HilE is required for synergistic activation of SPI-1 gene expression in Salmonella enterica serovar Typhimurium
BMC Microbiology volume 21, Article number: 49 (2021)
Salmonella enterica serovar Typhimurium is an intestinal pathogen capable of infecting a wide range of animals. It initiates infection by invading intestinal epithelial cells using a type III secretion system encoded within Salmonella pathogenicity island 1 (SPI-1). The SPI-1 genes are regulated by multiple interacting transcription factors. The master regulator is HilD. HilE represses SPI-1 gene expression by binding HilD and preventing it from activating its target promoters. Previous work found that acetate and nutrients synergistically induce SPI-1 gene expression. In the present study, we investigated the role of HilE, nominally a repressor of SPI-1 gene expression, in mediating this response to acetate and nutrients.
HilE is necessary for activation of SPI-1 gene expression by acetate and nutrients. In mutants lacking hilE, acetate and nutrients no longer increase SPI-1 gene expression but rather repress it. This puzzling response is not due to the BarA/SirA two component system, which governs the response to acetate. To identify the mechanism, we profiled gene expression using RNAseq in the wild type and a ΔhilE mutant under different growth conditions. Analysis of these data suggested that the Rcs system, which regulates gene expression in response to envelope stress, is involved. Consistent with this hypothesis, acetate and nutrients were able to induce SPI-1 gene expression in mutants lacking hilE and the Rcs system.
While the exact mechanism is unknown, these results demonstrate the HilE, nominally a repressor of SPI-1 gene expression, can also function as an activator under the growth conditions investigated. Collectively, these results provide new insights regarding SPI-1 gene regulation and demonstrate that HilE is more complex than initially envisioned.
Salmonella enterica serovar Typhimurium initiates infection by invading intestinal epithelial cells using a type III secretion system encoded within Salmonella pathogenicity island 1 (SPI-1) . Expression of the SPI-1 genes is tightly regulated by multiple transcription factors, ensuring that these genes are expressed at the right time and place using extracellular metabolites and environmental signals as sensory cues [2, 3]. HilA activates expression of the genes encoding the type III secretion system and associated effector proteins . HilA expression is positively regulated by three transcription factors: HilD, HilC, and RtsA [5,6,7,8]. These three regulators can independently activate hilA expression. In addition, they also positively regulate their own and each other’s expression. Among the three, HilD is the most significant. In mutants lacking hilD, hilA expression is weak. In addition to these positive regulators, there is also a negative regulator, HilE . This protein binds HilD and prevents it from binding its target promoters and activating transcription [10,11,12]. In addition to these SPI-1 specific regulators, a number of additional factors regulate SPI-1 gene expression, most by altering the expression of HilD (cf. ).
In previous work, we found that acetate and nutrients, provided as yeast extract, synergistically induce SPI-1 gene expression . Both acetate and yeast extract are individually capable of inducing SPI-1 gene expression. However, expression is far greater when both are present in the growth medium than would be expected from their individual contributions.
As a brief background, acetate is the most abundant short-chain fatty acid in the distal small intestine , the site of invasion, and Salmonella presumably uses this metabolite to know when it is within the small intestine. Acetate is known to induce SPI-1 gene expression via the BarA/SirA two-component system [14,15,16]. Yeast extract, on the other hand, is complex mixture of nutrients. It is known to induce flagellar gene expression via RflP (also known as YdiV) [17,18,19], though induction does not appear to result from a specific metabolite but rather from improved growth resulting these nutrients . Its role in invasion is unknown but nonetheless provide a chemical signal for tuning both SPI-1 and flagellar gene expression. Most likely, it provides a surrogate for other metabolite present in the distal small intestine.
Synergistic activation of SP1–1 gene expression by acetate and yeast extract results from transcriptional crosstalk with the flagellar genes , where expression of the flagellar regulator FliZ induces SPI-1 gene expression by post-translationally activating HilD  and HilD induces expression of the flagellar genes by activating the expression of the flagellar master operon flhDC .
