Original Research ARTICLE
Hydroxyurea treatment inhibits proliferation of Cryptococcus neoformans in mice
- 1 Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA
- 2 Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA
- 3 Department of Craniofacial Biology, Medical University of South Carolina, Charleston, SC, USA
- 4 Division of Infectious Diseases, Medical University of South Carolina, Charleston, SC, USA
The fungal pathogen Cryptococcus neoformans (Cn) is a serious threat to immunocompromised individuals, especially for HIV patients who develop meningoencephalitis. For effective cryptococcal treatment, novel antifungal drugs or innovative combination therapies are needed. Recently, sphingolipids have emerged as important bioactive molecules in the regulation of microbial pathogenesis. Previously we reported that the sphingolipid pathway gene, ISC1, which is responsible for ceramide production, is a major virulence factor in Cn infection. Here we report our studies of the role of ISC1 during genotoxic stress induced by the antineoplastic hydroxyurea (HU) and methyl methanesulfonate (MMS), which affect DNA replication and genome integrity. We observed that Cn cells lacking ISC1 are highly sensitive to HU and MMS in a rich culture medium. HU affected cell division of Cn cells lacking the ISC1 gene, resulting in cell clusters. Cn ISC1, when expressed in a Saccharomyces cerevisiae (Sc) strain lacking its own ISC1 gene, restored HU resistance. In macrophage-like cells, although HU affected the proliferation of wild type (WT) Cn cells by 50% at the concentration tested, HU completely inhibited Cn isc1Δ cell proliferation. Interestingly, our preliminary data show that mice infected with WT or Cn isc1Δ cells and subsequently treated with HU had longer lifespans than untreated, infected control mice. Our work suggests that the sphingolipid pathway gene, ISC1, is a likely target for combination therapy with traditional drugs such as HU.
Cryptococcus spp. are environmental fungal pathogens afflicting immunocompromised patients as well as immunocompetent individuals, causing life-threatening meningoencephalitis (Idnurm et al., 2005; Jarvis et al., 2008; Dadachova and Casadevall, 2011; Del Poeta and Casadevall, 2011; Kronstad et al., 2011; Kozubowski and Heitman, 2012). Cryptococcus causes approximately one million annual cases of meningoencephalitis globally among AIDS patients, leading to nearly 625,000 deaths (Park et al., 2009). Despite major developments in HIV treatment Cryptococcus infection still remains a major threat to AIDS patients, especially in sub-Saharan Africa (Warkentien and Crum-Cianflone, 2010).
Cryptococcus neoformans (Cn) is a ubiquitous fungus, found in tree hollows and pigeon droppings. It is present in the environment and in human hosts predominantly in the yeast form; however, Cn can assume hyphal and other shapes depending upon its life cycle state or environmental influences (Zaragoza et al., 2010; Kronstad et al., 2011; Kozubowski and Heitman, 2012). Pathogenic Cn infection initiates upon the inhalation of infectious Cn particles, which initially disseminate to the lungs and subsequently to the central nervous system via the circulation if the host’s immune response does not control fungal proliferation within the lung (Kronstad et al., 2011). An intracellular facultative pathogen, Cn can grow and replicate within the phagolysosome of phagocytic cells, such as alveolar macrophages (AMs) and it can also grow in extracellular spaces, such as within the alveoli or in the bloodstream (Feldmesser et al., 2000; Goldman et al., 2000; Levitz, 2001; Steenbergen et al., 2001; Shea et al., 2006). Because the pathogen rapidly develops drug resistance (Morschhauser, 2010), and because the number of immunocompromised patients is increasing, there is a constant need for innovative and effective antifungal therapies.
Hydroxyurea (HU), an antineoplastic drug used for treatment of HIV, cancer, and myeloproliferative diseases (Kovacic, 2011) slows the progression of DNA replication machinery by reducing the cell’s deoxyribonucleotide (dNTP) pool (Katou et al., 2003). HU treatment of the budding yeast Saccharomyces cerevisiae (Sc) results in DNA replication fork slowing, and the formation of a fork-protection complex to guard the cell’s replication machinery, activating the replication checkpoint (Alcasabas et al., 2001; Katou et al., 2003; Zegerman and Diffley, 2003; Bando et al., 2009). In the absence of replication proteins, yeast cells become HU sensitive. Interestingly, in addition to DNA replication genes, ~300 genes from various other pathways have been shown to play role in resistance to HU toxicity and the absence of these genes gives rise to HU sensitivity (Chang et al., 2002; Hartman and Tippery, 2004; Parsons et al., 2004; Woolstencroft et al., 2006).
