Extracellular Paracoccidioides brasiliensis phospholipase B involvement in alveolar macrophage interaction
© Soares et al; licensee BioMed Central Ltd. 2010
Received: 31 May 2010
Accepted: 15 September 2010
Published: 15 September 2010
Phospholipase B (PLB) has been reported to be one of the virulence factors for human pathogenic fungi and has also been described as necessary for the early events in infection. Based on these data, we investigated the role of PLB in virulence and modulation of the alveolar pulmonary immune response during infection using an in-vitro model of host-pathogen interaction, i.e. Paracoccidioides brasiliensis yeast cells infecting alveolar macrophage (MH-S) cells.
The effect of PLB was analyzed using the specific inhibitor alexidine dihydrochloride (0.25 μM), and pulmonary surfactant (100 μg mL-1), during 6 hours of co-cultivation of P. brasiliensis and MH-S cells. Alexidine dihydrochloride inhibited PLB activity by 66% and significantly decreased the adhesion and internalization of yeast cells by MH-S cells. Genes involved in phagocytosis (trl2, cd14) and the inflammatory response (nfkb, tnf-α, il-1β) were down-regulated in the presence of this PLB inhibitor. In contrast, PLB activity and internalization of yeast cells significantly increased in the presence of pulmonary surfactant; under this condition, genes such as clec 2 and the pro-inflammatory inhibitor (nkrf) were up-regulated. Also, the pulmonary surfactant did not alter cytokine production, while alexidine dihydrochloride decreased the levels of interleukin-10 (IL-10) and increased the levels of IL-12 and tumor necrosis factor-α (TNF-α). In addition, gene expression analysis of plb1, sod3 and icl1 suggests that P. brasiliensis gene re-programming is effective in facilitating adaptation to this inhospitable environment, which mimics the lung-environment interaction.
P. brasiliensis PLB activity is involved in the process of adhesion and internalization of yeast cells at the MH-S cell surface and may enhance virulence and subsequent down-regulation of macrophage activation.
Paracoccidioidomycosis (PCM) is the most prevalent systemic mycosis in Latin America. Epidemiological data indicate a broad geographic distribution in Central and South America, from Mexico to Argentina . It is estimated that as many as ten million individuals may be infected with P. brasiliensis in this part of the world. Infection occurs primarily in the lungs, from where it can disseminate via the bloodstream and/or lymphatic system to many organ systems, resulting in the disseminated form of PCM .
Considering the pathogenesis of this disease, the initial stages are of importance since this is when resident pulmonary macrophages interact with the fungus for the first time and become activated.
In this context, multiple characteristics have been proposed as virulence factors that enable the invading organism to cause disseminated infections in susceptible hosts. The ability to recognize and adhere to host tissues, to respond rapidly to changes in the external environment, and to secrete enzymes are all thought to play important roles in virulence. Secretion of enzymes, such as phospholipases, has been proposed as one of the strategies used by bacteria, parasites, and pathogenic fungi for invasion of the host and establishment of infection .
The role of extracellular phospholipases, particularly phospholipase B (PLB), as potential virulence factors for pathogenic fungi, including Candida albicans [4, 5], Cryptococcus neoformans [6–10], and Aspergillus fumigatus  has been reported, although the underlying mechanism has yet to be elucidated. Extracellular phospholipase activities have also been detected in in-vitro cultures of P. brasiliensis , and PLB has been postulated as a potential virulence factor for this pathogen by in-silico analysis .
Phospholipases are ubiquitous enzymes that are involved in a wide range of biological functions, such as membrane homeostasis, nutrient acquisition, and generation of bioactive molecules. These enzymes are known to contribute to bacterial and fungal virulence through a variety of different interactions with eukaryotic host cells,  and to modulate the innate and acquired immune response of the host by generating second messengers such as diacylglycerol or the eicosanoid precursor arachidonic acid . Furthermore, phospholipase-mediated IL-8 release induces the host inflammatory response .