In this work, we investigated the role of HilE in mediating synergistic induction of SPI-1 gene expression by acetate and yeast extract. We found that HilE is necessary for acetate and yeast extract to increase hilA expression. In mutants lacking HilE, acetate and yeast extract repressed hilA expression. To better understand the governing mechanism, we explored a number of regulatory mutants and also profiled gene expression using RNA-Seq. Our findings indicate that the Rcs system, involved in regulating the response to envelope stress, inhibits the activation of SPI-1 gene expression by acetate and yeast extract in mutants lacking HilE. These results further our understanding of SPI-1 gene regulation and also demonstrate that HilE has roles in addition to being a repressor of SPI-1 gene expression.
HilE is necessary for activation of hilA expression by acetate
We previously found that during growth on TB medium, the addition of yeast extract and acetate synergistically induce hilA expression . HilE negatively regulates HilA expression by binding to HilD and preventing it from activating hilA expression [10,11,12]. Other studies have shown that deleting hilE increases hilA expression . Therefore, we tested whether yeast extract and acetate would also induce hilA expression in a ΔhilE mutant. In these experiments, we measured SPI-1 gene expression using transcriptional fusion to β-galactosidase (LacZ) after 12 h of growth, which was chosen for consistency with our previous study and that it yielded strong SPI-1 gene expression . Consistent with these previous studies, we found that hilA expression was greater in a ΔhilE mutant than the wild type during growth on TB medium (Fig. 1). When yeast extract was added to the growth medium, hilA expression increased in both the wild type and ΔhilE mutant with expression higher in the ΔhilE mutant as expected. However, when acetate was added to the growth medium, hilA expression was reduced in the ΔhilE mutant even though it increased it in the wild type. The further addition of yeast extract further decreased hilA expression (> 2-fold) in the ΔhilE mutant.
In these experiments, we used transcriptional fusions to LacZ. One possibility is that these results are an artifact of using LacZ transcriptional fusions. Therefore, we repeated the same experiments using transcriptional fusions to the green fluorescent protein (GFP), the same reporter used in our previous study . Similar results were observed (Fig. S1). The one exception was that yeast extract weakly increased hilA expression (< 2-fold) in the presence of acetate in the ΔhilE mutant. As discussed below, we also observed a similar response when profiling gene expression using RNA-Seq (Fig. 2). Collectively, these results suggest that HilE is necessary for activation of hilA expression by acetate and that results are not an artifact of the method used to measure gene expression.
HilE is not necessary for activation of hilA expression by other short-chain fatty acids
Short-chain fatty acids are known to induce hilA expression . Therefore, we tested whether the same response occurred when acetate was replaced with formate or propionate using LacZ transcriptional fusions. Consistent with previous results, we found that formate and propionate induce hilA expression (Fig. 3a). In the case of formate, the addition of yeast extract further increased hilA expression whereas, in the case of propionate, the addition of yeast extract decreased hilA expression. The mechanism governing repression by propionate and yeast extract is not known though the same behavior was observed in the ΔhilE mutant as discussed below.
When the same experiments were performed with the ΔhilE mutant (Fig. 3b), the same general responses were observed. In the case of formate, expression was higher in the ΔhilE mutant than in the wild type, which is consistent with HilE being a negative regulator of hilA expression. The addition of yeast extract further increased hilA expression. In the case of propionate, the results were mixed. In the absence of yeast extract, propionate increased hilA expression in both the wild type and ΔhilE mutant. However, in the presence of yeast extract, hilA expression was higher in the wild type at some yeast extract concentration and lower at others. These results suggest that loss of HilE has only a minor effect on the response to propionate and yeast extract. Taken together, we conclude that the requirement of HilE for activation of hilA expression is specific for acetate though we cannot discount that there is also minor contribution in the case of propionate.
