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Prior studies have established that the Cryptococcus neoformans capsular polysaccharide component galactoxylomannan (GalXM) manifests serotype-related structural differences that translate into antigenic differences. We analyzed GalXM from acapsular serotype A and D strains by carbohydrate analysis and static and dynamic light scattering to determine mass, effective diameter, polydispersity, and diffusion coefficients. Multiangle laser light scattering showed that GalXM from C. neoformans var. grubii strain cap59 (serotype A) had larger molecular mass (4.21 × 106 ± 0.95 × 106 g/mol) and radius of gyration (207 ± 27 nm) than GalXM from C. neoformans var. neoformans cap67 (serotype D). cap67 GalXM had corresponding values of 0.70 × 106 ± 0.05 × 106 g/mol and 120 ± 22 nm, respectively. The effective diameter for GalXM and polydispersity from the two strains varied depending on temperature and medium growth conditions, indicating that GalXM structure can vary within a strain, depending on its environment. Zeta potential determinations were negative for GalXM from both strains under all conditions, consistent with the recently reported presence of glucuronic acid. These results imply that C. neoformans GalXM, like glucuronoxylomannan, can manifest variety- and growth condition-related variations. Analysis of 16 C. neoformans and 7 Cryptococcus gattii strains with polyclonal antibody to a GalXM strain revealed antigenic similarities among the C. neoformans variety neoformans and grubii strains and no reactivity with C. gattii. As a result of the deleterious effects of GalXM on immune function, structural and antigenic variability between serotypes may translate into differences in immunomodulatory effects.
The encapsulated fungal pathogen Cryptococcus neoformans causes disease primarily in individuals with impaired immunity (22). Cryptococcosis is relatively common in individuals with late-stage human immunodeficiency virus or certain cancers and in organ transplant recipients (22, 25, 31). C. neoformans has several well-defined virulence factors that include a polysaccharide (PS) capsule (23, 31). The capsular polysaccharide was classically defined as being composed of glucuronoxylomannan (GXM), galactoxylomannan (GalXM), and mannoproteins (MP) (19, 24, 29). However, this composition was inferred based on analysis of culture-shed exopolysaccharide (6, 18). Recent studies suggest that the capsule is made of GXM while GalXM and mannoproteins appear to be primarily export products (10, 17).
GXM has been extensively studied, but considerably less is known about GalXM (5, 6). Earlier structural studies of GalXM revealed that GalXM constitutes about 8% of the shed polysaccharide found in cryptococcal culture supernatants (1, 29) and has an α-1,6-galactan backbone containing four potential short oligosaccharide branch structures. The branches are 3-O-linked to the backbone and consist of an α-1,3-mannose, α-1,4-mannose, and β-galactosidase trisaccharide with variable amounts of β-1,2- or β-1,3-xylose side groups (1, 21, 29). The GalXM backbone consists of galactopyranose and a small amount of galactofuranose (29), unlike GXM, which contains only mannopyranose (1). Recently, it was found that the residue that is (1→3)-linked to the side chain galactose of GalXM is β-d-glucuronic acid, instead of β-d-xylose as previously determined. It was proposed that the GalXM polymer be renamed to “glucuronoxylomannogalactan” (GXMGal) due to the presence of glucuronic acid (16). Heiss et al. suggest that the nomenclature accurately represents both the polymer composition and structure (16). Although we agree that GXMGal is a better term for this polysaccharide based on the existing information, we will continue to use GalXM for now to maintain the continuity of the literature. It is conceivable that as structural knowledge accumulates, additional revisions to the nomenclature will be needed in the future. The latter concern is heightened by data presented in the manuscript showing considerable variability in GalXM structure under different conditions. Several recent studies indicate that GalXM is a potent immunomodulator with pleiotropic deleterious effects on the immune system (2, 9, 26, 30).
