Exocytosis and protein secretion in Trypanosoma
© Geiger et al; licensee BioMed Central Ltd. 2010
Received: 23 April 2009
Accepted: 26 January 2010
Published: 26 January 2010
Human African trypanosomiasis is a lethal disease caused by the extracellular parasite Trypanosoma brucei. The proteins secreted by T. brucei inhibit the maturation of dendritic cells and their ability to induce lymphocytic allogenic responses. To better understand the pathogenic process, we combined different approaches to characterize these secreted proteins.
Overall, 444 proteins were identified using mass spectrometry, the largest parasite secretome described to date. Functional analysis of these proteins revealed a strong bias toward folding and degradation processes and to a lesser extent toward nucleotide metabolism. These features were shared by different strains of T. brucei, but distinguished the secretome from published T. brucei whole proteome or glycosome. In addition, several proteins had not been previously described in Trypanosoma and some constitute novel potential therapeutic targets or diagnostic markers. Interestingly, a high proportion of these secreted proteins are known to have alternative roles once secreted. Furthermore, bioinformatic analysis showed that a significant proportion of proteins in the secretome lack transit peptide and are probably not secreted through the classical sorting pathway. Membrane vesicles from secretion buffer and infested rat serum were purified on sucrose gradient and electron microscopy pictures have shown 50- to 100-nm vesicles budding from the coated plasma membrane. Mass spectrometry confirmed the presence of Trypanosoma proteins in these microvesicles, showing that an active exocytosis might occur beyond the flagellar pocket.
This study brings out several unexpected features of the secreted proteins and opens novel perspectives concerning the survival strategy of Trypanosoma as well as possible ways to control the disease. In addition, concordant lines of evidence support the original hypothesis of the involvement of microvesicle-like bodies in the survival strategy allowing Trypanosoma to exchange proteins at least between parasites and/or to manipulate the host immune system.
The Trypanosomatidae family comprises genera that infect many kinds of eukaryotes: insects, fish, amphibians, reptiles, birds, mammals, and even plants. In the Trypanosoma genus, three species are pathogenic for humans (Trypanosoma brucei, T. cruzi, and T. evansi). Human African trypanosomiasis (HAT, or sleeping sickness) is caused by T. brucei and transmitted by tsetse flies (Glossina sp.). In contrast to most other insect-transmitted parasites, T. brucei spends its entire cycle as an extracellular parasite. To thwart the host immune system, the parasite has developed population survival strategies. Through antigenic variation, trypanosomes shield their plasma membrane with a continually switching densely packed layer of 5 × 106 dimers of variant surface glycoprotein (VSG), which constitutes a surface coat. This coat is indeed composed of a single protein, but the parasite genome has a repertoire of about 2,000 different potential VSG genes that are expressed in a mutually exclusive manner. The coat also prevents antibodies from gaining access to necessarily invariant surface molecules [1–3].
HAT is lethal when untreated and is a threat for over 60 million people living in sub-Saharan countries [4, 5]. Treatment of the disease is difficult and expensive and has potentially life-threatening side effects [6, 7]. Since today there is no prophylactic chemotherapy, specific, low-cost, and sensitive methods for the early diagnosis of the parasite in human blood samples are needed, as well as novel therapeutic targets for fighting the parasite. A class of particularly interesting proteins are the expressed/secreted proteins (ESPs), which are specifically secreted by parasites. Several ESPs are involved in various aspects of the pathogenesis [8–10]. In addition, we have previously shown that the secretome of T. brucei inhibits the maturation of dendritic cells and their ability to induce lymphocytic allogenic responses . As the majority of ESPs of the secretome remain unknown, we used a proteomics-based approach to analyze the entire secretome of the parasite.
In this study, we compared three different T. brucei gambiense strains, identified over 440 proteins and determined their protomeric status. We isolated microvesicles from the secretion medium and showed in microscopy the budding of these microvesicles at the parasite surface before and after incubation in the secretion medium. Moreover, microvesicles were also isolated directly from infected rat serum and the proteome of these microvesicles was similar to the secretome. This extended overview demonstrates that ESPs play an unexpected major role in the trypanosome survival strategy via these microvesicles and highlights a number of potential therapeutic strategies to control the disease.