HilC and RtsA are not involved in repressing hilA expression by acetate and yeast extract in a ΔhilE mutant
HilD is the master regulator of hilA expression. In a ΔhilD mutant, hilA expression is weak. HilD also activates two additional transcription factors, HilC and RtsA, that can independently activate hilA expression. HilC and RtsA appear to amplify hilA expression as opposed to HilD, which is necessary for turn hilA expression on [8, 22]. There is no evidence to suggest that HilE binds either HilC or RtsA . Nonetheless, we tested whether HilC or RtsA are necessary for repression of hilA expression by acetate and yeast extract in a ΔhilE mutant. Consistent with what we observed in the wild type, acetate and yeast extract synergistically induced hilA expression in ΔhilC and ΔrtsA mutants (Fig. S2). When hilE was also deleted, acetate and yeast extract repressed hilA expression in both mutants. These results indicate that neither HilC nor RtsA affect the response to acetate and yeast extract.
The Bar/SirA two-component system is not involved in repressing hilA expression by acetate and yeast extract in a ΔhilE mutant
The BarA/SirA two-component system regulates hilA expression in response to acetate . It specifically regulates HilD expression through the action of CsrA . Therefore, we tested whether the BarA/SirA two-component system is necessary for repressing hilA expression by acetate and yeast extract in a ΔhilE mutant. We first compared hilA expression in response to acetate and yeast extract in the wild type and a ΔsirA mutant (Figure S3). Overall, hilA expression was lower in the ΔsirA mutant than the wild type, consistent with previous observations. We next compared hilA expression in ΔhilE and ΔhilE ΔsirA mutants. Acetate and yeast extract reduced hilA expression in both mutants. These results suggest that repression of hilA expression by acetate and yeast extract in a ΔhilE mutant does not involve the BarA/SirA two-component system.
Expression profiling suggest that the Rcs is involved in inducing hilA expression by acetate and yeast extract
Our results suggest that HilE is necessary for activation of hilA expression by acetate and yeast extract under the growth conditions tested. In cells lacking HilE, acetate and yeast extract repress hilA expression. These results would naively suggest that HilE is a positive regulator of hilA expression. However, HilE is a known repressor of hilA expression, and there is no evidence to suggest that it is capable of activating hilA expression based on current models. In particular, HilE binds the upstream regulator HilD and prevents it from activating hilA expression [10,11,12]. Therefore, we hypothesized that loss of HilE is somehow affecting the expression of some other regulator of hilA expression. To identify such regulators, we profiled transcription using RNA-Seq in the wild type and ΔhilE mutant during growth (12 h time point) in TB medium alone, TB medium containing 1% yeast extract, TB medium containing 10 mM sodium acetate, and TB medium containing 1% yeast extract and 10 mM sodium acetate (Table S1). These concentrations of yeast extract and sodium acetate were previously shown to induce hilA expression during growth on TB medium.
A total of 522 million raw reads were obtained from 24 samples (3 biological replications for the two strains grown under the four conditions). Approximately 90% of the reads mapped to a unique location on the S. enterica genome. During growth on TB medium, we observed 85 genes with increased expression and 25 genes with reduced expression in the ΔhilE mutant as compared to the wild type. During growth on TB medium containing 1% yeast extract, we observed 95 genes with increased expression and 241 with decreased expression. During growth on TB medium containing 10 mM acetate, we observed 382 genes with increased expression and 144 with decreased expression. And, during growth on TB medium containing both 1% yeast extract and 10 mM acetate, we observed 457 genes with increased expression and 770 with decreased expression (Fig. S4).
Consistent with the data involving transcriptional fusions for the green fluorescent protein and LacZ, we found that acetate and yeast extract strongly inhibited the expression of the SPI-1 genes involved in the ΔhilE mutant relative to the wild type (Fig. 2). Otherwise, the expression of these genes was increased in the ΔhilE mutant relative to the wild type as expected. Similar results were also observed with regards to the expression of the flagellar genes, whose expression is coupled with the SPI-1 genes (Fig. S5).
