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J. Biol. Chem., Vol. 275, Issue 36, 27671-27680, September 8, 2000

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Trypanosoma cruzi Surface Mucins with Exposed Variant Epitopes^*

Guido D. Pollevick^§¶, Javier M. Di Noia^§, Maria L. Salto^**, Carlos Lima^**§§, M. Susana Leguizamón^¶¶¶, Rosa M. de Lederkremer^¶**, and Alberto C. C. Frasch^¶

From the  Instituto de Investigaciones Biotecnológicas, Instituto Tecnológico de Chascomús (CONICET), Universidad Nacional de General San Martín, Av. Gral. Paz s/n, INTI, Edificio 24, 1650, San Martín, Pcia. de Buenos Aires, ^** CIHIDECAR (CONICET) Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, and the ^¶¶ Departamento de Microbiología, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina

Received for publication, January 12, 2000, and in revised form, June 7, 2000

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

The protozoan parasite Trypanosoma cruzi, the agent of Chagas disease, has a large number of mucin molecules on its surface, whose expression is regulated during the life cycle. These mucins are the main acceptors of sialic acid, a monosaccharide that is required by the parasite to infect and survive in the mammalian host. A large mucin-like gene family named TcMUC containing about 500 members has been identified previously in T. cruzi. TcMUC can be divided into two subfamilies according to the presence or absence of tandem repeats in the central region of the genes. In this work, T. cruzi parasites were transfected with one tagged member of each subfamily. Only the product from the gene with repeats was highly O-glycosylated in vivo. The O-linked oligosaccharides consisted mainly of -D-Galp(14)GlcNAc and -D-Galp(14)[-D-Galp(16)]-D-GlcNAc. The same glycosyl moieties were found in endogenous mucins. The mature product was anchored by glycosylphosphatidylinositol to the plasma membrane and exposed to the medium. Sera from infected mice recognized the recombinant product of one repeats-containing gene thus showing that they are expressed during the infection. TcMUC genes encode a hypervariable region at the N terminus. We now show that the hypervariable region is indeed present in the exposed mature N termini of the mucins because sera from infected hosts recognized peptides having sequences from this region. The results are discussed in comparison with the mucins from the insect stages of the parasite (Di Noia, J. M., D'Orso, I., Sánchez, D. O., and Frasch, A. C. C. (2000) J. Biol. Chem. 275, 10218-10227) which do not have variable regions.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Mucins in vertebrate cells are highly O-glycosylated proteins having relevant roles in protection and in cell-cell interactions. The former function is accomplished mainly by high molecular weight epithelial mucins and the latter by the much smaller endothelial and leukocyte mucins, all of them encoded by a few dozen genes (1, 2). In the lower eukaryote Trypanosoma cruzi, the protozoan agent of Chagas disease, mucins seem to have essential functions and unusual characteristics. The parasite mucins, located on the surface membrane, are the main acceptors of sialic acid transferred from host's glycoconjugates by the trypanosomatid-specific enzyme trans-sialidase (3). Surface mucins seem to be involved, after acquiring sialic acid, in the invasion of host cells by the parasite and in the protection against the alternative complement pathway (4-7). Both steps are essential for parasite replication and survival in mammals.

Mucins from T. cruzi were first isolated with aqueous-phenol and called bands A, B, and C (8, 9). These glycoproteins were strongly labeled after intact parasites were treated with galactose oxidase/NaB³H₄, thus proving their surface location (10). More recently, the structure of the O-linked sugars (11-13) was described. The oligosaccharides are linked through GlcNAc, rather than the GalNAc commonly found in vertebrate mucins. Most of the O-linked GlcNAc residues are substituted with 1-5 galactosyl units. The structures of the O-linked oligosaccharides are conserved between epimastigotes (the form of the parasite present in the insect vector midgut) and metacyclic trypomastigotes (the infective form in the feces of the insect). However, there are some polymorphisms among the strains, the most important one being the presence of galactofuranose in the G strain (12, 13), whereas in the Y strain the O-linked oligosaccharides contain only galactopyranose (11). The mucins present in these forms of the parasite are glycoproteins of about 35-50 kDa, whereas those in cell culture-derived trypomastigotes are considerably larger (70-200 kDa). The latter molecules have O-linked oligosaccharides terminating with -Galp residues, epitopes that elicit a lytic antibody response in the human (14).

The largest gene family encoding mucin-like genes described so far is present in T. cruzi, showing diversity among and within strains of the parasite (15, 16). 500 mucin-like genes per haploid genome have been estimated to be present in this parasite (16), all members of a family named TcMUC because their overall structure resembled that of mucin genes in higher eukaryotic cells (17). They all have conserved 5'- and 3'-regions, encoding a predicted signal peptide at the N terminus, and a C-terminal region that includes a putative sequence for a GPI¹ anchor. Between the conserved ends, there is a variable central domain that characterizes two subfamilies within the mucin-like gene family. In one of these subfamilies, the central region encodes repetitive motifs with the consensus sequence T₈KP₂. In the second subfamily, the central domain codes for a region lacking amino acid repeats, which is rich in codons for Thr, Ser, and Pro residues, but which is variant in sequence among the members (16). Because of its organization and amino acid composition, these central regions were predicted to contain the target sites for O-glycosylation (17). This assumption is supported by the facts that a repeats-containing member became highly glycosylated when transfected in Vero cells (15) and that the synthetic peptide KP₂T₈KP₂ is a good substrate for the enzyme UDP-N-acetylglucosamine:peptide N-acetylglucosaminyl transferase, which starts O-glycosylation in T. cruzi (18). However, a direct demonstration that these genes indeed code for the core protein of parasite mucins is still lacking. The small sequence (8-16 amino acids) between the signal peptide and the repeats, likely to code for the mature N terminus of mucins, is highly variable among members of the family (16). Comparison of this hypervariable (HV) region from 32 cDNA clones showed 22 different variants (16).

A second gene family encoding mucin-type polypeptides (TcSMUG) was recently reported in T. cruzi. It is less complex than TcMUC and does not present any variable region. Several evidences suggest that TcSMUG probably encodes mucins from the insect stages of the parasite (19).

