- Research article
- Open Access
Isolation and characterization of Ehrlichia chaffeensis RNA polymerase and its use in evaluating p28 outer membrane protein gene promoters
© Faburay et al; licensee BioMed Central Ltd. 2011
- Received: 2 December 2010
- Accepted: 22 April 2011
- Published: 22 April 2011
Ehrlichia chaffeensis is a tick-transmitted rickettsial pathogen responsible for an important emerging disease, human monocytic ehrlichiosis. To date how E. chaffeensis and many related tick-borne rickettsial pathogens adapt and persist in vertebrate and tick hosts remain largely unknown. In recent studies, we demonstrated significant host-specific differences in protein expression in E. chaffeensis originating from its tick and vertebrate host cells. The adaptive response of the pathogen to different host environments entails switch of gene expression regulated at the level of transcription, possibly by altering RNA polymerase activity.
In an effort to understand the molecular basis of pathogen gene expression differences, we isolated native E. chaffeensis RNA polymerase using a heparin-agarose purification method and developed an in vitro transcription system to map promoter regions of two differentially expressed genes of the p28 outer membrane protein locus, p28-Omp14 and p28-Omp19. We also prepared a recombinant protein of E. chaffeensis σ70 homologue and used it for in vitro promoter analysis studies. The possible role of one or more proteins presents in E. chaffeensis lysates in binding to the promoter segments and on the modulation of in vitro transcription was also assessed.
Our experiments demonstrated that both the native and recombinant proteins are functional and have similar enzyme properties in driving the transcription from E. chaffeensis promoters. This is the first report of the functional characterization of E. chaffeensis RNA polymerase and in vitro mapping of the pathogen promoters using the enzyme. This study marks the beginning to broadly characterize the mechanisms controlling the transcription by Anaplasmataceae pathogens.
- Electrophoretic Mobility Shift Assay
- Sigma Factor
- Core Enzyme
- Electrophoretic Mobility Shift Assay Experiment
- Human Monocytic Ehrlichiosis
Ehrlichia chaffeensis is an obligate intracellular rickettsial pathogen and the causative agent of an important emerging zoonotic disease, human monocytic ehrlichiosis [1–4]. This Amblyomma americanum tick-transmitted pathogen causes infections in susceptible hosts (humans), host reservoirs (white-tailed deer), and less well described hosts such as the dog, goat and coyote [5–10]. E. chaffeensis has an unusual developmental cycle that requires growth and replication within eukaryotic cells of vertebrate and tick hosts . During its developmental cycle, there is conversion between two distinct morphological forms, the elementary bodies (EBs) and reticulate bodies (RBs) [12, 13]. The EBs are the infectious form and upon entry into a host cell, they differentiate into metabolically active reticulate bodies (RBs), which are larger compared to EBs and divide by binary fission [12–14]. The reticulate bodies are also non-infectious forms . Later in the developmental cycle, RBs convert back to EBs, which are released from infected cells [12, 14]. The transformation of RBs to EBs by E. chaffeensis is observed in both vertebrate and tick hosts .
The mechanism by which the pathogen survives in dual hosts by adapting to changes in different host environments is unclear. Recent studies described the differential gene and protein expression profiles of the pathogen originating from tick and mammalian cell environments [15–18]. Moreover, E. chaffeensis organisms recovered from infected tick cells produce longer-lasting infections in mice compared to the infection with organisms harvested from mammalian macrophages . Differentially expressed proteins of E. chaffeensis included the predominant expression from outer membrane protein genes p28-Omp19 and p28-Omp14 in mammalian and tick cell environments, respectively [15–19]. The adaptive response to different host environments requires altering the gene expression, often regulated at the transcriptional level by altering RNA polymerase (RNAP) activity . A typical bacterial RNAP consists of five polypeptide chains; two α subunits, one each of β and β' subunits, and a σ subunit. The enzyme can take two forms, a holoenzyme containing all four different subunits or core polymerase that lacks a σ subunit . The capacity to synthesize RNA resides in the core polymerase and the role of a σ subunit is to direct initiation of transcription from specific promoters [22, 23]. The genome of E. chaffeensis includes two sigma factor genes; the homologs of the major bacterial sigma factor, σ70, and an alternative sigma factor, σ32 . The current lack of established methods to stably transform, transfect, conjugate, or electroporate E. chaffeensis remain a major limiting factor to study mechanisms of gene expression by traditional methods. Mapping the functions of E. chaffeensis genes in vivo cannot be performed because genetic manipulation systems are yet to be established. To overcome this limitation, in a recent study we reported the utility of Escherichia coli RNAP as a surrogate enzyme to characterize E. chaffeensis gene promoters . Although the E. coli RNAP proved valuable for mapping E. chaffeensis gene promoters, the extrapolation of the data requires further validation using the E. chaffeensis RNAP.