Among the other differentially expressed genes, we found that acetate and yeast extract activate the expression of genes involved in the Rcs system in a ΔhilE mutant (Fig. 4). Consistent with increased expression of the Rcs system, we also observed increased expression of wca genes involved in the synthesis of extracellular polysaccharides, which are known to be induced by the Rcs system [23, 24]. Interestingly, the Rcs system is known to repress expression of the SPI-1 genes [25, 26].
The Rcs system is necessary for activation of hilA expression by acetate and yeast extract
Analysis of the RNA-Seq data suggest that the Rcs system may govern the response to acetate and yeast extract observed in the ΔhilE mutant (Fig. 4). To test this hypothesis, we measured hilA expression in ΔrcsBC and ΔrcsBC ΔhilE mutants, which lacks the RcsC histidine kinase necessary for signaling (Fig. 5). The response of hilA expression to acetate and yeast extract in the ΔrcsBC mutant was similar to the wild type, with acetate and yeast extract synergistically inducing expression. Consistent with a model where the Rcs system is necessary for repression of hilA expression by acetate and yeast extract in a ΔhilE mutant, we again observed that acetate and yeast extract synergistically induce hilA expression in a ΔrcsBC ΔhilE double mutant. These results demonstrate that the Rcs system is necessary for repression of hilA expression in the absence of HilE.
HilE is a repressor of SPI-1 gene expression [9, 10]. It is known to bind HilD and prevent it from activating hilA expression [11, 12] . HilA, in turn, activates expression of the genes encoding the SPI-1 type III secretion system and associated chaperone and effector proteins. A number of regulators tune SPI-1 gene expression by altering the expression of HilE. For example, LeuO and FimZ repress SPI-1 gene expression by increasing the expression of HilE [27,28,29] whereas Mlc and the small RNA isrM increase SPI-1 gene expression by decreasing the expression of HilE [30, 31]. All of these mechanisms are consistent with HilE being a repressor of SPI-1 gene expression.
In our work, we found that deleting hilE decreases SPI-1 gene expression during growth in TB medium containing acetate and yeast extract. These results suggest that HilE can also function as an activator of SPI-1 gene expression under the specific growth conditions tested, most likely through an indirect mechanism. By analyzing differentially expressed genes in the wild type and ΔhilE mutant during growth on different medias, we identified the Rcs phosphorelay system as a critical regulator. Expression of rcsA, rcsC, and rcsF was increased in the ΔhilE mutant as compared to the wild type during growth on TB medium containing acetate and yeast extract but not during growth of TB medium containing either acetate or yeast extract. The Rcs phosphorelay system normally represses SPI-1 gene expression in response to envelope stress . Indeed, a ΔrcsBC mutant exhibited the same response to acetate and yeast extract. Yet, hilA expression was not repressed by acetate and yeast extract in a ΔrcsBC ΔhilE mutant; rather, the behavior was similar to the wild type.
We also observed strong repression of the flagellar genes by acetate and yeast extract in the ΔhilE mutant (Fig. S5). Previous work demonstrated that synergistic activation of both SPI-1 and flagellar gene expression is due to transcriptional crosstalk between these two systems . Acetate activates SPI-1 gene expression via the BarA/SirA two-component system and yeast extract activates flagellar gene expression via RflP, also known as YdiV. Since gene expression is coupled in these two systems, the net effect is synergistic activation. Not surprisingly then, we also observed repression of flagellar gene expression by acetate and yeast extract.
The mechanism of repression of SPI-1 gene expression by the Rcs phosphorelay system is unknown though part is due to repression of the flagellar genes . In addition, it is not clear whether HilE directly interacts with components of the Rcs system or other proteins affecting its activity. Moreover, in the absence of acetate and yeast extract, SPI-1 gene expression is higher in a ΔhilE mutant than in the wild type during growth in TB medium, suggesting the observed behavior is specific to acetate and yeast extract. One possibility is that the response is due to crosstalk between the Bar/SirA and Rcs systems . However, the expressions patterns observed in the ΔhilE mutant are not due to the BarA/SirA two-component systems, suggesting some other regulatory system is involved.