Recently, lipid signaling, especially sphingolipid metabolism, has gained recognition for its role in fungal pathogenesis (Shea and Del Poeta, 2006; Rhome and Del Poeta, 2010; Singh and Del Poeta, 2011). All yeast cells, including Cn, produce inositol-containing sphingolipids instead of choline-containing sphingolipids (e.g., sphingomyelin), and the deletion of the inositol sphingophospholipid phospholipase C 1 (ISC1) gene in Sc (Sc isc1Δ) causes accumulation of inositol-containing sphingolipids (Sawai et al., 2000; Shea et al., 2006). Cn is a pathogenic yeast, and deletion of ISC1 renders it incapable of causing meningoencephalitis (Shea et al., 2006). Isc1 has been characterized in Sc (Sawai et al., 2000) and Cn (Henry et al., 2011) and in Leishmania (Zhang et al., 2009), indicating that this sphingolipid metabolizing enzyme has unique biochemical characteristics. The absence of the ISC1 gene in Sc increases fungal sensitivity to HU and methyl methanesulfonate (MMS) accompanied by cell division arrest and morphological aberrations (Chang et al., 2002; Matmati et al., 2009; Tripathi et al., 2011). Here, we report our studies into the role of Cn ISC1 in the fungal resistance to HU and MMS and their specific effects on the virulence of the pathogenic fungus Cn. We show that Cn cells lacking the ISC1 gene are highly sensitive to HU and MMS and form cell clusters upon HU exposure. The absence of ISC1 in conjunction with HU treatment synergistically reduced Cn infection of macrophage-like cells and immunocompetent mice.
Materials and Methods
Strains and Plasmids
Wild type (WT) Cn (var. grubii serotype A strain H99) and its isc1Δ derivative were used in the current study and have been described previously (Shea et al., 2006; Henry et al., 2011). The Sc strain Jk9-3d a (MATa trp1 leu2-3 his4 ura3 ade2 rme1) and its isc1Δ derivative were used and have been described previously (Matmati et al., 2009; Tripathi et al., 2011).
Exposure to HU and MMS
YPD plates (1% yeast extract, 2% peptone, and 2% glucose plus 2% agar) containing appropriate concentrations of HU (Sigma; 0, 25, 50, 100, and 200 mM) or MMS (Sigma; 0.033%) were prepared and used within 48 h. Overnight cultures were inoculated in fresh medium at A600 of 0.2 and grown at 30°C. Log-phase cultures were adjusted to A600 of 0.4 before making 10-fold serial dilutions and plate spotting (2.5 μl). Plasmids pYES-Sc ISC1 and pYES-Cn ISC1 that express Sc ISC1 and Cn ISC1 genes respectively have been described previously (Henry et al., 2011). The two plasmids and a control vector were transformed into appropriate strains (WT and isc1Δ of Sc) and plated on SD/Ura- plates. Then, 10-fold serial dilutions of log-phase liquid cultures in SD/Ura- liquid medium were spotted on SD/Ura- and SD/Ura-/HU plates, and the plates were incubated at 30°C, and analyzed at appropriate times before recording the data.
Cells were grown to log-phase as described above, HU (25–200 mM) or MMS (0.033% v/v) was added, and cells were incubated for 5 or 22 h before they were fixed with 3.7% formaldehyde. Cells were washed with phosphate buffered saline (PBS, 50 mM, pH 7) and further suspended in PBS before analyzing them under a Nikon Eclipse (TE2000-5) microscope with a 40×/100× objective lens.
