Journal of Bacteriology, February 2004, p . 794-802, Vol . 186, No . 3

Regulation of Transcription of Compatible Solute Transporters by the General Stress Sigma Factor, ^B, in Listeria monocytogenes

Mehmet Sevket Cetin, Chaomei Zhang, Robert W . Hutkins, and Andrew K . Benson^*

Department of Food Science and Technology, University of Nebraska, Lincoln, Nebraska 68583-0919

Received 31 July 2003/ Accepted 24 October 2003

 
Listeria monocytogenes is well known for its durable physiological characteristics, which allow the organism to grow at low temperature and pH and high osmolarity . Growth under high osmolarity depends on the accumulation of compatible solutes, among which glycine betaine and carnitine are the preferred solutes for this organism . Three different transport systems, Gbu, BetL, and OpuC, have been identified in L . monocytogenes which serve to scavenge the preferred compatible solutes . The general stress response regulator ^B has been shown to play an important role in osmotic adaptation in L . monocytogenes, presumably by directing transcription from one or more of the solute transport genes . In the studies presented here, we have used primer extension analyses to identify the promoter elements responsible for transcription of the opuC, gbuA, and betL genes . All three genes are osmotically inducible to some degree . betL is transcribed from a ^B-independent promoter, while gbuA is transcribed from dual promoters, one of which is ^B dependent . opuC is transcribed exclusively from a ^B-dependent promoter . The betL promoter is similar in sequence to the ^B-independent gbuAP1 promoter . Kinetic analysis of transcript accumulation after osmotic upshift demonstrated that ^B-dependent transcripts from gbuAP2 and sigB accumulate for an extended period after upshift, suggesting that ^B activity may provide a mechanism for sustained high-level expression during osmotic challenge . In contrast to osmotic upshift, expression from the ^B-dependent opuC and gbuAP2 promoters after temperature upshift and ethanol stress was minimal, suggesting that additional mechanisms may also participate in regulating transcription from these ^B-dependent promoters .

 
Listeria monocytogenes is a gram-positive food-borne pathogen that is ubiquitous in the environment and problematic to the food production industry due to its ability to grow at refrigeration temperatures, at low pH, and elevated osmolarity (10, 20, 22, 35) . Studies on growth and survival of L . monocytogenes under elevated osmolarity have shown a crucial role for transport of organic compounds such as glycine betaine (N,N,N-trimethylglycine) (7, 18) and carnitine (ß-hydroxy--N-trimethylaminobutyrate) (7, 32) . These compounds, known as compatible solutes or osmolytes, can accumulate to high intracellular concentrations and relieve turgor pressure without significantly affecting the activity or function of cellular components (36) . Although several structural analogs of glycine betaine, including dimethylhetin, ß-butyrobetaine, acetylcarnitine proline, proline betaine, glutamate, choline, small peptides, and trehalose can be used as osmoprotectants by different bacterial species (17), betaine and carnitine are the preferred compatible solutes in L . monocytogenes (7, 18, 32) . After osmotic upshift, these osmolytes, which are found primarily in plant and animal environments, accumulate to high intracellular concentrations via active transport in L . monocytogenes rather than by de novo synthesis (18, 19, 31, 32) .

