental conditions (Cabezas et al., 2018; Pardo-Esté et al., 2018).

MPOe Activity Quantification

To determine the activation of BMDNs infected with each bacterial strain separately we measured the enzymatic activity of MPO using the Neutrophil Myeloperoxidase Activity Assay Kit (Cayman Chemical). Briefly, infected BMDNs were incubated and at 1 and 3 hpi the color intensity of the 3,3′,5,5′-tetramethyl-benzidine (TMB), which is proportional to the amount of MPO in the sample and is detectable at 650 nm, obtaining the enzymatic activity, in μmoles/min./ml. To obtain the enzymatic specific activity, the results were normalized to the total protein concentration in the samples. Negative control of non-infected neutrophils and free bacteria were used for normalization, in addition to the negative controls with MPO inhibitor (4-aminobenzhydrazide) provided by the kit.

Protein Carbonylation, Lipid Peroxidation, and Total Glutathione Determination

As indicators of oxidative damage, we determined protein carbonylation, lipid peroxidation, and total glutathione using the Protein Carbonyl Colorimetric, TBARS, and Glutathione Assay Kits (Cayman Chemical), respectively. Briefly, we infected BMDNs with S. Typhimurium 14028s and ΔarcA separately, as described above. For protein carbonylation, we measured the absorbance at a wavelength of 375 nm of the hydrazone formed by the reaction between 2,4-dinitrophenylhydrazine and the target molecule to determine the concentration (nmol/ml) of protein carbonyls. For TBARS, we used an excitation wavelength of 530 nm and an emission wavelength of 550 nm, and lipid peroxidation was determined as the malondialdehyde concentration (μM) obtained. For glutathione, we used a 410 nm wavelength to read the microplate and obtain the rate of 5-thio-2-nitrobenzoic acid production, which is directly proportional to the concentration of total glutathione (μM). Measurements for each indicator were performed at 1 and 3 hpi. In all cases, negative controls of non-infected neutrophils and free bacteria were used for normalization.

Statistical Analyses

Gene expression (qRT-PCR) and detection of oxidative damage indicators from the mutant strain were calculated relative to the wild type strain. Gene-by-gene comparisons were performed as individual experiments for each time point using one-way ANOVA with α = 0.05 with the Bonferroni correction, comparing mutant strains with a wild-type strain separately at 1 and 3 hpi using GraphPad 5.01 (Prism1). Additionally, the R package pheatmap was used for results visualization (Kolde, 2015). Correlation analyses were performed using the R package Corrplot 0.84 (Wei and Simko, 2017).


ArcA Participates in the S. Typhimurium Response to NaOCl Stress by Regulating Bacterial Metabolism

To understand the role of ArcA during HOCl-related stress in vitro under conditions that could mimic those found in neutrophils, we sought to perform a transcriptomic analysis of the parental and ΔarcA mutant strains. We used NaOCl for these experiments since the sodium form of HOCl is more stable and dissociates into HOCl in solution (Fukuzaki, 2006). To investigate the optimal concentration of NaOCl in which both ΔarcA and the parental strain had similar growth rates, we first determined the minimal inhibitory concentration (MIC) of NaOCl for both strains (Figure 1A). With this information, strains grown to mid-log phase (OD600 of 0.4) were exposed to a sublethal NaOCl concentration of 1 mM corresponding to half of the MIC for ΔarcA. The growth rates of-ΔarcA and the parental strain under this condition were similar, and also the mutant could recover after the addition of NaOCl (Figure 1B).


Figure 1. Salmonella Typhimurium growth rate in response to NaOCl. (A) Minimal inhibitory concentrations (MIC) for the parental 14028s and ΔarcA mutant strains. t-test (∗∗∗P < 0.001). Values represent the average of three independent experiments ± SD each with three technical repeats. (B) Growth curves for the 14028s and ΔarcA mutant strains with and without 1 mM NaOCl treatment.

Next, we obtained transcriptomic datasets from parental and ΔarcA treated and untreated with 1 mM NaOCl, as explained in the Materials and Methods, which were mapped against the reference S. Typhimurium 14028S (GenBank: GCA_000022165.1). Our transcriptomic data covers 94.4% and 93.8% of the total Salmonella ORFs in the ΔarcA and parental strain, respectively (Supplementary Table S2). After matching the ORFs that change their expression (after FDR ≤ 0.1 and FC ± 2 filters) between ΔarcA (in response to NaOCl relative to the untreated control) and the parental strain (in response to NaOCl relative to the untreated control) to identify the unique ORFs that are dependent on ArcA regulation (ORFs that in the ΔarcA strain respond to NaOCl treatment but are not common with those found in the parental strain under stress). The estimated expression levels of these ORFs in the mutant strain suggest that ArcA acts predominantly as a repressor, since 60 ORFs showed higher expression levels, while the remaining 13 had reduced expression.

A gene-by-gene comparison revealed different gene expression patterns between the ΔarcA mutant and the S. Typhimurium parental in response to NaOCl treatment. Only the expression of four genes was shared between the parental strain and ΔarcA, while the expression of 82 and 76 genes was unique to ΔarcA and the parental strain, respectively. These data suggest that loss of arcA caused dysregulation of a different gene set in response to NaOCl. KEGG pathway enrichment analyses revealed that an important part of the transcriptional response to NaOCl mediated by ArcA corresponds to genes involved in metabolism (Figure 2).