In this study, we developed a functional in vitro transcription system by utilizing G-less transcription templates  to drive transcription from two E. chaffeensis promoters. We described the partial purification and characterization of E. chaffeensis RNAP and its use in characterizing the transcriptional profiles of two p28-Omp gene (p28-Omp) promoters. In this study, we also described the recombinantly expressed E. chaffeensis sigma factor, σ70, and its use in promoter analysis studies after its reconstitution with E. coli core enzyme. Modulatory effect of E. chaffeensis protein lysates on in vitro transcription is also described in this study to serve as the first step towards determining the regulatory mechanisms underlying gene expression in this pathogen.
Isolation of E. chaffeensis RNA polymerase (E. chaffeensisRNAP)
Primer pairs and probes used in this study
For cloning p28-Omp14 and p28-Omp19promoters into pMT504
For cloning RpoD gene into pET32
For TaqMan RT-PCR of test G-less transcripts
RRG765 (TaqMan Probe)
For TaqMan RT-PCR of control G-less transcripts
RRG768 (TaqMan Probe)
For sequencing pRG198
p28-Omp14 promoter EMSA probes
Full length probe
Probe 1 (P1)
Probe 2 (P2)
Probe 3 (P3)
Probe 4 (P4)
Probe 5 (P5)
p28-Omp19 promoter EMSA probes
Full length probe
Probe 6 (P6)
Probe 7 (P7)
In vitro transcription by recombinant E. chaffeensis-σ70
Modulation of E. chaffeensisRNAP activity by whole-cell protein
Effect of macrophage-culture grown E. chaffeensis whole-cell lysate on the transcription of p28-Omp14 (pRG147) and p28-Omp19 (pRG198) promoter constructs quantitated by densitometry and real-time RT-PCR (fold change)
(x ± std)
(x ± std)
(Ct ± std)
(Ct ± std)
83.3 ± 1.8
45.5 ± 1.9
17.51 ± 0.81
16.64 ± 0.23
76.9 ± 1.7
35.7 ± 1.6
17.48 ± 0.08
16.27 ± 0.06
EMSA analysis of upstream sequences of p28-Omp14 and p28-Omp19promoters
A major impediment to the study of regulation of gene expression in the human monocytic ehrlichiosis pathogen, E. chaffeensis, is the absence of an experimental genetic manipulation system due to the inability to stably transform the organism. To partially overcome this constraint, we constructed plasmid transcription templates by transcriptional fusion of p28-Omp14 and p28-Omp19 promoters to a G-less transcriptional template and isolated E. chaffeensis RNAP to create a system for transcriptional analysis in vitro, similar to studies reported for Chlamydia species [20, 26, 32–35]. We adapted the bacterial RNAP purification methods reported in the literature [21, 27, 36, 37] to recover functionally active E. chaffeensis RNAP. The procedure has been modified from a single-column purification method used for RNAP from E. coli, Bacillus subtilis, Chlamydia trachomatis, Rickettsia prowazekii and to recover the enzymes from several other bacterial organisms [21, 27, 37]. The purification steps involved the use of sodium deoxycholate, a bile salt often used in cell lysis but reportedly effective in the isolation of membrane proteins and in affinity chromatography by preventing non-specific binding . This property may be critical for the recovery of active enzyme, since previous studies in R. prowazekii, a closely related species, showed that up to 62% of total RNAP activity was associated with membrane proteins . The heparin-agarose purification step is known to remove RNAP inhibitors and endogenous DNA . The recovered E. chaffeensis enzyme showed transcriptional activity for both p28-Omp14 and p28-Omp19 promoters and marked the first study describing RNAP activity of E. chaffeensis. SDS-PAGE profile suggested that the enzyme is partially pure and E. chaffeensis RNAP has a typical bacterial holoenzyme composition with five major subunits, α2, β, β', and σ.