Transport of betaine and carnitine in L . monocytogenes has been studied at both the biochemical and genetic levels . Physiological studies have demonstrated the existence of an ATP-dependent carnitine transport system (32) and an ATP-dependent, salt-inducible betaine transporter in strain Scott A (19) . In addition, a sodium ion-driven betaine transport system was reported in membrane vesicles (14) . These biochemical observations have been confirmed recently by cloning of the three distinct transporters, BetL, Gbu, and OpuC (3, 11, 19, 26), and demonstration that these three genes likely encode the entire complement of betaine and carnitine transporters in L . monocytogenes (2, 34) . The BetL protein of strain LO28 is a betaine transporter, belonging to a Na⁺-dependent symport family of secondary transporters (26) . Deletion of betL in L . monocytogenes results in slow growth in media with elevated osmolarity but no significant effect on virulence (27) . Gbu, encoded by the gbuABC operon, is an ATP-dependent transporter belonging to the ATP binding cassette (ABC) superfamily of transporters, and it is homologous to OpuA in Bacillus subtilis and ProU in Escherichia coli (19) . Analysis of the gbu operon revealed the presence of three protein subunits . GbuA is an ATPase, GbuB is a transmembrane protein, and GbuC is a substrate-binding protein . Disruption of gbuA results in reduced growth and a low rate of accumulation of betaine when cells are grown in minimal media with 8% NaCl or at low temperatures (19) . Finally, two laboratories independently identified a gene encoding a third osmolyte transporter, opuC, which is an ABC transporter specific for carnitine (3, 11) . The opuCABCD operon is homologous to opuC and opuB of B . subtilis and is composed of genes encoding two permeases, one extracellular solute-binding protein, and one ATPase . OpuC is activated at low temperatures, and accumulation of carnitine is severely reduced in opuC null mutants (3, 12, 28) . Studies with opuC mutants and strains carrying multiple mutations in betL, gbuA, and opuC have recently shown that OpuC is the primary carnitine transporter in L . monocytogenes (2) .

In addition to the direct function of compatible solute transporters in the osmotic response of L . monocytogenes, the general stress response regulator, ^B, also participates in the response to osmotic upshift . Osmotic upshift is one of the most potent stimulators of ^B activity, and absence of ^B impairs the ability of cells to accumulate both betaine and carnitine as osmoprotectants and cryoprotectants (5, 6, 13) . DNA sequences upstream of the betL and opuC genes show some similarity to putative ^B-dependent promoters (11, 26, 29), and recent studies using promoter fusions and reverse transcription-PCR (RT-PCR) have confirmed the dependence of opuC and gbuA expression on ^B, providing a simple explanation for the participation of ^B (13) . To more precisely examine the role of ^B in the expression of these osmolyte transporters, we have used primer extension and RT-PCR analyses to map transcription start sites from the three transporter genes and to examine the kinetics of transcript accumulation during osmotic upshift . We show in strain 10403S that gbuA and opuC are transcribed from osmotically inducible, ^B-dependent promoters . The gbuA operon is also transcribed from a ^B-independent promoter that is highly similar in sequence to the ^B-independent promoter upstream of the betL gene . Kinetic analysis of transcript accumulation after osmotic upshift suggests that ^B activity is maintained for long periods of time after osmotic upshift and may therefore be the mechanism used for expression of gbuA during prolonged periods of osmotic stress .

 
Cloning of betL, opuC, and gbuA from L . monocytogenes. Prior to identification of betL (26) and publication of the L . monocytogenes strain EGDe genome sequence (15), we cloned the betL gene from strain 10403S using the B . subtilis opuD gene as a probe . A 1,084-base fragment of the opuD gene of B . subtilis was amplified by Taq DNA polymerase using primers BSOPUDF (5'-AAACAGAAACCCCCCAAG-3') and BSOPUDR (5'-GCAATCATCAGCAGGATAAC-3') . The product was blunt ended and cloned to the EcoRV site of the pBluescript KS(+) cloning vector . Preliminary Southern blot hybridization experiments with the cloned B . subtilis gene as a probe indicated that a single 4.5-kb HindIII fragment of the L . monocytogenes 10403S chromosome hybridized under conditions of moderate stringency . A plasmid library of 4- to 5-kb HindIII fragments was then constructed from gel-purified digested chromosomal DNA using the pUC19 vector . Approximately 400 colonies were screened using the B . subtilis opuD PCR product as a probe . One clone harboring a 5-kb HindIII fragment was obtained and designated p4B3 and used for further studies .

