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The Leishmania infantum PUF proteins are targets of the humoral response during visceral leishmaniasis
© Requena et al.; licensee BioMed Central Ltd. 2010
Received: 21 September 2009
Accepted: 21 January 2010
Published: 21 January 2010
RNA-binding proteins of the PUF family share a conserved domain consisting of tandemly repeated 36-40 amino acid motifs (typically eight) known as Puf repeats. Proteins containing tandem repeats are often dominant targets of humoral responses during infectious diseases. Thus, we considered of interest to analyze whether Leishmania PUF proteins result antigenic during visceral leishmaniasis (VL).
Here, employing whole-genome databases, we report the composition, and structural features, of the PUF family in Leishmania infantum. Additionally, the 10 genes of the L. infantum PUF family were cloned and used to express the Leishmania PUFs in bacteria as recombinant proteins. Finally, the antigenicity of these PUF proteins was evaluated by determining levels of specific antibodies in sera from experimentally infected hamsters. The Leishmania PUFs were all recognized by the sera, even though with different degree of reactivity and/or frequency of recognition. The reactivity of hamster sera against recombinant LiPUF1 and LiPUF2 was particularly prominent, and these proteins were subsequently assayed against sera from human patients. High antibody responses against rLiPUF1 and rLiPUF2 were found in sera from VL patients, but these proteins resulted also recognized by sera from Chagas' disease patients.
Our results suggest that Leishmania PUFs are targets of the humoral response during L. infantum infection and may represent candidates for serodiagnosis and/or vaccine reagents; however, it should be kept in mind the cross-reactivity of LiPUFs with antibodies induced against other trypanosomatids such as Trypanosoma cruzi.
Leishmaniases constitute a vast variety of diseases ranging from cutaneous manifestations to visceral dissemination that are caused by different species of the genus Leishmania. Visceral leishmaniasis (VL), the most severe form of leishmaniases (usually fatal if untreated), is typically caused by Leishmania donovani and Leishmania infantum (syn. Leishmania chagasi) . Leishmaniases constitute a worldwide public-health problem and 1.5 to 2 million new cases occur every year: 1 to 1.5 million cases of cutaneous forms and 500,000 cases of VL . These vector-borne diseases are endemic in large areas of the tropics, subtropics and the Mediterranean basin. Early and accurate diagnosis of leishmaniasis remains unresolved. Diagnostic tests should be highly sensitive and specific; furthermore, the tests should be able to make the distinction between acute disease and asymptomatic infection. Also, accurate diagnosis is relevant for monitoring success in the chemotherapeutic treatment of leishmaniases.
Parasite detection in tissue biopsies either by microscopic visualization of amastigotes or in vitro culturing of the parasite remains the gold standard in leishmaniasis diagnosis because of its high specificity [1, 3]. However, for VL diagnosis, aspirates of lymph nodes, bone marrow or spleen need to be obtained, being both risky and painful for patients. In addition, the sensitivity of microscopy and culture techniques tends to be low and variable, depending of many factors, among them the technical skills of the personnel. Given that leishmanial infections are accompanied by a dramatic humoral response, mainly in the visceral forms of leishmaniasis, serodiagnosis appears as an interesting alternative. In fact, a battery of immunological procedures have been developed and adapted for diagnosis and epidemiological surveys . Several Leishmania antigenic proteins have been expressed as recombinant proteins and their potential for serodiagnosis assayed [5–8]. However, so far, only a Leishmania recombinant protein (rK39) is being used for serodiagnosis of leishmaniasis in the field . rK39 is a subfragment within a 230-kDa kinesin-related protein (LcKin); it spans the LcKin C-terminal region, which contains seven 39-amino acid repeats . Many antigens of different protozoan parasites contains tandem repeats in their structure [10, 11], suggesting that repeated domains might be better inducers of B-cell activation and, therefore, resulting preferred targets of the humoral responses. Experimental support for this hypothesis has been obtained by Goto and co-workers . By screening an L. infantum expression library with sera from human VL patients or infected hamsters, they identified 43 genes encoding B-cell antigens, and, remarkably, 44% of those antigens contained tandem repeats in their structure. In a subsequent work, these authors, using a bioinformatic approach, directly searched in the L. infantum database for genes encoding proteins with tandem repeats. Among the 64 identified genes, the antigenicity for 6 of the encoded proteins was experimentally assayed using sera from VL patients, showing that 4 of them had significant and specific reactivity against VL sera .
