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Leptospirosis is considered a re-emerging infectious disease caused by pathogenic spirochaetes of the genus Leptospira. Pathogenic leptospires have the ability to survive and disseminate to multiple organs after penetrating the host. Leptospires were shown to express surface proteins that interact with the extracellular matrix (ECM) and to plasminogen (PLG). This study examined the interaction of two putative leptospiral proteins with laminin, collagen Type I, collagen Type IV, cellular fibronectin, plasma fibronectin, PLG, factor H and C4bp.
We show that two leptospiral proteins encoded by LIC11834 and LIC12253 genes interact with laminin in a dose - dependent and saturable mode, with dissociation equilibrium constants (KD) of 367.5 and 415.4 nM, respectively. These proteins were named Lsa33 and Lsa25 (Leptospiral surface adhesin) for LIC11834 and LIC12253, respectively. Metaperiodate - treated laminin reduced Lsa25 - laminin interaction, suggesting that sugar moieties of this ligand participate in this interaction. The Lsa33 is also PLG - binding receptor, with a KD of 23.53 nM, capable of generating plasmin in the presence of an activator. Although in a weak manner, both proteins interact with C4bp, a regulator of complement classical route. In silico analysis together with proteinase K and immunoflorescence data suggest that these proteins might be surface exposed. Moreover, the recombinant proteins partially inhibited leptospiral adherence to immobilized laminin and PLG.
We believe that these multifunctional proteins have the potential to participate in the interaction of leptospires to hosts by mediating adhesion and by helping the bacteria to escape the immune system and to overcome tissue barriers. To our knowledge, Lsa33 is the first leptospiral protein described to date with the capability of binding laminin, PLG and C4bp in vitro.
Leptospirosis is a zoonosis caused by pathogenic species of the genus Leptospira. Greater incidence of human infection occurs in tropical and subtropical countries [1,2]. The transmission of leptospirosis has been correlated with exposure of individuals in close proximity to wild or farm animals [1,3]. Recently, the disease became prevalent in cities with sanitation problems and large urban rodent reservoirs that contaminate the environment through their urine .
Pathogenic Leptospira spp. have ability to adhere and rapidly disseminate within the host during the early stage of infection. Surface - associated proteins are potential targets to mediate host - pathogen interactions, and therefore are likely to elicit several activities, including adhesion. The adhesion of leptospires to ECM components of the host was considered to be essential in the initial stage of the infection . Indeed, we have reported that pathogenic leptospires are capable of binding several ECM molecules . To date, several leptospiral ECM binding adhesins have been described [6-18]. After the adhesion, pathogens have to overcome tissue barriers in order to reach blood circulation and organs. We have reported that leptospires have the ability of binding PLG at their surface and that plasmin (PLA) can be generated in the presence of activator . In addition, Verma and colleagues  and our group have described several leptospiral proteins as PLG - binding receptors [17,18,21]. More recently, we have reported that PLA generation on Leptospira decreased opsonization and that it might be an important aspect of the immune escape strategy and survival .
L. interrogans serovar Copenhageni genome annotation identified many unknown coding sequences predicted to be surface exposed proteins. Characterization of these proteins, with no previously assigned function, should increase our understanding of this intriguing pathogen’s biology. In this work, we present our studies with two leptospiral coding sequences, LIC11834 and LIC12253, named Lsa33 and Lsa25, respectively. The genes were cloned and the proteins expressed using E. coli. The recombinant proteins were purified and their ability to bind various ECM and serum components was evaluated. We report that these proteins are novel surface adhesins capable of binding to laminin. In addition, Lsa33 can also interact to PLG and both proteins bind the complement regulator of the classical pathway C4bp. We believe that these proteins are likely to be involved in Leptospira - host interactions.
The selected coding sequences, LIC11834 and LIC12253, are genome annotated as hypothetical proteins, and one of them, LIC11834, is a putative lipoprotein, having lipoprotein signal peptide (signal peptidase II) and a cleavage site between amino acids 17–18. According to SMART web server, LIC11834 has a signal peptide from 1 to 21 amino acids and a FecR domain from amino acid 60 to 162. PFAM predicts that this domain is involved in regulation of iron dicitrate transport and that FecR is probably a sensor that recognizes iron dicitrate in the periplasm. LIC12253 presents a signal peptide from amino acid 1 to 21 and a DUF1566 (Domain of Unknown Function) from amino acid 58 to 164 [23,24]. The LIC11834 coding sequence can be classified as alpha - beta protein, being the percentage of 36.57 for alpha-helix and 29.13 for beta strands secondary structure. In the case of coding sequence LIC12253, the protein can be classified as mixed, having a predicted secondary structure composition percent of 11.01, 19.38 and 69.60 for alpha - helix, beta strands and others, respectively. Cellular localization predicts as extra - cellular (non-cytoplasmic branch) for both proteins. The solvent accessibility composition (core/surface ratio) for the CDs LIC11834 and LIC12253 is expected to be 59.87 and 66.52% of amino acid residues exposed with more than 16% of their surface, respectively. All the predictions above were performed with PrecitedProtein web server [25,26]. The presence and identity of both coding sequences among Leptospira sequenced genomes are depicted in Table1.
