Modulation of Phagosomal pH by Promotes Hyphal Morphogenesis and Requires Stp2p, a Regulator of Amino Acid Transport

Summary

The innate immune system represents a key barrier that fungal pathogens such as Candida albicans must overcome in order to disseminate through the host. C. albicans cells phagocytosed by macrophages initiate a complex program that involves a large-scale reprogramming of metabolism and transcription and results in the switch to a hyphal form that can penetrate and kill the macrophage. Though a number of signals are known to induce this morphological transition in vitro, what does so following phagocytosis has been unclear. We previously showed that C. albicans rapidly neutralizes acidic, nutrient-poor media that resembles the phagolysosome and that this is deficient in mutants impaired in amino acid import due to a mutation in STP2. In this paper, we investigate whether this happens within the macrophage as well. We show here that, in contrast to wild-type cells, stp2Δ mutants occupy an acidic phagosome and are unable to initiate hyphal differentiation. Because of this, they are more sensitive to killing and do less damage to the macrophages than cells that can neutralize the phagolysosome. We conclude that alteration of phagosomal pH is an important virulence adaptation in this species.

Introduction

Normally a benign commensal, Candida albicans is also the most prevalent fungal pathogen in humans. Common mucosal manifestations of candidiasis are oropharyngeal thrush and vaginitis, but C. albicans can infect virtually any body site [1], [2]. The most serious infection – disseminated hematogenous candidiasis – is the fourth most common acquired hospital infection with a mortality rate of about 40% [3], [4]. In healthy individuals the innate immune system maintains C. albicans as a commensal and, with the exception of vaginitis, C. albicans infections are associated with defects in innate immunity. A variety of factors such as neutropenia, chemotherapy, implanted medical devices, and several genetic disorders have been linked with increased risk for disseminated candidiasis, emphasizing the important role of the immune system, including phagocytes such as macrophages and neutrophils [5].

Phagocytosis is an important step in the process by which macrophages destroy foreign cells. Many pathogens have evolved strategies to avoid or subvert phagocytosis at various stages of this process. For instance, bacterial pathogens such as Pseudomonas aeruginosa and Yersinia enterolitica inhibit phagocytosis through direct inhibition or by altering cell surface structure [6], [7]. Other pathogens, such as Anaplasma phagocytophila, interfere with the endocytic process or with the activity of macrophage-derived antimicrobial factors [8], [9]. Mycobacterium tuberculosis, Salmonella typhimurium, Listeria monocytogenes and other pathogens have developed strategies to either withstand or modulate the acidic pH of the phagolysosome, and/or alter fusion of the phagosome with the lysosome to prevent killing [10]–[12]. Similarly, C. albicans has developed strategies to escape phagocytosis and killing by the macrophages. Inside the macrophage C. albicans differentiates into the filamentous hyphal form, which ruptures the macrophage allowing it to escape and resume proliferation. This morphogenetic switch is required for virulence and has therefore been well studied [13], [14]. A variety of factors can trigger morphogenesis in vitro, including neutral pH, serum, elevated CO₂ concentration, physiological temperature, and N-acetyl glucosamine [15]. While several of these inducing factors (37°C, elevated CO₂) act on phagocytosed cells, an acidic phagosome should inhibit germination and it has been unclear what stimulates this morphological transition. Understanding this phenomenon is further complicated by evidence suggesting that C. albicans might modulate the phagosomal milieu or alter endocytic trafficking [16]. In fact, the exact nature of the intracellular compartment(s) containing C. albicans is not clear; here we use the generic term phagosome for simplicity.

The morphogenetic change is only part of the response to phagocytosis. Genomic and proteomic profiling indicates that C. albicans responds to phagocytosis by a significant reorganization of metabolic processes [17]–[20]. The response of C. albicans within macrophages is broadly similar to that seen after nutrient starvation, including repression of translation and glycolysis and activation of metabolic pathways required to use less favored carbon sources, including the glyoxylate cycle, β-oxidation, and gluconeogenesis [17], [18], [21]. Some of these metabolic pathways have been shown to be required for full virulence or are induced in vivo in animal models of candidiasis indicating that cells experience carbon starvation in the context of the intact host [19], [22]–[24]. Growth in alternative carbon sources also alters recognition by phagocytes, drug resistance and other relevant phenotypes [25], [26].

In a recent study we demonstrated that C. albicans cells grown in acidic medium with a nutrient composition similar to that predicted to exist inside phagocytic cells rapidly alkalinize the environment [27]. This phenomenon requires amino acid catabolism and results in extrusion of as ammonia presumably derived from the amino acid. As the cells neutralize the media, they auto-induce a shift to the hyphal form [27]. We identified mutations in several genes that impaired or abolished alkalinization, with the most severe phenotype conferred by mutation of STP2, which encodes for a transcription factor that regulates expression of amino acid permeases. We previously postulated that C. albicans might modulate the pH of the phagosome [27], a suggestion also made by others [16]. Thus, the stp2Δ mutant is an excellent tool with which to probe the importance of extracellular alkalinization during contact with host phagocytes.