Effect of HU on Intracellular Growth of Cn
The murine reticulum sarcoma macrophage-like cell line J774A.1 cells were used up to passage #8. Cells were then plated in 96-well cell culture plates in Dulbecco’s minimal essential medium supplemented with 10% fetal bovine serum. WT Cn (H99) and its isc1Δ derivative were grown overnight in YPD at 30°C. Cells were washed three times in PBS and counted. Approximately 105 cells in DMEM + FBS medium were added with 10 μg/ml of anti-GXM monoclonal antibody 18B7 (kindly provided by Dr. Arturo Casadevall) with 1 mM HU or without HU. Meanwhile the macrophage-like cells were washed off the non-adhered cells and activated with 50 units/ml of recombinant murine gamma interferon (IFNγ) and 0.3 μg/ml of lipopolysaccharide (LPS). The antibody-opsonized Cn cells were added to the macrophage cells at an effector-to-target ratio of 1:1. After incubation for 2 h, extracellular Cn cells were washed with three changes of warm DMEM medium and fresh medium without or with 1 mM of HU. For one set of the experiments 200 μl sterile water was added to each well and the macrophage-like cells were lysed by pipetting several times. The samples were diluted and an aliquot was spread on YPD agar plate for determining colony forming units (CFUs); this set served as the time-point “zero.” The other time points were 6, 12, and 24 h, at which points the supernatant was aspirated and cells were rinsed once with DMEM. Macrophage cells were lysed by adding 200 μl of sterile water and pipetting several times. The samples were diluted and spread on YPD agar plate for determining the CFUs.
For the phagocytic indices (PI) and for photographs, the conditions were same as above except that the macrophage-like cells were grown on glass cover slips. After 2 h of the Cn challenge, the cells were washed three times with PBS, fixed with ice-cold methanol, and stained with Giemsa. For the 24-h experiment, cells were washed three times and fresh medium without HU or with 1 mM HU was added and incubated at 37°C in 5% CO2. After 24 h the cells were washed three times with PBS, fixed with ice-cold methanol, and stained with Giemsa. Photographs were taken using a Zeiss microscope equipped with charged-coupled device camera. Results for 0 and 24 h time points are shown in the text.
Survival Studies in Mouse Models
Mice were anesthetized with a xylazine–ketamine mixture (60 μl, i.p., 5 mg/kg xylazine, 95 mg/kg ketamine). All Cn strains were grown in YPD medium for 16–18 h at 30°C. Cells were washed and re-suspended in PBS. Mice were challenged intranasally with 20 μl of the inoculum containing 5 × 105 Cn cells. After Cn infection, mice were administered HU (0.8 mg/kg every 48 h). Mice were fed ad libitum and monitored twice daily for signs of morbidity or pain or clinical signs suggesting meningoencephalitis. Mice exhibiting any of these signs were immediately sacrificed using CO2 inhalation followed by cervical dislocation.
All data were analyzed by standard Student’s t-test with P values shown in appropriate figures.
Absence of ISC1 Causes Sensitivity to HU and MMS in Cn Cells
Cryptococcus neoformans WT and isc1Δ cells were analyzed for their response to long-term exposure to HU and MMS. As shown in Figures 1A,B, whereas WT Cn cells recovered from HU and MMS stress, isc1Δ cells were highly sensitive to both HU and MMS. The HU sensitivity of Cn isc1Δ cells was almost comparable to that of Sc isc1Δ cells (Figure 1A). To ensure that the sensitivity to HU and MMS was due to loss of the ISC1 gene, we examined a Cn isc1Δ strain containing reconstituted ISC1 for HU and MMS tolerance. As shown in Figures 1A,B, the reconstituted strain was resistant to HU and MMS similar to the WT strain, strongly suggesting a role for Cn ISC1 in HU/MMS tolerance. In addition to testing the role of the reconstituted strain for HU and MMS sensitivity, we tested the role of Cn ISC1 in HU tolerance independently: we expressed the Cn ISC1 gene in an Sc isc1Δ strain and examined whether the former complemented HU sensitivity. As shown in Figure 1C, whereas the Sc WT strain containing a vector showed HU resistance, its isc1Δ derivative containing the vector was HU sensitive. In contrast, the Sc isc1Δ strain expressing either Sc ISC1 or Cn ISC1 (in pYES vector; Henry et al., 2011) showed HU resistance, albeit with minor differences (Figure 1C). All these results show that Cn Isc1 plays a key role in HU/MMS tolerance.