Figure 2. Differential global gene expression in response to 1 mM NaOCl. KEGG pathway enrichment analyses with the differentially expressed genes, comparing the 14028s strain and the ΔarcA mutant. White bars show the expression on the 14028s and lavender bars show the expression on the mutant strain normalized by the control condition of the 14028s strain grown in LB medium.

By calculating the fold change expression of genes belonging to these pathways, as well as for genes encoding proteins with functions related to ROS-resistance, we observed a marked difference in expression levels on several of these genes as a consequence of the mutation on arcA (Figure 3). KEGG pathway enrichment analysis revealed that ArcA regulates genes involved in several metabolic pathways such as fatty-acid degradation, oxidative phosphorylation, lysine degradation, arginine-proline metabolism, pyruvate metabolism, and propanoate metabolism. We conclude that ArcA is involved in the bacterial adaptation to ROS by modulating the metabolic fingerprint to effectively reduce oxidative damage and ensure survival under ROS conditions.


Figure 3. Comparison of differentially expressed genes between the S. Typhimurium 14028s parental strain and the ΔarcA mutant, both treated with 1 mM of NaOCl relative to the control LB medium.

ArcA Mediates Bacterial ROS Resistance Inside Neutrophils, and the Participation of ArcA in Gene Expression Regulation Under HOCl Stress Is Consistent in All Conditions Studied

We used the transcriptome information in response to HOCl in vitro to evaluate the transcriptional profile of ΔarcA and parental bacteria inside neutrophils. The expression of genes representing the most relevant metabolic pathways found in response to NaOCl in vitro was compared by qRT-PCR to that of the same genes in bacteria harvested from infected neutrophils. For these experiments, gene expression was evaluated at 1 and 3 hpi, since these are the times of maximal oxidative burst and also when the Salmonella-containing vacuole (SCV) reaches maturation (Goldman, 1990; Eriksson et al., 2000; Vazquez-Torres et al., 2000).

The results show that ArcA negatively regulated fatty acid and lysine degradation, as well as arginine, proline, pyruvate, and propanoate metabolism. This is consistent with a study determining that aspartate, proline, and asparagine are available in the SCV in macrophages (Popp et al., 2015). Also, ArcA positively regulated oxidative phosphorylation (Oxphos) and the antiporter lysine/cadaverine cadB gene inside neutrophils (Figure 4). These results suggested the use of extracellular nutrients as TCA cycle intermediaries for the generation of ATP through Oxphos, since other classical pathways are inhibited in intracellular Salmonella (Garcia-Gutierrez et al., 2016). Therefore, we conclude that ArcA has a role in maintaining metabolic homeostasis intracellularly by modulating a similar metabolic gene set as seen in vitro.


Figure 4. Transcriptional expression of selected genes in ΔarcA relative to parental S. Typhimurium 14028s in BMDNs at 1 and 3 hpi. Panels show gene expression levels in each strain according to the heatmap scale. Expression data by qRT-PCR were normalized against the expression of talB (Cabezas et al., 2018; Pardo-Esté et al., 2018). Values represent the average of three independent experiments; three technical replicates per experiment. One-way ANOVA with the Bonferroni correction (P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).

We also investigated the expression of genes encoding proteins required for bacterial intracellular survival in phagocytes (Figure 4). The results demonstrated that during neutrophil infection, ArcA promotes the expression of trxB (involved in the repair of disulfide bonds, which are damaged by HOCl) (Gray et al., 2013). Also, expression of the sodC gene, which codes for a superoxide dismutase, is negatively regulated inside neutrophils at 3 hpi (Figure 4) but is required in response to HOCl bolus treatment; this could be a manifestation of the gradual production of ROS in the phagosome, contrary to the direct attack of the toxic compound in vitro that does not allow the bacteria to adapt efficiently, but rapidly responds to ROS-related stress. Also, ArcA upregulates virulence-related genes not classically associated with antioxidant responses, such as pagC and wzz (Figure 4). pagC encodes a virulence protein involved in intramacrophage survival (Miller, 1991). wzz encodes a protein involved in the regulation of O-antigen polysaccharide chain length (Batchelor et al., 1991; Whitfield and Trent, 2014), which is also required for full Salmonella virulence (May and Groisman, 2013).

Inside neutrophils, ArcA also repressed the expression of kgd (encoding α-ketoglutarate decarboxylase, an enzyme that participates in the TCA cycle) (Figure 4). This is consistent with previous evidence that Salmonella does not require an intact TCA cycle to survive intracellularly, as levels of metabolites related to glycolysis, the pentose phosphate pathway, and the TCA cycle decrease in bacteria under stress (Bowden et al., 2009, 2010; Jozefczuk et al., 2010; Garcia-Gutierrez et al., 2016).

We found a positive correlation between the genes expressed under 1 mM of NaOCl treatment in vitro and those expressed in bacteria harvested from infected neutrophils at 1 and 3 hpi (Figure 5). Only three genes, sodC, cadB, and cyoC, showed negative correlations between their expression levels under 1 mM of NaOCl and in qRT-PCR from bacteria harvested from infected neutrophils. This result was expected, as the conditions inside the neutrophils vary in many aspects compared to the in vitro conditions. Bacteria grown in aerobiosis in LB broth with NaOCl bolus treatment negatively regulate oxidative phosphorylation (Oxphos)-related genes, while, on the contrary, their expression is promoted inside neutrophils. Garcia-Gutierrez et al. (2016), demonstrated that under such conditions, Salmonella can rely on substrate-level phosphorylation (SLP) and/or Oxphos to fulfill ATP requirements. Also, sodC expression is differential, as superoxide concentration varies greatly between the conditionsevaluated, in particular as it is one of the substrates used to generate other ROS inside neutrophil phagosomes.