Here we test the ability of C. albicans cells to alkalinize the phagosomal space and the importance of neutral pH in escape from phagocytosis. We show that phagocytosed stp2Δ mutant cells do not underdo hyphal morphogenesis within macrophages, suggesting that amino acid uptake is necessary for this process. Cells lacking STP2 are defective in killing macrophages and show reduced survival upon phagocytosis. Finally, we show that wild type C. albicans cells can modulate the intraphagosomal pH, since these cells fail to co-localize with acidophilic dyes. In contrast, stp2Δ mutant cells inhabit acidic phagosomes, suggesting that the alteration of phagosomal pH by C. albicans requires amino acid catabolism, as does alkalinization in vitro. Pharmacological neutralization of the phagosome restored hyphal morphogenesis in the stp2Δ mutant cells, indicating that neutral pH is a critical inducing factor in this environment. Consistent with this, stp2Δ mutants were attenuated in virulence in a mouse model of disseminated candidiasis. Altogether our results suggest that during phagocytosis C. albicans utilizes amino acids to promote neutralization of the phagosome, stimulation of hyphal morphogenesis and escape from the macrophages and that this process contributes to fitness within the host.

Results

Construction and verification of new stp2Δ mutants

C. albicans cells grown in conditions that mimic the phagolysosome efficiently alkalinize the environment, resulting in induction of hyphal morphogenesis. We hypothesized that this phenomenon may occur within the phagosome to promote fungal survival and escape. To test this, we took advantage of cells carrying mutation in the STP2 gene, a regulator of amino acid permease expression [28], since cells lacking STP2 are defective in environmental alkalinization [27]. Because the existing stp2Δ mutant strain is apparently aneuploid [28] and uses URA3 as a disruption marker, which can be problematic when used for in vivo and ex vivo studies [29], [30], we generated two independent stp2Δ mutant strains (SVC17, SVC18) using the SAT-flipper method [31] as described in the Materials and Methods.

In order to confirm the phenotype in the newly generated strains we verified that they shared previously published phenotypes in amino acid assimilation, alkalinization and ammonia release [27], [28]. Our newly generated strains behaved identically to the previously published stp2Δ mutant strain PMRCA57 [28] when grown on multiple amino acids as the sole nitrogen source and phenotypes were fully complemented in the restored strain (Fig. S1). Next, we tested if the newly developed strains were able to alkalinize an acidic environment via production of ammonia. The stp2Δ mutant strains grew slightly more slowly than the wild type cells in alkalinization-inducing medium (YNB+1% CAA, pH 4.5), but the difference was not statistically significant (Fig. 1A). In contrast, the stp2Δ mutant cells showed a dramatic defect in alkalinization (Fig. 1B). In cultures with the wild type and complemented strains, the media pH rose from a starting pH of 4.5 to about 7.5 within seven hours, whereas cultures with the stp2Δ mutant reached only pH 5.4 at 24 hours (Fig. 1B). A similar environmental alkalinization defect was observed in the stp2Δ mutant when cells were grown in medium M199 (data not shown) and on the solid medium GM-BCP, pH 4.5 (Fig. S2). Alkalinization is associated with extrusion of volatile ammonia [27] and non-alkalinizing stp2Δ mutant colonies did not release significant quantities of ammonia when grown on GM-BCP medium (Fig. 1C). Overall, these results confirm that the newly generated stp2Δ mutant strain shows the expected phenotypes: impaired utilization of amino acids, a severe defect in the ability to modulate the environmental pH, and abrogated release of volatile ammonia during this process [27], [28].

By generating a neutral pH, alkalinization induces C. albicans to switch from yeast to hyphal form, which is not observed when alkalinization is repressed by glucose or buffering [27]. Therefore, we assessed the morphology of the stp2Δ mutant cells grown under alkalinizing conditions (Fig. 2A). As expected, the majority of the wild type cells (∼85%) and of the STP2 complemented cells (∼75%) switched to the hyphal morphology as the media neutralized. In contrast, fewer than 5% of the stp2Δ mutant cells had switched to the hyphal form within seven hours, at which point the pH of the medium was 4.8. Representative images of each strain prior to and after alkalinization of the medium are presented in Fig. 2B. To verify that the observed defect in morphological switch is due to the inability of the stp2Δ mutants to raise the environmental pH under these conditions and not due to an inherent defect in responding to neutral pH, we assessed hypha formation in the wild type and stp2Δ mutant cells in standard YPD medium at pH 4.5 or 7.3 (average pH achieved by wild-type cells). We did not observe any difference in the morphologies of the wild type and the stp2Δ mutant cells (Fig. 2C). Thus, the inability of the stp2Δ mutant cells to switch to the hyphal form in alkalinizing conditions is not due to a general morphological defect in these cells.

