The intracellular protozoan Leishmania replicates in parasitophorous vacuoles (PV) that share many features with late endosomes/lysosomes. L. amazonensis PVs expand markedly during infections, but the impact of PV size on parasite intracellular survival is still unknown. Here we show that host cells infected with L. amazonensis upregulate transcription of LYST/Beige, which was previously shown to regulate lysosome size. Mutations in LYST/Beige caused further PV expansion and enhanced L. amazonensis replication. In contrast, LYST/Beige overexpression led to small PVs that did not sustain parasite growth. Treatment of LYST/Beige over-expressing cells with vacuolin-1 reversed this phenotype, expanding PVs and promoting parasite growth. The opposite was seen with E-64d, which reduced PV size in LYST-Beige mutant cells and inhibited L. amazonensis replication. Enlarged PVs appear to protect parasites from oxidative damage, since inhibition of nitric oxide synthase had no effect on L. amazonensis viability within large PVs, but enhanced their growth within LYST/Beige-induced small PVs. Thus, the upregulation of LYST/Beige in infected cells functions as a host innate response to limit parasite growth, by reducing PV volume and inhibiting intracellular survival.
The protozoan parasite Leishmania causes serious infections in humans throughout the world. After being inoculated into the skin through the bite of infected sandflies, the parasites enter host cells and replicate. The lysosome-like intracellular vacuoles where Leishmania amazonensis replicates expand dramatically as the infection progresses. Here we studied the impact of vacuole expansion on the ability of the parasites to survive and replicate inside host cells. We found that the host cell responds to infection with Leishmania amazonensis by upregulating expression of LYST/Beige, a gene that regulates the size of lysosomes and of parasite-containing vacuoles. The parasites replicated more efficiently in the large vacuoles formed in cells that have a mutation in LYST/Beige, whereas the same cells overexpressing functional LYST/Beige generated small vacuoles that were not able to sustain parasite growth. Drug treatments that reduced or enhanced the size of parasite-containing vacuoles had a corresponding effect on intracellular replication, demonstrating that large vacuoles provide a growth advantage to Leishmania amazonensis. Our results indicate that host cells respond to Leishmania infections by producing a protein capable of reducing vacuole size, as a strategy to inhibit parasite growth.
Citation: Wilson J, Huynh C, Kennedy KA, Ward DM, Kaplan J, et al. (2008) Control of Parasitophorous Vacuole Expansion by LYST/Beige Restricts the Intracellular Growth of Leishmania amazonensis. PLoS Pathog 4(10): e1000179. doi:10.1371/journal.ppat.1000179
Editor: Stephen M. Beverley, Washington University School of Medicine, United States of America
Received: May 5, 2008; Accepted: September 16, 2008; Published: October 17, 2008
Copyright: © 2008 Wilson et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by NIH grants R37AI34867 and RO1GM64625 to NWA, 5RO1AI052286 to AA, and R37HL26922 to JK.
Competing interests: The authors have declared that no competing interests exist.
Infections with the trypanosomatid protozoan Leishmania cause a broad spectrum of human diseases throughout the world. Depending on the parasite species, and on the genetic and immunological composition of the host, the clinical form can range from self-healing cutaneous lesions to severe visceralizing disease. The parasites enter mammalian hosts through the bite of sandflies, and replicate intracellularly as amastigotes. Although macrophages are considered the major host cell type for Leishmania, fibroblasts also harbor parasites and are thought to play an important role during latent infections ). In both macrophages and fibroblasts, intracellular amastigotes replicate within parasitophorous vacuoles (PV) that share several properties with late endosomes/lysosomes, including low luminal pH and the presence of lysosome-specific membrane proteins and acidic hydrolases ,.
An important question in the study of Leishmania pathogenesis is how parasites persist indefinitely in the host, even after the development of immunity to reinfection . Their exclusively intracellular life style suggests that amastigotes possess mechanisms to avoid killing by the abundant microbicidal products produced by activated host cells. The mechanisms of in vivo persistence are of particular interest in relation to L. amazonensis, a species that causes cutaneous leishmaniasis in the new world. Several lines of evidence indicate that L. amazonensis is particularly adept at surviving intracellular killing mechanisms, when compared to other Leishmania species –. Interestingly, the morphology of the PVs harboring L. amazonensis amastigotes (and other species from the L. mexicana complex) also differs dramatically from PVs containing other Leishmania species, such as L. major and L. donovani. Amastigotes of L. mexicana and L. amazonensis replicate within very large, communal PVs that continuously undergo fusion with lysosomes and phagolysosomes. In contrast, PVs containing L. major and L. donovani amastigotes partition as the parasites replicate, resulting in small compartments containing only one parasite per vacuole ,. It was suggested that PV expansion might protect L. amazonensis from host killing mechanisms, by diluting microbicidal molecules . Here we directly investigated this hypothesis, by examining the expression pattern and role in infection of LYST/Beige, a gene known to regulate lysosome size in mammalian cells. Our results show that L. amazonensis infections upregulate LYST/Beige transcription, resulting in the control of PV expansion and inhibition of intracellular growth.