Three main questions about the TcMUC family are addressed in this work. First, do any of the mucin-like gene subfamilies code for parasite mucins, and what is the structure of these glycoproteins? Second, at which stages are the products expressed? Third, are the HV regions present in the mature products, and do they interact with the host immune system? Here we show that a gene representative of those encoding the repetitive T₈KP₂ central domain resulted in a highly O-glycosylated product, linked to the surface membrane through a GPI anchor. Sera reactivity with recombinant proteins indicates that these kinds of products are expressed during the vertebrate infection and that antibodies from natural and experimental infections can recognize the HV regions. Taken together, these results suggest a structural model for TcMUC-encoded mucins on the surface of the parasite and that the hypervariability in their exposed N terminus is driven by natural selection.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Parasites

Epimastigotes of the T. cruzi RA strain (20) and the CL-Brener cloned stock (21) were grown axenically with shaking at 28 °C in BHT medium (22) supplemented with 10% fetal calf serum (Life Technologies, Inc.). Cell-derived trypomastigotes, equivalent to the bloodstream forms of the parasite, were obtained by centrifugation from the supernatant of infected Vero cells at day 6-7 postinfection (19).

Construction of Epitope-tagged Mucin Genes and T. cruzi Transformation

Because sugars might hinder the access of antibodies to protein epitopes of molecules expected to be heavily O-glycosylated like TcMUC products in T. cruzi, a tag made up of the amino acid residues 21-44 of the HCV core protein (23), which lacks N- and O-glycosylation sites, was inserted within the sequence predicted to encode the mature N-terminal region of MUC-CA3 and MUC-RA2 (17). Gene fusions were generated by polymerase chain reaction following standard protocols (24) and using the oligonucleotides indicated in Table I. The region spanning the repeats and C-terminal domains of MUC-CA3 was amplified using primers MREcoRI and P2 and cloned into pBlueScript KS II+ (Stratagene, San Diego, CA). Primers MNREcoRI and P2 were used to do the same with the central and C-terminal domains of MUC-RA2. Oligonucleotides C21-44A and C21-44B were annealed to create a double-strand insert encoding the HCV core epitope that was cloned in-frame with both fragments mentioned above. Finally the corresponding N-terminal regions of MUC-CA3, amplified with primers MRatg and MRBglII, and MUC-RA2, amplified using primers MNRatg and MNRBglII, were added to the corresponding construct in-frame with the tag. These tagged versions of MUC-CA3 and MUC-RA2 were named MUC-R and MUC-NR, respectively, and subcloned into both the T. cruzi expression vector pRIBOTEX (25), kindly provided by Dr. R. Hernández (Universidad Nacional Autónoma de México, México), and the pET-25b(+) (Novagen, Madison, WI) Escherichia coli expression vector.

Epimastigotes of T. cruzi were transformed by electroporation with the Qiagen-purified (QIAGEN Inc, Chatworth, CA) recombinant pRIBOTEX plasmids, using a slight modification of described procedures (26). The transfected parasites were selected by the pRIBOTEX-encoded G418 resistance using 500 µg/ml Geneticin (Sigma) and used as populations after 40 days of selection. MUC-R and MUC-NR were transfected into epimastigotes of both RA strain and of CL-Brener clone of T. cruzi. A similar result was obtained when each gene was expressed in both strains of the parasite, although the levels of product expression were very different (results not shown). Transcription of the recombinant genes was analyzed by Northern blot washed at 65 °C in 0.1 × SSC, 0.1% SDS as described (19).

Antibodies and Serum Samples

Anti-tag is a polyclonal serum raised in rabbit against the purified recombinant 21-44 amino acid residues of HCV core protein (23) expressed in pGEX-1 (Amersham Pharmacia Biotech) as a fusion with the Schistosoma japonicum glutathione S-transferase (GST). This serum was preadsorbed with GST before use to prevent background signals from T. cruzi homologous enzymes. Anti-cross-reacting determinant (CRD) was obtained from Oxford GlycoSystem, Rosedale, NY. Anti-GST is a polyclonal serum raised in rabbit against purified recombinant GST expressed from the pGEX-1 plasmid vector. Monoclonal antibody 3F5 was a kindly gift from Dr R. Mortara (Escola Paulista de Medicina, Sao Paulo, Brazil).

Sera from 10 rabbits infected with different T. cruzi strains and bled at 15, 30, and 60 days postinfection (dpi) were kindly given by Dr. D. Sánchez (Instituto de Investigaciones Biotecnológicas, San Martín, Argentina). Sera from 12 infected humans in the chronic stage of the disease, as assessed by their differential reactivity against cruzipain and SAPA T. cruzi antigens (27), were used. Mice sera used in Table II were from 42 individuals, each one belonging to any of four different mice strains, infected with one of seven different T. cruzi strains and bled at postinfection times ranging from 8 to 210 days and so being from the chronic or acute stages of the infection (for details, see the Table II legend). Sera used in Table III were obtained from 13 1-month-old Rockland mice infected intraperitoneally with 10⁵ blood trypomastigotes of the Acosta population of T. cruzi and bled at three different times postinfection. Sera from noninfected individuals were used as controls (four from rabbits, eight from humans, and four from mice).

Immunoprecipitation and Endoglycosidase H Treatment of Recombinant Mucin

Conditioned culture medium from transfected T. cruzi epimastigotes was clarified for 10 min at 10,000 × g and concentrated 8 times by Polyethylene Glycol 8000 dialysis. Aliquots were immunoprecipitated using a 1/500 dilution of either anti-tag or anti-GST serum and protein A-agarose beads (Life Technologies, Inc.), following standard protocols (28). Immunoconjugates were analyzed by Western blot with anti-tag or anti-CRD serum. In another experiment, equally anti-tag immunoprecipitated proteins were eluted from protein A-Sepharose beads in 0.1 M sodium acetate, pH 5.5, 0.1% SDS, by boiling 5 min. The supernatant was treated with 5 milliunits of endoglycosidase H (New England Biolabs, Beverly, MA) for 16 h at 37 °C or mock treated as control. Reactions were analyzed with anti-tag by Western blot.

Expression and Purification of Recombinant Proteins

Protein M76-- The TcMUC repeats-containing gene MUC-M76 (GenBank accession number L20809) was cloned in pGEX-1T vector (Amersham Pharmacia Biotech). The resulting recombinant protein spanned from the HV region to the conserved C terminus fused with GST.

Proteins GST-E13, T15, T18, and NCA-- Two complementary oligonucleotides having the sequence encoding the HV region from clones EMUCe-13, EMUCt-15, EMUCt-18 (16), and MUC-CA2 (17) were synthesized. Sense and antisense oligonucleotides (Table I) were annealed and cloned in pGEX-2T. Their deduced amino acid sequences are AAEGGGQKQENT, SEEGKQET, TASGQKAEQDT, and AESVSQNN, respectively. All of the GST fusion proteins were purified identically by affinity chromatography on glutathione-Sepharose beads (Sigma) following manufacturer's instructions. Their purity was assessed by SDS-PAGE and they were quantified using Bradford reagent (Bio-Rad).