stp2Δ mutant cells fail to escape phagocytosis

The ability to change the environmental pH from acidic to neutral could have important effects on the host-pathogen interaction, since many niches in the host, such as oral cavity, vagina and the skin, have acidic pH. Another environment where pH is critical is the phagolysosome, where acidic pH activates lysosomal proteases and hydrolases, potent defensive enzymes, to destroy the pathogen [32]. Therefore, we asked whether the stp2Δ mutant cells have a morphogenetic defect upon internalization by macrophages. First, we monitored the interaction of stp2Δ mutant cells with the macrophages using live cell video microscopy. As expected, the majority of wild type C. albicans cells initiated hyphal morphogenesis within one hour of phagocytosis (Fig. 3A; Movies S1 and S2 are the wild-type and stp2Δ mutant, respectively). Hypha formation continued and eventually allowed C. albicans to escape phagocytosis by rupturing the macrophages. In contrast, the phagocytosed stp2Δ mutant cells showed a severely impaired ability to form hyphae. Importantly, stp2Δ cells that were not phagocytosed switched to the hyphal forms, indicating that stp2Δ mutant cells have no inherent defect in responding to hyphal-inducing conditions in this medium. To calculate what percentage of the cells underwent hyphal morphogenesis during phagocytosis, we carefully observed the time-lapse images of phagocytosed wild type or stp2Δ mutant cells and counted both total phagocytosis events and morphogenesis. At one hour of co-culture about 14% of the phagocytosed wild type cells and 8% of the stp2Δ mutant cells had initiated hyphal morphologensis (Table 1). However, significant differences in hyphal morphogenesis between the two strains were observed at later time points: at three hours of co-culture about 75% of the wild type cells were found as germ tubes or hyphae, whereas only 31% of the stp2Δ mutant cells have switched to the hyphal morphology. We noted that stp2Δ mutant cells that had begun to germinate prior to phagocytosis continued to form hyphae within the phagosomes, but those that were ingested as yeast rarely switched morphology (data not shown). Thus, stp2Δ mutant cells have a substantial reduction in hyphal morphogenesis following phagocytosis.

We sought to understand whether the impaired hyphal growth might be caused by altered recognition by macrophages, as has been observed in some mutations that affect the cell wall proteome [33], [34]. We monitored the uptake of C. albicans cells by macrophages by applying the membrane-impermeant chitin binding dye Calcofluor White (CW) to distinguish between external versus internalized cells. We did not observe any significant differences in uptake of live C. albicans cells tested, indicating that recognition of stp2Δ mutant cells by the macrophages is not impaired (Fig. 4). At 30 min about 30% of the wild type cells, stp2Δ mutant cells and STP2 complemented cells were internalized and this increased to about 60% at one hour. In contrast, phagocytosis of the heat killed cells was far more effective, with the majority of the cells internalized by 30 minutes (Fig. 4), which may be explained by alterations in the cell wall caused by the heat killing [35]. Thus, the observed morphogenesis defect in the stp2Δ mutants was not due to differential recognition by the RAW264.7 macrophages.

Hyphal growth permits C. albicans cells to escape phagocytosis by lysing the macrophage. We hypothesized that the hyphal growth defect of the stp2Δ mutant strain would result in less damage to the phagocyte. For this purpose we measured loss of macrophage membrane integrity based on lactate dehydrogenase (LDH) release by the cells after five hours of co-culture. At this point about 32% of the RAW264.7 macrophages were killed (Fig. 5A); in contrast, damage caused by the stp2Δ mutant strain was significantly reduced (16% killed). The complemented STP2 strain damaged macrophages to about the same extent as the wild type (Fig. 5A). This data clearly indicates that STP2 is required for successful escape from phagocytosis.

Since we observed that the stp2Δ mutant has a reduced ability to form hyphae and escape phagocytosis, we asked whether it was more efficiently killed by the immune cells. To test C. albicans survival following phagocytosis we used an end-point dilution survival assay as previously reported [36]. Only 54% of the stp2Δ mutant strains survived the macrophage attack while about 80% of the wild type cells and 78% of the STP2 complemented cells survived (Fig. 5B). Thus, the reduced ability to escape macrophages leads to more effective killing.

Growth of stp2Δ mutant cells is not impaired by different stress conditions mimicking the macrophage phagosome

The impaired interaction with macrophages could results from enhanced sensitivity to host-derived stresses, which we tested using in vitro growth assays. Phagocytosed C. albicans cells appear to utilize non-fermentable carbon sources for nutrition rather than glucose [18]. Therefore, we tested growth in minimal medium supplemented with ethanol, acetate or glucose as the sole carbon source and found no meaningful differences (Fig. S3). Further, the stp2Δ mutant strain was not more sensitive to conditions that mimic other aspects of the phagolysosomal environment, including oxidative stress, nitrosative stress, or iron depleting conditions (Fig. S4). Thus, the stp2Δ mutants are not more sensitive to conditions found in the macrophage phagosome.

