Abstract
Cryptococcus neoformans, an encapsulated basidiomycete fungus of medical importance, is capable of crossing the blood-brain barrier and causing meningitis in both immunocompetent and immunocompromised individuals. To gain insight into the adaptation of the fungus to the host central nervous system (CNS), serial analysis of gene expression (SAGE) was used to characterize the gene expression profile of C. neoformans cells recovered from the CNS of infected rabbits. A SAGE library was constructed, and 49,048 tags were sequenced; 16,207 of these tags were found to represent unique sequences or tag families. Of the 304 most-abundant tags, 164 were assigned to a putative gene for subsequent functional grouping. The results (as determined according to the number of tags that identified genes encoding proteins required for these functions) indicated that the C. neoformans cells were actively engaged in protein synthesis, protein degradation, stress response, small-molecule transport, and signaling. In addition, a high level of energy requirement of the fungal cells was suggested by a large number of tags that matched putative genes for energy production. Taken together, these findings provide the first insight into the transcriptional adaptation of C. neoformans to the host environment and identify the set of fungal genes most highly expressed during cerebrospinal fluid infection.
Cryptococcus neoformans is an opportunistic pathogen that primarily infects immunocompromised individuals. Infection is generally initiated by inhalation of basidiospores or poorly encapsulated yeast cells and is usually contained by granulomatous inflammation within the lung in immunocompetent individuals. In immunocompromised hosts, the fungus is frequently capable of disseminating into the bloodstream and then crossing the blood-brain barrier to cause meningoencephalitis (52). C. neoformans has emerged as a significant opportunistic pathogen because of the pandemic of AIDS and the widespread use of immunosuppressive therapy; this fungus now represents the most common cause of fungal infections of the central nervous system (CNS) (68). CNS cryptococcosis is fatal without treatment, and therapy with the antifungal drug amphotericin B has limitations due to potential host toxicity. Treatment failures with death in the first 3 months after diagnosis still range between 10 and 25%. The importance of identifying new targets for antifungal therapy is emphasized by a recent outbreak of C. neoformans infections on Vancouver Island in British Columbia, Canada. None of the approximately 60 cases involved people coinfected with human immunodeficiency virus, and the disease occurred primarily in immunocompetent individuals (84).
The best-characterized virulence factors for C. neoformans include the production of a polysaccharide capsule, the formation of melanin, and the ability to grow at 37°C (71). Capsule-defective mutants of C. neoformans and mutants defective in their ability to grow at 37°C are essentially avirulent; mutants defective in melanin production display attenuated virulence (19, 50, 63, 65, 96). The capsular polysaccharide is believed to be antiphagocytic, because phagocytes do not ingest the fungal cells in vitro in the absence of complement or antibodies (47, 48) and the capsule blocks the recruitment of inflammatory cells (reviewed by Rodrigues et al. [76]). Capsular polysaccharide also depletes complement and suppresses the delayed type of hypersensitivity response and may influence antibody production during fungal infection. In vitro studies have shown that compared with nonencapsulated cells, encapsulated cells are better able to resist phagocytosis. Recent in vivo studies indicate that C. neoformans is actually a facultative intracellular pathogen and that polysaccharide production within phagocytic cells contributes to fungal survival (reviewed by Feldmesser et al. [30]).
Melanin formation in C. neoformans is catalyzed by a laccase that uses diphenolic compounds such as catecholamines as substrates (77). Melanin is synthesized during infection and is hypothesized to serve a protective function by quenching free radicals (63, 95). The prevalence of substrates for laccase in the CNS has been proposed as a possible explanation for the neurotropism of the fungus (17, 62).
The mechanisms of thermotolerance in C. neoformans are starting to be explored. Genes such as RAS1 (encoding a small GTP-binding protein) and CNA1 (encoding calcineurin) have been implicated during growth at elevated temperatures (3, 65). Steen et al. have recently initiated a genome-wide analysis of the response of C. neoformans to host temperature (83). This analysis revealed striking differences in the levels of responsiveness of serotype A and D strains to growth at 25 versus 37°C. Our analysis of the response to the temperature difference in a serotype D strain revealed changes in transcript levels for histone genes, stress-related genes, and genes encoding translation components.
We are interested in identifying the factors that are important for C. neoformans to survive and proliferate in the cerebrospinal fluid (CSF) of an infected host. The rabbit is an excellent model for cryptococcal meningitis because it allows study of the yeast at the site of infection in a serial manner, and this is difficult to perform in smaller animals such as mice, rats, or guinea pigs (23). The body temperature of the rabbit (39.5°C) and the use of steroids in this model are meant to closely mimic the human host situation in which patients usually present with fever and are often undergoing steroid treatment (68). We applied the technique of serial analysis of gene expression (SAGE) to C. neoformans cells isolated from the CSF of rabbits to characterize the transcript abundance profile under these specific in vivo conditions.
SAGE was chosen instead of microarray analysis due to the limited number of expressed sequence tags (ESTs) and the availability of the genomic sequence of C. neoformans strain H99 at the start of our work. SAGE involves the construction and sequencing of libraries of short (10- to 14-bp) sequence tags in which each tag represents a single unique transcript in the cell. The number of times a unique tag sequence appears in a library of SAGE tags is directly proportional to and accurately represents the RNA expression level of the corresponding gene under the specified growth conditions (91). Recent studies indicate that the microSAGE and the SAGE methods are reproducible and accurate for libraries made separately from the same starting material (13, 88).
Our preliminary analysis of the 304 most highly expressed SAGE tags from C. neoformans cells isolated from the rabbit CSF revealed several categories of gene functions, including protein biosynthesis and degradation, energy production, stress response, signaling, and small-molecule transport as well as carbohydrate, amino acid, and lipid metabolism. The high level of expression of genes in these categories suggested that these are functions that C. neoformans requires to survive and proliferate within the host environment. These findings will be important for the C. neoformans research community, and further functional analysis of the genes that we have identified may shed light on the propensity of C. neoformans to cause life-threatening meningitis. In addition, our SAGE data are valuable for the annotation of the H99 genome because they identify transcribed regions.