The enhanced RNAP activity following addition of E. chaffeensis recombinant sigma 70 suggests that the preparation had less than stoichiometric amounts of the sigma factor, which is consistent with findings of the recovery of E. coli RNAP when employing similar procedures [22, 27]. Previous studies suggest that RNAPs purified by heparin-agarose chromatography methods are only about 30% saturated with the major sigma factor, σ70  and do not co-purify with alternative sigma factors, such as a σ32 homolog .
In this study, we presented evidence that the major E. chaffeensis sigma subunit, σ70, was also recognized by a heterologous E. coli anti-σ70 monoclonal antibody, 2G10. Functional studies with the 2G10 suggest that this antibody can effectively inhibit in vitro transcriptional activity of E. coli  and C. trachomatis RNAP holoenzymes . Similarly, this antibody inhibited the E. chaffeensis RNAP activity. These data are consistent with our bioinformatic analysis that the putative 2G10 antibody binding site sequences of E. coli and E. chaffeensis σ70 subunits of RNAP share high degree of homology. Transcriptional inhibition of the enzyme by the anti- σ70monoclonal antibody and rifampin, a potent inhibitor of prokaryotic RNAP [27, 38], demonstrates that the in vitro transcriptional activity in our study was due to the isolated E. chaffeensis RNAP.
Transcriptional profiles depicting salt tolerance of purified enzymes have been described for prokaryotes, such as, C. trachomatis and E. coli [20, 39]. In E. coli, transcription of a σ70-regulated promoter decreases dramatically between 100 mM and 150 mM potassium acetate , whereas σ66-dependent promoter activity of Chlamydia is completely inhibited at 400 mM concentration . The purified E. chaffeensis RNAP, reported in this study, also showed a similar range of salt tolerance as observed for other bacterial σ70 dependent RNAPs. For example, the enzyme showed optimum transcriptional activity at 80 mM sodium chloride, a slight difference from the optimal 50 mM concentration reported for the R. prowazekii RNAP . The minor differences in the salt tolerance properties may be unique to E. chaffeensis RNAP.
Previous studies suggest that RNAP fractions purified by heparin-agarose chromatography methods are typically about 30% saturated with the major sigma subunit . Thus the presence of free core enzymes in the preparation allows reconstitution studies or saturation with recombinant sigma factors to enhance transcription in vitro. Thus we prepared a purified recombinant E. chaffeensis σ70 subunit and used for assessing transcriptional activity by saturation of the native enzyme or by reconstitution with E. coli core enzyme. Saturation of the purified RNAP with the recombinant subunit resulted in enhanced transcriptional signals. Reconstitution of E. coli core enzyme with E. chaffeensis recombinant σ70 subunit had similar salt sensitivities to that of purified E. chaffeensis RNAP before and after saturating with the recombinant subunit. These data are consistent with earlier reports indicating that purified C. psittacci σ66 was effective in stimulating transcription by C. trachomatis and C. psittaci RNAP preparations  and highlights that E. coli core enzyme reconstituted with E. chaffeensis sigma factor offers an alternative approach to in vitro characterization of E. chaffeensis promoters as described for C. trachomatis [20, 33]. Previously, we and others reported the use of E. coli system in characterizing the promoters of E. chaffeensis [25, 40]. The current study offers an additional advantage over the E. coli system in that it uses E. chaffeensis RNAP or E. coli core enzyme with E. chaffeensis recombinant σ70.