Phagosomal neutralization promotes C. albicans escape from the macrophages

Given the Stp2p-mediated alkalinization in vitro, we hypothesized that the defect in hyphal growth in phagocytosed cells reflected a difference in the pH of phagosomes containing wild type versus stp2Δ mutant cells, i.e. neutral versus acidic. To test our hypothesis we pretreated RAW264.7 macrophages with the acidophilic dye Lysotracker Red DN99 (LR) to allow accumulation of the dye in acidic organelles (lysosomes). FITC-labeled C. albicans cells were allowed to interact with the LR-loaded macrophages for up to two hours. As expected, heat killed cells were found in acidic phagosomes one hour after co-culture (Fig. 6). In contrast, C. albicans wild type cells rarely localized to acidic phagosomes as noted by the diffuse LR staining, suggesting that the pH of the C. albicans-containing phagosome is over 5.5 and that these cells alter the nature of this compartment relative to heat-killed cells. In contract, cells lacking STP2 localized to acidic phagosomes, similar to the heat killed cells; complementation of STP2 restored the wild type phenotype (Fig. 6). To estimate the difference in the pH of phagosomes containing wild-type versus stp2Δ mutant cells, we measured the fluorescence intensity of LR relative to FITC surrounding phagocytosed cells, with the rationale that a higher ratio indicated a lower pH (Fig. 7). The LR:FITC ratio for heat killed cells in acidic phagosomes was about 2.0 at 60 min (Fig. 7). In contrast, the LR:FITC ratio for wild-type or STP2 complemented cells was 1.2 and 0.8 respectively, while the stp2Δ mutant cells had an LR/FITC ratio of 1.9, close to that of heat killed cells. Stp2p-dependent phagosomal neutralization by C. albicans was also observed following phagocytosis by bone marrow-derived macrophages (data not shown). Thus, there is a substantial difference in the pH of phagosomes containing wild-type versus stp2Δ mutants, suggesting that the alkalinization process we have described in vitro also occurs within the phagocyte.

Next, we asked if failure to neutralize the phagosomal environment alone explains the hyphal defect of stp2Δ cells. To test this, we created neutral phagosomes by specifically inhibiting the vacuolar ATPase (v-ATPase) of the macrophages using bafilomycin A. We verified that the phagosomes were neutralized by obtaining the LR/FITC ratio after one hour of co-culture of C. albicans, which was about 1.0 for all the cells tested (Fig. S5). Importantly, bafilomycin A completely suppressed the hyphal morphogenesis defects of phagocytosed stp2Δ mutant cells (Fig. 8). Indeed, the proportion of stp2Δ hyphal cells in bafilomycin-treated macrophages was essentially the same as that of the wild-type control, indicating that neutralization of the phagosome is a key factor for hyphal morphogenesis in these cells (Table 1). Bafilomycin A1 did not affect C. albicans growth or morphogenesis in macrophage-free RPMI medium (data not shown). Altogether, our data suggests that the observed differences in stp2Δ morphogenesis, macrophage survival and reduced macrophage killing are due to inability to neutralize the phagosomal environment. More importantly, neutralization of the phagosome promotes hyphal morphogenesis and phagosomal escape in the fungal pathogen.

Environmental alkalinization can occur in body niches colonized by C. albicans

Since C. albicans can alkalinize the phagosome and this process contributes to hyphae formation and escape from the macrophages, we asked if alkalinization may alter the host-pathogen interaction in other body niches colonized by C. albicans. Because both the oral and vaginal cavities are acidic, we tested C. albicans alkalinization on media that mimics the composition of vaginal fluid (vaginal simulating fluid or VSF) and human saliva (artificial saliva or AS). Alkalinization in AS was remarkably rapid, rising from pH 4.5 to 7.0 within five hours and further to pH 8.4 at 24 hours of incubation (Fig. 9A). Similarly, these cells steadily raised the pH of the VSF from starting pH of 4.2 to 7.0 (Fig. 9B), though this was much slower, occurring over 72 hours. Interestingly, stp2Δ mutant cells showed a marked delay in alkalinization on AS, where the pH reached only 5.3 at five hours (Fig. 9A), but the alkalinization of VSF did not differ from that of the controls (Fig. 9B). The significant difference in the time required to fully alkalinize VS and AS, and the differential requirement of Stp2p in the alkalinization processes, suggests that multiple mechanisms for environmental alkalinization by C. albicans may exist.

Stp2p is important for full virulence in a mouse model

The decreased survival upon phagocytosis by the macrophages of stp2Δ mutants raised the question whether these strains would be impaired during disseminated infection. Therefore, we tested stp2Δ mutant strains in the standard mouse tail-vein injection model of disseminated hematogenous candidiasis. The stp2Δ mutant strain SVC23 was attenuated in virulence compared to the STP2 complemented or the wild type strain SVC21 (Fig. 10), with a mean time to death of 2.4 days for the wild-type strain compared to 5.9 days for the mutant strain, indicating that Stp2p is required for full virulence in this animal model of infection. The statistical analysis showed that the survival curve for this mutant is significantly different compared to the wild type or the complemented cells (p = 0.0011 or 0.0024, respectively). We also tested the survival of a second, independent stp2Δ mutant strain SVC22, which had a mean time to death 5.3 days (data not shown). This modest attenuation is consistent with the partial reduction of hyphal induction and macrophage toxicity in phagocytosed cells.