FIGURE 1. Cryptococcus neoformans cells lacking the ISC1 gene are sensitive to HU and MMS. (A) Ten-fold serial dilutions of log-phase cultures of C. neoformans (WT, isc1Δ, and isc1Δ + Cn ISC1 reconstituted) and S. cerevisiae (WT and isc1Δ strains) were spotted on plates containing YPD and YPD + HU (50 mM). (B) Ten-fold serial dilutions of log-phase cultures of C. neoformans (WT, isc1Δ, and isc1Δ + Cn ISC1 reconstituted) were spotted on YPD and YPD + 0.033% MMS plates. (C) Cn ISC1 complements HU sensitivity of the S. cerevisiae isc1Δ strain. Ten-fold serial dilutions of following log-phase cultures were spotted on SD/Ura- and SD/Ura-/HU plates: Sc WT cells containing pYES vector, Sc isc1Δ cells containing the pYES vector, Sc isc1Δ cells containing pYES-Sc ISC1 and Sc isc1Δ cells containing pYES-Cn ISC1.
Absence of ISC1 Affects Cell Morphology and Cell Division in Cn Cells Upon Exposure to HU and MMS
We examined whether Cn ISC1 controls cell division and cellular morphology under HU stress. Cn WT and isc1Δ cells were grown in the presence of various concentrations of HU in liquid media and cell morphology was analyzed microscopically. As shown in Figures 2A,B, HU did not affect cell division of WT cells at 25–50 mM concentrations; however, the bud size was relatively large compared to the untreated WT cells. At higher concentrations of HU (100–200 mM) some WT cells had defects in cell division resulting in cell chains. In contrast to the WT cells, cell division in isc1Δ cells was severely inhibited at low HU concentrations (25–50 mM) resulting in cell chains and lawns (Figures 2A,B); a few misshapen cells were also seen (data not shown). These data suggest a synergism between HU and the absence of ISC1 in inhibiting cell division.
FIGURE 2. Cryptococcus neoformans cells show HU-induced defects in morphology and cell division. (A) Cn WT and isc1Δ cells were treated with HU overnight and observed under phase contrast microscope (×1000). Cn isc1Δ cells formed cell chains and clumps upon HU exposure. (B) Bar diagrams showing morphological aberrations in untreated and HU-treated Cn WT and Cn isc1Δ cells.
Synergistic Effects of HU and ISC1 Deletion on Macrophage Infection
One mechanism by which Isc1 protects Cn cells against the host immune response is by increasing the resistance to antifungal activity of macrophages by favoring fungal intracellular growth (Shea et al., 2006). HU treatment of macrophages infected by Toxoplasma gondii, Leishmania amazonensis, Trypanosoma cruzi, and L. mexicana has been shown to drastically reduce the number of infected cells (Melo and Beiral, 2003; Martinez-Rojano et al., 2008). Therefore, we tested whether HU would compromise the intracellular growth of Cn cells. We first allowed macrophages to internalize Cn cells and then treated the macrophages with HU. HU treatment diminished the intracellular growth of WT Cn by ~3.5-fold (Figure 3A). Interestingly, HU treatment completely abolished the growth of Cn isc1Δ cells within the macrophages suggesting a strong synergism between HU and ISC1 deletion. Representative macrophages with Cn infection are shown in Figure 3B. Importantly, inhibition of intracellular growth was not due to HU’s effect on phagocytosis because the drug did not inhibit macrophage ingestion of Cn (data not shown). We have already demonstrated that a Cn isc1Δ strain reconstituted with Cn ISC1 behaves like the WT Cn strain in macrophages (Shea et al., 2006). Because the in vitro experiments were carried out at 30°C and in vivo experiments were performed at 37°C, we needed to ensure that the loss of isc1Δ cell viability in macrophages was not temperature dependent. Thus, we grew WT and isc1Δ cells at 37°C and compared these data with those obtained at 30°C. We observed that the growth pattern of WT and isc1Δ at 37°C was similar to those patterns observed at 30°C (data not shown).
FIGURE 3. Synergistic role of HU and ISC1 deletion on Cryptococcus infection of the macrophage-like cell line J774A.1. (A) Phagocytosis assay with macrophage-like cell line J774A.1 cells infected with Cn WT or isc1Δ cells in the presence/absence of HU (see Materials and Methods). (B) Cn cells phagocytosed by J774A.1 were grown in the presence/absence of HU and stained with Giemsa after 24 h. Photographs were taken with a Zeiss microscope equipped with a CCD camera. All images were captured under oil immersion (×100). Red arrows indicate the presence/absence of Cryptococcus in the phagolysosomes of macrophages. Most phagolysosomes in untreated WT cells contained Cn cells, whereas some HU-treated WT cells still contained Cn cells. In contrast, most macrophages did not contain Cn isc1Δ cells regardless of HU treatment.