It has been shown that secreted PLB1, a proven virulence determinant of C. neoformans, is required for the initiation of interstitial pulmonary cryptococcosis, being important for the binding of this fungus to human lung epithelial cells prior to its internalization . PLB1, the product of the CnPLB1 gene, is a multifunctional enzyme which can degrade dipalmitoylphosphatidylcholine (DPPC), the main component of lung surfactant .
The goal of this work was to determine whether P. brasiliensis PLB is involved in adhesion of this fungus to and internalization by alveolar macrophage (MH-S) cells. Also, we investigated the role of this enzyme in virulence and modulation of the alveolar pulmonary immune response during infection using alexidine dihydrochloride as a specific PLB inhibitor, as well as pulmonary surfactant (Survanta) as a substrate rich in phospholipids.
Results and discussion
The first contact between P.brasiliensis and the host occurs by inhalation of the infectious propagules from the environment. PLB has been reported as a potential virulence factor by transcriptome analysis in P. brasiliensis [13, 16]. Furthermore, experiments performed by our group showed that the plb1 gene is up-regulated during the early events of murine pulmonary infection in a paracoccidioidomycosis model (data not shown), suggesting a possible role for this enzyme in the host-pathogen interaction and reinforcing the hypothesis that PLB could be an important virulence factor for P. brasiliensis.
In C. neoformans, PLB is necessary for the early events of pulmonary infection and for dissemination from the lung via the lymphatic system and blood [9, 17]. Specifically, adhesion to alveolar macrophage cells is reduced in a PLB deletion mutant of C. neoformans and also in the presence of selective chemical inhibitors of PLB and a specific anti-PLB antibody. The extent of adhesion was correlated with PLB activity, but not with lysophospholipase (LPL) or lysophospholipase transacylase (LPTA) activity .
Lack of established protocols for conducting experiments that might lead to gene disruption or silencing in P. brasiliensis hinders the validation of the plb gene functionality in this pathogen. In view of this fact, we decided to investigate the role of PLB using an in-vitro model of host-pathogen interaction, i.e. the yeast cells of P. brasiliensis infecting MH-S cells. The use of a specific inhibitor and/or an activator of PLB could be an effective strategy for investigating the possible role of this enzyme during host-pathogen interaction.
Effects of alexidine dihydrochloride and pulmonary surfactant on cell viability, adhesion, internalization, and PLB activity during co-cultivation of P. brasiliensis and MH-S cells
Phospholipase B activities secreted under the experimental conditions used for Phagocytic test
Specific activity of PLB
1.21 ± 0.02
Pulmonary surfactant (100 μg mL-1)
1.55 ± 0.06* (28% activation)
Alexidine dihydrochloride (0.25 μM)
0.41 ± 0.08* (66% inhibition)
A role for PLB activity in adhesion of C. neoformans to lung epithelial cells has already been proposed ; DPPC is predicted to be the favored lipid substrate for PLB, leading to the production of glycerophosphocholine and free palmitic acid. In this context, it is hypothesized that the addition of pulmonary surfactant (rich in DPPC) would increase the adhesion of P. brasiliensis yeast cells to MH-S cells. These results strongly suggest that PLB activity is important in P. brasiliensis adhesion to and/or internalization by MH-S cells.
In the present study, enzyme activities were tested under conditions used for adhesion (Table 1). P. brasiliensis produced high levels of PLB at 6 h post-infection. 0.25 μM Alexidine dihydrochloride selectively inhibited PLB activity by 66%. In contrast, PLB activity in the presence of 100 μg mL-1 pulmonary surfactant was significantly increased (28%) compared to the control experiment.