The presence of LIC11834 and LIC12253 genes in pathogenic strains and in one saprophytic strain was examined by PCR with a pair of primers designed according to L. interrogans serovar Copenhageni genome sequences. The gene LIC11834 was amplified by PCR in all strains belonging to the pathogenic species excluding in L. santarosai serovar Shermani (Figure (Figure1A).1A). No DNA amplification was detected in the non - pathogenic L. biflexa serovar Patoc. In the case of LIC12253 gene, DNA band was amplified in all pathogenic strains and a less intense band was detected in the saprophytic strain (Figure (Figure1A).1A). The expression of LIC11834 and LIC12253 genes was evaluated by PCR amplification of reversely transcribed total RNA. LIC11834 gene product was detected only in L. interrogans specie serovars Canicola, Pomona, Copenhageni, Icterohaemorrhagiae and Hardjo. No expression was observed in non-pathogenic strain. LIC12253 gene expression could be identified in all pathogenic strain tested (Figure (Figure1B).1B). Integrity of total RNA used in RT - PCR experiments was assured by the presence of a 1,042 - bp 16S ribosomal cDNA fragment in all samples (Figure (Figure11B).
The amplified DNA sequences of LIC11834 and LIC12253 were cloned into an E. coli pAE vector  and the corresponding proteins were expressed as full-length with 6X His sequence tag at their N - terminal. Expression of recombinant proteins was elicited from cultures of E. coli BL21 SI after addition of NaCl (300mM). Recombinant protein Lsa33 is expressed in its soluble form, while Lsa25 is expressed in its insoluble form, as inclusion bodies (data not shown). Protein Lsa25 was recovered from inclusion bodies after solubilization with 8M urea. The purification was performed by metal chelating chromatography under normal (Lsa33) or denaturing condition, followed by refolding by gradually removal of urea (Lsa25). The proteins were recovered with 1.0M imidazol. Evaluation of protein purification has shown that most of the contaminants were washed away and proteins were represented as single major bands. The recombinant protein bands were further confirmed by western blotting probed with monoclonal anti - His tag antibodies and with polyclonal antiserum raised against each protein (data shown). The calculated 33.1kDa and 24.07kDa molecular masses of the recombinant proteins comprise the vector fusion plus the encoded amino acids. Structural integrity of the purified proteins was assessed by circular dichroism (CD) spectroscopy. The minima at 208 and 222nm, and the maximum at 192nm in the CD spectrum showed the high α - helical secondary structure content of both recombinant proteins (data not shown).
The assessment of the selected CDSs on the bacterial cell membrane was performed using living organisms and the liquid - phase immunofluorescence method. Leptospires were visualized by propidium iodide staining (Figure (Figure2,2, column A) followed by protein detection with polyclonal mouse antiserum raised against each protein in the presence of anti - mouse IgG antibodies conjugated to FITC. Green fluorescence could be observed in Figure Figure22 column B, for LIC11834, LIC12253 and LipL32, an outer membrane protein used as a positive control , but not with GroEL, a protoplasmic - cylinder marker, used as a negative control . The localization of the protein - green light lying on the leptospires was achieved by merging both fields and the results obtained are shown in Figure Figure2,2, column C.
We have performed proteinase K accessibility assay by using the previously described assay (37, 41) with some modifications. Live leptospires were treated with 25μg/ml of proteinase K and aliquots of the bacterial suspensions were taken at time 0, 1, 3 and 5h; the suspensions were sedimented and the ressuspended bacteria were used to coat microplates, followed by incubation with polyclonal antibodies against each protein, including the controls, LipL32 and DnaK, for outer  and cytoplasmic  protein. The reactions proceeded as described in Methods. The leptospiral coding sequences LIC11834 and LIC12253 were both susceptible to protease treatment after 1h incubation, similar to the positive control LipL32 (Figure (Figure3).3). Almost no reduction was observed with DnaK cytoplasmic protein (Figure (Figure33).
To examine whether LIC11834 and LIC12253 leptospiral coding sequences are able to elicit an immune response from an infected host, we evaluated the reactivity of the recombinant proteins Lsa25 and Lsa33 with antibodies present in serum samples of early (MAT -) and convalescent (MAT +) phases of leptospirosis patients. ELISA was performed using 24 and 33 serum samples of negative MAT and of positive MAT, respectively. The recombinant protein Lsa33 was almost non-reactive with samples from both phases of the disease (Figure (Figure4A),4A), while Lsa25 showed 46 and 48% reactivity for negative and positive MAT, respectively (Figure (Figure4B).4B). When the two proteins were assayed together, a small increment was observed for positive MAT samples (58%) (Figure (Figure4C).4C). Our data suggest that Lsa25 might be an interesting protein for early diagnose of leptospirosis.