MATERIALS AND METHODS
Strains and growth conditions.
The C. neoformans serotype A, MATα strain H99 was used for the rabbit infection. The growth conditions for the in vitro 25°C and 37°C SAGE libraries have been described previously (83). Briefly, cells were cultured overnight with shaking in yeast nitrogen base (YNB) broth at either 25°C or 37°C until the cells reached log phase. Cells were harvested by centrifugation, snap frozen, and then lyophilized.
Rabbit cryptococcal meningitis model.
New Zealand White rabbits were housed in separate cages and provided with water and Purina rabbit chow ad libitum. Each rabbit weighed between 2 and 3 kg. H99 cells were grown for 3 to 4 days on YPD plates and then transferred to YNB broth supplemented with 2% glucose (with shaking at 30°C for 48 h). The cells were pelleted and washed once in phosphate-buffered saline and then suspended in phosphate-buffered saline at a concentration of 3.25 × 109 cells per ml. New Zealand White rabbits were immunosuppressed with betamethasone acetate-phosphate (Schering-Plough, Kenilworth, N.J.) 24 h prior to inoculation with H99 and then daily throughout the infection. After sedation with ketamine (Fort Dodge Laboratories, Fort Dodge, Iowa) and xylazine (Vedco, St. Joseph, Mo.), 1.3 × 109 viable C. neoformans cells in a volume of 0.4 ml were inoculated intracisternally into each of 12 rabbits. The rabbits were sedated on days 5, 7, and 9 after inoculation, and the CSF (0.3 to 0.7 ml) was withdrawn from the subarachnoid space, pooled, and immediately placed on ice until RNA processing was performed. Cryptococci in the pooled CSF samples were counted, with the following results: on day 5, 5.2 × 107 yeast cells were found; on day 7, 2.2 × 107 yeast cells were found, and on day 9, 4.0 × 106 yeast cells were found. Samples were split into two aliquots, pelleted at 4°C, washed in chilled water, and allowed to sit on ice for 5 to 10 min to lyse any rabbit cells that may have been present. The supernatant was then withdrawn, and the pellet was frozen at −80°C for lyophilization.
RNA isolation.
One-half of the lyophilized cells from days 5, 7, and 9 of infection were pooled and vortexed with 1.0-mm-diameter acid-washed, RNase-free silica matrix beads for 15 min. Beads and yeast cells were resuspended in 1.0 ml of TRIzol (Gibco BRL) and incubated at room temperature for 15 min. Total RNA was isolated according to the instructions of the manufacturer (Gibco BRL), and the pellet was dissolved in 1.0 ml of lysis-binding buffer from a Dynabeads mRNA DIRECT kit (Dynal). Beads were prepared per the instructions of the manufacturer (Dynal), and mRNA was added to the beads. Poly(A)+ RNA was isolated per the microSAGE method (detailed protocol version 1.0e; available at www.sagenet.org).
SAGE analysis.
The microSAGE method was performed per the microSAGE protocol. A total of 35 PCR cycles were performed to amplify the ditags during the construction of the library. The library of clones was sequenced by BigDye primer cycle sequencing on an ABI PRISM 3700 DNA analyzer. Sequence chromatograms were processed using PHRED software (28, 29), and the vector sequence was detected and removed using CROSS_MATCH software (36). Tags (10 bp) (plus the 4-bp NlaIII site) were extracted, and each tag was given a quality (accuracy) score based on the cumulative PHRED score. Only tags with an accuracy of more than 99% were used in this study. P values for comparisons of levels of tag abundance between libraries were determined and represented the probability that the difference in tag numbers was due to random fluctuation (10).
Tag identification.
For preliminary assignment of tags to putative genes, we used the EST database available for strain H99 at the University of Oklahoma's Advanced Center for Genome Technology (http://www.genome.ou.edu/cneo.html [funded under cooperative agreement UO1 AI 485 94-01]). When an EST sequence could not be identified for a particular tag, we used the genomic sequence available for H99 at the Duke University Center for Genome Technology (http://cgt.genetics.duke.edu/data/index.html) and the Whitehead Institute Center for Genomic Research (http://www-genome.wi.mit.edu/annotation/fungi/cryptococcus_neoformans/index.html) to identify contigs with unambiguous tag assignments. Once an EST or genomic sequence had been identified, the BLASTx (Basic Local Alignment Search Tool) algorithm was employed to find proteins of high levels of sequence similarity in the nonredundant database at the National Center for Biotechnology Information (NCBI). Each BLASTx result was inspected individually and recorded. In the case of genomic DNA sequences where introns are present, the expected values recorded were higher than would have been expected if the introns had been removed. The same was true for the results determined for both genomic DNA sequences and ESTs compared to those that would have been expected if the sequences had been translated and the BLASTp algorithm were employed rather than a BLASTx algorithm.
RESULTS AND DISCUSSION
Overview of highly expressed SAGE tags in vivo.
C. neoformans H99 cells were pooled from the CSF of 12 rabbits on days 5, 7, and 9 postinfection, and the microSAGE method was used to generate a library of cDNA tags. The microSAGE method was used rather than the standard protocol due to the small number of cells obtained from infected animals (8.3 × 107 cells) and the difficulty of obtaining large amounts of RNA from C. neoformans due to its large polysaccharide capsule. The microSAGE library was sequenced to generate C. neoformans gene expression data. The total number of tags for this library was 49,048, and 16,207 of these tag sequences were unique in the library, 10,305 tags occurred once, and 5,902 tags occurred more than once. These numbers provide an approximation of the total number of genes expressed under these growth conditions, although it is difficult to estimate gene numbers from SAGE data (85).