HU Treatment Inhibits Growth of Cn WT and isc1Δ Cells in Mice
We tested the effects of HU on survival and virulence of Cn WT and isc1Δ strains in mice. Mice were infected with fungal cells and treated with HU as described in Section “Materials and Methods.” Interestingly, HU inhibited the proliferation of WT Cn cells in mice and significantly prolonged their survival. In addition, we observed that HU acted synergistically when the ISC1 gene was absent to inhibit Cn cell growth. We performed survival and tissue burden studies in mice by infecting them intranasally with Cn WT or the isc1Δ strain and then treated the mice with HU (0.8 mg/kg every other day). As expected, untreated mice died within 30 days whereas HU-treated mice survived up to 60 days (Figure 4A). Interestingly, mice infected with Cn isc1Δ cells also survived for 60 days regardless of HU treatment (Figure 4B). HU significantly reduced fungal burden, especially in the lung tissue. Specifically, HU-treatment reduced the number of CFUs in the lung infected with Cn WT by ~10-fold from the initial inoculum (Figure 4C). Remarkably the number of Cn isc1Δ CFU decreased by ~1,700 fold in HU-treated mice compared to untreated mice. These data suggest a synergistic effect of HU treatment with ISC1 deletion in increasing host survival by decreasing organ fungal load. The survival of mice infected with WT Cn and treated with HU suggests that exposure to HU (at the HU concentration tested) slows down DNA replication and growth of WT cells, allowing the host’s immunity to take over the pathogen. The role of Cn ISC1 in mice experiments was revealed by the CFU of HU-treated WT Cn, untreated isc1Δ and HU-treated isc1Δ cells recovered from lung tissues.
FIGURE 4. Role of HU and ISC1 deletion on the survival of mice and on lung tissue burden. (A) Survival curve of CBA/J mice upon infection with WT Cn in the presence (green) or absence (black) of HU; (B) Survival curve of CBA/J mice upon infection with Cn isc1Δ cells in the presence (red) or absence (blue) of HU. (C) Survival of Cn cells in lung tissue of CBA/J mice after 60 days of infection. Lung t-issues were collected from mice and Cn CFU was counted by plating on YPD plates.
Our results show that HU slows down growth of WT Cn cells, which helps both mice and macrophages to inhibit further pathogenic growth. This effect is enhanced by deletion of ISC1, suggesting that Isc1 and the sphingolipid metabolic pathway in general should be exploited as novel targets for antifungal drug development, either alone or in combination with existing drugs (e.g., HU) to better control cryptococcosis. Of note, all experiments conducted with mice ended on the 60th day of infection when all surviving mice were sacrificed. Thus, we observed no differences in survival between WT and isc1Δ cells upon HU treatment; the isc1Δ has a significant defect in virulence. However, treatment with HU profoundly diminished Cn proliferation in the lung environment compared to untreated cells.
At present, the molecular mechanism of HU inhibition of Cn growth is unknown. We hypothesize that isc1Δ may be more susceptible than the WT strain because it controls phytoceramide generation (Garcia et al., 2008) and its decrease in the deletion mutant could affect membrane permeability and thus HU transport. However, this hypothesis was not supported by studies in budding yeast in which the inhibition of DNA synthesis by HU was not enhanced by deletion of ISC1 (Matmati et al., 2009).
Of note, HU has been shown to have an anti-proliferative activity on T cells (Benito et al., 2007) and to cause neutropenia in humans and mice (Hermans et al., 1999). Because neutropenia is associated with prolonged survival of Cn-infected mice (Mednick et al., 2003) HU could increase mice survival through neutropenia. However, the neutropenic effect of HU is remarkably linked to the administered HU dose. Almost all patients will develop neutropenia when the administered dose is 20–30 mg/kg/day or greater. However, several studies have shown that such toxicity can be dramatically reduced if the HU dose is decreased to 4–5 mg/kg/day. In mice, HU at 50 mg/kg/day in a sickle cell model does cause a moderate neutropenia, whereas a lower dose of 25 mg/kg/day does not cause neutropenia (Lebensburger et al., 2012). The dose used in our mouse experiment was 0.8 mg/kg/every other day, a dose that is 10-fold less that the HU dose that does not produce neutropenia in people and 25- to 50-fold less than the dose that does not produce neutropenia in mice. Thus, due to the very low dose of HU used in our experimentations, we hypothesize that the increased mouse survival is not due to an effect of HU on neutrophils.
