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Infect Immun. 2009 September; 77(9): 3552–3568.
Published online 2009 July 6. doi:  10.1128/IAI.00418-09
PMCID: PMC2737987

The RNA Binding Protein CsrA Is a Pleiotropic Regulator of the Locus of Enterocyte Effacement Pathogenicity Island of Enteropathogenic Escherichia coli[down-pointing small open triangle]


The attaching and effacing (A/E) pathogen enteropathogenic Escherichia coli (EPEC) forms characteristic actin-filled membranous protrusions upon infection of host cells termed pedestals. Here we examine the role of the RNA binding protein CsrA in the expression of virulence genes and proteins that are necessary for pedestal formation. The csrA mutant was defective in forming actin pedestals on epithelial cells and in disrupting transepithelial resistance across polarized epithelial cells. Consistent with reduced pedestal formation, secretion of the translocators EspA, EspB, and EspD and the effector Tir was substantially reduced in the csrA mutant. Purified CsrA specifically bound to the sepL espADB mRNA leader, and the corresponding transcript levels were reduced in the csrA mutant. In contrast, Tir synthesis was unaffected in the csrA mutant. Reduced secretion of Tir appeared to be in part due to decreased synthesis of EscD, an inner membrane architectural protein of the type III secretion system (TTSS) and EscF, a protein that forms the protruding needle complex of the TTSS. These effects were not mediated through the locus of enterocyte effacement (LEE) transcriptional regulator GrlA or Ler. In contrast to the csrA mutant, multicopy expression of csrA repressed transcription from LEE1, grlRA, LEE2, LEE5, escD, and LEE4, an effect mediated by GrlA and Ler. Consistent with its role in other organisms, CsrA also regulated flagellar motility and glycogen levels. Our findings suggest that CsrA governs virulence factor expression in an A/E pathogen by regulating mRNAs encoding translocators, effectors, or transcription factors.

Enteropathogenic Escherichia coli (EPEC) is a major etiologic agent of infantile diarrhea in developing countries, causing the deaths of several hundred thousand children per year (13, 71). EPEC and the related bacterium enterohemorrhagic E. coli (EHEC) cause attaching and effacing (A/E) lesions that are characterized by disruption of the intestinal microvilli and reorganization of the cytoskeleton in infected cells to form actin-filled membrane protrusions, termed “pedestals,” that emanate beneath bacteria attached to the cell surface (48, 69).

The locus of enterocyte effacement (LEE) of EPEC is a pathogenicity island that is necessary and sufficient for the formation of pedestals (63). It consists of five major polycistronic operons, including LEE1, LEE2, LEE3, LEE5, and LEE4; the bicistronic operon grlRA; and several monocistronic genes (21, 26, 67). The LEE1, LEE2, and LEE3 operons encode the architectural components of a type III secretion system (TTSS), whereas LEE4 encodes the translocator exporter SepL; the secreted translocators EspA, EspB, and EspD; the chaperones CesD2 and L0017; the needle complex-forming component of the TTSS EscF; and the effector protein EspF. SepL, along with SepD, forms a molecular switch that coordinates the hierarchical secretion of EspA, EspB, and EspD over effectors in response to calcium and other environmental signals (20, 22). EspA is secreted to form a hollow filamentous organelle that connects the protruding EscF needle of the bacterial TTSS to the host cell membrane (17, 50, 82). EspB and EspD are translocated through this filamentous TTSS and integrated into the host cell membrane, where they form a pore that allows effector molecules to be injected directly into the host cytosol (39, 96). The LEE5 operon encodes the effector Tir, its ligand, the adhesin intimin, and the Tir chaperone CesT (67). Tir is translocated into the host cytosol via the TTSS and subsequently integrated into the host cell membrane, where it serves as a receptor for intimin, which is present on the outer bacterial membrane (44). The interaction of Tir and intimin results in firm attachment of the bacterium to the infected cell. Tir recruits cellular factors, such as tyrosine kinases, Nck, and N-WASP, that activate the Arp2/3 complex and initiate actin polymerization beneath the attached bacteria (9, 32, 42, 93), culminating with the formation of pedestals.

Coordinated spatiotemporal expression from the LEE is critical for pedestal formation by EPEC. Such a mode of regulation is achieved by the presence of a plethora of transcription factors such as Ler, PerC, GrlA, GrlR, QseA, IHF, Fis, and H-NS (21, 29, 30, 67, 83, 94) in response to diverse environmental conditions, including pH, osmolarity, Fe(NO3)3, Ca2+, temperature, quorum sensing, and HCO3 (1, 43, 85-90, 94). Most of these transcription factors affect the expression from the LEE by activating the transcription of ler, which in turn activates transcription from grlRA, LEE2, LEE3, LEE5, escD, and LEE4 (see Fig. Fig.9)9) (7, 11, 21, 26, 35, 65, 67).

FIG. 9.
Model of LEE regulation by csrA. When expressed in monocopy, binding of CsrA to the LEE4 operon encoding sepL espADB and escF transcript results in their increased steady-state transcript levels. However, activation of escD occurs indirectly via an intermediate ...

Whereas our understanding of the mechanisms of transcriptional regulation of the LEE is extensive, information about posttranscriptional and posttranslational regulation is more limited. Posttranscriptional control has been suggested in the negative regulation of espADB mRNA in EHEC strains that secrete high levels of EspA. However, the mechanistic basis for this phenomenon has not been established (78). In terms of posttranscriptional and posttranslational regulation, the detailed molecular mechanisms for only the endoribonuclease RNase E (60) and the protease ClpXP have been elucidated (40). Whereas in EHEC RNase E generates the sepL and espADB transcripts by splicing at the C-terminal end of sepL in the precursor sepL espADB transcript (60), the protease ClpXP positively regulates the LEE posttranslationally by affecting the expression of RpoS and GrlR (40). The ribosome binding GTPase BipA and the noncoding RNA DsrA have also been shown to upregulate the expression of the LEE in EPEC and EHEC, respectively, although the detailed molecular mechanisms involved in this regulation have yet to be elucidated (31, 53).

We have identified csrA as a posttranscriptional regulator of EPEC necessary for paralyzing and killing the nematode Caenorhabditis elegans (S. Bhatt and D. Kalman, unpublished data). Previous studies have demonstrated that genes involved in nematode pathogenesis may also facilitate pedestal formation on mammalian cells (3, 66). This latter observation prompted us to investigate the possible role of csrA in mammalian pathogenesis.

