Immunoreactivity of the AAA+ chaperone ClpB from Leptospira interrogans with sera from Leptospira-infected animals
© The Author(s). 2016
Received: 24 February 2016
Accepted: 12 July 2016
Published: 16 July 2016
Leptospira interrogans is a spirochaete responsible for leptospirosis in mammals. The molecular mechanisms of the Leptospira virulence remain mostly unknown. Recently, it has been demonstrated that L. interrogans ClpB (ClpBLi) is essential for bacterial survival under stressful conditions and also during infection. The aim of this study was to provide further insight into the role of ClpB in L. interrogans and answer the question whether ClpBLi as a potential virulence factor may be a target of the humoral immune response during leptospiral infections in mammals.
ClpBLi consists of 860 amino acid residues with a predicted molecular mass of 96.3 kDa and shows multi-domain organization similar to that of the well-characterized ClpB from Escherichia coli. The amino acid sequence identity between ClpBLi and E. coli ClpB is 52 %. The coding sequence of the clpB Li gene was cloned and expressed in E. coli BL21(DE3) strain. Immunoreactivity of the recombinant ClpBLi protein was assessed with the sera collected from Leptospira-infected animals and uninfected healthy controls. Western blotting and ELISA analysis demonstrated that ClpBLi activates the host immune system, as evidenced by an increased level of antibodies against ClpBLi in the sera from infected animals, as compared to the control group. Additionally, ClpBLi was found in kidney tissues of Leptospira-infected hamsters.
ClpBLi is both synthesized and immunogenic during the infectious process, further supporting its involvement in the pathogenicity of Leptospira. In addition, the immunological properties of ClpBLi point to its potential value as a diagnostic antigen for the detection of leptospirosis.
Leptospira interrogans belongs to pathogenic spirochaetes causing a serious disease in both humans and animals known as leptospirosis that is considered the most widespread zoonosis of worldwide importance . The vectors of this pathogen are mostly wild rodents and domestic animals, which harbor the spirochetes in the proximal renal tubules of the kidneys and chronically excrete the leptospires with urine into the environment . It is worth noting that leptospirosis is also a serious economic problem, because it causes abortions, stillbirths, infertility, failure to thrive, reduced milk production, and death in domestic animals such as cows, pigs, sheep, goats, horses and dogs [3–6]. In humans the disease varies from an asymptomatic flu-like illness to an acute life-threatening infection. Despite its severity and global importance, the molecular mechanisms of leptospiral pathogenesis remain largely unknown . To date, only a few proteins have been identified as potential virulence factors in Leptospira. Among them, there is the chaperone ClpB, a member the Hsp100/Clp subfamily of the AAA+ ATPases that reactivates stress-aggregated proteins in cooperation with the DnaK system . Recently, ClpB from L. interrogans (ClpBLi) has been shown to be essential for bacterial survival under stressful conditions (nutrient restriction, oxidative and heat stresses) and also for the pathogen’s virulence . The involvement of ClpB in the response of L. interrogans to oxidative stress suggests that this chaperone may be one of key mediators of stress resistance, which is a prerequisite for Leptospira pathogenesis. The present study provides further insight into the role of ClpBLi during the infectious process. It is known that heat shock proteins (Hsps) play important roles during bacterial infections. They help pathogens to overcome stressful conditions to which they are exposed within the host cells, and represent major targets of the host’s immune system. Taking into account the fact that the chaperone ClpB from some pathogenic bacteria, Francisella tularensis and Mycoplasma pneumoniae, has been shown to be immunoreactive [9, 10], we decided to investigate an immunogenic potential of ClpBLi, which could point to this chaperone’s role in the pathogenicity of Leptospira and may translate into diagnostic applications.