We predict that HU (at the concentration tested here) slows Cn DNA replication and cell division while host immunity overtakes the pathogen. This effect appears to be enhanced when Cn cells are intracellular. This hypothesis is supported by our experiment with macrophage-like cell line showing that HU significantly suppresses fungal cell division within macrophages. Very interestingly, HU has been tested against various intracellular parasites such as Toxoplasma gondii, L. amazonensis, Trypanosoma cruzi, and L. mexicana (Melo and Beiral, 2003; Martinez-Rojano et al., 2008). Not only did HU induce morphological changes in these parasites, but also it inhibited intracellular multiplication of these microbes, similar to the phenotype observed with Cn in macrophages illustrated in this paper. In addition, in L. mexicana HU induced cell cycle arrest suggesting that the mechanism by which HU inhibits the synthesis of the DNA replication and cell division has been maintained in different microbial species.
A recent study points to an important aspect concerning the use of HU to control cryptococcosis. The authors found that HU enhances post-fusion hyphal extension in Cn cells, but not in haploid cells (Zulkifli et al., 2012). HU is known to induce morphological changes such as hyphal generation in Candida albicans (Shi et al., 2007; Sun et al., 2011) but in Sc it generates limited morphological aberrations (in 1–3% cells) and extensive morphological aberrations are seen in Sc mutants on checkpoint, budding and, notably, in the isc1Δ deletion mutant (Jiang and Kang, 2003; Enserink et al., 2006; Tripathi et al., 2011). It seems that Cn behaves similar to Sc; morphological changes by HU (at low concentrations) only occur in isc1Δ cells and not in WT cells. In another study it has been shown that certain Cn mutants such as ras1Δ were sensitive to HU and MMS (Maeng et al., 2010).
Intriguingly, the morphological changes ascribed to HU are strictly linked to defects in yeast cell division. Possibly, in addition to the inhibition of DNA synthesis, HU also affects actin polymerization/depolymerization during Cn cell division and cell wall synthesis (Enserink et al., 2006; Tripathi et al., 2011). This hypothesis is supported by our previous studies in Sc in which we showed that actin depolymerization is inhibited by HU especially in conditions in which ISC1 is deleted. This will ultimately block cell division or cell proliferation (Tripathi et al., 2011), possibly through the regulation of morphogenesis and DNA integrity checkpoint proteins. The latter hypothesis is also supported by the results presented in this paper in which we show that HU delays the separation of Cn isc1Δ daughter cells from the mother cell (Figures 2A,B). This delay in cell division of Cn cells may expose the isc1Δ cells for longer time to intracellular inhibitors (e.g., hydrogen peroxide, nitric oxide) rendering isc1Δ even more susceptible to the intracellular compared to the extracellular environment. Considering that the Cn isc1Δ is already hypersusceptible to hydrogen peroxide and nitric oxide (Shea et al., 2006), the treatment with HU may render the isc1Δ cells even more sensitive than WT cells. Thus, it is possible that HU does increase the killing capacity of macrophages indirectly by increasing the exposure of undivided Cn cells to intracellular toxins. Finally, in Sc HU affects chitin deposition on the cell wall (Tripathi et al., 2011) particularly when ISC1 is deleted. This observation further supports a role for Isc1 under HU stress in cell division as chitin is an important regulator of cell morphology and cell division in yeasts (Roh et al., 2002). These are exciting possibilities that we will explore in the future.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We thank Aimee Guillotte in Del Poeta’s laboratory for helping with the animal experiments. We thank Dr. Jennifer Schnellmann and Dr. Ashley Cowart for editing the manuscript. This work was performed in part by the National Institute of Health (NIH) awards AI056168, AI071142, AI078493, and AI087541 to Maurizio Del Poeta and, in part, by pilot research funding from an American Cancer Society Institutional Research Grant (ACS-IRG# 97-219-08) awarded to the Hollings Cancer Center, Medical University of South Carolina, and in part by a Center of Biological Research Excellence (COBRE P20 RR17677) pilot grant to Bidyut K. Mohanty. Kaushlendra Tripathi is thankful to the American Society for Biochemistry and Molecular Biology (ASBMB) for a travel award. This work was conducted in a facility constructed with support from the NIH C06 RR015455 from the Extramural Research Facilities Program of the National Center for Research Resources. Maurizio Del Poeta is a Burroughs Welcome New Investigator in the Pathogenesis of Infectious Diseases.