CsrA and its orthologue RsmA are homodimeric RNA binding proteins (4, 33, 36, 59, 77) that regulate gene expression posttranscriptionally by binding to sites containing the AGGA/ANGGA motif in the leader segment of transcripts and altering their stability and/or translation (5, 6, 23, 59, 62, 97, 98). Transcripts such as flhDC, whose expression is activated by CsrA, have a putative CsrA binding site(s) located distantly from the Shine-Dalgarno sequence. Binding of CsrA enhances their stability and leads to an increase in the steady-state levels of such transcripts (79, 98). For transcripts that are negatively regulated, CsrA binds to sequences that overlap or lie in close proximity to the Shine-Dalgarno sequence, thereby preventing the 30S ribosomal subunit from binding to the transcript and inhibiting translation and/or facilitating mRNA decay (5, 6, 24, 97).

The carbon storage regulation (Csr) system also includes the noncoding small RNAs CsrB and CsrC, which bind tightly to and sequester 9-10 and 4-5 CsrA dimers, respectively, thereby preventing CsrA from exerting its effect on the mRNAs in its regulon (58, 99). The expression of CsrB and CsrC is activated by CsrA through the BarA-UvrY two-component regulatory system (74, 92, 99). The last component of the Csr system is CsrD, a protein containing vestigial GGDEF and EAL domains, which targets CsrB and CsrC for degradation by the endoribonuclease RNase E, thereby increasing intracellular CsrA activity (91). These negative feedback loops of the Csr system demonstrate that CsrA activity is finely tuned and suggest that the Csr system functions as a homeostatic circuit (91, 92). The role of CsrA and RsmA in regulating virulence factors and host interactions of mammalian and plant pathogens is well established in Salmonella enterica serovar Typhimurium, Erwinia carotovora, Pseudomonas aeruginosa, Helicobacter pylori, Legionella pneumophila, and Yersinia pseudotuberculosis (2, 8, 10, 16, 27, 37, 47, 56, 75).

In this report, we provide evidence that in EPEC, a functional csrA allele is necessary for the formation of pedestals and for membrane depolarization of epithelial cells. CsrA exerts its effect by binding to the leader segment of the sepL espADB mRNA and enhancing the steady-state transcript and protein levels. In contrast to the csrA mutant phenotype, modest overexpression of csrA globally repressed transcription from the LEE operons by binding to and repressing the expression of the global regulator of the LEE activator GrlA. Furthermore, we also provide evidence that CsrA-mediated effects appear through at least one other regulatory factor. Lastly, we show that csrA also regulates other virulence-associated traits such as motility and glycogen biosynthesis. Our results extend the role of csrA as a regulator of virulence of the LEE genes of EPEC and likely other A/E pathogens, which also possess highly conserved csrA orthologs and putative CsrA binding sites in the leader segment of LEE genes.


Bacterial strains, plasmids, primers, and media.

Bacteria were grown in Luria-Bertani (LB) broth or Dulbecco modified Eagle medium (DMEM) containing phenol red (for immunofluorescence microscopy) or lacking glutamine and phenol red (for Western blotting and real-time quantitative reverse transcription [qRT]-PCR) with appropriate antibiotic supplements when needed. The antibiotics used were streptomycin (100 μg/ml), chloramphenicol (25 or 50 μg/ml), kanamycin (50 μg/ml), tetracycline (15 μg/ml), and ampicillin (50 or 100 μg/ml).

To determine growth rates, bacterial cultures were grown overnight at 37°C at 250 rpm in LB broth or in LB broth supplemented with the appropriate antibiotic. Overnight cultures were diluted to a starting optical density (OD) of approximately 0.01 in DMEM containing glucose (4.5 g/liter) but lacking phenol red and glutamine. The cultures were grown standing at 37°C in a 5% CO2 incubator, and growth was measured every hour and intermittently at half-hour intervals over a period of 24 h. The growth curve of each strain was determined at least twice with different experimental samples by assaying each sample in duplicate. Growth curves are representative of one such experiment. The strains, plasmids, and oligonucleotides used are listed in Tables Tables11 and and22.

Bacterial strains and plasmids used in this study
Oligonucleotides used in this study

csrA was disrupted by the one-step gene inactivation method described by Datsenko and Wanner and modified for EPEC by Murphy and Campellone (18, 70). Briefly, plasmid pKD3 was used as the template to amplify a chloramphenicol (cat) resistance cassette flanked on its 5′ side with 51 nucleotides (101 to 151 nucleotides downstream of the translation initiation codon of the csrA open reading frame [ORF]) and on its 3′ side with 49 nucleotides (152 to 186 nucleotides downstream of the translation initiation codon of the csrA ORF and 14 nucleotides downstream of the translation termination codon) by using primers 5′csrAP2(Wanner) and 3′csrAP1(Wanner). The PCR product was gel purified, and 250 to 500 ng of the product was electroporated into EPEC expressing the lambda red recombinase proteins Gam, Exo, and Bet from plasmid pTP223 under the control of an isopropyl-β-d-thiogalactopyranoside (IPTG)-inducible promoter (76). Expression of the lambda red recombinase system promotes the site-specific substitution of the wild-type csrA allele with the mutant csrA::Cmr PCR product because of the presence of identical flanking sequences in the PCR product. Recombinants were selected on LB broth plates containing chloramphenicol. grlA was tagged in the chromosome with a 3XFLAG tag in a similar manner by using pKD4 as the template (40, 70, 95). The csrA disruption was verified by locus-specific PCR with primer pair 5′csrA and c2 or 3′csrA(EPEC) and c1, whereas grlA tagging was verified by using the primer pair 5′grlA(qRT-PCR) and k1 (18). PCR products of the expected size were generated and verified by sequencing.

Construction of pCRA16 has been described previously (91). Briefly, a BamHI-EcoRI fragment of approximately 500 bp containing the K-12 csrA gene under the control of its putative promoter(s) was restricted from pCSR10 (80), end filled with the Klenow fragment of DNA polymerase I, and cloned into the blunt VspI site of the bla gene of pBR322 to generate pCRA16. The csrA ORF is oriented in the same direction as the bla gene (91).