The RNA-binding proteins of the PUF family constitute an evolutionarily conserved group of proteins present in all eukaryotic phyla . PUF proteins bind to sequence motifs in the 3'-UTR of specific mRNAs and control their localization, stability and translation . The distinctive feature of PUF proteins is the RNA-binding domain known as the Pumilio homology domain (PUM-HD), which is composed of several consecutive imperfect repeats (typically eight) of around 36-40 amino acids (Puf repeats). Recently, Caro and co-workers  identified up to 10 different PUF proteins in the genome of Trypanosoma cruzi, and an equivalent complement of PUF proteins has been also described for two other trypanosomatids, Trypanosoma brucei and Leishmania major. Because of the existence of many repeated motifs in this class of proteins, we questioned whether the PUF proteins would be antigenic during Leishmania infection. For this purpose, we have identified the putative PUF genes existing in the L. infantum genome and expressed them as recombinant proteins. Afterwards, the antigenicity of the different L. infantum PUFs was assayed using the sera from experimentally infected hamsters. Interestingly, all the PUFs were specifically recognized by immune sera, even though individual differences were observed.
Parasites and sera
L. infantum promastigotes were cultured at 26°C in RPMI containing 10% heat-inactivated, fetal bovine serum. Hamsters were infected intracardially with stationary-phase promastigotes (strain M/CAN/ES/96/BNC150) and the animals were monitored for 1-year follow-up period. At the onset of clear symptoms of visceral leishmaniasis (emaciation and asthenia) hamsters 1, 2, 3, 4, 5, 7 and 8 were sacrificed; high parasite loads were found in both liver and spleen of these animals. At the end of the study, even though hamsters 9 and 10 did not show external signs of disease, significant parasite loads were found in their livers and spleens. Hamster 6 was a particular case, no parasites were observed after microscopic examination of liver or spleen preparations at the moment of sacrifice; thus, it was assumed that this animal had resolved the infection. Before infection (preimmune serum) and at the time of sacrifice (immune serum), sera were collected. See reference  for further details of this infection experiment (code correspondence: 1 = A2, 2 = A3, 3 = A4, 4 = B1, 5 = B3, 6 = B4, 7 = C3, 8 = C4, 9 = A5, 10 = A7). All experimental animals were housed, fed and used in accordance with the Federation of European Laboratory Animal Science Association (FELASA) Guidelines. The animal study protocol was approved by the Ethics Committee of the Universidad Autónoma de Madrid.
Human sera were provided by Dr. Carmen Cañavate (WHO Collaborating Centre for Leishmaniasis, Servicio de Parasitología, Centro Nacional de Microbiología, Madrid). VL sera were collected from Spanish patients with active disease that was diagnosed by serological and parasitological methods. Chagasic sera were obtained from Latin American immigrants showing signs of cardiomyopathy and proven serologically positive by IFI and commercial ELISA kits. Normal sera were obtained from healthy individuals in Spain.
Identification and bioinformatic analyses of the L. infantum PUF proteins
T. brucei, T. cruzi, L. braziliensis, L. infantum and L. major PUF sequences were obtained from GeneDB . Searches for structural motifs in Leishmania PUF sequences were performed using the PROSITE database and resources . Potential N-terminal signal peptides were predicted by Signal P program .
Cloning of L. infantum PUF genes and expression of recombinant proteins
The complete coding sequences of LinJ06_V3.1830, LinJ11_V3.0470, LinJ12_V3.0330, LinJ18_V3.1400, LinJ20_V3.1420, LinJ21_V3.2050, LinJ25_V3.2470, LinJ32_V3.1830 and LinJ33_V3.1210 genes were amplified by PCR. The sequences of the oligonucleotide primers used in this study are listed in the Additional file 1. As template, genomic DNA from L. infantum JPC strain (MCAN/ES/98/LLM-724) was used.