Alcasabas, A. A., Osborn, A. J., Bachant, J., Hu, F., Werler, P. J., Bousset, K., Furuya, K., Diffley, J. F., Carr, A. M., and Elledge, S. J. (2001). Mrc1 transduces signals of DNA replication stress to activate Rad53. Nat. Cell Biol. 3, 958–965.
Bando, M., Katou, Y., Komata, M., Tanaka, H., Itoh, T., Sutani, T., and Shirahige, K. (2009). Csm3, Tof1, and Mrc1 form a heterotrimeric mediator complex that associates with DNA replication forks. J. Biol. Chem. 284, 34355–34365.
Benito, J. M., Lopez, M., Lozano, S., Ballesteros, C., Gonzalez-Lahoz, J., and Soriano, V. (2007). Hydroxyurea exerts an anti-proliferative effect on T cells but has no direct impact on cellular activation. Clin. Exp. Immunol. 149, 171–177.
Chang, M., Bellaoui, M., Boone, C., and Brown, G. W. (2002). A genome-wide screen for methyl methanesulfonate-sensitive mutants reveals genes required for S phase progression in the presence of DNA damage. Proc. Natl. Acad. Sci. U.S.A. 99, 16934–16939.
Enserink, J. M., Smolka, M. B., Zhou, H., and Kolodner, R. D. (2006). Checkpoint proteins control morphogenetic events during DNA replication stress in Saccharomyces cerevisiae. J. Cell Biol. 175, 729–741.
Goldman, D. L., Lee, S. C., Mednick, A. J., Montella, L., and Casadevall, A. (2000). Persistent Cryptococcus neoformans pulmonary infection in the rat is associated with intracellular parasitism, decreased inducible nitric oxide synthase expression, and altered antibody responsiveness to cryptococcal polysaccharide. Infect. Immun. 68, 832–838.
Henry, J., Guillotte, A., Luberto, C., and Del Poeta, M. (2011). Characterization of inositol phospho-sphingolipid-phospholipase C 1 (Isc1) in Cryptococcus neoformans reveals unique biochemical features. FEBS Lett. 585, 635–640.
Katou, Y., Kanoh, Y., Bando, M., Noguchi, H., Tanaka, H., Ashikari, T., Sugimoto, K., and Shirahige, K. (2003). S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex. Nature 424, 1078–1083.
Kronstad, J. W., Attarian, R., Cadieux, B., Choi, J., D’Souza, C. A., Griffiths, E. J., Geddes, J. M., Hu, G., Jung, W. H., Kretschmer, M., Saikia, S., and Wang, J. (2011). Expanding fungal pathogenesis: Cryptococcus breaks out of the opportunistic box. Nat. Rev. Microbiol. 9, 193–203.
Lebensburger, J. D., Pestina, T. I., Ware, R. E., Boyd, K. L., and Persons, D. A. (2012). Hydroxyurea therapy requires HbF induction for clinical benefit in a sickle cell mouse model. Haematologica 95, 1599–1603.
Maeng, S., Ko, Y. J., Kim, G. B., Jung, K. W., Floyd, A., Heitman, J., and Bahn, Y. S. (2010). Comparative transcriptome analysis reveals novel roles of the Ras and cyclic AMP signaling pathways in environmental stress response and antifungal drug sensitivity in Cryptococcus neoformans. Eukaryot. Cell 9, 360–378.
Mednick, A. J., Feldmesser, M., Rivera, J., and Casadevall, A. (2003). Neutropenia alters lung cytokine production in mice and reduces their susceptibility to pulmonary cryptococcosis. Eur. J. Immunol. 33, 1744–1753.
Melo, E. J., and Beiral, H. J. (2003). Effect of hydroxyurea on the intracellular multiplication of Toxoplasma gondii, Leishmania amazonensis and Trypanosoma cruzi. Braz. J. Med. Biol. Res. 36, 65–69.
Park, B. J., Wannemuehler, K. A., Marston, B. J., Govender, N., Pappas, P. G., and Chiller, T. M. (2009). Estimation of the current global burden of cryptococcal meningitis among persons living with HIV/AIDS. AIDS 23, 525–530.