Modulation of P. brasiliensis and MH-S genes in the host-pathogen interaction
P. brasiliensis metabolic adaptation in response to phagocytosis involves the induction of sod 3, which encodes a putative Cu, Zn SOD, an enzyme participating in the elimination of superoxide anions. In-silico analysis showed that P. brasiliensis sod 3 corresponds to a putative membrane-bound, glycosylphosphatidylinisotol (GPI)-anchored Cu, Zn SOD, which would allow for better accessibility to host-derived superoxide anions and subsequent rapid detoxification of reactive oxygen intermediates (ROI) [18, 19]. The up-regulation of sod 3 expression in P. brasiliensis internalized by pulmonary surfactant-treated MH-S cells provides evidence that sod 3 may also be needed for the elimination of generated superoxides, thus increasing yeast cell survival. This suggests that the sod3 gene is probably involved in the survival of P. brasiliensis, corroborating previous data .
Induction of the glyoxylate cycle upon phagocytosis has been described as an important adaptation by pathogens to the glucose-poor environment within macrophages, since it facilitates the assimilation of two-carbon compounds, the product of fatty acid degradation [20, 21]. In P. brasiliensis, both isocitrate lyase and the entire glyoxylate pathway have been shown to be enhanced under low glucose and oxygen tension, in the presence of acetate and high temperature, as well as during intracellular growth [16, 22, 23]. Our results showed that the icl1 gene was up-regulated under increased PLB activity, which could be correlated with the fungal survival inside macrophage cells.
The results observed for the gene expression of plb1, sod3, and icl1 suggest that, under in-vitro conditions mimicking the lung-environment interaction, gene re-programming was similar to that described for peritoneal macrophages [18, 24], corroborating the importance and effective participation of those genes in the process of adaptation by the fungus to this inhospitable environment.
The process of recognition of pathogen-associated molecular patterns (PAMP) depends on the pattern recognition receptors (PRR) present in great diversity in the plasma membrane of phagocytes . The two main members of this family that recognize fungal components are the C-type lectin-like receptors (CLRs) and toll-like receptors (TLRs) .
To investigate whether P. brasiliensis PLB is able to affect the inflammatory response of MH-S cells, we assessed the transcription level of the following key genes: tnf-α (tumor necrosis factor-alpha), il-1β (Interleukin-1β), nkrf (NFKappaB repressing factor), and nfkb (P50 subunit of NFKappaB), known to be involved in the phagocytic process, and trl2 (toll-like receptor 2), cd14 (glycosyl-phosphatidylinositol-anchored glycoprotein), and clec 2 (C-type lectin-like receptor), signal receptors involved in controlling the immune response. These genes had already been reported to be differentially expressed by peritoneal macrophages infected with P. brasiliensis .
NFkB is a key transcription factor involved in TLR-mediated innate immunity and together with its repressor Nkrf is an important regulator of the inflammatory process, a powerful protective mechanism coordinated and controlled by cytokines and chemokines. Our data showed an up-regulation of the nkrf gene in the presence of the pulmonary surfactant, suggesting a possible modulation of the innate immune response under conditions of increased PLB activity.
Cytokine production by MH-S cells during host-pathogen interaction
In the course of experimental fungus infection, cell-mediated immunity is critical for host defense . The successful resolution of P. brasiliensis infection depends on a strong Th1 immune response and down-regulation of Th2 cytokine production. The immune response involving a preferential Th1 activation, with IFN-γ production and efficient macrophage activation, is able to control fungal dissemination. IFN-γ production is partly dependent on IL-12 production in macrophages .
Our results demonstrated that the interaction between MH-S and yeast cells, in the presence of PLB, is capable of shaping macrophage activation, compromising the induction of the Th1 response and strongly suggesting a pathogen evasion mechanism.