While the mechanism is unknown, our results nonetheless demonstrate that HilE has additional functions to being a repressor of HilD. In particular, HilE is required for activation of SPI-1 gene expression by acetate and yeast extract. At this stage, we have few insights regarding the mechanism beyond the involvement of the Rcs system (Fig. 6). One possibility is that HilE is somehow interacting with specific components of Rcs system, preventing them from repressing SPI-1 gene expression or, alternatively, inducing expression. Indeed, RcsB can associate with other transcriptional regulators [33,34,35,36], and perhaps HilE binds these complexes and prevents them from binding their target promoters. In addition, acetate and yeast extract may affect the response of the Rcs system, which nominally responds to envelope stress, via direct phosphorylation or acetylation by acetyl-P [37, 38]. However, the Rcs system has little effect on hilA expression in presence of HilE. This would suggest, that HilE perhaps interacts with other proteins that affect the response of the Rcs system. Clearly, more studies are required to elucidate the mechanism.
We found that HilE is required for activation of SPI-1 gene expression by acetate and yeast extract in S. enterica. The mechanism does not involve the BarA/SirA two-component system, which normally induces SPI-1 gene expression in response to acetate. Rather, the Rcs system is involved. Deletion of the Rcs system removes the HilE requirement for SPI-1 activation by acetate and yeast extract. While the exact mechanism is unknown, these results demonstrate the HilE, nominally a repressor of SPI-1 gene expression, can also function as an activator under the growth conditions investigated. Collectively, these results provide new insights regarding SP1 gene regulation and demonstrate that HilE is more complex than initially envisioned.
Bacterial strains and growth conditions
All strains were derived from Salmonella enterica serovar Typhimurium ATCC 14028 (American Type Culture Collection) and are listed in Table S2. Mutants were constructed using P22 transduction with previously developed strains as the donor. All growth experiments were perform at 37 °C using tryptone broth (10 g/L tryptone) buffered at pH 7 using 100 mM 3-(N-morpholino) propanesulfonic acid (MOPS) as the base medium. Sodium acetate, sodium formate, and sodium propionate were added at concentrations of 10 mM; yeast extract was added at the specified concentrations.
β-Galactosidase and fluorescence assays
Cells were grown overnight in TB medium and subcultured 1:500 into fresh TB medium containing the specified concentrations of sodium acetate and yeast extract. The cells were then harvested after 12 h growth. The β-galactosidase was performed as previously described using 96-well microplates . Fluorescence was measured using a BD LRS II flow cytometer (BD Biosciences) as previously described [13, 40]. Briefly, we recorded the fluorescence from 50,000–100,000 cells and reported the mean fluorescence. Data extraction and analysis was performed using FCS Express Version 6 (Denovo Software) and to OriginPro 2019. All experiments report the mean and standard deviation from three biological replicates.
RNA samples were isolated from cells, three biological replicates, after 12 h growth. First, the cells were pelleted by centrifugation at 3200×g for 10 min and then resuspended in 1 mL of RNAlater solution (Sigma-Aldrich). The total RNA was then extracted using RiboPure™-Bacteria Kit (ThermoFisher) following the manufacturer’s instruction. The concentration and quality of the extracted RNA were evaluated using an Invitrogen Qubit 4 Fluorometer and a Thermo Scientific NanoDrop One. RNA integrity numbers were determined using an Agilent Bioanalyzer 2100.
RNA samples were sequenced at the Roy J. Carver Biotechnology Center, University of Illinois at Urbana-Champaign. Briefly, ribosomal RNA was removed using the Ribozero Bacteria Kit (Illumina). The RNAseq libraries were prepared with Illumina’s “TruSeq Stranded mRNAseq Sample Prep Kit”. The libraries were quantitated by qPCR and sequenced on one lane for 101 cycles from each end of the fragments on a NovaSeq 6000 using a NovaSeq SP reagent kit. FASTQ files were generated and demultiplexed with the bcl2fastq v2.20 Conversion Software (Illumina).