LYST/Beige mRNA transcription is upregulated in macrophages infected with Leishmania
Human mutations in LYST (also known as lysosomal trafficking regulator) are responsible for the Chediak-Higashi syndrome (CHS), an autosomal recessive disease characterized by severe immune deficiency, partial albinism and recurrent bacterial infections. Cells from CHS patients and their mouse counterparts, beige, have abnormally enlarged lysosomes and lysosome-related organelles –. LYST/Beige overexpression reduces the size of lysosomes, suggesting that this large cytosolic protein (~430 kDa) is involved in regulating the size of these organelles . Although the LYST/Beige mechanism of action is still unknown, yeast two-hybrid screens , expression of truncated constructs , and functional analysis of homologs containing similar BEACH domains , suggest that it may provide an anchoring scaffold for kinases and other molecules controlling membrane fusion/fission reactions. To investigate a possible role of LYST/Beige in the regulation of L. amazonensis PVs, we initially focused our investigations on the expression levels of this gene in infected macrophages.
Oligonucleotide DNA microarray analysis demonstrated that LYST/Beige transcription was increased in C57BL/6 mouse bone marrow macrophages (BMM) infected with L. amazonensis axenic amastigotes for 48 h (results not shown). These findings were confirmed using real time PCR (qPCR). Infection of BMM with L. amazonensis amastigotes induced a gradual enhancement in LYST/Beige messenger RNA transcription, reaching a ~3 fold increase 72 h after infection (Figure 1A). As previously described for L. amazonensis , amastigotes replicating intracellularly during this period were visualized attached to the Lamp1-positive limiting membrane of large communal PVs (Figure 1B and 1C).
(A) Upregulation of LYST/Beige transcripts in BMM infected with L. amazonensis. BMM were infected for 30 min with axenic amastigotes, washed and incubated for the indicated periods, followed by RNA extraction and quantitative real-time PCR (qPCR) analysis. The data represents the mean +/− SD of triplicate determinations. Asterisks indicate significant differences from non-infected samples (NI): ** P<0.005 (Student t test). (B) Increased PV expansion in LYST/Beige-deficient BMM (bgJ/bgJ). BMM were infected for 30 min with axenic amastigotes and the size of PVs was determined microscopically after the indicated periods. The values represent the mean of 50 independent PV measurements, asterisks indicate significant differences from the same time points in wild type BMM: * P<0.05, ** P<0.01 (Student t test). (C) Wild type and bgJ/bgJ BMM infected with L. amazonensis were fixed immediately or after 48–72 h, and stained with anti-Lamp1 mAb (green) and DAPI (DNA, blue) stain. Arrows point to heterogeneously sized Lamp1-positive PVs in bgJ/bgJ BMM. Bar = 15 µm. (D) Phase-contrast images showing higher magnifications of parasite-containing PVs (arrows) in wild type or bgJ/bgJ BMM 48 h after infection. (Bar = 5 µm). (E) L. amazonensis intracellular growth is enhanced in bgJ/bgJ BMM. BMM were infected for 60 min and the number of intracellular parasites was determined after the indicated periods. The data (expressed as fold increase in parasite numbers over the 60 min values) corresponds to the mean +/− SD of triplicates. Asterisks indicate significant differences from the corresponding time points in wild type BMM: * P<0.05 (Student t test).
The Beige mutation causes expansion of Leishmania-containing parasitophorous vacuoles and enhances parasite growth
To directly examine the role of LYST/Beige in controlling L. amazonensis PV expansion, we measured the size of parasite-containing vacuoles in BMM from wild type or beige mice (bgJ/bgJ). In wild type BMM infected with L. amazonensis, PVs expanded rapidly between 1 and 48 h after infection, and more slowly between 48 and 72 h (Figure 1B, wild type). In contrast, PV expansion in infected bgJ/bgJ BMM appeared to be enhanced, with several significantly larger PVs observed at all time points (Figure 1B–1D, bgJ/bgJ). The PV size distribution in bgJ/bgJ BMM, however, was heterogeneous (Figure 1B), with markedly enlarged PVs observed side-by-side smaller ones (arrows, Figure 1C). This pattern was consistent with the overall morphology of the lysosomal compartment in bgJ/bgJ BMM, which is also heterogeneous in size (results not shown), probably due to the highly dynamic nature of the tubular lysosomes of macrophages . When we analyzed the impact of LYST/Beige deficiency on L. amazonensis intracellular survival and growth in bgJ/bgJ BMM, we found a small but statistically significant increase in the number of intracellular parasites at 48 and 72 h after infection (Figure 1E). Although the size heterogeneity of PVs in BMM did not allow a definitive conclusion, these data suggested that PV expansion might favor L. amazonensis survival and replication within host cells.