The ability of Lsa33 and Lsa25 proteins to mediate host colonization by adhering to extracellular matrix proteins was examined by ELISA. Laminin, collagen Type I, collagen Type IV, cellular fibronectin, plasma fibronectin, and the control proteins fetuin and gelatin were immobilized on microdilution wells and recombinant protein attachment was assessed by ELISA using antibodies against the proteins. As shown in Figure Figure5A,5A, both recombinant proteins exhibited adhesiveness to laminin, while no statistically significant binding was observed with these proteins when wells were coated with collagen Type I and IV, cellular and plasma fibronectin, gelatin or with the highly glycosylated control protein fetuin. The interaction of recombinant proteins with laminin was also observed when anti - polyhistidine monoclonal antibodies were employed to probe the ligands (Figure (Figure5B).5B). The binding between Lsa33 and Lsa25 with laminin was also evaluated on a quantitative basis as depicted in Figure Figure5C.5C. A dose - dependent and saturable binding was observed when increasing concentrations of the recombinant proteins (0–6μM) were allowed to adhere to a fixed laminin concentration (1μg) (Figure (Figure5C).5C). Binding saturation level was achieved by protein concentration of ~4 and 5μM for Lsa33 and Lsa25, respectively. Based on ELISA data, the calculated dissociation equilibrium constants (KD) for the recombinant protein Lsa33 and Lsa25 with laminin is 367.5 and 415.4nM, respectively. The role of laminin sugar moieties in the binding with Lsa33 and Lsa25 was assessed with laminin previously oxidized by increasing concentrations of sodium metaperiodate, ranging from 5 to 100mM. The effect of metaperiodate concentration on the interaction is displayed in Figure Figure5D.5D. Laminin oxidation had some effect on the interaction with Lsa25, being the reduction of 40% achieved at the highest metaperiodate concentration employed (100mM). However, the attachment of Lsa33 to metaperiodate - treated laminin had no interference on the binding. These results indicate that the binding of the proteins to laminin occur in a different manner and that sugar residues contribute to some extent for the interaction of Lsa25 with this ECM glycoprotein.
Our group has recently reported that leptospires interact with PLG and that several proteins could act as PLG - receptors [17-19,21]. Protein binding to complement regulators factor H and C4bp have also been shown [31,32]. Therefore, we set out to evaluate whether the recombinant proteins Lsa33 and Lsa25 were capable of binding human PLG, factor H and C4bp in vitro. The components, human PLG, factor H and C4bp and the control proteins, gelatin and fetuin, were individually immobilized onto 96 - wells plates followed by incubation with the recombinant leptospiral proteins. The results obtained using polyclonal antibodies against each protein to probe the reactions showed that Lsa33 and Lsa25 interact with C4bp while only Lsa33 appears to bind to PLG (Figure (Figure6A).6A). No reaction was observed with factor H and the control proteins (Figure (Figure6A).6A). Similar results were achieved when binding was performed using monoclonal anti - his tag antibodies (Figure (Figure6B).6B). Both data show that while Lsa33 protein depicted a statistically significant absorption value for the interaction with PLG, the Lsa25 appears to have only a weak or no adherence to this component. These data were further confirmed when the reaction between the recombinant proteins and PLG were assessed on a quantitative basis as illustrated in Figure Figure6C.6C. Dose - dependent and saturable binding was observed when increasing concentrations (0 to 1.0μM) of the recombinant protein Lsa33 were allowed to adhere to a fixed PLG amount (1μg), while very low absorption was detected with Lsa25 (Figure (Figure6C).6C). Based on the ELISA data, the calculated KD for the recombinant proteinLsa33 with PLG is 23.53±4.66nM (Figure (Figure6C).6C). This KD value is in the same order of magnitude with the ones obtained with several recombinant proteins in our laboratory .
PLG bound to leptospires and to several recombinant proteins, acting as PLG receptor, can acquire proteolytic activity in the presence of an activator, as we have previously shown [17-19,21]. Therefore, we investigated whether Lsa33 bound to PLG could also generate the enzymatically active plasmin. As a negative control, we have included the recombinant protein Lsa63, previously shown to be non-reactive with PLG . Microplates were coated with the test protein, blocked, and then incubated with PLG. Unbound PLG was washed away and the urokinase - type PLG activator (uPA) was added together with a plasmin - specific chromogenic substrate. The reaction was carried out overnight and the plasmin activity was evaluated by measuring the cleavage of the substrate (absorbance at 405nm). As shown in Figure Figure6D,6D, the PLG captured by the Lsa33 protein could be converted into plasmin, as demonstrated indirectly by specific proteolytic activity. The negative controls Lsa63 and BSA did not show any proteolytic activity, similar to the controls lacking PLG, uPA or the chromogenic substrate.
The interaction of recombinant proteins with C4bp was studied in function of protein concentration. We have employed anti –Lsa33 and anti-Lsa25 polyclonal (Figure (Figure6E)6E) and anti-His tag monoclonal antibodies (Figure (Figure6F)6F) to probe the binding. Dose - response curves were obtained with both antibodies but the best response was achieved with anti-His tag monoclonal (Figure (Figure6F),6F), probably because of their homogeneous nature. However, C4bp was not saturated with the protein concentration range employed and therefore the KD could not be calculated. Lsa63, a His - tag recombinant protein that does not bind C4bp was also included, as a negative control, showed very low interaction and did not respond to increase protein concentration.
It has been reported that the several recombinant proteins with adhesin activity revealed an inhibitory effect on the binding of leptospires to ECM macromolecules . We therefore performed experiments to assess whether the recombinant proteins had an effect on the binding of Leptospira to laminin or PLG by employing ELISA to detect the interaction in function of protein concentration (0–10μg). The results demonstrate that the addition of increasing concentrations of Lsa33 reduced the leptospiral binding to laminin and to PLG molecules in a dose - dependent manner (Figure (Figure7A).7A). Binding decrease in the number of leptospires interacting to laminin and PLG was statistically significant with 1.25μg of Lsa33 (*, P<0.05). This interference was also evaluated with the binding of leptospires to laminin in the presence of increasing concentrations of Lsa25 (0–10μg), resulting in a similar effect as obtained with Lsa33 (*, P<0.05) (Figure (Figure7B).7B). We have also assessed the competition for the binding of Lsa33 to PLG by increasing laminin concentration (0 to 1.0μg). The results revealed that both ligands compete for the binding with Lsa33 as a decrease of 40% in the binding was already detected with 0.25μg of laminin (*, P<0.05) (Figure (Figure7C).7C). These experiments were performed in triplicate and Figure Figure77 shows one representative data of two independent experiments.