An overview of the abundance classes for the in vivo library is presented in Table 1. Both the number of different tag sequences and the total number of tags present in each abundance class are indicated. For example, in the largest abundance class, 685 SAGE tag sequences appear between 10 and 99 times for a total of 16,651 tags. The in vivo library tag distribution is slightly different from that of the abundance classes for the temperature SAGE libraries that were previously characterized (83). Figure 1 presents the distribution of the tags in abundance classes for the in vivo library, as well as those of the 25 and 37°C in vitro libraries for comparison. To do the direct comparisons, the libraries were normalized to the size of the smallest library and tags that appeared less than one time in any given library were removed. The most striking difference occurs upon comparison of the in vivo data with that of the 37°C in vitro library; by contrast, the in vivo library appears to be more similar to the 25°C in vitro library in terms of overall tag abundance.
TABLE 1.
Interval | Tag sequence count | Total no. of tags |
---|---|---|
1 | 10,305 | 10,305 |
2-4 | 4,183 | 10,426 |
5-9 | 1,007 | 6,436 |
10-99 | 685 | 16,651 |
100-99 | 27 | 5,230 |
Total | 16,207 | 49,048 |
To study further the relationship between in vivo and in vitro growth, a global comparison of the numbers of shared tags among the three libraries was performed to generate an overview of the SAGE data (Fig. 2). The Venn diagram shows that the in vivo library shared 1,885 SAGE tag sequences with the 25°C library alone and 632 SAGE tag sequences with the 37°C library alone. Of the remaining in vivo tags, 12,231 were unique to the in vivo library and 1,459 were shared by all three libraries. As well, this analysis revealed that the 25°C in vitro library was 92.3% similar to the in vivo library in terms of overall gene expression patterns relative to an 88.1% similarity between the 37°C library and the in vivo library. Importantly, we have found that a large proportion of the most highly expressed genes in vivo (described below) were also found among the most highly expressed genes in vitro at 25°C (B. Steen, unpublished observations). Specifically, 69% of those tags that are more abundant at 25 than at 37°C are also found in the most abundant tags of the in vivo library. This suggests that much of the similarity between the in vivo and the 25°C libraries is represented in the most abundant tags (83). Taken together, these data support the hypothesis that the C. neoformans transcription profile from cells grown in vivo is more similar to that of cells grown in vitro at 25°C than to that of those grown at 37°C.
To gain an understanding of the predisposition of C. neoformans for the CNS, we attempted to determine which genes were highly expressed during CNS infection by strain H99. To do so, we chose the 304 most-abundant tags and used those to predict genes from the EST and genomic sequences of strain H99. We then determined what the abundance of these same tags was in the in vitro temperature libraries.
An assembly of shotgun sequence data recently became available for the genome of C. neoformans strain H99 (18 February 2003, 2× coverage, Duke Center for Genome Technology; 13 June 2003, 11× coverage, Whitehead Institute Center for Genome Research). Combined with an EST database (Cryptococcus neoformans cDNA Sequencing Project, University of Oklahoma), these resources allowed us to give preliminary gene assignments to 164 of the top 304 most-abundant SAGE tags in the C. neoformans in vivo library. The remaining 140 tags yielded four types of results in BLAST searches. First, 31 (10%) of the top 304 SAGE tags did not hit any of the sequences in either the H99 genomic or EST databases. These tags were then used in a BLAST search of the available Oryctolagus cuniculus (rabbit) EST sequences at NCBI and of the genomic sequence (sequenced by the National Cancer Institute; available at the ENSEMBLE trace server). We were able to confirm that these tags were not a result of the presence of contaminating cells from the rabbit CSF. Second, 85 (28%) of the SAGE tags corresponding to ESTs or genomic contigs did not result in significant BLAST scores in searches of the nonredundant database at NCBI. Third, 13 (4%) of the tags were significantly similar to uncharacterized, hypothetical proteins. Finally, 11 (3.6%) of the tags hit more than one EST or genomic contig such that further characterization was not possible.
Table 2 shows the 164 tags that were given putative gene identifications; these results were then classified according to the controlled vocabulary determined by the Gene Ontology (GO) Consortium (9). Normalization of the data to the size of the smallest library (the 25°C in vitro library) allowed a comparison of tag abundance in vivo to the abundance of the same tags in vitro at either 25 or 37°C. It should be noted, however, that this comparison involved libraries prepared from cells grown under different conditions of temperature (e.g., 39.5°C in the rabbit) and nutrition (i.e., YNB broth for the in vitro libraries).
TABLE 2.
Numbers have been normalized to the size of the smallest library for comparison (30,468 tags). Tag abundance is presented for each library in shaded boxes in which the shading is proportional to the abundance of that tag such that darker shading corresponds to higher levels of abundance.
Values in parentheses refer to the number of BLAST hits within the proteins that were divided by introns.
Protein biosynthesis.
Of the 164 annotated SAGE tags, 46 were assigned to ribosomal protein genes and 5 more were assigned to genes for two translation elongation factors, two translation initiation factors, and a poly(A)-binding protein. The expectation of this abundance of transcripts encoding translation factors was determined on the basis of SAGE experiments for Saccharomyces cerevisiae grown in rich medium in vitro at 30°C. For example, SAGE analysis of S. cerevisiae revealed that mRNAs for ribosomal proteins represented 18 of the 30 most abundant transcripts (92). Our results indicated that the C. neoformans cells were proliferating in the CSF of rabbits and carrying out protein biosynthesis. Little is known about the regulation of protein biosynthesis in C. neoformans. The results of several studies with S. cerevisiae indicate that ribosome production is a major consumer of cellular resources and is a key component of the energy budget of the cell. Several factors regulate the production of ribosomal proteins in yeast, including nutrients such as nitrogen via the TOR signaling pathway (16, 79) and carbon source through the cyclic AMP (cAMP)/protein kinase A (PKA) signaling pathway (46). Additionally, the interruption of secretory pathway signals (mediated by protein kinase C) results in the repression of ribosomal protein biosynthesis (53). Finally, it is known that the levels of ribosomal protein mRNAs are significantly higher in rapidly growing cells than in cells that are growing more slowly (99).