Figure 5. Correlation index between gene expression found in vitro with NaOCl treatment (RNAseq) and in intracellular bacteria (qRT-PCR). Data obtained from RNA-seq in response to 1 mM of NaOCl, and gene expression in bacteria harvested from neutrophils evaluated by qRT-PCR at 1 and 3 hpi. Positive correlations are displayed in blue, and negative correlations in red. Color intensity and circle size are proportional to the correlation coefficients relative to RNA-seq values.

The other gene with differential expression in both conditions is cadB, a transporter related to pH maintenance. Its expression is required inside neutrophils but is not activated in vitro, as the conditions in regards to pH change considerably. In particular, neutrophils maintain a near-neutral pH for maintenance of their secreted enzymes, and it has been demonstrated that Salmonella is able to sense and acidify in macrophages acidic phagosomes (Chakraborty et al., 2017). Our results suggest that it could also modulate the intraphagosomal pH in neutrophils.

ArcA Participates in the Defense and Resistance S. Typhimurium to Oxidative Damage

Since ArcA regulates several important genes in response to ROS inside neutrophils, we determined the MPO activity in infected neutrophils at the same times post-infection used for transcriptional analyses, which provides an estimation of the HOCl production. The results indicate that MPO activity is detectable at similarly high levels in neutrophils infected with either ΔarcA or the parental strain at 1 hpi (Figure 6A). In contrast, at 3 hpi, MPO activity decreases by up to 75% in neutrophils infected with ΔarcA compared to those infected with the parental strain (Figure 6A). The lower MPO activation suggests that neutrophils infected with bacteria lacking arcA are more susceptible to oxidative damage and therefore killed more rapidly.


Figure 6. Myeloperoxidase activation and oxidative damage found in Salmonella Typhimurium 14028s and ΔarcA infecting BMDNs at 1 and 3 hpi. (A) Myeloperoxidase enzyme-specific activity in BMDNs infected with S. Typhimurium 14028s and ΔarcA. Measured as the protein units (μmol/ml) normalized by total protein concentration. (B) Thiobarbituric acid reactive substances (TBARS) as an indicator of oxidative damage in ΔarcA relative to S. Typhimurium 14028s harvested from infected BMDNs at 1 and 3 hpi. (C) Protein carbonylation as an indicator of oxidative damage in ΔarcA relative to S. Typhimurium 14028s harvested from infected BMNs at 1 and 3 hpi. (D) Glutathione as an indicator of cellular redox state in ΔarcA relative to S. Typhimurium 14028s harvested from infected BMDNs at 1 and 3 hpi. One-way ANOVA with the Bonferroni correction (P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001). Values represent the average of five independent experiments ± SD, three technical replicates per experiment.

Lipid peroxidation, protein carbonylation, and total glutathione are indicators of oxidative damage in bacteria. The ΔarcA mutant shows a greater amount of oxidative damage in lipids and proteins as measured by lipid peroxidation and protein carbonylation (Figures 6B,C). However, the cellular redox state, determined as the amount of total glutathione, remains similar in all strains (Figure 6D). There is a positive correlation between MPO activity and increased lipid peroxidation (Morales et al., 2012; Drazic et al., 2015; Okada et al., 2016) and protein carbonylation (Levine et al., 1990; Shacter et al., 1994; Wilkie-Grantham et al., 2015; Beavers and Skaar, 2016). These results further support the notion that ArcA plays a pivotal role in oxidative damage resistance. Indeed, mutant bacteria activate significantly less MPO in neutrophils and display a higher amount of oxidative-associated damage.


Neutrophils play an important role in the innate immune response to S. Typhimurium infection (Conlan, 1997) in particular by producing HOCl, a short-lived toxic compound that rapidly targets and damages key macromolecules (Davies, 2005). The transcription factor ArcA is required for bacterial survival in epithelial cells, macrophages, and neutrophils by regulating detoxification-, membrane permeability-, and virulence-related genes inside macrophages and neutrophils (Pardo-Esté et al., 2018). In this work, we show that ArcA is also relevant in the metabolic fingerprint of S. Typhimurium in response to HOCl. This was revealed by a clear dysregulation of the transcriptomic profile under NaOCl treatment in the absence of arcA and by showing that ArcA also influences the metabolic adaptation of bacteria upon phagocytosis by neutrophils.

In this study, we evaluated three very specific conditions concerning HOCl concentrations, namely bolus treatment and 1 hpi and 3 hpi in neutrophils, and determined that the participation of ArcA in these conditions is similar. Further, there was a predominantly positive correlation between expression patterns from bacteria treated with sub-lethal concentrations of NaOCl in vitro and those found in bacteria at 1 and 3 hpi in infected neutrophils. We have previously reported that, at these hpi times, infected neutrophils produce increasing amounts of HOCl, reaching up to 200 μM at 3 hpi (Pardo-Esté et al., 2018).