The opuC and gbuA promoter regions were amplified by PCR using OpuCF (5'-ATCGATGTCACACGTGCCACAAGTAC-3'), OpuCR (5'-TCTCGATAATGTCCATAACAGAAG-3'), Gbu5 (5'-TTTGTCCACATCCCTTTGA-3'), and Gbu3 (5'-ATATTGATCGCCGTAACCAG-3') . Primer design was based on the sequences from strain EGDe (15) . The primers corresponded to positions -367 to -348 upstream and +427 to +447 downstream of the initiation codon of gbuA and -181 to -154 and +948 to + 926 of opuC, respectively . The opuC and gbuA amplicons were subsequently cloned into the pTOPO cloning vector using the topoisomerase-mediated ligation reaction (Invitrogen, Carlsbad, Calif.), and the plasmids were designated as pOPUC and pGBUA, respectively .

DNA sequence analysis. Plasmid p4B3 was digested by ClaI, and the resulting two fragments were ligated separately to the ClaI site of pBluescript KS(+), designated as pCla2 and pCla3, and sequenced using universal primers . The remaining vector was self ligated, designated as pCla1, and sequenced using M13 forward and reverse primers . The PCR products from gbuA and opuC were also confirmed by DNA sequencing using the T3 and T7 primers . All DNA sequence analyses were performed using end-labeled sequencing in conjunction with a LiCor 4200 automated sequencer (LiCor, Inc., Lincoln, Nebr.), and the contigs were assembled using Sequencher (Gene Codes, Inc., Ann Arbor, Mich.) .

Growth conditions and preparation of RNA. Cells of L . monocytogenes 10403S were inoculated into 200 ml of brain heart infusion (BHI) medium with 1% of an overnight BHI-grown culture and incubated at 37°C with shaking at 200 rpm . At mid-logarithmic phase (optical density at 600 nm [OD₆₀₀] of 0.5), the cells were harvested at room temperature and washed twice in 50 mM potassium phosphate buffer, pH 6.8 . Cells were resuspended in the same buffer with 5 mM glucose for 20 min . Separate aliquots of the cells were then treated for 20 min by the addition of NaCl (3% final concentration) . After 20 min, the cells were harvested by centrifugation at 6,000 x g for 5 min, and the cell pellets were frozen at -70°C overnight . The cells were subsequently resuspended in 1 ml of Tri reagent (Molecular Research Center, Inc., Cincinnati, Ohio) solution and disrupted by homogenization with beads four times at 1-min intervals on ice . Total RNA was extracted according to the manufacturer's directions .

Primer extension analysis of betL, opuC, and gbuA transcripts. Primers (100 pmol each) complementary to the 5' ends of the betL (PEX3, 5'-ATTCTCTGTATCTATTTCCCCATG-3'), opuCA (CEX3, 5'-AATTCTCCTTTATCGATGTTAAGTG-3'), and gbuA (AEX3, 5'-CACCAATTGTCGCGCCTGTTTTCTTTC-3') coding regions were end labeled with 50 µCi of [-³²P]ATP . For each extension reaction, 10 pmol of labeled primer was then mixed with 50 µg of RNA, heated to 80°C for 5 min, chilled on ice for 5 min, and incubated at 42°C with 3 U of SuperScript II RNase H-reverse transcriptase (Invitrogen) . After 1 h of extension, the products were precipitated with ethanol, washed in 70% ethanol, and dissolved in loading buffer, as described previously (5) . Sequencing ladders were generated by double-strand sequencing reactions using Sequenase 2.0 (U.S . Biochemicals, Cincinnati, Ohio) . Ladders were primed with unlabeled PEX3, CEX3, and AEX3 primers using the pCla1, pOPUC, and pGBUA plasmids, respectively, as templates . Each of the primer extension reactions was performed on RNA samples extracted from at least two independent cultures or treatments . For band quantification, bands were excised using an autoradiogram as a guide . Portions of the lanes with no apparent band were also excised and used to estimate background (three slices averaged for each background measurement) . The quantification was performed at least twice on independent RNA samples . The graphs shown are derived from a single experiment and are representative of the results from independent experiments .