The PCR products were digested with restriction enzymes (specific restriction sites were added to the 5'-end of the primers) and cloned directionally in the appropriate expression vector (pQE30, pQE31 or pQE32; Qiagen). The sequences of the inserts were determined by automatic sequencing (Servicio de Genómica, Parque Tecnológico de Madrid-UAM). The expression clones were used to transform Escherichia coli M15-pREP4 strain bacteria. The optimum conditions for expression were determined by varying the IPTG (isopropyl-β-D-thiogalactopyranose) concentration, length of induction and growth temperature. The recombinant proteins were then purified by Ni-nitrilotriacetic acid agarose chromatography, using denaturing conditions according to the manufacturer's protocol (Qiagen). The purity of the proteins was assayed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Coomassie blue staining of the gels. The concentration of proteins was determined by the Bradford dye assay (Bio-Rad) using bovine serum albumin (BSA) as standard.
Enzyme-linked immunosorbent assay (ELISA)
The recombinant PUF proteins were analyzed for seroreactivity using sera from 10 hamsters with VL symptoms that were experimentally infected with L. infantum promastigotes (see above). Preimmune sera from the same animals were used as negative controls. In addition, L. infantum soluble lysate antigen (SLA) was used as a positive control. Each sample was assayed in triplicate. Proteins were diluted in coating buffer (15 mM Na2CO3, 28 mM NaHCO3, pH = 9.6), and plates were coated overnight at 4°C with 50 ng of SLA or 200 ng of recombinant protein. After removing the coating solution, free binding sites were blocked with 200 μl of 5% milk in PBS containing 0.3% Tween 20 (T-PBS) for 1 h at room temperature. The plates were then washed two times in T-PBS. Sera diluted 1:200 in T-PBS and 0.5% nonfat milk were added (100 μl/well), and plates were incubated at room temperature for 1 h. After three washes, horseradish peroxidase-conjugated rabbit anti-hamster IgG (Nordic Immunological Lab.), diluted 1:1500 in T-PBS and 0.5% nonfat milk were added (100 μl/well). After incubation at room temperature for 1 h, plates were washed three times. Finally, the antibody binding was revealed with ortho-phenylenediamine (OPD) and hydrogen peroxide. The reaction was left to proceed for 15 min and then stopped by addition of 100 μl of H2SO4 1 M. The absorbance of the reaction was measured at 450 nm in an ELISA reader (Bio-Rad). The lower limit of positivity (cutoff) was determined by the mean of the negative controls (pre-immune sera) plus three standard deviations. Human sera were also assayed in ELISA at 1:200 dilution, using horseradish peroxidase-conjugated goat anti-human IgG (Nordic Immunological Lab.) as secondary antibody (1:1500 dilution).
Results and Discussion
L. infantum has an equivalent complement of PUF proteins to those predicted in other trypanosomes
Putative PUF proteins in pathogenic trypanosomatids
On the other hand, it is remarkable the existence of two isoforms for PUF9 in L. major and L. infantum. We named these isoforms as PUF9a (LmjF20.1365 and LinJ20_V3.1410; see Table 1) and PUF9b (LmjF20.1370 and LinJ20_V3.1420). Phylogenetic analysis (not shown) suggests that PUF9a/b isoforms are derived from a recent duplication of the ancestral PUF9 gene that occurred in the L. infantum/L. major evolutionary line. In fact, both genes are contiguous in the L. infantum/L. major chromosome 20. However, multiple alignment of the sequences for the Leishmania PUF9 isoforms evidenced a conspicuous structural difference between L. infantum and L. major PUF9 proteins: L. infantum LiPUF9 isoforms have an N-terminal extension that is absent from the L. major counterparts. However, since the sequences upstream of the assigned start codons for LmjPUF9a and LmjPUF9b are extremely conserved with the sequences coding for the N-terminal regions of the LiPUF9a and LiPUF9b (data not shown), the differences in the predicted sequences may be due to annotation errors in the L. major database. In fact, even though with low sequence conservation, the T. brucei and T. cruzi PUF9 proteins have N-terminal extensions equivalent in size to those existing in the L. infantum isoforms.
Structural features of the L. infantum PUF proteins
Recognition of the L. infantum PUF proteins by sera from experimentally infected hamsters
The repeated nature of PUF proteins prompted us to analyze whether, as hypothesized by other authors , they can be targeted by the immune system during Leishmania infection. In order to determine the antigenicity of the L. infantum PUF proteins, we cloned the complete coding regions of 10 out of the 11 PUF genes existing in this Leishmania species (Table 1). Since LiPUF9a and LiPUF9b are essentially identical in sequence and, presumably, antigenically cross-reactive, we selected one gene (i.e. LiPUF9b) for cloning and expression. The different PUF genes were successfully expressed as His-tagged recombinant proteins in E. coli (see Methods for details). After affinity chromatography purification, the recombinant PUF (rPUF) proteins were assayed by SDS-polyacrylamide gel electrophoresis, showing apparent molecular masses similar to those deduced from the amino acid sequence [see Additional file 1].