Salmonella Typhimurium metabolism is very flexible, and T3SS1 expression is also influenced by metabolism. For example, cell invasion increases when pyruvate metabolism is abolished (Abernathy et al., 2013). Here, we determined that ArcA inhibits genes related to pyruvate metabolism (Figure 4). Additionally, intracellular S. Typhimurium might fulfil its ATP requirements via substrate-level phosphorylation (SLP) and/or Oxphos (Garcia-Gutierrez et al., 2016), and TCA cycle enzymes do not appear to be essential inside macrophages (Bowden et al., 2009, 2010; Garcia-Gutierrez et al., 2016). Our results agree with this notion, several metabolic pathways are inhibited by ArcA in bacteria inside neutrophils, while genes related to Oxphos are upregulated. This indicates that the ability of the pathogen to resist HOCl-related stress is associated with its capacity to metabolically adapt and use the available metabolites to withstand oxidative damage.

We have determined that ArcA negatively regulates pyruvate metabolism, fatty acid degradation, and at least part of the TCA cycle in response to HOCl-related stress and oxygen availability inside neutrophils (Figure 4). Evidence shows that Salmonella does not use the β-oxidation pathway during RAW 264.7 macrophage infection in DMEM medium with high levels of glucose (Diacovich et al., 2017). During infection, the bacterium allocates resources very tightly, especially to protein production and pathway usage. As sugars are the primary carbon sources of S. Typhimurium, here we demonstrate that ArcA represses the β-oxidation pathway in favor of sugar uptake and further catabolism in response to oxidative stress. The intracellular redox state also requires a balanced pool of (NADH/NAD+), as well as the conversion of pyruvate to acetyl-CoA, which finally fuels the TCA cycle. Thus, the pyruvate node is essential in regulating both the cofactor ratio and the rate of carbon conversion within the TCA cycle. These results confirm that ArcA controls the redox state of the cell, as it is involved in regulating at least part of the TCA cycle. ArcA also appears to govern the metabolism of various amino acids, such as proline, arginine, lysine, and threonine, inside neutrophils (Figure 4). The proline and arginine biosynthesis pathways require ATP and NADP(H) for their synthesis. The latter cofactor is critical to counteract oxidative damage and is also required for glutathione synthesis.

Salmonella Typhimurium can utilize amino acids obtained from the host during intracellular life (Das et al., 2010), enabling an efficient mechanism for intracellular proliferation. In fact, intracellular S. Typhimurium utilizes medium-derived amino acid rather than host cell-derived amino acids in an SPI-2-dependent manner (Popp et al., 2015), a bacterial strategy for host cell endosomal transport for intracellular nutrition. In agreement with this notion, we found the antiporter of lysine/cadaverine cadB to be upregulated by ArcA (Figure 4), which would allow a continuous amino acid supply from the host cell’s cytoplasm of the host cell into the bacteria-containing vacuoles which is key for survival and, at the same time, limiting, because hypochlorite exposure causes methionine and alanine to significantly decrease in treated cells (Drazic et al., 2015).

Further, the use of oxidative phosphorylation for energy production inside the vacuole is suggested by the upregulation of cyoC and cyoA (Figure 4), indicating that the environment in vivo is somewhat anaerobic and requires oxidative phosphorylation for ATP generation. To obtain the NAD and FADH required for Oxphos, the bacteria under these conditions might be using amino acids obtained from the host cell (Popp et al., 2015). In addition to energy sources, intracellular S. Typhimurium requires other virulence traits involved in manipulating the host cell (Holden, 2002; Fabrega and Vila, 2013; Hurley et al., 2014).

One unexpected finding was that the MPO activity was lower in ΔarcA-infected neutrophils compared to neutrophils infected with the parental strain. Despite this, neutrophils cause more oxidative damage to the bacterial mutant than to the parental strain. We speculate that the loss of ArcA may affect the mechanism of MPO activation directly or indirectly, thus explaining the lower enzymatic activity, but this observation will require additional experimentation.

Collectively, our results indicate that the transcription factor ArcA is required for the resistance of S. Typhimurium to HOCl-related stress in general and, in particular, to the conditions found inside neutrophils. This response regulator modulates the gene expression of metabolic pathways that enable the bacteria to obtain ATP and also controls some additional virulence- and repair-related genes, which together provide resistance to oxidative damage during the pathogen’s infection cycle. Therefore, ArcA-mediated modulation of metabolic homeostasis contributes to the virulence repertoire that Salmonella uses to evade antimicrobial strategies in the host.

Data Availability Statement

The datasets generated for this study can be found in the NCBI SRA database under accession numbers SRR9188680 and SRR9188681 (Bioproject PRJNA357075).

Ethics Statement

The animal study was reviewed and approved by the Bioethics Committee of Universidad Andrés Bello, Protocol 06/2016 in the framework of FONDECYT Grant #1160315.

Author Contributions

CS and CP-E conceived and designed the study. CP-E, JC-S, GK, CA, and YS carried out experiments. CC, AB, and MB extracted in vitro RNA samples. NM, AH, CM, IP-C, EC-N, and MV contributed with the reagents, materials, and analysis tools. CP-E, JC-S, IP-C, MV, and CS wrote the manuscript. All authors read and approved the final manuscript.


CS was funded by CONICYT FONDECYT 1160315, UNAB Nucleo Grant DI-3-17/N, and ECOS-CONICYT 170023. CP-E, JC-S, CC, AB, and YS were funded by the CONICYT National Doctoral Fellowship. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Conflict of Interest

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


We would like to thank Guido Mora for providing the parental bacteria strain Salmonella Typhimurium 14028s. We also gratefully acknowledge the sequencing service from Centro de Biotecnología Vegetal, Universidad Andres Bello.