Complement is a key component of the innate immune system responsible for protection against pathogenic microorganisms . Factor H is a host fluid - phase regulator of the alternative complement pathway. Pathogenic leptospiral complement - resistant strains were found to bind factor H from human serum and this interaction seems to be associated to their serum resistance [31,34]. C4b - binding protein is an inhibitor of complement classical pathway system. This protein controls the complement classical pathway by interfering with the formation and regeneration of C3 convertase and acting as a cofactor to the serine proteinase factor I in the proteolytic inactivation of C4b [33,35]. It has been shown that pathogenic leptospiral strains can obtain C4bp from the host and that this acquisition preserves its cofactor activity . The surface bound C4bp elicits factor I mediated cleavage of C4b, an interaction that appears to contribute to complement resistance by Leptospira, through the classical route . Leptospiral binding proteins to C4bp, factor H and factor H - like have also been identified in Leptospira[9,31,32]. Interaction of C4bp and of factor H with other pathogens has been described, including the spirochetes Borrelia spp. [33,37-41].
The capacity of the leptospires to adhere to extracellular matrix components has been reported and to date, several leptospiral adhesins have been identified. These include 36 - kDa fibronectin - binding protein , LfhA/Lsa24 [6,31], LigA and LigB proteins [7,8], Len-family proteins , Lsa21 , LipL32 [12,43], Lsa27 , Lp95 , TlyC , LipL53 , Lsa63 , OmpL37 , Lsa66  and Lsa20 . We have reported that Leptospira species were also capable to bind PLG and generating plasmin, in the presence of host activator, on the outer surface in vitro. In addition, we have described that plasmin - coated virulent L.interrogans bacteria were capable to degrade purified extracellular matrix components fibronectin  and laminin (Vieira et al., unpublished data), a step that may contribute for dissemination of the bacteria through the host tissues. More recently, we have shown that plasmin generation on the bacterial surface decreases the deposition of C3b and IgG and hence, opsonization and phagocytosis, a process that could facilitate leptospires to evade the immune system . Several PLG-receptor proteins in Leptospira have been identified [17,18,20,21].
By data mining the genome sequences of L. interrogans, searching for surface exposed proteins that could mediate host - pathogen interactions, we have identified two proteins annotated as Leptospira conserved hypothetical, one of them, predicted to be a novel lipoprotein, LIC11834, and the other, LIC12253, has recently been shown to be non-protective in leptospiral challenge assay . Both selected coding sequences were cloned and the recombinant proteins expressed in E. coli. We report that these proteins, Lsa33 and Lsa25, are laminin - binding adhesins and in the case of Lsa33, capable to bind PLG generating enzymatically active plasmin. Although weak, both proteins showed the ability to bind human purified C4bp, suggesting that these proteins have the potential to participate in leptospiral immune evasion by interfering with the complement classical pathway.
Due to the high degree of antigenic variation among leptospires, we examined the gene/protein conservation among important species of Leptospira. The LIC11834 and LIC12253 genes are conserved in five serovars of L. interrogans and in other species tested but in the case of L. santarosai serovar Shermani the gene LIC11834 is absent. However, LIC11834 transcripts were detected only in serovars of L. interrogans, while LIC12253 appears to be expressed in all strains evaluated. None of the proteins seems to be expressed in the saprophytic strain, L. biflexa serovar Patoc.
The recombinant proteins Lsa33 and Lsa25 were expressed with molecular mass of 33 - and 24 - kDa, respectively, having a 6XHis tag at N - terminal. The purified proteins exhibited single major bands in SDS - PAGE and were recognized by anti - His tag monoclonal antibodies and by homolog sera from mice immunized with each recombinant protein. Secondary structure of the recombinant proteins after the purification process was evaluated by CD spectroscopy and showed a predominance of alpha helices in both cases, similar to the data predicted by bioinformatics, indicating the suitability of recombinant proteins for further studies. The LIC12253 coding sequence is probably higher immunogenic than LIC11834 because it was recognized by approximately 45% of serum samples of both phases, initial and convalescent, of confirmed leptospirosis’s cases. Interestingly, the LIC11834 protein although presented almost no reactivity among these serum samples, showed a slightly augment effect on serum reactivity when was assayed together with LIC12253. Immunofluorescence using live leptospires showed LIC11834 and LIC12253 coding sequences at the surface of bacteria, as a result of antiserum recognition raised against each protein. In silico analysis, proteinase K accessibility and immunofluorescence data together suggest that these proteins are likely to be surface exposed. In addition, the recombinant proteins partially inhibited leptospiral adherence to immobilized laminin and PLG.
Merien and colleagues  identified a 36-kDa fibronectin-binding protein expressed by a virulent variant of Leptospira. Our group described the first leptospiral laminin - binding protein, named Lsa24 . These studies were followed by the identification of several extracellular matrix binding proteins [7,9-18]. The recombinant proteins Lsa33 and Lsa25 exhibited extracellular matrix - binding properties, and are laminin - binding proteins. The binding affinity dissociation constants estimated for both proteins to laminin showed similar KD value of that reported for OmpL 37 (410±81 nM) and the same ECM molecule . Thus, it is possible that these proteins have a role in the adhesion of leptospires to hosts.