RT-PCR analyses. For each sample, 10 µg of total RNA was treated twice to remove the trace contaminating DNA using the DNA-free kit (Ambion, The RNA Company, Austin, Tex.) according to the manufacturer's instructions . cDNA was synthesized from 5 µg of total RNA using SuperScript II RNase H-reverse transcriptase (Gibco, BRL, Cleveland, Ohio) and 250 ng of random hexamer primers according to the manufacturer's instructions . One microliter of the cDNA reaction mixture was used as a template for amplification in PCR . The specific primers used for PCR amplification were the following: SigB1, 5'-GCGCCGAATCAAAGAGTTAGG-3'; SigB2, 5'-CCACTTCCTCATTCTGCAACG-3'; BetL1, 5'-AAGTCCGATTGGCTCGATTC-3', BetL2, 5'-ATCAAGTCCGGACATAGCCG-3'; OpuCA1, 5'-AATGGAGGTGTGTAGGCGTG-3' OpuCA2, 5'-GTAATTGGATCTAGCGCGCC-3'; GbuAP1-1, 5'-TGGGCCGAATTTTTGACCTAG-3' GbuAP1-2, 5'-CGCTCTTCTTTGTCCATTCC-3'; GbuAP2-1, 5'-CTAATTGAGCCTACGAGCGG-3'; and GbuAP2-2, 5'-TGAACGACAGAACCATCACG-3' .

The PCRs were performed in a total volume of 20 µl containing 20 pmol of each primer, 100 µM deoxynucleoside triphosphate, 1.5 mM MgCl₂, 10 mM Tris-HCl (pH 8.3), 50 mM KCl, and 1 U of Taq DNA polymerase (Sigma, St . Louis, Mo.) . The PCR cycling protocol was 95°C for 2 min; 21 cycles of 95°C for 30 s, 55°C for 1 min, and 72°C for 45 s; and 72°C for 5 min for final extension . PCR products were electrophoresed on 0.7% agarose gels, poststained with ethidium bromide (0.5 µg/ml), and visualized under UV . Control reactions to confirm absence of DNA were performed using each of the RNA samples with no cDNA synthesis step and yielded no distinguishable amplification products (data not shown) . Each experiment was repeated at least twice using independent RNA samples .

 
BetL expression is constitutive and independent of ^B. In a previous study, our investigators showed that the absence of ^B in L . monocytogenes impaired the ability of these cells to use betaine as an osmoprotectant and specifically that the sigB mutation blocked osmotically inducible betaine accumulation (5) . Slot blot and RT-PCR analysis of betL expression in strains LO28 and 10403S, respectively, showed that expression was slightly osmotically inducible and independent of ^B (13, 26) . To identify the promoter element, we used primer extension with a primer (PEX3) that is complementary to positions -39 to -17 relative to the start codon . As shown in Fig . 1, extension of this primer on mRNA extracted from logarithmically growing 10403S and LMA2B (sigB::Kan) cells yielded a 134-base product before and after the strains were subjected to an osmotic upshift . Although a prominent product was present prior to osmotic upshift, addition of 3% salt in both strains increased the abundance of the primer extension product, indicating that accumulation of the transcript is osmotically inducible . Since the primer extension product was present in the sigB::Kan mutant, we conclude that it is not dependent on ^B . Using the PEX3 and four additional primers, we were never able to observe a primer extension product in the 10403S strain mapping to the putative ^B-dependent promoter proposed by Sleator et al . (26) . Inspection of the sequences at -10 and -35 relative to the transcription start site (Fig . 1) revealed sequence elements that do not display substantial similarity to known promoters in other gram-positive bacteria .