EPEC csrA lacZ csrA+ is the csrA disruptant expressing the wild-type csrA allele under the control of its putative promoter(s). csrA was amplified from EPEC by colony PCR with primers 5′csrA-EcoRV and 3′csrA-EcoRV. The 685-bp PCR product contains the intergenic sequence spanning the region from the last 11 nucleotides of the csrA upstream gene alaS to the −35 region of the csrA downstream gene serV and includes csrA under the control of its native cis regulatory elements (as determined by qRT-PCR and Western blotting for LEE-encoding genes regulated by CsrA). The PCR product was gel purified, treated with EcoRV, and cloned into the EcoRV site of the lacZ gene in plasmid pJRlacZins (51) to generate pJRcsrA6. The cloned csrA gene is oriented opposite to the direction of transcription of the lacZ gene. The csrA sequence in pJRcsrA6 was verified by sequencing with the same set of primers. pJRcsrA6 contains the R6Kγ origin of replication and can only replicate in π protein-expressing strains such as S17-1λpir (84). This plasmid was transferred into the csrA mutant of EPEC by conjugation as described previously (51). Integrants were selected by plating dilutions onto LB broth plates supplemented with chloramphenicol, ampicillin, 5-bromo-4-chloro-3-indolyl-β-d-galactopyranoside (X-Gal; 40 μg/ml), and IPTG (5 mM) and incubated overnight at 37°C. Transconjugants that arose on these plates were confirmed to be EPEC derivatives and contained both the wild-type and csrA mutant alleles. One such colony was selectively purified, and serial dilutions were plated onto LB broth plates devoid of NaCl but supplemented with 5% sucrose to counterselect for loss of the sacB gene carried on the plasmid backbone. One such colony that arose was confirmed to be ampicillin sensitive, chloramphenicol resistant, sucrose resistant (sacB mutant), and white when plated onto LB broth plates containing X-Gal and IPTG (lacZ mutant) and contained both the wild-type and mutant csrA alleles as determined by PCR and was used for all subsequent experiments.

Cell culture and immunofluorescence microscopy.

3T3 cells were maintained and passaged under standard culture conditions in DMEM supplemented with 10% fetal bovine serum and penicillin and streptomycin. Pedestal formation by EPEC and its isogenic derivatives on 3T3 cells was performed as described previously (3).

Preparation of cell lysates, trichloroacetic acid precipitation, and Western blotting.

Synthesis of EspA and Tir and secretion of EspA, EspB, EspD, and Tir were analyzed by Western blotting. Bacterial cultures were grown under standing conditions at 37°C in a 5% CO2 incubator to an OD of 0.2 to 0.3, 0.5, or 1.0 and pelleted by centrifugation at 3,000 rpm. The proteins in the supernatant were precipitated at −20°C by the addition of trichloroacetic acid to a final concentration of 10%. The precipitated proteins were pelleted and washed with acetone and centrifuged. The pellets were air dried to ensure complete evaporation of the acetone prior to suspending them in 100 μl of a 1:1 volumetric ratio of 2× Laemmli buffer containing ß-mercaptoethanol (54) and 1 M Tris-HCl (pH 6.8). The suspensions were boiled for 10 min prior to 12% sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis. To ensure equal loading, the volume of the sample loaded was normalized to the OD of the cultures when harvested.

To determine protein levels in the cell lysate, the cell pellets were suspended in 200 μl of 50 mM Tris-HCl (pH ~7.5) and sonicated to disrupt the cell membrane. Cell debris was pelleted by centrifugation, and the supernatant was transferred to a fresh Eppendorf tube. Protein concentrations were determined by the Lowry assay (61) as recommended by the manufacturer (Bio-Rad), after which the lysates were mixed with an equal volume of 2× Laemmli buffer containing ß-mercaptoethanol. The lysates were boiled at 95°C for 10 min. Equal amounts of protein were subjected to 12% SDS-polyacrylamide gel electrophoresis. Proteins were electroblotted onto a polyvinylidene difluoride membrane and probed with one of the following antibodies: mouse monoclonal anti-FLAG M2 (F-3165; 10 μg/ml), rabbit anti-Ler (1:2500), rabbit anti-EspA (1:50,000), rabbit anti-EspB (1:10,000), rat anti-EspD (1:500), or rabbit anti-Tir (1:50,000). The anti-FLAG antibody was purchased from Sigma. Each experiment was repeated at least three times with similar results each time.

RNA isolation.

RNA isolation was performed by using the MasterPure RNA purification kit from EPICENTRE as recommended by the manufacturer, with the exception that the DNase I treatment was performed for 45 min and then an additional 5 μl of DNase I was added to the samples and the reaction was allowed to continue for another 45 min prior to inactivation of the DNase I. The DNase I-treated RNA was subjected to phenol-chloroform extraction, followed by isopropanol precipitation, and the procedure was repeated. Precipitated RNA was resuspended in 50 μl of TE buffer (10 mM Tris-HCl [pH 7.8],1 mM EDTA), and 1 μl of ScriptGuard RNase inhibitor was added to the RNA samples.

Real-time qRT-PCR.

The iScript One-Step real-time qRT-PCR kit with SYBR green (Bio-Rad) was used to determine the transcript levels of genes as recommended by the manufacturer, with some modifications. Each reaction mixture had a total volume of 25 μl. The reaction mixture consisted of 1× SYBR green RT-PCR mix (12.5 μl of 2× reaction buffer containing 0.4 mM dATP, dCTP, dGTP, and dTTP; magnesium ions; iTaq DNA polymerase, 20 nM fluorescein; SYBR green I dye; and stabilizers), a primer pair (0.75 μl at a final concentration of 300 nM), nuclease-free water, iScript reverse transcriptase (0.5 μl), and DNase I-treated RNA (50 ng). The reaction conditions were (i) 53°C for 20 min, (ii) 95°C for 10 min, (iii) 40 cycles of 95°C for 0.5 min and 60°C for 1 min, and (iv) 4°C for ∞. Melting curve analysis were done to ensure the specificity of the generated product. The melting curve conditions were (i) 95°C for 1 min, (ii) 55°C for 1 min, and (iii) 40 cycles of 55°C for 10 s with an increment of 0.5°C. Control reactions were conducted to ensure the absence of genomic DNA contamination in purified RNA and that the observed fluorescence was not the result of primer dimer formation. Real-time qRT-PCR was performed in duplicate or triplicate with multiple experimental samples. The cycle threshold method 2−ΔΔCt was used to quantify the transcript levels after normalizing them to the housekeeping gene rrsB. The relative transcript level for EPEC or EPEC(pBR322) in the first sample of the first experiment was defined as 1, and all other values were determined relative to this. The unpaired Student t test was used to assay for the statistical significance of differences. A P value of <0.01 was considered statistically significant for real-time qRT-PCR-based analysis.

In vitro transcription and RNA electrophoretic mobility shift assay (EMSA).