Regulation of gene transcription in prokaryotes involves a complex network and is controlled at the stage of RNA synthesis in which transcription factors (TFs) are key components [41, 42]. TFs play an important role in regulating the transcription of specific genes by acting on the DNA regulatory sequences within the gene promoters [41, 42]. When a transcription factor binds to a specific promoter, it can either activate or repress transcription [35, 43, 44]. To investigate the possible modulatory role of E. chaffeensis proteins on transcription of promoters of two differentially expressed genes, p28-Omp14 and p28-Omp19, we prepared E. chaffeensis whole-cell protein lysate from macrophage-derived bacteria and evaluated its effect on transcription in vitro. Addition of the macrophage cell infection-derived E. chaffeensis protein extracts resulted in enhanced transcription suggesting that promoters of the p28-Omp14 and p28-Omp19 genes may be regulated in response to changing environments of the pathogen. Importantly, the enhanced in vitro transcription observed in this study in response to addition of protein extracts suggests that the lysates contain transcription regulators. Given the differential expression of p28-Omp14 and p28-Omp19 genes  in vertebrate and invertebrate hosts, the hypothesis that promoters of these genes may be under both positive and negative regulation in response to the changing host environments is also plausible. This hypothesis requires additional investigations, including the evaluation of the impact of tick cell environment. As an organism may express diverse array of transcription factors, it is highly likely that E. chaffeensis may regulate its gene expression via modulating the expression of transcription factors in support of maintaining its existence in dual hosts. Transcription regulation of a gene is a dynamic process and is responsive to environmental cues under which TFs trigger regulation [39, 45–47]. This study shows the first evidence of stimulatory effect of E. chaffeensis whole-cell protein extract on the transcription of both p28-Omp14 and p28-Omp19 promoters in vitro. In our previous studies, we reported that the expression levels of the p28-Omp14 and p28-Omp19 genes are different in macrophage and tick cell environments [16, 19]. Although both the genes are transcriptionally active in macrophage host cell environment under in vitro and in vivo conditions, the expression levels for p28-Omp19 is higher for the bacteria in infected macrophages, whereas in tick cells p28-Omp14 is the predominantly expressed protein [16, 19]. Consistent with those observations, the promoter constructs of both p28-Omp14 and p28-Omp19 genes remained active and enhanced when E. chaffeensis protein lysates prepared from macrophage culture derived organisms were added. Additional investigations are needed to further define the differences in the expression levels for the p28-Omp14 and p28-Omp19 genes in macrophage and tick cell environments. A gene in a cell may be regulated by different TFs, and the contribution from different TFs may be variable under different environmental conditions . Thus, more detailed investigations are needed to map quantitative differences in the transcription and to further assess the complex regulatory network of transcription in E. chaffeensis.
The current study provides the first evidence suggesting that E. chaffeensis whole-cell protein lysates contain regulatory proteins which modulate transcription of p28-Omp14 and p28-Omp19 promoters in vitro. In support of further testing the hypothesis that E. chaffeensis whole-cell protein lysates contain proteins that bind to putative regulatory DNA sequences of these promoters, EMSA experiments were performed. A shift in mobility of DNA fragments was observed for several partial or complete DNA segments of the promoter regions of both p28-Omp14 and p28-Omp19 genes. These data suggest that the promoter region contained regulatory DNA sequences that allowed binding of one or more E. chaffeensis proteins. The binding was specific as the addition of specific competitors considerably reduced the shift and the addition of a non-specific protein did not cause a shift. The binding of E. chaffeensis regulatory proteins to the DNA segments spanning putative DNA binding elements is consistent with previous studies on this organism  as well as in several other bacteria, including Anaplasma phagocytophilum [50–52], C. trachomatis [34, 35]and B. subtilis [53, 54]in which interaction of regulatory proteins with regulatory sequences have been demonstrated. The identity of DNA binding proteins and the location of protein binding sites remain to be determined.
In this study, we developed in vitro transcription assays using a G-less cassette and described methods to isolate native RNAP and the recombinant RNAP σ70 subunit of E. chaffeensis. The value of using these tools in evaluating the promoters of two differentially expressed genes has been demonstrated. The application of these tools to the study of E. chaffeensis is new and important for furthering our understanding of the regulation of gene expression in this pathogen. Specifically, the tools will be valuable in studies to map specific interactions of E. chaffeensis proteins in driving differential gene expression influenced by vertebrate and tick host cell environments. This is the first report of in vitro transcription using native E. chaffeensis RNAP and E. coli RNAP core enzyme reconstituted with the recombinant E. chaffeensis σ70 subunit. This study marks the beginning of a greater effort to broadly characterize the mechanisms that control the transcription in Anaplasmataceae pathogens in support of their growth in vertebrate and tick hosts.
PCRs for amplification of E. chaffeensis p28-Omp14 and p28-Omp19 promoters were carried out in a 25 μl reaction volume containing 0.2 μM of each primer, 250 ng of purified E. chaffeensis (Arkansas isolate) genomic DNA, 400 μM of each of the four deoxyribonucleoside triphosphates, 1.5 mM MgSO4, 1x native HiFi PCR buffer (60 mM Tris-SO4, 18 mM (NH4)2SO4), 2.5 units HiFi polymerase. After the first denaturation step of DNA at 95°C for 2 min, amplification was carried out for 45 cycles of denaturation at 95°C for 30 s, annealing at 40°C for 30 s and extension at 72°C for 50 s and a final extension at 72°C for 2 min.