Supplementary Material

The Supplementary Material for this article can be found online at:


Anders, S., Pyl, P. T., and Huber, W. (2015). HTSeq—a Python framework to work with high-throughput sequencing data. Bioinformatics 31, 166–169. doi: 10.1093/bioinformatics/btu638

PubMed Abstract | CrossRef Full Text | Google Scholar

Andrews, S. (2010). FastQC a Quality-Control Tool for High-Throughput Sequence Data. Available at: (accessed November, 2017).

Google Scholar

Abernathy, J., Corkill, C., Hinojosa, C., Li, X., and Zhou, H. (2013). Deletions in the pyruvate pathway of Salmonella typhimurium alter SPI1-mediated gene expression and infectivity. J. Anim. Sci. Biotechnol. 4:5. doi: 10.1186/2049-1891-4-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Batchelor, R. A., Haraguchi, G. E., Hull, R. A., and Hull, S. I. (1991). Regulation by a novel protein of the bimodal distribution of lipopolysaccharide in the outer membrane of Escherichia coli. J. Bacteriol. 173, 5699–5704. doi: 10.1128/jb.173.18.5699-5704.1991

PubMed Abstract | CrossRef Full Text | Google Scholar

Beavers, W. N., and Skaar, E. P. (2016). Neutrophil-generated oxidative stress and protein damage in Staphylococcus aureus. Pathog. Dis. 74:ftw060. doi: 10.1093/femspd/ftw060

PubMed Abstract | CrossRef Full Text | Google Scholar

Behnsen, J., Perez-Lopez, A., Nuccio, S. P., and Raffatellu, M. (2015). Exploiting host immunity: the Salmonella paradigm. Trends. Immunol. 36, 112–120. doi: 10.1016/

PubMed Abstract | CrossRef Full Text | Google Scholar

Bindea, G., Mlecnik, B., Hackl, H., Charoentong, P., Tosolini, M., Kirilovsky, A., et al. (2009). ClueGO: a Cytoscape plug-in to decipher functionally grouped gene ontology and pathway annotation networks. Bioinformatics 25, 1091–1093. doi: 10.1093/bioinformatics/btp101

PubMed Abstract | CrossRef Full Text | Google Scholar

Bowden, S. D., Ramachandran, V. K., Knudsen, G. M., Hinton, J. C., and Thompson, A. (2010). An incomplete TCA cycle increases survival of Salmonella Typhimurium during infection of resting and activated murine macrophages. PLoS One 5:e13871. doi: 10.1371/journal.pone.0013871

PubMed Abstract | CrossRef Full Text | Google Scholar

Bowden, S. D., Rowley, G., Hinton, J. C., and Thompson, A. (2009). Glucose and glycolysis are required for the successful infection of macrophages and mice by Salmonella enterica serovar Typhimurium. Infect. Immun. 77, 3117–3126. doi: 10.1128/IAI.00093-09

PubMed Abstract | CrossRef Full Text | Google Scholar

Cabezas, C. E., Briones, A. C., Aguirre, C., Pardo-Esté, C., Castro-Severyn, J., Salinas, C. R., et al. (2018). The transcription factor SlyA from Salmonella Typhimurium regulates genes in response to hydrogen peroxide and sodium hypochlorite. Res. Microbiol. 169, 263–278. doi: 10.1016/j.resmic.2018.04.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Calderon, I. L., Morales, E., Caro, N. J., Chahuan, C. A., Collao, B., Gil, F., Villareal, J. M., Ipinza, F., Mora, G. C., and Saavedra, CP. (2011). Response regulator ArcA of Salmonella enterica serovar Typhimurium downregulates expression of OmpD, a porin facilitating uptake of hydrogen peroxide. Res. Microbiol. 162, 214–222. doi: 10.1016/j.resmic.2010.11.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Chakraborty, S., Winardhi, R. S., Morgan, L. K., Yan, J., and Kenney, L. J. (2017). Non-canonical activation of OmpR drives acid and osmotic stress responses in single bacterial cells. Nat. Commun. 8:1587. doi: 10.1038/s41467-017-02030-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Chaudhuri, R. R., Peters, S. E., Pleasance, S. J., Northen, H., Willers, C., Paterson, G. K., et al. (2009). Comprehensive identification of Salmonella enterica serovar Typhimurium genes required for infection of BALB/c mice. PLoS Pathog. 5:e1000529. doi: 10.1371/journal.ppat.1000529

PubMed Abstract | CrossRef Full Text | Google Scholar

Conlan, J. W. (1997). Critical roles of neutrophils in host defense against experimental systemic infections of mice by Listeria monocytogenes, Salmonella typhimurium, and Yersinia enterocolitica. Infect. Immun. 65, 630–635.

PubMed Abstract | Google Scholar

Das, P., Lahiri, A., Lahiri, A., Sen, M., Iyer, N., Kapoor, N., et al. (2010). Cationic amino acid transporters and Salmonella typhimurium ArgT collectively regulate arginine availability towards intracellular Salmonella growth. PLoS One 5:e15466. doi: 10.1371/journal.pone.0015466

PubMed Abstract | CrossRef Full Text | Google Scholar

Davies, M. J. (2005). The oxidative environment and protein damage. Biochim. Biophys. Acta. 1703, 93–109.