Parsons, A. B., Brost, R. L., Ding, H., Li, Z., Zhang, C., Sheikh, B., Brown, G. W., Kane, P. M., Hughes, T. R., and Boone, C. (2004). Integration of chemical-genetic and genetic interaction data links bioactive compounds to cellular target pathways. Nat. Biotechnol. 22, 62–69.
Sawai, H., Okamoto, Y., Luberto, C., Mao, C., Bielawska, A., Domae, N., and Hannun, Y. A. (2000). Identification of ISC1 (YER019w) as inositol phosphosphingolipid phospholipase C in Saccharomyces cerevisiae. J. Biol. Chem. 275, 39793–39798.
Shea, J. M., Kechichian, T. B., Luberto, C., and Del Poeta, M. (2006). The cryptococcal enzyme inositol phosphosphingolipid-phospholipase C confers resistance to the antifungal effects of macrophages and promotes fungal dissemination to the central nervous system. Infect. Immun. 74, 5977–5988.
Shi, Q. M., Wang, Y. M., Zheng, X. D., Lee, R. T., and Wang, Y. (2007). Critical role of DNA checkpoints in mediating genotoxic-stress-induced filamentous growth in Candida albicans. Mol. Biol. Cell 18, 815–826.
Steenbergen, J. N., Shuman, H. A., and Casadevall, A. (2001). Cryptococcus neoformans interactions with amoebae suggest an explanation for its virulence and intracellular pathogenic strategy in macrophages. Proc. Natl. Acad. Sci. U.S.A. 98, 15245–15250.
Sun, L. L., Li, W. J., Wang, H. T., Chen, J., Deng, P., Wang, Y., and Sang, J. L. (2011). Protein phosphatase Pph3 and its regulatory subunit Psy2 regulate Rad53 dephosphorylation and cell morphogenesis during recovery from DNA damage in Candida albicans. Eukaryot. Cell 10, 1565–1573.
Tripathi, K., Matmati, N., Zheng, W. J., Hannun, Y. A., and Mohanty, B. K. (2011). Cellular morphogenesis under stress is influenced by the sphingolipid pathway gene ISC1 and DNA integrity checkpoint genes in Saccharomyces cerevisiae. Genetics 189, 533–547.
Woolstencroft, R. N., Beilharz, T. H., Cook, M. A., Preiss, T., Durocher, D., and Tyers, M. (2006). Ccr4 contributes to tolerance of replication stress through control of CRT1 mRNA poly(A) tail length. J. Cell Sci. 119, 5178–5192.
Zaragoza, O., Garcia-Rodas, R., Nosanchuk, J. D., Cuenca-Estrella, M., Rodriguez-Tudela, J. L., and Casadevall, A. (2010). Fungal cell gigantism during mammalian infection. PLoS Pathog. 6, e1000945. doi: 10.1371/journal.ppat.1000945
Zhang, O., Wilson, M. C., Xu, W., Hsu, F. F., Turk, J., Kuhlmann, F. M., Wang, Y., Soong, L., Key, P., Beverley, S. M., and Zhang, K. (2009). Degradation of host sphingomyelin is essential for Leishmania virulence. PLoS Pathog. 5, e1000692. doi: 10.1371/journal.ppat.1000692
Keywords: Cryptococcus, ISC1, hydroxyurea, morphology
Citation: Tripathi K, Mor V, Bairwa NK, Del Poeta M and Mohanty BK (2012) Hydroxyurea treatment inhibits proliferation of Cryptococcus neoformans in mice. Front. Microbio. 3:187. doi: 10.3389/fmicb.2012.00187
Received: 11 April 2012; Accepted: 08 May 2012;
Published online: 24 May 2012.
Edited by:Joshua D. Nosanchuk, Albert Einstein College of Medicine, USA
Reviewed by:Andrew Alspaugh, Duke University School of Medicine, USA
John C. Panepinto, State University of New York at Buffalo, USA
Copyright: © 2012 Tripathi, Mor, Bairwa, Del Poeta and Mohanty. This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
*Correspondence: Maurizio Del Poeta and Bidyut K. Mohanty, Department of Biochemistry and Molecular Biology, Medical University of South Carolina, 173 Ashley Avenue, Charleston, SC 29412, USA. e-mail: firstname.lastname@example.org; email@example.com