The MEGAshortscript kit from Ambion was used for in vitro transcription as recommended by the manufacturer. Briefly, a PCR product containing the T7 promoter at its 5′ end and the entire leader segment encompassing the putative CsrA binding sites of grlR, sepL, and escD was generated. Transcripts were run on a 5% polyacrylamide gel, the band corresponding to the correct-size transcript was excised, and the gel fragment was suspended in 250 μl of elution buffer (0.5 M ammonium acetate, 1 mM EDTA, 0.2% SDS) along with 2 μl of Superase-in (Ambion) and eluted overnight at 4°C and then at room temperature for 30 min. The eluate was subjected to phenol-chloroform extraction and ethanol precipitation and suspended in TE (10 mM Tris-HCl [pH 8.0], 1 mM EDTA) buffer. Five hundred nanograms of the RNA was run on a gel to verify the size and integrity of the RNA. Thirty to 40 pmol of the RNA was dephosphorylated, and the RNA was purified by another round of phenol-chloroform extraction and ethanol precipitation. The purified RNA was suspended in 10 μl of nuclease-free water. RNA was radioactively labeled and suspended in 10 μl of TE buffer. Because the csrA ORF and the CsrA protein are identical between EPEC and K-12, C-terminally His-tagged CsrA, purified from E. coli K-12, was used for the binding reactions. Purification of recombinant His-tagged CsrA has been described elsewhere (68). His-tagged CsrA was suspended in protein dilution buffer (10 mM Tris-HCl [pH 7.5], 2 mM dithiothreitol, 10% glycerol). RNA was denatured at 85°C and slowly cooled to 25°C over 25 min in a Bio-Rad ICycler prior to addition to the binding reaction mixture. The components of the binding reaction mixture included 50 pM RNA in TE, 1× binding buffer (10 mM Tris-HCl [pH 7.5], 10 mM MgCl2, 100 mM KCl), 3.25 ng/μl total yeast RNA, 20 mM dithiothreitol, 7.5% glycerol, 0.01 μl of Superase-in (Ambion), and 2 μl of different concentrations of His-tagged CsrA in a total volume of 10 μl. The reaction mixtures were incubated at 37°C for 30 min, after which the samples were loaded onto a 10% native polyacrylamide gel. The gel was exposed to a PhosphorImager plate overnight, and the bands were detected with a PhosphorImager. ImageQuaNT (Molecular Dynamics) was used to perform densitometric analysis. The apparent equilibrium dissociation constant (KD) for CsrA was determined from two independent experiments with the equation Y = {Ymax × [(x/KD)n]}/{1 + [(x/KD)n]}. For competition-based gel shift experiments, unlabeled specific and nonspecific (phoB) transcripts were added at final concentrations of 500 pM, 5 nM, and 50 nM, which represent 10-, 100-, and 1,000-fold excesses relative to the labeled transcript.

Transepithelial resistance (TER) assay.

The resistance of cells in response to wild-type and mutant EPEC strains was monitored in real time with the electric cell substrate impedance sensing (ECIS) 1600R device (Applied BioPhysics, Troy, NY). Caco2-BBE cells were seeded into ECIS 8W1E electrodes (5 × 105 cells/400 μl/electrode) and kept at 37°C in 5% CO2 and 90% humidity. When the cells were confluent, they were washed and changed to serum-free, antibiotic-free DMEM. Cell resistance was measured at a frequency of 500 Hz and a voltage of 1 V. Details of the operation, equivalent resistance-capacitance circuit, and modification of the ECIS system can be found in the manufacturer's instructions. Bacterial strains were grown overnight in LB broth and transferred to serum-free and antibiotic-free DMEM, and confluent Caco2-BBE monolayers were infected at a multiplicity of infection of 10. TER was measured continuously postinfection. TER assays were conducted at least three times with separate experimental samples with each sample assayed in triplicate per experiment. The depicted results are representative of one such experiment.

Motility assay.

Cultures were grown to an OD at 600 nm (OD600) of 1.0, and 1 μl of the culture was stabbed onto 0.3% 0.5× DMEM containing glucose (2.25 g/liter) and sodium pyruvate (0.5 mM) but lacking phenol red and glutamine. The stabbed agar plates were incubated upright overnight at 37°C, and the diameter of the “diffusion halo” was measured 30 h later to determine the extent of motility of the bacterium. Motility assays were performed on three separate occasions.

Glycogen biosynthesis assay.

A loopful of a bacterial culture grown to an OD600 of 1.0 was streaked onto Kornberg medium (1.1% K2HPO4, 0.85% KH2PO4, 0.6% yeast extract, 2% glucose, 1.5% agar) (83), after which the plates were incubated overnight at 37°C. The plates were then exposed to iodine crystals to determine the extent of glycogen biosynthesis in the different bacterial strains. Iodine forms complexes with glycogen, as a result of which strains producing glycogen appear blackish-brown whereas strains that do not synthesize glycogen do not exhibit any color change after exposure to iodine. Glycogen biosynthesis assays were performed on three separate occasions. The pictures shown are representative of one such experiment.


csrA regulates adherence and pedestal formation on mammalian cells.

Disruption of csrA does not affect the growth of EPEC, as evident from similar doubling times for the wild type (48.04 ± 0.8 min) and the csrA mutant (41.15 ± 9.2 min) (Fig. 1A, B, and C). Because csrA was necessary for virulence against C. elegans (data not shown, unpublished data), we next assessed whether disruption of csrA affected virulence in mammalian cells. To do this, we assessed the capacity of EPEC to adhere to and form pedestals on mammalian 3T3 cells (49) and to disrupt the resistance across polarized epithelial cells (12, 34). Although cells were infected with the same number of bacteria, the csrA mutant exhibited reduced adherence compared to that of EPEC or the single-copy complemented strain (n = 4; Fig. Fig.1D,1D, compare 4′,6-diamidino-2-phenylindole [DAPI] staining in column 2, row 3 [csrA mutant], with column 1, row 3 [EPEC], or column 3, row 3 [csrA lacZ csrA+]). Furthermore, whereas clustering of the bacteria was evident for the wild-type strain and the complemented strain (yellow arrows), the csrA mutant primarily appeared as solitary isolated cells.

FIG. 1.
Inactivation of csrA does not affect EPEC growth but greatly diminishes adherence, pedestal formation, and disruption of TER. (A and B) Bacterial cultures grown overnight were diluted in DMEM (lacking phenol red) to a starting OD600 of ~0.01, ...

Using fluorescence microscopy in conjunction with antibodies against phosphotyrosine (pY) and Tir and fluorescein isothiocyanate-phalloidin to visualize polymerized actin, we next assessed the formation of actin pedestals. In cells infected with EPEC, >80% of the cells displayed >10 pedestals per cell (Fig. (Fig.1E),1E), and Tir and pY staining was evident directly beneath attached bacteria and at the tips of actin pedestals (Fig. (Fig.1D,1D, column 1). By contrast, with the csrA mutant, the percentage of cells displaying pedestals was reduced by ~35-fold (Fig. (Fig.1E),1E), as was the number of pedestals per cell (Fig. (Fig.1D).1D). Accordingly, pY and Tir staining was diminished in cells infected with the csrA mutant compared to that in cells infected with wild-type EPEC (Fig. (Fig.1D,1D, column 2). Complementation of the mutant with csrA in a single copy restored adherence, pedestal formation, and localization of pY and Tir to the levels seen with wild-type EPEC (Fig. (Fig.1D,1D, column 3, and E).

