Transcriptional regulators: SlyA as an example

Proteins of the MarR/SlyA family are known to regulate the expression of virulence genes in many Gram-positive and Gram-negative organisms. Evidence of such a regulator existing in enterococci arose with the examination of the crystal structure of an E. faecalis transcriptional factor (EF3002) in 2003 (Wu, et al., 2003). The 150 amino acid SlyA protein is encoded by an open reading frame that begins with a GTG initiator codon. The crystal structure of SlyA was determined without its DNA target or signal molecule bound, and the unliganded crystal structure revealed that SlyA consists of two monomers in an asymmetric unit (Wu, et al., 2003) (Figure 1). In the SlyA crystal, key arginine residues thought to play a role in DNA binding were found to point away from the major groove, as was determined for the crystal structure of MarR (Alekshun, Levy, Mealy, Seaton, & Head, 2001), but differs from that of the MexR (Lim, Poole, & Strynadka, 2002) transcriptional regulator of Pseudomonas aeruginosa. The high degree of flexibility observed between the crystal structures of the various DNA-binding domains provides indirect evidence of the ability of this fold to adapt in order to recognize various DNA targets. Conserved residues among the various transcriptional regulator structures suggest that this fold could make contact with the phosphate groups or bases. Comparison of the SlyA-Ef structure with the structure of MarR and MexR suggest they are similar, which indicates that the MarR/SlyA family shares a common fold and similar DNA-binding properties, despite their low amino acid sequence similarity (Wu, et al., 2003) (Figure 1).

Figure 1.

Structure of SlyA dimer and comparison of the structure to the transcriptional factors MexR and MarR. A. The SlyA dimer from E. faecalis with the subunits labeled in shades of blue and orange. The structural models were created from the structure under (more...)

The promoter region of SlyA suggests that it is a part of a bicistronic operon that also serves as the promoter for EF3001, which encodes an N¹-acetyltransferase enzyme. This transcriptional organization is conserved in other Gram positive species (Michaux, et al., 2011). It is thought that over-expression of EF3001 would be an advantage to the ΔslyA mutant as it shows homology to PaiA, a protein from Bacillus subtilis, that encodes for an N¹-spermidine acetyltransferase (Forouhar, et al., 2005) involved in polyamine homeostasis (excess of this molecule is toxic to the cell).

Recent functional analyses of the SlyA regulator (ef3002) (Michaux, et al., 2011; Michaux, Martini, Hanin, Auffray, Hartke, & Giard, 2011) have illustrated that SlyA activity is part of a complex regulatory network. Observations have suggested that the involvement of SlyA is linked to virulence and persistence inside the host (Michaux, et al., 2011). SlyA mutant strains were found to be more virulent than the parental wild type strain in a wax moth (Galleria mellonella) model (Michaux, et al., 2011). The immune response of G. mellonella has a number of structural and functional similarities to the innate immune response of mammals (reviewed in (Vogel, Altincicek, Glöckner, & Vilcinskas, 2011)). The ΔslyA mutant was also found to survive better in mouse organs and in macrophages (Michaux, et al., 2011). DNA microarray experiments revealed that 117 genes were deregulated in the ΔslyA mutant as compared to the parental strain, a finding that suggests that SlyA acts as a repressor and activator (Michaux, et al., 2011)—although it should be noted that the expression of most of these genes changed by only two fold. EF3001 was the only gene in this analysis where expression in the ΔslyA mutant was up-regulated by 16.62-fold as compared to the parental wild type strain, suggesting that the enzyme it encodes may provide an important advantage during infection (Michaux, et al., 2011). Another gene encoding a helicase (EF3217) in the ΔslyA mutant was strongly down-regulated, but its role in virulence is unclear. This particular gene is associated with a mobile element and is not conserved across a number of the sequenced enterococcal genomes (Michaux, et al., 2011).

Further work using a pVEPhoZ-PslyA strain revealed that the expression level of the slyA operon was increased in the presence of bile salts (Michaux, Martini, Hanin, Auffray, Hartke, & Giard, 2011). Under the stressed conditions induced by the presence of 0.08% bile salts, the growth of the ΔslyA mutant was impaired, with the doubling time of the strain decreased by a factor of two. Under these growth conditions, the bile salt hydrolase (BSH) encoded by EF3005 in the E. faecalis V583 genome was found to be induced in the ΔslyA mutant by six-fold in comparison to the wild type parental strain, which is somewhat puzzling, given the growth phenotype of the ΔslyA mutant in the presence of bile salts (Michaux, Martini, Hanin, Auffray, Hartke, & Giard, 2011). In the E. faecalis V583 genome, there are two BSHs encoded by EF0521 and EF3005. In wild-type E. faecalis V583, the BSH encoded by EF0521 is induced at a higher level than EF3005, which suggests that the BSH encoded by EF3005 plays a minor role in the bile salt stress response. SlyA may in fact give a selective advantage to bacterial development in the intestine, as E. faecalis is naturally present in the gastrointestinal tract (Jones, Begley, Hill, Gahan, & Marchesi, 2008). However, other experiments using microarrays (Solheim, Aakra, Vebo, Snipen, & Nes, 2007) or a proteomic approach (Bøhle, et al., 2010) have produced contrary results, where the expression of these genes was not seen to be inducible by exposure to bile salt conditions. Differences in the results may be attributable to differences in experimental procedure or the detection limits of the various assays. The down-regulation of a number of genes was also observed, with a number of these being hypotheticals and with a majority related to protein synthesis (i.e. tRNA synthetases). However, expression of one of the tryptophanyl-tRNA- synthetases (EF2679, trpS) was found to be up-regulated at all time points studied, as compared to the initial start time. Further work is required to clarify the role of SlyA under different environmental conditions.