The PLG activation system with generation of plasmin was described for virus, parasites and bacteria, including the spirochetes Borrelia spp. and with Treponema denticola[47-50]. Plasmin is a serine protease with the capacity to degrade a broad spectrum of substrates, including fibrin clots, connective tissue and components of extracellular matrices [51-53]. We have reported that Leptospira spp. bind PLG at their surface generating plasmin, when host activator is available, making the bacteria capable to degrade fibronectin  and laminin (Vieira, M.L., unpublished results). Verma et al.  have demonstrated that the protein LenA of L. interrogans is a surface receptor for human PLG. Moreover, we have reported several novel PLG - receptor proteins of Leptospira[17,18,21]. We now describe Lsa33 as a novel PLG - binding protein. Similar to the previously reported proteins, bound PLG could be converted to plasmin by the addition of urokinase - type PLG activator (uPA), showing specific proteolytic activity. It is thus possible that the Lsa33 besides playing a role in the attachment to host and acting as PLG - receptor, may also help leptospires to surmount tissue barriers.
The inhibitory effect exerted on the binding of leptospires to laminin and PLG by the recombinant proteins was statistically significant with both, in the case of Lsa33, and with laminin for the Lsa25. The intensity of the interference upon the binding is expected given the presence of several ECM - or PLG-binding proteins in Leptospira. These data are comparable to the ones already reported in the literature [6,7,16-18,21]. Partial inhibitory effect was observed by laminin on the binding of Lsa33 to PLG, suggesting a competition for the same binding site.
We report in these studies a characterization of two leptospiral proteins, genome annotated as proteins of unknown function. The recombinant proteins Lsa33 and Lsa25 are laminin binding proteins that might be involved in the attachment to host. Moreover, both proteins showed the ability to bind C4bp, a feature suggesting their possible involvement in the immune evasion of leptospires. The recombinant Lsa33 is also PLG - binding protein that could help the bacteria during the infection process. Thus, it appears that Lsa33 and to a lesser degree, Lsa25, are multifaceted proteins that might have multiple functions in the leptospiral pathogenesis. To date, Lsa33 is the first described laminin -, PLG - and C4bp - leptospiral binding protein.
The pathogenic Leptospira strains used were: L. interrogans serovar Canicola strain Hound Utrech IV, L. interrogans serovar Copenhageni strain M 20, L. interrogans serovar Hardjo strain Hardjoprajitno, L. interrogans serovar Icterohaemorrhagiae strain RGA, L. interrogans serovar Pomona strain Pomona, L. borgpetersenii serovar Whitcombi strain Whitcomb and serovar Grippothyphosa strain Moskva V, L. kirshneri serovar Cynoptery strain 3522C, L. santarosai serovar Shermani strain 1342K, L. noguchi serovar Panama strain CZ 214 and L. biflexa serovar Patoc strain Patoc, were cultured at 28°C under aerobic conditions in liquid EMJH medium (Difco®) with 10% rabbit serum, enriched with L - asparagine (wt/vol: 0.015%), sodium pyruvate (wt/vol: 0.001%), calcium chloride (wt/vol: 0,001%), magnesium chloride (wt/vol: 0.001%), peptone (wt/vol:0.03%) and meat extract (wt/vol: 0.02%) (Turner LH. Leptospirosis. 3. Maintenance, isolation and demonstration of leptospires. Trans R Soc Trop Med Hyg 1970; 64: 623–646). Leptospira cultures are maintained in Faculdade de Medicina Veterinária e Zootecnia, USP, São Paulo, SP, Brazil. Confirmed - leptospirosis serum samples were from Instituto Adolfo Lutz collection, São Paulo, Brazil.
The microscopic agglutination test was performed according to . In brief, an array of 22 serovars of Leptospira spp. as antigens were employed: Australis, Autumnalis, Bataviae, Canicola, Castellonis, Celledoni, Copenhageni, Cynopteri, Djasiman, Grippotyphosa, Hardjo, Hebdomadis, Icterohaemorrhagiae, Javanica, Panama, Patoc, Pomona, Pyrogenes, Sejroe, Shermani, Tarassovi and Wolffi. All the strains were maintained in EMJH liquid medium (Difco, USA) at 29°C. A laboratory - confirmed case of leptospirosis was defined by the demonstration of a four - fold microagglutination titer rise between paired serum samples. The probable predominant serovar was considered to be the one with the highest dilution that could cause 50% of agglutination. MAT was considered negative when the titer was below 100.
Predicted coding sequence (CDSs) LIC11834 and LIC12253 were identified on L. interrogans serovar Copenhageni and selection was based on cellular localization; cellular localization prediction was performed by PSORT, http://psort.nibb.ac.jp and PredictProtein web server, https://www.predictprotein.org/. The SMART http://smart.embl-heidelbergde/ and PFAM http://www.sanger.ac.uk/Software/Pfam/ web servers were used to search for predicted functional and structural domains. The presence of lipobox putative sequence was evaluated by use of the LipoP program http://www.cbs.dtu.dk/services/LipoP/. The predicted sequence of the lipobox was also assessed by use of the SpLip program, as described by Setubal et al. . Secondary structure, solvent accessibility and cellular localization predictions were also performed by using PredictProtein web server, https://www.predictprotein.org/.