Disruption of TER across polarized Caco-2BBe cells depends on csrA.

Previous reports have shown that adherence, pedestal formation, and the effectors EspF and Map mediate the capacity of EPEC to disrupt TER across polarized Caco-2BBe cells (12, 19, 64). Because mutation of csrA diminishes the ability of EPEC to adhere and form pedestals, we next examined its effects on TER. For EPEC, the time required to disrupt the TER to 50% of the value at the point of infection (t1/2) was ~5.5 h, whereas the csrA mutant required approximately 2.5 times as long (t1/2 of ~14.3 h; Fig. Fig.2).2). By 9.5 h postinfection, EPEC decreased the resistance across the cells by over 76% (more than fourfold), whereas the csrA mutant reduced the TER by less than 15% during the same period. The complemented strain regained the ability to disrupt the TER with significantly faster kinetics than those of the csrA mutant (t1/2 of ~7.9 h), and by 9.5 h it had decreased the TER by over 63% (Fig. (Fig.2).2). Interestingly, even after prolonged infection by the csrA mutant, there was still some residual endpoint resistance (~12,000 Ω) that was reproducibly higher than that observed in cells infected with EPEC (7,000 Ω) or with the complemented strain (5,000 Ω) (Fig. (Fig.2).2). Taken together, these data suggest that csrA not only regulates the time of onset but also the kinetics and extent of membrane depolarization of mammalian cells in vitro.

FIG. 2.
csrA is necessary for disruption of TER across Caco-2BBe cells. Caco-2BBe cells were seeded into ECIS 8W1E electrodes (5 × 105 cells/400 μl/electrode) and kept at 37°C in a 5% CO2 incubator with 90% humidity. Bacterial ...

csrA is necessary for synthesis and secretion of translocators but only affects the secretion of the effector Tir.

Mutations in espA, espB, espD, or tir negate the ability of EPEC and Citrobacter rodentium to form pedestals on tissue culture cells in vitro or to colonize mice, respectively (14, 21, 28, 44-46, 50, 55). Disruption of csrA reduced the secreted (Fig. (Fig.3A),3A), as well as the bacterium-associated (Fig. (Fig.3B),3B), levels of EspA, EspB, and EspD. Complementation of the csrA mutant with csrA expressed in a single copy under the control of its putative promoter(s) restored both the secreted (Fig. (Fig.3A)3A) and the bacterium-associated (Fig. (Fig.3B)3B) amounts of EspA, EspB, and EspD to nearly wild-type levels.

FIG. 3.
Secretion of EspA, EspB, EspD, and Tir is diminished in the csrA mutant. (A and B) EPEC, the csrA mutant, and the csrA lacZ csrA+ monocopy complemented strain were grown in DMEM lacking phenol red at 37°C in a 5% CO2 incubator ...

Two prominent bands corresponding to Tir were visible in the secreted fraction of the wild type and the complemented strain (Fig. (Fig.3A,3A, lanes 1 and 3) but absent in the tir mutant (data not shown). Whereas the slower-migrating band displayed a modest reduction, the faster-migrating band was absent in the csrA mutant (Fig. (Fig.3A,3A, compare lane 1 with lane 2). Our results are consistent with previous observations identifying at least two variants of Tir in EPEC, of which one migrates at 80 kDa (upper band) and the other, likely representing a truncated form, migrates at 70 kDa (lower band) (25, 26). Both bands were routinely observed in the secreted fraction (Fig. (Fig.3A),3A), but only the 80-kDa band was consistently observed in cell lysates (Fig. (Fig.3B).3B). In contrast to the secretion of Tir, the bacterium-associated level of Tir was not substantially affected by the disruption of csrA (Fig. (Fig.3B).3B). Overall, these data suggest that disruption of csrA reduces the secretion of Tir without appreciably affecting the amount of Tir protein associated with the bacterium or its synthesis (see below).

csrA regulates the transcript levels of the architectural components of the TTSS.

Because the bacterium-associated levels of EspA, EspB, and EspD were reduced in the csrA mutant, we next explored the possibility that reduced levels of protein were due to reduced transcript levels. Real-time qRT-PCR for espA, espD, and espB demonstrated that transcript levels for these genes were reduced by approximately 16-, 28-, and 14-fold, respectively, in the csrA mutant (Fig. (Fig.4A).4A). Complementation with csrA in a single copy restored the transcript levels to those seen in the parental strain (Fig. (Fig.4A).4A). Thus, reduced steady-state protein levels of the translocators in the mutant can be accounted for by reduced transcript levels. Interestingly, whereas espA and espB showed similar n-fold reductions in transcript levels, espD exhibited a 1.75-fold greater reduction (Fig. (Fig.4A4A).

FIG. 4.
sepL, espA, espD, espB, escD, and escF, but not tir, transcript levels are reduced in the csrA mutant. (A and B) RNA was isolated from bacterial cultures grown to an OD of ~1.0, and real-time qRT-PCR was performed as described in Materials and ...

A σ70 promoter for the LEE4 operon is located upstream of sepL, which is the first gene in the operon (67). In EPEC and EHEC, sepL, espA, espD, and espB are transcribed as a single polycistronic transcript (60, 67). In EHEC, this polycistronic transcript is processed at the C terminus of sepL to yield two transcripts containing sepL and espADB, respectively (60), whereas for EPEC this phenomenon has yet to be demonstrated. SepL facilitates the secretion of translocators (20, 52, 72) without affecting their synthesis. Because CsrA binds to the 5′ leader segment of transcripts and affects gene expression, we scanned the RNA sequence in the leader segment of the sepL transcript for putative CsrA binding sites. Two such sites were identified (Fig. 5A and B), suggesting that CsrA might bind to and affect the sepL espADB transcript levels. Consistent with this prediction, sepL transcript levels were reduced by ~17.2-fold in the csrA mutant (Fig. (Fig.4A).4A). Together, these data suggest that csrA not only regulates the synthesis of EspA, EspB, and EspD but may directly affect their export by regulating the levels of SepL. Consistent with data showing similar levels of bacterium-associated Tir in the wild type and the csrA mutant, no significant differences in the tir transcript levels in these strains were observed (Fig. (Fig.4B).4B). Thus, reduced secretion of Tir in the mutant is likely due to an effect of csrA on a regulator or a component of the TTSS.