Characterization of the secretome of T. brucei gambiense
1- Comparison of different T. brucei strains reveals potential strain markers
2- Secreted proteins form stable complexes
Another striking feature concerned the proteasome, which we identified in two forms (spots 48-55 and 56-65) in the secretome. The 20S proteasome is a 28-mer composed of two stacked heptameric rings of proteolytically active beta subunits, surmounted at each end by another heptameric ring of structural alpha subunits. Seven alpha and seven beta paralogs exist in the T. brucei genome and all of the 14 different subunits were identified in both lanes, except alpha3 in the highest MW complex. The 20S core is regulated by additional 19S or 11S complexes. In T. brucei, a form of the 20S proteasome showing enhanced peptidase activity was previously described, and a 26-kDa protein, PA26 (26-kDa proteasome activator protein), was proposed to correspond to the 11S activator known in mammals [16, 17]. We identified PA26 in both complexes. Because of the sizes of the two proteasome complexes (300-350 kDa) and the average size of the alpha and beta subunits (~25 kDa), the two forms of the proteasome complex identified here probably contain a single ring of alpha and beta subunits. Moreover, from the size of the highest MW complex and the apparent stoichiometry between PA26 and the other subunits in the complex, the highest MW complex may represent the activated form of the complex. Finally, it should be pointed out that the 19S and 20S subunits were also identified in the unresolved part of the gel (spots 1-18), corresponding to complexes above 1000 kDa, and they could reveal a minor form of the 26S proteasome that has not been identified in T. brucei to date.
3- Secreted proteins correspond to a specific subset of the trypanosome proteome
A few proteomic data sets were recently published for members of the Trypanosomatidae family, including the total proteome of T. brucei in the procyclic (insect) stage , that of the glycosome, a specialized compartment similar to peroxisomes and involved in sugar metabolism , and the secretome of the promastigote Leishmania donovani, where authors were able to distinguish between actively secreted proteins and cell-associated proteins .
To cross-correlate between the secretome and proteome data sets, we first searched for Leishmania orthologs in T. brucei using BLAST (Basic Local Alignment Search Tool) analysis. 281 out of the 358 Leishmania secretome entries were found to have an ortholog in Trypanosoma (additional file 3, Table S3), including 115 actively secreted proteins and 166 cell-associated proteins. Interestingly, a high proportion (61%) of the former was present in our Trypanosoma secretome, suggesting a close relationship between the actively secreted proteins in Leishmania and the Trypanosoma secreted proteins.
In summary, comparison of both the protein accessions and the functional categories similarly demonstrated features specific to the different compartments, and a close relationship between the secretome of Trypanosoma and Leishmania.
How are Trypanosoma proteins secreted?
1- Secreted proteins do not contain a transit peptide
If trypanosomes use the classical secretion pathway, most secreted proteins should carry an N-terminal extension (transit peptide). SignalP is currently the most popular software for predicting the presence of a N-terminal transit peptide and the associated cleavage site . We performed a genome-wide screen of the Trypanosoma proteome using SignalP and identified 1445 proteins as predicted to contain a transit peptide (see additional file 6, Table S6), 61% without any known function. Of the remaining 561 proteins, many were known to be secreted or located at the plasma membrane, including 128 VSGs, 16 invariant surface proteins (ISG), 15 procyclin surface proteins, 14 bloodstream stage alanine-rich surface proteins (BARPs), 36 receptors for adenylate cyclase (GRESAGs), 28 transporters, 13 cysteine peptidases/clan CA/family C1 and family C2, seven transialidases, and many enzymes involved in lipid modification, glycosylation, and GPI (Glycosylphosphatidylinositol) anchoring. To focus specifically on the secreted proteins, i.e., proteins with no transmembrane span, we further assessed the occurrence of such domains using the transmembrane predictor TMHMM (transmembrane protein topology with a Hidden Markov Model) . 660 proteins were simultaneously predicted to contain a transit peptide by SignalP and not to contain transmembrane domains by TMHMM. Quite unexpectedly, only 30 out of the 444 secretome proteins experimentally identified in this work belonged to the predicted secretome.