 
gbuA is transcribed from dual promoters. Since betL transcription is not dependent on ^B, we postulated that the sigB phenotype of impaired betaine transport must be due to its effect on gbuA . We therefore investigated transcription of the gbuA operon in wild-type and sigB mutant cells using primer AEX3, which is complementary to positions +100 to +126 relative to the start codon . As shown in Fig. 2, three different primer extension products were detected . The largest product was induced after osmotic upshift (compare lanes 1 and 2 in Fig . 2A) and was present in the sigB mutant background, indicating that it is osmotically inducible but does not depend on ^B . Inspection of the sequences upstream of this start site showed that this promoter region, termed gbuAP1, is unique in sequence and does not conform to a consensus ^A-like promoter from the closely related species B . subtilis (Fig. 2A) .

 
In contrast to gbuAP1, the remaining extension products (Fig . 2B) were osmotically inducible but absent in the sigB null mutant background (compare lanes 3 and 4) . Mapping of the ^B-dependent primer extension products to the gbuA sequence showed that the longer product maps to a position -20 relative to the initiation codon, while the shorter product maps to +5 relative to the start codon . Alignment of sequences 5' to these extension products showed that sequences at -10 and -35 relative to the -20 extension product aligned with ^B-dependent promoters, while the sequences relative to the +5 extension product did not . Therefore, we conclude that the +5 extension product is likely derived from premature termination of the reverse transcriptase or due to a breakdown product derived from the longer transcript . Identification of the ^B-dependent promoter, which we have termed gbuAP2, therefore provides an explanation for the phenotype of impaired osmotically inducible accumulation of betaine in sigB mutant strains .

Mapping of the ^B-dependent opuC promoter. Genetic and expression analyses of the opuC transport system, which is the primary carnitine transport system in L . monocytogenes, have previously shown that carnitine transport depends on ^B and that opuC expression is also ^B dependent (6, 13) . Sequences upstream of the coding region also display similarity to known ^B promoters (13), supporting the idea that ^B may be solely responsible for expression of the primary carnitine transporter in L . monocytogenes . Indeed, RT-PCR analyses in sigB mutant strains showed that the product from the opuC gene is nearly undetectable (13) . To confirm the location of the start site, and to assess whether other promoters may drive opuC transcription, we mapped transcripts originating upstream of the opuCA gene using primer extension . A primer (CEX3) that is complementary to positions +63 to +88 relative to the start codon was end labeled and used for primer extension analysis . As shown in Fig . 3, a primer extension product was observed mapping to position -100 relative to the opuCA-coding region . This was the only product that was observed in our experiments, and it was not observed in the sigB mutant background . Alignments of the sequences upstream of this transcription start site revealed -10 and -35 elements that resembled known ^B-dependent promoters but did not correspond to the start site predicted from the sequence analysis by Fraser et al . (11) . Based on the results of our primer extension analyses, we conclude that the opuCABCD operon is transcribed exclusively from a ^B-dependent promoter in the 10403S strain, which would explain the primary dependence of carnitine transport on sigB (6, 13) .

