BosR Functions as a Repressor of the ospAB Operon in Borrelia burgdorferi

The Lyme disease spirochete, Borrelia burgdorferi, must abundantly produce outer surface lipoprotein A (OspA) in the tick vector but downregulate OspA in mammals in order to evade the immune system and maintain its natural enzootic cycle. Here, we show that BosR binds two regulatory elements of the ospAB operon and that increasing BosR expression leads to downregulation of OspA. Both regulatory sequences, cisI and cisII, showed strong BosR-binding and cisII bound much tighter than cisI. A promoterless bosR gene fused with an inducible promoter was introduced into an rpoS mutant and a wild-type strain to assess RpoS-independent and -dependent downregulation of OspA by BosR. With the induction of BosR expression, OspA expression was reduced more significantly in the RpoS-deficient than wild-type background, but not completely repressed. In the presence of constitutive expression of OspC, DbpA and DbpB, increasing BosR production resulted in complete repression of OspA in the RpoS mutant. Taken together, the study clearly demonstrated BosR serves as a repressor that binds both regulatory elements of the ospAB operon and shuts off expression.


Introduction
Outer surface proteins (Osps) A and B, encoded by a 2-gene operon [1], are among the most abundantly produced outer surface antigens by the Lyme disease spirochete, Borrelia burgdorferi, in engorged and unfed Ixodes ticks [2][3][4][5]. In response to a fresh bloodmeal, B. burgdorferi downregulates OspA/B and upregulates OspC and other proteins, a process that prepares B. burgdorferi for infection of a mammal [6][7][8]. Repressing ospAB expression during mammalian infection is critical for B. burgdorferi to evade the immune system, cause persistent infection, and maintain the enzootic cycle, as both OspA and OspB, even expressed at a low level, may ultimately induce a strong humoral response due to their high immunogenicity. The specific response can pose tremendous pressure on the pathogen or even clear infection [9,10]. Even by chance, the anti-OspA/B humoral response may not effectively target spirochetes with very low OspA/B expression in mammalian tissues. Once acquired by the tick vector, the pathogen has to dramatically upregulate OspA/B and consequently becomes extremely vulnerable to the specific antibodies in bloodmeal [11], whereby potentially leading to the eradication of the organism and a discontinuation of the enzootic cycle.
Expression of the ospAB operon is driven by a s 70 -dependent promoter [12]. B. burgdorferi has only two alternative s factors, RpoN and RpoS, which form a regulatory network, in which RpoS expression depends on RpoN and controls expression of many important Osps, including OspC, DbpA and DbpB [13]. A study by Radolf and colleagues suggested that RpoS is involved in repression of OspA expression [14]. Given the fact that RpoS activates expression of many Osps, the indirect effect on OspA expression due to their absence could be significant. The inability of rpoS mutants to downregulate OspA may be caused by an indirect effect resulting from the lack of RpoS-dependent Osps. There has been no evidence showing any interaction of RpoS with DNA sequences associated the ospAB operon, essentially ruling out direct involvement of RpoS in OspA downregulation.
Successful identification of two regulatory sequences, namely cisI and cisII, which flank the ospAB promoter, indicates the existence of a repressor(s), which should bind the two elements and shut off expression during murine infection [15]. Our recent study revealed that more than 156 genes in the B. burgdorferi genome have at least one putative BosR-binding site, among which is the ospAB locus [16]. Interestingly, one of the two putative BosRbinding sites associated with the ospAB operon is completely included within the previously identified cisII regulatory sequence [15], and the second partially overlaps with cisII and the -10 region of the promoter [16].
As a key regulator, BosR functions to bind the rpoS promoter region and positively regulate the alternative s factor, which in turn upregulates a number of Osps, including OspC, DbpA and DbpB [17][18][19]. Although in vitro grown B. burgdorferi does not produce BosR during early growth phase, once grown to late log phase, the pathogen dramatically upregulates the regulator. This dramatic BosR upregulation thus far has not been correlated with OspA downregulation, seriously challenging the notion that BosR, in addition to the identified function, may also serve as a repressor of the ospAB operon. The current study first demonstrated that BosR bound both cisI and cisII and then showed that increased BosR expression indeed led to a shutoff of OspA.