Leptospira cultures were harvested by centrifugation at 11,500g for 30min and gently washed in sterile PBS twice. Genomic DNA was isolated from the pellets by guanidine - detergent lysing method using DNAzol® Reagent (Invitrogen), according to the manufacturer’s instructions. Primers were designed according to L. interrogans serovar Copenhageni genome sequences (GenBank accession AE016823) and are listed in Table1. PCR was performed in a reaction volume of 25μl containing 100ng of genomic DNA, 1×PCR buffer (20mM Tris - HCl, pH8.4, 50mM KCl), 2mM MgCl2, 20pmol of each specific primer, 200μM of each dNTP, and 2.5 U Taq DNA Polymerase (Invitrogen). Cycling conditions were: 94° C - 4min, followed by 40 cycles at 94°C - 50sec, 57°C (LIC11834) or 56°C (LIC12253) - 50sec, 72°C - 90sec, and a final extension cycle of 7min at 72°C. PCR amplified products were loaded on a 1% agarose gel for electrophoresis and visualization with ethidium bromide.
For reverse transcription RT - PCR, total RNA was isolated by the acid guanidinium thiocyanate phenol - chloroform method using TRIzol® Reagent (Invitrogen) according to the manufacturer’s recommendations. 1μg of RNA from each sample was treated with 1 U of DNAse I Amplification Grade (Invitrogen) for 15min at room temperature. DNAse I was inactivated by the addition of 1μl of 25mM EDTA solution followed by an incubation at 65° C for 10min. DNAse - treated RNAs were reversely transcribed using the SuperScript™ III First - Strand Synthesis System for RT-PCR (Invitrogen). One tenth of RT products were amplified in a 25μl reaction mix using oligonucleotides LIC11834 - F/LIC11834 - R or LIC12253 - F/LIC12253 - R, as described above. Samples quantity and integrity were verified by amplification of a 1,042bp 16S ribosomal cDNA fragment using oligomers:
16S - F 5′CAAGTCAAGCGGAGTAGCAATACTCAGC 3′ and 16S - R 5′GATGGCAACATAAGGTGAGGGTTGC 3′.
Predicted CDSs LIC11834 and LIC12253, without signal peptides, were amplified by the PCR from L. interrogans serovar Copenhageni strain Fiocruz L1 - 130 genomic DNA using the primer pairs depicted in Table1. The PCR products obtained for each corresponding gene were cloned into pGEM-T easy vector (Promega) and subcloned into the pAE expression vector  at the restriction sites shown in Table1. The pAE vector allows the expression of recombinant proteins with a minimal 6X His - tag at the N - terminus. All cloned sequences were confirmed by DNA sequencing with an ABI 3100 automatic sequencer (PE Applied Biosystems, Foster city, CA). Protein expression of rLIC11834 and rLIC12253 was achieved in E. coli BL21 (SI) strain by the action of T7 DNA polymerase under control of the osmotically induced promoter proU . E. coli BL21 (SI) containing recombinant plasmids were grown at 30°C in Luria - Bertani broth without NaCl and with 100μg/ml ampicillin with continuous shaking until an optical density at 600nm of 0.6 to 0.8 was reached. Recombinant protein synthesis was induced by the addition of 300mM NaCl. After three hours, the cells were harvested by centrifugation and the bacterial pellets resuspended in lysis buffer (200μg/ml of lysozyme, 1% Triton X - 100, 2mM phenylmethylsulfonyl fluoride [PMSF]). The bacterial cell pellets were lysed on ice with the aid of a sonicator (Ultrasonic Processor; GE Healthcare). The insoluble fractions were washed with 20ml of buffer (20mM Tris - HCl, pH 8.0, 500mM NaCl, 1M urea and 1% Triton X-100) and resuspended in a buffer containing 20mM Tris - HCl, pH 8.0, 500mM NaCl, 5mM Imidazole, 1mM β - mercaptoethanol and 8M urea. The proteins were then purified through metal chelating chromatography in a Sepharose fast flow column (GE Healthcare) and fractions were analyzed in 12% SDS-PAGE. The rLIC12253 protein was refolded by 500 times dilution with 20mM Tris - HCL, pH 8.0, and 500mM NaCl before chromatographic purification. The purified recombinant proteins were extensively dialyzed against phosphate - buffered saline (PBS), pH 7.4, 0.1% (wt/vol) glycine solution (1:100), pooled and stored at −20°C.
Purified recombinant proteins were dialyzed against sodium phosphate buffer (pH 7.4). Circular dichroism (CD) spectroscopy measurements were performed at 20°C using a Jasco J-810 spectropolarimeter (Japan Spectroscopic, Tokyo) equipped with a Peltier unit for temperature control. Far-UV CD spectra were measured using a 1mm - path - length cell at 0.5nm intervals. The spectra were presented as an average of five scans recorded from 185 to 260nm. The molar ellipticity (Φ) is expressed in deg.cm.dmol1.
Five female BALB/c mice (4–6weeks old) were immunized subcutaneously with 10μg of the recombinant proteins. The recombinant proteins were adsorbed in 10% (vol/vol) of Alhydrogel (2% Al(OH)3, Brenntag Biosector, Denmark), used as adjuvant. Two subsequent booster injections were given at two - week intervals with the same preparation of 10μg of the proteins. Negative - control mice were injected with PBS. One week after each immunization, the mice were bled from the retro - orbital plexus and the pooled sera were analyzed by enzyme -linked immunosorbent assay (ELISA) for determination of antibody titers. All animal studies were approved by the Ethics Committee of the Instituto Butantan, São Paulo, SP, Brazil. The Committee in Animal Research in Instituto Butantan adopts the guidelines of the Brazilian College of Animal Experimentation.