Although not secreted by the classical secretory pathway, proteins devoid of an N-terminal signal peptide may still be secreted. We used the SecretomeP software  to predict such proteins in the Trypanosoma genome (additional file 6, Table S6). Depending on the selected threshold score, different proportions of known proteins and proteins having unassigned functions were computed. A score between 0.8 and 0.9 was taken as a convenient trade-off between sensitivity and specificity, so that enough known proteins were identified for validation and avoiding obvious false predictions. In this way, 583 proteins were predicted as secreted, 79% of which had unassigned functions. Of the remaining 125 proteins, 18 transporters were found, as well as three procyclins. However, only 13 proteins from this set were found to match our experimental data.
Thus, taken together, less than 20% of the secreted proteins from our data set were predicted to have a transit peptide (SignalP) and no transmembrane domain (TMHMM) or to be secreted via the nonclassical pathway (SecretomeP), suggesting that most Trypanosoma secreted proteins purified so far are secreted by a novel mechanism.
2-Possible exocytosis of microvesicles
We also looked at proteins specifically involved in endocytosis/exosome formation, and identified nine proteins, including ubiquitin (which serves as an important sorting signal during endocytosis and early endosomal protein trafficking ), clathrin heavy chain (involved in vesicle traffic ), a dynamin (a GTPase involved in the fission of clathrin-coated vesicles ), two adaptins (one of the major proteins of clathrin-coated vesicles ), two RAB proteins (small GTPases playing an essential role in the regulation of membrane traffic [34, 35]), a protein called CAP (cyclase-associated protein) (implicated in vesicle trafficking and endocytosis ), and Hsc70 (a chaperone regulating the disassembly of clathrin coats and participating in the translocation of cytoplasmic protein substrates into a subset of lysosome-like organelles ).
Finally, a modest proportion (~5%) of secreted proteins found in this study contains at least one predicted transmembrane span (TMHMM), supporting the idea that vesicles are present in the sample. Thus, our secretome data support the hypothesis that Trypanosoma could use microvesicles to secrete proteins.
The secretome of Trypanosoma displays unique features
In this study, we combined different proteomics approaches, resulting in the identification of a total of 444 proteins excreted or secreted by T. brucei gambiense. These data make up the largest set of secreted proteins characterized to date in Trypanosoma and identify a specific pattern of functional categories that differs from the total proteome and from specific subcellular compartments such as the glycosome. In addition, this functional distribution is not a special case, but is shared by different strains covering the two subgroups of T. brucei gambiense. Thus, ESPs may be used as a general identifier of the Trypanosoma strains. The analysis of native proteins shows that many of them are in multiprotein complexes and form heteroligomers, again suggesting that this specific set of proteins is functional. Furthermore, in some cases, a different or original oligomeric status is observed. Taken together, these data strongly suggest that ESPs are not simply a population of unrelated proteins, but are a functionally oriented set of active proteins. Finally, genome-wide bioinformatics shows that although a number of Trypanosoma proteins are predicted to be secreted, few ESPs possess a transit peptide and most probably use a nonclassical secretion pathway. Thus, several lines of evidence converge to identify the Trypanosoma secretome as an original proteome, showing unique features both in terms of function and origin. It is noteworthy that some of the characteristics above, including the function of proteins and the absence of a transit peptide, were recently observed in the Leishmania secretome. This raises the question as to whether these features reveal a generic trait and whether the two parasites share common survival strategies.
Function of secreted proteins
Our results showed that most ESPs delineate a quite limited set of functions. Generally speaking, the functions identified are not unexpected given the known physiology of Trypanosoma and the parasite's requirement for defense mechanisms against its host. However, for a number of proteins, previous evidence exists that they may also have other roles. Below we discuss a few examples.
Diversity of peptidase families found in the secretome of T. brucei gambiense bloodstream form and their distribution in other organisms.