 
Response of opuC and gbuA to heat and ethanol shock. Because ^B activity is induced by a number of different stress conditions (5), we hypothesized that induction of ^B activity by nonosmotic stress would also lead to ^B-dependent transcription of the gbuA and opuC osmolyte transporters, unless additional mechanisms were present to prevent induction . To test this hypothesis, we used primer extension and RT-PCR to examine transcripts originating from the ^B-dependent gbuAP2 and opuC promoters after cells had been subjected to osmotic or temperature upshift . Cells for these experiments were grown in BHI at 37°C to mid-log phase, washed, and resuspended in transport buffer with glucose . After equilibration, the cells were subjected to osmotic upshift or temperature upshift to 47°C for 20 min . As shown in Fig . 4, transcripts originating from the ^B-dependent opuC and gbuAP2 accumulated substantially after osmotic upshift but were barely detectable after temperature upshift . Since ^B activity is induced significantly by heat shock (5), it is surprising that its activities at opuC and gbuAP2 were not detectable after the temperature upshift . To confirm the primer extension results, we also used RT-PCR to examine transcripts from gbuA, opuC, and sigB . To differentiate transcription originating at gbuAP1 from gbuAP2, we compared RT-PCR products using two different sets of primers . Primers gbuAP1-1 and gbuAP1-2, which are immediately 3' to gbuAP1, were used to detect transcripts originating at gbuAP1 . Primers gbuAP2-1 and gbuAP2-2, positioned 3' to gbuAP2, were used to detect transcripts originating at both gbuAP1 and gbuAP2 promoters . As shown in Fig . 5, none of the products from gbuAP1 or gbuAP2 increased significantly in abundance when log-phase cells were compared to cells subjected to temperature upshift or addition of ethanol . RT-PCR products from opuC showed a slight increase in abundance after addition of ethanol but not after temperature upshift . In contrast, RT-PCR products from sigB increased substantially after either temperature upshift or addition of ethanol . Therefore, both the primer extension and the RT-PCR data suggest that ^B is necessary for directing transcription from opuC and gbuAP2, but additional mechanisms likely control the ability of the ^B RNA polymerase holoenzyme to form transcription-competent complexes at these promoters . These mechanisms presumably serve to restrict upregulation of transcription to osmotic stress conditions .

 
Kinetics of gbuA and opuC transcription. In B . subtilis, measurement of ^B activity from promoter fusions and accumulation by Western blot analyses suggests that its activity at most promoters peaks between 10 and 20 min after exposure to activating conditions and then falls to a new level that is higher than before the shock (9) . The ^B-dependent promoter of the proline transporter, opuE, in B . subtilis follows this temporal pattern of activity after osmotic upshift, since transcripts accumulate for up to 20 min but are undetectable after 40 min (30) . In contrast, transcripts originating from the osmotically inducible ^A-dependent promoter upstream of opuE continue to accumulate for an extended period after the upshift (30) . Our discovery of the dual gbuAP1 and gbuAP2 promoters provided an opportunity to similarly compare kinetics of osmotic activation of ^B and another holoenzyme form in L . monocytogenes. We therefore measured transcripts originating from these promoters and the ^B-dependent transcript from the sigB operon over time after an osmotic upshift . Surprisingly, the ^B-dependent transcript from both sigB and the gbuAP2 promoters in L . monocytogenes did not accumulate transiently but continued to accumulate even up to 40 min postinduction (Fig . 6) . Measurement of the band intensity by excision and scintillation counting demonstrated that the intensity of the labeled bands indeed increased significantly throughout the measurement period, suggesting that the transcript accumulated due to prolonged ^B activity . In contrast, transcript levels from the osmotically inducible gbuAP1 promoter remained relatively constant after induction . Thus, kinetic analysis of transcript accumulation was consistent with the conclusion that the ^B-dependent gbuAP2 is largely responsible for expression of gbuA during long-term osmotic stress . Similar experiments at the opuC promoter also demonstrated continued accumulation of ^B-dependent transcripts after osmotic upshift, indicating that the response is not peculiar to the gbuAP2 or sigB promoters (data not shown) .

 
To confirm the kinetics of transcript accumulation observed by primer extension, we also performed RT-PCR on RNA samples from cells subjected to osmotic upshift . As shown in Fig . 7, RT-PCR analysis using primers 3' to the ^B-dependent promoter of the sigB operon showed product accumulation for the first 20 min, with saturated signal for the latter time points . Likewise, RT-PCR products amplified using primers 3' to the gbuAP2 promoter (which would include transcripts initiating from gbuAP1 and gbuAP2) showed increasing signal intensity during the 5- to 30-min time period and saturation thereafter . In contrast, RT-PCR products amplified from segments of transcripts immediately 3' to the gbuAP1 promoter were relatively constant during the upshift, with a minor peak occurring 30 min after upshift . These results suggest that the accumulating product derived from the gbuAP2 primers must be due to transcripts originating at gbuAP2 . This supports the findings from the primer extension assays and further supports our hypothesis that ^B activity remains high for extended periods after osmotic upshift .