Expression and purification of recombinant BosR
The entire bosR-coding region was amplified from genomic DNA of B. burgdorferi B31 with the use of primers P5F and P5R ( Table 1). The resultant PCR product was digested, purified and cloned into pET-23a vector (EMD Chemicals Inc., Darmstadt, Germany), generating a construct that contained the bosR-coding region fused with a C-terminal His 6 tag. One Shot BL21(DE3)-pLysS Chemically Competent E. coli cells (Life Technologies, Grand Island, NY) were transformed with the construct and induced with 1.0 mM isopropyl-beta-D-thiogalactopyranoside (IPTG) (Sigma Chemical Co., St. Louis, MO). Recombinant BosR was affinity-purified with the use of HiTrap Chelating HP following the manufacturer's instruction (GE Healthcare Bio-Sciences, Pittsburgh, PA). Protein concentration was measured using Quick Start Bradford Dye Reagent following the manufacturer's protocol (Bio-Rad Laboratories, Hercules, CA).

Gel mobility shift assay
Each strand of the probes CisI, CisII and IRs was synthesized by Integrated DNA Technologies, Inc. (Coralville, IA). One strand of each complementary pair was incorporated with 59 digoxigenin during synthesis. Complementary strands were allowed to anneal to form a double-strand probe. The binding assay reaction volume was set in 20 ml, in which 1.0 nM DNA probe was allowed to bind 400 nM of recombinant BosR at room temperature for 10 min. The binding buffer contained 50 mg/ml salmon sperm DNA, 100 mg/ml BSA, 1.0 mM DTT, 50 mM KCl, 10 mM Tris (pH 7.5) and 5% glycerol. In the competition assay, 10 nM DNA competitor was first added to a reaction volume of 20 ml and allowed to interact with 400 nM of recombinant BosR at room temperature for 10 min before 1.0 nM DNA probe was supplemented and incubated for an additional 10 min. Resultant mixtures were separated by electrophoresis on 10% polyacrylamide gels prepared with 0.5x TBE buffer. Separated DNA was transferred to a nylon membrane and probed with the use of the DIG High Prime DNA Labeling and Detection Starter Kit I per the manufacturer's instructions (Roche Applied Science, Mannheim, Germany).
Construction of pIBM-rpoS in , pME22-bosR' and pME22-C'B'A'-bosR' As diagrammed in Fig. 1A, to construct pIBM-bosR in , a 554-bp DNA fragment covering the entire coding region of the bosR gene was amplified with the use of primers P1F and P1R (Table 1) and DNA template extracted from B. burgdorferi B31. The resultant PCR product was purified, digested with NcoI and XhoI, repurified and cloned into pIBM, which was created in a previous study [20], and pre-digested with the same enzymes.
To construct pME22-bosR', the plasmid that conferred constitutive BosR expression, a 597-bp DNA fragment containing the entire coding sequence of the bosR gene was amplified with the use of primers P2F and P2R (Table 1) and DNA template purified from B. burgdorferi B31. The resultant amplicon was purified, digested with BspHI and BamHI, repurified and cloned into pME22, which was created in an earlier study [21], and predigested with NcoI and BamHI. The construction process was summarized in Fig. 1B.

Generation of transformants
The rpoS mutant, DrpoS, which was generated in our previous study [20], was grown to late logarithmic (log) phase in Barbour-Stoenner-Kelly H (BSK-H) complete medium (Sigma). Spirochetes were harvested from approximately 40 ml of culture and transformed with pIBM-bosR in , pME22-bosR' or pME22-C'B'A'-bosR' as described previously [22]. Transformants were identified by PCR using a primer pair specific for either streptomycin or kanamycin cassette and their plasmid content was analyzed as described previously [22].

Growth rate estimation
The spirochete culture was grown at 33uC to late log phase (approximately 10 8 cells/ml) in BSK-H complete medium and diluted to 10 5 cells/ml with the medium. A total of fifteen 1.3-ml aliquots were prepared and IPTG was then added at final concentrations of 0, 0.02, 0.05, 0.10 and 0.20 mM. Each inducer concentration was in triplicate. All aliquots were incubated at 33uC and cell numbers were counted daily for 10 days. Either the parental clone 13A or the transformant DrpoS/rpoS was used as a control.