PubMed Abstract | Google Scholar

Diacovich, L., Lorenzi, L., Tomassetti, M., Méresse, S., and Gramajo, H. (2017). The infectious intracellular lifestyle of Salmonella enterica relies on the adaptation to nutritional conditions within the Salmonella-containing vacuole. Virulence 8, 975–992. doi: 10.1080/21505594.2016.1270493

PubMed Abstract | CrossRef Full Text | Google Scholar

Drazic, A., Kutzner, E., Winter, J., and Eisenreich, W. (2015). Metabolic response of Escherichia coli upon treatment with hypochlorite at sub-lethal concentrations. PLoS One 10:e0125823. doi: 10.1371/journal.pone.0125823

PubMed Abstract | CrossRef Full Text | Google Scholar

Eriksson, S., Björkman, J., Borg, S., Syk, A., Pettersson, S., Andersson, D., et al. (2000). Salmonella typhimurium mutants that downregulate phagocyte nitric oxide production. Cell. Microbiol. 2, 239–250. doi: 10.1046/j.1462-5822.2000.00051.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Eriksson, S., Lucchini, S., Thompson, A., Rhen, M., and Hinton, J. C. (2003). Unravelling the biology of macrophage infection by gene expression profiling of intracellular Salmonella enterica. Mol. Microbiol. 47, 103–118. doi: 10.1046/j.1365-2958.2003.03313.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Evans, M. R., Fink, R. C., Vazquez-Torres, A., Porwollik, S., Jones-Carson, J., McClelland, M., et al. (2011). Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium. BMC Microbiol. 11:58. doi: 10.1186/1471-2180-11-58

PubMed Abstract | CrossRef Full Text | Google Scholar

Fabrega, A., and Vila, J. (2013). Salmonella enterica serovar Typhimurium skills to succeed in the host: virulence and regulation. Clin. Microbiol. Rev. 26, 308–341. doi: 10.1128/CMR.00066-12

PubMed Abstract | CrossRef Full Text | Google Scholar

Fukuzaki, S. (2006). Mechanism of actions of Sodium Hypochlorite in cleaning and disinfection processes. Biocontrol Sci. 11, 147–157. doi: 10.4265/bio.11.147

PubMed Abstract | CrossRef Full Text | Google Scholar

Garcia-Gutierrez, E., Chidlaw, A. C., Le Gall, G., Bowden, S. D., Tedin, K., Kelly, D. J., et al. (2016). A comparison of the ATP generating pathways used by S. Typhimurium to fuel replication within human and murine macrophage and epithelial cell lines. PLoS One. 11:e0150687. doi: 10.1371/journal.pone.0150687

PubMed Abstract | CrossRef Full Text | Google Scholar

Gebendorfer, K. M., Drazic, A., Le, Y., Gundlach, J., Bepperling, A., Kastenmüller, A., et al. (2012). Identification of a hypochlorite-specific transcription factor from Escherichia coli. J. Biol. Chem. 287, 6892–6903. doi: 10.1074/jbc.M111.287219

PubMed Abstract | CrossRef Full Text | Google Scholar

Goldman, R. (1990). Control of lipoprotein lipase secretion by macrophages: effect of macrophage differentiation agents. J. Leukoc. Biol. 86, 79–86. doi: 10.1002/jlb.47.1.79

PubMed Abstract | CrossRef Full Text | Google Scholar

Gray, M. J., Wholey, W. Y., and Jakob, U. (2013). Bacterial responses to reactive chlorine species. Annu. Rev. Microbiol. 67, 141–160. doi: 10.1146/annurev-micro-102912-142520

PubMed Abstract | CrossRef Full Text | Google Scholar

Hawkins, C. L., and Davies, M. J. (2002). Hypochlorite-induced damage to DNA, RNA, and polynucleotides: formation of chloramines and nitrogen-centered radicals. Chem. Res. Toxicol. 15, 83–92. doi: 10.1021/tx015548d

PubMed Abstract | CrossRef Full Text | Google Scholar

Hébrard, M., Kröger, C., Sivasankaran, S. K., Händler, K., and Hinton, J. C. D. (2011). The challenge of relating gene expression to the virulence of Salmonella enterica serovar Typhimurium. Curr. Opin. Biotechnol. 22, 200–210. doi: 10.1016/j.copbio.2011.02.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Holden, D. W. (2002). Trafficking of the Salmonella vacuole in macrophages. Traffic 3, 161–169. doi: 10.1034/j.1600-0854.2002.030301.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hurley, D., McCusker, M. P., Fanning, S., and Martins, M. (2014). Salmonella–host interactions–modulation of the host innate immune system. Front. Immunol. 5:481. doi: 10.3389/fimmu.2014.00481

PubMed Abstract | CrossRef Full Text | Google Scholar

Ibarra, J. A., and Steele-Mortimer, O. (2009). Salmonella–the ultimate insider. Salmonella virulence factors that modulate intracellular survival. Cell. Microbiol. 11, 1579–1586. doi: 10.1111/j.1462-5822.2009.01368.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Ipinza, F., Collao, B., Monsalva, D., Bustamante, V. H., Luraschi, R., Alegría-Arcos, M., et al. (2014). Participation of the Salmonella OmpD porin in the infection of RAW264. 7 macrophages and BALB/c mice. PloS one. 9:e111062. doi: 10.1371/journal.pome.0111062