Gel Electrophoresis and Western Blots

Gel electrophoresis was performed in 7.5 or 12.5% polyacrylamide in the presence of 0.1% SDS (SDS-PAGE). When needed, gels were prepared for fluorography (29), dried, and exposed to Kodak X-Omat AR-5 films at 70 °C. For Western blot, parasites were resuspended in lysis buffer (150 mM NaCl, 1% Nonidet P-40, 50 mM Tris-HCl, pH 7.5, in the presence of 50 µM E64 and 1 mM phenylmethylsulfonyl fluoride), at 10⁶ parasites/µl, and 5 × 10⁷ epimastigotes were loaded in each lane. After SDS-PAGE, lysates were transferred to nitrocellulose filters (Life Technologies, Inc.), reacted with the appropriate sera, and developed with ¹²⁵I-protein A (NEN Life Science Products).

Dot-Spot Immunoassays

1 µl containing 200 ng of each indicated recombinant protein in TBS (50 mM Tris-HCl, pH 7.6, 150 mM NaCl) was spotted on nitrocellulose filters and air dried. Filters were processed as in Western blots using sera from different infected animals diluted 1/100 and ¹²⁵I-protein A. Recombinant GST-SAPA (30) and epimastigote-purified cruzipain (31) antigens were always included as controls of positive infection. Sera from noninfected individuals were included in each assay as background controls. Internal negative controls consisting of GST derived from pGEX-1, 2T, and 1T were also included. Only those signals clearly above those obtained with the noninfected sera and GST were recorded as positive.

Oligosaccharide Standards

-D-Galp(14)GlcNAc and -D-Galp(13)GlcNAc were from Sigma. The disaccharides -D-Galf(14)GlcNAc (32), -D-Galf(16)GlcNAc and -D-Galf(13)GlcNAc (33), -D-Galp(16)GlcNAc (34) and the trisaccharides -D-Galf(14)[-D-Galp(16)]-D-GlcNAc (34) and -D-Galp(13)[-D-Galp(16)]-D-GlcNAc were kindly given by C. Gallo-Rodriguez. Labeled -D-Galp(14)[-D-Galp(16)]-D-GlcNAcol was kindly provided by Drs J. O. Previato and Lucia Mendonça-Previato (Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil).

Preparation of Unlabeled and Labeled Alditols

The corresponding alditols were prepared by reduction of 0.2 mmol of disaccharide or trisaccharide in 9/1 methanol/water (10 ml) with NaBH₄ (2 mM). The mixture was left overnight at room temperature, and the solution was decationized by elution through a column of Bio-Rad AG 50W-X12 (H⁺ form) resin. The solvent was evaporated, and the boric acid was eliminated by five successive coevaporations with methanol. The purity of the alditol was checked by TLC. For the preparation of the labeled alditols, 100 µg of the sugars was reduced with 500 µCi of NaB³H₄ (NEN Life Science Products) in water for 1 h at room temperature, followed by the addition of unlabeled NaBH₄ and processing as above.

Thin Layer Chromatography and High pH Anion Exchange Chromatography with Pulse Amperometric Detection (HPAEC-PAD)

Analysis by TLC and HPAEC-PAD were performed as described (35).

Galactose Oxidase/NaB³H₄

In Vivo Labeling-- For the galactose oxidase labeling experiments 10⁸ T. cruzi cells were resuspended in 0.5 ml of PBS containing 22 units of galactose oxidase (Sigma) and incubated for 90 min at 30 °C with gentle agitation. The cells were washed three times with PBS, suspended in 0.5 ml of PBS, and 1 mCi of NaB³H₄ was added, and incubation proceeded for 30 min at room temperature. The reaction was stopped with 0.5 ml of cold PBS, and the cells were washed with a solution of 1% NaBH₄ in 7% NaCl and then twice with 7% NaCl. The final pellet was lysed directly with the electrophoresis sample buffer under reducing conditions and applied onto polyacrylamide gels.

Labeling of Isolated Glycoconjugates-- A sample of glycoconjugate (5 µg) was suspended in 0.5 ml of PBS containing 20 units of galactose oxidase (Sigma) and incubated overnight at 37 °C. The solution was adjusted to pH 8 with 2.5 M NH₄OH; 1 mCi of NaB³H₄ was added, and incubation proceeded for 3 h at room temperature. Reduction was completed with NaBH₄ for 4 h and dialyzed against water with gentle agitation. The sample was lyophilized and applied to a column of octyl-Sepharose CL-4B with 50 µg of nonlabeled material.

Purification of Mucins from T. cruzi

Mucins from Wild Type Epimastigotes-- Mucins were extracted from lyophilized cells (~10¹¹) and purified as described (35).

Mucins from Transfected Epimastigotes-- The pellet obtained after extraction with water/butanol as described under "In Vivo Labeling" was extracted further with 44% aqueous phenol as described previously (8). The aqueous extracts in each case were lyophilized and purified by affinity chromatography, using rabbit IgG anti-tag bound to Sepharose 4B.

PI-Phospholipase C Treatment

The pellet obtained after extraction with water/butanol was digested with 1 unit of PI-phospholipase C from Bacillus thuringiensis (Oxford GlycoSciences, Inc) in 50 µl of Tris-HCl, pH 7.2, containing 0.1% deoxycholate at 37 °C. After centrifugation the supernatant was analyzed by Western blot.

Reductive -Elimination of O-linked Oligosaccharides

The glycoproteins were treated with a solution (0.2 ml) of 0.05 M NaOH containing 500 µCi of NaB³H₄ at 37 °C. After 1 h, a solution of 0.6 M NaBH₄ (0.2 ml) was added, and the reaction mixture was kept for 24 h at 37 °C, acidified with 1 M acetic acid, N-acetylated (36), decationized by passage through AG 50-W-X12 (H⁺), and dried in vacuo at room temperature. Boric acid was removed by repeated coevaporations with methanol. The labeled sugar alditols were purified by Bio-Gel P-2 chromatography.