Interestingly, upon comparison of the abundance of the 51 translation-related tags with results from in vitro temperature libraries, we found that 37 (73%) were most abundant in vivo relative to the in vitro situation. Six of the remaining ribosomal protein tags (RPS12, RPL1, RPL30, RPL36A, RPL37B, and RPL41 plus TEF1) were most abundant at 37°C relative to both the 25°C library and the in vivo library. RPL18 and RPS26 were most abundant at 25°C, and the remaining tags were equally abundant both at 25°C and in vivo. It is interesting that all six of the ribosomal protein transcripts and TEF1 (which are more abundant at 37°C than in vivo) exhibit a significantly higher abundance overall than all of the other ribosomal protein transcripts at the same temperature. This suggests that not all ribosomal protein genes are transcribed equally at 37°C and that novel regulatory functions influence the transcription of these seven genes.
A tag for the phosphomannomutase gene was highly abundant under in vivo conditions relative to in vitro conditions. In S. cerevisiae, this enzyme is known to be required for O-linked glycosylation of proteins and is involved in protein secretion. A phosphomannomutase mutant in yeast displays defective ribosomal protein synthesis due to the strong regulatory link between protein biosynthesis and secretion pathways (60). Our findings here suggest that the protein biosynthesis and secretory pathways are also tightly linked in C. neoformans.
Protein catabolism.
In addition to the evidence for active protein biosynthesis in vivo, several tags identified genes encoding proteins required for protein degradation. For example, the presence of abundant tags for ubiquitin pathway genes suggests proteosome activity in the C. neoformans cells in the host environment. Ubiquitin is transferred to proteins that are targeted for degradation by ubiquitin-conjugating or -ligating enzymes (identified by our SAGE tags), and proteosome activity is involved in several cell processes, including regulation of the cell cycle, transcription, signal transduction, and apoptosis (reviewed in reference 37). We also identified a SAGE tag corresponding to ubiquitin/S27a fusion protein; ubiquitin serves to aid in the assembly of S27a into the ribosome, and this result suggests a possible connection with the translation machinery (31).
In the context of proteolysis, we also identified tags for four proteases that were abundant in vivo. The two metalloproteases that we identified were not abundant in vitro regardless of temperature. The carboxypeptidase tag was abundant in vitro, but to a lesser extent relative to the abundance seen under in vivo conditions, and the proteinase A gene was temperature regulated and abundant both in vivo and at 25°C in vitro. These proteases may be important virulence factors because of their potential involvement in the degradation of host tissues and the proteolysis of immunologically important host proteins such as antibodies and complement. It is known that C. neoformans produces many extracellular enzymes that may contribute to its ability to invade host tissues (21, 22, 76). In the context of in vivo growth, the CSF contains some plasma-derived proteins, including low concentrations of immunoglobulins and C′3 complement. However, the concentration of these and other proteins in the CSF is significantly less than the concentration of the same proteins in the plasma, such that the CSF is regarded as protein poor (24). Therefore, C. neoformans may secrete proteases for the assimilation of carbon and nitrogen to enable growth in the relatively nutrient-deficient CSF. There is evidence to support the supposition that C. neoformans secretes proteases to use proteins as a nitrogen source (8). In addition, we identified tags for glutamine synthetase and glutamine-dependent NAD+ synthase (both categorized under the GO heading amino acid metabolism; see Table 2). Glutamine synthetase exhibits increased activity under conditions of nitrogen starvation in Candida albicans (38). Glutamine-dependent NAD+ synthase is responsible for the use of glutamine as an ammonia source (98). As determined on the basis of tag abundance, our findings support the hypothesis that protease production is an important requirement for survival of C. neoformans in the CSF.
Response to stress.
Several tags corresponded to genes known to be involved in protein folding and the response to heat stress (Table 2). Heat shock proteins are produced in cells under conditions of stress and allow cells to survive under conditions that would otherwise be lethal (35, 66). They play a role in the folding and unfolding of proteins, the degradation of unstable proteins, the prevention of protein aggregation, and the transport of proteins within the cell. Interestingly, the two most-abundant tags overall corresponded to two different putative heat shock protein 12 genes (HSP12) and both were more abundant in strain H99 at 25 than at 37°C. This is similar to what was observed in the SAGE temperature libraries for one of the HSP12 genes in the serotype D strain B3501 (83). Although a second HSP12 has also been identified in the genomic DNA sequence of strain B3501, no SAGE tag was identified in the serotype D in vitro temperature data. A SAGE tag for heat shock protein 60 (Hsp60p) was also identified; this protein is known to produce a strong immune response in the host during infection with Coccidioides immitis (87) and Histoplasma capsulatum (78). Studies of H. capsulatum demonstrate the use of Hsp60p and fragments of this protein as an effective vaccine (25). In addition, the identification of HSP90 in our SAGE data is interesting, because the C. albicans Hsp90p is immunogenic and can confer protective immunity in a mouse model (58). HSP70 was also identified as highly abundant in vivo and is known to be a major immunogenic antigen during pulmonary cryptococcosis (42, 43). Taken together, these studies with Hsp60p, Hsp70p, and Hsp90p in other fungi and our SAGE data suggest that all of these proteins can thus serve as good vaccine candidates for patients at risk for cryptococcal meningitis.
The comparison of our in vivo and in vitro data indicated a surprising difference in the regulation of RNA levels for the HSP60, HSP70, and HSP90 genes. Specifically, these tags do not appear to be abundant in strain H99 at 37°C. This result supports the hypothesis that serotype A strains of C. neoformans such as H99 are not stressed at 37°C, whereas serotype D strains are stressed at 37°C. The latter observation is corroborated by the fact that transcript levels of HSP60, HSP70, and HSP80/90 genes are all elevated at 37°C relative to 25°C in vitro in the serotype D strain B3501A (83). It is possible that the increased body temperature of the rabbit (39.5°C) causes a stress response in the serotype A H99 strain or that there is some other aspect of in vivo growth conditions that caused the increase in transcript levels for stress response genes in H99. We have been able to show that the induction of HSP60, HSP70, and HSP80/90 occurred at 37°C in H99 under low-iron growth conditions (unpublished observations). This supports the hypothesis that the low-iron environment of the host is a key contributing factor in the induction of transcription of these heat shock protein genes in vivo. This difference between serotype A and D strains in temperature stress responses further supports the known differences between serotype A and D strains in their growth abilities at high temperature (57).