Discussion

Here we show that C. albicans can neutralize the macrophage phagosome to induce hyphal morphogenesis and escape from the immune cell and we propose the first mechanism for this phenomenon: extrusion of ammonia as a byproduct of amino acid catabolism within the host cell. This conclusion comes from the analysis of strains lacking Stp2p, a transcriptional regulator of amino acid permease genes that is required for amino acid-driven alkalinization in vitro [27]. Cells lacking Stp2p are defective in hypha formation during phagocytosis, show reduced survival upon interaction with the immune cell and are defective in killing the macrophages. These cells grow at wild type rates on alternative carbon sources and show normal resistance to a variety of stress conditions encountered in the phagosome, indicating that the observed defects are not due to an enhanced sensitivity to macrophage-derived stresses. However, stp2Δ mutant cells switched to the hyphal form when within neutral phagosomes, indicating a key role for pH in inducing germination of phagocytosed cells. Alkalinization is also observed in artificial saliva and vaginal simulating fluid, indicating that there may be Candida-induced pH changes at body sites normally occupied by C. albicans, such as the oropharyngeal tract and vulvovaginal tract, underlining the effect of this phenomenon on microbial and human physiology. These defects are reflected in a modest attenuation of virulence in a mouse model of disseminated candidiasis.

The intracellular fate of C. albicans cells is not well understood. A few studies on the phagosome-lysosome fusion following C. albicans ingestion by macrophages exist: two studies concluded that the fusion is inhibited, two studies concluded that fusion occurs, while another got both results depending on the assay used [37]–[41]. A key distinction in these papers was whether fusion was monitored by acidification using dyes such as acridine orange or lysotracker or by colocalization with endocytic markers such as LAMP-1. Our data provides a possible explanation for these contradictory reports, since we show that C. albicans can alkalinize the phagosome and that neutralization of the phagosome promotes hyphal morphogenesis and escape from the host cell. The exact fate of C. albicans after phagocytosis remains unclear: studies report C. albicans localization in mature phagolysosmes [37], late endosomes [39], or the endoplasmic reticulum [16]. Our data does not directly address this question, which clearly requires additional study, but we demonstrate a difference in the pH of the Candida-containing compartment between the wild-type strain and stp2Δ mutants, the latter of which behave similarly to killed cells. The simplest explanation is that the wild-type cells occupy a fused phagolysosome in which acidification is outcompeted by ammonia release from the fungal cell, though we cannot exclude differences in trafficking between these two strains.

We indicate here the importance phagosomal neutralization for C. albicans escape from the macrophages, however additional factors may also contribute to this process, including nutrient availability, CO₂ concentration, presence of reactive oxygen species, and modulation of the iron content. The effect of these morphogenetic stimuli is likely combined, since mutants in hyphal morphogenesis, cell wall synthesis, or nutrient assimilation fail to escape from phagocytosis [16], [33]. The exact role of each of these factors on hyphal morphogenesis during phagocytosis is yet to be determined, but here we provide for the first time evidence that neutral pH is a critical component since mutants defective in environmental alkalinization remain in acidic phagosomes and do not switch to the hyphal form.

It has been well documented that pathogens manipulate the phagosomal environment to promote survival by neutralizing the phagolysosome, preventing phagosome-lysosome fusion and/or reducing the production of reactive oxygen or nitrogen species [42]–[45]. Phagosomal neutralization is also observed with Helicobacter pylori, which uses an extracellular urease to produce ammonia to elevate phagosomal pH and retard acquisition of late endosomal markers, allowing survival [43], [46]. Other fungal pathogens, such as Candida glabrata, Histoplasma capsulatum, and Cryptococcus neoformans alter phagosomal pH, but the mechanisms to achieve the pH increase differ from the one reported here. For instance, C. glabrata inhibits phagolysosomal fusion and survives phagocytosis without damaging the host cells or eliciting a proinflammatory immune response but, surprisingly, this does not require viable cells [47]. In contrast, H. capsulatum resides in neutralized mature phagosomes [48], [49]. The mechanism for this is unknown, but may involve permeabilization of the phagosomal membrane via the saposin-like protein Cbp1, which is secreted into the phagosomal space [50]. Similarly, C. neoformans appears to destabilize the phagosomal membrane such that there is exchange of luminal contents with the cytosol [51]. Thus, our findings are consistent with other fungal pathogens, though the mechanism we propose is quite different. Pharmacological inhibition of acidification also compromises macrophage antimicrobial activity: artificial elevation of the phagosomal pH using NH₄Cl, chloroquine or Bafilomycin A1 has also been found to impair killing of phagocytosed Staphylococcus aureus, Bordetella pertusis and the fungal pathogen Aspergillus fumigatus [42], [44], [45]. Further, addition of NH₄Cl to normal resident mouse peritoneal macrophages reduced the rate of killing of the non-pathogenic S. cerevisiae [52]. Likewise, we observe hypha formation and escape from Bafilomycin A1-treated phagosomes of the stp2Δ mutant cells that normally are defective in these processes. In the context of C. albicans the elevated pH of the phagosome will promote hyphal morphogenesis and escape from phagocytosis.