Acetolysis

A sample was acetylated with acetic anhydride/pyridine (1/1) for 30 min at 100 °C and dried under a stream of N₂. A mixture of acetic anhydride/acetic acid/concentrated H₂SO₄ (10/10/1) was added, and incubation proceeded for 8 h at 37 °C. After the addition of 40 µl of pyridine and evaporation (three times with additions of toluene), partition was performed with 1 ml of water and chloroform. The organic phase was evaporated and deacetylated with sodium methoxide at room temperature for 1 h. The mixture was decationized by passage through AG 50W-X12 (H⁺).

Metabolic Labeling of T. cruzi

CL-Brener epimastigotes in the logarithmic growth phase, and cell-derived trypomastigotes from 1-week-infected Vero cells monolayers were harvested, washed twice with PBS, and resuspended at 10⁸/ml in minimal essential medium/Select-amine (Life Technologies, Inc.) Thr- and fetal calf serum-free, supplemented with 1.5 mg/ml glucose. After a 30-min incubation at 37 °C, a pulse of [¹⁴C]Thr (NEN Life Science Products) was added and incubated further for 10 min, after which a 2-h chase was done by adding Thr to 0.5 mM and 2% fetal calf serum. Parasites were harvested, washed twice in PBS, resuspended in lysis buffer (50 mM Tris-HCl, pH 7.6, 150 mM NaCl, 1% Triton X-100, 1% sodium deoxycholate with 1 mM phenylmethylsulfonyl fluoride and 0.5 mM N-p-tosyl-L-lysine chloromethyl ketone) and submitted to aqueous phenol extraction. The aqueous layer was dialyzed, lyophilized, resuspended in water, and analyzed by SDS-PAGE stained by periodic acid-Schiff (36), after which fluorography was performed using EN³HANCE (NEN Life Science Products).

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Expression of Two Tagged TcMUC Genes in T. cruzi.-- Two representative members of the TcMUC gene family, one belonging to subfamily encoding T₈KP₂ repeats (MUC-R) and a second one coding for a nonrepetitive central domain but still rich in Ser, Thr, and Pro (MUC-NR) (Fig. 1A), were tagged and cloned in the vector pRIBOTEX (25) and transfected into T. cruzi epimastigotes. After selection with G418, the tag probe detected bands in Northern blots of the transfected parasite population (Fig. 1B). The repetitive TcMUC genes like MUC-R show their highest level of mRNA at the trypomastigote stage in wild type parasites (17, 37). The nonrepetitive genes should be considered individually as they differ widely in sequence, and their mRNA level can be different for each member at a given stage (16). MUC-RA2, the gene used for MUC-NR construction, mRNA level is similar, although very low, in both epimastigotes and trypomastigotes.² Notwithstanding this, the coding regions cloned into pRIBOTEX, devoid of any extragenic region, are expressed irrespectively of the expression of their endogenous homologous.

View larger version (25K): [in this window] [in a new window]   Fig. 1.   A, schematic representation of proteins derived from the transfected repetitive (MUC-R) and nonrepeated (MUC-NR) MUC genes of T. cruzi. The structure of the two deduced products is represented with their different regions indicated. The dashed line indicates a gap for best alignment. Degenerate repeats are indicated as black boxes. The deduced sequence of the central and Thr-rich regions is indicated above or below the corresponding representative box. The triangles indicate N-glycosylation consensus sequences. The percentage of similarity is indicated for each region below the scheme. Calculations were done using the program DNASTAR (DNASTAR Inc., Madison, WI). The drawing is not in scale. B, Northern blot analysis of transfected populations. Total RNA from transfected (MUC-R and MUC-NR transfected with pMUC-R and pMUC-NR respectively) and wild type (wt) T. cruzi populations were hybridized with an antisense oligonucleotide of the tag.

Antibodies directed to the tag detected two broad bands of 85 and 90 kDa for the pRMUC-R repetitive gene expressed in T. cruzi (Fig. 2A, lane 2). The product from this same gene expressed in E. coli migrated as a band of 35 kDa (Fig. 2A, lane 1), thus suggesting that post-translational modifications were occurring when expressed in T. cruzi. Moreover, MUC-R products were probed with sera raised against the untagged recombinant protein fused to GST and expressed in E. coli. None was detected after expression in T. cruzi, whereas the E. coli-expressed protein was readily detected (not shown), further supporting the presence of extensive post-translational modifications. The product of pRMUC-NR (nonrepetitive gene) transfected in T. cruzi showed three to four bands from 35 to 55 kDa after reaction with the anti-tag serum (Fig. 2A, lane 7). The lower molecular mass band migrated in the same position as the product of this construct expressed in E. coli, but the presence of bands migrating at higher positions suggested that this product has also undergone some post-translational modifications when expressed in T. cruzi. Wild type epimastigotes used as controls produced no signal when probed with the anti-tag serum (Fig. 2A, lane 4).

View larger version (67K): [in this window] [in a new window]   Fig. 2.   Expression and purification of tagged products from transfected T. cruzi epimastigotes. A, Western blot analysis of total lysate of E. coli-expressing MUC-R (lane 1), total lysate of 5 × 107 pRMUC-R-transfected parasites (lane 2), medium from pRMUC-R-transfected parasites (lane 3), total lysate of 5 × 107 wild type (wt) parasites (lane 4), medium from wild type parasites (lane 5), total lysate of E. coli-expressing MUC-NR (lane 6), total lysate of 5 × 107 pRMUC-NR-transfected parasites (lane 7), and medium from pRMUC-NR-transfected parasites (lane 8). Molecular mass markers are indicated at the left. B, phenol/water extraction of parasites expressing MUC-R. Phenolic (Ph) and aqueous (Aq) phases were loaded on SDS-PAGE, transferred to nylon membrane, and, after probing with the anti-tag serum, revealed with 125I-protein A. C, identical to B for MUC-NR-expressing parasites. D, affinity purification of MUC-R product. The aqueous phase of phenolic extraction was applied to an anti-tag affinity column. The eluted (lane 1) and percolated material (lane 2) was analyzed by Western blot with the anti-tag serum. The calculated molecular mass of the observed bands is indicated in panels B, C, and D.

Only the product from the repetitive gene MUC-R was detectable in the culture medium from transfected epimastigotes as a 90-kDa band (Fig. 2A, lane 3). Furthermore, although two products were detected in the parasite lysate, only the upper band was observed in conditioned medium from transfected parasites. This behavior is analogous to that reported for soluble variable surface glycoprotein, which lacking the lipid anchor, showed a decreased electrophoretic migration (38).