FIG. 5.
CsrA binds to the leader segment of the LEE4 operon. (A) Cartoon depicting the location of putative CsrA binding sites in the leader segment of the LEE4 transcript. The thick black arrows depict the genetic organization of sepL, espA, espD, espB, cesD2 ...

EscF forms the needle complex of the TTSS that connects the EscC outer membrane protein of the TTSS to the EspA filament. Inactivation of escF diminishes the secretion of EspA, EspB, and EspD and pedestal formation by EPEC (100). escF is present on the same polycistronic transcript as sepL espADB (67), suggesting that its transcript levels might also be reduced in the csrA mutant. However, the transcript levels of escF did not show the same extent of reduction as sepL espADB and were reduced by only ~5.5-fold in the csrA mutant (Fig. (Fig.4B).4B). It is possible that besides being present on the longer transcript, escF is also transcribed from an additional promoter(s) in the intergenic region between espB and escF and this transcript is not subject to CsrA-mediated regulation.

Besides escF, we also assayed for the transcript levels of escD. EscD is homologous to the Yersinia YscD protein, both of which are predicted to be inner membrane proteins and components of the TTSS necessary for the secretion of translocators and effectors (73). escD is located between the eae gene of the LEE5 operon and the sepL gene of the LEE4 operon (67). escD and LEE4 have overlapping divergent promoters, and their transcriptional initiation nucleotides are adjacent to one another, albeit on opposite strands (67). We found that escD transcript levels were reduced ~2.5-fold in the csrA mutant (Fig. (Fig.4B)4B) and restored when the mutant was complemented with csrA in single copy. Overall, these data suggest that reduced synthesis of EscF and EscD in the csrA mutant may, in part, be responsible for reduced secretion of Tir and the translocators by affecting assembly of the TTSS. Expression from the LEE1 and LEE2 operons, which encode other components of the TTSS, was not significantly affected in the csrA mutant (data not shown).

Purified CsrA binds to the leader segment of the sepL espADB, but not the escD, transcript.

Two putative CsrA binding sites were identified in the 5′ leader segment of sepL (Fig. 5A and B), suggesting that CsrA might regulate sepL espADB mRNA levels by directly binding to the transcript. Binding of CsrA to the leader segment of the sepL transcript was detectable at a protein concentration of 10 nM (Fig. (Fig.5C),5C), with an apparent equilibrium binding constant of 23 ± 1.7 nM (Fig. (Fig.5E).5E). No unbound transcript was evident at a CsrA concentration of 80 nM (Fig. (Fig.5C),5C), and multiple shifted ribonucleoprotein complexes were evident at concentrations of ≥160 nM (Fig. (Fig.5C).5C). The binding of CsrA to the sepL transcript was specific, as shown by competition assays with unlabeled sepL and the nonspecific phoB RNA, to which CsrA does not bind (Fig. (Fig.5D).5D). The binding data and real-time qRT-PCR results suggest that increased steady-state levels of sepL, espA, espD, espB, and escF in the wild-type strain are the result of direct interaction between CsrA and the polycistronic transcript. CsrA failed to bind to the escD transcript (data not shown), suggesting that csrA-mediated activation of escD occurred through an intermediate regulator.

The transcription factor GrlA activates the transcription of ler (7, 21, 38), which in turn upregulates the steady-state transcript levels of escD (21, 26, 67). To determine whether the effect of csrA on escD and LEE4 may also be occurring through grlA and ler, we assayed for the expression of these genes. Protein levels of Ler and FLAG-tagged GrlA were unchanged in the csrA mutant (Fig. 5F and G), suggesting that the effects of csrA on escD and LEE4 occurred independently of Ler and GrlA.

Overexpression of csrA globally represses expression from the LEE.

Previous studies with csrA suggest that fine tuning of the activity of CsrA is critical for the virulence of S. enterica serovar Typhimurium (2). This observation prompted us to assess the effect of increasing the activity of CsrA in EPEC. The noncoding small RNAs CsrB and CsrC bind to and sequester CsrA, thereby inhibiting its activity. These RNAs are strongly regulated in vivo, and deletion of both csrB and csrC increases CsrA activity in the cell, a condition that would be more relevant for in vivo interpretation (92, 99). Because CsrB and CsrC exhibit compensatory regulation, loss of either RNA leads to an increase in the remaining RNA (99). Thus, single deletions have weak or negligible effects on CsrA-regulated genes and processes. In this regard, isogenic csrB or csrC single mutants show no difference in the expression of Tir (data not shown), and we were unable to construct a csrB csrC double mutant of EPEC, for unknown reasons. Thus, high activity of CsrA was achieved by increasing the levels of CsrA via expression of csrA from a plasmid. Multicopy expression of csrA resulted in a modest ~1.5-fold ± 0.1-fold increase in CsrA protein levels above that of the empty-vector-containing strain (Fig. (Fig.6A).6A). Overexpression of CsrA reduced the transcript levels of escJ, tir, and espA in the LEE2, LEE5, and LEE4 operons and the monocistronic gene escD by 76-, 43-, 13-, and 45-fold, respectively (Fig. (Fig.6B).6B). Consistent with the observed reduction in transcript levels of tir and espA, the overall steady-state protein levels were also reduced (data not shown). Reduced tir transcript levels in the overexpressor, but not the csrA mutant (compare Fig. Fig.6B6B with 4B), suggest that at some level of regulation, disruption and overexpression of csrA affect Tir levels via distinct pathways.

FIG. 6.
Expression of csrA from a multicopy plasmid globally represses expression from the LEE via GrlA. (A) Cultures of EPEC(pBR322) and EPEC(pCRA16) grown overnight were diluted in DMEM and allowed to grow to an OD of ~1.0. CsrA protein levels were ...

In EPEC, grlR and grlA are on the same bicistronic transcript because a PCR product was generated in a real-time qRT-PCR with a primer specific for grlR and another specific for grlA (data not shown). The grlRA operon encodes a repressor, GrlR, and an activator, GrlA (21). GrlA activates the expression from the LEE by upregulating the transcription of ler (7, 21), whereas binding of GrlR to GrlA has been proposed to prevent such activation (15, 38, 41). Ler, in turn, upregulates the transcription from LEE2, LEE3, LEE5, LEE4, and escD (26, 67). Because we observed reduced transcript levels of genes under the control of the ler regulon, we assessed the expression of ler, grlR, and grlA in the csrA-overexpressing strain. The transcript levels of the three genes were reduced by 7-, 14-, and 29-fold, respectively, in the overexpressor, as determined by real-time qRT-PCR (Fig. (Fig.6C).6C). The corresponding protein levels of Ler and 3XFLAG-tagged GrlA were also substantially reduced (Fig. (Fig.6D),6D), suggesting that overexpression of csrA globally shuts off the transcription from the LEE by repressing the expression of grlA. We were unable to assay for GrlR because no antibody was available, and we were unable to epitope tag grlR on the chromosome. Notably, no Ler protein was detectable in the csrA overexpressor, even when ler was expressed from a multicopy plasmid, despite the fact that complementation of EPEC Δler with the same plasmid resulted in Ler protein levels that were ~17-fold higher than those of EPEC containing a single chromosomal copy of ler (data not shown).