Another remarkable finding of this study is that the PUF antigens are differentially recognized by each one of the hamster sera. Thus, for example, rLiPUF1 was highly recognized by serum from animals 2, 7 and 9, whereas rLiPUF2 was recognized better by sera 4 and 5. Additional variations can be easily deduced from a visual inspection of figure 2. Individual differences in the antigens targeted by the immune system are not unexpected findings, at least, for non inbred animals . Furthermore, this variability of recognition indicates that different LiPUFs are priming specific humoral responses in hamsters, and that the cross-reactivity of the elicited anti-PUF antibodies seems to be low.
Antigenicity and specificity of rLiPUF1 and rLiPUF2 in human patients
Given the prominent recognition of rLiPUF1 and rLiPUF2 by sera from L. infantum-infected hamsters, we assayed the reactivity of 10 sera from VL patients against each one of these recombinant proteins (figure 3B). Remarkably, 8/10 and 5/10 of the VL sera reacted with rLiPUF1 and rLiPUF2, respectively, with absorbance values higher than the cut-off value of the healthy controls (0.49). Some of the human VL sera yielded absorbance values higher than 1, indicating that these proteins are strong immunogens for the immune system of some individuals. Since the LiPUF proteins have well-conserved homologues in other trypanosomatids (Table 1), we further analyzed whether specific antibodies are present in the sera from Chagas' disease patients. Not surprisingly, positive reactivity against rLiPUF1 and rLiPUF2 was observed in 3/5 and 2/5, respectively, of the sera from chagasic patients. This cross-reactivity may be a hurdle for the use of these two proteins as diagnostic antigens, at least in regions where leishmaniasis and Chagas's disease are endemic. Nevertheless, they should not be absolutely discarded before determining the location of B-cell epitopes recognized by antibodies elicited in VL and chagasic patients. For example, acidic ribosomal proteins are prominent and cross-reactive antigens during both leishmaniasis and Chagas' disease, but the recognized epitopes are different for each group of patients, allowing that a truncated form of the Leishmania P2 protein could be used for differential serodiagnosis of these diseases .
In order to evaluate the diagnosis usefulness of these proteins, it remains to determine the recognition of the Leishmania PUFs by sera from patients with different forms of leishmaniasis and/or VL dogs. Currently, we are planning those studies with the hope that some of these proteins can be used together with other well characterized Leishmania antigens for designing new serodiagnosis devices. Diagnostic arrays based on antigens that most often are targeted by human immune system are expected to be far more sensitive and informative than simple monospecific diagnostics such as the currently widely applied rK39 dipstick, as single antigens that are recognized by all individuals infected by any pathogen appear to be rare.
L. infantum shares with other Leishmania species and related trypanosomatids (e.g. T. brucei and T. cruzi) a PUF family consisting of ten members. All ten L.infantum PUF are B-cell antigens during parasite infection in hamster model of VL, even though with variable strength. Thus, rLiPUF1 and rLiPUF2 showed strong reactivity, rLiPUF4, rLiPUF5 and rLiPUF8 showed intermediate reactivity, whereas rLiPUF3, rLiPUF6, rLiPUF7, rLiPUF9b and rLiPUF10 showed low reactivity. We also showed that rLiPUF1 and rLiPUF2 are recognized by sera from VL patients, but also by sera from Chagas' disease patients. In conclusion, this study has shown that PUFs are targets of the immune system during L. infantum infection and, therefore, might have usefulness in diagnosis and/or vaccine developments.
Genome sequence data from the Sanger Institute sequencing projects (GeneDB) were invaluable for this work and their provision in the public domain is gratefully acknowledged. This work was funded by grants from the Ministerio de Ciencia y Tecnología (BFU2006-08346), and the Spanish Ministry of Science and Innovation and the Instituto de Salud Carlos III within the Network of Tropical Diseases Research (RICET RD06/0021/0008 - FEDER). Also, an institutional grant from Fundación Ramón Areces is acknowledged.
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