The Repetitive Member of the TcMUC Family Is Expressed in Transfected T. cruzi Epimastigotes as a Surface Mucin-- To analyze if the recombinant proteins behaved as mucins, they were isolated from delipidated cells by extraction with water saturated with 1-butanol as reported previously (35). The extract was analyzed by Western blotting, using the anti-tag serum. The product of the repetitive gene (MUC-R), but not the one from the nonrepetitive gene (MUC-NR), was detected in the extract, as expected for a highly O-glycosylated molecule. Nonetheless, the majority remained in the pellet (data not shown). Therefore, a second extraction with 44% phenol/water was conducted. Only the MUC-R product, but not the MUC-NR product, was detected in the aqueous phase, and after this second step only traces remained in the phenol phase (Fig. 2, B and C). From these experiments, we concluded that only the product of the MUC gene having the repetitive central domain behaved as a typical mucin, and so this one was purified further and characterized. MUC-NR could still have a mucin domain in the Thr-rich degenerated repeats (Fig. 1A) and/or N-glycosylated as it has two NXT consensus sequences, probably causing the observed shift when expressed in T. cruzi. However, as our goal was to identify mucin genes, the MUC-NR product was not analyzed further in this work.

The second purification step for MUC-R was an affinity column chromatography on immobilized antibodies directed against the HCV tag. The aqueous phase of both, water/butanol and phenol extraction were loaded. As shown in Fig. 2D, the antibodies directed to the molecular tag detected the recombinant mucin only in the samples retained in the column. Possible contamination of the samples with epimastigote endogenous mucins was checked using the monoclonal antibody 3F5, which specifically detects the epimastigote endogenous 35/50-kDa mucins (39). This antibody did not detect the 35-50-kDa mucins in the sample retained by the anti-tag antibody column, indicating that the recombinant mucin was not contaminated with endogenous mucins (data not shown).

Parasite surface mucins were labeled in vivo using galactose oxidase and NaB³H₄, in the wild type and pRMUC-R transfected cells, as reported previously (10). Besides the endogenous mucins of 35/50 kDa, a parasite surface glycoprotein of about 85 kDa was slightly and differentially labeled in the transfected parasites (Fig. 3A). Labeling was not improved by previous treatment with neuraminidase. The apparent molecular mass observed corresponded with that of the lower band detected by anti-tag in extracts from pMUC-R epimastigotes in Fig. 2A. The reason for the different behavior in SDS-PAGE migration of MUC-R and endogenous epimastigote mucins will be discussed later.

View larger version (34K): [in this window] [in a new window]   Fig. 3.   Labeling of pRMUC-R-transfected and wild type T. cruzi epimastigotes. A, intact transfected (MUC-R) or wild type (wt) epimastigotes were surface labeled by galactose oxidase/NaB3H4. Total lysates were separated by 10% SDS-PAGE and revealed by fluorography. NA, Clostridium perfringens neuraminidase. B, T. cruzi epimastigotes (E) and trypomastigotes (T) were metabolically labeled with [14C]Thr and submitted to phenol/water extraction. Extracted material was separated by 10% SDS-PAGE and revealed by fluorography. The molecular mass of standards is indicated on the right.

Comparison of the Carbohydrate Structure between Endogenous and Recombinant Mucins of T. cruzi-- Analysis of the sugars obtained from endogenous and recombinant MUC-R mucins by reductive -elimination was performed by HPAEC and TLC. The mucins, obtained from wild type cells labeled by the galactose oxidase/NaB³ H₄ method, were purified on octyl-Sepharose as reported previously (35). The recombinant MUC-R mucin was purified using the affinity column. In this case a low amount of radioactivity was recovered; thus, reductive -elimination was performed in the presence of NaB³H₄. The products obtained were separated from the radioactive contaminants on a Bio-Gel P-2 column (not shown). From the recombinant mucin an included peak was obtained, eluting between maltotriose and maltose (Fig. 4, lane 1). An excluded peak was also eluted. Analysis by paper electrophoresis of the void radioactivity showed that no negatively charged molecules were present, excluding the presence of sialic acid. This fraction was not analyzed further.

View larger version (49K): [in this window] [in a new window]   Fig. 4.   Thin layer chromatography of O-linked sugar alditols obtained from the recombinant and wild type mucins of T. cruzi epimastigotes. Lane 1, O-linked sugars released from the recombinant mucins by -elimination in the presence of NaB3H4; lane 2, O-linked sugars released from galactose oxidase/NaB3H4-labeled mucins; lane 3, authentic sample of [1-3H]--D-Galp(14)GlcNAcol; lane 4, [1-3H]GlcNAcol. The products were analyzed by TLC with propyl alcohol/NH3/water (7/1/2), double development, and fluorography. The migration of nonradioactive standards is shown on the right. I, -D-Galf(13)GlcNAcol; II, glucitol; III, -D-Galp(13)GlcNAcol; IV, -D-Galp(14)GlcNAcol; V, -D-Galp(16)GlcNAcol. The origin is indicated by an arrow.

On the other hand, it was interesting to investigate the presence of galactofuranose-containing oligosaccharides because this sugar is important in antibody recognition (40). Galactofuranose was detected in the mucins of one parasite strain (12). Analysis by HPAEC (Dionex) allows the easy identification of galactofuranose-containing disaccharitols and trisaccharitols because they elute later than the galactopyranose-containing isomeric oligosaccharitols (35). No galactofuranose-containing disaccharide or trisaccharide was detected (Fig. 5). The presence of -D-Galp(14)GlcNAcol was shown by TLC (Fig. 4, lanes 1 and 2) and HPAEC (Fig. 5), by comparison with an authentic sample of the disaccharitol (Fig. 4, lane 3, and Fig. 5, standard 3). The sugar alditols obtained from the recombinant mucin were eluted separately from the plate (major compounds in Fig. 4, lane 1) and treated with -galactosidase. Both oligosaccharitols were hydrolyzed by the enzyme (not shown). The fast compound (Fig. 4, lane 1) was identified as glucitol by HPAEC, utilizing the column MA-1, which differentiates alditols (Dionex, Application Note 117). Glucose, originating labeled glucitol, is a common contaminant in the analysis of glycoconjugates. When analyzing the oligosaccharitols of the recombinant mucin by HPAEC in the PA-10 column (Fig. 5), besides the -D-Galp(14)-D-GlcNAcol, a peak with the elution position of -D-Galp(14)[-D-Galp(16)]-D-GlcNAcol was detected. This trisaccharitol was obtained previously from the mucins of the Y strain (11). The higher oligosaccharitols obtained from the wild type mucins (Fig. 4, lane 2) were extracted from the TLC (except the origin) and subjected to partial acetolysis, which selectively hydrolyzed 16 linkages. A main product comigrating with the disaccharitol -D-Galp(14)-D-GlcNAcol was obtained (not shown). These data suggested that they all have the same disaccharide core.