Our data suggests that this alkalinization phenomenon is driven by metabolic changes resulting from nutrient starvation imposed by the phagocyte; metabolism of non-fermentable carbon sources appears to be important during infection as disruption of some these carbon metabolic pathways impairs virulence [19], [21]–[23]. Glucose limitation within the phagosome might be one of the mechanisms macrophages use to prevent survival of the ingested cells in a manner analogous to iron limitation within the host. For example, enzymes involved in the gluconeogenesis and the glyoxylate shunt are also required for colonization and persistence of the phagosomal pathogens Leishmania manor and M. tuberculosis [53], [54]. Similarly, 3-hydroxy-methylglutaryl coenzyme A lyase, the enzyme catalyzing the last step of leucine catabolism, is important for survival of the fungal pathogen Histoplasma capsulatum within macrophages [55]. Amino acid utilization is important for C. albicans pathogenicity too, since we show that stp2Δ mutants have reduced survival during phagocytosis and a modest reduction in virulence. Similarly, cells lacking DUR1,2 and ATO5, genes involved in detoxification and export of excess amines produced during amino acid catabolism, exhibit significant delay in hyphal morphogenesis and survival upon phagocytosis, further highlighting the importance of amino acid utilization within the host ([56]; H. Danhof and M. Lorenz, unpublished).

The source of amino acids within the macrophage is not clear, but they are a potentially plentiful nutrient source in the host. Numerous amino acid auxotrophic mutants retain full virulence in the mouse model, including those for leucine, arginine, tryptophan, and histidine [57]–[60]; this is the basis for the genetic methodology developed by Noble and Johnson [61]. This demonstrates that sufficient amino acids are accessible in the host to support growth of the pathogen, in decided contrast to the profound avirulence of nucleotide auxotrophs [29], [30], [60], [62]. We note that previous transcriptional profiling of phagocytosed cells suggested that they were starved for carbon but not for amino acids, as no amino acid biosynthetic genes were upregulated, with the exception of the arginine pathway, which we have shown is induced by oxidative stress [18], [63]. Importantly, we propose these amino acids are being used as a source of carbon and not just as the building blocks of proteins. Consistent with this, mutations of both STP2 and CSH3, an ER chaperone for amino acid permeases, block alkalinization and confer virulence defects [27], [64]. The presence of extracellular amino acids activates STP2 post-translationally to increase the relative levels of the amino acid permeases CAN1, GAP1 and GAP2, the oligopeptide transporters OPT1 and OPT3, and the secreted aspartyl protease SAP2; most of these genes are significantly induced in phagocytosed cells [18], [28]. Together, these indicate that amino acids are a key source of carbon, nitrogen or both within the host. Our preliminary results showing Stp2p-independent alkalinization during growth in vaginal simulating fluid indicates some redundancy with other processes; perhaps transport and utilization of oligopeptides generated from the protein in this media. In summary, we show here that catabolism of amino acids as a primary nutrient is a key determinant of the host-pathogen interaction with both phagocytes and in whole animal models. Further studies are necessary to define the most important catabolic pathways and host niches in which amino acid-driven pH changes have the biggest impact.

Materials and Methods

Strains and growth media

C. albicans strains were propagated under standard conditions in YPD medium (1% yeast extract, 2% peptone, 2% glucose). For growth on plates, 2% agar was added to the medium. To select for nourseothricin-resistant (Nou^R) transformants, 200 µg/ml of nourseothricin (Werner Bioagents, Jena, Germany) was added to the YPD agar plates [31]. Alkalinization experiments were performed in minimal yeast nitrogen base (YNB) medium (0.17% yeast nitrogen base, 0.5% ammonium sulfate) prepared without glucose and supplemented with 1% casamino acids as the sole carbon source. For alkalinization on solid medium and for assessment of NH₃ release by alkalinizing colonies cells were grown on GM-BCP medium, which contained 1% yeast extract, 30 mM CaCl₂, 3% glycerol, 0.01% bromocresol purple, 2% agar and adjusted pH 4.5 [65]. Other carbon sources or chemical stressors were added to YNB medium as indicated in the results and figures. In some experiments environmental alkalinization was monitored in artificial saliva, pH 4.5 (which included, per liter, 1.7 g yeast nitrogen base without amino acids and ammonium sulfate, 5.0 g casamino acids, 1.1 g KCl, 0.5 g NaCl, 14 mg choline chloride, 10 mg sodium citrate, 1.0 mg ascorbate, 2.5 g mucin), a formulation modified from [66] or in vaginal simulating fluid, pH 4.2 (per liter, 2 g glucose, 0.16 g glycerol, 2 g lactic acid, 1 g acetic acid, 0.018 g bovine serum albumin, 0.4 g urea, 1.4 g KOH, 0.222 CaCl₂, 3.51 g NaCl, 0.25 g mucin), a formulation modified from [67]. Utilization of different amino acids as the sole nitrogen source was assessed as previously described [28], using succinate buffered YNB medium supplemented with 2% glucose and 50 µM histidine, pH 6.0 and supplemented with the indicated amino acids at 1 mM. RAW264.7 macrophages were maintained in RPMI with glutamine and HEPES, supplemented with Penicillin/Streptomycin and 10% inactivated Fetal Bovine Serum.

