Contribution of Three Bile-Associated Loci, bsh, pva, and btlB, to Gastrointestinal Persistence and Bile Tolerance of Listeria monocytogenes

Media, chemicals, and growth conditions.Bacterial strains and plasmids used in the present study are listed in Table 1. Escherichia coli strains were grown in Luria-Bertani (LB) medium. L. monocytogenes strains were grown in brain heart infusion (BHI) broth (Oxoid) shaking at 37°C (aerobic growth conditions). When necessary, anaerobic conditions were created by using BBL anaerobic jars and the Merck Anaerocult A Gas Pak system, and the absence of oxygen was verified by using Anaerotest strips (Merck). Chloramphenicol, erythromycin, and rifampin were made up as concentrated stocks and added to media at the required levels. Bile acids (sodium salts of glycodeoxycholic acid [GDCA] and taurodeoxycholic acid [TDCA]; Sigma G3258 and T0875, respectively), penicillin G (benzylpenicillin; Sigma PEN-NA), and penicillin V (phenoxymethylpenicillinic acid; Sigma P-1376) were solubilized in water, and filter-sterilized stocks were added to cooled autoclaved media. Bovine bile (oxgall; Sigma B3883) was added to broth prior to autoclaving.

Genetic manipulations and sequence analyses.Sequencing upstream of the groESL operon revealed the presence of a gene (designated bsh) with significant homology to cbh, a Lactobacillus plantarum BSH gene. Inverse PCR was used to obtain the full sequence of the gene. Genomic DNA was digested with AccI. After self-ligation, a PCR was performed with primers CBH1 and CBH2, and the resulting product was purified with the Qiaex II gel extraction kit (Qiagen, Hilden, Germany) and cloned into the pCR2.1 vector by using the TOPO TA cloning kit (Invitrogen, San Diego, Calif.). Plasmids were isolated with the Qiagen QIAprep Spin Miniprep Kit. Nucleotide sequence determination was performed on an ABI 373 automated sequencer. Sequencing upstream of gadA revealed the presence of a BSH-PVA homolog. The remainder of the gene (designated pva) was cloned and sequenced by using a single-specific-primer-PCR approach. Genomic DNA was digested with EcoRI, cloned into similarily digested pORI13, and electroporated into E. coli EC1000 to create a random bank. Plasmids were purified and used as a template for PCRs with primers P1 or P3, situated on either side of the pORI13 multiple cloning site, and PBH3 (a primer situated at the 5′ end of the pva gene). A P1-PBH3 amplicon, ∼1.3 kb in size, was cloned into the pCR2.1 vector and sequenced. The bile acid dehydratase homolog (designated btlB for bile tolerance locus [see below]) was sequenced in L. monocytogenes LO28 by using primers based on the corresponding gene in L. monocytogenes EGDe (lmo0754). Various web-based programs were used to analyze sequences (http://psort.nibb.ac.jp/ , http://www.sbc.su.se/∼miklos/DAS/maindas.html , http://.cbs.dtu.dk/services/TMHMM/ , http://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml , and www.ncbi.nlm.nih.gov/BLAST ). Restriction enzymes, T4 DNA ligase, and PCR reagents were purchased from Boehringer Mannheim, Mannheim, Germany, and used according to the manufacturer's recommendations. PCR was carried out by using a Hybaid (Middlesex, United Kingdom) PCR express system. Colony PCRs were performed after the lysis of cells with IGEPAL CA-630 (Sigma).

Construction of L. monocytogenes deletion mutants.Isogenic nonpolar deletion mutants of bsh, pva, and btlB with 783-, 804-, and 534-bp deletions, respectively, were created by using plasmid constructs generated by the splicing by overlap extension (SOEing) PCR procedure described by Horton et al. (29). In each case primers SOE AB and SOE CD (Table 2) were used to amplify regions flanking the sequence to be deleted. The resulting products were gel extracted, mixed in a 1:1 ratio, and reamplified with the SOE A and D primers. The product was digested with the appropriate restriction enzymes, cloned into the temperature-sensitive shuttle vector pKSV7, and transformed into E. coli DH5α. The resulting plasmids were electroporated into L. monocytogenes, and transformants were selected on BHI plates containing 10 μg of chloramphenicol/ml (BHI/Cm). Chromosomal integration of the plasmids at 42°C was selected for by serial passage of a transformant in prewarmed BHI/Cm broth and streaking onto prewarmed BHI/Cm plates. Plasmid excision and curing was brought about by continuous passage in BHI at 30°C and spreading at intervals on BHI agar at the same temperature. Replica plating onto BHI and BHI/Cm was used to select for the appropriate deletion events. The mutations were confirmed by using primers upstream of SOE A and downstream of SOE D. Double and triple mutants were created by sequential deletions.