Fungal PLB exhibits a function related to the regulation of immune responses via the liberation of fatty acid precursors (arachidonic acid, linolenic acid, or eicosanopentaenoic acid) for host eicosanoid synthesis . The production of eicosanoids, potent regulators of host immune responses, including prostaglandins and leukotrienes by fungi in the lungs, may also play a role in modulating the Th1-Th2 balance in the immune response, and may promote eosinophil recruitment or survival of the fungus in the lungs . In-vivo and ex-vivo P. brasiliensis infection has been recently proven to induce leukotriene synthesis, which could explain the low levels of cytokines IL-10, IL-12, and TNF-α, and confirm a pattern capable of interfering in the host response to the fungus . Thus, in the presence of surfactant there is increased activity of PLB, and probably a greater release of substrates for lipid synthesis and production of leukotrienes, which act as suppressors of the innate immune response, confirming the low expression levels of the cytokine tnf-α and il-1 β genes. In the proposed model, the genes related to phagocytosis and oxidative burst are up-regulated providing an efficient mechanism for fungal survival. The increase in IL-12 and decrease in IL-10 after inhibition of PLB participate in the enhancement of IFN-γ activity, which is capable of inducing a cellular immune response. These data confirm the participation of PLB in the mechanism of fungal evasion, interfering with an adequate immune response by the host.
Based on these data, we conclude that P. brasiliensis PLB is important for adhesion and internalization of yeast cells by MH-S cells. Whether PLB activity results from the production of eicosanoids or leukotrienes or not remains unknown, although studies are in progress to investigate this possibility. Nevertheless, our study clearly identified activities of fungal PLB that may enhance virulence and subsequent down-regulation of macrophage activation.
Strains, cultures and reagents
P. brasiliensis Pb18 (ATCC 32069) yeast cells were cultivated in Fava-Netto semisolid medium for 7 days at 37°C and used in in-vitro infection. Alveolar macrophage lineage MH-S (ATCC CRL-2019) was grown in RPMI-1640 tissue culture medium (Sigma-Aldrich, Inc., St. Louis, MO, USA) supplemented with 20 mM HEPES, 1.5 g L-1 sodium bicarbonate, 2.5 mg mL-1 gentamicin, and 10 U mL-1 heparin. The viability of MH-S cells was determined by trypan blue exclusion. All assays used the bovine pulmonary surfactant Survanta (Abbott Laboratories, Inc., Columbus, OH, USA), which is an extract of bovine lung containing about 75% DPPC and 45% phosphatidylcholine (PC), generating substrates for phospholipases. The specific inhibitor of PLB - alexidine dihydrochloride (Toronto Research Chemicals, Inc., Toronto, Ontario, Canada) - was prepared as a stock solution at 10 mM in dimethyl sulfoxide (DMSO), which was then diluted to the required concentration with RPMI medium.
Infection of MH-S cells with P. brasiliensis yeast cells
MH-S cells were seeded in 24-well (0.2 × 105 cells/well) or in 150 cm2 (0.4 × 107 cells/well) cells culture flasks and incubated at 37°C for 6 h. Non-adherent cells were removed by washing, whereas the adherent cells were incubated in RPMI supplemented as stated above, with 10% heat-inactivated fetal calf serum, at 37°C. P. brasiliensis yeast cells were suspended in RPMI medium containing 20% fresh mouse serum. The opsonization protocol was carried out by incubation of yeast cell suspension at 37°C for 30 min. MH-S cell monolayers were infected with 4 × 106 yeast cells, representing a yeast-to-macrophage ratio of 1:5 . Incubation was carried out at 37°C in a humidified 5% CO2 atmosphere.
The influence of PLB on the phagocytic indices was evaluated by adding different concentrations of the surfactant (100 μg mL-1 and 200 μg mL-1) and alexidine dihydrochloride (0.25 μM and 0.50 μM) to the culture medium at the beginning (T0) of the experiments.
We selected a 6-hour period for infection because it represents an early time point of fungal cell internalization by macrophages . After infection, the culture was fixed with methanol and stained with Wright-Giemsa (Sigma-Aldrich, Inc., St. Louis, MO, USA). P. brasiliensis cells were counted in order to evaluate the percentage of attached or internalized yeast cells after infection. Experiments were performed in triplicate, and 12 microscopic fields were assessed. The results are presented as mean ± SEM (standard error of the mean).