Immunoblotting and Coomassie staining
Spirochetes were harvested by centrifugation at 5,0006g for 10 min at 4uC. Resultant pellets were dissolved in a SDS-PAGE sample buffer, separated by electrophoresis and electrotransferred onto nitrocellulose membranes. Blots were probed either with a mixture of FlaB mAb and mouse anti-BosR sera or OspC mAb, mouse anti-DbpA or anti-DbpB sera alone as described in our previous study [23]. Mouse BosR sera was prepared in an earlier study [16]. For protein analysis, proteins separated on SDS-PAGE gels were directly stained with Coomassie Brilliant Blue G-250 (Amresco, Inc., Solon, OH).

qRT-PCR
Total RNA was prepared from cultured spirochetes, converted to cDNA through reverse-transcription and quantified for the mRNA copy numbers of flaB and ospA by quantitative PCR as described previously [24].

Results
Both ospA regulatory sequences, cisI and cisII, bind BosR, albeit cisII shows much stronger binding Our previous study identified two regulatory sequences contributing to downregulation of ospA expression in the mammalian host located upstream of the ospAB promoter and located between the promoter and the translational start codon, namely cisI and cisII, respectively [15]. Our most recent study revealed the existence of two putative BosR-binding sites associated with the ospAB locus [16]. One of the sites is completely included within cisII and the second covers the entire -10 region of the ospAB promoter and the first two base pairs of cisII ( Fig. 2A). As the second site of the 14-bp putative BosR-binding sequence overlaps with the -10 region, it is impossible to entirely remove it without inactivation of the ospAB promoter. For this particular reason, only 2 bps of this putative binding site were identified as a part of cisII in the previous study [15].
The regulatory sequence cisI contains no putative BosR-binding site but showed a critical role in repression of ospA transcription during murine infection, albeit it is less effective than cisII in this regard [15]. To examine if the previously identified regulatory elements were able to bind BosR, three 70-bp DNA probes, namely cisI, cisII and IRs, were designed and synthesized as diagrammed in Fig. 2. Probe cisI covered the entire cisI sequence and additional 14 bps up-and downstream sequences. Probe cisII included the entire cisII sequence and extended upstream to include the -35 region of the ospAB promoter. Probe IRs contained the ospC IRs and extended few bps up-and downstream to make up a total of 70 bps. The IRs sequence was previously identified as an operator of the ospC gene and was not expected to bind BosR; thus, it was chosen as a negative control [25]. To minimize nonspecific DNA interaction with BosR, the binding buffer was supplemented with 50 mg/ml salmon sperm DNA. As shown in Fig. 3, the presence of sperm DNA completely eliminated the interaction of IRs probe with BosR. In contrast, the mobility of both cisI and cisII probes was restrained by BosR, a result that clearly indicates that both cisI and cisII are able to effectively bind BosR.
Next, the ospAB regulatory sequences were compared for BosR binding affinity. The IRs probe was first added as a competitor. As shown in Fig. 3, although IRs DNA was added at a concentration of 10-fold greater than cisI or cisII, it did not significantly reduce the interaction of BosR with either cisI or cisII, reiterating the results showing that IRs do not bind with BosR. When cisI and cisII probes were added as a competitor, cisI was unable to significantly reduce the interaction of cisII with BosR, but the addition of cisII essentially eliminated the interaction of cisI with bosR, allowing for the conclusion that cisII more effectively binds BosR than cisI.
Our previous study showed no effect of the presence or absence of Zn 2+ on the DNA-binding activity of BosR [16]. Nevertheless, the influence of Zn 2+ on the binding of BosR to both cisI and cisII was investigated. At concentrations below 10 mM, Zn 2+ had no effect on binding. When Zn 2+ was added to 100 mM, however, the binding of BosR to either cisI or cisII was significantly inhibited (date not shown).