Adaptors were trimmed from the 3′-end of the reads using Trimmomatic  and then analyzed by FastQC . Genome alignments were performed using STAR (STAR/2.7.3a-IGB-gcc-8.2.0)  and RNA reads were counted using the featureCounts-subread package. Salmonella enterica subsp. enterica serovar Typhimurium (ASM386401v1) was used as the reference genome. FASTA files are available at NCBI (NCBI Accession: PRJNA663059 ID: 663059 SAMN16116301 to SAMN16116324).
Statistical analysis was performed using R (Version 3.6). The edgR function “DGEList” was used to count data obtained from featureCount and the “objectreadDGE” function to calculate the sum counts for each sample, normalized to the library size with low-information genes filtered out. The edgeR-quasi pipeline needs to create a design matrix with one coefficient (column) for each of the eight groups, and growth in TB medium was used as the baseline for comparison and specified the contrast of interest using limma vignette section 9.6. Differential expression was performed using edgeR as follows: the estimateDisp function was used to determine the variance among replicates and perform empirical Bayesian “shrinkage” of variances. Test statistics were calculated using the glmLRT function. Finally, decideTestsDGE function was used to identify differentially expressed genes by setting the p-value threshold to be 0.1 and log fold-change to be at least two.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. The RNA-Seq dataset are available at NCBI: https://www.ncbi.nlm.nih.gov/Traces/study/?acc=PRJNA663059.
Lostroh CP, Lee CA. The Salmonella pathogenicity island-1 type III secretion system. Microbes Infect. 2001;3(14–15):1281–91.
Jones BD. Salmonella invasion gene regulation: a story of environmental awareness. J Microbiol. 2005;43:110–7.
Golubeva YA, Sadik AY, Ellermeier JR, Slauch JM. Integrating global regulatory input into the Salmonella pathogenicity island 1 type III secretion system. Genetics. 2012;190(1):79–90.
Bajaj V, Hwang C, Lee CA. hilA is a novel ompR/toxR family member that activates the expression of Salmonella typhimurium invasion genes. Mol Microbiol. 1995;18(4):715–27.
Schechter LM, Lee CA. AraC/XylS family members, HilC and HilD, directly bind and derepress the Salmonella typhimurium hilA promoter. Mol Microbiol. 2001;40(6):1289–99.
Olekhnovich IN, Kadner RJ. DNA-binding activities of the HilC and HilD virulence regulatory proteins of Salmonella enterica serovar Typhimurium. J Bacteriol. 2002;184(15):4148–60.
Ellermeier CD, Slauch JM. RtsA and RtsB coordinately regulate expression of the invasion and flagellar genes in Salmonella enterica serovar Typhimurium. J Bacteriol. 2003;185(17):5096–108.
Ellermeier CD, Ellermeier JR, Slauch JM. HilD, HilC and RtsA constitute a feed forward loop that controls expression of the SPI1 type three secretion system regulator hilA in Salmonella enterica serovar Typhimurium. Mol Microbiol. 2005;57(3):691–705.
Fahlen TF, Mathur N, Jones BD. Identification and characterization of mutants with increased expression of hilA, the invasion gene transcriptional activator of Salmonella typhimurium. FEMS Immunol Med Microbiol. 2000;28(1):25–35.
Baxter MA, Fahlen TF, Wilson RL, Jones BD. HilE interacts with HilD and negatively regulates hilA transcription and expression of the Salmonella enterica serovar Typhimurium invasive phenotype. Infect Immun. 2003;71(3):1295–305.
Grenz JR, Cott Chubiz JE, Thaprawat P, Slauch JM. HilE Regulates HilD by Blocking DNA Binding in Salmonella enterica Serovar Typhimurium. J Bacteriol. 2018;200(8):e00750.