We studied archived serum samples from rabbits and cattle. Rabbit antisera (n = 8) against L. interrogans serovars: Icterohaemorrhagiae, Hardjo, and Canicola, and L. borgpetersenii serovars: Hardjo, Javanica, were prepared as described by . Polyclonal rabbit antiserum prepared against the L. interrogans ClpB (residues 158–334; anti-ClpBLi158–334 serum)  and provided by M. Picardeau was used as a positive control and the pre-immune serum was used as a negative control. Bovine sera were collected from cattle (n = 10) experimentally infected with L. borgpetersenii serovar Hardjo via conjunctival instillation of 1 x 106 bacteria. Blood samples were collected 28 days after the challenge and in one case 210 days after the challenge (this serum was used as a positive control showing the highest OD in ELISA). Sera from uninfected cattle (n = 8) and also a fetal bovine serum were used as negative controls. To confirm the serological status of leptospiral infection, the sera were subjected to the microscopic agglutination test (MAT) [11, 12] and used at dilutions 1:100 for Western blotting or 1:200 for ELISA.
Kidney homogenate preparation
For detection of ClpBLi in kidney tissues from Leptospira-infected hamsters, the kidneys were macerated with nine parts of a 1 % BSA diluent and inoculated into Tween80/40/ LH semi-solid medium. Cultures were incubated at 28–30 °C, for up to 10 weeks and examined weekly by dark-field microscopy to detect the growth of leptospires. The same macerated kidney tissues (20 μg sample of homogenate) were used for Western-blotting analysis. Total protein concentration in the homogenates was determined by the method of Bradford .
Plasmid construction for protein overproduction
L. interrogans clpB gene (2583 bp) was amplified from genomic DNA of L. interrogans by PCR using AccuTaq LA polymerase MIX (Sigma) with the following primers: CATATGAAATTAGATAAACTTACATCCAAATT with the NdeI restriction site underlined, and AAGCTTTTAAACTACAACAACTACC with the HindIII restriction site underlined. DNA primers were synthesized by Genomed S.A. (Warsaw, Poland). First, the PCR product was cloned into pJET1.2 blunt vector (Fermentas), then digested with NdeI, HindIII, and ligated with the linearized pET NdeI-HindIII vector. The sequence of the resulting construct was confirmed by DNA sequencing (Genomed S.A.). Leptospira genomic DNA was extracted with a QIAamp DNA Mini Kit (Qiagen).
DNA plasmid preparation and transformation of E. coli cells were done according to .
Purification of the recombinant ClpBL
L. interrogans ClpB protein was overproduced in E. coli BL21(DE3) strain (Novagen) and purified according to the procedure similar to that used to obtain ClpB from Ehrlichia chaffeensis . Briefly, bacteria were grown at 37 °C to OD600 = 0.6 and then induced with 0.5 mM IPTG for 2 h. Next, the cells were collected and suspended in 50 mM Tris–HCl (pH 7.4), 300 mM NaCl, 20 mM imidazole and 0.1 % Triton X-100, then disrupted by sonication in the presence of the protease inhibitor PMSF and centrifuged to collect the soluble extract. Next, polyethyleneimine (PEI) was added to precipitate nucleic acids. After centrifugation (20 000 g, 1 h), the supernatant was applied to a Ni-NTA column (Qiagen) and the bound protein was eluted with 50 mM Tris–HCl (pH 7.4), 300 mM NaCl, and 0.1 % Triton X-100 and 250 mM imidazole. Fractions containing a 6His-tagged ClpBLi (a calculated molecular mass of 98 488.59 Da) were identified with SDS-PAGE electrophoresis and Coomassie blue staining, then combined and further purified by gel filtration on Superdex 200 (Sigma) equilibrated with 50 mM Tris–HCl (pH 7.5), 10 % glycerol, 1 mM EDTA and 1 mM DTT. The pooled fractions containing ClpBLi were dialyzed against dialysis buffer (50 mM Tris–HCl pH 7.5, 1 mM EDTA, 1 mM DTT, 20 mM MgCl2, 200 mM KCl, 10 % glycerol) and stored at −70 °C. The N-terminal histidine tag was removed by proteolytic digestion using the Thrombin Cleavage Capture Kit (Novagen) according to the manufacturer’s protocol. The identity of the purified ClpBLi was confirmed by a liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis of tryptic peptides obtained after trypsin cleavage of the protein, performed at the MS LAB IBB PAN (Warsaw, Poland). The equipment used was sponsored in part by the Centre for Preclinical Research and Technology (CePT), a project co-sponsored by European Regional Development Fund and Innovative Economy, The National Cohesion Strategy of Poland.