Excessive BosR expression causes cell death in B. burgdorferi
To specifically regulate BosR expression, pIBM-bosR in was constructed as illustrated in Fig. 1A. Within the construct, BosR expression was under the control of an inducible promoter. Production of BosR should not occur from the construct in the absence of the inducer IPTG, although the native bosR gene may produce BosR as normal. The construct pIBM-bosR in was easily introduced into DrpoS. This mutant was used because any RpoS involvement in OspA downregulation was readily ruled out in this way. It was also electroporated into 13A, the parental clone of DrpoS, as a control. In a single transformation experiment with DrpoS, five transformants were obtained. Plasmid analyses led to the identification of one clone, namely, DrpoS/bosR in , which lost cp9, lp5, lp21, lp25 and lp56 as DrpoS, in addition to lp28-1. Transformation of 13A led to the selection of seven transformants, one of which, namely 13A/bosRin, lost cp9, lp5, lp21, lp25, lp56 and lp28-1 and was chosen for further studies. There has been no evidence that any of these lost plasmids affects gene regulation although both lp25 and lp28-1 are critical for murine infection [26]. However, there is a possibility that additional complexity of Osp-BosR regulation exists in wild-type spirochetes.
Our previous study reported that increasing RpoS expression causes cell death [27]. To investigate whether high BosR expression is toxic, both DrpoS/bosR in and 13A/bosR in were grown to early log phase (10 7 cells/ml) in BSK-H medium and diluted to 10 5 cells/ml before IPTG was added to final concentrations ranging from 0 to 0.2 mM. When IPTG reached as low as 0.05 mM, DrpoS/bosR in growth was affected (Fig. 4A). When the concentration increased to 0.1 mM, growth was essentially arrested within a couple of days after induction and all spirochetes eventually died during the subsequent week. The location of cisI, cisII and putative BosR-binding sites and the sequences of cisI and cisII probes. The regulatory sequences upstream of the coding region of the ospAB operon include cisI and cisII (both in bold) and two putative BosR-binding sites (italic). One putative site overlaps with the -10 region and cisII, and the other is contained within cisII. The -35 and -10 regions of the promoter, transcriptional initiation site, and start codon ATG all are underlined. The sequences of cisI and cisII probes are marked with brackets. (B) The IRs were identified as the ospC operator in a previous study [25], and used as a control probe. The sequence of the probe is marked with a bracket. doi:10.1371/journal.pone.0109307.g002 Although at lower concentrations IPTG did not affect early growth, its presence reduced the stationary cell density.
At 0.1 mM, the inducer showed little effect on growth of 13A/ bosR in , indicating that this strain was less sensitive than DrpoS/ bosR in to induction with IPTG (Fig. 4B). Even at 0.2 mM, the 13A/bosR in spirochetes continued to grow for a couple of days before beginning to die; induced spirochetes became uncountable within a week.

Inducing BosR expression leads to dramatic downregulation of OspA
As shown above, excessive BosR expression caused a lethal consequence to B. burgdorferi, therefore it is important to use appropriate concentrations of the inducer to treat the bacteria. At 0.2 mM, IPTG significantly inhibited both DrpoS/bosR in and 13A/bosR in growth shortly after induction and killed them within a week. This concentration was chosen for the investigation of how induction of BosR influenced OspA expression. The DrpoS/bosR in and 13A/bosR in spirochetes were grown to 10 7 cells/ml before supplementing with IPTG at 0.2 mM. Induction was allowed to proceed for three days, during which time the spirochete density reached approximately 10 8 cells/ml, reflecting a three-fold increase. As shown in Fig. 5, as BosR was induced, OspA expression dramatically reduced in DrpoS/bosR in , but had a lesser effect in 13A/bosR in . However, the reduction in the detected protein amount may primarily depend on the dilution effect of cell division as OspA may be stable in live cells. Therefore, a reduction in the total OspA amount may not be greater than three-fold even if the transcriptional process could be fully stopped immediately upon induction. Moreover, the abundant ospA mRNA accumu-lated before induction would continue to be translated into protein until it was degraded.
Total RNA was also prepared and analyzed. As shown in Fig. 5C, induced BosR expression led to a reduction in ospA transcription greater than 86% in DrpoS/bosR in and 65% in 13A/ bosR in . Unlike protein, mRNA is less stable and its level would be better reflected in the magnitude of ospA gene downregulation resulting from increased BosR expression.
Although induction led to a dramatic increase in BosR production, OspC expression did not significantly increase (Fig. 5A), probably because RpoS was also regulated by other regulators, such as RpoN, small RNAs and BadR [13,[28][29][30]. An unbalanced increase in BosR expression might not significantly increase RpoS production if the other regulators were not actively involved.
Increasing BosR expression completely shuts off OspA production when constitutive expression of other Osps simultaneously occurs Although increasing BosR expression, even to a toxic level, leads to dramatic downregulation of OspA, it does not abolish it. To completely downregulate OspA with increased BosR, we designed an experiment based on our hypothesis that the Osp layer homeostasis of B. burgdorferi overwrites the normal regulatory programs. In other words, as OspAB are the most dominantly expressed Osps in cultured spirochetes, B. burgdorferi cannot completely downregulated them without dramatically increasing expression of other Osps. Based on the hypothesis, two additional constructs, pBBE22-bosR' and pBBE22-C'B'A'-bosR', were created as shown in Fig. 1. Within the former, the fused bosR gene was designed to express driven by the flaB promoter, while in the latter, in addition to a fused bosR gene, three osp genes, ospC, dbpA and dbpB, were all engineered to transcribe under the control of a fused flaB promoter.
After these constructs were introduced into DrpoS, five and eight transformants were obtained, respectively. Plasmid analyses led to the identification of two clones, namely, DrpoS/bosR' and DrpoS/C'B'A'-bosR', which lost cp9, lp5, lp21, lp25 and lp56 as DrpoS. In addition, both clones also lost lp28-1. As shown in Fig. 6, a high level of BosR expression driven by the fused flaB promoter greatly downregulated OspA, but was unable to completely shut off expression, consistent with the result obtained with the inducible promoter shown in Fig. 5. In the presence of constitutive expression of OspC, DbpA and DbpB, increased BosR production led to complete shutoff of OspA production.

Discussion
OspA is highly immunogenic and would induce a strong immune response even if expressed at a very low level during mammalian infection [31,32]. Even though OspA antibodies may not effectively kill the spirochetes with low OspA expression in mammalian tissues, once acquired by the tick vector, the pathogen is extremely sensitive to the specific antibodies [5,33]. In order to maintain its infectious life cycle, B. burgdorferi must abundantly produce OspA during this stage in the tick vector and downregulate to below the immune system detectable level during infection of the mammalian host. The current study revealed OspA downregulation can be achieved through binding BosR to the regulatory elements of the ospAB operon. Clearly, BosR functions as a repressor and the two regulatory elements, cisI and cisII, serve as operators of the ospAB operon.
Our previous study identified both cisI and cisII as the regulatory sequences of the ospAB operon and showed that the presence of both was required for maximum downregulation during murine infection [15]. The study also showed that the two elements do not contribute equally to ospA downregulation as cisII exhibits a four-fold greater reduction in ospA transcription when compared to cisI [15]. These previous findings appear consistent with those of the current study, indicating that both elements bind BosR with cisII having more binding affinity than cisI. This double-operator system with use of a single common repressor may ensure full shutoff of the ospAB operon and, thus providing the pathogen with a secure mechanism to completely conceal the highly immunogenic antigens during mammalian infection.
BosR is required for expression of RpoS, which in turn activates ospC, dbpBA and many other genes encoding Osp proteins [17,19]. The regulator is not expressed in early growth phases, but is dramatically upregulated in the late log phase. No significant OspA downregulation has been observed in cultured spirochetes, despite BosR reaching its highest level in the stationary phase. Even in the tick's midgut, no more than 50% of the spirochete population downregulate OspA during any period of the transmission bloodmeal [4]. Most of the remaining spirochetes highly express OspC, an indication that BosR is actively expressed, but they do not show OspA downregulation. Given these previous observations, the process of inducing OspA downregulation should not be oversimplified just based on the fact B. burgdorferi readily shuts off OspA either during mammalian infection or being grown in the host-adapted conditions [31,34]. As a matter of fact, to induce OspA downregulation, BosR expression was increased to a level that nearly kills B. burgdorferi. Under this in vitro condition, OspA expression was significantly downregulated but was not shut off.
When cycling between the two distinct hosts, B. burgdorferi must adapt bacterial survival strategies to extremely different environments. Without a doubt, spirochetal adaptation must dramatically change its gene expression. Under normal conditions, complete OspA downregulation occurs only during mammalian infection, in which OspC and other RpoS-dependent Osps are dramatically upregulated. The mammalian host apparently provides an extreme environment as these specific alternation signals, which may be unachievable under any in vitro conditions. While either excessive RpoS or BosR expression is lethal to B. burgdorferi in vitro, these high levels of expression may be essential for the pathogen to achieve downregulation of the ospAB operon and to greatly upregulate RpoS-dependent virulence factors, and ultimately allow B. burgdorferi to survive better in the mammalian host. To achieve OspA downregulation in B. burgdorferi grown in vitro, a high level of BosR expression in combination with simultaneous expression of OspC and other Osps may be required.