 
The ability of L . monocytogenes to grow at high osmolarity and to accumulate compatible osmoprotectant molecules favors its growth in contaminated food products and promotes survival during transit through the gastrointestinal tract of animal and human hosts . In this report, we used primer extension analyses and physiological studies to examine how the general stress sigma factor, ^B, controls accumulation of osmolytes through its activity in directing transcription from the genes encoding the primary osmolyte transporters . In strain 10403S, we showed that transcription of betL originates from a single promoter and that expression is modestly osmotically inducible, but not dependent on ^B . Sequences upstream of the transcription start site showed some similarity to those recognized by the housekeeping sigma factor, ^A, in B . subtilis but also deviated significantly from the consensus (Fig . 8B) . It is therefore unclear if this promoter is recognized by the ^A ortholog in L . monocytogenes . Although the betL extension product accumulated after osmotic upshift (Fig . 1), the fact that the transcript was quite detectable prior to osmotic upshift suggests that BetL is the primary transporter synthesized in unshocked cells and is likely to be the primary mechanism for transport of betaine during the early stages of osmotic upshift .

 
Unlike betL, expression of the gbuA operon was almost exclusively osmotically inducible . After osmotic upshift, the gbuA transporter was expressed from both ^B-independent (gbuAP1) and ^B-dependent (gbuAP2) promoters (Fig . 2) . This finding is congruent with the fact that sigB mutants are defective only in osmotically inducible betaine transport .

In contrast to the betaine transport systems, expression of the carnitine transporter gene, opuC, was primarily dependent on ^B in the 10403S strain background . This finding is particularly interesting, since a majority of stress response genes are typically under control of dual promoters to sustain flexible transcription under all conditions, particularly for those genes that are essential (25) . Only a few genes, in fact, are known to rely solely upon ^B for their transcription (1, 21, 24) . The dependence of opuC on ^B provides a mechanism for preferential use of betaine to maintain osmotic balance under normal growth conditions, since ^B activity is minimal under those conditions . However, once the cells encounter osmotic stress, gbuA and opuC expression increases, providing the cells with an enhanced array of transporters and potential osmolytes .

Structure of ^B-dependent gbuAP2 and opuC promoters. Alignment of the gbuAP2 and opuC promoters with known ^B-dependent promoters showed that both are quite deviant from consensus ^B recognition sequences (Fig . 8A) . The opuC -35 region is well aligned, whereas the -10 region deviates from consensus ^B promoter sequences . In contrast, the -35 and -10 regions of gbuA both deviate somewhat from the consensus ^B promoter sequences . This could imply that formation of closed complexes or isomerization to open complexes at these promoters is relatively inefficient . Since osmotic strength and counter ion concentration are known to affect the properties of RNA polymerase (8), it seems possible that changes in osmotic strength of the cytoplasm alter the affinity of ^B holoenzyme for these promoters or the kinetics of open complex formation . While speculative, this could provide one explanation for why temperature upshift, which is a potent inducer of ^B activity in L . monocytogenes, does not lead to significant transcript accumulation from gbuAP2 and opuC .

Perhaps of equal interest is the similarity between the ^B-independent betL and gbuAP1 promoters . Alignment showed that the -10 and -35 regions are nearly identical (Fig . 8B) . It is not yet clear if these promoters are recognized by the housekeeping form of RNA polymerase, since its specificity in L . monocytogenes has not been characterized . However, based on the canonical -10 and -35 sequences of B . subtilis ^A promoters, the gbuAP1 and betL promoters show only limited similarity and thus may be utilized by a secondary form of RNA polymerase . Since the genome sequence from L . monocytogenes strain EGDe identified only five sigma factor paralogs, including the previously identified rpoD and sigB genes, the list of possible candidates is not overly large .