LYST/Beige overexpression reduces parasitophorous vacuole size and inhibits parasite growth
Fibroblasts have been implicated as important host cells during latent infections with Leishmania . Consistent with this finding, primary and immortalized fibroblast cell lines are susceptible to L. amazonensis infection ,. Examining in parallel primary BMM and murine embryonic fibroblasts (MEF) infected with L. amazonensis axenic amastigotes, we found that both cell types sustain PV expansion and parasite intracellular proliferation (Figure 2A and 2D). We also observed that in fibroblasts PVs expand faster, and are significantly more homogeneous in size (Figure 2C and 2D, compare to Figure 2A and 2B). This finding allowed us to examine in detail the impact of LYST/Beige expression on L. amazonensis intracellular growth.
(A,C) Intracellular growth of L. amazonensis amastigotes in mouse BMM (A) or MEF (embryonic fibroblasts) (C). BMM or MEFs were exposed to amastigotes at a MOI = 1 for 30 min or MOI = 10 for 60 min, respectively. Cells were washed, incubated for 1, 24, 48, and 72 h, and the number of intracellular parasites was determined. In fibroblasts parasites per microscopic field were quantified, to compensate for cell division during the experimental period. The data corresponds to the mean +/− SD of triplicates. (B,D) The average size of the parasitophorous vacuole (PV) in BMM (B) and MEFs (D) increases in parallel with the number of intracellular amastigotes. In MEFs the maximum PV expansion is reached earlier than in BMM. The values represent the mean of 50 independent measurements. (E) Phase contrast images illustrating the rapid expansion of a L. amazonensis PV in a fibroblast (arrows). Bar = 5 µm.
Fibroblasts derived from beige mice complemented (YAC-bgJ/bgJ) or not (bgJ/bgJ) with a wild copy of LYST/Beige  were infected with L. amazonensis axenic amastigotes. The size of L. amazonensis-containing PVs in the YAC-bgJ/bgJ fibroblasts was markedly reduced, when compared to the PVs found in LYST/Beige-deficient bgJ/bgJ cells (Figure 3A and 3B). Importantly, the overexpression of LYST/Beige, which is known to reduce lysosome size in this cell line , caused a reduction in PV size that was significantly below the size normally seen in L. amazonensis-infected wild type fibroblasts (compare Figure 3B with Figure 2D). This reduction in PV size had a strong impact on parasite growth, since no intracellular replication was detected in the YAC-bgJ/bgJ cells overexpressing LYST/Beige, in several independent experiments (Figure 3C). A cell line derived in parallel from wild type mice also supported L. amazonensis intracellular replication, but the parasite population grew slower than in the mutant bgJ/bgJ cells (Figure 3C). Collectively, these results support a role of LYST/Beige in restricting the intracellular survival of L. amazonensis.
(A) Phase contrast images showing that the PV expansion observed in bgJ/bgJ fibroblasts is inhibited in YAC-bgJ/bgJ fibroblasts overexpressing LYST/Beige. Arrows point to individual PVs. Bar = 10 µm. (B) Analysis of PV size in infected bgJ/bgJ or YAC-bgJ/bgJ fibroblasts, showing the markedly reduced PV expansion in cells overexpressing LYST/Beige. Fibroblasts were infected for 30 min, and PV size was determined microscopically after the indicated time points. The values represent the mean of 50 independent measurements. Asterisks indicate significant differences from the corresponding time points in bgJ/bgJ fibroblasts: * P<0.05, ** P<0.01 (Student t test). (C) L. amazonensis amastigotes proliferate slowly in wild type and more vigorously in bgJ/bgJ fibroblasts lacking a functional LYST/Beige protein, but not in YAC-bgJ/bgJ fibroblasts that over-express LYST/Beige. Fibroblasts were exposed to L. amazonensis amastigotes for 60 min, washed, and incubated for the indicated periods followed by determination of the number of intracellular parasites. The data corresponds to the mean +/− SD of triplicates. The results shown are representative of several independent experiments. (D) Upregulation of the mutant LYST/Beige transcripts in bgJ/bgJ fibroblasts infected with L. amazonensis. The cells were exposed for 30 min to axenic amastigotes, washed, and incubated for the indicated periods, followed by RNA extraction and analysis by qualitative RT-PCR (left) and quantitative real-time qPCR (right). The data on the right panel represents the mean +/− SD of triplicate determinations. Asterisks indicate significant differences from non-infected samples (NI): * P<0.05 (Student t test).