Regulation of E. faecalis Ebp pilus

The E. faecalis endocarditis and biofilm-associated pili (Ebp) is a major virulence factor that plays an important role in cell adhesion, biofilm formation, and the development of endocarditis. Many environmental factors affect the levels of Ebp surface expression, including culture media (TSB vs. BHI), serum, and bicarbonate levels, which suggests that this is a tightly regulated process (Nallapareddy, et al., 2006; Bourgogne, Thomson, & Murray, 2010). Three genes (ebpA, B and C) that encode the E. faecalis pilus structural proteins are located in the same polycistron, with the divergent promoter region shared with the ebpR gene.The ebpR gene encodes a protein that is a member of the AtxA/Mga family of transcriptional regulators. It has been demonstrated that the deletion of the ebpR gene leads to reduced levels of ebpABC mRNA and Ebp production, as evaluated by qRT-PCR and Western blot analysis, respectively (Bourgogne, Singh, Kox, Pflughoeft, Murray, & Garsin, 2007). As a result, the mutant ebpR gene displays phenotypes of reduced biofilm formation and attenuated primary adherence. In a recent study, Bourgogne et al. demonstrated that the addition of bicarbonate to culture media enhanced the expression of the ebpR and ebpABC loci. However, the authors did not observe a strong direct relationship between ebpR expression and ebpA expression, suggesting that the activation effect of bicarbonate to ebpABC may be through other unidentified factors other than ebpR (Bourgogne, Thomson, & Murray, 2010). Another recent study by Gao et al. identified RNase J2 as a positive regulator of Ebp expression (Gao, Pinkston, Nallapareddy, van Hoof, Murray, & Harey, 2010). Similar to ebpR, the deletion of E. faecalis rnjB resulted in a 30-fold decrease in ebpABC mRNA expression and significantly decreased Ebp surface display. RT-PCR and a reporter gene assay demonstrated that the mRNA level of ebpR is not affected by the deletion of RNase J2, excluding the possibility that RNase J2 affects ebpR at the RNA level through transcriptional regulation or RNA processing. It is likely, however, that RNase J2 affects epbR expression at the translational level through an as-yet unidentified regulatory or antisense RNA.

Erythromycin

Erythromycin is a macrolide antibiotic which acts by reversibly binding to the P site of the 50S subunit of the bacterial ribosome. Resistance mechanisms identified in Gram-positives to subvert the inhibitory effects of erythromycin include target modification by methylation, which changes the P site of the rRNA, as well as a macrolide efflux resistance mechanism (Pechère, 2001). E. faecalis V583 carries a plasmid known as pTEF1 that encodes an rRNA adenine dimethylase family protein (EF0007), which may aid in its resistance to this drug.

E. faecalis strain V583 is resistant to relatively high concentrations of erythromycin; however, the treatment does retard its growth. A drastic change in gene transcription was seen with erythromycin-treated V583, as compared to untreated cells, over a 90 minute period (Aakra Å. , et al., 2005). In the presence of 50 μg/ml of erythromycin (V583 is resistant to > 400 μg/ml), Aakra et al. (Aakra Å. , et al., 2005) found that 260 genes were down-regulated at one or more time points, while 340 genes were up-regulated. From this set, genes encoding for hypothetical proteins, as well as genes encoding for transport and binding proteins, were the two most dominant groups of differentially expressed genes. Surprisingly, in this experiment, the EF0007 gene that encodes for an rRNA adenine dimethylase family protein (ErmB), was not up-regulated in the presence of erythromycin, but was constitutively expressed in V583 even in the absence of erythromycin. This would suggest that the expression of genes other than ermB is important for the survival and growth of V583 in the presence of erythromycin.

Although changes in transcriptional levels of many genes with differential expression identified upon erythromycin exposure is assumed to occur mainly due to a change in growth conditions (Aakra Å. , et al., 2005), a number of these changes could be linked to survival in the presence of erythromycin. For example, the induction of ribosomal proteins and two protein Ala-acetyltransferases indicate that the overproduction of ribosomal proteins is one way to evade the effects of erythromycin. Interestingly, a MsrC-like protein (EF1413) was up-regulated at all time points studied. MsrC homologs found in E. faecium are thought to encode an efflux pump that is involved in low-level macrolide resistance (Portillo, Ruiz-Larrea, Zarazaga, Alonso, Martinez, & Torres, 2000; Singh, Malathum, & Murray, 2001). However, when compared to the MrsC homolog from E. faecium, the protein sequence of EF1413 from E. faecalis V583 is found to be only 40% identical (60% similar). Other specific genes found to be up-regulated were genes that encode ABC transporters that belong to the MDR family (EF1732 and EF1733) (Aakra Å. , et al., 2005). Another MDR efflux pump, EmeA (EF1078), is also induced at all time points, excluding time zero in V583 exposed to erythromycin, and is most likely involved in mediating resistance. This finding supports previous observations that the efflux pump could extrude erythromycin (Jonas, Murray, & Weinstock, 2001). A number of two-component signal transduction pathways were also found to be up- or down-regulated in the presence of erythromycin—although further work is required to clarify their roles in E. faecalis. It is assumed that these factors all play some role in mediating erythromycin resistance.

Another interesting observation made by Aakra et al. (Aakra Å. , et al., 2005) is that in the presence of erythromycin, six genes related to fatty acid and phospholipid metabolism were up-regulated. In Gram-negative bacteria, such intrinsic resistance to macrolides is achieved due to the impermeability of the cellular outer membrane to this hydrophobic drug (Roberts M. C., 2008), and it may be that changes in membrane biochemistry in enterococci also impede the entry of this class of drug into the cell.

Chloramphenicol

Chloramphenicol is a broad-spectrum antibiotic that inhibits the peptidyl transferase reaction of the large subunit of the ribosome. This antibiotic currently has limited use in treating bacterial infections in humans, due to widespread acquisition of resistance mechanisms. Bacterial resistance to chloramphenicol may be mediated by several mechanisms, including inactivation by an enzyme (acetyltransferase or phosphotransferase), the excretion of the drug by an efflux pump, and mutations in the 23S rRNA that result in an altered target site in the cell. The well-studied E. faecalis strain V583 is resistant to chloramphenicol, but no specific chloramphenicol resistance genes have been identified in the genome sequence, and resistance cannot be solely attributed to mutations in the 23S rRNA gene. Interestingly, the growth of V583 in the presence of chloramphenicol is decreased, which suggests that chloramphenicol does create stress on the cells. In the presence of chloramphenicol, over 609 genes were up-regulated and down-regulated at one or more of three time points (t=0, 90, and 180 minutes), and these genes were identified through two different methods to undergo transcriptional changes (Aakra A. , et al., 2010).