Complementation of deletion mutants.The site-specific phage integration vector pPL2 (34) was used for complementation of deletion mutants. The entire bsh, pva, and btlB genes and flanking regions were amplified from a parental L. monocytogenes LO28 genomic DNA preparation by using Pwo DNA polymerase (Roche) and primers (CBH SOEA and CBH SOED, PVA SOEA and PVA pPL2R, and BtlB pPL2F and BtlB pPL2R, respectively; Table 2) that were modified to contain restriction sites. Gel-extracted PCR products were cut and ligated to similarly digested pPL2 (since the plasmid does not have an XbaI-cut site, it was digested with SpeI which generates an identical 5′ overhang). The resulting ligation mixes were electroporated into freshly competent E. coli DH5α, and transformants were selected on Luria-Bertani plates containing 15 μg of chloramphenicol/ml. Plasmids were extracted with the Qiagen QIAprep Spin Miniprep kit and sequenced with primers T3 and T7 to ensure the validity of inserts. Then, 50 μl of each plasmid preparation was ethanol precipitated and resuspended in 5 μl of elution buffer (10 mM Tris-Cl [pH 8.5]) and transformed into freshly competent mutant cells. Wild-type cells were transformed with pPL2 containing no insert to use as a control. Transformants were selected on BHI plates containing 7.5 μg of chloramphenicol/ml. Integration of constructs at the appropriate chromosomal site was confirmed by PCR with a primer that anneals 5′ of the integration site tRNA^Arg-attB′ (PL102) and primers that anneal to the cloned fragments. The additional primer sets BSH F and BSH R, PVA F and PVA R, and BtlB F and BtlB R were used to specifically detect bsh, pva, and btlB, respectively. Each of these primer sets does not amplify a product in the relevant deletion mutant, e.g., BSH F and BSH R do not amplify a product in Δbsh.

Construction of L. monocytogenes insertional mutants.Plasmid pORI19 mutants were constructed as previously described (7, 35). Internal fragments of prfA and sigB were generated by PCR with primers PrfAF and PrfAR and SigBF and SigBR, respectively (Table 2), which were modified to contain restriction sites. The PCR products were cut and ligated to similarly digested pORI19. The resulting plasmids were transformed into E. coli EC101 and subsequently into L. monocytogenes harboring pVE6007. For each gene, one transformant was grown overnight in 10 ml of BHI broth prewarmed to 42°C (the nonpermissive temperature for pVE6007 replication in Listeria) and plated onto BHI containing 5 μg of erythromycin/ml. This selected for chromosomal integration at the point of homology with prfA and sigB. The mutations were confirmed by PCR analysis.

RNA procedures.Cultures were inoculated from single colonies and grown overnight in BHI shaking at 37°C. The cultures were diluted 1:100 in BHI and grown either aerobically or anaerobically. Total RNA was extracted from exponential-phase (optical density at 600 nm of ca. 0.2) and stationary-phase (overnight) cultures by using the RNeasy kit (Qiagen). Samples were treated with the RNase-free DNase I set (Qiagen) according to the manufacturer's recommendations. The absence of DNA was confirmed by PCR. For reverse transcriptase PCR (RT-PCR) analysis, cDNA was synthesized from RNA by using Expand RT and a random primer p(dN)₆ (Roche). Primers BSH F and R, PVA F and R, and BtlB F and R were used for PCR amplification of bsh, pva, and btlB cDNA, respectively. cDNA template was added to PCRs at levels which gave similar band intensities for control reactions performed with primers U141 and L142 (rrnA) (18). PCRs were carried out for 16, 22, 30, and 35 cycles to allow optimal quantitation of products. Densitometric analyses were performed by using Phoretix ID Advanced software. For ex vivo RNA experiments, 6-week-old BALB/c mice were orally infected with ca. 10¹⁰L. monocytogenes LO28 cells that were grown overnight shaking in brain heart broth (Merck) at 37°C. An aliquot of the inoculum was flash frozen in an ethanol bath at −80°C. After 2 h mice were sacrificed and each entire intestine was removed and immediately placed in a sterile petri dish containing 1 ml of RNAprotect Bacteria Reagent (Qiagen). Intestinal contents were flushed out by using a sterile forceps and scissors and flash frozen. Approximately 5 min elapsed between the beginning of dissections and freezing. After thawing on ice, samples from three mice were pooled and centrifuged (10,000 rpm for 6 min), and pellets were resuspended in 500 μl of TE (10 mM Tris, 1 mM EDTA [pH 8.0]). In order to obtain higher RNA yields, total RNA was extracted by using the Macaloid method as outlined by Raya et al. (45). Briefly, the cell suspension was added to a 2-ml screw-cap microcentrifuge tube containing 0.5 g of 425- to 600-nm glass beads (Sigma), 50 μl of 10% sodium dodecyl sulfate (SDS), 500 μl of acid phenol-chloroform (5:1; Sigma), and 150 μl of a 2% Macaloid slurry (Bentone MA; Kronos), and cells were disrupted in a Mini-Beadbeater-8 (Biospec Products). After centrifugation at 13,200 rpm for 10 min, the aqueous supernatant was extracted with 500 μl of phenol chloroform, reextracted with 500 μl of chloroform-isoamyl alcohol (24:1; Sigma), precipitated with ethanol, and resuspended in 30 μl of TE. Mammalian RNA was removed with the MICROBEnrich kit (Ambion), and DNA was removed by using DNA-free (Ambion). RNA was extracted from the aliquot of the inoculum for comparison purposes. The RT reaction and ensuing PCR analyses were performed as described earlier except control PCRs were performed with L. monocytogenes-specific 16S RNA primers MONO7-F and LisR (50). For control purposes the entire procedure was also performed with intestines from noninfected mice.