Colony forming unit (CFU) determination
The number of viable fungal cells after phagocytosis by MH-S cells was assessed by CFU counts. MH-S cells were challenged with P. brasiliensis yeast cells and incubated for 6 h as described for the phagocytic test. After this time, cultures were rinsed with RPMI to remove non-internalized yeast cells and distilled water was added to lyse the macrophages. The cellular suspension was harvested, washed in phosphate buffered saline (PBS), and the final pellets were resuspended in 1 mL of PBS. Aliquots of 100 μL of each sample were added to agar plates (4% SFB, 5% BHI solid medium) and colonies per plate were counted after 8-10 days of incubation at 37°C.
Total RNA from P. brasiliensis yeast cells internalized by MH-S cells and RNA from MH-S cells were extracted after 6 h of co-cultivation with pulmonary surfactant (100 μg mL-1) and alexidine dihydrochloride (0.25 μM), as well as without treatment (control). Extracellular and weakly adherent fungal cells were removed by washing with pre-warmed RPMI. Macrophages were then lysed with a guanidine thiocyanate-based solution  and intact fungal cells were harvested by centrifugation (8000 × g for 10 min) immediately followed by Trizol total RNA extraction (Invitrogen Corp., Carlsbad, CA, USA) according to the manufacturer's instructions. Total RNA from in-vitro grown P. brasiliensis yeast cells and MH-S cells was also extracted with Trizol, to be used as controls.
Phospholipase B assay
Supernatants were obtained after cell centrifugation at 10000 × g for 15 min and assayed for PLB activity using DPPC as a substrate by the radiometric assay method . The carriers, DPPC (800 mM) and 1,2-di [1-14C] palmitoyl-phosphatidylcholine (20,000 dpm), were dried under nitrogen and resuspended in 125 mM imidazole-acetate buffer, pH 4.0. The reaction was initiated by adding culture supernatant (1 mg of total protein), and after incubation for 30 min the rate of radiolabeled PC loss was measured.
Reaction products were extracted, separated by thin-layer chromatography (TLC), and quantified. Measurements were repeated in three experiments for each treatment and the data were presented as the average of the three. PLB activity was expressed as mM of substrate hydrolyzed per minute, per milligram of protein. Total protein concentrations were measured using the Protein Assay kit (Quant-iT - Invitrogen Corp., Carlsbad, CA, USA). Significance tests were carried out comparing each treatment with the control value (100%) using a one-sample Student's t-test. P < 0.05 was taken as the limit to indicate significance.
Real-time RT-PCR validation of differentially expressed genes
Primers Paracoccidioides brasiliensis used for real time RT-PCR
Forward primer (5'-3')
Reverse primer (5'-3')
Primers for real time RT-PCR to measure gene expression using RNA from alveolar macrophage (MH-S) cells
Forward primer (5'-3')
Reverse primer (5'-3')
The comparative crossing threshold (CT) method, employing the constitutive ribosomal Rps9 macrophage gene or P. brasiliensis α-tubulin gene, was used in order to normalize the expression value of each gene of interest in the macrophage infected sample compared with the non-infected control. Real time RT-PCR experiments were carried out in triplicate for all analyzed genes.
Analysis of cytokine secretion by MH-S cells
Supernatants of co-cultured cells from the different treatments, obtained as described above, were used for the detection of cytokine production. The levels of cytokines IL-10, IL-12, and TNF-α were measured using a commercial ELISA kit (BD Biosciences, San Diego, CA, USA) according to the manufacturer's guidelines. The cytokine levels in the supernatant from MH-S cells were calculated based on a standard curve provided with the commercial kit. Data are expressed as mean ± SEM.
Statistical comparisons were performed by the paired 2-tailed Student's t-test. All values are reported as mean ± SEM, with significance assumed at p < 0.05.
We are most indebted to H. R. Muller for helping with the experiments. This work was supported by CNPq. DAS received a grant from CAPES.
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