In response to the addition of chloramphenicol to the growth medium, it would be expected that the bacterial cells would want to adapt to the conditions, potentially through changes in the cell wall, as was observed for treatment with other agents, such as sodium dodecyl sulfate (Solheim, Aakra, Vebo, Snipen, & Nes, 2007) and erythromycin (Aakra Å. , et al., 2005). Two genes (ef1732 and ef1733) that encode potential transporters of chloramphenicol out of the V583 cells were strongly induced in cells treated with the drug at 90 minutes. These genes encode for an ABC transporter that belongs to the MDR family of transporters, and were also seen to be up-regulated in the presence of erythromycin (Aakra Å. , et al., 2005). Genes involved in fatty acid biosynthesis were up-regulated in E. faecalis V583 cells at 180 minutes (Aakra A. , et al., 2010), and a similar response was noted for the growth of E. faecalis in the presence of sodium dodecyl sulfate (Solheim, Aakra, Vebo, Snipen, & Nes, 2007) and erythromycin (Aakra Å. , et al., 2005). The up-regulation of these genes suggests that V583 is adapting to the stress induced by chloramphenicol by altering the membrane, which may change the transport capabilities of the cell as a result. This change in membrane composition may also partly explain the relatively low number of induced genes that specify transport and binding proteins. Interestingly, a number of phage genes were also up-regulated in the cells exposed to chloramphenicol, potentially indicating that the potential for cell lysis induces the phage to leave the cell. There are a number of phage-encoded genes in the V583 genome, including one phage that is found in many different E. faecalis strains (phage 02); however, the transcriptional profile for the phage 02 genes was not found to change in the time course of chloramphenicol exposure.

The genome of V583 carries the vanB operon, which encodes for resistance to vancomycin. In the presence of chloramphenicol, 8 of the 11 genes encoded in the operon were induced, including the genes encoding for the histidine kinase and the cognate response regulator, which are responsible for sensing vancomycin and inducing the expression of the rest of the operon.

The addition of chloramphenicol to the medium led to the up-regulation of the pyrimidine biosynthesis operon (ef1721 to ef1712). Interestingly, the precursor for pyrimidine synthesis, carbamoyl phosphate, is also the precursor of arginine biosynthesis. Arginine biosynthesis in chloramphenicol-treated V583 cells was down-regulated (Aakra A. , et al., 2010). This response is different than what was seen in erythromycin exposed E. faecalis V583 (Aakra Å. , et al., 2005), suggesting that it is specific to the presence of chloramphenicol.

As the target of chloramphenicol is the ribosomal protein, it was hypothesized that transcriptional changes would be seen in a number of ribosomal proteins. Although the increased transcription of the ribosomal proteins were noted by Aakra et al. (Aakra A. , et al., 2010), it is also important to keep in mind that microarray analysis may not actually reflect the level of ribosomal proteins in the cells, as many proteins may also be regulated at the translational level.

Vancomycin

Sub-inhibitory concentrations of vancomycin are known to trigger changes in cell wall biosynthesis genes in Gram-positive bacteria, including in E. faecalis. Vancomycin is known to inhibit cell wall synthesis by covalently binding to the D-alanyl-D-alanine chain of the cell wall pentapeptide (Reynolds P. E., 1989). Vancomycin resistance in E. faecalis and E. faecium can be mediated by either the vanA or vanB operon. Both operons encode for the expression of polypeptides that are involved in aiding in the transposition of the transposon that encodes the van genes, as well as genes encoding for the modification of the cell wall pentapeptide to prevent vancomycin from binding to its target (reviewed in (Courvalin, 2006)). The difference between the vanA and vanB operons is that the vanA operon can also be induced by the related glycopeptide antibiotic teicoplanin (Baptista, Depardieu, Reynolds, Courvalin, & Arthur, 1997; Baptista, Rodrigues, Depardieu, Courvalin, & Arthur, 1999).

Transcription of the vancomycin-resistant gene cluster is regulated by the VanRS two-component system that is found at the beginning of the gene cluster (Arthur, Molinas, & Courvalin, 1992; Evers & Courvalin, 1996). Phosphorylation of the VanR response regulator enhances the affinity of the protein for the regulatory regions of the promoter regions of the vanA gene cluster; namely, for vanRS (P_R) and vanHAXYZ (P_H) (Arthur, Depardieu, Gerbaud, Galimand, Leclercq, & Courvalin, 1997; Holman, Wu, Wanner, & Walsh, 1994). A similar setup is also found to regulate the expression of the vanB gene cluster (Baptista, Depardieu, Reynolds, Courvalin, & Arthur, 1997; Arthur, Depardieu, Gerbaud, Galimand, Leclercq, & Courvalin, 1997; Wright, Holman, & Walsh, 1993). The response regulators of both van operons can also be activated by kinases encoded by the host chromosome in the absence of their partner sensor (Baptista, Rodrigues, Depardieu, Courvalin, & Arthur, 1999; Arthur, Depardieu, Gerbaud, Galimand, Leclercq, & Courvalin, 1997; Silva, Haldimann, Prahalad, Walsh, & Wanner, 1998).

The activation of the promoters in the vanA operon by VanR is inducible by vancomycin, teicoplanin, and moenomycin in wild-type strains of E. faecalis, and these are constitutively expressed in vanS mutants (Arthur, Depardieu, Gerbaud, Galimand, Leclercq, & Courvalin, 1997). The vanB cluster differs with the operon being inducible only by the addition of vancomycin, whereas in a vanS_B mutant, vancomycin, teicoplanin, and moenomycin can all activate transcription of the operon from the two promoter sites (Baptista, Rodrigues, Depardieu, Courvalin, & Arthur, 1999; Evers & Courvalin, 1996). Activation of the vanA operon by glycopeptides and moenomycin occurs as these drugs inhibit the transglycosylation reaction, but by different mechanisms, as the structure of moenomycin is unrelated to that of the glycopeptides (Handwerger & Kolokathis, 1990). It is thought that the VanS_A sensor kinase in the vanA operon is not involved in direct interaction with the stimulating drugs (Handwerger & Kolokathis, 1990). With the vanB operon, the VanS_B sensor kinase does appear to interact with vancomycin, which distinguishes the transcriptional differences between these two operons. Amino acid substitution of the N-terminal sensing domain of VanS_B allows for the induction of the vanB operon by the other glycopeptide teicoplanin, but not by moenomycin (Baptista, Depardieu, Reynolds, Courvalin, & Arthur, 1997; Baptista, Rodrigues, Depardieu, Courvalin, & Arthur, 1999). Experiments completed both in vitro and in vivo have shown that carriage of the transposon encoding for the vanB operon, when uninduced, was not significantly costly to the host (Foucault, Depardieu, Courvalin, & Grillot-Courvalin, 2010). Induction of the resistance genes leads to a major reduction in growth rate, colonization, and transmission in Enterococcus sp. (Foucault, Depardieu, Courvalin, & Grillot-Courvalin, 2010). Overall, tight regulation mediated by a two-component regulatory system effectively reduces the biological costs that are associated with vancomycin resistance.