Studies with GalXM from cap67 revealed an average mass of 1 × 105 Da (1, 21), which was significantly smaller than that of GXM (1.7 × 106 Da) (21). Since GalXM has a smaller molecular mass, GalXM is the most numerous component among shed capsular polysaccharide fractions on a molar basis, with 2 to 3.5 mol of GalXM for each mole of GXM (21). Recently, we showed that GalXM is primarily an exopolysaccharide and that there are serotype-related structural differences in GalXM, based on nuclear magnetic resonance (NMR) analysis, that could translate into antigenic variability (10). Here, we follow up on that lead using carbohydrate analysis, light scattering, and zeta potential measurements to show that there are strain- and serotype-related differences in GalXM structure that could be enhanced by growth conditions.
(The data in this paper are from a thesis submitted by M. De Jesus (Ph.D. awarded in June 2009) and S.-K. Chow in partial fulfillment of the requirements for a Ph.D. from the Albert Einstein College of Medicine, Yeshiva University, Bronx, NY.)
C. neoformans var. grubii acapsular mutant cap59 was derived from strain H99 (MATα and hygromycin resistant; serotype A) and was a kind gift of Joseph Heitman at Duke University. C. neoformans var. neoformans acapsular mutant cap67 was derived from strain B3501 (serotype D) and was obtained from the American Type Culture Collection (Manassas, VA). cap67 is also known in the literature as B-4131, and its capsular phenotype in this strain can be restored by the CAP59 gene (3). Hence, cap59 and cap67 are derived from serotype A and D strains that are both complemented with the same gene, which appears to function in capsular polysaccharide export (15). In the immunofluorescence studies, eight C. neoformans var. grubii (serotype A), eight C. neoformans var. neoformans (serotype D), and seven C. gattii (serotype B and C) strains were used. H99 (serotype A) was obtained from the New York State Herbarium, Albany, NY, and the rest of the serotype A isolates were obtained from cryptococcal meningitis patients from New York City hospitals (28). Strains 24067, B3501, and Jec21 and five other clinical isolates were used in the serotype D group. The C. gattii strains included NIH isolates 18, 34, 112, 191, 444, 1343, and 3939. These isolates have been described previously (4).
GalXM was isolated as previously described (10). Briefly, a 400-ml culture of a C. neoformans acapsular mutant of strain cap67 or cap59 was grown under one of the following conditions: peptone medium supplemented with 2% galactose, minimal medium (15 mM glucose, 10 mM MgSO4, 29.4 mM KH2PO4, 13 mM glycine, and 3 μM thiamine-HCl; pH 5.5), yeast extract-peptone-dextrose (YPD; Difco Laboratories, Detroit, MI), or Sabouraud's dextrose broth (Difco Laboratories, Detroit, MI) for 7 days. For the experiments to evaluate the effect of temperature, C. neoformans was grown in peptone supplemented with 2% galactose at 25, 30, 37, or 40°C for 7 days. The culture supernatant was separated from the cells by centrifugation at 900 × g for 15 min at room temperature and then concentrated using an Amicon centrifugal filter with a 10,000-molecular-weight (MW)cutoff (Millipore, Bedford, MA). The material was then dialyzed for 1 week against distilled water, and the 10-kDa retentate, containing GalXM and mannoproteins, was passed through a 0.2-μm-pore-size filter. The resulting filtrate was then lyophilized and stored at room temperature. The freeze-dried mixture was dissolved in 25 ml of start buffer [0.01 M Tris base and 0.5 M NaCl solution, pH 7.2, to which CaCl2 and Mn(II)Cl2 was sequentially added to final concentrations of 1 mM]. To separate the GalXM and mannoproteins, the solution was then continuously passed through a concanavalin A-Sepharose 4B column (2.5 by 10 cm) (Sigma) for 16 h at 4°C using a peristaltic pump with a flow rate of 16 ml/h. The flowthrough as well as five column washes with start buffer were collected as 25-ml fractions (21). To identify carbohydrate-containing fractions, we tested these using a phenol-sulfuric acid assay (11). The fractions were combined, concentrated by ultrafiltration, and dialyzed against water for 3 days. GalXM was then recovered by lyophilization.