In addition to genes that play a role in the response to heat stress, we also identified genes that play a role in oxidative stress. These included genes encoding thioredoxin (67), glutathione peroxidase (40), and a peroxisomal membrane protein. The RNA for the peroxisomal membrane protein is induced in response to four different stress conditions (metal, heat shock, osmotic, and DNA damage stresses) in Schizosaccharomyces pombe (20). In C. neoformans the tags corresponding to these genes were abundant at 37°C, suggesting a global increase in transcript levels for oxidative stress response genes when cells are placed at higher temperatures. The possibility that the C. neoformans cells in the CSF are under stress is further supported by the identification of tags for three enzymes (i.e., trehalose-6-phosphate synthase and two trehalose phosphate synthases) known to be involved in the synthesis of trehalose, the stress-protective sugar. Microarray analysis has shown that these genes are upregulated in S. cerevisiae in response to several other stresses besides temperature (18).
The production of stress-related proteins in vivo may be important in protecting the fungus from oxidative radicals produced by macrophages and neutrophils which occur in the CSF of rabbits during meningitis (70). The C. neoformans cells that we used were isolated at times of infection in which the number of inflammatory cells would be expected to be the highest in the CSF (although the immune response was suppressed by cortisone treatment in the experiment of Perfect et al. [70]). Previous work has demonstrated that cortisone-treated rabbits develop chronic progressive meningitis that can be fatal after 2 to 12 weeks, and all of the pathological findings in this rabbit model resemble those of fatal human cryptococcal meningitis cases (70). Following infection with a pathogen, the CSF becomes infiltrated with neutrophils and macrophages and, under pathological conditions, monocytes in the CSF are capable of phagocytosis and production of reactive oxygen species (69). It has been shown that the presence of C. albicans increases the transcription of genes known to be involved in antioxidant response when exposed to blood and that this response is dependent on the presence of host blood cells rather than the plasma. This is suggestive of a response of C. albicans to the production of oxygen radicals from phagocytic cells (33). It is likely that under the conditions found in the rabbit model, C. neoformans was responding to oxidative radicals produced by phagocytic cells in the CSF by an upregulation of transcription of oxidative stress response genes.
Cellular respiration.
C. neoformans is considered to be an obligate aerobe, and oxygen is a limiting nutrient for growth in vitro (64). The brain is known to consume 25% of the available oxygen in the body, and oxygen and glucose are rapidly transported from the bloodstream to the CSF. Several tags for genes encoding mitochondrial proteins (including components of the electron transport chain such as NADH dehydrogenase, different cytochrome c subunits, and ATP synthase subunits) were highly abundant in vivo. Upon comparison with the abundance of the same tags in vitro, it was found that the cytochrome oxidoreductase subunits and the NADH oxidoreductase tags were present in vitro at 25°C but were present at very low levels (or not at all) at 37°C. If transcript abundance can be correlated with protein abundance, then the respiration rate may be higher at lower temperatures in C. neoformans.
The abundance of two tags corresponding to two different isocitrate dehydrogenases correlates well with the putative high level of energy requirement of these cells, because this enzyme is associated with the tricarboxylic acid cycle of the mitochondria and is essential for respiration. Together, these results suggest that energy requirements of yeast cells in the CSF are high. This is expected for actively growing and respiring cells, and this result is consistent with abundant expression levels of ribosomal proteins.
Signal transduction.
Several tags corresponding to genes encoding small G proteins were abundant, including those encoding members of the RAS and RHO superfamilies. Small G proteins play an important role in the development and pathogenesis of fungi. For example, C. neoformans Ras1p has been shown to control both the mitogen-activated protein (MAP) kinase cascade and cAMP-PKA signaling pathway and is involved in cross talk between the two pathways (5). Both the cAMP-PKA pathway and a MAP kinase pathway are implicated in regulating morphogenesis and virulence in C. neoformans (5, 26, 94). During the induction of filamentous growth in S. cerevisiae, a MAP kinase cascade is activated by a RAS protein (Ras2p) (61) and a 14-3-3 protein (Bmh1p) that is highly similar to the 14-3-3 protein identified in our SAGE data (75). Comparison of the abundance of tags for cell signaling genes identified in vivo relative to those identified in vitro showed that seven out of eight tags are most abundant in vivo. Further, six tags displayed a statistically significant (P < 0.05) increase in abundance in vivo. These tags correspond to the homologues for a Rho2 GTP-binding protein, Rho GDP-dissociation inhibitor, small GTP-binding protein, 14-3-3 pro tein, and the multiprotein binding factor. It is not surprising that several genes involved in cell signaling are highly expressed in vivo due to the requirement of signaling pathways in the regulation of ribosomal protein biosynthesis, the cell cycle, the cell stress response, and the production of known virulence factors (melanin and the polysaccharide capsule) (4, 6, 26). The identification of a tag which corresponds to a unique putative cyclophilin A is interesting, because two other cyclophilins have been identified in C. neoformans and one of these is important for virulence (93).
Transport.