We could not attribute the observed differences in gene expression from the LEE simply to the subtle alteration in growth exhibited by the csrA-overexpressing strain. While barely observable on a logarithmic scale (Fig. (Fig.1A),1A), in a linear plot of growth, the csrA-overexpressing strain exhibited biphasic growth (black arrows in Fig. Fig.1B),1B), which resulted in a mild but detectable growth defect (Fig. (Fig.1B).1B). This growth defect was evident only after the strain had grown past the early log phase beyond an OD600 of ~0.25 as both strains grew at similar rates in the early log phase, with doubling times of ~51.61 ± 8.3 and ~54.70 ± 6.4 min for EPEC(pBR322) and EPEC(pCRA16), respectively (Fig. (Fig.1C).1C). Steady-state levels of Ler protein were reduced in the csrA overexpressor (Fig. (Fig.6E),6E), even when both strains were growing at the same rate (OD600, ~0.2).

CsrA binds to the 5′ leader segment of the grlRA transcript.

Three predicted CsrA binding sites were identified in the leader segment of the grlRA transcript (Fig. 7A and B). Transcripts that are repressed by CsrA often have binding sites that overlap the Shine-Dalgarno sequence or are located nearby (5, 97). One of the predicted CsrA binding sites in grlRA is located one codon downstream of the translation initiation codon in EPEC (Fig. (Fig.7B).7B). Bioinformatic analysis, together with the observation that grlR and grlA transcript levels were reduced in the csrA-overexpressing strain (Fig. 6C and D), suggested that CsrA, when present at high levels, might repress these genes by binding to the leader segment of the grlRA transcript. Binding of CsrA to the grlRA leader segment was evident at a CsrA concentration of 2.5 nM; at 80 nM, all of the transcript was present in the bound form (Fig. (Fig.7C).7C). Multiple shifted ribonucleoprotein species were evident at CsrA concentrations as low as 20 nM (Fig. (Fig.7C,7C, S1 and S2). On further increasing the CsrA concentration (≥320 nM), the transcript was evident in supershifted CsrA-RNA complexes S3 and S4 (Fig. (Fig.7C).7C). Binding to the grlRA leader was specific because unlabeled grlRA, but not phoB, RNA competed with the labeled transcript (Fig. (Fig.7D).7D). The apparent equilibrium binding constant of CsrA for grlRA was 6 ± 0.8 nM (Fig. (Fig.7E).7E). Taken together, these data suggest that overexpression of CsrA globally represses transcription from the LEE in part by binding to the grlRA transcript and repressing the expression of GrlA.

FIG. 7.
Purified CsrA binds to the leader segment of the grlRA transcript. (A) Cartoon depicting the locations of putative CsrA binding sites in the leader segment of the grlRA transcript. The thick black arrows depict the genetic organization of grlR and grlA ...

csrA regulates motility and glycogen biosynthesis in EPEC.

In nonpathogenic E. coli K-12, CsrA activates flagellar biogenesis by directly binding to the untranslated leader segment of the flhDC transcript and increasing its half-life (98). Similarly, inactivation of csrA rendered EPEC nonmotile, whereas complementation of the mutant with csrA restored motility (Fig. (Fig.8A).8A). High levels of CsrA appeared to have a dose-dependent effect on motility, as the overexpressor was hypermotile compared to the empty-vector-containing strain (Fig. (Fig.8A).8A). Consistent with the observed reduction in motility, flhD transcript levels exhibited an approximately sixfold reduction in the csrA mutant and the transcript levels were restored in the complemented strain (Fig. (Fig.8B).8B). Besides motility, csrA also regulated glycogen biosynthesis in EPEC, with a csrA mutation resulting in elevated glycogen levels (Fig. (Fig.8C).8C). Glycogen biosynthesis was repressed in a dose-dependent manner as multicopy presence of csrA in EPEC [EPEC(pCRA16)] did not elicit any color change on exposure to iodine in comparison to EPEC containing the empty vector [EPEC(pBR322)] (Fig. (Fig.8C8C).

FIG. 8.
csrA activates motility and represses glycogen biosynthesis in EPEC. (A) For motility assays, cultures grown overnight were diluted in LB broth or in LB broth supplemented with the appropriate antibiotic and allowed to grow to an OD of 1.0. One microliter ...


We have shown that csrA regulates gene expression from the LEE pathogenicity island of EPEC and is necessary for pedestal formation and disruption of TER, two in vitro correlates of pathogenesis. Whereas disruption and multicopy expression of csrA lead to a reduction in the levels of the LEE4-encoded transcripts, the mechanistic basis differs. The two predicted CsrA binding sites observed in the leader segment of the sepL transcript do not overlap the predicted Shine-Dalgarno sequence of sepL and are located 17 and 45 nucleotides upstream. Our results suggest that binding of CsrA to the leader segment of the sepL espADB transcript results in increased steady-state transcript levels in EPEC. In contrast, multicopy expression of csrA decreases transcription from the LEE operons, including LEE4, by repressing the expression of the transcriptional activator GrlA (Fig. (Fig.99).

csrA disruption and overexpression also differentially regulate the expression of Tir. Whereas tir transcript and bacterium-associated Tir protein levels are unaffected in the csrA mutant, reduced secretion of Tir in the csrA mutant is partly due to reduced synthesis of EscD and EscF. In the multicopy expressor, by contrast, tir transcript levels are greatly diminished, resulting in reduced Tir synthesis.