Distinct roles of ^B in L . monocytogenes. Relative to the well-studied ^B regulon in B . subtilis, much less is known about the role of ^B in the biology of L . monocytogenes . Perhaps the most significant differences identified to date are the relative magnitude and roles of ^B in response to different stress in these two species . Our studies in this report now extend these observations to show that ^B plays a role in long-term osmotic stress in L . monocytogenes (Fig . 6 and 7) . Primer extension studies on the promoters of the opuE gene in B . subtilis have shown that the ^B-dependent transcript accumulates only transiently after induction and is almost undetectable 40 min later, while the ^A-dependent transcript remains at high levels 40 min postinduction (30, 33) . In contrast, our studies showed that the ^B-dependent transcript of the gbuAP2 promoter continued to accumulate at 40 min after induction, while the ^B-independent gbuAP1 transcript remained constant . The similarity in transcript accumulation profiles at both sigB and gbuAP2 implies that ^B activity may remain at high levels for long periods after upshift . Thus, the difference in ^B kinetics at the opuE and gbuAP2 promoters in B . subtilis and L . monocytogenes, respectively, could imply that ^B plays a primary role in directing gene expression in response to osmotic shock in L . monocytogenes but only an ancillary role in osmotic responses in B . subtilis . In support of an extended role for ^B in directing stress response gene transcription in L . monocytogenes, we note that its activity profile during temperature downshift also displays continued transcript accumulation for hours after the downshift (6), suggesting that the long-term activity postinduction may be a general feature of ^B induction in this organism . If this is indeed the case, then the role of ^B in L . monocytogenes may be as a primary response to stress, whereas its role in B . subtilis is relegated to an ancillary and transient role to augment the many additional adaptive response pathways available in that organism .

Understanding the role and function of stress adaptation systems from a phylogenetic perspective may also provide significant insight as to the adaptive characteristics of different microorganisms . Indeed, this may provide an understanding of important characteristics of different subpopulations of the same species . Moorhead and Dykes (23) recently suggested that variations in the responses of different L . monocytogenes serotypes to osmotic stress may be due to differences in the magnitude of ^B activation . Collectively, these studies underscore the importance of comparative analyses of the function and activation of ^B in different species of gram-positive bacteria as well as within phylogenetic lineages of a single species, such as L . monocytogenes .

 
This work was supported by HATCH funds (project number NEB-16-077) from the United States Department of Agriculture Cooperative State Research, Education, and Extension Service to A.K.B .

We thank John Wise for assistance in preparation of the figures .

 
* Corresponding author . Mailing address: Department of Food Science and Technology, University of Nebraska, 330 Food Industry Complex, Lincoln, NE 68583-0919 . Phone: (402) 472-5637 . Fax: (402) 472-1693 . E-mail: abenson1@unl.edu .

A contribution of the University of Nebraska Agricultural Research Division, Lincoln (journal series number 14326) .

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What Is Molecular Microbiology?, What Is Molecular Biology?, What Is Genetic Engineering?, What Is Pcr?, What Is Water Purification?, a, Bacteriology, a, Bacterium, a, Microorganisms, o, Bacteria, i, Microbiology, c, Listeriosis, r, Escherichia coli, c, Staphylococcus aureus, n, Gram negative, a, Listeriosis, n, Yeasts, e, Listeriosis, r, Escherichia coli, n, Antimicrobials, c, Microorganism, r, Salmonella, n, Rhodococci, i, Agrobacterium, n, Bactericidal, o, Growth media, a, Listeriosis, c, Escherichia coli, o, Salmonella, a, Rhodococci, s, Streptococcal, o, Escherichia coli




 

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