Strain construction

C. albicans strains lacking STP2 were generated using the SAT-flipper method as described previously [31]. In short, approximately 300 bp of homology immediately to the 5′ or 3′ of the STP2 ORF were amplified by PCR and cloned between the ApaI/XhoI and SacI/SacII sites of pSFS1. The resulting SAT1–FLP cassette was used to transform C. albicans SC5314 strain by electroporation with selection on YPD-Nou. Genomic DNA was isolated and cassette integration confirmed in the selected candidates via PCR. To eliminate the nourseothricin selection marker, the mutant strain was induced with 1% BSA in YNB medium for 4 days and the Nou^S colonies were selected. This process was repeated to generate the independently-derived homozygous disruptants SVC17 and SVC18 (stp2Δ::FRT/stp2Δ::FRT).

Complementation of the mutant strain used plasmid pSV-4, a SAT1-marked version of CIp10 expressing STP2 under its native promoter. To generate this plasmid the URA3 gene from Cip10 [68] was excised using BamHI and SacI and replaced by the SAT1 gene from the plasmid pSFS1 [31] to generate pAG6. Next, pSV-4 was generated by cloning the entire STP2 ORF into the ApaI and XhoI sites of pAG6. This plasmid was linearized with StuI and used to transform SC5413 or stp2Δ mutant cells to generate the strains SVC21 (STP2/STP2 RPS10/rps10:Clp10-SAT1) and SVC20 (stp2Δ::FRT/stp2Δ::FRT RPS10/rps10::Clp10-STP2-SAT1), respectively. The stp2Δ mutant strain was also transformed with linearized pAG6 to produce the stp2Δ strains SVC22 and SVC23 (stp2Δ::FRT/stp2Δ::FRT RPS10/rps10::Clp10). The previously generated stp2Δ mutant strain PMRCA57 (stp2Δ4::dpl200-URA3/stp2Δ2::CaNAT1/stp2Δ5::MPA) [28], was used for phenotype comparison where noted.

Alkalinization and ammonia release assays

Alkalinization experiments were performed as previously described [27], with the following modifications: The minimal medium YNB was supplemented with 1% casamino acids as the sole carbon source and pH adjusted to 4.5. C. albicans cells were grown in YPD medium overnight, washed in dH₂O and diluted to OD₆₀₀ = 0.2 in the alkalinization medium. Cells were incubated at 37°C with aeration and growth, pH changes, and cellular morphology were assessed at the indicated times. Cellular morphology was scored by analyzing photomicrographs of at least 150 cells per condition. Experiments were performed at least in triplicate and analyzed using Prism 5.0 (GraphPad) software.

Ammonia release by C. albicans cells during alkalinization was assessed using acid traps as previously described [27], [65]. In brief, cells were grown in YPD medium overnight, washed in dH₂O and resuspended at an OD₆₀₀ of 1.0 in dH₂O. Cells were spotted onto solid GM-BCP medium at pH 4.5; reservoirs containing 10% citric acid were placed underneath the colonies. Cells were incubated at 37°C and samples from the acid trap collected at 24, 48 or 72 hours after initiation of the experiment. Ammonia was quantified using Nessler's reagent, as described [27]. Experiments were performed in triplicate and data plotted using GraphPad Prism software.

Growth assays

C. albicans strains were grown in YPD medium overnight, washed in dH₂O and diluted in the testing medium to final OD₆₀₀ of 0.2. For growth on alternative carbon sources we tested YNB medium supplemented with 0.01% or 0.1% acetate, 0.2% or 2% ethanol or 2% glucose. To test the effect of different stress conditions on growth, YNB medium was supplemented with 2% glucose and H₂O₂, DETA NONOate (Cayman Chemical), or bathophenanthroline disulfonate (BPS; Acros Organics), as indicated in the figures. Assays were performed in triplicate in 96 well plate format using a SynergyMx (Biotek) plate reader at 30°C with 1 minute agitation prior to the OD₆₀₀ reading every 10 minutes for 16 hours.