The purified recombinant proteins were loaded into 12% SDS - PAGE and transferred to nitrocellulose membranes (Hybond ECL; GE Healthcare) in semi - dry equipment. Membranes were blocked with 5% non-fat dried milk and 2.5% BSA in PBS containing 0.05% Tween 20 (PBS - T) and then incubated with anti - rLIC11834 (1:500), anti - rLIC12253 (1:500) mouse serum or anti - his antibody (1:1,000) (GE Healthcare) for 2h at room temperature. After washing, the membranes were incubated with horseradish peroxidase (HRP) - conjugated anti - mouse IgG (1:5,000; Sigma) in PBS - T for 1h. The protein’s reactivity was revealed by ECL reagent kit chemiluminescence substrate (GE Healthcare) with subsequent exposition to X - Ray film.
Human IgG antibodies against Lsa33 or Lsa25 were detected by ELISA as previously described . In brief, serum samples of negative (24) and positive (33) MAT from confirmed - leptospirosis patients were diluted 1:400 and evaluated for total IgG using goat HRP - conjugated anti-human IgG antibodies (1:5,000, Sigma). Cutoff values were set at three standard deviations above the mean OD492nm of sera from 11 health individuals, unexposed to leptospirosis, from the city of São Paulo, Brazil and one pool of normal serum samples from USA (Sigma).
Suspensions of 5ml live leptospires/per treatment (~108cells/ml) were harvested at 10,000rpm for 15min at room temperature, washed once with PBS (with 50mM NaCl), resuspended in 5ml of PBS (with 50mM NaCl) plus with 25μg/ml of proteinase K (PK) (Sigma Aldrich). Four similar test tubes were then incubated for 0 to 5h at 37°C and aliquots were taken at 0, 1, 3 and 5h before the addition of 100mM of phenylmethylsulfonyl fluoride (PMSF) to stop PK activity. The suspensions were subsequently pelleted by centrifugation at 10,000rpm for 5min, washed twice with PBS (with 50mM NaCl) and resuspended in 1ml PBS (with 50mM NaCl) for ELISA analysis using antibodies against Lsa33, Lsa25, Lip32 and DnaK, as described below. LipL32 and DnaK are membrane and cytoplasmic leptospiral proteins that were employed in our experiment as positive and negative control, respectively.
Leptospires were coated onto microplates and allowed to stand at room temperature for 16h. The plates were washed three times with PBS (with 50mM NaCl) and blocked with 5% non-fat dry milk and 1% BSA for 2h at 37°C. After incubated for 2h at 37°C with polyclonal mouse anti - serum against Lsa33, Lsa25, LipL32 or DnaK (dilution of an OD equal to 1). The leptospires were washed three times with PBS (with 50mM NaCl) and incubated with 50μL of a 1:5,000 dilution of HRP - conjugated goat anti - mouse IgG (Sigma) in PBS (with 50mM NaCl) for 1h at 37°C. The wells were washed three times with PBS (with 50mM NaCl), and o - phenylenediamine (OPD) (1mg/mL) in citrate phosphate buffer (pH 5.0) plus 1μL/mL H2O2 was added (100μL per well). The reaction proceeded for 5min and was interrupted by the addition of 50μL of 4N H2SO4. The absorbance at 492nm was determined in a microplate reader (TP - reader, Thermo) against the O.D. of blanks, containing all the reaction mixture but antibodies against the proteins. For statistical analyses, the binding of polyclonal mouse anti - serum against Lsa33, Lsa25, LipL32 or DnaK at 0h incubation was compared with other incubations by Student’s two - tailed t test.
Protein attachment to individual macromolecules of the extracellular matrix was analyzed according to a previously published protocol  with some modifications. Briefly, 96 - well plates (Costar High Binding, Corning) were coated with 1μg of laminin, collagen type I, collagen type IV, cellular fibronectin, plasma fibronectin, human PLG, factor H, C4bp, or gelatin (negative control) and fetuin (highly glycosylated attachment - negative control protein) in 100μL of PBS for 3h at 37°C. The wells were washed three times with PBS - T and then blocked with 200μL of 10% (wt/vol) non-fat dry milk (overnight at 4°C). One microgram of each recombinant protein was added per well in 100μL of PBS, and protein was allowed to attach to the different substrates for 2h at 37°C. After washing six times with PBS - T, bound Lsa33 or Lsa25 was detected by adding mouse anti - recombinant proteins (1:750) in 100 μL of PBS or anti - His tag monoclonal (1:200) in 100μL of PBS. Incubation proceeded for 1h at 37°C. After three washings with PBS - T, 100μL of a 1:5,000 dilution of HRP - conjugated goat anti - mouse IgG (Sigma) in PBS was added per well for 1h at 37°C. The wells were washed three times, and o - phenylenediamine (OPD) (1mg/mL) in citrate phosphate buffer (pH 5.0) plus 1μL/mL H2O2 was added (100μL per well). The reaction proceeded for 10min and was interrupted by the addition of 50μL of 4N H2SO4. The absorbance at 492nm was determined in a microplate reader (TP - reader, Thermo). For statistical analyses, the binding of recombinant proteins to ECM macromolecules and to serum components were compared to its binding to gelatin and by Student’s two - tailed t test.