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiang, L., Feng, L., Yang, B., Zhang, W., Wang, P., Jiang, X., et al. (2017). Signal transduction pathway mediated by the novel regulator LoiA for low oxygen tension induced Salmonella Typhimurium invasion. PLoS Pathog. 13:e1007997. doi: 10.1371/journal.ppat.1006429

PubMed Abstract | CrossRef Full Text | Google Scholar

Jozefczuk, S., Klie, S., Catchpole, G., Szymanski, J., Cuadros-Inostroza, A., Steinhauser, D., et al. (2010). Metabolomic and transcriptomic stress response of Escherichia coli. Mol. Syst Biol. 6:364. doi: 10.1038/msb.2010.18

PubMed Abstract | CrossRef Full Text | Google Scholar

Kolde, R. (2015). pheatmap: Pretty Heatmaps. R Package Version 1.0.8. Available at: (accessed November, 2017).

Google Scholar

Koronakis, V., and Hughes, C. (1988). Identification of the promotors directing in vivo expression of hemolysin genes in Proteus vulgaris and Escherichia coli. MGG Mol. Gen. Genet. 213, 99–104. doi: 10.1007/bf00333404

PubMed Abstract | CrossRef Full Text | Google Scholar

Langmead, B., and Salzberg, S. L. (2012). Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–359. doi: 10.1038/nmeth.1923

PubMed Abstract | CrossRef Full Text | Google Scholar

LaRock, D. L., Chaudhary, A., and Miller, S. I. (2015). Salmonellae interactions with host processes. Nat. Rev. Microbiol. 13:191. doi: 10.1038/nrmicro3450

PubMed Abstract | CrossRef Full Text | Google Scholar

Levine, R. L., Garland, D., Oliver, C. N., Amici, A., Climent, I., Lenz, A. G., et al. (1990). Determination of carbonyl content in oxidatively modified proteins. Meth. Enzymol. 186, 464–478. doi: 10.1016/0076-6879(90)86141-h

CrossRef Full Text | Google Scholar

May, J. F., and Groisman, E. A. (2013). Conflicting roles for a cell surface modification in Salmonella. Mol. Microbiol. 88:5. doi: 10.1111/mmi.12236

PubMed Abstract | CrossRef Full Text | Google Scholar

Miller, S. I. (1991). PhoP/PhoQ: macrophage-specific modulators of Salmonella virulence? Mol. Microbiol. 5, 2073–2078. doi: 10.1111/j.1365-2958.1991.tb02135.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Morales, E. H., Calderón, I. L., Collao, B., Gil, F., Porwollik, S., McClelland, M., et al. (2012). Hypochlorous acid and hydrogen peroxide-induced negative regulation of Salmonella enterica serovar Typhimurium ompW by the response regulator ArcA. BMC Microbiol. 12:63. doi: 10.1186/1471-2180-12-63

PubMed Abstract | CrossRef Full Text | Google Scholar

Morales, E. H., Collao, B., Desai, P. T., Calderón, I. L., Gil, F., Luraschi, R., et al. (2013). Probing the ArcA regulon under aerobic/ROS conditions in Salmonella enterica serovar Typhimurium. BMC Genomics 14:626. doi: 10.1186/1471-2164-12-626

PubMed Abstract | CrossRef Full Text | Google Scholar

Okada, S. S., de Oliveira, E. M., de Araújo, T. H., Rodrigues, M. R., Albuquerque, R. C., Mortara, R. A., et al. (2016). Myeloperoxidase in human peripheral blood lymphocytes: production and subcellular localization. Cell. Imunol. 300, 18–25. doi: 10.1016/j.cellimm.2015.11.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Pardo-Esté, P., Hidalgo, A., Aguirre, C., Inostroza, A., Briones, A., Cabezas, C., et al. (2018). The ArcAB two-component regulatory system promotes resistance to reactive oxygen species and systemic infection by Salmonella Typhimurium. PLoS One 13:e0203497. doi: 10.1371/journal.pone.0203497

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, D. M., Akhtar, M. S., Ansari, A. Z., Landick, R., and Kiley, P. J. (2013). The bacterial response regulator ArcA uses a diverse binding site architecture to regulate carbon oxidation globally. PLoS Genetics. 9:e1003839. doi: 10.1371/journal.pgen.1003839

PubMed Abstract | CrossRef Full Text | Google Scholar

Pattison, D. I., and Davies, M. J. (2001). Absolute rate constants for the reaction of hypochlorous acid with protein side chains and peptide bonds. Chem. Res. Toxicol. 14, 1453–1464. doi: 10.1021/tx0155451

PubMed Abstract | CrossRef Full Text | Google Scholar

Pfaffl, M. W. (2011). A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 29:e45. doi: 10.1093/nar/29.9.e45

PubMed Abstract | CrossRef Full Text | Google Scholar

Popp, J., Noster, J., Bush, K., Kehl, A., Gero zur, H., and Hensel, M. (2015). Role of host cell-derived amino acids in nutrition of intracellular Salmonella enterica. Infect. Immun. 83, 4466–4475. doi: 10.1128/IAI.00624-15

PubMed Abstract | CrossRef Full Text | Google Scholar

Robinson, M. D., McCarthy, D. J., and Smyth, G. K. (2010). edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26, 139–140. doi: 10.1093/bioinformatics/btp616