We next examined whether the bgJ/bgJ fibroblasts that sustain L. amazonensis growth also responded to infection by upregulating LYST/Beige, as seen in macrophages (Figure 1A). This determination was possible because the mutation causing LYST/Beige functional inactivation in bgJ/bgJ fibroblasts would lead to a truncated protein, lacking approximately 1400 amino acids . A single transcript corresponding to the truncated form of LYST/Beige was detected in bgJ/bgJ fibroblasts (Figure 3D, left panel, not infected), and infection with L. amazonensis amastigotes markedly enhanced this signal (Figure 3D, left panel, infected, and Figure 3D, right panel). Thus, L. amazonensis infection triggers in host cells an innate response that upregulates LYST/Beige expression, a process that blocks parasite replication if the expressed protein is functional.
The intracellular survival of Leishmania is regulated by parasitophorous vacuole size
The data discussed above suggested that PV expansion facilitates the intracellular survival and growth of Leishmania. To further investigate this possibility, we examined the effects of reducing PV size in bgJ/bgJ fibroblasts and, conversely, increasing the size of PVs in YAC-bgJ/bgJ fibroblasts. Previous studies showed that treatment of bgJ/bgJ cells with the thiol proteinase inhibitor E-64d reduces the size of the enlarged lysosomes normally observed in these cells ,. A reduction in PV size after pre-treatment with E-64d was evident in bgJ/bgJ fibroblasts (Figure 4A and 4B), and this coincided with a reduction of ~3 fold in the number of intracellular amastigotes detected after 24 h, when compared to untreated bgJ/bgJ cells (Figure 4C, bgJ/bgJ). In contrast, there was no apparent effect of E-64d on the smaller PVs within the YAC-bgJ/bgJ fibroblasts (Figure 4B, YAC-bgJ/bgJ), and no effect on parasite numbers in these cells (Figure 4C, YAC-bgJ/bgJ).
(A) Phase contrast images showing that pretreatment with E64d reduces the large vacuoles observed in bgJ/bgJ fibroblasts. Arrows point to individual PVs. Bar = 5 µm. (B) Analysis of PV size in infected bgJ/bgJ or YAC-bgJ/bgJ fibroblasts pretreated or not with E64d. Fibroblasts were exposed to L. amazonensis amastigotes for 30 min, washed, and further incubated for 24 h followed by microscopic determination of PV size. The values above the symbols represent the mean of 50 independent measurements. Asterisks indicate significant differences from the non-treated controls (NT): ** P<0.01 (Student t test). (C) PV reduction with E64d inhibits the intracellular growth of L. amazonensis in bgJ/bgJ fibroblasts. After E64d pretreatment the fibroblasts were exposed to amastigotes for 1 h, washed, and further incubated for 24 h, followed by determination of the number of intracellular parasites. The data corresponds to the mean +/− SD of triplicates. Asterisks indicate significant differences from the non-treated controls (NT): * P<0.05 (Student t test). (D) Analysis of PV size in infected bgJ/bgJ or YAC-bgJ/bgJ fibroblasts pretreated or not with 1 µM vacuolin-1. Fibroblasts were exposed to L. amazonensis amastigotes for 30 min, washed, and further incubated for 24 h followed by microscopic determination of PV size. The values above the symbols represent the mean of 50 independent measurements. Asterisks indicate significant differences from non-treated controls (NT): ** P<0.01 (Student t test). (E) Phase contrast images showing that pretreatment with 1 µM vacuolin-1 enlarges the small vacuoles observed in L. amazonensis-infected YAC-bgJ/bgJ fibroblasts. Arrows point to individual PVs. Bars = 10 µm. (F) After vacuolin-1 pretreatment the fibroblasts were infected for 1 h, washed, and further incubated for 24 h, followed by determination of the number of intracellular parasites. The data corresponds to the mean +/− SD of triplicates. Asterisks indicate significant differences from the non-treated controls (NT): ** P<0.01 (Student t test).