Construction of transcription plasmids
The plasmid pMT504 is a G-less cassette plasmid containing two transcription templates cloned in opposite directions to aid in driving transcription from promoters introduced upstream of the G-less cassette sequences . We constructed in vitro transcription templates, pRG147 and pRG198, by cloning the promoter regions of p28-Omp14 and p28-Omp19, respectively, into the pMT504 plasmid at EcoRV site (Figure 1). The promoter sequences selected for preparing these constructs included the sequences starting from the downstream first nucleotide of the termination codon of the upstream gene and up to the transcription start sites of the genes mapped in our previous study . Plasmid pRG147 contained a 553 bp promoter region of p28-Omp14 amplified from genomic DNA using primers RRG217 and RRG695 (Table 1). Similarly, plasmid pRG198 contained a 306 bp promoter region of p28-Omp19 amplified by primers RRG185 and RRG696. All oligonucleotide primers used in this study were designed from the genome sequence data  and were synthesized at Integrated DNA Technologies, Inc. (Coralville, Iowa). Reverse primers for promoter segments included the transcription start sites of the respective promoters but excluding any guanosine residue downstream of the transcription initiation sites. This is to avoid transcription termination caused by incorporation methylated guanosine triphosphate present in the transcription reactions (outlined below under in vitro transcription). The promoter inserts were also cloned in opposite orientation (pRG147R and pRG198R) to serve as negative controls to demonstrate promoter-specific in vitro transcription.
Transcription from pRG147, pRG198 or pMT504 plasmids results in a shorter 125-nucleotide transcripts encoded by a control transcription template positioned downstream of the Chlamydia trachomatis rRNA P1 promoter. The test transcription template contains a 153-nucleotide G-less cassette segments in the opposite direction to the control transcription template. This synthetic template results in the transcription of a 162-nucleotide transcript from the transcription start site for both the p28-Omp14 and 19 gene promoters. Supercoiled plasmids for use in the in vitro transcription assays were prepared using the QIAprep Spin Miniprep kit (Qiagen Inc., Valencia, CA) according to the manufacturer's instructions. The DNA sequences of the promoter templates were verified by restriction enzyme and sequencing analysis.
In vitrotranscription assays
In vitro transcription reactions were performed in a 10 μl final reaction volume with the following components; 50 mM Tris-acetate buffer pH 8.0 containing 50 mM potassium acetate, 8.1 mM magnesium acetate, 27 mM ammonium acetate, 80 mM NaCl, 2 mM DTT, 400 μM ATP, 400 μM UTP, 2.1 μM [α-32P]-CTP (800 Ci mmol-1 for radioisotope detection method) or 400 μM CTP (for detection and quantification by real-time reverse transcription PCR), 100 μM sodium salt of 3'-O-methylguanosine 5'-triphosphate, 18 units of RNasin, 5% glycerol, 0.13 pmol of supercoiled DNA template and 1 μl (360 ng) of heparin-agarose purified E. chaffeensis RNAP or 0.5 μl of 1:10 dilution of E. coli core enzyme (Epicenter, Madison, WI) or 0.5 μl of 1:10 dilution of E. coli σ70-saturated holoenzyme (Epicenter, Madison, WI). For enzyme salt tolerance assays, potassium acetate and NaCl concentrations were varied over a range from 0 to 600 mM and 0 to 120 mM, respectively. In transcription reactions using E. chaffeensis recombinant σ70, RNAP holoenzyme was reconstituted by adding 360 ng of recombinant protein to 0.5 μl of 1:10 diluted E. coli core enzyme. Holoenzyme formation was allowed to occur by incubating the mixture on ice for 20 min. To assess the modulatory effect on transcription, 4.0 μg of E. chaffeensis protein lysate (preparation described below) was incubated for 20 min at room temperature with the transcription reaction mixture in the absence of an RNAP to allow binding of proteins to DNA elements of promoter segments. Next, 1 μl of the purified E. chaffeensis RNAP was added to reaction mixture. In general, transcription reactions were incubated at 37°C for varying times of 7.5 min, 15 min or 30 min and the reactions were terminated by adding 7 μl of stop solution (95% formamide, 20 mM EDTA, 0.05% bromophenol blue and 0.05% xylene cyanol). Six microliters of the sample was electrophoresed on a 6% polyacrylamide sequencing gel containing 7 M urea. The gels were dried and transcripts were visualized by exposing an X-ray film to the gels. Autoradiographs were scanned on a HP SCANJET 5550 scanner (Hewlett-Packard®).
Isolation of E. chaffeensisRNAP
The RNAP isolation method was a modified version from the heparin-agarose procedure described in [21, 27, 55]. E. chaffeensis Arkansas isolate was grown in confluent DH82 cells (malignant canine monocyte/macrophage cells) in 300 cm2 culture flasks in 1 litre MEM tissue culture medium containing 7% fetal bovine serum (Gibco BRL®) and 1.2 mM L-glutamine . DH82 cultures infected with E. chaffeensis having predominantly reticulate bodies (RB) were harvested 48 h post-infection by centrifugation at 1,000 × g for 10 min at 4°C in an Eppendorf 5810R centrifuge. (All centrifugation steps were performed using this centrifuge.) The purification steps were all performed at 4°C. The pellet was resuspended in 25 ml sucrose potassium glutamate (SPG) buffer (218 mM sucrose, 3.76 mM KH2PO4, 7.1 mM K2HPO4, 5 mM potassium glutamate, pH 7.0) and host cells were lysed in a 40 ml Wheaton homogenizer with pestle A. The lysate was centrifuged at 800 × g for 10 min in 50 ml conical tubes to pellet host cell debris. Subsequent supernatant was centrifuged at 15,000 × g for 10 min to pellet the organisms. The RB pellet was resuspended in 2 ml of freshly prepared lysis buffer [10 mM Tris-HCl (pH 8.0), 10 mM MgCl2,1 mM EDTA, 0.3 mM dithiothreitol (DTT), 7.5% glycerol (vol/vol), 50 mM NaCl, 1x Amersham protease inhibitor mixture, and 150 μg per ml of lysozyme]. Lysis was facilitated by three passages through 27.5 G needle. Sodium deoxycholate (at final concentration of 0.05%) was added to the lysate and the suspension incubated for 30 min at 4°C. The lysate was centrifuged at 10,000 × g for 10 min and the supernatant was collected and clarified by an additional centrifugation step for 5 min.
The clarified supernatant was loaded onto pre-packed heparin-agarose column (type I-S, Sigma®) previously equilibrated with buffer A [10 mM Tris HCl (pH 8.0),10 mM MgCl2,1 mM EDTA, 0.3 mM DTT, 7.5% glycerol and 50 mM NaCl]. The suspension was adsorbed for 60 min at 4°C and the column was washed by gravity with 20 ml of buffer A for complete removal of unbound proteins. The bound proteins from the column were eluted by gravity with buffer A containing 0.6 M NaCl and 0.5 ml fractions were collected. Based on previous analysis and calculation of the void volume of the column, fractions 3-6 were pooled and dialyzed overnight against storage buffer [10 mM Tris-HCl (pH 8.0), 10 mM MgCl2, 0.1 mM EDTA, 0.1 mM DTT, 50% glycerol and 100 mM NaCl] using Slide-A-Lyzer Gamma Irradiated Dialysis Cassette (Thermo Scientific, Illinois, USA). The fractions were stored at -80°C. RNAP activity of the dialyzed fraction was determined by in vitro transcription assay.
Protein concentration of the HA purified RNAP fractions and E. chaffeensis whole-protein lysates were measured with the bicinchoninic acid protein assay reagent (Thermo Scientific, Illinois, USA) with bovine serum albumin as the protein standard.
Proteins were analyzed by electrophoresis in 7.5% sodium dodecyl sulphate-polyacrylamide gel (SDS-PAGE), followed by silver staining according to the procedures provided by the manufacturer (G Biosciences, USA) or resolved proteins were transferred onto a nitrocellulose membrane, Hybond-ECL (Amersham Biosciences, Germany), for immunoblot analysis.
Western blot (immunoblot) of RNAP extracts
E. chaffeensis RNAP purified above was subjected to SDS-PAGE and the proteins were electroblotted for 2 h at 70 V to a sheet of nitrocellulose membrane. The membrane blot was blocked in a solution containing 10% nonfat dried milk (NFDM) freshly made in TTBS [0.1% Tween-20 in 100 mM Tris-HCl (pH 7.5) and 0.9% NaCl] for 1 h at room temperature with gentle agitation. The blot was rinsed three times in TTBS and then was incubated for 1 h at room temperature or overnight at 4°C with anti-E. coli σ70 antibody, 2G10 (Santa Cruz Biotechnology Inc., Santa Cruz, CA), diluted 1: 500 in 1% NFDM in TTBS solution. The blot was washed again three times with washing solution and then incubated for 1 h at room temperature with horseradish peroxidase-conjugated anti-mouse immunoglobulin G diluted 1:5000 in 1% NFDM in TTBS solution. The blot was rinsed again three more times with TTBS to remove excess secondary antibody and detection was carried out using chemiluminescent detection reagents (Amersham ECL™, GE Healthcare).
Properties of isolated E. chaffeensisRNAP
Assays to determine the salt tolerance of the purified enzyme have been described above. Rifampin/rifampicin is a potent inhibitor of prokaryotic RNAPs, but not for eukaryotic RNAP . As E. chaffeensis RNAP was recovered from organisms grown in eukaryotic cells (DH82), it may be potentially contaminated with eukaryotic RNAP. To confirm that the transcript formation is from E. chaffeensis RNAP but not from eukaryotic RNAP, in vitro transcription assays were performed in the presence of rifampin at a concentration of 25 μg ml-1.
Functional studies with an E. coli RNAP monoclonal antibody (2G10) demonstrated that it can effectively bind to E. coli σ70 and markedly inhibit in vitro transcriptional activity by RNAPs of E. coli  and C. trachomatis . To further assess that in vitro transcriptional activity was due to E. chaffeensis purified RNAP but not from eukaryotic RNAP, we utilized the E. coli monoclonal antibody 2G10 in inhibition assays assuming that it blocks the E. chaffeensis RNAP similar to C. trachomatis RNAP. For this experiment, 4 μg of 2G10-antibody was added in transcription reactions and the production of transcripts were assessed by following the methods described above.
Overexpression and purification of E. chaffeensis RpoD (σ70)
The entire RpoD (σ70 subunit gene) protein coding sequence, identified from the E. chaffeensis Arkansas isolate genome , was amplified by PCR and cloned into the pET32 plasmid (Novagen, Madison, WI) for producing recombinant protein. The PCR was performed using pfu DNA polymerase (Promega, Madison, WI) and with the gene-specific PCR primers, RRG742 and RRG 743 (Table 1). To facilitate directional cloning, NcoI and XhoI restriction enzyme sites were engineered in the PCR product. The PCR product was subsequently cloned into pET32 plasmid at the above restriction sites after digesting both plasmid and inserts and ligating using T4 DNA ligase. Over expression of RpoD protein and its purification was carried out with methods similarly described elsewhere [20, 57]. The concentration of the purified RpoD protein was approximately 180 ng/μl, as determined by protein estimation method (described above).
Quantification of transcription
We carried out quantification of in vitro-generated RNA transcripts of p28-Omp14 and p28-Omp19 promoters by densitometry and TaqMan probe-based real-time RT-PCR. For densitometric analysis, we quantitated the signal intensity of radio actively labelled transcripts on X-ray films using ImageQuant software 5.2 (Molecular Dynamics, Inc., Sunnyvale, CA). For real-time RT-PCR analysis, primers and TaqMan probes for the 162 and 125 nucleotide (nt) G-less cassettes were designed manually and optimized using Vector NTI Advance 11 software (Invitrogen, Carlsbad, CA). The primers and probes used for these assays were listed in Table 1. The TaqMan probe for the 162 nt cassette (RRG765) and the probe for the 125 nt cassette (RRG768) have been labelled with reporter fluorescent dyes TET and ROX and quencher dyes Iowa Black FQ and Iowa Black RQ-Sp, respectively. Real-time RT-PCR was carried out using the SuperScript™ III One-Step RT-PCR reagents (Invitrogen, Carlsbad, CA). Each RT-PCR reaction contained the following: 1x reaction mix (containing 200 μM dNTPs), 5 mM MgSO4, 100 nM of each primer, 150 nM of each TaqMan probe, 1 μl of SuperScript III reverse transcriptase/Platinum Taq mix and 1 μl of in-vitro transcribed RNA sample in a 25 μl volume. Reverse transcription was carried out for 30 min at 48°C followed by a denaturation step of 2 min at 95°C. The PCR amplification was then performed for 40 cycles with each cycle at 94°C for 15 s and 60°C for 30 s. All reactions were carried out in triplicate using a Smart Cycler system (Cepheid, Sunnyvale, CA). The threshold cycle, Ct, values of the samples (containing 4.0 μg of E. chaffeensis protein lysate) were averaged from values obtained from each reaction, and the promoter activity was calculated as a relative level of expression to the reference control in a separate tube. The relative level of expression was calculated using the mathematical model of relative expression ratio in real-time PCR under constant reference gene expression : Ratio = (Etarget)ΔCTtarget (control-sample) , where E represents the PCR efficiency of one cycle in the exponential phase and was calculated according to the equation: E = 10[-1/slope].