Experiments that used sub-inhibitory concentrations of vancomycin on the E. faecalis strain V583, which carries the vanB operon, revealed that the open reading frame EF2292 (named vanV) located 3’ to the vanX gene exhibited the same level of induction as the vancomycin resistance genes (Ribeiro, Santos, Marques, Gilmore, & de Fátima Silva Lopes, 2011). Analysis of this gene suggests that it might be involved in some regulation process of the vanB operon in strains that carry vanV, although it is not consistently found in all vanB-carrying strains. It also appears that vanV does not have an effect on the resistance of the carrying strain to vancomycin (Ribeiro, Santos, Marques, Gilmore, & de Fátima Silva Lopes, 2011). Further screening of vanB-resistant enterococci for the presence of this gene is required, and may unravel a particular function for this gene.

It should be noted that many enterococcal species can carry other van operons, which encode for low-level or constitutive resistance to vancomycin. One of these operons is the vanD operon, which encodes for the constitutive production of the peptidoglycan precursor ending in D-alanyl-D-lactate (Depardieu, Bonora, Reynolds, & Courvalin, 2003). Mutations in the sensor kinase and response regulator, as well as the native D-alanyl-D-alanine ligase (involved in native cell wall synthesis), lead to the constitutive expression of the van operon and the cell wall that contains only the D-alanyl-D-lactate pentapeptide structure (Depardieu, Reynolds, & Courvalin, 2003; Depardieu, Kolbert, Pruul, Bell, & Courvalin, 2004).

Another van operon carried by E. casseliflavus, E. gallinarum, and E. flavescens is the vanC operon. The vanC phenotype is inducible and constitutive, and results in the production of a peptidoglycan precursor ending in D-Alanyl-D-Serine (Reynolds & Courvalin, 2005). Other van operons that encode for a pentapeptide ending in a serine residue are found in E. faecalis and are referred to as the vanE and vanG operons. The vanE operon has an organization identical to the vanC operon (Patiño, Courvalin, & Perichon, 2002). The vanG operon has a unique gene organization and appears to encode a predicted transcriptional activator upstream of the two component regulatory system (Depardieu, Bonora, Reynolds, & Courvalin, 2003).

The expansion of the van operon alphabet is continually expanding with vanL (Boyd, Willey, Fawcett, Gillani, & Mulvey, 2008), vanM (Xu, et al., 2010), and vanN (Lebreton, et al., 2011) gene clusters being reported. Transcriptional regulation of these operons appears to be similarly regulated by a two component transduction system and promoters, as in the van operons discussed above.

Bacteriocins

Bacteriocins are peptides secreted by bacteria with the intent of inhibiting the growth of similar or closely related bacterial species. Many lactic acid bacteria produce bacteriocins that have the ability to inhibit the bacterium beyond the genus level, and also have the potential to be used medically for the prevention of growth of unwanted microflora. With the spread of antibiotic resistance, bacteriocins are ideal candidates for use as alternative antimicrobials. In addition, resistance to bacteriocins is not common in nature. Class IIa bacteriocins encompass the non-lantibiotic bacteriocins that have regular amino acid residues. A well-characterized class IIa bacteriocin is pediocin, which is produced by Pediococcus acidilactici (Marugg, et al., 1992). Many of these bacteriocins are produced by lactic acid bacteria and have been found to inhibit other Gram-positive organisms, including Enterococcus spp. Bacteriocins act by permeabilizing the cell membrane, which leads to the killing of the cell. The target for class IIa bacteriocins is the mannose phosphate transport (mpt-PTS), and mutants that lack this system are insensitive to the effects (Diep, Skaugen, Salehian, Holo, & Nes, 2007; Gravesen, et al., 2002; Héchard & Sahl, 2002; Ramnath, Beukes, Tamura, & Hastings, 2000). The PTS is a major uptake system for mannose and glucose, and many of the components are also involved in gene regulation of catabolic operons. In the laboratory, deletion mutants of mptR and the mpt operon are known to be resistant to the effects of bacteriocins.

Transcriptional analysis has been completed on pediocin-resistant strains of E. faecalis generated in the laboratory environment to test the efficacy of this bacteriocin in the treatment of hospital-acquired enterococcal infections. A comparison of wild-type V583, spontaneously resistant isolates, and an ΔmptD mutant, which is known to render E. faecalis strains resistant to the effects of the class IIa bacteriocin pediocin, was completed (Opsata, Nes, & Holo, 2010). In E. faecalis, the mpt operon is under transcriptional control of a promoter recognized by σ⁵⁴, and is dependent upon the activator MptR. The spontaneous bacteriocin resistant isolates contained a mutation in mptR (EF0018; A356G mutation) causing the down-regulation of the expression of the mpt operon. The expression of several other genes were also down-regulated, and included the components of the mpt operon (EF0019-EF0022); the downstream mannose operon regulator (manO; EF0024); a major facilitator family transporter (EF0082); glyceraldehyde-3-phosphate dehydrogenase (gap-2; EF1964); phosphoglycerate kinase (pgk EF1963); triosephosphate isomerase (triA; EF1962); enolase (eno, EF1961); phosphoglycerate mutase (gpm,EF0195); pyruvate kinase (pyk; EF1046); and L-lactate dehydrogenase (ldh-1; EF0255); a majority of which encode for sugar metabolism. A study by Opsata et al. (Opsata, Nes, & Holo, 2010) found the reduced consumption of glucose as a carbon source in the mpt mutants, which demonstrated the important role of Mpt in glucose metabolism in E. faecalis. The reduced glucose uptake results in changes in the concentrations of glycolytic metabolites, which subsequently affects the energy status of the cell. Putative carbon catabolite regulation (cre)-sites were located upstream of three of the differentially expressed genes, and some with cre-sites were located downstream of the genes, supporting the idea that an altered energy status sensed by a histidine protein-kinase/phosphorylase and implemented on the PTS phospho-carrier protein does occur. However, this is also the first time that cre-sites have been reported downstream of the regulated gene (Opsata, Nes, & Holo, 2010). In E. faecalis, disruption of the mannose PTS altered the transcription of about 90 cre-sites, with about 65% of these being involved in the uptake and metabolism of alternative energy sources. A number of these genes were also found to encode transcriptional regulators, and may indicate that a regulatory cascade has been triggered. A number of the genes found to be differentially regulated in the E. faecalis V583 mpt bacteriocin-resistant mutants were also found to be similarly expressed in a transcriptome study of a Streptococcus mutans EIIAB mannose-PTS mutant; however, some differences were found that may be attributed to niche preferences (Opsata, Nes, & Holo, 2010).