Growth experiments.For bile broth assays, overnight cultures were inoculated (3%) into BHI broth containing various concentrations of bile or bile acids. Cell growth was measured by performing viable cell counts by diluting cultures in one-quarter-strength Ringer solution and enumeration on BHI. To examine the pH dependency of bile salt toxicity, the effect of 5 mM GDCA and TDCA on cultures was investigated in BHI broth set at initial pH values ranging from 4.5 to 7.5 with 3 M lactic acid. Broth was inoculated (2%) with cells from an overnight culture and incubated anaerobically. Viable cell counts were performed at intervals. The pH was not controlled during the experiment. For all other growth experiments (acid, salt, and penicillin), overnight cultures were inoculated (2%) into BHI supplemented with the relevant stressor, and cell growth was measured spectrophotometrically over 24-h periods by using a Spectra Max 340 spectrophotometer (Molecular Devices, Sunnyvale, Calif.).

BSH plate assays.The plate assay developed by Dashkevicz and Feighner (12) was used to examine bile hydrolase activity. Bacteria were grown on BHI agar and subsequently patch inoculated onto BHI or Man Rogosa and Sharpe (MRS) agar (Merck) supplemented with 0.5% (wt/vol) GDCA or TDCA. Plates were incubated anaerobically at 37°C. Strains with BSH activity were surrounded with white precipitate halos of unconjugated bile acids.

Virulence assays.Spontaneous rifampin-resistant (Rif^r) mutants of wild-type and bsh, pva, and btlB mutant strains were isolated by centrifuging 10 ml of overnight cultures, resuspending the cell pellets in 200 μl of phosphate-buffered saline (PBS) and plating them onto BHI supplemented with 50 μg of rifampin/ml (BHI/RIF). For each strain, four BALB/c mice were infected with ∼10¹⁰ cells by oral gavage. Excretion of viable Listeria was measured in fecal samples collected for 3 days postinfection. Samples were weighed, homogenized in PBS, diluted, and plated onto BHI/RIF. Bacterial numbers in the spleens were determined on the third day by spread plating homogenized organs onto BHI.

Identification and analysis of genes encoding putative bile-degrading enzymes.As part of another study undertaken in our laboratory, a region upstream of groESL was sequenced in L. monocytogenes LO28 and revealed the presence of an open reading frame designated bsh (lmo2067 in L. monocytogenes EGDe) (21). Further analysis revealed a putative ribosomal binding site (AGGAG-14 nucleotides [nt]-ATG), which in turn is preceded by a consensus σ^B-dependent promoter binding site (GTTTTAN₁₃GGGTAC-66 nt-ATG) and a putative PrfA box (TTAAAAATTTTTAA-147 nt-ATG). A 27-nt symmetric sequence followed by a stretch of T residues was identified 9 bp downstream of the stop codon and may function as a Rho-independent transcription termination signal. Further sequence analyses, using computer-aided approaches, suggest that bsh encodes an intracellular enzyme (designated BSH) that is a member of the choloylglycine hydrolase family (PSORT, Pfam02275, COG3049, ProDom009912). Searches for similarity and identity reveal that BSH shows most homology to BSHs of Enterococcus faecium, Enterococcus faecalis, and Lactobacillus plantarum (74, 70, and 66% identities, respectively). It also exhibits lower, yet significant, homology to the Bacillus sphaericus PVA (30% identity). This is in agreement with the previous annotation of EGDe lmo2067 as a BSH (23) and is consistent with the bile hydrolase activity ascribed previously to this locus (18).