Families of Peptidases
Serine peptidase family S9
Bacteria, Archaea, Protozoa, Fungi, Plants, Animals, Viruse
Cysteine peptidase family C2
Bacteria, ----------, Protozoa, Fungi, Plants, Animals, --------
Cysteine peptidase family C13
Bacteria, Archaea, Protozoa, Fungi, Plants, Animals, --------
Cysteine peptidase family C19
Bacteria, ----------, Protozoa, Fungi, Plants, Animals, Viruse
Metallo-peptidase family M1
Bacteria, Archaea, Protozoa, Fungi, Plants, Animals, --------
Metallo-peptidase family M3
Bacteria, Archaea, Protozoa, Fungi, Plants, Animals, --------
Metallo-peptidase family M16
Bacteria, Archaea, Protozoa, Fungi, Plants, Animals, Viruse
Metallo-peptidase family M17
Bacteria, Archaea, Protozoa, Fungi, Plants, Animals, --------
Metallo-peptidase family M20
Bacteria, Archaea, Protozoa, Fungi, Plants, Animals, --------
Metallo-peptidase family M24
Bacteria, Archaea, Protozoa, Fungi, Plants, Animals, --------
Metallo-peptidase family M32
Bacteria, Archaea, Protozoa, -------, Plants, ----------, --------
Among metallopeptidases, the thimet oligopeptidase A is the first member of the M3 family to be identified in Protozoa. Thus, this protease, which processes neuropeptides in humans , may be a good candidate for a specific diagnostic marker. Another metallopeptidase in the secretome belongs to the M32 family, absent in eukaryotic genomes other than trypanosomatids . Although of unknown biological function, it might offer attractive drug targets against Trypanosoma.
Proteins involved in folding and degradation are the major class of secreted proteins. Apart from contributing to protecting the parasite against the defense mechanisms of the host, many of them also appear to have the capacity to induce perturbations in the host physiology. Given their abundance, one may speculate that they play a genuine role in the pathology. Some of these proteins may be promising candidates for diagnosis or therapy. As well as degrading proteins, proteases perform highly specific processing tasks that can affect protein structure, function, life span, and localization. By limited and specific cleavage, proteases can act as switches, turning protein activity on or off, or can modulate protein function in more complex ways, regulating vital processes. Indeed, more than 53 specific hereditary diseases of proteolysis are recognized and it is therefore not surprising that proteases are implicated in many pathologies. Hence, proteases account for 5-10% of drug targets, with protease inhibitor drugs already in use to treat AIDS (acquired immunodeficiency syndrome) by blocking HIV (human immunodeficiency virus) protease-1, cardiovascular disease by targeting angiotensin convertase enzyme and rennin, and multiple myeloma by the reversible covalent proteasome inhibitor. In addition, many biomarkers of disease, especially in cancer, are stable fragments generated by proteolysis and found in biological fluids .
Enzymes of nucleotide metabolism are another major class of ESPs represented here by more than 46 protein accessions. This is not unexpected, as T. brucei is incapable of de novo purine nucleotide synthesis and expresses purine salvage enzymes to recover host purines . However, extracellular nucleotides are also signaling molecules that modulate a wide variety of physiological responses in mammalian tissues  and are archetypal activators of the innate immune system . In this context, both hematophagous insects and endoparasites secrete enzymes degrading nucleotides, thus minimizing inflammatory reactions or purinergic signaling provoked by these mediators [56, 57]. As such, the identification of several nucleotide-metabolizing enzymes in the secretome raises the question of whether T. brucei might exploit such strategies to modulate the concentration of extracellular nucleotides, hence affecting a range of inflammatory responses. If so, Trypanosoma would not only divert the host nucleotides for its own requirements, but also to evade an immune response.
Enzymes involved in glycolysis and carbohydrate metabolism are not a major class of the secretome, but this category still numbers more than 36 accessions. Trypanosoma have a simplified energy metabolism entirely dependent on external carbohydrate sources, such as blood glucose.
Most glycolysis enzymes are compartmented in glycosomes , but three are cytosolic: phosphoglycerate mutase, enolase, and pyruvate kinase . We found all three in the T. brucei secretome, together with phosphoglycerate kinase, yet this secretome strongly differs from glycosomes. Although not yet reported as being secreted in Trypanosoma, all four enzymes are secreted by other organisms and may be involved in functions unrelated to glycolysis, such as peptide cleavage or immunosuppressive activity [60–63]. Therefore, it cannot be excluded that Trypanosoma might use part of its energy metabolism machinery for alternative purposes.