Live interaction with the macrophages

To assess the interaction of single C. albicans cells with the macrophages we seeded 3×10⁶ cells RAW264.7 macrophages to 35 mm glass bottom dishes (MatTek) and allowed them to adhere for four hours. C. albicans cells were grown in YPD medium overnight, diluted 1∶100 in fresh medium and grown for 3 hours at 30°C. Cells were then washed in dH₂O and 3×10⁶ cells were resuspended in CO₂-independent RPMI medium (HyClone) and co-cultured with the macrophages at 37°C. Images of the Candida-macrophage interaction were taken at 3 minute intervals for up to 10 hours using an Olympus IX81 automated inverted microscope with a temperature-controlled stage. Images from at least 10 fields were analyzed using SlideBook software. Percent hyphal morhogenesis during phagocytosis was calculated by obtaining percentage of phagocytosed cells using the following formula: (germ tubes + hyphal cells/total amount of cells)×100. Experiments were performed in triplicate.

Macrophage cytotoxicity assay

C. albicans toxicity on macrophages was assessed using CytoTox96 Non-Radioactive Cytotoxicity assay (Promega) as follows: tissue culture macrophages were seeded at 2.5×10⁵ cells per well of a 96 well plate in phenol red-free RPMI and incubated overnight at 37°C, 5% CO_2. C. albicans cells were grown to log phase in YPD media, washed in PBS and co-cultured with macrophages at a 3∶1 ratio for 5 hours. Calculation of lactate dehydrogenase (LDH) release by infected macrophages was then determined according to the manufacturer's protocol relative to maximum LDH release from lysed macrophages and corrected for spontaneous release of LDH by the macrophages or C. albicans alone. The experiment was performed in triplicate.

End-point dilution assay

C. albicans survival during interaction with the RAW264.7 macrophages was assessed as previously described [36]. Briefly, macrophages were collected and resuspended in fresh RPMI medium. Cells were seeded at 2.5×10⁴ cells/well in 96 well plates and grown overnight at 37°C, 5% CO₂. Log-phase C. albicans cells were washed in dH₂O and resuspended in fresh RPMI medium. 1×10⁴ cells/well were added to wells with or without macrophages, followed by six serial 1∶5 dilutions. After 48 hours at 37°C in 5% CO₂, microcolonies of C. albicans were counted using an inverted microscope in wells in which individual colonies could be distinguished. Results were presented as the ratio of (number of colonies in the presence of macrophages/number of colonies without macrophages)×100. The experiment was performed in triplicate.

Lysotracker Red assay

For co-cultures with RAW264.7 cells, 1×10⁶ cells/ml were seeded onto glass coverslips in 12-well plates and allowed to adhere for 2 hours. Next, 1 mM Lysotracker Red DM99 (Molecular Probes) was added to the cells and incubated for 2 hours to ensure concentration of the dye in the lysosomes. In some experiments 50 nM Bafilocymin A1 (Alexis Biochemicals) was added to the cells and incubated for 30 minutes prior to co-culture. C. albicans cells were grown overnight in YPD, diluted 1∶100 in fresh YPD, and grown for 3 hours at 30°C. Then cells were washed in dH₂O, stained with 1 µM FITC for 15 minutes and excess dye was removed by washing three times in PBS. Control cells were heat killed by incubation for 60 minutes at 65°C. Cells were diluted to 1×10⁶ cells/ml in phenol red-free RPMI medium and co-cultured with macrophages for the indicated time points. Cultures were washed once in PBS, stained with Calcofluor white (35 µg/ml for 1 minute) to label non-phagocytosed cells, and fixed in 2.7% paraformaldehyde for 20 minutes. To estimate the relative phagosomal pH, regions that included a phagocytosed C. albicans cell and including approximately 0.5 µm of the adjoining area were selected for at least 100 cells per condition. Lysotracker Red (LR) and FITC intensities were determined and corrected by subtracting background intensities in an area without phagocytosed C. albicans cells before calculating the LR/FITC ratio. Percentage of phagocytosed cells was calculated as (Calcofluor White stained cells/total cells)×100. Image analysis was performed using SlideBook 5.0 Image Software. All experiments were performed at least in triplicate.

In vivo virulence assays

Disseminated infections with C. albicans were performed as previously described [23]. Briefly, C. albicans strains were grown to mid-log phase in YPD overnight. Next, cells were collected via centrifugation, washed, and resuspended in phosphate-buffered saline. Ten female 21–25 g ICR mice per strain were infected via tail vein injection with 1×10⁶ C. albicans cells in 100 µl PBS. The mice were monitored twice daily for signs of infection and euthanized when moribund. Survival data were plotted using Prism 5 (GraphPad Software) and analyzed using the log-rank test.

Ethics statement

All animal work was performed under protocols approved by the Animal Welfare Committee of the University of Texas Health Science Center at Houston (protocol HSC-AWC-12-099). Procedures adhered to the U.S National Institutes of Health Guide for the Care and Use of Laboratory Animals, Eighth Edition.

Supporting Information

Attachment 1

Attachment 2

Attachment 3

Attachment 4

Attachment 5

Attachment 6

Attachment 7