Preparation of E. chaffeensiswhole-cell soluble protein lysates
E. chaffeensis organisms were cultivated in vitro in canine macrophage (DH82) cell lines at 37°C or in ISE6 tick cells as described previously [18, 56]. The protocols for E. chaffeensis cell lysate preparations were similar to previously described methods for E. chaffeensis, A. phagocytophilum and other Gram negative bacterial organisms [49, 52, 58]. Twenty five ml of about 80-100% E. chaffeensis infected cultures were harvested using glass beads. The cultures were centrifuged at 15,560 × g for 15 min to recover infected host cells and cell free E. chaffeensis organisms. To release the organisms from host cells, the pellet was resuspended in 10 ml SPK buffer (0.5 K2HPO4, 0.5 M KH2PO4, and 0.38 M sucrose) and sonicated twice for 30 sec at a setting of 6.5 in a Sonic Dismembrator (Fisher Scientific, Pittsburgh, PA). The cell lysates were centrifuged at 400 × g for 5 min and the supernatant containing cell free E. chaffeensis was filtered through a 5 μm and 3 μm sterile isopore membrane filters (Millipore, Billerica, MA). The filtrate containing cell free organisms was centrifuged at 15,560 × g for 15 min at 4°C. The pellet containing E. chaffeensis organisms was washed twice with 1.5 ml of lysis buffer (150 mM Tris-HCl pH 8.0, 100 mM KCl, 10 mM Magnesium Acetate, 1 mM EDTA, 2 mM DTT and 10% glycerol) and the pellet was resuspended in 1 ml of lysis buffer containing protease inhibitors (Roche Diagnostic Labs, Indianapolis, IN). The cell suspension was sonicated four times at 8.5 setting, 30 sec each time to lyse E. chaffeensis organisms. The cell lysates were centrifuged at 15,560 × g for 15 min at 4°C to pellet the insoluble fraction and the supernatant containing soluble proteins of E. chaffeensis was collected into sterile micro centrifuge tubes as 25 μl aliquots containing protease inhibitor mix and stored at -80°C until use. Protein concentration of the protein lysates, prior to adding the protease inhibitor mix, was estimated as described above.
Electrophoretic mobility shift assay (EMSA)
DNA sequence segments spanning one or more putative regulatory sequences of p28-Omp14 or p28-Omp19 gene promoters were amplified from E. chaffeensis Arkansas isolate genomic DNA using sequence specific primers and 5'end biotin-labeled reverse primers (Table 1) and evaluated for their interaction with the protein lysates. EMSA experiments and detection were carried out according to established protocols [57, 58] with a radioactive nucleotide incorporated DNA probes or using the LightShift Chemiluminescent EMSA kit (Pierce Biotechnology, Rockford, Illinois, USA) according to the specifications of the manufacturer. The assay mixtures included a non-specific DNA (salmon sperm DNA or poly dI.dC at a high concentration of 240 μg/ml or 50 μg/ml, respectively) to eliminate non-specific interactions. Briefly, about 1 ng of each of the full length or biotin-labeled partial upstream sequences was used in each reaction together with 5 μg of the E. chaffeensis whole-cell protein lysate. About 50 ng of unlabeled specific probe sequences were used as competitors. Bovine serum albumin (BSA) was included in each experiment as a non-specific protein control. The protein concentration in E. chaffeensis protein lysates used in these experiments was similar to the work reported earlier [41, 49, 58].
We carried out two-tailed t-tests with equal variances for densitometry analysis and unequal variances for the real-time RT-PCR analysis to comparatively analyse the effect of addition of E. chaffeensis whole cell protein lysate on transcription of p28-Omp14 (pRG147) and p28-Omp19 (pRG198) promoters.
This work is supported by National Institutes of Health grant AI070908. We thank Dr. Ming Tan of the University of California, Irvine, CA for providing the G-less cassette parent plasmid, pMT504. We also acknowledge Chuanmin Cheng for her technical assistance. This manuscript is a contribution from the Kansas Agricultural Experiment Station, number 11-283-J.
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