Enzymes involved in signaling constitute another group of proteins identified in the T. brucei secretome (26 accessions), and some could also play physiopathological roles. Two notable examples here concern calreticulin (CRT) and prostaglandin F (PGF) synthase. Autoantibodies against CRT are found in the sera of human hosts of a number of parasitic diseases  and it was suggested that the parasite-derived CRT could trigger an inappropriate immune response against self-antigens through molecular mimicry . The gene encoding PGF synthase is present in T. brucei, and we show that this enzyme can be secreted. Given that African trypanosomiasis is characterized by miscarriage, due to PGF overproduction correlated with parasitemia peaks , the finding that T. brucei secretes a PGF synthase suggests that this enzyme may well play a role in pathogenesis.
One trivial role of protein secretion in hosts is usually associated with trophic purposes for the benefit of the parasites. Several recent proteomics studies highlighted other features, depending on the parasite. For instance, whereas for Brugia malayi a large fraction of the 80 proteins found to be secreted are involved in energy metabolism , for the helminth Schistosoma mansoni the 188 proteins identified include proteins involved in metabolic pathways and in protein folding, development, and signaling, or immune response modulation , and the secretome of Plasmodium falciparum is predicted to encompass several hundred proteins to both import nutrients and remodel the host erythrocyte . In this work, the 444 identified T. brucei-secreted proteins display a specific pattern and, for a number of these, there is evidence for possible alternative functions. The various examples detailed above support the hypothesis that, far from being fortuitous, these features probably reveal an additional role for the secretome in manipulating the host in order to overcome its defenses. As such, the secretome would also play a key role in the pathogenicity of the parasite. More generally, this suggests that, apart from the production of VSGs to elude the host immune system, the secretome might also be another authentic component of the survival strategy of Trypanosoma.
Origin and significance of the identified secretome for the survival strategy of Trypanosoma
Only a minority of ESPs appear to possess a transit peptide, raising the question of the nature of the secretory pathway in Trypanosoma. Several arguments support the hypothesis that secretion could take place by the release of microvesicles. Such small vesicles contain cytosol and proteins from the plasma membrane, but no protein from intracellular organelles. On the one hand, apart from the nine proteins specifically involved in vesicle transport and trafficking, we identified 13 out of the 22 most common exosome proteins. On the other hand, we found very few proteins from intracellular compartments (1% of the secretome). The viability of Trypanosoma tested with flow cytofluorometric analysis and microscopic analysis suggests that the nonspecific release of material from lysed cells is modest and the yield of secreted proteins is not correlated to viability but is strain-specific (for example, Biyamina produced 4 times less secreted proteins than other strains). Moreover, the comparison between the total proteome and the secretome showed in this study also suggests that contaminations from nonspecific release would be relevant only if the kinetics of release is highly protein-specific. In addition, ubiquitin seems to play a key role in the sorting of proteins into exosomes , and we identified ubiquitin and 25 related proteins of the ubiquitin/proteasome pathway. Thus, the overall picture of the Trypanosoma secretome shows homologies with exocytosis occurring in the flagellar pocket and with exosome-related proteomes. Interestingly, we have successfully demonstrated for the first time the presence of vesicles at the trypanosome surface using electron microscopy and further shown that similar vesicles are present in the secretion medium. Moreover, proteomic analysis of TIRSP confirmed the presence of a set of proteins that is very similar (71%, 46/65) to ESPs purified from isolated parasites. Thus, both approaches converge to strengthen the hypothesis of a new secretion pathway in Trypanosoma. Indeed, the size of the vesicle-like structure observed on electronic microscopy pictures fits with microvesicles (50-100 nm). This situation seems to be shared with Leishmania, a close relative of Trypanosoma, where the absence of transit peptides in secreted proteins and the presence of microvesicles at the promastigote surface were recently demonstrated . This differs from the case of P. falciparum, where a specific host-targeting motif was described for secreted proteins .
This could be hypothesized to present several advantages for Trypanosoma, in comparison to the classical secretory pathway: it may deliver an avalanche of new epitopes to overwhelm the host immune system or to communicate between trypanosomes themselves by exchanging receptors in the form of non-protein cytosolic compounds or even potentially genomic information. As such, microvesicles could be a flexible way for Trypanosoma to reversibly adapt its machinery and to homogenize the survival strategy at the population level.
This study provides the first overview of proteins secreted by Trypanosoma brucei. Several of them had not yet been discovered and studied in trypanosomes, and some may be new potential therapeutic targets or diagnostic markers. Strikingly, some proteins do not use the classical secretory pathway and many probably play additional roles once secreted. Collectively, these data lead to novel hypotheses concerning both the pathogenic role of secreted proteins and the secretion pathway in trypanosomatids, providing insight into the complex survival strategy of T. brucei.
Ethical statement: all the experiments on animals reported in this article were performed according to internationally recognized guidelines; the experimental protocols were approved by the Ethical Committee on Animal Experiments and the Veterinary Department of the Centre International de Recherche Agronomique pour le Développement (CIRAD), Montpellier-France. No experiment was performed on human.
Male Wistar rats (6-12 weeks old) were purchased from Charles Rivers (France).
Feo [72, 73], OK  and Biyamina  parasite bloodstream strains were used for the experiment. The parasites were intraperitoneally injected into rats. When their multiplication reached the logarithmic growth stage, the parasites were purified from blood by chromatography on a DEAE (diethylaminoethyl) cellulose column, as previously described . After elution, the parasites were washed three times in sterile phosphate-buffered saline (PBS) solution. This resulted in a complete elimination of the rat blood proteins.
Excreted/secreted protein (ESP) production
The parasites were resuspended at a concentration of 200.106 cells/ml in a secretion buffer (Ringer lactate, glucose 0.6%, Kcl 0.4%, NaHCO3 0.125%, polymixin B 5 μg/ml, L-glutamine 2 mM, MEM nonessential amino acids, pH 8) . The secretion of ESPs was performed at 37°C/5% CO2 for 2 h. At the end of the experiment, the reaction was stopped by centrifugation of parasites at 4°C, 1000 g for 10 min. The supernatant was collected and filtered on a 0.2-μm filter and immediately mixed with a protease inhibitor mix. ESPs were concentrated by ultrafiltration using a PM - 10-kDa membrane (Amicon). The protein concentration was determined by the Bradford dye binding procedure (Bio-Rad). Concentrated ESPs were analyzed further by SDS- and BN-PAGE and visualized after staining with coomassie blue.
The percentage of apoptotic parasites was quantitated every 15 min by flow cytofluorometric analysis using the DNA intercalant propidium iodide (IP), as recommended by the manufacturer (Immunotech, Marseille, France). Cells were immediately analyzed with a FACScan (fluorescence-activated cell sorting) flow cytometer (Becton Dickinson, Ivry, France) using an argon-ion laser. Parasite viability, determined every 15 min, remained constant for 2 h and was more than 95%. Moreover, cellular integrity was controlled by microscopic examination of aliquots of the incubation medium during the 2-h period of trypanosome incubation.
One-dimensional electrophoretic analysis
Proteins from the different samples were heated at 100°C for 2 min and spun for 5 min at 14,000 g prior to separation by one-dimensional SDS-PAGE. Proteins were separated on 24 × 18-cm Tricine/SDS-PAGE (12% acrylamide) .
After migration, the gels were fixed, and the proteins were visualized by coomassie brilliant blue R-250. Images of the gels were taken with a high-resolution scanner (Amersham Biosciences).
Proteins were concentrated and directly loaded on native PAGE gradients 6-15% acrylamide for the first dimension and on a 12% Tricine-SDS-PAGE for the second dimension, as described in Peltier et al., 2004 . Proteins were visualized by coomassie blue staining.
Protein identification by mass spectrometry
Stained protein spots were manually excised, washed, digested with trypsin, and extracted using formic acid. Protein digests were analyzed using either a hybrid triple-quadrupole linear ion trap mass spectrometer (Q-TRAP 4000; Applied Biosystems), coupled to a nano-chromatography system (Dionex), or an ion trap mass spectrometer (Esquire HCT; Bruker), interfaced with an HPLC (high-performance liquid chromatography) chip system (Agilent). MS/MS data were searched against NCBI (National Center for Biotechnology Information) and Trypanosoma brucei databases using Mascot software. Raw data were analyzed using Data Analysis software (Bruker) to generate a peak list for searching a Trypanosoma database extracted from the Sanger Institute. The Mascot (v2.2) search engine was used with the following parameters: one missed cleavage allowed for trypsin, carboxymethylation of cyst as fixed modification, methionine oxidation as variable modification, and a 0.6-Da tolerance range for mass accuracy in MS/MS. At least one matching sequence tags of high quality was needed for positive identification of proteins. Potential false positive identifications have been addressed as described in Elias et al., 2005  using identical search parameters against a database in which the sequences have been reversed. We set a false discovery rate (FDR) of 1%. When the Mascot peptide score was below (and even above) the Mascot peptide score indicated for a FDR of 1%, a systematic manual validation was done with stringent parameters (at least 6 y or b ions, at least 4 consecutive ions, and peptidic sequence formed of more than 7 amino acids). The proteins were classified according to MapMan http://mapman.gabipd.org. Raw data will be made available upon request for research purposes. Additional data on identified proteins are supplied in additional file 8 (Table S8).