Paredes-Amaya CC, Valdes-Garcia G, Juarez-Gonzalez VR, Rudino-Pinera E, Bustamante VH. The Hcp-like protein HilE inhibits homodimerization and DNA binding of the virulence-associated transcriptional regulator HilD in Salmonella. J Biol Chem. 2018;293(17):6578–92.
Hamed S, Wang X, Shawky RM, Emara M, Aldridge PD, Rao CV. Synergistic action of SPI-1 gene expression in Salmonella enterica serovar typhimurium through transcriptional crosstalk with the flagellar system. BMC Microbiol. 2019;19(1):211.
Lawhon SD, Maurer R, Suyemoto M, Altier C. Intestinal short-chain fatty acids alter Salmonella typhimurium invasion gene expression and virulence through BarA/SirA. Mol Microbiol. 2002;46(5):1451–64.
Martinez LC, Yakhnin H, Camacho MI, Georgellis D, Babitzke P, Puente JL, Bustamante VH. Integration of a complex regulatory cascade involving the SirA/BarA and Csr global regulatory systems that controls expression of the Salmonella SPI-1 and SPI-2 virulence regulons through HilD. Mol Microbiol. 2011;80(6):1637–56.
Teplitski M, Goodier RI, Ahmer BM. Pathways leading from BarA/SirA to motility and virulence gene expression in Salmonella. J Bacteriol. 2003;185(24):7257–65.
Koirala S, Mears P, Sim M, Golding I, Chemla YR, Aldridge PD, Rao CV. A nutrient-tunable bistable switch controls motility in Salmonella enterica serovar Typhimurium. mBio. 2014;5(5):e01611–4.
Wada T, Tanabe Y, Kutsukake K. FliZ acts as a repressor of the ydiV gene, which encodes an anti-FlhD4C2 factor of the flagellar regulon in Salmonella enterica serovar typhimurium. J Bacteriol. 2011;193(19):5191–8.
Takaya A, Erhardt M, Karata K, Winterberg K, Yamamoto T, Hughes KT. YdiV: a dual function protein that targets FlhDC for ClpXP-dependent degradation by promoting release of DNA-bound FlhDC complex. Mol Microbiol. 2012;83(6):1268–84.
Chubiz JE, Golubeva YA, Lin D, Miller LD, Slauch JM. FliZ regulates expression of the Salmonella pathogenicity island 1 invasion locus by controlling HilD protein activity in Salmonella enterica serovar typhimurium. J Bacteriol. 2010;192(23):6261–70.
Singer HM, Kuhne C, Deditius JA, Hughes KT, Erhardt M. The Salmonella Spi1 virulence regulatory protein HilD directly activates transcription of the flagellar master operon flhDC. J Bacteriol. 2014;196(7):1448–57.
Saini S, Ellermeier JR, Slauch JM, Rao CV. The role of coupled positive feedback in the expression of the SPI1 type three secretion system in Salmonella. PLoS Pathog. 2010;6(7):e1001025.
Ebel W, Trempy JE. Escherichia coli RcsA, a positive activator of colanic acid capsular polysaccharide synthesis, functions to activate its own expression. J Bacteriol. 1999;181(2):577–84.
Cano DA, Dominguez-Bernal G, Tierrez A, Garcia-Del Portillo F, Casadesus J. Regulation of capsule synthesis and cell motility in Salmonella enterica by the essential gene igaA. Genetics. 2002;162(4):1513–23.
Palmer AD, Slauch JM. Envelope Stress and Regulation of the Salmonella Pathogenicity Island 1 Type III Secretion System. J Bacteriol. 2020;202(17):e00272.
Lin D, Rao CV, Slauch JM. The Salmonella SPI1 type three secretion system responds to periplasmic disulfide bond status via the flagellar apparatus and the RcsCDB system. J Bacteriol. 2008;190(1):87–97.