Copper

Metal ions are crucial for bacteria to maintain transcriptional control of regulatory networks that govern gene expression. Maintaining homeostasis between the intra- and extracellular concentration of metal ions is critical in adaptations to intracellular survival and replication among pathogenic bacteria. Copper is useful as a cofactor for redox enzymes in reactions, due to its ability to accept and donate electrons; however, this very reactivity also makes it a toxic metal (Urbański & Beresewicz, 2000; Linder & Hazegh-Azam, 1996). It is therefore crucial for cells to maintain control over copper by means of uptake, storage, and efflux.

Copper uptake and regulation in E. hirae is a well-studied system. The regulation of intracellular copper in this species is mediated by the cop operon, which consists of four open reading frames (Solioz & Stoyanov, 2003) (Figure 3). The four genes encode two P-type ATPase copper transporters (copA and copB), a copper chaperone protein (copZ), and a copper-dependent transcriptional regulator (copY) (70). This operon is conserved between all members of the Lactobacillales and includes at least homologues of the copA and copY genes (Reyes, Leiva, Cambiazo, Méndez, & González, 2006).

Figure 3.

The cop operon. A. Regulation of the cop operon under low copper conditions (physiological). The CopA repressor is bound to Zn(II) and to the promoter, turning transcription of the cop operon down. B. Regulation of the cop operon under high copper conditions. (more...)

The transporters in the cop operon are responsible for opposite processes. CopA takes up copper (I) when it is limiting, and structural information for this ATPase is available (Lübben, Portmann, Kock, Stoll, Young, & Solioz, 2009; Tsuda & Toyoshima, 2009). CopB extrudes copper (I) when it reaches toxic concentrations (Odermatt & Solioz, 1995; Solioz & Odermatt, 1995). CopY is a bipartite repressor, where the N-terminal half of the protein exhibits 20% identity to bacterial repressors of β-lactamases, such as MecI (Solioz & Stoyanov, 2003). The N-terminal region also contains a QQ motif found in the phage repressors (lambda and 434), and has been shown to tightly interact with an ACA triplet of the DNA binding site (Anderson, Ptashne, & Harrison, 1987). Mutations of the DNA binding site of CopY abolish the ability of the repressor to interact with DNA in vitro (Wunderli-Ye & Solioz, 1999). The C-terminal end of CopY has multiple cysteine residues arranged in a pattern commonly seen in other copper-responsive transcriptional activators that have been studied in yeast (CxCx₃CxC) (Zhou & Thiele, 1991; Dobi, Dameron, Hu, Hamer, & Winge, 1995). CopY functions as a dimer (Strausak & Solioz, 1997), binding to an inverted repeat sequence upstream of the cop operon when bound to zinc (Zn (II)) (Cobine, Jones, & Dameron, 2002), suppressing transcription. Figure 3 illustrates the role of CopY in the presence of high copper concentrations and low (physiological) copper concentrations. CopZ or another appropriate copper complex can donate two copper (Cu(I)) to CopY, displacing the bound Zn(II), which results in CopY releasing itself from the DNA and allows expression of the downstream cop genes (Cobine, Jones, & Dameron, 2002). The interaction of CopY and CopZ carrying Cu(I) is dependent on electrostatic interactions, and transfer of the Cu(I) occurs due to affinity differences for this metal, as well as charged-based interactions between the two proteins (reviewed in (Solioz & Stoyanov, 2003)).An interesting detail pertaining to CopZ is that it more easily degraded when bound to Cu(I) by a cellular protease under high copper stress (Lu & Solioz, 2001). It is hypothesized that CopZ degradation prevents cell damage from occurring as a result of the exposed Cu(I) in the protein metal ion complex, which can participate in Fenton-type reactions leading to formation of reactive hydroxyl radicals and cell damage (Lu, Dameron, & Solioz, 2003; Solioz M. , 2002).

With the emergence of microarray technology, the effect of copper on the transcriptome of enterococci species has been more closely studied. Two recent publications have looked at the transcriptional response of E. faecalis OG1RF (Reyes-Jara, et al., 2010) and V583 (Abrantes, Lopes, & Kok, 2011) in the presence of copper. Not surprisingly in both studies, the cop operon (EF0297-EF0299) was the most up-regulated operon. In V583, in the presence of 0.05 mM CuSO₄, other induced operons included the following: genes involved in potassium transport (kpdA and kpdB); an operon encoding for two ABC transporters, a hypothetical protein and a GntR family transcriptional regulator (EF1673-EF1676); an operon of V-type ATP enzymes (EF1492-EF1500); nine genes related to cell wall biosynthesis; and several virulence-associated genes, including LemA (EF0468), a cell-envelope associated acid phosphatase (EF3245), and a cell wall surface anchor family protein (EF3314) (Abrantes, Lopes, & Kok, 2011). In the study conducted by Reyes-Jara et al. (Reyes-Jara, et al., 2010), the authors found that an OG1RF ΔcopY mutants’ response to the presence of 0.5 mM CuSO₄ was similar to the wild-type copY strain, with the exception of the cop operon being constitutively expressed in the absence of copper. Several other transcriptional elongation factors were also induced shortly after the CuSO₄ exposure, including GreA (EF2914), Rrf2 (EF3175), the Cro/CI (EF0873), Sor/DeoR (EF1965) and a hypothetical protein of COG class K (EF1752). The induction of these genes may not occur as a result of increased copper concentration, but may be induced in response to a secondary signal, such as the oxidative stress generated by copper exposure. Comparison between the two strains’ responses to copper is difficult, given that the experimental conditions were different.