Microtitre wells were coated with 1μg of laminin in 50mM sodium acetate buffer, pH 5.0, and incubated for 16h at 4°C. Wells were washed three times with the same buffer, and laminin was treated with different sodium metaperiodate concentrations (0–100mM) in the same buffer for 15min at 4°C in the dark. After three washes with 50mM sodium acetate buffer, wells were blocked with 200μl of 1% BSA for 1h at 37°C. Binding of recombinant proteins (1μg in PBS per well) to periodate - treated laminin was evaluated as described above.
First, 96 - well plates were coated overnight in PBS at 4°C with 100μl of 10μg/ml PLG, laminin or C4bp. Plates were then blocked and increasing concentrations of the purified recombinant proteins (0–6μM) were added (100μl/well in PBS). The assessment of bound proteins was performed by incubation for 1h at 37°C with the antiserum raised against each protein at the dilution of 1:750, followed by HRP - conjugated goat anti-mouse IgG (Sigma) (1:5,000 in PBS). The reactions were detected with OPD as describe above. The ELISA data were used to calculate the dissociation constant (KD) according to the method described by Pathirana et al.  and Lin et al. , based on the equation: , where A is the absorbance at a given protein concentration, Amax is the maximum absorbance for the ELISA plate reader (equilibrium), [protein] is the protein concentration and KD is the dissociation equilibrium constant for a given absorbance at a given protein concentration (ELISA data point).
96 - well ELISA plates were coated overnight with 10μg/ml recombinant proteins in PBS at 4°C. Lsa63, which does not bind PLG  and BSA were employed as negative control. Plates were washed once with PBS - T and blocked for 2h at 37°C with PBS with 10% (wt/vol) non - fat dry milk. The blocking solution was discarded and 100μl/well of 10μg/ml human PLG was added, followed by incubation for 2h at 37°C. Wells were washed three times with PBS - T, and then 4ng/well of human uPA (Sigma - Aldrich) were added. Subsequently, 100μl/well of plasmin - specific substrate D - valyl - leucyl – lysine - p - nitroanilide dihydrochloride (Sigma - Aldrich) were added at a final concentration of 0.4mM in PBS. Plates were incubated overnight at 37°C and substrate degradation was measured by readings at 405nm.
ELISA plates were coated with laminin or PLG (1μg/well). The plates were washed and blocked with 10% non - fat dry milk in PBS - T for 2h at 37°C. The blocking solution was discarded, and the wells were incubated for 90min at 37°C with increasing concentrations of proteins (0 to 10μg). After three washings, 50μL/well of 4×107 live low - passage virulent L. interrogans serovar Copenhageni strain M20 were added for 90min at 37°C. The unbound leptospires were washed and the quantification of bound leptospires was performed indirectly by anti - LipL32 antibodies produced in mice (1:4,000), given the fact that LipL32 is a major outer membrane leptospiral protein ; the procedure was followed by horseradish peroxidase - conjugated anti - mouse IgG antibodies, essentially as described in Barbosa et al. . The detection was performed by OPD as previously described.
The localization of LIC11834 and LIC12253 encoded proteins by L - IFA was performed as described by Oliveira et al. . In brief, suspensions of 2.5ml live leptospires (~109cells/ml) were harvested at 10,000rpm for 15min, washed twice with PBS (with 50mM NaCl), resuspended in 200μl of PBS with 6μg/ml propidium iodide to stain the nuclei, and incubated for 45min at 37°C. After incubation, the leptospires were washed gently with PBS and incubated for 30min at 4°C with polyclonal mouse anti - serum against Lsa33, Lsa25, LipL32 or GroEL at a 1:50 dilution. The leptospires were washed and incubated with goat anti - mouse IgG antibodies conjugated to fluorescein isothiocyante (FITC, Sigma) at a dilution 1:50 for 30min at 4°C. After incubation with secondary antibody, the leptospires were washed and resuspended in PBS - antifading solution (ProLong Gold, Molecular Probes). The immunofluorescence - labeled leptospires were examined by employ of a confocal LSM 510 META immunofluorescence microscope (Zeiss, Germany).
GenBank accession numbers for protein sequences LIC11834 and LIC12235 are AAS70420 and AAS70825, respectively. The protein can also be accessed by the genome nomenclature for the gene locus, LIC number (Leptospira interrogans serovar Copenhageni).
The control proteins fetuin and gelatin, were purchased from Sigma Chemical Co. (St. Louis, Mo.) and Difco®, respectively. Laminin - 1 and collagen Type IV were derived from the basement membrane of Engelbreth - Holm-Swarm mouse sarcoma, cellular fibronectin was derived from human foreskin fibroblasts, plasma fibronectin was isolated from human plasma and collagen Type I was isolated from rat tail. PLG, purified from human plasma, was purchased from Merck. Human Factor H was from Calbiochem. C4bp was from Complement Technology, INC.
RFD performed the molecular cloning studies, protein expression, ECM assays and animal immunizations. MLV carried out the PLG assays and help with the manuscript. ECR evaluated MAT of the collection serum samples. APG and ZMM were responsible for bacteria growth, identification and virulence strain maintenance. SAV participated in the design of the study and help drafted the manuscript. ALTON conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
We are deeply indebted to Alexsander Seixas de Souza (Departamento de Parasitologia, Instituto Butantan, Sao Paulo, Brazil) for use of Confocal facilities and helpful discussion. This work was supported by FAPESP, CNPq and Fundaçao Butantan, Brazil; RFD and MLV have fellowships from FAPESP.