A second gene, also annotated as a BSH, was designated pva (lmo0446 in L. monocytogenes EGDe). This gene encodes a putative choloylglycine hydrolase family enzyme, PVA (COG3049, Pfam02275, ProDom009912), which also shows homology to the B. sphaericus PVA (37% identity). The presence of an N-terminal sequence signal suggests an extracellular location (PSORT). Recently, members of the choloylglycine hydrolase enzyme family have been classified as N-terminal nucleophilic (Ntn) hydrolases, and the crystal structure of B. sphaericus PVA has been elucidated (52). The amino acids of the active site were identified as Cys-1 (thought to play an essential role in catalysis), Asp-20, Tyr-82, Asn-175, and Arg-228. Significantly, a CLUSTAL alignment of the L. monocytogenes BSH and PVA amino acid sequences with PVA of B. sphaericus showed that all five amino acids are conserved (not shown). No potential PrfA or σ^B consensus promoters were identified upstream of this locus.

A third locus designated btlB (for bile tolerance locus [see below]; lmo0754 in L. monocytogenes EGDe) was amplified and subsequently sequenced in L. monocytogenes LO28. A putative PrfA box (TTAAAAAGTGTTAC) was identified 365 bp upstream of the predicted start codon. This locus shows no significant homology to genes in the public databases and was annotated as being weakly homologous to bile acid dehydratase genes (baiE) (23). To date, these genes have only been identified and characterized in specific members of the genera Clostridium and Eubacterium. In both, the baiE genes are part of large operons with other genes involved in bile dehydroxylation (17), several regions upstream of the promoters are highly conserved (56), and the bile acid dehydratase enzymes possess lipocalin motifs that are thought to function as bile acid-binding sites (13). However, homologs of the remaining genes in the bile dehydroxylation pathway could not be found in the L. monocytogenes genome. In addition, neither the highly conserved promoter region nor the lipocalin motif could be located. Thus, although detailed computational analyses provided no further insight into a possible function for the encoded protein, it was one of only three loci identified by the European Listeria Genome Consortium as being possibly involved in bile responses and, as such, was deemed appropriate to be included in our investigation.

Comparison of the genomes of L. monocytogenes EGDe and the nonpathogenic strain L. innocua Clip 11262 revealed that all three genes (bsh, pva, and btlB) are specific to L. monocytogenes (23). Further analyses showed that the pva and btlB genes are part of islets present in L. monocytogenes but absent from L. innocua (See Fig. 1). The areas surrounding the bsh gene and pva and bltB gene islets are identical in both species; all upstream and downstream genes are orthologues of identical size. The “pva islet” consists of five genes (lmo0444 to lmo0448) and the “btlB islet” consists of nine as-yet-uncharacterized genes (lmo0746 to lmo07554). Notably, the bsh gene and pva and btlB islets have lower G+C contents than the flanking regions (36%, averages of 37 and 34%, respectively, as opposed to 39%), suggesting their recent acquisition through horizontal gene transfer from low G+C content bacteria.

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FIG. 1.

Genomic organization of bsh, pva, and btlB regions. This figure was drawn approximately to scale by using L. monocytogenes EGDe and L. innocua Clip 11262 genome sequence data. The numbers are National Center for Biotechnology Information annotation numbers. Arrows indicate orientation of genes. Hairpins depict putative terminators. Black open reading frames are orthologs. Open reading frames present in L. monocytogenes but absent from L. innocua are in white. Those present in L. innocua but not L. monocytogenes are in gray. Hatched arrows represent the three genes examined in the present study.

Genetic distribution of bsh, pva, and btlB among Listeria species.The observation that all three genes are absent from the sequenced L. innocua strain led us to examine, by PCR, the distribution of the genes among the six Listeria species, of which monocytogenes, ivanovii, and seeligeri are potentially pathogenic. In all cases, at least two sets of primers were used for each gene. In addition, negative results (i.e., the absence of bsh or of pva and btlB islets) were verified by amplifying products of expected sizes by using primers based upstream and downstream of bsh and of pva and btlB islets. bsh products were amplified in all L. monocytogenes, L. ivanovii, and L. seeligeri strains tested but not in strains of L. innocua, L. grayi, or L. welshimeri (Table 3). Primers based on pva generated products of the predicted size for 22 of the 45 L. monocytogenes strains tested (Table 3). Of the remaining strains, pva products were only obtained for four L. welshimeri strains. Finally, btlB primers generated products in all L. monocytogenes strains, two L. seeligeri strains, and one L. ivanovii strain (Table 3).

Bile tolerance of bsh, pva, and btlB mutants.The splicing by overlap extension (SOEing) procedure was used to create appropriate plasmid constructs to generate isogenic in-frame deletion mutants of bsh, pva, and btlB in L. monocytogenes LO28. Double and triple mutants were created by sequential deletions. The bile tolerance of the resulting mutants was assessed by determining their survival in 30% oxgall (bovine bile). As expected from previous results (6), on initial exposure to the bile there was almost a half-log-unit reduction in numbers of the parent (Fig. 2A). However, Δbsh, Δpva, and ΔbtlB mutants are all significantly more sensitive (P < 0.05 as determined by the Student t test), demonstrating ∼2.5-log-unit reductions in numbers (Fig. 2A), indicating that all three genes play an important role in tolerating the acute toxicity of these high concentrations of bile. Interestingly, a subpopulation of each mutant survived the exposure to bile; however, when these survivors were recultured and reexposed to bile, they were not more resistant than the original deletion mutant cultures (data not shown). The integration vector pPL2 (34) was used to complement mutant strains by inserting the relevant wild-type gene as a single copy at the PSA bacteriophage attachment site. The bile tolerance of all complemented strains was comparable to the wild type, confirming that the bile-sensitive phenotype of Δbsh, Δpva, and ΔbtlB deletion mutants resulted from direct mutation of the loci in question (data not shown). Interestingly, multiple deletion of bsh, pva, or btlB did not result in an additive effect since double (Δbsh Δpva) and triple (Δbsh Δpva ΔbtlB) mutants were only as bile sensitive as single mutants (Fig. 2A). The type of bile used (oxgall) is a crude extract obtained from bovine gallbladders. Though it is composed of a mix of individual bile acids, oxgall's exact composition is unknown (Sigma technical support). In vivo bile acids are typically conjugated to either glycine (glycoconjugated) or taurine (tauroconjugated) before secretion into the duodenum (28). Survival of parent and mutants was therefore compared in BHI broth supplemented with a 5 mM concentration of a typical glycoconjugated bile acid (GDCA) and 5 mM concentration of a typical tauroconjugated bile acid (TDCA). The 5 mM concentration was chosen because this is considered the average concentration prevailing in the intestinal tract (14), and since a wide range of pHs may be encountered in vivo in the lumen the broth was adjusted to various pHs with lactic acid. Figure 2B and C show viable plate counts after 16 h of anaerobic incubation. As we have previously observed, TDCA did not prevent growth of the parent strain at any pH tested (6). Growth of the mutants was also not affected compared to the parent (Fig. 2B). Again, in agreement with our previous observations (6), GDCA inhibited the growth of wild-type cells (Fig. 2C). The toxicity of this bile acid increased at low pH, and at pH 5.5 a 2-log-unit reduction in numbers was observed. All mutants were significantly more sensitive at this pH (P < 0.05, as determined by the Student t test), each demonstrating ∼3.5-log-unit reductions in numbers. This observation reinforces the suggestion that all three genes play a role in tolerating the acute toxicity of bile. Again, double and triple mutants were only as sensitive as single mutants (data not shown). It was observed that mutant numbers were significantly higher than the parent in GDCA-supplemented broth at pH values above pH 5.5 (Fig. 2C). Similar results were observed when strains were patched onto a solid medium (BHI adjusted to the appropriate pH with lactic acid and supplemented with GDCA).

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FIG. 2.

Role of L. monocytogenes LO28 bsh, pva, and btlB genes in bile tolerance. Overnight cultures were inoculated into BHI supplemented with 30% oxgall (A) or BHI adjusted to various pHs and supplemented with either 5 mM TDCA (B) or 5 mM GDCA (C). Viable plate counts were performed at intervals (A) or after 16 h (B and C) by serial dilution in Ringer solution and enumeration on BHI agar. The horizontal lines in panels B and C represent the initial inoculum. The error bars represent the standard deviations of triplicate experiments.

General physiological analyses of mutants.All mutants (Δbsh, Δpva, ΔbtlB, Δbsh Δpva, and Δbsh Δpva ΔbtlB) displayed growth rates (doubling times) similar to that of the wild-type when grown in BHI (pH 7) at 37°C, indicating that the disrupted genes were not necessary for growth under normal physiological conditions (data not shown). In addition, no obvious differences in cell or colony morphologies were observed between wild-type and mutant strains. The growth rate of the individual mutants was also comparable to that of the wild type under acidic conditions (BHI adjusted to pH 5.5 with 3 M lactic acid) and salt stress (BHI supplemented with 7% NaCl) (data not shown), confirming that the decreased survival observed in bile-supplemented broth was actually due to the presence of bile and did not result from associated pH or osmolarity effects.

Disk diffusion assays were used to examine antibiotic resistances. Mutants exhibited resistance identical to that of the parent strain against all antibiotics tested (results not shown). Since pva was annotated as a putative PVA, the growth of Δpva was compared to the wild-type in BHI broth supplemented with various concentrations (ranging from 25 to 125 ng/ml) of penicillin G or V. It was observed that the mutant was significantly more sensitive to all concentrations of penicillin V examined but behaved identically to the parent with all levels of penicillin G tested. Figure 3 shows representative growth curves obtained. The ΔbtlB and Δbsh mutants were not affected in penicillin V or penicillin G resistance (data not shown).

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FIG. 3.

Growth of L. monocytogenes LO28 wild-type (squares) and pva mutant (triangles) in BHI broth supplemented with 50 ng of penicillin G (open symbols) or 50 ng of penicillin V (closed symbols)/ml. Cell growth was measured spectrophotometrically by the determining optical density at 595 nm (OD₅₉₅). The error bars represent the standard deviations of triplicate experiments.

Since bile acids function as biological detergents in vivo, the general detergent resistance of mutants was compared to the parent as outlined by De Smet et al. (15). Briefly, viable cell counts were determined after a 5-min exposure of strains to equivalent concentrations (critical micellar concentration plus 10% [wt/vol]) of four biological detergents: sodium dodecyl sulfate (anionic), Triton X-100 (nonionic), CHAPS {3-[(3-cholamidopropyl)-dimethylammonio]-1-propanesulfonate} (zwitterionic), and cetylpyridinium bromide (cationic). Mutants did not show any enhanced sensitivity (data not shown), implying that the three genes do not form part of a general response to detergent stress.

The growth of mutants were also compared to the parent under combined stress conditions (BHI broth adjusted to various pHs with lactic acid and supplemented with either various levels of salt or sodium dodecyl sulfate). Mutants behaved similarly to parent cells under all conditions examined (data not shown).

BSH activity of wild-type and bsh, pva, and btlB mutants.The agar plate assay developed by Dashkevicz and Feighner (12) was used to investigate BSH activity of the wild-type and mutants. In this assay, bacteria that possess BSH enzymes hydrolyze conjugated bile acids in the agar to the unconjugated form that precipitates at low pH, giving rise to a halo surrounding the colony. Patch inoculation of wild-type L. monocytogenes LO28 or EGDe (the strain used in the European Listeria genome sequencing project) onto BHI supplemented with a glycoconjugated bile acid GDCA resulted in the formation of identical translucent halos with small irregular precipitates, suggesting that both strains have similar BSH activity. Since it proved difficult to photographically document this phenomenon (Fig. 4), other media were investigated. Patch inoculation of the strains onto MRS supplemented with the same concentration of GDCA resulted in much more pronounced white precipitates; however, it was observed that the LO28 halo was smaller than that of EGDe. The reason for this difference on MRS is unclear, but it does not appear to be a consequence of the bile tolerance of each strain since LO28 is significantly more tolerant of bile than EGDe. In addition, halo sizes observed for eight L. monocytogenes strains randomly chosen from our laboratory culture collection did not correlate with their relative bile tolerance profiles (data not shown). Nevertheless, to confirm and accentuate results obtained for strain LO28, all genes in the present study were also mutated in strain EGDe, and these mutants were used solely for BSH plate assays. It was observed that only bsh mutants were incapable of GDCA hydrolysis (Fig. 4). However, since it was possible that pva could encode another BSH enzyme that specifically hydrolyzes tauroconjugated bile salts (similar to the BSH of Bacteroides vulgatus [31]), the agar plate assay was repeated with a tauroconjugated bile acid TDCA. It was again observed that only bsh mutants were incapable of hydrolysis (not shown), indicating that bsh encodes an enzyme that can deconjugate both glycoconjugated and tauroconjugated bile salts. Although PVA has been annotated as a BSH, loss of the pva gene does not affect hydrolysis of either the glyco- or tauroconjugated bile salts tested, demonstrating unambiguously that L. monocytogenes BSH activity results solely from the bsh gene. Deletion of btlB did not affect bile salt hydrolysis.

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FIG. 4.

BSH activity of L. monocytogenes LO28 and EGDe bsh, pva, and btlB mutants. Strains were patch inoculated onto BHI or MRS agar supplemented with 0.5% (wt/vol) GDCA and incubated anaerobically for 48 h. Strains with BSH activity are surrounded with white precipitate halos of unconjugated bile acids.

Expression and regulation of bsh, pva, and btlB genes.Expression of bsh, pva, and btlB was examined by using RT-PCR. cDNA was synthesized from RNA isolated from exponential- and stationary-phase cells grown anaerobically in BHI broth at 37°C. Control PCRs performed with rrn primers (16S RNA primers) confirmed that DNA concentrations were comparable in all samples (Fig. 5A). PCRs were then carried out with primers specific for bsh, pva, and btlB genes. All reactions were performed in triplicate and repeated at least once. It was observed that all three genes were expressed in wild-type cells during both exponential and stationary phases. Figure 5A shows the products obtained after 30 (bsh and btlB) or 35 cycles (pva). The intense band obtained for bsh suggests very high levels of transcription under the conditions examined. In contrast, a product was not amplified for pva until 35 cycles of PCR, indicating relatively low levels of transcription.

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FIG. 5.

(A) Analysis of expression and regulation of bsh, pva, and btlB genes by using RT-PCR. cDNA was synthesized from RNA isolated from L. monocytogenes LO28 wild-type and prfA and sigB mutant cells grown anaerobically to exponential and stationary phases in BHI broth at 37°C. (B) Expression of sigB in cells grown to exponential phase either aerobically or anaerobically in BHI broth at 37°C. (C) Expression of sigB during murine infection. cDNA was synthesized from RNA that was extracted from intestines 2 h after oral infection with 10¹⁰L. monocytogenes LO28 cells. In all cases, control PCRs were performed with 16S RNA primers to confirm identical template DNA levels. The number of PCR cycles are shown in parentheses.

Sequence analysis revealed that the bsh gene is preceded by a consensus binding site for PrfA, the global regulator of virulence gene expression in Listeria spp. Indeed, Dussurget et al. (18) demonstrated a role for PrfA in transcription of the L. monocytogenes EGDe bsh gene during exponential growth. A consensus PrfA box was also identified upstream of the btlB gene, prompting us to determine the effect of inactivating prfA on expression of all three genes. We determined that bsh transcription was reduced in an LO28 prfA mutant during exponential phase (∼1.8-fold) (Fig. 5A); however, this reduction did not appear to be as dramatic as that reported by Dussurget et al. (18) for strain EGDe. The differences between studies may be a result of variances in experimental conditions (in our study cultures were grown anaerobically, whereas Dussurget et al. grew cultures microaerophilically) or differences between strains LO28 and EGDe. Levels of bsh transcript were also lower in the prfA mutant in stationary phase (∼2-fold), suggesting that PrfA regulates transcription of this gene during both stages of growth. Transcription of btlB was reduced in a prfA mutant in exponential phase (∼1.5-fold), whereas stationary-phase expression of btlB was moderately increased in the prfA mutant (Fig. 5A). Transcription of pva was not affected by mutating prfA.

Given the role of σ^B in regulation of bsh (51), we examined expression of the three genes in a sigB mutant. Although pva is not preceded by a σ^B consensus sequence, transcription of the gene was reduced significantly (∼4-fold) in stationary-phase cultures of the sigB mutant. It is possible that the σ^B binding site for pva differs from that of known listerial σ^B-regulated genes or, alternatively, that pva transcription is not controlled directly by σ^B but rather indirectly by a member of its regulon. In the present study, btlB transcription was not reduced by inactivating sigB but was marginally increased (∼1.2-fold) in stationary phase relative to the wild type (Fig. 5A). Transcription of bsh was markedly reduced during exponential phase (∼7.5-fold) and eliminated during stationary phase. Although roles for both PrfA (18) and σ^B (51) in the regulation of bsh have been demonstrated previously, our data suggest a greater role for σ^B in the regulation of this locus under anaerobic conditions that mimic the intestinal environment. This evidence is supported by bile hydrolysis (Fig. 6A) and bile resistance (Fig. 6B) assays outlined below.

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FIG. 6.

(A) BSH activity of prfA and sigB mutants. Strains were patched onto MRS agar supplemented with 0.5% (wt/vol) GDCA and then incubated anaerobically for 48 h. White precipitate halos indicate BSH activity. (B) Bile tolerance of the wild type and of prfA and sigB mutants. Overnight cultures were inoculated into BHI (pH 6) supplemented with 5 mM GDCA and incubated anaerobically at 37°C. Viable plate counts were performed after 4 h. The error bars represent the standard deviations of triplicate experiments.

Expression of sigB under anaerobic conditions and during murine infection.The role of σ^B in the regulation of bsh in exponential phase was unexpected, since sigB is generally not expressed to high levels during exponential phase (3). Further RT-PCR analyses revealed that sigB transcript levels were increased in exponential phase by the anaerobic conditions used in our experiments (Fig. 5B). To our knowledge, this is the first report of sigB induction by anaerobiosis. Although it has been shown that σ^B regulates loci that contribute to the survival of L. monocytogenes in the intestine (30, 51), expression of sigB during infection has not been investigated to date. To address this, we examined sigB expression in ex vivo L. monocytogenes cells isolated directly from the intestine of orally infected mice. The data clearly indicate that sigB is upregulated within the intestine during the early stages of colonization (Fig. 5C). PCR products were not amplified with any of the primer pairs (16S or sigB) when the entire experiment was repeated on RNA extracted from the intestines of noninfected mice, confirming the validity of our observations.

BSH activity and bile tolerance of prfA and sigB mutants.Since PrfA and σ^B were shown to regulate transcription of bsh, the affect of inactivating either of these genes on BSH activity was investigated by using the agar plate assay. Although halo size of both LO28 and EGDe prfA mutants were measurably smaller than those of the corresponding wild-type on agar supplemented with either GDCA (Fig. 6A) or TDCA (not shown), halos were not observed for the sigB mutants (Fig. 6A). This is consistent with transcriptional studies and confirms that σ^B plays a greater role in bsh regulation than does PrfA under the conditions tested. The bile tolerances of the prfA and sigB mutants were assessed by determining their survival in broth adjusted to pH 6 and supplemented with 5 mM GDCA. Figure 6B shows that the prfA mutant was significantly more sensitive to bile than the parent (56% versus 71% survival). However, mutating sigB was more detrimental to cells and survival of the sigB mutant was over 2-log-units lower than the parent (0.65% versus 71%). The growth of mutants was not affected in broth at pH 6 without bile (data not shown), confirming that the observed affects were due to exposure to bile and not pH effects.

Investigation of the role of bsh, pva, and btlB in gastrointestinal persistence.The persistence of wild-type and mutants in the murine intestinal tract was assessed by measuring excreted bacteria in fecal samples for 3 days after oral inoculation. In order to detect Listeria from the background flora, all strains were marked with rifampin. These rifampin-resistant (Rif^r) strains behaved in a manner identical to that of the non-drug-marked strains under all conditions examined (growth in BHI broth alone, growth in BHI supplemented with various levels of salt or adjusted to various pHs with lactic acid, and survival in BHI supplemented with 30% oxgall; data not shown). The virulence potential of the Rif^r parent strain was comparable to that of the non-drug-marked parent (data not shown). Figure 7 shows that numbers of the wild-type were reduced by 1-log-unit over the 72 h of the experiment. Although numbers of Δpva were slightly lower, differences were not statistically significant (Student t test). In contrast, ΔbtlB and Δbsh cells were not detected after 48 and 72 h, respectively. This represents 4-log-unit reductions in numbers of each strain demonstrating that BSH and BtlB play a significant role in the persistence of L. monocytogenes LO28 in the murine gastrointestinal tract. Significantly, bacterial numbers in the spleens of inoculated mice after 72 h mirrored these observations in that Δbsh and ΔbtlB were not recovered from spleens, whereas the wild-type and Δpva were isolated at levels of 2.7 × 10³ and 3.5 × 10³ CFU/organ, respectively.

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FIG. 7.

Role of bsh, pva, and btlB in persistence in the murine gastrointestinal tract. Excretion of rifampin-marked strains was measured in fecal samples collected 24, 48, and 72 h after oral infection of BALB/c mice. The error bars represent the standard deviations of triplicate experiments.