PubMed Abstract | CrossRef Full Text | Google Scholar

Ruby, T., McLaughlin, L., Gopinath, S., and Monack, D. (2012). Salmonella’s long-term relationship with its host. FEMS Microbiol. Rev. 36, 600–615. doi: 10.1111/j.1574-6976.2012.00332.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmieder, R., and Edwards, R. (2011). Quality control and preprocessing of metagenomic datasets. Bioinformatics 27, 863–864. doi: 10.1093/bioinformatics/btr026

PubMed Abstract | CrossRef Full Text | Google Scholar

Shacter, E., Williams, J. A., Lim, M., and Levine, R. L. (1994). Differential susceptibility of plasma proteins to oxidative modification: examination by western blot immunoassay. Radic. Biol. Med. 17, 429–437. doi: 10.1016/0891-5849(94)90169-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Shalel-Levanon, S., San, K. Y., and Bennett, G. N. (2005). Effect of oxygen, and ArcA and FNR regulators on the expression of genes related to the electron transfer chain and the TCA cycle in Escherichia coli. Metab. Eng. 7, 364–374. doi: 10.1016/j.ymben.2005.07.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Shannon, P., Markiel, A., Ozier, O., Baliga, N. S., Wang, J. T., Ramage, D., et al. (2003). Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res. 13, 2498–2504. doi: 10.1101/gr.1239303

PubMed Abstract | CrossRef Full Text | Google Scholar

Srikumar, S., Kröger, C., Hebrard, M., Colgan, A., Owen, S. V., Sivasankaran, S. K., et al. (2015). RNA-seq brings new insights to the intra-macrophage transcriptome of Salmonella Typhimurium. PLoS Pathog. 11:e1005262. doi: 10.1371/journal.ppat.1005262

PubMed Abstract | CrossRef Full Text | Google Scholar

Swamydas, M., and Lionakis, M. S. (2013). Isolation, purification and labeling of mouse bone marrow neutrophils for functional studies and adoptive transfer experiments. J. Vis. Exp. 77:e50586. doi: 10.3791/50586

PubMed Abstract | CrossRef Full Text | Google Scholar

Vazquez-Torres, A., Xu, Y., Jones-Carson, J., Holden, D. W., Lucia, S. M., Dinauer, M. C., et al. (2000). Salmonella pathogenicity island 2-dependent evasion of the phagocyte NADPH oxidase. Science 287, 1655–1658. doi: 10.1126/science.287.5458.1655

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, S., Phillippy, A., Deng, K., Rui, X., Li, Z., Tortorello, M., et al. (2010). Transcriptomic responses of Salmonella enterica serovars enteritidis and Typhimurium to chlorine-based oxidative stress. Appl. Environ. Microbiol. 76, 5013–5024. doi: 10.1128/AEM.00823-10

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Z., Sun, J., Xia, T., Liu, Y., Fu, J., Lo, Y. K., et al. (2018). Proteomic delineation of the ArcA regulon in Salmonella Typhimurium during anaerobiosis. Mol. Cell. Prot. 17, 1937–1947. doi: 10.1074/mcp.RA117.000563

PubMed Abstract | CrossRef Full Text | Google Scholar

Wei, T., and Simko, V. (2017). R Package “corrplot”: Visualization of a Correlation Matrix. Available at: (accessed November, 2017).

Google Scholar

Whitfield, C., and Trent, M. (2014). Biosynthesis and export of bacterial lipopolysaccharides. Annu. Rev. Biochem. 83, 99–128. doi: 10.1146/annurev-biochem-060713-035600

PubMed Abstract | CrossRef Full Text | Google Scholar

Wilkie-Grantham, R., Magon, N., Harwood, D., Kettle, A., Vissers, M., Winterbourn, C., et al. (2015). Myeloperoxidase-dependent lipid peroxidation promotes the oxidative modification of cytosolic proteins in phagocytic neutrophils. J. Biol. Chem. 290, 9896–9905. doi: 10.1074/jbc.M114.613422

PubMed Abstract | CrossRef Full Text | Google Scholar

Winterbourn, C. C., and Kettle, A. J. (2013). Redox reactions and microbial killing in the neutrophil phagosome. Antioxid. Redox Sign. 18, 642–660. doi: 10.1089/ars.2012.4827

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: ArcA, neutrophils, Salmonella, transcription factor, hypochlorous acid

Citation: Pardo-Esté C, Castro-Severyn J, Krüger GI, Cabezas CE, Briones AC, Aguirre C, Morales N, Baquedano MS, Sulbaran YN, Hidalgo AA, Meneses C, Poblete-Castro I, Castro-Nallar E, Valvano MA and Saavedra CP (2019) The Transcription Factor ArcA Modulates Salmonella’s Metabolism in Response to Neutrophil Hypochlorous Acid-Mediated Stress. Front. Microbiol. 10:2754. doi: 10.3389/fmicb.2019.02754

Received: 12 September 2019; Accepted: 12 November 2019;
Published: 05 December 2019.

Edited by:

Dieter Jahn, Technische Universität Braunschweig, Germany

Reviewed by:

Dimitris Georgellis, National Autonomous University of Mexico, Mexico
Guang Zhao, Qingdao Institute of Bioenergy and Bioprocess Technology (CAS), China

Copyright © 2019 Pardo-Esté, Castro-Severyn, Krüger, Cabezas, Briones, Aguirre, Morales, Baquedano, Sulbaran, Hidalgo, Meneses, Poblete-Castro, Castro-Nallar, Valvano and Saavedra. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Claudia P. Saavedra,