E-64d was washed out prior to infection, to prevent an effect of this irreversible cysteine protease inhibitor on the parasites. However, we cannot completely rule out the possibility that a small pool of the inhibitor remained inside host cells. For this reason, we examined the effect of a drug that has the opposite effect of E-64d, enlarging lysosomes. YAC-bgJ/bgJ fibroblasts were pre-treated with vacuolin-1, a small molecule that causes rapid expansion of late endosomes/lysosomes in mammalian cells . We infected bgJ/bgJ and YAC-bgJ/bgJ fibroblasts pre-treated with vacuolin-1 with L. amazonensis, and determined PV size and the number of intracellular parasites after a 24 h period. Vacuolin-1 pre-treatment of bgJ/bgJ fibroblasts did not further increase the mean PV size, nor did it cause an enhancement in the number of intracellular amastigotes (Figure 4D and 4F, bgJ/bgJ). In contrast, in the LYST/Beige overexpressing YAC-bgJ/bgJ fibroblasts, vacuolin-1 caused a significant increase in PV size (Figure 4D–4E, YAC-bgJ/bgJ) and a ~3 fold enhancement in parasite numbers (Figure 4F, YAC-bgJ/bgJ).
In these experiments, fibroblasts were pre-treated with E-64d or vacuolin-1 before infection to avoid any adverse effects on the parasites. For this reason, parasite development was not followed beyond 24 h. Since Leishmania has an intracellular doubling time of approximately 12 h, the strong impact of PV size on the number of parasites detected after only 24 h suggests that the mechanism involves direct modulation of early intracellular survival.
PV enlargement may protect Leishmania from nitric oxide (NO)-mediated killing
A major mechanism underlying the leishmanicidal activity of murine macrophages is the IFN-gamma and TNF-alpha-mediated activation of nitric oxide synthase (iNOS or NOS2), which generates the potent microbicidal agent nitric oxide (NO) ,. Recent evidence indicates that iNOS is recruited to the membrane of recently formed pathogen-containing phagosomes, in a process thought to be critical for its microbicidal action ,. The strong reactivity of NO implies that it has to be generated in close proximity to targets, in order to be effective. Interestingly, L. amazonensis is significantly less susceptible to IFNgamma-mediated killing, when compared to species that reside in small PVs such as L. major ,. Thus, PV enlargement may have a role in reducing the concentration of NO in direct contact with intracellular amastigotes.
Since L. amazonensis is capable of productively infecting both macrophages and fibroblasts in culture (Figure 2), and PV enlargement enhances the early survival and replication of L. amazonensis in these two cell types (Figures 3 and 4), it is conceivable that PV enlargement protects Leishmania from a microbicidal mechanism common to both macrophages and fibroblasts. Although NO production in response to IFN-gamma and TNF-alpha is much more robust in macrophages, fibroblasts are also capable of mounting this response . To investigate whether NO production plays a role in the enhanced survival of Leishmania in fibroblasts, we quantified intracellular amastigotes in L. amazonensis-infected bgJ/bgJ and YAC-bgJ/bgJ fibroblasts pre-treated with the iNOS inhibitors L-NMMA and L-NAME. These inhibitors were previously shown to promote the intracellular growth of Leishmania in macrophages by blocking NO production ,. Quantification of the number of intracellular amastigotes after 24 h showed that these inhibitors did not alter the parasite population size in bgJ/bgJ fibroblasts, which exhibit large PVs (Figure 5A). However, amastigote survival and replication was significantly enhanced in YAC-bgJ/bgJ fibroblasts pre-treated with the iNOS inhibitors (Figure 5B), consistent with the observation of several parasites inside each of the small PVs found in these cells (Figure 5D). Importantly, the size of the small PVs induced by L. amazonensis in the YAC-bgJ/bgJ fibroblasts overexpressing LYST/Beige remained unchanged after treatment with the iNOS inhibitors (Figure 5C), suggesting that inhibition of NO production can promote L. amazonensis survival/growth in the absence of PV expansion. Future studies are required to investigate the possibility that LYST expression might also impact the trafficking of iNOS to L. amazonensis-containing PVs.
(A) Treatment with iNOS inhibitors does not affect L. amazonensis growth in the enlarged PVs of bgJ/bgJ fibroblasts, but rescues growth in the small PVs of YAC-bgJ/bgJ fibroblasts. After pretreatment with 50 µM L-NMMA or 50 µM L-NAME, the fibroblasts were infected for 1 h, washed and incubated for 24 h, followed by determination of the number of intracellular parasites. The data corresponds to the mean +/− SD of triplicates. Asterisks indicate significant differences from non-treated controls (NT): * P<0.05 (Student t test). (B) iNOS inhibitors do not alter PV size in bgJ/bgJ or YAC-bgJ/bgJ fibroblasts. Cells were exposed to L. amazonensis amastigotes for 30 min, washed, and further incubated for 24 h followed by microscopic determination of PV size. The values represent the mean of 50 independent measurements. (C) Phase contrast images of bgJ/bgJ or YAC-bgJ/bgJ fibroblasts pretreated or not with L-NMMA or L-NAME, exposed to L. amazonensis amastigotes for 1 h and fixed after 24 h. Arrows point to individual PVs. Bars = 5 µm.