It is noteworthy that csrA, when expressed in a single copy, upregulates the expression of genes that form the architectural components of the TTSS (e.g., escD and escF), translocators that form a filamentous conduit between the EscF needle of the TTSS and the host cytosol (e.g., espA, espB, and espD) and the “gatekeeper switch” sepL. SepL and SepD interact (20, 72) to facilitate the hierarchical secretion of translocators over the effectors in response to changes in calcium and possibly other environmental signals (20), perhaps as a means of ensuring the formation of a functional secretion apparatus and subsequent delivery of effectors directly into the host cytosol rather than the medium. EPEC with a mutation in sepL is insensitive to the presence or absence of calcium and displays dysregulated secretion of effectors and translocators (20). Thus, SepL may be a component of a sensor apparatus that detects a reduced intracellular calcium concentration in the host cell and then promotes the release of effectors. Our results suggest that csrA is immediately proximal to sepL in a regulatory cascade, and thus it might play a role in coordinating this hierarchical secretion of translocators over effectors by posttranscriptionally regulating the expression of sepL in response to different environmental stimuli. Future experiments aimed at addressing whether csrA transcript or CsrA protein levels are affected by environmental factors known to regulate the expression and/or secretion of the proteins encoded by LEE4 genes will shed light on the possible involvement of CsrA in such a hierarchical secretion mechanism.

We have demonstrated that multicopy expression of csrA globally represses expression from the LEE locus, likely via GrlA. A grlA mutation might be expected to act epistatically with respect to a grlR mutation, because GrlR affects expression from the LEE locus by binding to and inhibiting GrlA activity (15, 38). Hence, a reduction in GrlR and GrlA should lead to overall transcriptional repression from lee1, resulting in reduced levels of the master regulator Ler. Consistent with this idea, ler transcript and Ler protein levels, as well as transcription from all of the LEE operons tested, were reduced in the CsrA overexpressor.

It is intriguing that the affinity of CsrA for the grlRA transcript is higher than that for the sepL transcript, especially as the repression of grlRA by CsrA appears to occur only at high CsrA concentrations. A likely explanation is that although CsrA initially binds to the grlRA transcript at low concentrations (KD, ~6 nM), it does not produce physiologically relevant changes in gene expression, as evidenced by unchanged GrlA and Ler protein levels in the csrA mutant and the wild-type strain. However, at higher CsrA concentrations, higher-order complexes that affect gene expression may form. Consistent with this idea, multiple CsrA-grlRA ribonucleoprotein species are observed in gel shifts at higher CsrA concentrations (40 nM) (Fig. (Fig.7C,7C, band S2). It is unlikely that S2 represents an artifact resulting from nonspecific aggregates of CsrA because whereas almost all of the grlRA leader transcript is evident in the supershifted species S2 at 80 nM, the sepL transcript remained in the S1 form. Notably, a concentration of 40 nM is within the range in which CsrA binds to other E. coli mRNAs (5). Our data also raise the possibility of at least one additional CsrA-regulated factor that affects gene expression from the LEE in lieu of the fact that escD transcript levels are reduced in the csrA mutant but purified CsrA does not bind to its leader segment.

CsrA is a pleiotropic regulator in EPEC as it also regulates motility and glycogen metabolism. The flhDC mRNA leader segment contains binding sites for CsrA that mediate its effects on motility in E. coli K-12 (98). These binding sites are conserved in EPEC. Thus, it is likely that in EPEC, as in K-12, flagellar biogenesis and consequent motility are mediated by the direct binding of CsrA to the flhDC leader transcript. However, there may also be differences in the CsrA-mediated regulation of motility between EPEC and K-12. E. coli K-12 is motile under diverse environmental conditions, including LB and LB supplemented with exogenous carbon sources such as acetate and succinate, whereas a glucose concentration of 10 mM represses motility (98). By contrast, EPEC remains motile on 0.5× DMEM, which contains 12.5 mM glucose, whereas an isogenic csrA mutant is nonmotile.

Thus, CsrA represents a novel posttranscriptional regulatory molecule in A/E pathogens that activates and represses the expression of the LEE-encoded genes in a concentration-dependent manner. Based on putatively identified CsrA binding sites in the leader segment of sepL and grlRA of EHEC and C. rodentium (Fig. (Fig.5B5B and and7B),7B), and the conserved mode of regulation of ler by GrlR and GrlA (7, 21), we predict that CsrA functions similarly in these A/E pathogens.

An outstanding question is how EPEC and other A/E pathogens integrate transcriptional and posttranscriptional control of the LEE with motility and metabolism as they transit through the digestive tract. Our results raise the possibility that an important component of this coordinated regulatory system may be CsrA. Thus, regulation of the concentration or activity of CsrA, through transcriptional control or via its binding partners CsrB/C, in response to extracellular signals from other bacteria, or even signals from the host, may have pronounced effects on pathogenesis in vivo. We speculate that it would be advantageous for EPEC to mimic commensal strains, perhaps in a manner akin to the csrA overexpressor, during passage through the upper gastrointestinal tract. Thus, increased expression or activity of CsrA would be expected to repress the expression of virulence factors encoded on the LEE (Fig. (Fig.9),9), thereby minimizing energy expenditures on unneeded transcripts and reducing the possibility of detection of pathogen-specific antigens by the innate immune system. Moreover, increased flagellar motility might facilitate transit to the sites of colonization. As EPEC approaches the small intestine, decreasing CsrA protein levels or activity may prove advantageous. Thus, reducing flagellar motility in coordination with increased transcription and translation of translocators, followed by effectors, would permit the bacteria to efficiently attach and colonize. Using the mutants we have developed, we are currently testing how coordinated regulation of flagellar motility, metabolism, and LEE expression by CsrA contributes to pathogenesis and immune evasion in vivo.


We thank Bernie Weiss and Phil Rather for critical evaluation of the manuscript and Guy Benian, Charlie Moran, and the members of the Kalman, Romeo, and Weiss labs for helpful discussions and suggestions. We are grateful to June Scott (Emory University) for providing the wild-type strain EPEC 2348/69, Jim Kaper and Michael Donnenberg (University of Maryland) for strains (EPEC ΔespA, EPEC ΔespB, and EPEC ΔespD), and antibodies (anti-Tir, anti-EspA, and anti-EspB), B. Brett Finlay (University of British Columbia) for EPEC Δtir, Jay Mellies (Reed College) for EPEC Δler, Vanessa Sperandio (UT-Southwestern, Dallas) for pJRLacZIns, Rebekah DeVinney (University of Calgary) for the anti-EspD antibody, Phil Rather (Emory University) for S17-1λpir, Bettina Bommarius (Emory University) for DH5α, and Ilan Rosenshine (The Hebrew University, Jerusalem) for anti-Ler.

This work was supported by NIH grants R01DK074731-01 and R01-A1056067-01 to D.K. and R01-GM059969 to T.R. S.B. is the recipient of National Science Foundation award 0450303 and subaward I-66-606-63 to Emory University.


Editor: A. J. Bäumler


[down-pointing small open triangle]Published ahead of print on 6 July 2009.


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