GalXM samples were dissolved in methanol–1 M HCl and incubated at 80°C for 18 h. Methanolyzed samples were then per-O-trimethylsilylated by treatment with Tri-Sil (Pierce) for 30 min at 80°C. The per-O-trimethylsilyl (TMS) derivatives were analyzed by gas chromatography coupled to mass spectrometry (GC-MS). The derivatized structures were first separated on an HP 5890 gas chromatograph using a Supelco DB-1 fused silica capillary column (30 m by 0.25-mm internal diameter). Peaks detected by GC were fragmented in a 5970 MSD mass spectrometer, interfaced to the gas chromatograph. Carbohydrate standards included arabinose, rhamnose, fucose, xylose, glucuronic acid, galacturonic acid, mannose, galactose, glucose, mannitol, dulcitol, and sorbitol.
Zeta potential (ζ), particle mobility, and shift frequency of polysaccharide samples were calculated in a zeta potential analyzer (ZetaPlus; Brookhaven Instruments Corp., Holtsville, NY). Zeta is a measurement of charge (in millivolts) defined as the potential gradient that develops across the interface between a boundary liquid in contact with a solid and the mobile diffuse layer in the body of the liquid. Derivation of zeta potential is described in Frases et al. (12).
The effective diameter and the polydispersity of GalXM preparations were measured by quasi-electric light scattering (QELS) or multiangle laser light scattering in a 90Plus/BI-MAS Multi-Angle Particle Sizing analyzer (Brookhaven Instruments Corp., Holtsville, NY). The protocol used to measure particle size is described in Frases et al. (12, 13). Both GalXM samples were analyzed under the same conditions.
Sixteen C. neoformans strains (eight each of serotypes A and D, respectively) and seven C. gattii strains (three of serotype B and four of serotype C) were grown in Sabouraud dextrose broth (Difco Laboratories, Detroit, MI) for 1 day at 30°C. The cells were then transferred to capsule-inducing medium (1:10 Sabouraud broth-morpholinepropanesulfonic acid [MOPS], 50 mM, pH 7.3) for another day of incubation at 30°C. In the experiment associated with the growth curve study, the strains were grown in 1:1 Sabouraud broth–50 mM MOPS, pH 7.3, to optimize cell growth and capsule induction. The cells were washed three times with phosphate-buffered saline (PBS; pH 7.4) and counted with a hemocytometer. For GalXM staining using GalXM-PA (where PA is protective antigen) polyclonal serum (10), 2 × 106 cells in 100 μl of immunofluorescence buffer (1% bovine serum albumin [BSA] and 0.05% goat serum in PBS) were incubated with 4 μl of serum for 1 h at room temperature. Cells were washed three times with buffer and incubated with a 1:25 dilution of goat anti-rat IgM-fluorescein isothiocyanate (FITC) as the secondary antibody for 1 h at room temperature. Cells were then washed and incubated with 1:10,000 Uvitex 2B (Polysciences Inc.) in PBS for 20 min. Stained cells were suspended in mounting medium (50% glycerol and 50 mM N-propyl gallate in PBS) and imaged by epifluorescence microscopy on a Zeiss Axioskop 200 inverted microscope equipped with a cool charge-coupled device using a 63×, 1.4-numerical aperture (NA) objective with a 1.6× optovar. Images were acquired using the same exposure times and microscopic settings and processed by Axio Vision, version 4.6, software (Carl Zeiss Micro Imaging, New York, NY).
Fifteen randomly selected fields of view were imaged for each strain. The cells were stained with Uvitex 2B, and the images were focused on the plane of the cell wall to avoid bias in locating GalXM staining. The total number of cells and the number of GalXM-labeled cells in the field of view were recorded digitally and counted, and the percentage of labeled cells was calculated in each strain. To study the GalXM staining pattern with polyclonal antibody, the number of discrete fluorescent signals on the capsule (expressed in dots) was counted on each labeled cell and categorized into four groups (1 to 5, 6 to 10, 11 to 15, and >15 dots) (see Fig. 7). This method did not count all the fluorescent signals on the labeled cell but was limited to those signals on the equatorial plane defined by focusing the microscope on the cell wall. In the experiment associated with the growth curve study, optical density was read at 620 nm for 2.5 days with six time points (0, 12, 24, 36, 48, and 60 h). At each interval except 0 h, cells were stained as described above and imaged using the same microscope setting. Thirty randomly selected fields of view were imaged followed by GalXM staining quantification.
Statistical and computation analyses of light scattering measurements were carried out with Bi-ZPMwA Zimm Plot software (Brookhaven Instruments Corp., Holtsville, NY) to calculate Mw, radius of gyration (Rg) and the second virial coefficient (A2). The software 90Plus/BI-MAS was used for effective diameter, polydispersity, and diffusion coefficient parameters (Brookhaven Instruments Corp., Holtsville, NY). For each sample we isolated two different preparations of GalXM per condition. We then examined each polysaccharide preparation per condition and took 10 measurements for each sample. Error was calculated from 10 measurements of one sample. Zeta Plus software was used for zeta potential, mobility, and frequency shift data (Brookhaven Instruments Corp., Holtsville, NY). Student's t test was used in the immunofluorescence study comparing serotypes A and D.
GalXM samples were subjected to acidic methanolysis, and their monosaccharide constituents were analyzed by gas chromatography. This analysis allows the potential detection of four different forms for each sugar derivative, corresponding to the α- and β-forms of furanose and pyranose rings. In association with mass spectrometry analysis, each peak can be identified precisely, based on the profile of fragmentation observed. Fragmentation of TMS derivatives of hexoses usually generates diagnostic peaks at m/z 217 and 214. Pyranose rings give rise to a ratio of (m/z 204)/(m/z 217) of >1, whereas the ratio of furanose rings is <1. Peaks with retention times corresponding to standard derivatives of the typical cryptococcal GalXM components, mannose (Man), xylose (Xyl), galactose (Gal), and glucuronic acid (GlcA) were detected in the hydrolysates. For GalXM samples, Gal was the major monosaccharide constituent, followed by Man and Xyl. Proportions of monosaccharide constituents were similar in cap59 and cap67 GalXMs, which presented Gal/Man/Xyl average molar ratios of 3.5:1.2:1 and 3.2:1.6:1, respectively (Table 1). GlcA was present in most of the GalXM samples derived from growing cultures at different temperatures, with an average molar ratio of 2.2%. Glucuronic acid was not present under all medium conditions tested. N-Acetyl galactosamine was the only sugar other than Man, Gal, and Xyl detected in the cap59, with a molar ratio of 3.6% (data not shown). The method used significantly underestimates glucuronic content, and these numbers should be considered in light of this fact.
Multiangle laser light scattering was used to determine the average molecular mass (Mw) of GalXM from cap59 and cap67 acapsular mutants. The masses of the different GalXM preparations were calculated from Zimm plots (Table 2). The mass for GalXM for cap59 was about 8-fold greater than that for cap67 (Table 2). The radius of gyration (Rg) and the second virial coefficient (A2) were also calculated from the light scattering data (Table 2). The Rg can be described as the average distance from the center point of PS to the outer edge of the molecule (average measure of the molecular size). The Rg for the different GalXM samples manifested significant differences, with 207 nm and 120 nm for cap59 and cap67, respectively. The Rg was used in conjunction with the Mw to calculate the mass density of each GalXM sample. This analysis revealed that cap59 GalXM was 4-fold denser than the GalXM obtained from cap67 (Table 2). The second virial coefficient (A2) is a property which describes the interaction strength between the molecule and a solvent, hence giving insights into the tendency of PS aggregation in that solvent. A2 measurements for the different GalXM samples showed important differences. GalXM PS purified from the cap59 mutant was 0.26 × 10−3 ± 0.12 × 10−3 cm3 mol/g2, suggesting higher molecule-solvent interaction strengths than PS isolated from cap67, which manifested a negative A2 value (−4.20 × 10−3 ± 3.6 × 10−3 cm3 mol/g2), suggesting that molecule-solvent interaction strengths in cap67 are much lower than the molecule-molecule interaction strengths, resulting in a higher tendency for PS aggregation.
Zeta potential was determined for GalXM preparations from both cap67 and cap59 under different medium conditions and temperatures. For strain cap59 the zeta potentials were −13.40 ± 0.88 mV (mean ± standard error of the mean [SEM]) in minimal medium, −8.04 ± 0.96 mV in Sabouraud's broth, −13.09 ± 3.34 mV in peptone supplemented with galactose, and −7.67 ± 0.26 mV in YPD medium. For cap67 the zeta potential values were −10.39 ± 0.44 mV in minimal medium, −5.75 ± 0.28 mV in Sabouraud's broth, −15.51 mV in peptone supplemented with galactose, and −5.97 ± 0.85 mV in YPD medium. These results suggest that the cryptococcal growth medium can affect the zeta potential of the GalXM produced (Fig. 1). When the glycosyl composition was analyzed, we found that the samples with the most negative zeta potential were most likely to test positive for glucuronic acid in the glycosyl analysis, consistent with the notion that such samples had higher content of this negatively charged constituent. We tested whether growth temperature could also alter the zeta potential of the GalXM produced. For GalXM from strain cap59, zeta potential measurements were −16.91 ± 0.92 at 25°C, −13.09 ± 3.34 mV at 30°C, −19.26 ± 2.64 at 37°C, and −15.17 ± 1.49 mV at 40°C. For GalXM from strain cap67, zeta potential measurements were −15.04 ± 1.01 at 25°C, −11.43 ± 1.23 mV at 30°C, −14.63 ± 1.01 at 37°C, and −11.63 ± 0.92 mV at 40°C. These results suggest that growth temperature had as smaller effect on the GalXM zeta potentials than growth medium (Fig. 1).
To gain additional insight into the structural relationship between cap59 and cap67 GalXMs, we determined average effective diameters and size distributions of PS in different media and at different temperatures using multiangle light scattering. Although GalXM from both strains was comprised of populations of various diameters, it is clear that both the culture medium and growth temperature could affect the effective diameter and polydispersity of GalXM preparations. The effective diameter of GalXM from cap67 in minimal medium could not be determined since GalXM extractions under these conditions did not yield any polysaccharide. Polydispersity is a measure of the particle size distribution. We observed variation in GalXM effective diameters for both strains depending on growth medium conditions. This variation was most apparent for cap59 GalXM. We observed modest shifts in effective diameters as growth temperature was increased. The largest diameters were detected at 30°C for both cap59 and cap67 GalXM (Fig. 2 and and33 and Tables 3 and and4).4). The dynamic light-scattering parameters of cap59 and cap67 GalXMs derived from cultures grown in peptone and galactose at 30°C were measured as a function of salt concentration. The results revealed different responses for cap59 and cap67 GalXM as a function of salt concentration (Fig. 4 and Table 5).
A polyclonal serum against GalXM was obtained from mice immunized with a GalXM-Bacillus anthracis protective antigen (PA) conjugate (9, 10). The polyclonal antibody to GalXM was slightly reactive with cap59 GalXM and strongly reactive with cap67 GalXM by ELISA (data not shown). The immunofluorescence pattern of antibody binding to GalXM in encapsulated cryptococcal cells is dot- or punctate-like (10). When we compared different strains, we noted wide discrepancies in the number of dots surrounding individual cells and estimated the reactivity of the polyclonal antibody and/or amount of GalXM/cell by counting the average number of dots per cell. We tested eight strains each of serotype A and D and looked at the percentage of labeled cells. Using this measurement, we found that the percentages of labeling differed between A and D serotypes (P < 0.01) (Fig. 5). Seven strains of C. gattii (serotypes B and C) were also studied, and none stained with the polyclonal antibody to serotype D GalXM (data not shown).
To investigate the dynamics of GalXM production in C. neoformans, we studied antibody to GalXM binding as a function of growth time for strains B3501 (serotype D), 24067 (serotype D), and H99 (serotype A) in 12-h intervals for 2.5 days. The results revealed a sigmoidal pattern in GalXM staining as a function of time, which paralleled the shape of the C. neoformans growth curve except that it occurred 12 to 24 h later (Fig. 6). The highest percentage of GalXM staining was found in the stationary phase (Fig. 6A, B, and C). To further quantify GalXM production, we categorized the labeled cells into four groups depending on their number of fluorescence dots (Fig. 6D, E, and F). The results revealed a change in GalXM production with time. Toward the end of log phase at 24 h, the labeled C. neoformans showed a high percentage of the weakly labeled group, i.e., 1 to 5 dots per cell, indicating the low GalXM production during the active replication of the fungal population (Fig. 6D, E, and F). In contrast, in stationary phase, i.e., at >36 h, the labeled cell possessed a much stronger labeling pattern, as shown by the increasing number of fluorescence dots with time. Figure 7 shows representative examples of the cells counted in this assay. Despite these growth effects on GalXM expression, we note that the quantitative differences in staining described above were not a consequence of the kinetics of fungal growth since all studies used cells from 48-h or stationary-phase cell cultures.
Earlier studies suggested that GalXM was structurally heterogeneous since its galactose, mannose, and xylose components could potentially be linked in 15 different ways (17). The biochemical complexity of that data suggested that the purified GalXM fractions could be part of a composite of several closely related antigens (17). Using proton NMR in an earlier study, we also found subtle differences among the different GalXM molecules (10). These data in turn implied that fine structural differences in the GalXM molecule could translate into antigenic variability (10). Here, we explore these differences using composition analysis, molecular weight, zeta potential, polydispersity measurements, and immunofluorescence.
GalXM derived from the acapsular C. neoformans var. neoformans and C. neoformans var. grubii strains each contained galactose, mannose, and xylose but differed in the molar percentage of these components. Different media resulted in the production of GalXMs with different structural and physical properties, suggesting that studies of GalXM function should carefully control for nutritional conditions during culture growth. In contrast, the GalXM structure was more stable with respect to growth temperature. We also confirmed the presence of glucuronic acid in our GalXM preparations, as reported in a recent study (16). Since glucuronic acid is difficult to measure accurately relative to the other monosaccharide components, we used zeta potential measurements as a surrogate measure for the presence of negatively charged constituents in GalXM. Zeta potential measurements revealed a negative charge for all GalXM preparations from both cap67 and cap59 under different medium conditions. GalXM samples with the highest negative zeta potential were more likely to show the presence of glucuronic acid. These results, together with the prior report of glucuronic acid in GalXM, establish that this polysaccharide, like GXM, is negatively charged.
We explored the structural relationship between GalXM derived from cap59 (serotype A) and cap67 (serotype D). Static light-scattering measurements revealed that the average molecular mass of the GalXM from variety C. neoformans var. grubii was ~8-fold larger than that of C. neoformans var. neoformans. From the Rg and Mw we calculated the mass density, and the results revealed that cap59 GalXM was 4-fold denser than the cap67 GalXM. These differences might also suggest differences in internal structure conformations (or shape factor) between both PS. Dynamic light scattering revealed that GalXM from both strains was comprised of a population of various diameters and that the relative distribution of diameters and extent of polydispersity were affected by both the growth medium and temperature. The ionic strength also affected the measured polydispersity, suggesting that GalXM conformational variability is a function of anion and cation concentration. In this regard, the effective diameters in cap59 become smaller as salt concentration is increased while in cap67 the effective diameters increased. This difference in response may reflect differences in charge positioning in the GalXMs of these strains, which in turn would imply differences in primary structural arrangements of the monosaccharide constituents.
We note that the mass of the cap67 GalXM reported here is larger than that reported in our prior study (21). Given all the structural variability uncovered by the current study, we attribute that difference to the culture growth conditions used to prepare GalXM in the prior and current study. In the earlier study cap67 cultures were grown in Sabouraud's dextrose broth; in this study we used peptone supplemented with 2% galactose since we found that this medium gave a higher yield of purified GalXM. Lastly, we note differences in the sign of the second virial coefficient value for GalXMs from cap59 and cap67 measured by static light scattering. Positive and negative values for the second virial coefficient reflect globally repulsive and attractive intermolecular interactions, respectively, providing an additional parameter for differences between the GalXMs produced by these strains.
In considering the biological implications of these results, it is important to note one potential limitation of the work described here, namely, reliance on GalXM derived from acapsular strains. This reliance on using GalXM from acapsular strains is necessitated by the fact that there are currently no methodologies that completely separate GalXM from GXM, especially given data that these two polysaccharides can interact (12). Since culture supernatants from encapsulated strains contain copious amounts of GXM, all structural studies of GalXM have relied on material from acapsular strains. However, this introduces a potential systematic problem for GalXM studies because the phenotype of acapsular strains like cap67 and cap59 may reflect a secretion defect (15). Hence, it is conceivable that the GalXM from acapsular strains has structural differences from that of wild-type strains. Currently, there is no methodology to ascertain whether this concern is real since attempts to develop better serological reagents in the form of monoclonal antibodies (MAbs) have not proved successful, and we lack reagents to compare the GalXM structures in capsular and their acapsular mutants (10).
Given the potential limitations inherent in working with acapsular strains noted above and the paucity of well-characterized acapsular mutants expressing the same genetic defect such as strains cap67 and cap59, we investigated GalXM variability in wild-type strains by evaluating their reactivity for immune serum reactive with GalXM. All serotype A and D strains reacted with immune serum generated against GalXM from serotype D, with serotype D strains producing stronger reactivity. Serum reactivity with cryptococcal cells was a function of growth phase for both serotype A and D strains, and was most prominent in stationary-phase cells. In contrast, no immunoreactivity was observed with any of the C. gattii strains. We interpret these results as indicating that GalXMs from serotypes A and D share antigenic determinants that presumably reflect the presence of common structural motifs not found in C. gattii strains. Hence, the serological studies imply quantitative differences in GalXM epitope content between A and D strains that could reflect differences in GalXM amount and/or chemical structure.
In summary, we report large intra- and interstrain variability in the structure, serological reactivity, and physical properties of GalXM as a function of growth conditions. One practical consequence of these results is that experiments comparing GalXM structural properties must take into account growth conditions. Given this structural variability, it is possible that GalXM made in vivo is structurally different from that made in culture. In fact, it is conceivable that interstrain and growth-related differences in GalXM structure are responsible for discrepant results observed regarding serological cross-reactivity of the polysaccharide with other antigens (7, 8). Given that GalXM has now been associated with profound immunological derangements (26, 27, 30), it is likely that this polysaccharide makes a contribution to the virulence composition of C. neoformans (9, 20, 23). Since the biological properties of GalXM must reflect its structure, we suspect that structural variability could translate into variable effects in host damaging effects.
Funding for this project was provided by NIH awards AI033774, 5R01HL059842, and 2R37AI033142. R.J.B.C. was supported by the Training Program in Cellular and Molecular Biology and Genetics, T32 GM007491. Carbohydrate and NMR analyses were performed at the Complex Carbohydrate Research Center, University of Georgia in Atlanta. The Complex Carbohydrate Research Center is supported by the Department of Energy Center for Plant and Microbial Complex Carbohydrates, DE-FG09-93ER-20097.
Published ahead of print on 8 January 2010.