Bile

Bile is a digestive juice secreted by the liver and stored in the gallbladder, and it functions both to assist the digestion and absorption of fat in the gut and as a means for the body to excrete waste from the blood. The concentrations of bile present in the small intestines range from 0.2–2%, but can get up to 8% in the gall bladder (Bowen, 1998). The ability to resist the deleterious action of various bile components is thus an absolute need for E. faecalis in its commensal lifestyle. The mechanisms involved in bile resistance in E. faecalis V583 were previously assessed in a genome-wide transcriptional analysis over a time course of 120 min. after the addition of 1% bovine bile to the growth medium (Solheim, Aakra, Vebo, Snipen, & Nes, 2007). The detergent-like action of bile acids was reflected as an enrichment of V583 genes that code for proteins with membrane-associated functions and/or locations among the differentially transcribed genes. In particular, the functional categories of genes involved in fatty acid and lipid metabolism and signal transduction were strongly affected. Studies in lactobacilli (Bron, Molenaar, de Vos, & Kleerebezem, 2006; Pfeiler, Azcarate-Peril, & Klaenhammer, 2007; Whitehead, Versalovic, Roos, & Britton, 2008) and Bifidobacterium breve (Ruiz, Zomer, O'Connell-Motherway, van Sinderen, & Margolles, 2012) also suggest that cell envelope stress is one of several aspects of the bile response that is conserved among Gram-positive bacteria.

Active extrusion of bile appears to be another common strategy to counteract bile toxicity in bacteria (Storz, 2000). Transcriptional profiling has previously been used to identify bile efflux proteins in Lactobacillus reuteri and B. breve (Whitehead, Versalovic, Roos, & Britton, 2008; Ruiz, Zomer, O'Connell-Motherway, van Sinderen, & Margolles, 2012), for example. Several candidate transporters were also reported in E. faecalis V583, including two members of the EmrB/QacA subfamily of the major facilitator superfamily of multidrug resistance transporters (Solheim, Aakra, Vebo, Snipen, & Nes, 2007). In E. coli, EmrB was shown to play a role in bile resistance and efflux of bile (Lomovskaya & Lewis, 1992; Thanassi, Cheng, & Nikaido, 1997), but the study of Solheim et al. (Solheim, Aakra, Vebo, Snipen, & Nes, 2007) was the first report of a proton motive force dependent transport system involved in bile resistance in Gram-positive bacteria. Shortly after this study, however, a similar induction of a gene coding for an EmrB/QacA-like multidrug resistance transporter (lr1584) was observed in L. reuteri (Whitehead, Versalovic, Roos, & Britton, 2008). Interestingly, lr1584 is part of an operon structure which was up-regulated during bile exposure in Lactobacillus acidophilus, as well as in L. reuteri and E. faecalis. Inactivation of both lr1584 and lr1582 resulted in an impaired adaptation phenotype in L. reuteri. Another V583-encoded transport system (EF2641-42) with significant homology to the well characterized bile responsive bilE system in Listeria monocytogenes (Sleator, Wemekamp-Kamphuis, Gahan, Abee, & Hill, 2005), also displayed differential expression in V583. This operon codes for proteins involved in glycine betaine uptake. The role of compatible solutes in bacterial stress management, such as glycine betaine, was recently reviewed by Sleator and Hill (Sleator & Hill, 2010).

Bile salt hydrolases (BSH) have also been implicated in bile resistance in other Gram- positive bacteria. These enzymes have been proposed to confer the ability to detoxify bile salts, and studies with a Δbsh mutant revealed an important role for BSH in the intestinal persistence of L. monocytogenes (Begley, Sleator, Gahan, & Hill, 2005). None of the two bsh homologs in V583 (EF0521 and EF3005) showed significant differential expression during exposure to bovine bile (Solheim, Aakra, Vebo, Snipen, & Nes, 2007); however, the bile-sensitive phenotype of an E. faecalis ΔslyA mutant was recently connected to the regulation of ef3005 by the transcriptional regulator SlyA (Michaux, Martini, Hanin, Auffray, Hartke, & Giard, 2011), which suggests the potential role of BSH in E. faecalis bile response after all. The diverging result can most likely be attributed to the increased sensitivity associated with real-time PCR, as compared to the microarray-based approach. As a result, further characterization of the loci in question will be needed to conclude whether BSH constitutes a mechanism for bile resistance in E. faecalis.

Urine

The urinary tract is among the most common sites of bacterial infection in humans, and urinary tract infections (UTIs) are the type of infection most commonly caused by enterococci (Malani, Kauffman, & Zervis, 2002). In order to identify genetic traits that may distinguish pathogenic and non-pathogenic E. faecalis in their ability to cause UTIs, the global transcription signatures of a probiotic (Symbioflor 1) and two pathogenic (MMH594 and OG1RF) strains during cultivation in human urine were compared (Vebø, Solheim, Snipen, Nes, & Brede, 2010). The non-pathogenic strain grew at the same rate as the pathogenic strains, which indicates that the pathogenic potential is not related to newly required mechanisms that enable growth in this environment. Although the three strains have different strategies in relation to their host, their transcriptional signatures towards urine as a growth medium were surprisingly similar. However, some potentially significant differences were reported. The highest number of differentially expressed genes was observed after 5min in OG1RF, whereas the process took 30min in MMH594 and Symbioflor 1. Consequently, it may be inferred that OG1RF adapts more rapidly to growth in urine. This rationale was further supported by the swift derepression of genes involved in macromolecular biosynthesis (i.e. transcription and protein synthesis) in OG1RF, as compared to the two other strains.

More than 50% of all microbial infections have been associated with the formation of biofilms, and biofilm formation appears to also be clinically relevant for UTIs. A particularly problematic aspect of biofilm formation is the ability of sessile bacteria to withstand host defense mechanisms and the increased resistance to antibiotics, biocides, and hydrodynamic shear forces observed for bacteria in biofilm (Bitsori, Maraki, Raissaki, Bakantaki, & Galanakis, 2005). Several genetic determinants with impact on biofilm formation in E. faecalis were differentially transcribed during growth in human urine, as compared to the rich medium 2×YT: bopABCD (biofilm on plastic; EF0954 to -57) this process was partially up-regulated in OG1RF, while srtA (EF3056) was induced in MMH594 and Symbioflor 1. Data from knock-out mutant studies also inferred a role for salA (EF3060), salB (EF0394) and altA (EF0799) in biofilm production, all of which were down-regulated in response to urine (Vebø, Solheim, Snipen, Nes, & Brede, 2010; Mohamed, Tenq, Nallapareddy, & Murray, 2006).

SalB was initially characterized as a stress-inducible protein in E. faecalis (Breton, Mazé, Harte, Lemarinier, Auffray, & Rincé, 2002). Its growth in urine also affected the expression of a large number of other genes with a proven or predicted function in stress responses in E. faecalis. One of the most pronounced effects was the stimulation of an oxidative stress response. Mn²⁺-depletion has been reported as a regulator of oxidative stress regulons in other bacteria. Interestingly, the pathogenic strain MMH594 seemed slightly better equipped with genes involved in manganese acquisition than the two other isolates: while efaABC and two other genes encoding Mn²⁺/Fe²⁺ transporters (EF1057 and EF1901) were induced during growth in human urine in all three strains, the putative uptake system for manganese encoded by EF0575 to -78, located on the pathogenicity island, is specific to MMH594. Vebø and coworkers reported the latter system to be induced in MMH594 during cultivation in urine (Vebø, Solheim, Snipen, Nes, & Brede, 2010). Taken together with the differential regulation of several iron transporters, these observations may be indicative of urine as an iron- and manganese depleted environment. This hypothesis was further supported by up-regulation of genes involved in the uptake and assimilation of iron in E. coli during growth in the urinary tract (Snyder, et al., 2004).

Surface structures are major determinants of virulence for many pathogens: namely, the presence of a capsule may allow the microorganism to evade the host immune system. Indeed, several cell wall polysaccharides with implications in the pathogenesis of enterococcal infections have been reported (Hancock & Gilmore, 2002; Huebner, et al., 1999; Xu, Murray, & Weinstock, 1998; Xu, Singh, Murray, & Weinstock, 2000), two of which showed differential expression upon the encounter with urine. Both the cps (capsular polysaccharide) and the epa (enterococcal polysaccharide) loci were down-regulated during growth in urine. The data from the transcriptional analysis also suggested that E. faecalis adjusts the fatty acid and phospholipid composition of the membrane in response to urine as a growth medium. This was manifested as an up-regulation of two gene clusters (EF0282-84 and EF2886-75) that were responsible for type II fatty acid biosynthesis (FASII) and isomerization of membrane phospholipids (Vebø, Solheim, Snipen, Nes, & Brede, 2010).

Urine is a complex medium consisting of a mixture of carbon sources (Tasevska, Runswick, McTaggart, & Bingham, 2005; Wishart, et al., 2009) that are likely to change over time, and the ability of the bacteria to exploit available carbon and energy sources may be crucial for virulence. The final cell density reached by E. faecalis in urine compared to those in 2× YT growth medium suggests that important growth factors are absent in urine; however, supplementary growth experiments disproved glucose as a major limiting factor for growth of E. faecalis in urine, as elevated glucose levels alone did not significantly augment bacterial growth (Solheim, unpublished). Nevertheless, the induction of EF3215 to -22 pointed towards citrate as a significant carbon source for E. faecalis during growth in urine. The cit operon is responsive to carbon catabolite repression (CCR) (Blancato, Repizo, Suárez, & Magni, 2008; Suárez, Blancato, Poncet, Deutscher, & Magni, 2011), and this observation is indicative of low glucose levels in urine. Furthermore, the transcriptional data suggested that E. faecalis uses available peptides as a source of amino acids.

The encounter with urine also had a considerable impact on the expression of a number of genes with a potential implication in virulence; however, among the established enterococcal virulence traits, only the fsr operon displayed significant changes in transcription. From the microarray data, a modest up-regulation of the fsrABC genes (EF1822 to -20) was seen in MMH594 at t₃₀. The fsrA gene was also up-regulated at t₅. The regulation of fsrB (EF1821) in MMH594 at t₃₀ was, however, not confirmed by real time quantitative PCR (QPCR)—thus the importance of this observation remains uncertain. On the other hand, QPCR revealed significant up-regulation of fsrB in OG1RF after 30 minutes exposure to urine. As mentioned previously, the fsr system modulates expression of gelE-sprE operon through a classic quorum sensing signaling cascade. Secretion of these proteases that damage host tissue may contribute to bacterial migration and invasion. The gelE gene has been shown to be predominant among clinical enterococcal isolates; however, contradictory results have later been reported (Roberts, Singh, Okhuysen, & Murray, 2004; Coque, Patterson, Steckelberg, & Murray, 1995). Moreover, isogenic strains of E. faecalis divergent in gelatinase and serine protease production exhibited attenuated killing in nematode- and mice infection models (Qin X. , Singh, Weinstock, & Murray, 2000; Sifri, et al., 2002). An up-regulation of the gelE-sprE operon after prolonged exposure to urine is in line with the work by Shepard and Gilmore (115) which used QPCR to show that gelE transcription was 7-fold induced during logarithmic growth in urine.

Blood

E. faecalis is also a significant cause of hospital-acquired bacteremia (Malani, Kauffman, & Zervis, 2002; Wisplinghoff, Bischoff, Tallent, Seifert, Wenzel, & Edmond, 2004), and with this in mind, Vebø et al. conducted a whole-genome transcription study on the adaptation of E. faecalis to blood (Vebø, Snipen, Nes, & Brede, 2009). Interestingly, several aspects of the transcriptional signature of E. faecalis grown in blood were similar to that of E. faecalis grown in urine. An activation of many of the same genes implicated in stress responses was observed, with an overrepresentation of genes involved in oxidative stress adaptation (e.g. ohr, npr, sodA, ahpFC and nox). Moreover, many of the observed changes in gene expression could also be related to an extensive remodeling of the cell envelope. The changes detected among genes involved in FASII were also particularly pronounced. Other differentially transcribed operons with membrane-associated functions included lrgAB (EF3194-93), cps (EF2492-84), epa (EF2200-2189 and EF2184-77), and dltABCD (EF2749-46). D-alanylation of cell wall teichoic acids and lipoteichoic acids by the Dlt complex leads to a reduced negative charge of the bacterial surface. In this case, the reduced content of D-alanine esters in the teichoic acid may have resulted in an increased net negative charge on the bacterial cell surface, which in turn may have affected several bacterial properties, such as susceptibility to cationic antimicrobial peptides and biofilm formation (Theilacker, et al., 2006). The microarray data also showed that genes related to iron acquisition represented one of the major changes related to E. faecalis’s adaptation to blood, despite the fact that iron is not essential for the growth of most lactic acid bacteria. A similar trend was also observed during growth in urine, but the transcriptional changes provoked by blood were more pronounced. The induction of the genes responsible for citrate metabolism was observed in both the blood and urine experiments. In addition, genes involved in the breakdown of other CCR regulated substrates also displayed enhanced transcription in blood, including arginine (Barcelona-Andrés, Marina, & Rubio, 2002) and glycerol (Opsata, Nes, & Holo, 2010), along with possibly other C3-glycerides present in blood. As a result, the glucose concentration in body fluids such as blood and urine appears to be below the threshold for release of CCR. As for the established enterococcal virulence factors, QPCR analysis showed that fsrB and gelE were down-regulated in response to growth in blood, the opposite of what was observed in urine. Whereas cues present in urine stimulate fsr expression, factors present in blood seemingly interfere with its expression. This is the opposite effect from growth in serum by the E. faecalis MMH594 strain (Shepard & Gilmore, 2002).

EutV, an ANTAR-family member with RNA-binding antiterminator activity

Upregulation of the E. faecalis eut genes is partially controlled by a two-component system. This consists of a soluble histidine kinase, eutW, and its cognate response regulator, eutV. Experiments showed that this two-component system specifically senses ethanolamine. In vitro, purified eutW underwent autophosphorylation in the presence of ethanolamine and was also able to transfer the phosphate residue to eutV (Del Papa & Perego, 2008; Fox, et al., 2009). In vivo, eut gene expression was demonstrated to be dependent on ethanolamine, eutV, and eutW (Del Papa & Perego, 2008; Fox, et al., 2009; Baker & Perego, 2011; Ramesh, et al., 2012). EutV belongs to the AmiR and NasR transcriptional anti-terminator regulator (ANTAR) family of response regulators, and its output domain controls gene expression by RNA binding (Shu & Zhulin, 2002). ANTAR proteins interact with nascent transcripts to prevent formation of transcriptional terminators that precede certain genes, allowing RNA polymerase to transit into the coding regions. The E. faecalis eut locus contains four of these rho-independent terminators, and significant evidence supports that they are the targets for antitermination by the eutV ANTAR protein (Fox, et al., 2009; Baker & Perego, 2011; Ramesh, et al., 2012). As already mentioned, expression of the genes downstream of the terminators is dependent on ethanolamine and the two-component system. Deletion of the terminators preceding eutP, eutS and eutG resulted in constitutive expression (Baker & Perego, 2011; Ramesh, et al., 2012). Finally, eutV binds to the RNA in a region just upstream and overlapping these terminators (Ramesh, et al., 2012). These data support an antitermination function for eutV and validates a model in which the eut locus is partially regulated by a series of rho-independent transcriptional terminators interspersed throughout the operon. A major focus of recent studies has been elucidating the details of the antiterminator structure that eutV recognizes.

Analysis of the sequences of the 5’ untranslated regions (UTR) of the E. faecalis eut genes revealed a hairpin structure with a short stem region and a hexanucleotide loop, with the first and fourth loop residues conserved among the E. faecalis eut genes (Ramesh, et al., 2012). A similar hairpin structure have been reported in the substrate of a previously characterized ANTAR protein, NasR from Klebsiella oxytoca (Chai & Stewart, 1999), and the loop sequences found to be conserved in the E. faecalis eut genes were shown to be important for the binding of NasR (Ramesh, et al., 2012; Chai & Stewart, 1999). A second, similar stem-loop structure was identified just downstream of the first hairpin, which also had a hexamer loop with similar conservation of loop residues. This second hairpin overlapped the 5’ end of the intrinsic terminator that precedes the ORF, such that formation of the hairpin and the terminator became mutually exclusive. This second stem-loop also contains a motif, called the ANTAR recognition sequence, that was predicted to be the site of recognition by eutV based on sequence conservation among eut genes present in Firmicutes (Chai & Stewart, 1999). This dual-hairpin motif and its conserved loop residues can be identified in the leaders of the eut genes from Clostridium species and Listeria monocytogenes, as well as in the substrates of the previously characterized ANTAR proteins, NasR and AmiR. This led to the hypothesis that upon activation, the eutV ANTAR protein bound the eut RNA, specifically interacting with the two terminal loops of the dual-hairpin motif in the nascent transcripts to stabilize an antiterminator structure and exclude terminator formation (Ramesh, et al., 2012; Aymerich & Steinmetz, 1992; Babitzke & Gollnick, 2001). This dual-hairpin motif is unique, as compared to the antiterminators employed by other bacterial regulators such as the Sac/Bgl and TRAP proteins (Aymerich & Steinmetz, 1992; Babitzke & Gollnick, 2001). In most previously characterized systems, the antiterminator is a single alternative structure that overlaps with the terminator in a manner such that only a single hairpin can exist.

Using a lacZ-based reporter assay, it was demonstrated that both stem-loops and the four conserved loop residues are critical for successful antitermination in vivo by eutV in the presence of ethanolamine and AdoCbl (Ramesh, et al., 2012). This was also supported by in vitro EMSA studies. In vivo data also showed that the terminal closing base pairs of the first hairpin may result in sequence-specific interactions with eutV. In addition, an optimal distance between the two stem-loops was required, and such an alteration resulted in reduced efficiency of antitermination. Hence, the current model for the mechanism of antitermination by the eutV ANTAR protein is formation of a protein-RNA complex involving the dual hairpin structure in the eut RNA, which prevents the formation of the terminator, resulting in expression of the downstream genes (Ramesh, et al., 2012).

The dual nature of the eut RNA substrate hinted at the possibility of interaction with a dimer of eutV (123). SEC-MALLS (Size Exclusion Chromatography – Multi-Angle Laser Light Scattering) analysis of full-length eutV indicated that it exists as a monomer in the unphosphorylated state. Phosphoryl transfer from the cognate sensor kinase, eutW, induced dimerization of eutV. DRaCALA (Differential radial capillary action of ligand assay) assays in turn showed that phospho-eutV bound the RNA substrate with significantly higher affinity, as compared to the unphosphorylated form of the protein. Interestingly, eutV that lacks the N-terminal domain is capable of dimerizing and binding the RNA substrate with higher affinity, as compared to unphosphorylated full-length protein, suggesting that the unphosphorylated receiver domain actively inhibits dimerization and therefore RNA binding. Overall, signal-induced dimerization of the eutV ANTAR protein seems to be essential for recognition of a symmetric, dual-hairpin RNA ligand, which is conceptually similar to the molecular mechanism exhibited by many DNA-binding response regulator proteins that dimerize and recognize paired sequences in the DNA. The E. faecalis eutV/eutW TCS provides, for the first time, a mechanistic model of antitermination employed by ANTAR proteins, validated by in vitro and in vivo techniques (Ramesh, et al., 2012).