One feature of B. burgdorferi is to coat itself with lipoproteins. A decade ago, we hypothesized that the pathogen must maintain its Osp expression level in order to keep it viable [35]. In other words, B. burgdorferi must upregulate other Osps to compensate for the loss resulting from downregulation of some Osps. Our previous study designed based on the hypothesis successfully revealed dramatic upregulation of VlsE with OspC expression being shut off by B. burgdorferi reacting to an amounting specific humoral response [35]. Another study based on the same hypothesis successfully restored OspC-deficient spirochetes with infectivity by increasing expression of an Osp, such as OspA, VlsE, DbpA or ErpA [36]. Based on the same hypothesis, we designed experiments and modified the DrpoS spirochete to simultaneously expression BosR and three major Osps to successfully achieve full shutoff of OspA in B. burgdorferi grown under in vitro conditions. As a key regulator, BosR, like RpoS, must be strictly regulated. As the current study demonstrated, BosR causes cell death when expressed at a very high level as RpoS does [27]. The cell death caused by excessive RpoS expression may be simply attributed to s factor competition, but there is no simple explanation for BosRrelated death. While the biological significance of induced cell death remains to be addressed, the possibility that it is to control cell populations less diverse in the same environment should be considered. For instance, the death strategy would select out subpopulations with a phenotype that highly expresses RpoS-or BosR-dependent genes when in the tick vector. However, cell death resulting from increased RpoS or BosR expression is observed only in vitro. Given that B. burgdorferi cycles between the extremely different environments encountered in the tick vector and a mammal, in vitro growth conditions may only constitute an abnormal environment. As emphasized above, it is possible that a high level of BosR and RpoS expression may provide an essential strategy for the pathogen to survive. Especially during infection of the mammalian host, B. burgdorferi may have to highly produce BosR to achieve shutoff of OspAB expression, as well as dramatic upregulation of RpoS-dependent virulence genes, in order to adapt to the extreme environment.
An RpoS-deficient background was used initially to rule out any involvement of RpoS in OspA downregulation, as a previous study suggested the alternative s factor may be involved in the regulation [14]. The current study clearly showed that there is no direct involvement of RpoS in OspA downregulation. BosR positively affects expression of many Osps, including OspC, DbpA and DbpB, through activation of RpoS expression [17,18]. We did expect that induced BosR expression would more effectively cause downregulation of OspA in 13A/bosR in than DrpoS/bosR in as BosR also increases RpoS expression, which, in turn, increases OspC, DbpA and DbpB expression and increased production of these Osps would compensate for the loss of OspAB. However, the current study showed that induced BosR more effectively causes OspA downregulation in DrpoS/bosR in than 13A/bosR in , suggesting that gene regulation in B. burgdorferi is more complicated than previously thought. Our immunoblotting result showed BosR expression significantly stronger in the RpoS-deficient background than in 13A/bosR in , suggesting that the presence of RpoS may produce a negative feedback on BosR expression. Such a feedback may include multiple regulators, which are either directly or indirectly regulated by RpoS.
As a critical regulator, BosR binds the rpoS promoter region and activates its transcription with an involvement of other regulators, such as RpoN. The current study demonstrated that via binding of the two regulatory sequences of the ospAB operon, BosR shuts off gene expression. Elucidating the function of this regulator, which operates in two opposite ways, remains to be addressed. Our previous study showed the presence of cisI and cisII enhanced ospA transcription in spirochetes grown in vitro, albeit the effect was very minor, suggesting that BosR may be involved in upregulation of the gene, suggestive of another regulatory function of BosR when it is expressed at a relatively low level [15].
Taken together with our previous study showing that the presence of both cisI and cisII is required for maximum ospA downregulation in the murine host [15], the current study clearly demonstrates BosR functioning as a repressor of the ospAB operon by binding both regulatory elements and shutting off OspA expression. In combination with a series of studies by others showing that BosR positively regulates many Osps via upregulation of RpoS [17,19], the current study provides sufficient evidence allowing for the conclusion that BosR, in general, functions as a coordinator by indirectly upregulating RpoSdependent Osps, such as OspC, DbpA and DbpB, and directly repressing expression of OspAB.