Tags corresponding to eight genes that encoded proteins involved in small-molecule transport were identified. These included proteins involved in transport functions for inorganic phosphate, transition metals, and monomeric sugars and an amino acid transporter probably specific for basic amino acids. Transition metals such as copper, iron, and zinc are important for the function of multiple proteins, because they stabilize protein structure and facilitate redox reactions (73). Five of the eight tags for small-molecule transport proteins identified here were abundant in vivo but were found at low levels in vitro at both temperatures. Exceptions included a putative membrane protein (similar to Pho88p of S. cerevisiae and abundant at 25°C) involved in phosphate transport, a putative metal transporter, a probable (as determined on the basis of BLAST searches) zinc transporter (also abundant at 25°C), and a hexose transporter (with similar levels of abundance in vivo and at 25°C). These findings suggest that there is a significant requirement for metals and phosphate during growth in the CSF and that these molecules are limiting. Phosphate is important for energy generation in the mitochondria. The phosphate transporter identified by our SAGE analysis is most similar to phosphate transporters of the mitochondrial carrier family. The increased abundance of a tag corresponding to the phosphate transporter in vivo correlates well with our identification of an increased abundance of tags for genes encoding the electron transport chain. Iron in the CSF is bound to brain-derived transferrin, and the availability of iron for C. neoformans is thought to be limited during infection (1).
This finding correlated with the significant increase in the abundance of a tag corresponding to an iron permease gene observed under in vivo conditions relative to in vitro conditions. Zinc is important in the brain, where it functions as a neurotransmitter due to its secretion from synaptic vesicles and interaction with specific receptors. In addition to being temperature regulated (with increased abundance at 25°C), the probable zinc transporter transcript is abundant under all growth conditions. This is similar to what was observed for the same gene in the serotype D strain (83). Glucose transport to the brain occurs at high levels due to the large energy requirement. However, the concentration of glucose in the CSF is lower than that in plasma. This may be related to the presence of a tag that corresponds to a hexose transporter in the top 304 tags found during in vivo growth of C. neoformans.
Carbohydrate metabolism.
One of the most intriguing tags identified a gene encoding mannitol-1-phosphate dehydrogenase. This tag was most abundant in vivo and at 25°C but not at 37°C. The enzyme has also been implicated in the response to heat stress in C. neoformans (86), and d-mannitol is produced by C. neoformans in the CSF of rabbits during experimental meningitis (97). In fact, the accumulation of mannitol during infection has been correlated with the outcome of meningitis and may act as an antioxidant and/or osmoticum.
A tag for myo-inositol 1-phosphate synthase (MYO1) was also identified by our analysis as abundant in vivo. This gene is temperature regulated such that the tag is most abundant at 25°C relative to 37°C, and this is similar to what was observed in the serotype D strain B3501 (83). This finding suggests that the abundance of the MYO1 gene in vivo is not due to temperature regulation but rather to some other aspect of the in vivo environment. Interestingly, a tag that was found uniquely in vivo relative to in vitro corresponded to an inositol monophosphatase (Table 3). Inositol monophosphatase is involved in the inositol cycle of calcium signaling in S. cerevisiae (55). The CSF is known to be an inositol-rich environment (82), and C. neoformans is capable of using inositol as a sole carbon and energy source (12). Thus, it is possible that inositol utilization is an important mechanism for survival of C. neoformans as a fungal pathogen in the CSF. It has also been shown that inositol phosphoryl ceramide synthase plays a direct role in intracellular growth and melanin production in C. neoformans (56). This also correlated with the identification of a hexose transporter tag abundant in the C. neoformans in vivo SAGE library (classified under transporters in Table 2).
TABLE 3.
Tag | No. of tags detected in vivo | BLAST result | Species | E value | % Identity | % Similarity | GO biological process | |
---|---|---|---|---|---|---|---|---|
TGATTATGAA | 25 | Glutamine-dependent NAD+ synthase | Saccharomyces cerevisiae | 1.0E-116 | 50 | 59 | Amino acid metabolism | |
CATATTATGT | 22 | Hypothetical protein | Neurospora crassa | 1.0E-24 | 46 | 75 | Uncharacterized | |
TATCTATGTA | 18 | Receptor-associated protein | Schizosaccharomyces pombe | 1.0E-13 | 40 | 62 | Antiapoptosis | |
CATTTGTATA | 17 | G10 protein homolog | Pleurotus ostreatus | 2.0E-42 | 85 | 96 | mRNA splicing | |
CCAATGATTA | 17 | Aconitase protein | Bacteroides fragilis | 3.0E-06 | 50 | 75 | Carbohydrate metabolism | |
GACATATGAA | 17 | Alpha-amylase | Debaryomyces occidentalis | 1.0E-21 | 33 | 55 | Carbohydrate metabolism | |
TGTTATATGA | 17 | Inositol monophosphatase | Rattus norvegicus | 1.0E-37 | 39-44 | 59-61 | Carbohydrate metabolism | |
GAGAGTGTTA | 16 | VHS domain protein | S. pombe | 5.0E-17 | 33 | 52 | Vesicle transport | |
ATTAGTTAAT | 15 | Clathrin coat assembly protein | S. pombe | 5.0E-19 | 40-53 (3)a | 58-79 (3) | Vesicle transport | |
TAACATACAT | 15 | Oligosaccharyltransferase subunit | Mus musculus | 3.0E-05 | 31-63 (3) | 41-72 (3) | Antiapoptosis | |
ATTATAACGA | 14 | Proteasome component PUP2 | S. pombe | 2.0E-27 | 60-95 (2) | 74-95 (2) | Protein catabolism | |
ATTCACAGGA | 14 | Regulatory particle non-ATPase; Rpn9p | S. cerevisiae | 8.0E-21 | 46 | 68 | Protein catabolism | |
CATATTATGT | 14 | Amino acid transporter | Uromyces viciae fabae | 1.0E-119 | 38-64 (3) | 61-78 (3) | Transport | |
CATCTTAGAT | 13 | UMP-CMP kinase | Lentinula edodes | 7.0E-50 | 65 | 80 | Signal transduction | |
TATTCTACAC | 13 | Predicted protein | N. crassa | 8.0E-12 | 45 | 57 | Uncharacterized | |
ATTTTCAGAA | 12 | Dynamin-related protein | S. pombe | 3.0E-16 | 50 | 69 | Mitochondrial organization-biogenesis | |
CATAGAATTA | 12 | RNA polymerase II subunit RPB9 | S. cerevisiae | 4.0E-07 | 48 | 63 | Transcription | |
GAATTGATAG | 12 | Arc1p | S. cerevisiae | 2.0E-18 | 44 | 58 | Amino acid metabolism | |
TACTTCTTGA | 12 | Related to BET1 protein | N. crassa | 1.0E-09 | 34 | 52 | Vesicle transport | |
AATTATTATT | 11 | Hypothetical protein | S. pombe | 2.0E-06 | 24 | 45 | Uncharacterized | |
GGTCAGTCGA | 11 | Hypothetical protein | Plasmodium yoelii yoelii | 1.0E-17 | 72-77 (2) | 85-89 (2) | Uncharacterized | |
TATTTCATTT | 11 | U3 small nucleolar RNP protein IMP3 | S. cerevisiae | 9.0E-50 | 59 | 74 | RNA splicing | |
TTATGGGTAG | 11 | Bud20p | S. cerevisiae | 7.0E-11 | 44 | 57 | Nuclear pore | |
AATGTATTAA | 10 | Stomatin-like protein | Gibberella fujikuroi | 2.0E-13 | 57-63 (2) | 72-79 (2) | Cell wall maintenance | |
CAATCAATAT | 10 | FKBP-70; immunophilin | S. cerevisiae | 9.0E-39 | 70 | 81 | Protein biosynthesis | |
CATAGATGCC | 10 | Hypothetical protein | N. crassa | 5.0E-11 | 35 | 54 | Uncharacterized | |
CATTGTTACT | 10 | NADH/ubiquinone oxidoreductase | N. crassa | 2.0E-45 | 63 | 78 | Cellular respiration | |
CATTTTGACT | 10 | Ribosomal protein L27 | Filobasidium floriforme | 5.0E-77 | 84 | 85 | Protein biosynthesis | |
TTTATAGATC | 10 | Mitochondrial carrier | N. crassa | 3.0E-53 | 67 | 78 | Mitochondrial organization-biogenesis |
Values in parentheses refer to the number of BLAST hits within the proteins that were divided by introns.
Several enzymes identified by our SAGE tags are known to be involved in the pentose-phosphate shunt, including two transaldolases, 6-phosphate gluconate dehydrogenase, and 6-phosphogluconolactonase. The major function of the pentose-phosphate shunt is the generation of NADPH (energy in the form of reducing power) and the supply of ribose-5-phosphates to the cell for nucleic acid synthesis. Cells that are undergoing fatty acid and sterol synthesis also require high amounts of NADH. Furthermore, cells growing rapidly require high rates of nucleic acid synthesis and therefore have a highly active pentose-phosphate shunt. In addition, it has been shown for S. cerevisiae that the pentose-phosphate shunt plays a role in the protection of cells against oxidative stresses (41, 80).
The tag for enolase was abundant in vivo relative to the levels of abundance seen at both in vitro temperatures, and the tag displayed temperature-regulated changes in abundance, with a higher level at 25 than at 37°C. In addition to its role in glycolysis, enolase has been implicated as a potent allergen in Aspergillus fumigatus (51), C. albicans (27), Pneumocystis carinii, and P. ratti (32). Enolase has been localized to both the cytoplasm and cell wall of C. albicans (7), and heat shock does not induce enolase gene expression in this fungus (34). Similarly, our C. neoformans SAGE data indicated that transcript levels for the gene are not higher at 37°C. In addition, enolase is involved in plasminogen binding and degradation of host tissues (fibrinolysis) in P. carinii and P. ratti (32). Thus, the high level of enolase tag abundance in our SAGE library is suggestive of a role in C. neoformans pathogenesis.
Amino acid metabolism.
Several amino acid metabolism genes were identified as abundant in vivo but not in vitro. Two of these genes encoded enzymes such as a glycine cleavage system protein precursor and glycine-hydroxymethyltransferase involved in the mitochondrial glycine cleavage system which mediates the entry of one-carbon units into folate-dependent pathways (45). Reduced folates are found in higher concentrations in the CSF (32 ng/ml) than in the plasma (6.5 ng/ml) (81). In addition to the importance of glycine in the metabolism of one-carbon fragments, peptides, and nucleotides within the cell, free glycine plays an important role in the mammalian brain as a neurotransmitter and neuromodulator such that disruption of glycine metabolism in the brain leads to a severe neurological disorder (49).
Aromatic compound degradation.
We have identified two tags corresponding to enzymes involved in aromatic compound degradation. Dienelactone hydrolase degrades chlorinated aromatic compounds, and 1,4-benzoquinone reductase is involved in the degradation of the aromatic intermediates produced from lignin degradation in Phanerochaete chrysosporium, the wood-rotting basidiomycete fungus (2). It is well documented in the literature that basidiomycete fungi are capable of the degradation of aromatic compounds, and the potential use of these fungi in bioremediation is being explored (72). In the natural environment, these enzymes are important for the degradation of polymeric lignin and its intermediates (such as quinines, hydroquinones, benzaldehydes, benzoic acids, and ring-opened fragments) by P. chrysosporium (15). C. neoformans may degrade lignin in the environment, and this idea correlates well with the natural tree habitat for C. neoformans (74). Our observed abundance of the corresponding SAGE tags in vivo suggests a possible requirement for similar functions during C. neoformans infection of the mammalian host.
Cell wall.
One tag identified the gene for C. neoformans MP98, an intriguing secreted mannoprotein that shows similarity to chitin deacetylases and that probably stimulates the T-cell response (39). Chitin deacetylases hydrolyze N-acetoamido bonds of chitin during cell wall formation. Chitin deacetylase is also thought to play a role in plant-pathogen interaction involving the fungus Colletotrichum lindemuthianum; the enzyme is extracellular in this case and acts on chitin oligomers that induce plant defense mechanisms (11, 44, 89, 90). Along with the high transcript level of the MP98 gene, a second chitin deacetylase gene (GACATTTTGA) was also abundant in vivo. Both of the tags for these genes did not show significant abundance under in vitro growth conditions, emphasizing their possible importance in vivo. The identification of a tag that corresponded to a GDP-mannose pyrophosphorylase is interesting in the context of capsule biosynthesis in C. neoformans, because mannose is the main component of sugar backbone of the capsule (14). This also may be related to the identification of the Golgi-GDP mannose transporter classified under the GO term heading of transport. Both of these tags were most abundant under in vivo growth conditions relative to in vitro growth conditions.
Unclassified.
Two poorly characterized proteins have been identified by our SAGE data as potentially important in pathogenesis. The CipC protein was originally identified in Aspergillus nidulans as a protein that is produced in high amounts in the presence of the antifungal agent concanamycin A (59). Expression of the C. neoformans CIPC gene in the serotype D strain B3501A is induced 55-fold at 37°C relative to levels seen at 25°C (83). We did not observe similar temperature regulation for the serotype A strain; however, the abundance of the tag for this gene was significantly elevated in vivo relative to that seen in vitro and represents the third-most-abundant tag in our in vivo SAGE library. This result strongly implicates this gene as serving an important role during growth in vivo. We have knocked out the CIPC gene in the B3501A strain and found that mutants exhibited a temperature-sensitive growth phenotype (B. Steen, unpublished results). The gene for the second protein was already described in GenBank (AJ345095) as encoding cytokine-inducing glycoprotein. The tag for this gene was abundant under in vitro growth conditions at both 25 and 37°C, and it was found to be one of the most abundant tags when C. neoformans cells were growing in vivo.
A SAGE tag (identifying a gene with similarity to the entire OV-16 antigen of Onchocerca volvulus, the causative agent of onchocerciasis [“river blindness”], which affects 18 million Africans and Latin Americans) was also unclassified. OV-16 antigen is highly immunogenic during the early stages of infection prior to the detection of the parasite (54). It is interesting that the gene for this protein exists in C. neoformans.
Transcripts that are unique to the in vivo library.
From the list of tags that are unique to the in vivo library relative to those in the temperature in vitro libraries, we have annotated the 100 most abundant tags. Of these tags, we found that 29 did not match any H99 genomic contigs at the Duke Center for Genome Technology or at the Whitehead Institute Center for Genome Research or any ESTs at The University of Oklahoma, four tags matched more than one contig, and 35 tags had no significant BLAST results at NCBI. Of the 29 tags that did not hit a corresponding EST or genomic sequence, 7 were due to rabbit sequences from contaminating rabbit cells from the CSF, as determined by searches of rabbit ESTs and the genomic sequence. This suggests that the uniqueness of 7% of the tags in the in vivo library was due to the presence of rabbit sequences. It is also possible that these tags correspond to sequences currently not available in existing H99 databases. That 35% of the tags were found to correspond to gene sequences without a BLAST result at NCBI suggested the existence of a large subset of undiscovered genes that were expressed by the fungus during growth in the host CSF. Investigations of the remaining 24 tags resulted in annotations that could be classified under different previously discussed categories, such as protein biosynthesis, protein catabolism, cellular respiration, signal transduction, and cell wall maintenance (Table 3). In addition, tags that were classified under new categories, including genes with predicted roles in antiapoptosis, mRNA splicing, vesicle transport, mitochondrial organization, and biogenesis and transcription, were identified. A nuclear pore protein was also identified. The unique expression suggests specific roles for these functions during growth of C. neoformans in the CSF of rabbits.
Conclusions.
Our work explored the hypothesis that genes that are turned on or expressed at high levels during infection belong to genetic pathways or networks important for survival and the progression of infection during rabbit cryptococcal meningitis. In this context, we identified several functions that are potentially important during infection, including protein catabolism, the heat stress response, and the oxidative stress response. Additionally, we identified abundant transcripts for genes involved in nutrient acquisition and transport that provide clues about metabolic limitations for C. neoformans growth in the CSF. Our SAGE data also confirmed in vivo abundance for some previously identified genes with suggested roles in infection. These included genes for MP98, mannitol dehydrogenase, heat shock proteins, enolase, and myo-inositol phosphate synthase. These results help to validate SAGE as a discovery tool to understand the infection process and to identify potential antifungal drug targets or strategies. We are now pursuing functional tests to examine the roles of selected genes identified by our work. In particular, we are interested in studying the roles of the CIPC and HSP12 orthologs because of their high transcript levels. We are also targeting functions that may be key for nutrient acquisition, including the proteases and the transporters. Finally, we believe that our findings will be an important resource for the medical mycology research community and will form a strong foundation for more detailed explorations of fungal gene expression during infection.
Acknowledgments
We thank the C. neoformans cDNA Sequencing Project at The University of Oklahoma (Bruce A. Roe, Doris Kupfer, Heather Bell, Sun So, Yuong Tang, Jennifer Lewis, Sola Yu, Kent Buchanan, Dave Dyer, and Juneann Murphy) for access to the EST information that was essential in the analysis of the SAGE data. We also thank Fred Dietrich at the Duke Center for Genome Technology for access to the Duke University database for H99 genome sequence. We are grateful to the Whitehead Institute/MIT Center for Genome Research (http://www-genome.wi.mit.edu) for access to genomic sequence data. Thanks also to Cletus D'Souza for critical review of the manuscript, Aliya Hasham for SAGE data analysis, Kristin Tangen for her SAGE information for H99 grown in low-iron conditions, and Tian Lian and Kim MacDonald for their work with the temperature libraries.
This work was funded by a Scholar Award (to J.K.) from the Burroughs Wellcome Fund and by Public Health Service grant AI28388 (J.R.P.). Additional funding was obtained from the Canadian Institutes of Health Research. M. Marra and S. J. M. Jones are Biomedical Scholars of the Michael Smith Foundation for Health Research.
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