Espinosa E, Casadesus J. Regulation of Salmonella enterica pathogenicity island 1 (SPI-1) by the LysR-type regulator LeuO. Mol Microbiol. 2014;91(6):1057–69.
Baxter MA, Jones BD. The fimYZ genes regulate Salmonella enterica Serovar Typhimurium invasion in addition to type 1 fimbrial expression and bacterial motility. Infect Immun. 2005;73(3):1377–85.
Baxter MA, Jones BD. Two-component regulators control hilA expression by controlling fimZ and hilE expression within Salmonella enterica serovar Typhimurium. Infect Immun. 2015;83(3):978–85.
Lim S, Yun J, Yoon H, Park C, Kim B, Jeon B, Kim D, Ryu S. Mlc regulation of Salmonella pathogenicity island I gene expression via hilE repression. Nucleic Acids Res. 2007;35(6):1822–32.
Gong H, Vu GP, Bai Y, Chan E, Wu R, Yang E, Liu F, Lu S. A Salmonella small non-coding RNA facilitates bacterial invasion and intracellular replication by modulating the expression of virulence factors. PLoS Pathog. 2011;7(9):e1002120.
Salvail H, Groisman EA. The phosphorelay BarA/SirA activates the non-cognate regulator RcsB in Salmonella enterica. PLoS Genet. 2020;16(5):e1008722.
Kuhne C, Singer HM, Grabisch E, Codutti L, Carlomagno T, Scrima A, Erhardt M. RflM mediates target specificity of the RcsCDB phosphorelay system for transcriptional repression of flagellar synthesis in Salmonella enterica. Mol Microbiol. 2016;101(5):841–55.
Castanie-Cornet MP, Cam K, Bastiat B, Cros A, Bordes P, Gutierrez C. Acid stress response in Escherichia coli: mechanism of regulation of gadA transcription by RcsB and GadE. Nucleic Acids Res. 2010;38(11):3546–54.
Salscheider SL, Jahn A, Schnetz K. Transcriptional regulation by BglJ-RcsB, a pleiotropic heteromeric activator in Escherichia coli. Nucleic Acids Res. 2014;42(5):2999–3008.
Pannen D, Fabisch M, Gausling L, Schnetz K. Interaction of the RcsB response regulator with auxiliary transcription regulators in Escherichia coli. J Biol Chem. 2016;291(5):2357–70.
Fredericks CE, Shibata S, Aizawa S, Reimann SA, Wolfe AJ. Acetyl phosphate-sensitive regulation of flagellar biogenesis and capsular biosynthesis depends on the Rcs phosphorelay. Mol Microbiol. 2006;61(3):734–47.
Hu LI, Chi BK, Kuhn ML, Filippova EV, Walker-Peddakotla AJ, Basell K, Becher D, Anderson WF, Antelmann H, Wolfe AJ. Acetylation of the response regulator RcsB controls transcription from a small RNA promoter. J Bacteriol. 2013;195(18):4174–86.
Slauch JM, Silhavy TJ. cis-acting ompF mutations that result in OmpR-dependent constitutive expression. J Bacteriol. 1991;173(13):4039–48.
Koirala S, Rao CV. Dynamic measures of Flagellar gene expression. Methods Mol Biol. 2017;1593:73–83.
Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30(15):2114–20.
Dobin A, Davis CA, Schlesinger F, Drenkow J, Zaleski C, Jha S, Batut P, Chaisson M, Gingeras TR. STAR: ultrafast universal RNA-seq aligner. Bioinformatics. 2013;29(1):15–21.
This work was supported by a visiting fellowship from the Egyptian cultural and educational bureau – Washington, DC.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Hamed, S., Shawky, R.M., Emara, M. et al. HilE is required for synergistic activation of SPI-1 gene expression in Salmonella enterica serovar Typhimurium. BMC Microbiol 21, 49 (2021). https://doi.org/10.1186/s12866-021-02110-8
- Gene regulation