View larger version (8K): [in this window] [in a new window]   Fig. 5.   HPAEC-PAD analysis of the radioactive O-linked sugars obtained by NaB3H4 reductive -elimination of the mucins from MUC-R transfected epimastigotes. The sample was desalted on Bio-Gel P-2 and chromatographed on a CarboPac PA-10 column with the conditions indicated under "Materials and Methods." The numbers correspond to the sugar alditol standards. 1, glucitol; 2, -D-Galp(13)GlcNAcol; 3, -D-Galp(14)GlcNAcol; 4, -D-Galp(13)[-D-Galp(16)]GlcNAcol; 5, -D-Galp(14)[-D-Galp(16)]GlcNAcol; 6, -D-Galf(13)GlcNAcol; 7, -D-Galf(14)GlcNAcol; 8, -D-Galp(14)[-D-Galf(16)]GlcNAcol.

The MUC-R-encoded Mucin Is Anchored by GPI and N-Glycosylated-- To find out if the transfected repetitive mucin was GPI-anchored, as predicted from primary sequence, conditioned culture media from pRMUC-R-transfected epimastigotes was immunoprecipitated with anti-tag serum and probed with an anti-CRD polyclonal antibody. This antibody reacts with a carbohydrate epitope whose key structural feature is an inositol 1,2-cyclic phosphate moiety that is found uniquely in PI-phospholipase C-cleaved GPI glycoproteins (41). As shown in Fig. 6A, antibodies directed to the tag and CRD moiety detected the same protein. Furthermore, MUC-R was enriched significantly in supernatants of transfected parasite lysates treated with PI-phospholipase C in comparison with mock treated lysates (Fig. 6B). Thus, the recombinant mucin MUC-R is anchored by GPI to the membrane and shed into the medium by the action of some endogenous phospholipase of the parasite.

View larger version (63K): [in this window] [in a new window]   Fig. 6.   The MUC-R mucin is anchored by GPI and N-glycosylated. Immunoprecipitation of culture medium from MUC-R-transfected epimastigotes of T. cruzi is shown. A, the immunoprecipitated material was revealed with 125I-protein A after SDS-PAGE separation and Western blotting. Left panel, probed with anti-tag serum; right panel, probed with anti-CRD serum. Lanes 1, immunoprecipitated with anti-tag serum; lanes 2, immunoprecipitated with anti-GST control serum. B, MUC-R-transfected parasite extracts were incubated in the absence (lane 1) or presence (lane 2) of B. thuringiensis PI-phospholipase C and the supernatants probed with anti-tag after Western blot. Lysate from nontransfected parasites treated with PI-phospholipase C was included as a further control (lane 3). C, anti-tag immunoprecipitated proteins were eluted from protein A-Sepharose beads, treated with endoglycosidase H, and probed with anti-tag serum after Western blot. The apparent molecular mass calculated from the markers migration is indicated by arrows.

As three consensus N-glycosylation sites were present in the C terminus of the MUC-R product (Fig. 1), we analyzed if they had an attached oligosaccharide. MUC-R immunoprecipitated with anti-tag from conditioned culture medium was treated with endoglycosidase H and then analyzed by Western blot with anti-tag serum. This treatment increased the electrophoretic mobility of the tag-containing band by 10 kDa (Fig. 6C), suggesting that all of the N-glycosylation sites have attached oligosaccharides.

TcMUC Genes Encode Mucins Present in the Mammalian Stage of the Parasite-- From the experiments described above, it can be concluded that the product of the MUC-R-tagged gene encodes the protein core of a mucin glycoprotein in T. cruzi. However, the mobility of the tagged product (about 90 kDa) is different from that of the endogenous mucins observed in the epimastigote stage (35/50 kDa). When mucins extracted by aqueous-phenol from [¹⁴C]Thr metabolically labeled T. cruzi CL-Brener were compared, the radioactive bands present in epimastigotes showed the same pattern as those labeled by galactose oxidase on parasites (see Fig. 3, A and B). On the other hand, the Thr-rich mucins from cell-derived trypomastigotes presented a different pattern composed of bands of slower mobility, encompassing the size of the MUC-R product (Fig. 3B). This, along with the level of the mRNA of TcMUC encoding T₈KP₂ repeats, which is much higher in cell-derived trypomastigotes (37), suggested that MUC-R-encoded mucins are present in this stage.

To analyze further if the natural products of TcMUC repetitive members, like MUC-R, were present in the stages associated with the vertebrate infection we used a second strategy. A recombinant TcMUC product (M76) containing four T₈KP₂ repeats was expressed in E. coli fused to GST, affinity purified, and probed in dot spots with sera from human and experimental (rabbits and mice) infections. We employed a panel of sera from animals infected with different parasite strains and from a wide range of times postinfection. The results indicated a different response to M76 depending on the species analyzed. It was recognized by almost all sera from infected mice tested (43/45), independently of the parasite strain or the genetic background of mice used. Sera obtained as early as 25 dpi to up to 6 months postinfection recognized M76. Only 3 out of 10 rabbit sera detected M76, and none of the 12 human sera used here did, despite the fact that M76 was isolated by immunological screening of an expression library using human infection sera (42). These results showed that TcMUC repetitive products are present in the stages of the parasite related to the infection (trypomastigote and/or amastigote) as they can elicit an antibody response in mice, although their antigenic properties can vary with the host.