SDS-PAGE and Western blotting analysis
To assess immune reactivity of ClpBLi, SDS-PAGE electrophoresis was performed according to  using 10 % polyacrylamide gels and Western blotting was performed as described . The blots were blocked with 0.1 % Tween 20 in Tris-buffered saline (TBS) for 1 h at room temperature and then incubated overnight at 4 °C with anti-ClpBLi158–334 serum (1: 2000 dilution)  or polyclonal rabbit and bovine sera (1:100 dilution) against Leptospira strains. After primary antibody incubation, the blots were washed three times with TBS containing 0.05 % Tween 20 and incubated for 1 h at room temperature with the goat anti-rabbit IgG horseradish peroxidase (HRP) conjugate (Sigma) diluted 1: 3000 or the polyclonal rabbit anti-cow Ig/HRP conjugate (DakoCytomation) diluted 1: 1000. The blots were then washed three times as described above and were developed using 3,3′-diaminobenzidine (Sigma), and H2O2 as substrates.
ELISA (enzyme-linked immunosorbent assay), was performed to analyze the immune response in animals experimentally exposed to L. interrogans serovars. Costar 96 well EIA/RIA polystyrene high-binding plates were coated with 100 μl of 0.625 μg/ml of the recombinant ClpBLi (a capture antigen) resuspended in phosphate-buffered saline (PBS) by incubation overnight at 4 °C. The plates were then washed five times with PBST buffer (PBS containing 0.05 % Tween 20) and non-specific binding sites were blocked by incubation with 100 μl of 0.1 % Tween 20 in PBS buffer for 1 h at room temperature. The wells were washed five times with PBST buffer. Control and duplicate animal serum samples were diluted 200-fold in PBST buffer and 50 μl of the diluted sera (in duplicate) were applied to each well and incubated at 37 ° C for 1 h, followed by five rinses with PBST buffer. Next, secondary HRP-conjugated anti-rabbit (Abcam) (diluted 1:10 000) or anti-cow IgG (DakoCytomation) (diluted 1:2000) were added to each well and incubated for 1 h at 37 °C. The plates were then washed five times with PBS buffer and 3,3′,5,5′-tetramethylbenzidine (TMB) (Sigma-Aldrich) was added to detect the antibodies. The reaction was stopped after 10 min by the addition of 50 μl of 1 M H2SO4. The absorbance at 450 nm was measured using PerkinElmer Multimode Plate Reader (Enspire). The assay was performed three times for each serum.
The statistical significance of differences between the ELISA results obtained for sera collected from uninfected and infected animals were determined using the Welch’s adjusted one-way ANOVA followed by the post-hoc Scheffe multiple comparison test. P < 0.05 was considered statistically significant. Results of data analysis are presented in the graphs as the median values. All statistical analyses were performed using STATISTICA PL program.
Analysis of the amino-acid sequence of the molecular chaperone ClpB from L. interrogans
Expression of the clpB Li gene in E. coli cells and purification of ClpBLi
Immunogenic capacity of ClpBLi
Detection of ClpBLi in Leptospira-infected animals
In summary, our data indicate that the molecular chaperone ClpBLi is immunogenic and detectable in animals infected with pathogenic Leptospira spp.