This study demonstrates that transcription of LYST/Beige, a gene previously implicated in regulating lysosome size, is upregulated in macrophages and fibroblasts infected by L. amazonensis. Examining the impact of PV expansion on the fate of the parasites, we found that PV size is an important determinant of intracellular survival. Collectively, our findings provide direct experimental evidence for the idea that increased expression of LYST/Beige functions as a host innate response to restrict Leishmania growth, by counteracting PV expansion. Our findings suggest that a search for drugs capable of specifically blocking L. amazonensis PV expansion might lead to novel therapeutic strategies against the human infections caused by this pathogen.
Materials and Methods
Parasites and mammalian cells
Leishmania amazonensis (IFLA/BR/67/PH8) were obtained from David Sacks (Laboratory of Parasitic Diseases, National Institutes of Health) and propagated as promastigotes at 27°C in M199 media supplemented with 5% penicillin/streptomycin, 0.1% hemin (25 mg/ml in 0.1N NaOH), 10 mM adenine, pH 7.5 and 10% FBS. To generate amastigotes, metacyclics were incubated in M199 media supplemented with 0.25% glucose, 0.5% trypticase, 40 mM sodium succinate (pH 5.4), 20% FBS, 5% penicillin/streptomycin at 2×106/ml at 31°C for a minimum of 6 days, and passaged axenically at 31°C. All parasites were washed 3 times in PBS before use in experiments.
Bone marrow-derived macrophages (BMM) were isolated from the femurs of 8-10 week-old C57BL/6 wild type mice or beige mice (in the C57BL/6 background) and cultured for 7 days in RPMI 1640 containing 30% L-fibroblast culture supernatant and 20% FBS. Mouse murine embryonic fibroblasts (MEFs) were prepared from day 13.5 mouse embryos  and cultured in high glucose DMEM (GIBCO BRL) with 10% FBS, 1% penicillin/streptomycin, and 2 mM glutamine. Fibroblast lines from wild type C57BL/6J mice and from beige-J mice lacking the Beige gene (bgJ/bgJ) (in the C57BL/6J background), and the bgJ/bgJ line complemented with a yeast artificial chromosome (YAC) carrying the Beige gene (YAC-bgJ/bgJ) (NCBI AAL40134 accession number) were generated in J.K.'s laboratory at the University of Utah  and maintained in DMEM 10% FBS, 1% penicillin/streptomycin and 2 mM glutamine (1 mg/ml G418 was kept in the growing medium of the YAC-bgJ/bgJ line, but removed prior to infection with Leishmania, followed by several washes).
Affimetrix GeneChip analysis and quantitative real-time PCR
C57BL/6 BMM plated at 2.5×105 in 10 cm dishes were exposed or not to L. amazonensis amastigotes at MOI:10 for 30 min at 34°C. After infection cells were washed 3 times in PBS and further incubated for the appropriate times. Total RNA was isolated using Trizol (Invitrogen). The Affymetrix protocol, used to analyse RNA extracted from BMM infected for 48 h with L. amazonensis amastigotes, was essentially as described (GeneChip Expression Analysis Technical Manual, Affymetrix). cRNA was hybridized for 16 h to Affymetrix Genechip Mouse Genome 430 2.0 Array (Affymetrix), which contain 45,000 probe sets for the analysis of 39,000 transcripts and variants from over 34,000 mouse genes. Normalization was performed using GeneChip robust multi-array analysis, followed by GC-robust multi-array average (GC-RMA) normalization. Identification of significantly perturbed genes was done using significance analysis of microarrays. The false positive rate was 0.1%. Real-time PCR was performed using a BioRad iQ icycler Detection system (BioRad Laboratories, Ltd) with SYBR green fluorophore (BioRad Laboratories, Ltd) according to the manufacturer's instructions. Oligonucleotide primers 5′- AGCAGAAGGTGATAGACCAGAA and 5′-CCCACACTTGGATCATCAATGC were used to amplify a 119 base pair portion of LYST or 5′-TCAGTCAACGGGGGACATAAA and 5′-GGGGCTGTACTGCTTAACCAG to amplify a 142 base pair of the control cDNA HPRT1. The reaction was incubated for 3 min at 95°C, and then for 45 cycles of 20 s each at 95°C and for 1 min at 55°C. Fluorescence was detected at each annealing step and cycle threshold (Ct) was calculated by determining the point at which the fluorescence exceeded a threshold limit. All reactions were run in triplicate and negative controls (no template cDNA) were included in each experiment. Data were normalized by the level of GAPDH expression in individual samples.
BMM were plated at 1.25×105 and fibroblasts at 2.5×104 on 12-mm diameter glass coverslips in 24-well dishes, 24 h prior to experiments. Vacuolin-1 (compound 5114069, ChemBridge San Diego, CA) (23), was added to fibroblasts at 1.0 µM for 1 h prior to infection. E-64d (Sigma) was added to fibroblasts at 1.0 µM for 1 h prior to infection. Immediately before infection the cells were washed 3 times in PBS. N-methyl-L-arginine (L-NMMA) or N-nitro-L-arginine methyl ester (L-NAME) (Sigma), two nitric oxide synthase inhibitors ,, were added to cells at 50 µM for 1 h. Cells were washed in PBS prior to infection.
Leishmania infection assays
For invasion of BMM, purified axenic amastigotes were added at a multiplicity of infection (MOI):1 in RPMI 10% FBS for 1 h at 34°C. For invasion of fibroblasts, amastigotes were added at an MOI = 10 for 1 h in high glucose DMEM supplemented with 10% FBS at 34°C. After invasion, cells were washed 3 times in PBS and incubated for indicated times at the appropriate temperature. Coverslips were then fixed in 2% paraformaldehyde, and host cell and parasite DNA were stained with 10 µg/ml DAPI for 5 min, after permeabilization with 0.05% Triton-X 100 for 10 min. At least 300 host cells, in triplicate, were analyzed for each time point. Images were acquired through a 100× objective using a Zeiss Axiovert microscope equipped with a Hamamatsu Orca II cooled CCD camera controlled by Metamorph Software (Molecular Devices). For parasite growth curves in fibroblasts the data was expressed as intracellular parasites per microscopic field, to compensate for host cell division . For Lamp-1 immunofluorescence, cells on coverslips were permeabilized with PBS/ 2% BSA/ 0.5% saponin for 20 min, incubated with anti-Lamp1 mAb 1D4B (Developmental Studies Hybridoma Bank) 1:50 in PBS/2% BSA/0.5% saponin for 45 min, followed by Alexa 488- goat anti-rat secondary antibodies (Invitrogen). Host and parasite DNA were stained with DAPI. Individual parasitophorous vacuoles (PVs) were measured using the Metamorph draw function. A line was drawn on phase contrast images straight across the length of the PV, and the Metamorph calculate function was used to convert the values to µm. A total of 50 PVs were measured for each sample.
We thank David Sacks (NIH) for helpful discussions, critical reading of the manuscript, and for the Leishmania amazonensis strain.
Conceived and designed the experiments: JW CH DMW JK AA NWA. Performed the experiments: JW CH KAK. Analyzed the data: JW CH KAK AA NWA. Contributed reagents/materials/analysis tools: DMW JK AA. Wrote the paper: JW CH NWA.
- 1. Bogdan C, Donhauser N, Doring R, Rollinghoff M, Diefenbach A, Rittig MG (2000) Fibroblasts as host cells in latent leishmaniosis. J Exp Med 191: 2121.
- 2. Antoine JC, Prina E, Lang T, Courret N (1998) The biogenesis and properties of the parasitophorous vacuoles that harbour Leishmania in murine macrophages. Trends Microbiol 6: 392.
- 3. Morehead J, Coppens I, Andrews NW (2002) Opsonization modulates Rac-1 activation during cell entry by Leishmania amazonensis. Infect Immun 70: 4571.
- 4. Sacks D, Noben-Trauth N (2002) The immunology of susceptibility and resistance to Leishmania major in mice. Nat Rev Immunol 2: 845.
- 5. Gomes IN, Calabrich AF, Tavares Rda S, Wietzerbin J, de Freitas L A, et al. (2003) Differential properties of CBA/J mononuclear phagocytes recovered from an inflammatory site and probed with two different species of Leishmania. Microbes Infect 5: 251.
- 6. Qi H, Ji J, Wanasen N, Soong L (2004) Enhanced replication of Leishmania amazonensis amastigotes in gamma interferon-stimulated murine macrophages: implications for the pathogenesis of cutaneous leishmaniasis. Infect Immun 72: 988.
- 7. McMahon-Pratt D, Alexander J (2004) Does the Leishmania major paradigm of pathogenesis and protection hold for New World cutaneous leishmaniases or the visceral disease? Immunol Rev 201: 206.
- 8. Veras PS, de Chastellier C, Rabinovitch M (1992) Transfer of zymosan (yeast cell walls) to the parasitophorous vacuoles of macrophages infected with Leishmania amazonensis. J Exp Med 176: 639.
- 9. Sacks D, Sher A (2002) Evasion of innate immunity by parasitic protozoa. Nat Immunol 3: 1041.
- 10. Barbosa MD, Nguyen QA, Tchernev VT, Ashley JA, Detter JC, et al. (1996) Identification of the homologous beige and Cheiak-Higashi syndrome genes. Nature 382: 262.
- 11. Nagle DJ, Karim MA, Wolf EA, Holmgren L, Bork P, et al. (1996) Identification and mutation analysis of the complete gene for Chediak Higashi syndrome. Nature Genetics 14: 307.
- 12. Ward DM, Griffiths GM, Stinchcombe JC, Kaplan J (2000) Analysis of the lysosomal storage disease Chediak-Higashi syndrome. Traffic 1: 816.
- 13. Perou CM, Leslie JD, Green W, Li L, Ward DM, et al. (1997) The Beige/Chediak-Higashi syndrome gene encodes a widely expressed cytosolic protein. J Biol Chem 272: 29790.
- 14. Tchernev VT, Mansfield TA, Giot L, Kumar AM, Nandabalan K, et al. (2002) The Chediak-Higashi protein interacts with SNARE complex and signal transduction proteins. Mol Med 8: 56.
- 15. Ward DM, Shiflett SL, Huynh D, Vaughn MB, Prestwich G, et al. (2003) Use of expression constructs to dissect the functional domains of the CHS/beige protein: identification of multiple phenotypes. Traffic 4: 403.
- 16. Han JD, Baker NE, Rubin CS (1997) Molecular characterization of a novel A kinase anchor protein from Drosophila melanogaster. J Biol Chem 272: 26611.
- 17. Wang X, Herberg FW, Laue MM, Wullner C, Hu B, et al. (2000) Neurobeachin: A protein kinase A-anchoring, beige/Chediak-higashi protein homolog implicated in neuronal membrane traffic. J Neurosci 20: 8551.
- 18. Hollenbeck PJ, Swanson JA (1990) Radial extension of macrophage tubular lysosomes supported by kinesin. Nature 346: 864.
- 19. Veras PS, de Chastellier C, Moreau MF, Villiers V, Thibon M, et al. (1994) Fusion between large phagocytic vesicles: targeting of yeast and other particulates to phagolysosomes that shelter the bacterium Coxiella burnetii or the protozoan Leishmania amazonensis in Chinese hamster ovary cells. J Cell Sci 107: 3065.
- 20. Perou CM, Moore KJ, Nagle DL, Misumi DJ, Woolf EA, et al. (1996) Identification of the murine beige gene by YAC complementation and positional cloning. Nat Genet 13: 303.
- 21. Tanabe F, Cui SH, Ito M (2000) Abnormal down-regulation of PKC is responsible for giant granule formation in fibroblasts from CHS (beige) mice–a thiol proteinase inhibitor, E-64-d, prevents giant granule formation in beige fibroblasts. J Leukoc Biol 67: 749.
- 22. Huynh C, Roth D, Ward DM, Kaplan J, Andrews NW (2004) Defective lysosomal exocytosis and plasma membrane repair in Chediak-Higashi/beige cells. Proc Natl Acad Sci U S A 101: 16795.
- 23. Huynh C, Andrews NW (2005) The small chemical vacuolin-1 alters the morphology of lysosomes without inhibiting Ca(2+)-regulated exocytosis. EMBO Rep 6: 843.
- 24. Bogdan C, Rollinghoff M, Diefenbach A (2000) The role of nitric oxide in innate immunity. Immunol Rev 173: 17.
- 25. Liew FY, O'Donnell CA (1993) Immunology of leishmaniasis. Adv Parasitol 32: 161.
- 26. Chakravortty D, Hansen-Wester I, Hensel M (2002) Salmonella pathogenicity island 2 mediates protection of intracellular Salmonella from reactive nitrogen intermediates. J Exp Med 195: 1155.
- 27. Miller BH, Fratti RA, Poschet JF, Timmins GS, Master SS, Burgos M, Marletta MA, Deretic V (2004) Mycobacteria inhibit nitric oxide synthase recruitment to phagosomes during macrophage infection. Infect Immun 72: 2872.
- 28. Gantt KR, Goldman TL, McCormick ML, Miller MA, Jeronimo SM, et al. (2001) Oxidative responses of human and murine macrophages during phagocytosis of Leishmania chagasi. J Immunol 167: 893.
- 29. Tournier C, Hess P, Yang DD, Xu J, Turner TK, et al. (2000) Requirement of JNK for stress-induced activation of the cytochrome c-mediated death pathway. Science 288: 870.
- 30. Koblish HK, Hunter CA, Wysocka M, Trinchieri G, Lee WM (1998) Immune suppression by recombinant interleukin (rIL)-12 involves interferon gamma induction of nitric oxide synthase 2 (iNOS) activity: inhibitors of NO generation reveal the extent of rIL-12 vaccine adjuvant effect. J Exp Med 188: 1603.