Hypervariable Regions Present in Mature Mucins Are Antigenic during the Infection-- The above mentioned results showed that membrane-located mucins, encoded by TcMUC genes, might be present in the trypomastigote stage, which is exposed to the vertebrate's immune system. The repetitive TcMUC genes encoding these molecules are all highly similar, except for the region predicted to be nonglycosylated and at the mature N terminus; this is the HV region (16). Two mice infected with parasites expressing MUC-R produced antibodies against the HCV tag as assessed by dot spot (not shown), suggesting that the HV region was present in the mature protein and could be immunogenic during the infection. To determine if the natural HV region was indeed expressed and remained in the mature product during natural and experimental infections and gave rise to an antibody response, GST fusion proteins having a single randomly chosen HV region (proteins E13, T15, T18, and NCA2, see "Materials and Methods") were generated and assayed by dot spot against sera obtained from different infected hosts. Because of the hypervariability there was the possibility that some strain-specific expression or temporal regulation could influence the response to different HV regions, as well as host species and/or haplotype dependence that could not be known a priori. So, in a first set of assays, a heterogeneous sera collection from human and experimental infections (mice and rabbits) covering many of these possibilities were employed, and the results are summarized in Table II. The four HV regions chosen were detected by more than one serum. Human sera were all obtained from patients during the chronic stage of the disease, and both rabbit positive sera were collected from 60 dpi. This tendency of anti-HV regions antibodies to appear late during the infection is clearly seen in mice infection, with all of the positive sera observed at times over 60 dpi. Some sera that detected more than one HV region were all obtained from chronic infections. None of the eight human, four rabbit, and four mice noninfected sera tested detected any of the HV regions. Furthermore, three GST, from plasmids pGEX-1, pGEX-2T, and pGEX-1T, with different C termini having similar size than, but unrelated sequences to, HV regions were used as specificity controls, and none of them was detected by any serum.

To study further the humoral response against these antigens, sera from a follow-up in infected mice were analyzed. Infected mice were bled at 15, 52, and 150 dpi and sera analyzed by dot spot. No reactivity was detected early during the infection, but antibodies against HV regions were detected at 52 dpi and remained at 150 dpi (Table III). Most of the sera (9/11) detected more than one fusion protein by day 150. Signals against HV regions were positive but weaker than those obtained against M76 protein. Taken together, these results confirmed the presence of the TcMUC repetitive products during the infection and showed that the HV region was retained in the mature product in vivo. They also showed that more than one HV region could be expressed in a parasite population during the infection and that they could be targets of specific antibodies.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

There are a few examples in protozoan parasites of large and variable gene families coding for proteins with similar function, as is the case in African trypanosomes and Plasmodium falciparum (43, 44). In both, the large number of genes is directly related to a requirement for parasite survival in the host and sequence variability is the naturally selected character. The N-terminal region of these proteins, the one exposed to the host antibodies, differs largely in sequence among members of these families. The finding that T. cruzi contains a large family of mucin-type genes with their putative mature N terminus having HV regions (16) raised the question of the reason for this diversity. Tempting possibilities could be antigenic variation or some related immunoevasive role and ligand diversity generation. However, several necessary prerequisites must be demonstrated to sustain any of these hypotheses, including the mucin nature of TcMUC gene products, the persistence of the HV region at the protein level, and their exposure to the host antibody response. In this paper, structural and serology data were obtained answering these questions.

Two different representative TcMUC products (MUC-R and MUC-NR) were traced in vivo by the use of T. cruzi transfection with tagged genes. The MUC-R gene product behaved as a mucin in phenol/water extractions, and its O-glycosylation was studied, consisting mainly of -D-Galp(14)GlcNAc and -D-Galp(14)[-D-Galp(16)]-D-GlcNAc. This post-translational modification, along with the presence of N-glycosylation and GPI anchor and the finding of a secreted form, are indications that the transfected MUC-R yielded a mucin able to traverse the secretory pathway when expressed under these conditions. The MUC-R product is likely to be highly O-glycosylated in the repeats region because the reactivity with a serum recognizing the recombinant protein expressed in E. coli is lost when expressed in T. cruzi. All of the products from TcMUC repetitive genes, like MUC-R, are highly conserved, differing only in the number of repeats and the sequence of the HV region (16). So they would be expected to be processed equally in vivo. Differences in the repeat number may contribute to the heterogeneity in the apparent molecular mass of T. cruzi mucins.

A second transfected gene that lacks repeats (MUC-NR) is translated into a product that, albeit not behaving as a typical mucin in the phenol/water extraction, is likely to have undergone some post-translational modifications in vivo (Fig. 2). The high identity in the leader sequence and GPI anchor signal of MUC-NR with those of MUC-R suggests that they should also be functional. MUC-NR may still have a mucin domain because its mature C-terminal region is very similar to the one in MUC-R product (see Fig. 1). It has been suggested that the nonrepetitive TcMUC genes would not be translated (37). Our results are not conclusive to this respect, and the nature of non-repetitive TcMUC products is still undetermined. It is difficult to imagine that T. cruzi would have conserved a subfamily composed of more than 200 genes, most of them found as mature mRNAs with an intact open reading frame (16), without any function. In relation to the different behavior between MUC-R and MUC-NR, it is worth noting that the ratio of Thr/Ser codons in the central domain is around 2 in deduced products from nonrepeated genes, far from the value around 7 in repeats-containing genes. Thr seems to be the main target for O-glycosylation in T. cruzi, but Ser was also found to be thus modified (3, 14). The T₈KP₂ motif is an excellent substrate for an UDP-N-acetylglucosamine:peptide:N-acetylglucosaminyl transferase, the only so far described O-glycosylation initiating enzyme of T. cruzi present in both epimastigotes and cell-derived trypomastigotes (18). MUC-NR, which is rich in Ser (Fig. 1) could be O-glycosylated by a different, still noncharacterized, transferase expressed in other developmental stage but not in epimastigotes. In this work, the same di- and trisaccharide structures were obtained from the endogenous mucins present in the epimastigote stage and the MUC-R product, even though evidences are provided that MUC-R encode mucins from the trypomastigote stage (see below) whose O-linked oligosaccharides have a more complex structure (14). This is in agreement with state of the art knowledge about O-glycosylation in vertebrate cells, where O-linked structures are in general tissue- or cell-specific depending on the expressed transferases (45) even when some sequence influence could exist because of secondary structures (46).

The evidence indicating that MUC-R-like products are expressed in the stages of the vertebrate infection, most probably in the trypomastigote are as follows. (i) The apparent molecular mass of MUC-R expressed in epimastigotes is different from endogenous mucins expressed in this stage (35-50 kDa) but within the size range of mucins expressed in cell-derived trypomastigotes (60-200 kDa). (ii) The molecular mass of the mature polypeptide deduced from TcMUC repetitive genes is around 13-18 kDa, in agreement with that calculated for the trypomastigotes apomucins (14) and not with the 5-7 kDa determined for epimastigote mucins (3, 15). (iii) T₈KP₂-containing TcMUC transcripts have their highest level in the trypomastigote stage (17, 37). (iv) The amino acid sequence of the predicted GPI anchor point of TcMUC genes is consistent with the mature C termini of trypomastigote mucins, which was determined recently to be Ile-Asp with the GPI attached to the latter amino acid (47). (v) A repeats-containing recombinant protein encoded by one of these genes (M76) was recognized by 43 out of 45 sera from infected mice. (vi) HV regions present at the mature N terminus of TcMUC repetitive products were recognized by sera from different infected hosts.