Preparation of vesicles by ultracentrifugation and sucrose gradient
Secretion buffer and infected rat serum after parasite depletion were filtered (0.2 μm). Membranes were isolated from secretion buffer and serum of Trypanosoma-infected rats by a 140,000 g ultracentrifugation for 30 min at 4°C. Pellets were resuspended in 20 mM Tris/Hcl buffer pH 7.8 and layered on top of a step sucrose gradient (20-30-40-60% sucrose [Sigma-Aldrich]). Gradients were centrifuged for 2 h at 100,000 g at 4°C. Fractions were collected at the interface 20/30%, 30/40%, and 40/60%, diluted in 20 mM Tris-Hcl buffer pH 7.8, and pelleted (140,000 g for 30 min at 4°C). Pellets were resuspended in Tris buffer and loaded on SDS-PAGE. After staining protein bands were picked and washed and proteins were trypsinated. Peptides were analyzed by LC-MS/MS on an orbitrap.
Transmission electron microscopy
Sample preparation for ultrastructure
Observations on whole trypanosomes obtained after incubation in secretion medium or directly from blood of infected rat were conducted as described previously . After centrifugation, pellets of trypanosomes were fixed in 4% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.2) overnight at 4°C, washed in fixation buffer, postfixed in osmium tetroxide for 1 h at 4°C and washed. Pellets were dehydrated in an acetone series and embedded in TAAB 812 epon resin .
Thin sections, mounted on 75 mesh collodion carbon-coated copper grids, were contrasted with uranyl acetate and lead citrate and examined at 80 KV with a transmission electron microscope (Jeol 100CX II).
The stains were prepared according to Brun et al., 2008 . Basically, 2-3 μl of sample (vesicles obtained by ultracentrifugation and sucrose gradient) were layered onto a 200-formvar-coated grids for 1 min. Liquid was remove with filter paper. The grid was incubated with a negative stain (1.5% uranylacetate in 70% ethanol for 1 min) and washed 3 times with water. The preparation was observed with a Hitachi H. 7100 transmission electron microscope.
acquired immunodeficiency syndrome
blue native-sodium dodecyl sulfate-polyacrylamide gel electrophoresis
Basic Local Alignment Search Tool
bloodstream stage alanine-rich surface protein
fluorescence-activated cell sorting
receptor for adenylate cyclase
human African trypanosomiasis
heat shock protein
human immunodeficiency virus
high performance liquid chromatography
invariant surface glycoprotein
- LC-ESI MS/MS:
liquid chromatography-electrospray tandem mass spectrometry
National Center for Biotechnology Information
proteasome activator protein with a molecular mass of 26-kDa
transmembrane protein topology with a Hidden Markov Model
translationally controlled tumor protein
Trypanosoma infected rat serum
variant surface glycoprotein
This work was funded by the Foundation for Medical Research (FRM). We sincerely thank Dr Daniel Fisher for his kind proofreading of the manuscript. We thank Pr Philippe Vincendeau and Dr Philippe Holzmuller for providing secretion buffer and Dr Sophie Ravel for her technical help. We thank Dr Chantal Cazevieille from the CRIC (Centre Régional d'Imagerie Cellulaire) laboratory in Montpellier for the electronic microscopy negative stain picture analysis, the Pôle Proteome de Montpellier, particularly Dr Serge Urbach and Martial Seveno for the MS/MS analysis of the TIRSP fraction on Orbitrap, and Dr Nicolas Sommerer for making complementary MS facilities available and for expert advice.
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