Leptospires like many other pathogenic bacteria are exposed to a significant stress during infection of host cells, frequently resulting in protein misfolding and aggregation. Despite being exposed to stressful conditions, pathogens survive, overcome host defense mechanisms, and cause the disease symptoms. The specific mechanisms of the host invasion by leptospires are not well defined. In particular, the molecular basis for virulence remains unknown, due to the lack of genetic tools for the manipulation of Leptospira. The fact that ClpB is usually up-regulated in pathogenic microorganisms [8, 15] suggests that the disaggregase activity of ClpB may be essential for their virulence. Moreover, the involvement of ClpB in the response of L. interrogans to oxidative stress  suggests that this chaperone may be one of key mediators of stress resistance, which is a prerequisite for Leptospira pathogenesis. The chaperone ClpB may function either as a true virulence factor directly involved in causing the disease or a virulence-associated protein that can be essential for colonization of the host. Virulence gene products are often immunogenic and responsible for acquired immunity that protects against disease . At this point it should be also noted that molecular chaperones despite their cytosolic localization are strongly immunogenic in a number of bacterial infections . It has been reported that some chaperones (e.g. GroEL) may be associated with the outer membrane of the pathogenic bacteria or exported from the bacterial cell after heat shock . Therefore, exposure of bacterial Hsps to the host’s immune system is possible during infection. Indeed, ClpB from some pathogens (i.e. Mycoplasma pneumoniae, Francisella tularensis) is an immunoreactive protein [9, 10]. The total sequence identity between ClpB proteins from these pathogens is only ~40 %. It is likely that ClpB as an important mediator of resistance to oxidative stress could be also a potential target for the host immune response during leptospiral infections in mammals. Therefore, we decided to investigate an immunogenic potential of this chaperone in Leptospira. The use of the E. coli expression system allowed us to produce the recombinant ClpBLi protein and to assess its immune reactivity with sera collected from Leptospira-infected animals and the uninfected healthy controls. Our results show that ClpB is immunogenic during leptospiral infections because it was recognized by sera collected from experimentally infected animals (see Figs. 4 and 5). Thus, among the antibodies raised against leptospiral proteins, there were specific antibodies against ClpBLi. This is the first study where ClpB from pathogenic Leptospira species was evaluated for its ability to elicit immune responses in animals. Moreover, our results suggest that ClpBLi could be considered as a potential antigen candidate for a diagnostic test. We postulate that the presence of species-specific domains (e.g. ND or MD, see Fig. 1) in the antigen could minimize a cross-reactivity of antibodies with ClpB from different bacteria. Further prospective studies are needed to assess the ClpBLi’s predictive value in leptospirosis diagnostics. In addition, the presence of ClpBLi in the infected hamster kidney tissues (see Fig. 6) demonstrates that the chaperone is produced by pathogen during infection of the host further confirming the involvement of ClpB in the pathogenicity of Leptospira.
Identification of Leptospira virulence factors and understanding their properties is crucial for uncovering the diseases mechanisms. This study underlines the potential importance of the chaperone ClpB in leptospiral infections. We believe that our data provide new information, which may lead to a better understanding of the role of ClpB and possibly other stress-response factors in the life cycle of the pathogenic bacterium L. interrogans. It is worth noting that since ClpB does not exist in animal cells, it might become a promising target for novel therapies against pathogenic Leptospira species. Further studies are needed to determine the biological role of ClpB during leptospiral infection in mammals and its diagnostic or even immunoprotective potential. The recombinant ClpBLi produced in this work will help in further biochemical characterization of this chaperone and the analysis of its function in the pathogen.
We thank M. Picardeau (Institut Pasteur, Unité de Biologie des Spirochètes) for the generous gift of ClpBLi antiserum. We are very grateful to S. Barańska (University of Gdańsk) for her excellent assistance in the statistical analyses.
This work was supported by the Preludium Grant number 2015/17/N/NZ6/03493 (to JK) from the National Science Center (Poland).
Availability of supporting data
The DNA sequence of L. interrogans clpB gene was retrieved from the EMBL-EBI (accession number AAS70592.1) website (http://www.ebi.ac.uk/ena/data/view/AAS70592). The protein sequences of L. interrogans and E. coli ClpB were retrieved from UniProtKB (accession number Q72QU2 (CLPB_LEPIC)/http://www.uniprot.org/uniprot/Q72QU2 and P63284 (CLPB_ECOLI)/ http:// www.uniprot.org/uniprot/P63284).
JK, ZA, DW performed the experiments. SKM designed the experiments, analyzed the data and drafted the manuscript. MZ assisted in data analyses and the preparation of manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The sera and kidney tissues used in this work were originally collected during another study (project license number PPL2608, date of approval 15 October 2008). All operators involved in the study, protocols, and premises were licensed under the Animals (Scientific Procedures) Act (1986) (ASPA).
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