This last mentioned evidence showed not only that the HV region is present in the mature mucin but that it is able to elicit a humoral response. Differences were found in reactivity between the complete protein and HV regions when probed with mice sera. Antibodies directed to M76 showed an early and strong reactivity and remained positive through the chronic phase of the infection. On the other hand, antibodies recognizing HV regions showed weaker signals and were displayed later during the infection, something not unexpected given the difference in size and abundance of each region. Although repeats are present in several copies in each protein and, along with the mature C termini, are conserved in all members of the family, HV regions are small epitopes restricted to a subset of TcMUC proteins. The four HV regions tested, chosen at random out of the many described (16), were detected by more than one sera. As the sera used were from different animals infected with different strains of the parasite, it is possible that the same HV regions could be expressed by different populations or, more likely, that closely related HV regions elicit cross-reacting antibodies. At least one identical HV region exists in the Y (37) and CL-Brener (16) populations of the parasite. Also, several variant but clearly related HV regions were described within one parasite clone (16). Many sera detected more than one HV region, indicating that multiple variants are expressed in the same parasite population during the infection. However, if they appear sequentially or simultaneously or if the distribution is homogeneous or heterogeneous among individual parasites cannot be said now.

O-Glycosylation has predictable consequences on the glycoprotein structure. Sugar proximity to the protein backbone and hydrophilic interactions between sugars cause structural restrictions resulting in protein backbone stiffness (45, 48). The rod-like structure of densely O-glycosylated domains is due to the first attached sugar and independent of the composition of the oligosaccharide, and its length has been measured for many mucins (49-51). An average length of 0.25 nm/amino acid residue was established (45, 48). It is reasonable to assume that O-GlcNAc in T. cruzi would have a structural effect similar to that of O-GalNAc in vertebrate mucins. Therefore, we can estimate the length of a TcMUC repetitive product with the average number of three T₈KP₂ repeats, plus the 37 amino acids that follow up to the likely GPI addition site and 10 residues an HV region. No secondary structure is predicted for these regions using the available algorithms, supporting their extended or random coil nature. The result would be a rod with a length of about 20 nm, highly glycosylated, GPI-anchored to the membrane, and exposing to the medium the HV N terminus. In agreement with this prediction, T. cruzi trypomastigotes are covered by a dense 20-nm-thick coat of mucins (52).

When a protein from a pathogen has a variant region exposed to the medium that is associated with the presence of specific antibodies or lymphocytes, this is usually taken as evidence that the immune system pressure is causing the appearance of variants as a way of evading the immune response. This was described in Plasmodium spp. (53, 54), Streptococcus (55), the hepatitis C virus (56), and the simian immunodeficiency virus (57), among others. The presence of antibodies against the exposed N-terminal HV region of TcMUC-encoded mucins in sera from infected individual suggests that variation is being selected by the immune system of the vertebrate.

We have recently identified a novel mucin-type gene family in T. cruzi, named TcSMUG, whose deduced products have all of the characteristics of epimastigote apomucins (19). Beside the presence of two groups of genes, all members within each group showed no sequence variability. The sequence of one of the groups of TcSMUG-deduced proteins coincided with peptide sequences obtained from the 35-50-kDa mucins purified from epimastigotes,³ suggesting that this new family encodes the mucins from the insect stages of the parasite. Mucins are also the main surface glycoprotein in epimastigotes (52), but variant sequences would not represent an adaptive advantage in an insect host, which has a nonspecific immune response. On the other hand, a large number of identical N termini in molecules covering the parasite surface would be dangerous for the trypomastigote under a high affinity specific immune response, and having to survive in the blood long enough to invade different tissues and for being available to the insect vector. We presented herein evidence that the parasite expresses different mucins in this stage, encoded by TcMUC repeats-containing genes, with variant exposed HV regions probably selected to delay the maturation of the immune response. In relation with this, trypomastigote-specific surface glycoproteins belonging to the trans-sialidase superfamily (58) displayed variant but related epitopes at defined regions of different family members (59). These variants are expressed simultaneously in a single parasite, indicating that a potentially protective CD4⁺ response becomes anergic (60). So, the presence of variant but related epitopes in the surface of the trypomastigote might be a general strategy of T. cruzi to evade an early immune response and allow the infection to be established.

	ACKNOWLEDGEMENTS

We acknowledge Drs. J. J. Cazzulo, A. Parodi, and O. Campetella for critically reading the manuscript. We thank Dr. D. Sánchez for helpful discussions and suggestions and for sera from infected rabbits, Dr. R. Mortara for providing the 3F5 antibody, Dr. R. Hernández for pRIBOTEX plasmid, and Dr. I. C. Almeida for letting us include unpublished results. We thank L. Sferco and B. Franke de Cazzulo for technical assistance and I. D'Orso and C. Ascencio for help in some of the electrophoresis assays.

	FOOTNOTES

^* This work was supported in part by grants from the Agencia Nacional de Promoción Científica y Tecnológica, Argentina, the Swedish Agency for Research Cooperation with Developing Countries (SAREC-SIDA), the International Atomic Energy Agency, the Consejo Nacional de Investigaciones Científicas y Técnicas, and the University of Buenos Aires.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

^§ The first two authors contributed equally to this work.

^¶ CONICET researchers.

CONICET fellow.

University of Buenos Aires fellow.

^§§ CONICET principal professional.

Supported in part by an International Research Scholar grant from the Howard Hughes Medical Institute. To whom correspondence should be addressed. Tel.: 54-11-4580-7255; Fax: 54-11-4752-9639; E-mail: cfrasch@iib.unsam.edu.ar.

Published, JBC Papers in Press, June 7, 2000, DOI 10.1074/jbc.M000253200

² G. D. Pollevick, J. M. Di Noia, M. L. Salto, C. Lima, M. S. Leguizamón, R. M. de Lederkremer, and A. C. C. Frasch, unpublished results.

³ I. Almeida, personal communication.

	ABBREVIATIONS

The abbreviations used are: GPI, glycophosphatidylinositol; HV, hypervariable; GST, glutathione S-transferase; CRD, cross-reacting determinant; dpi, days postinfection; PAGE, polyacrylamide gel electrophoresis; HPAEC-PAD, high pH anion exchange chromatography with pulse amperometric detection; PBS, phosphate-buffered saline; PI, phosphatidylinositol.

	REFERENCES

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES