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Open Access

Peer-reviewed

Research Article

Toxoplasma gondii Proliferation Require Down-Regulation of Host Nox4 Expression via Activation of PI3 Kinase/Akt Signaling Pathway

  • Wei Zhou ,

    Contributed equally to this work with: Wei Zhou, Juan-Hua Quan, Young-Ha Lee

    Affiliation Department of Infection Biology, Chungnam National University School of Medicine, Daejeon, Korea

    ⨯
  • Juan-Hua Quan ,

    Contributed equally to this work with: Wei Zhou, Juan-Hua Quan, Young-Ha Lee

    Affiliations Department of Infection Biology, Chungnam National University School of Medicine, Daejeon, Korea, Department of Gastroenterology, The Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong, China

    ⨯
  • Young-Ha Lee ,

    Contributed equally to this work with: Wei Zhou, Juan-Hua Quan, Young-Ha Lee

    Affiliation Department of Infection Biology, Chungnam National University School of Medicine, Daejeon, Korea

    ⨯
  • Dae-Whan Shin,

    Affiliation Department of Infection Biology, Chungnam National University School of Medicine, Daejeon, Korea

    ⨯
  • Guang-Ho Cha

    gcha@cnu.ac.kr

    Affiliation Department of Infection Biology, Chungnam National University School of Medicine, Daejeon, Korea

    ⨯

Abstract

Toxoplasma gondii results in ocular toxoplasmosis characterized by chorioretinitis with inflammation and necrosis of the neuroretina, pigment epithelium, and choroid. After invasion, T. gondii replicates in host cells before cell lysis, which releases the parasites to invade neighboring cells to repeat the life cycle and establish a chronic retinal infection. The mechanism by which T. gondii avoids innate immune defense, however, is unknown. Therefore, we determined whether PI3K/Akt signaling pathway activation by T. gondii is essential for subversion of host immunity and parasite proliferation. T. gondii infection or excretory/secretory protein (ESP) treatment of the human retinal pigment epithelium cell line ARPE-19 induced Akt phosphorylation, and PI3K inhibitors effectively reduced T. gondii proliferation in host cells. Furthermore, T. gondii reduced intracellular reactive oxygen species (ROS) while activating the PI3K/Akt signaling pathway. While searching for the main source of these ROS, we found that NADPH oxidase 4 (Nox4) was prominently expressed in ARPE-19 cells, and this expression was significantly reduced by T. gondii infection or ESP treatment along with decreased ROS levels. In addition, artificial reduction of host Nox4 levels with specific siRNA increased replication of intracellular T. gondii compared to controls. Interestingly, these T. gondii-induced effects were reversed by PI3K inhibitors, suggesting that activation of the PI3K/Akt signaling pathway is important for suppression of both Nox4 expression and ROS levels by T. gondii infection. These findings demonstrate that manipulation of the host PI3K/Akt signaling pathway and Nox4 gene expression is a novel mechanism involved in T. gondii survival and proliferation.

Citation: Zhou W, Quan J-H, Lee Y-H, Shin D-W, Cha G-H (2013) Toxoplasma gondii Proliferation Require Down-Regulation of Host Nox4 Expression via Activation of PI3 Kinase/Akt Signaling Pathway. PLoS ONE 8(6): e66306. https://doi.org/10.1371/journal.pone.0066306

Editor: Ira J. Blader, University of Oklahoma Health Sciences Center, United States of America

Received: January 17, 2013; Accepted: May 3, 2013; Published: June 18, 2013

Copyright: © 2013 Zhou 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 the Basic Science Research Program through the National Research Foundation of Korea funded by the Ministry of Education, Science, and Technology (2007-0054932, 2009-0068747, 2011-0006228, 2011-0023501) and Korea Health Technology Research & Development Project, Ministry of Health & Welfare, Republic of Korea (A100876-1102-0000100). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors have declared that no competing interests exist.

Introduction

Toxoplasma gondii is one of the most widespread zoonotic pathogens in the world. The tachyzoite is a rapidly dividing haploid form of T. gondii that can infect a wide range of mammalian host cells, including immune and non-immune cells [1], [2]. Inside the host cell, parasites reside within a specialized parasitophorous vacuole (PV) that resists endosomal acidification and lysosomal fusion, and these parasites exhibit rapid intracellular replication, redistributes host intracellular organelles and cytoskeleton, and modulates host cell gene expression [3] in the PV. T. gondii is an obligate intracellular parasite that competes with host cells for metabolites, such as glucose, lipids, and amino acids, as well as nucleotides for its survival [4]. To win this fierce competition for survival, the parasite displays a highly sophisticated ability to distort host responses and their underlying signal transduction cascades. However, the cellular factors involved in its intracellular replication are not well defined.

Recently, several reports demonstrated that the host PI3K/Akt signaling pathway is stimulated by T. gondii infection [5]. PI3K is a ubiquitously expressed enzyme that is responsible for the regulation of various intracellular processes, such as insulin-dependent cell growth, membrane trafficking, and endosome fusion [6]. The serine/threonine protein kinase B (PKB)/Akt is one of the major downstream targets of PI3K and is a central player in growth regulation of cells [7]. Phosphorylation at Ser473 and Thr308 activates the kinase activity of Akt, which regulates multiple cellular processes that increase metabolism, growth, and synthetic processes and suppress apoptosis [8]. PI3K/Akt signaling plays an important role in T. gondii invasion of host cells because phosphatidylinositol (3, 4, 5)-trisphosphate (PIP3) rapidly accumulates in host cells in response to infective tachyzoites and more importantly, PI3K inhibitors partially reduce parasite entry [9], [10]. Another study showed that excretory/secretory proteins (ESP) from T. gondii play an important role in generating suitable conditions for parasite invasion into host cells [11].

Ocular toxoplasmosis is an inflammatory process that involves the interior of the eye and is caused by infection with T. gondii. This disease is the most common posterior uveitis in immunocompent individuals [12]. Although ocular toxoplasmosis usually consists of a self-limited retinochoroiditis, sight-threatening complications occur, and this disease is the foremost cause of unilateral vision loss in patients with uveitis [13]. The intensity of damage to the retina and choroid depends on the severity of infection and associated inflammatory reaction. In the most severe form of T. gondii-induced uveitis, degeneration of large segments of the outer retina and pigment epithelium are often observed [14].

The retinal pigment epithelium (RPE) forms a single-cell layer between the retinal photoreceptors and the vascular-rich choroids, thereby forming the blood-retinal barrier. RPE normally functions under relatively high oxygen tensions in postnatal life. Several animal models showed that T. gondii tachyzoites reach the retina via both choroidal and retinal circulation. Upon injection of tachyzoites into the suprachoroidal space in rabbits, outer retinal lesions and localized foci of retinal pigment epitheliosis were observed within 48 h [15]. This result suggests that tachyzoites penetrate the RPE-Bruchs membrane barrier from the choroid to the retina. Histopathological examination of toxoplasma retinochoroiditis patients showed the presence of free tachyzoites and cysts in the RPE and the retina [16]. These reports support the idea that RPE is one of the preferred infection sites for T. gondii, although whether the RPE is an ideal environment for T. gondii survival and proliferation is not known. Therefore, in the present study, we used a human RPE cell line (ARPE-19) as a model for ocular toxoplasmosis to study host defense in response to parasite invasion and intracellular replication.

Reactive oxygen species (ROS), which occurs as byproducts of metabolic reactions, normally participate in various cellular physiological events. ROS regulate certain essential signaling pathway, targeting Akt [17], NF-κB [18] and MAPK [19], etc. However, ROS are chemically reactive and therefore, can easily damage DNA, lipids, and proteins when present at high concentrations. Therefore, high levels of ROS are a well-known cause of oxidative damage in eye disorders including age-related macular degeneration (AMD) and uveitis [20]. To the contrary, this hazardous effect of ROS is an important component of the innate immune defense response of immune cells and is utilized to cope with infectious pathogens from the outside environment. In phagocytes, the rapid ROS production, which is termed “oxidative burst”, is one of the earliest cellular responses to infection. Apoplastic generation of superoxide (O2−) or its dismutation product hydrogen peroxide (H2O2) can kill invading T. gondii in vitro and in vivo [21]. A variety of nonphagocytic cells also possess superoxide-producing enzymes, which generate low levels of ROS in response to various extracellular stimuli [22], [23]. Notable, RPE itself and its neighboring photoreceptors produce considerable ROS, because of photochemical reactions that converts light energy to chemoelectrical signals [24].

The sources of ROS include NADPH oxidases, the mitochondria electron transport chain, xanthine oxidase, and endothelial nitric oxide synthase [23], [25]. Although these enzymes contribute to the oxidative burden, evidence suggests that NADPH oxidase is the main enzymatic source of ROS production in human RPE cell lines [26]. Recent studies have demonstrated that NADPH-dependent oxidative stress induces apoptotic signaling pathways in RPE cells and that NADPH oxidase is mechanistically involved in the pathogenesis of some types of retinal degeneration in vivo [27]. NADPH oxidase activity occurs in all cells of the vascular wall, but the distribution of the subunits of this enzyme is cell-specific. The family of NADPH oxidases (Nox/Duox) consists of Nox1, Nox2 (gp91phox), Nox3, Nox4, and Nox5 as well as Duox1 and Duox2 [23].

In the present study, we provide evidence that activation of the host cell PI3K/Akt pathway by T. gondii infection contributes to the replication of this parasite. Nox4 is the primary source of sustained ROS in RPE cells and thereby is the main target used by T. gondii to disarm the oxidative immune system of the host cell for its benefit.

Materials and Methods

Reagents and Antibodies

Akt and Phosphospecific Akt (Ser473) antibodies were obtained from Cell Signaling Tech., Inc. (Beverly, MA, USA). Anti-Nox4 was obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Monoclonal anti-actin, HRP-conjugated anti-rabbit and anti-mouse secondary antibodies were purchased from Jackson ImmunoResearch Laboratories (West Grove, PA, USA). PI3K inhibitors, LY294002 and wortmannin, were obtained from Sigma (St. Louis, MO, USA) and PI3K-specific inhibitors, GDC-0941 and ZSTK474, were purchased from Selleck Chemical. Co.

Cell Culture

Human retinal pigment epithelial cells, ARPE-19 (ATCC, Manassas, VA, USA), were cultured in a 1∶1 mixture of DMEM and nutrient mixture F12 (DMEM/F12) supplemented with 10% heat-inactivated FBS and antibiotic–antimycotic reagents (all from Life Technologies Corporation, CA, USA). One day before treatment, the culture medium was changed to DMEM/F12 medium without FBS.

Parasites

Tachyzoites of T. gondii RH strain that expresses transgenic green fluorescent protein (GFP-RH) were kindly provided by Dr. Yoshifumi Nishikawa (Obihiro University of Agriculture and Veterinary Medicine, Japan). ARPE-19 cells were infected with the GFP-RH strain of T. gondii (parasite:cell ratio = 5∶1) and incubated at 37°C and 5% CO2 for 2–3 days. Following spontaneous host cell rupture, parasites and host cellular debris were washed in cold PBS. After centrifugation, the final pellet was resuspended in cold DMEM/F12, and the resuspension was passed through a 26-gauge needle and a 5.0-µm pore filter (Millipore, Billerica, MA, USA).

Preparation of ESP

Purified tachyzoites (3 × 108) were incubated at 37°C for 1 hr under mild agitation in 0.5 ml Hank’s balanced salt solution (HBSS) (Gibco BRL, Rockville, MD, USA). After centrifugation for 5 min at 6,000 rpm, the supernatant containing ESP was saved. The protein concentration was determined with Bradford assay method using BSA as the standard, and samples were stored at −70°C until use.

Mycoplasma and Endotoxin Detection Assay

To assess mycoplasma and endotoxin levels in the different samples, commercial EZ-PCR Mycoplasma Test kit (Biological Industries, Beit Haemek, Israel) and quantitative chromogenic method (Pierce LAL (Limulus amebocyte lysate) Chromogenic Endotoxin Quantification Kit (Thermo Scientific Co, PO)) were used. The Limulus amebocyte lysate contains an enzymatic system that is activated in the presence of endotoxin. The lower limit of detection of this assay is 0.1 EU/ml. No contamination of mycoplasma or endotoxin was detected in cell or parasite culture systems (Fig. S1).

Immunoblot

ARPE-19 cells were grown in 6-well plates and were serum starved overnight to remove any stimulation from serum factors. Cells were infected with tachyzoites or treated with ESP as indicated. After the cells were washed with ice cold PBS, proteins were extracted with PRO-PREP Protein Extraction Solution (iNtRON Biotechnology, Korea) and then incubated on ice for 20 min followed by centrifugation for 5 min at 13,000 rpm at 4°C. Equal amount of protein from each sample were loaded onto a 12% SDS-PAGE gel and separated by electrophoresis. Proteins were then transferred to a polyvinylidene fluoride (PVDF) membrane. Membranes were blocked with 5% nonfat skim milk in TBS containing 0.1% Tween 20 (TBST) for 1 h at room temperature. After being washed once in TBST, membranes were incubated with primary antibody diluted in TBST supplemented with 5% BSA for 2 h at room temperature or overnight at 4°C. After three washes with TBST, membranes were incubated with HRP-conjugated secondary antibody (Jackson ImmunoResearch Laboratories, Inc., USA) for 2 h at room temperature. After three washes with TBST, protein bands were visualized by an ECL chemiluminescence kit (Amersham Biosciences, Freiburg, Germany) according to the manufacturer’s instructions. The bands were scanned and quantified using an imaging densitometer (Bio-Rad Laboratories, Inc., Hercules, CA, USA).

Proliferation of T. gondii

ARPE-19 cells were cultured in 24-well plates containing glass coverslips and serum-starved overnight prior to infection with T. gondii at a multiplicity of infection (moi) of 5. Some sets of cells were pretreated with PI3Kinase inhibitors for 1 h and then rinsed 3 times with PBS before infection with T. gondii. In order to “synchronize” the T. gondii replication starting point, we have designed very narrow window for T. gondii infection (2 h infection then wash off free-, uninfected-T. gondii). By this process, we were also able to eliminate the side effect from secreted ESP of free-, uninfected T. gondii and possible invasion rate difference can be ignored, because the proliferation rate of only “infected” T. gondii was measured.

After 24 h of incubation, the coverslips were washed with PBS and then fixed with 4% formaldehyde. Cells were stained with Texas Red®-X phalloidin (Life Technologies Corporation, CA, USA) to label F-actin and mounted on slides using mounting medium with DAPI (Vector Laboratories, USA). Cells were then imaged using fluorescence microscopy or confocal microscopy. One to two hundred PVs were randomly selected in each preparation, and parasite replication was monitored by counting the number of tachyzoites per PV. Three separate experiments were performed for statistical analysis of the results.

Fluorescence Microscopy

ARPE-19 cells were cultured in 24-well plates containing glass coverslips overnight and then infected with GFP-RH tachyzoites for 23 h or with ESP for 1 h. Cells were then exposed to 100 µM H2O2 (Sigma Chemical Co) for 1 h. Following washing with HBSS, cells were incubated with 10 µM ROS-sensitive dye dihydroethidium (DHE; Life Technologies Corporation) for 30 min at 37°C in the dark. The stained cells were imaged using an Olympus BX-51 fluorescence microscope. All images of the DHE staining were taken using the same exposure time.

Flow Cytometry

Cell were cultured in 6-well dishes and treated with ESP according to the experimental design. The cultured cells were stained with 10 µM DHE and washed with HBSS. Cells were trypsinized and centrifuged. Then cells were resuspended in HBSS and analyzed on a FACS (BD Biosciences, San Diego, CA).

NADPH Oxidase Expression Analysis by RT-PCR

Total RNA from stimulated cells was prepared using the Trizol reagent (Invitrogen, Carlsbad, CA, USA), and RNA was reverse transcribed using ReverTra Ace RT kit (Toyobo, Osaka, Japan). All PCR reactions were performed with a MyCycler (Bio-Rad) for 25 cycles. The Nox1-4 and p22phox primer sequences for RT-PCR were described by Claudia Piccoli et al. [28]. Nox5 RT-PCR primer sequences were described by Chou et al. [29]. The other primer sequences (5′-3′) are as follows: Duox1 forward, ATCAATCGGAACTCAAGTGTCTC; Duox1 reverse, AACCAACACATGGTCCTCTCG; Duox2 forward, GCTACCATGTTCTTTCCGACG; and Duox2 reverse, GAGTGCGAGGAGCCATAGAT. Amplified products were electrophoresed in a 2% agarose gel and visualized with ethidium bromide. The relative intensity of bands for each mRNA was related to the intensity of the autoradiogram band of the internal control, GAPDH. Quantification of mRNA was performed using an imaging densitometer (Bio-Rad Laboratories, Inc.).

siRNA Transfection

Two different duplex sequences against human Nox4 were used as Weyemi et al. reported [30]. Cells were transfected with siRNA duplexes specific for human Nox4, using LipofectamineTM RNAiMAX (Life Technologies Corporation) according to the manufacturer’s protocol. Briefly, cells were seeded in 6-well plates, grown for 24 h (70% confluence), and then transfected with 6–24 nM Nox4-specific siRNA or negative control siRNA (Santa Cruz, CA) for 48 h. Then, cells were infected with T. gondii for 24 hours, and then T. gondii proliferation was evaluated. The knockdown efficiency was determined by RT-PCR and western blot.

Statistical Analysis

The data were analyzed using GraphPad Prism data analysis program. For the comparison of statistical significance between two groups, independent sample Student’s t-test was used. For multiple comparison, one-way ANOVA followed by post hoc comparisons of the group means according to the method of Tukey was used. P-values <0.05 were considered significant.

Results

Activation of Host PI3/Akt by T. gondii Infection and ESP Treatment

As an intracellular parasite, T. gondii relies on the growth environment provided by the host cell. The serine/threonine kinase Akt plays a central role in growth regulation of cells, and its activity is regulated by phospholipid binding and activation phosphorylation at Thr308 by PDK1 and by phosphorylation within the carboxy terminus at Ser473 [31]. To identify intracellular signaling mechanisms of the host cell that are responsible for the proliferation of T. gondii, we determined whether T. gondii infection induces Akt phosphorylation in ARPE-19 cells using immunoblot analysis with phosphospecific Ser473 Akt antibody. In addition, the effects of T. gondii ESP on Akt signaling were examined as well. ESP plays an essential function to provide appropriate environment for the entry of the parasite into host cell [11].

To minimize basal Akt activity, these experiments were performed in serum-starved cells. After T. gondii infection for 24 h or ESP stimulation for 1 h, cells were collected for immunoblot analysis to measure host Akt activation. The ratios between the intensities of phosphorylated Akt and total Akt in the infected and stimulated samples compared with those in the uninfected or unstimulated samples as determined by densitometric analysis are shown in Fig. 1A and, B. Phosphorylation of Akt occurred in cells infected with T. gondii for 24 h, and host Akt activity was significantly increased according to the number of T. gondii per infected cell. ESP also increased Akt phosphorylation in a dose-dependent manner, and this finding is consistent with the T. gondii infection experiment. Host cell ciability was tested with MTT assay and proved that viability of ARPE-19 was not significantly reduced by T. gondii infection (moi 15) after 24 h (Fig. S2A).

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Figure 1. T. gondii and ESP activate the PI3K/Akt pathway in ARPE-19 cells.

ARPE-19 cells were deprived of serum for 1 day before use in subsequent experiments. (A) Cells were infected with GFP-RH tachyzoites at the indicated moi for 24 h. Two hours after infection, the extracellular tachyzoites were immediately removed by washing with PBS and then incubated in the absence of serum media for 22 h. (B) Cells were stimulated for 1 h with various concentrations of GFP-RH tachyzoites ESP ranging from 0.1 to 10 µg/ml. (C) ARPE-19 cells were infected with T. gondii (moi 15) for 24 h and treated with increasing concentrations of LY294002 for the final 1 h. (D) Cells were pretreated with wortmannin for 1 h, and then after washing, cells were stimulated with 1 µg/ml ESP for 1 h. Whole cell lysates were collected and analyzed by western blot using primary antibodies against phospho-Akt and total Akt. Akt phosphorylation levels were calculated as the ratio of untreated control cells after normalization to the amount of total Akt. (E) Cells were infected at moi of 15 for 23 h and then treated with either inhibitor for 1 h. Values represent the mean ± SD values of triplicates. Data are representative of three independent experiments. * denotes p<0.05 and indicates that differences were considered significant.

https://doi.org/10.1371/journal.pone.0066306.g001

As T. gondii infection resulted in Akt phosphorylation in the host ARPE-19 cell, we analyzed the impact of T. gondii infection or ESP treatment on an upstream component of Akt signaling. Wortmannin and LY294002 are well-known inhibitors for PI3K, which is the upstream activator of Akt. We examined whether blocking host cell PI3K activation results in inhibition of T. gondii-induced Akt phosphorylation. ARPE-19 cells were infected with T. gondii for 24 h and treated with LY294002 during the final 1 h. Indeed, sequential increases in LY294002 concentration led to inhibition of the T. gondii infection-induced Akt phosphorylation (Fig. 1C). In a similar manner, pretreatment with wortmannin blocked Akt phosphorylation induced by T. gondii ESP treatment (Fig. 1D). Although wortmannin and LY294002 are well-known inhibitor for PI3K, it is also known that they are not specific to PI3K and can inhibit mTOR pathway. In order to confirm that PI3K/Akt pathway is indeed involved in T. gondii induced events, GDC-0941 and ZSTK474 were tested for their effect on T. gondii induced host cell response, GDC-0941 and ZSTK474 successfully inhibited Akt phosphorylation by T. gondii in a dose-dependent manner (Fig. S3) but S6 phosphorylation which is under control of mTOR was not affected (Fig. 1E). These results suggest that T. gondii and ESP activate host Akt in a PI3K-dependent manner.

Roles of Akt/PKB Signaling in Intracellular T. gondii Proliferation in the Host

Several independent lines of evidence indicate that T. gondii infection renders cells resistant to proapoptotic stimuli [32]. This effect is presumed to be beneficiary to T. gondii survival and proliferation in the host cell. Following phosphorylation by activating kinases, Akt affects multiple cellular targets that increase metabolism, growth, and synthetic processes and suppress apoptosis [33]. T. gondii, as an intracellular parasite, relies on the growth environment provided by the host. As a result, we initially investigated the effect of PI3K inhibitors on T. gondii proliferation in ARPE-19 cells. Statistically significant inhibition of T. gondii growth and proliferation by LY294002 and wortmannin was detected (Fig. 2). The numbers of tachyzoites in ARPE-19 cells, which had been pre-incubated with PI3K inhibitors for 1 h, washed, and then infected with T. gondii at an moi of 5, were counted 24 h post-infection. Without inhibitor pretreatment, most tachyzoites divided two times to generate four parasites per PV. PI3K-specific inhibitors, GDC-0941 and ZSTK474, also showed similar effect as LY294002 and wortmannin on T. gondii proliferation that inhibition of the PI3K/Akt pathway reduced the rate of T. gondii division, and most PVs only contained one or two T. gondii. Proliferation rate observation at different time point (12 h) also showed that PI3K inhibitors delay the proliferation of T. gondii compared to untreated (Fig. S2B). These results suggest that T. gondii-induced PI3K/Akt signaling is important for T. gondii proliferation in the host cell.

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Figure 2. PI3K inhibitors inhibited T. gondii proliferation in ARPE-19 cells.

The proliferation of tachyzoites in ARPE-19 cells was examined by fluorescence microscopy. Cells were pre-incubated with PI3K inhibitors, either 10 µM LY294002, 200 nM wortmannin (A), or 250 nM GDC-0941, 10 nM ZSTK474 (B) for 1 h. After washing, the cells were then infected with T. gondii at moi of 5 for 24 h. Cells were fixed and stained with Texas Red®-X phalloidin for labeling F-actin (red), and nuclei were stained with DAPI (blue). The number of parasites per vacuole were counted and converted to percentage. Data are representative of three independent experiments. Scale bar = 100 µM.

https://doi.org/10.1371/journal.pone.0066306.g002

Finally, given that the presence of mycoplasma and endotoxin could affect PI3K signaling and response to ROS, we quantified the levels of mycoplasma and endotoxin in the culture medium, cell, parasite and ESP. The results were shown in Figure S1 that no contamination detected in our experimental systems.

T. gondii-induced Activation of Host PI3K/Akt Signaling Pathway Reduced Intracellular ROS Levels of ARPE-19 Cells Under Oxidative Stress

The host cell generates various threats to attack parasite infection, and production of ROS is one very effective way to kill the infiltrators [21]. Since the PI3K/Akt pathway is involved in cell survival signaling and is important for T. gondii proliferation, we studied the effect of host PI3K/Akt signaling induced by T. gondii against H2O2 oxidative stress in ARPE-19 cells. ARPE-19 cells were stimulated with 100 µM H2O2 and then labeled with the cell-permeable fluorescent dye DHE as a cytosolic superoxide indicator. Intracellular levels of ROS were analyzed by fluorescent microscopy. The positive control, which received only H2O2 treatment, exhibited high DHE fluorescent signal. However, T. gondii infection or ESP treatment markedly reduced the host cytosolic ROS even in the presence of H2O2 treatment (Fig. 3A, B). Intriguingly, additional treatment with the PI3K inhibitors wortmannin, LY294002, GDC-0941 or ZSTK474 blocked the reduced ROS level induced by T. gondii infection or ESP treatment (Fig. 3A, B).

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Figure 3. T. gondii and ESP inhibited H2O2-induced ROS generation via activation of PI3K/Akt signaling.

Fluorescence microscopy images of cells stained with 10 µM DHE and treated with different conditions. ARPE-19 cells were infected with GFP-RH for 23 h (A, B), or ARPE-19 cells were stimulated with ESP for 1 h (C, D). These cell were exposed to 100 µM H2O2 with or without inhibitor for 1 h. The ROS level change by ESP and PI3K inhibitors under oxidative stress (H2O2) were quantitatively analyzed by flow cytometry (E). Results are representative of three independent experiments. * denotes p<0.05, and these differences were considered significant. Scale bar = 100 µM.

https://doi.org/10.1371/journal.pone.0066306.g003

Additionally, the flow cytometry were performed to quantitatively analyze the effect of ESP and PI3K inhibitors on host intracellular ROS level after H2O2 treatment (Fig. 3C). Flow cytometrical analysis with T. gondii infected cell was excluded because it is found that T. gondii itself can be strongly labeled by DHE (Fig. 3 and Fig. S4), and it interfered the reading the fluorescence intensities of DHE labeled- host cell cytoplasm by FACS. These results suggest that activation of host Akt/PKB signaling by T. gondii provides a protective function for infected T. gondii by blocking the ROS-dependent host defense system.

T. gondii ESP-induced Activation of Host PI3K/Akt Signaling Pathway Reduced Basal Intracellular ROS Levels of ARPE-19 Cells

Next, we tested whether ESP can reduce the basal ROS level of host cell (H2O2 untreated) into even lower level. Because it is reported that oxidative stress in ARPE-19 cells can activates mTOR signaling pathway [34], we wanted to test the ROS-reducing ctivity of ESP under the condition which possible side effect of H2O2 is minimized. Flow cytometric analysis indicated an approximately 50% decrease in ROS levels 5 h after 1 µg/ml ESP treatment (Fig. 4). This result was in agreement with the fluorescent microscopy analysis, indicating that the host intracellular ROS decreased markedly after T. gondii infection (Fig. 3B).

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Figure 4. T. gondii ESP decreased endogenous ROS levels in ARPE-19 cells.

(A) Cells were stimulated with ESP for 1 h and then incubated with PI3K inhibitors for 1 h. Intracellular superoxide was measured by DHE staining followed by flow cytometry. (B) Relative fluorescence intensity of the population of DHE-stained cells corresponding to A. The results are expressed as mean ± SD of three independent experiments. * denotes p<0.05, and these differences were considered significant.

https://doi.org/10.1371/journal.pone.0066306.g004

Next, we examined whether PI3K inhibitors blocked the ROS reduction by T. gondii ESP treatment in ARPE-19 cells. As expected from the previous results, the decrease in ROS induced by T. gondii ESP 5 h after treatment was almost completely reversed by incubation with LY294002, wortmannin, GDS-0941 or ZSTK474 (Fig. 4). Taken together, these data indicate that infection with T. gondii stimulates host PI3K/Akt signaling to suppress ROS generation and that this process may play an important role in the survival and proliferation of infected T. gondii.

T. gondii Targets Nox4 to Decrease Host ROS Levels via Activation of PI3K/Akt Signaling

Since T. gondii infection activated PI3K/Akt signaling and intracellular ROS levels were significantly reduced under both unstressed conditions and oxidative challenge, we sought to identify the ROS generator that is under control of PI3K/Akt signaling. Our experiments indicated the presence of a major oxidase to generate ROS, which may suppress T. gondii replication in host cells. To explore this idea, the mRNA levels of Nox/Duox family of ROS-generating NADPH oxidases were examined in ARPE-19 cells by RT-PCR. Nox4 was abundantly expressed in ARPE-19 cells, whereas the expression levels of the other Nox and Duox oxidases were undetectable (Figure S5). Interestingly, expression of Nox4 and its functional partner p22phox were suppressed by T. gondii infection in a moi-dependent manner. Also, PI3K inhibitor treatment experiment revealed that Nox4 gene expression was regulated by the PI3K/Akt signaling pathway (Fig. 5A). To confirm that the Nox4 protein level was decreased in agreement with the decrease in its mRNA level, immunofluorescence and immunoblot analysis were performed using anti-Nox4-specific antibody. Indeed, the Nox4 protein level was significantly reduced after T. gondii ESP treatment for 5 h (Fig. 5B, C). These findings demonstrated that T. gondii specifically suppresses host Nox4 gene expression via the PI3K/Akt signaling pathway in ARPE-19 cells.

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Figure 5. T. gondii and ESP suppressed host Nox4 expression via the PI3K/Akt pathway.

(A) RT-PCR analysis of the host Nox4 and P22phox mRNA levels in ARPE-19 cells. GAPDH was used as an internal control. (B) Cells were stimulated with 1 µg/ml ESP for the indicated times. Nox4 protein levels were analyzed by western blot, and β-actin was used as a loading control. (C) Immunocytochemistry of Nox4 in the ESP-stimulated cells. ARPE-19 cells were stimulated with 1 µg/ml ESP for 5 h. Cells were subsequently stained with anti-Nox4 antibody (green) and Texas Red®-X phalloidin for labeling F-actin (red). Nuclei were stained with DAPI (blue). The results are expressed as mean ± SD of three independent experiments. Scale bar = 100 µM. * denotes p<0.05, and these differences were considered significant.

https://doi.org/10.1371/journal.pone.0066306.g005

Nox4 Expression is Important for T. gondii Intracellular Replication

Experiments using specific siRNA duplexes to silence Nox4 expression in ARPE-19 cells were performed to determine whether Nox4-dependent production of ROS is important for intracellular replication of T. gondii. A series of candidate siRNA molecules was transfected into ARPE-19 cells for 48 h, and Nox4 protein levels were determined by immunoblot using a rabbit antibody raised against Nox4 (Fig. 6A). Both siRNA2 and siRNA3 (24 nM) consistently resulted in a 75–85% decrease in Nox4 protein expression, and thus, these siRNAs were selected for use in subsequent experiments. Intracellular ROS levels in ARPE-19 cells were significantly reduced by more than 40% following transfection with Nox4 siRNA, demonstrating that Nox4 plays a important role in the production of ROS in ARPE-19 cells (Fig. 6B).

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Figure 6. Nox4 gene knockdown promoted T. gondii replication.

ARPE-19 cells were transfected with Nox4-specific siRNA for 48 h. (A) Nox4 knockdown efficiency was determined by western blot. (B) Intracellular ROS levels were measured by flow cytometry after DHE staining. (C) ARPE-19 cells transfected with control siRNA or specific Nox4 siRNAs were infected with T. gondii for 24 h, and fluorescence micrographs of intracellular tachyzoite replication 24 h post-infection were obtained. The results are expressed as mean ± SD of three independent experiments.

https://doi.org/10.1371/journal.pone.0066306.g006

To determine the role of Nox4 in T. gondii proliferation, ARPE-19 cells, which were incubated 48 h after transfection with Nox4 siRNA, were infected for another 24 h with T. gondii, and the proliferation of T. gondii was evaluated under fluorescence microscope (Fig. 6C). In untranfected cells and in control siRNA treated cells, the PVs with 8 tachyzoites are approximately 40% of total PV population; however, in Nox4 siRNA-transfected cells, more than 50% of PVs contained 8 tachyzoites and even PVs with 16 tachyzoites (approx 10%) were observed after 24 h infection, demonstrating accelerated replication of T. gondii in these cells. These results indicated that infection with T. gondii suppresses the gene expression of Nox4 in host cells to reduce ROS generation and to generate a favorable intracellular environment for T. gondii growth and proliferation.

Discussion

It is common to find cysts and tachyzoites in the retina of T. gondii infected patients. Necrotic lesions are often observed which come with degeneration of the neuronal retina and choroids structure (retinochordoiditis) [35]. Mouse model studies have reported that retinal lesions are the results of inflammation reaction caused by mononuclear cells at the site of infection. Although, T. gondii favorably infiltrate and reside in the eye structures, for example, retinal pigment epithelium (RPE) to show dramatic symptoms, it is known that eye is an immune privileged organ which is protected from immune mediated inflammation and damage by various mechanisms [36]. The cells of the retinal pigment epithelium play important role in the physiology of the retina by recycling light-induced all-trans-retina from photoreceptor cells into 11-cis-retina and providing functional photopigments back to photoreceptors, and by eliminates oxidatively damaged materials from photoreceptors [24]. This means that RPE cells are basically prone to oxidative stress and capable to produce reactive oxygen species under certain condition [37]. For example, exposure to bright light may generate free radical and increase ROS production, which further induces oxidative stress in RPE cells [38]. Based on these facts, we tried to reveal how T. gondii’s survived and proliferate in such harsh condition.

T. gondii, like many other pathogens, forms a membranous vacuole to reside in when it infiltrates into host cell in order to avoid lysosomal attack from the host cell. The parasitophorous vacuolar membrane (PVM) itself works as physical barrier but also in order to increase their survivability, various signal related events occurs around the PVM. It has been reported that ADP-ribosylation factor-6 (ARF6) activate PI3K and recruit PIP(2) and PIP(3) to parasitophorous vacuole of invading parasites [39]. Other studies also showed that upon infection with T. gondii, host PI3K/Akt pathway was activated, and this activation was required for host cell resistance to apoptosis [32], and Akt activation was also required for T. gondii to coordinate control of host centrosome position, organelle distribution, and migratory response [40]. These reports suggest that host PI3k/Akt pathway is one major target for T. gondii to modify and utilize for its own beneficial events.

Our new finding is that PI3K/Akt signaling pathway activation is essential for intracellular T. gondii proliferation. In order to examine the intracellular tachyzoite replication rate, the replication number of GFP-labeled-T. gondii in each PV was monitored by fluorescent microscopy. This method was also useful to exclude the multi-infected T. gondii and count exact number of each T. gondii in each PV (More useful than FACS which just measuring the intensity of GFP to evaluate the number of T. gondii).

Most of intracellular tachyzoites divides twice to generate four individuals 24 h after infection. Inhibition of PI3K/Akt pathway by pre-treatment of LY294002 and wortmannin significantly reduced its dividing rate that T. gondii replication occurred only once after 24 h infection to generate two parasites in one PV compare to untreated control groups. These data suggest that PI3K/Akt signaling pathway activation by T. gondii is important for its proliferation against host innate immune defense system.

GDC-0941 inhibits all class 1 PI3K isoforms but does not significantly suppress the activity of any other lipid or protein kinase tested including mTOR [41]. ZSTK474 is known as an ATP-competing inhibitor of PI3K, and the inhibitory activity of ZSTK474 is even isoform-specific [42]. To the contrary, it is reported that even at a concentration of 100 µM, ZSTK474 inhibited mTOR activity rather weekly. The unique properties of GDC-0941 and ZSTK474, specific inhibition on PI3K activity but non-inhibitory effect on mTOR, were also confirmed by ourselves (Fig. 1E) and the experiments with these PI3K- specific inhibitors provided us more confidence on our hypothesis that PI3K/Akt pathway rather than mTOR pathway is important in regulation of host ROS and later Nox4 expression by T. gondii.

For the next step, we focused on unknown, underlying host mechanism which might hinder the infected T. gondii from its growth. It has long been known that ROS plays essential role in innate immune responses against pathogens, such as bacteria or intracellular parasites, through the production of superoxide by reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. Because of that, in the view of intracellular parasites, reducing, removal or intoxicating the intracellular ROS is the urgent requirement for their survival and proliferation [20]. It has been reported that proliferation of T. gondii can diminish oxygen radical production in the macrophage cell in vivo, but the most of the mechanisms and pathways related to the event is not fully understood yet [43].

Our data clearly showed that not just T. gondii only, but ESP also can reduce the host ROS level in the presence or absence of oxidative stress stimuli condition. Surprisingly, treatment of PI3K inhibitors significantly suppressed the T. gondii or ESP activity to reduce host ROS level. By combining these two results, we were able to deduce a hypothesis that for the T. gondii proliferation in RPE, ROS level reduction in host cell is important and this environmental regulation is achieved by activating host PI3K/Akt signaling pathway.

When we started the T. gondii-involved host ROS regulation study, it was our plan to combine data from immunocytochemistry and FACS analysis was used in order to cross-check the results from each experiments, respectively. Though, T. gondii itself contains large amount of ROS inside and T. gondii infected cell was therefore, not suitable for FACS analysis. In order to detour the problem, treatment of ESP to ARPE cell, instead of infecting live T. gondii, was established as a very useful model system to study the action of parasite infection on host ROS level modulation.

Next, all these data strongly suggests that T. gondii induced signal activation has specific target to reduce the generation of ROS in host ARPE19 cell. As described in introduction, mammalian cells have developed many ROS generating enzymes during the evolution process and NADPH oxidases have been known as one of the major player for ROS production in RPE and other mammalian cells. The family of NADPH oxidases (Nox/Duox) consists of Nox1-5, as well as the Duox1 and Duox2 [33]. Among these candidates, in order to identify a NADPH oxidase which is regulated by PI3k/AKT signaling pathway, first, we checked the mRNA expression level of each enzymes in ARPE19 cells. Surprisingly, Nox4 turned out to be the only NADPH oxidase which has significant amount of mRNA transcript in ARPE19 cell (Fig. S5). Other NADPH oxidases, including the Nox2, a well-known inducible NADPH oxidase in macrophage, did not show any change in its level even after T. gondii infection. Instead, T. gondii infection caused significant reduction of Nox4 mRNA and protein level, and intracellular ROS level of the host. These results suggest that Nox4 is the main target for T. gondii in reducing host intracellular ROS level, and PI3K/Akt signaling pathway is responsible for the suppression of Nox4 expression. Another interesting finding is that P22Phox transcription was suppressed by T. gondii infection. P22Phox is a required component for NADPH oxidases to express full enzymatic activity and stabilization of the enzyme complex. For example, in phagocytes, a well-characterized mulitcomponent enzyme, in which the catalytic subunit gp61/Nox2 and P22Phox form an integral complex called flavocytochrome b558 [23]. Not surprisingly, some pathogens have developed strategies to counter the Nox2 response by either inhibiting Nox2 assembly on the phagosome, as in the case for Salmonella typhimurium [44] and Helicobacter pylori [45], or reducing steady-state level of Nox2 components as illustrated by Anaplasma phagocytophilia [46] or Ehrlichia caffeensis [47].

However, there is a report that forms of P22Phox mutated in the proline-rich region inhibited ROS production for Nox1, Nox2, and Nox3, but not for Nox4 [23]. There are other reports that Nox4 does not require other components, such as P40Phox, P47Phox, P67Phox, or Rac, for its activation [48]. Given the fact that Nox4 generates substantial amounts of ROS without a need for cell stimulation and cofactors, it implies that T. gondii has developed a unique mechanism to suppress the ROS generation by elimination of constantly active Nox4 at the transcription level rather than by regulating its activity in RPE. Down-regulation of P22Phox transcription level by T. gondii would be a sub-system for tissues with traceable amount or inducible Nox enzyme(s) inside. This question would need further study. Silencing Nox4 expression with Nox4 siRNA demonstrated that down-regulation of Nox4 transcription is sufficient enough to reduce the intracellular ROS level and as a consequence, it was observed that in Nox4 siRNA treated host cell, T. gondii proliferated more rapidly, compare to T. gondii in untreated cell or in control siRNA treated cells.

Previous studies have suggested that multiple transcription factors, such as NF-κB, GATA, AP-1, Ets1, C/EBP, and STAT1/3 are coordinately involved in the regulation of Nox expression and function [49]. These data indicate that cooperation among multiple transcription factors, co-activators, and co-repressors is essential for precise control of Nox transcription and function. Nevertheless, the precise mechanisms of Nox regulation are not entirely defined. Our data demonstrating the involvement of PI3K/Akt pathway in Nox4 transcription imply the possibility that Forkhead Box O (FoxO) transcription factors are need to be added on the list of components which regulate Nox4 transcription. FoxO transcription factors have been associated with redox signaling and regulation of proliferation and apoptosis. These transcription factors share the ability to be inhibited and translocated out of the nucleus on phosphorylation by Akt/PKB in the PI3K signaling pathway. According to our preliminary data, T. gondii infection, indeed, induced the phosphorylation of FoxO and relocation of FoxO out of nucleus to cytosol (data not shown) in correlation with intracellular ROS level.

In conclusion, our findings demonstrate that T. gondii can manipulate host PI3K/Akt signaling pathway to reduce intracellular ROS level and to generate beneficial microenvironment for their proliferation. According to Nox4 siRNA experiments, it is also indicated that Nox4 is the important component for innate immune defense mechanism of host cell against parasite infection and it is the major target for T. gondii to suppress hostile intracellular ROS level. Down-regulation of Nox4 in T. gondii infected human RPE cell may represent a novel mechanism of blood-retinal barrier breakdown and pathological retinal in ocular toxoplasmosis.

Supporting Information

Figure S1.

Examination of Mycoplasma and Endotoxin. (A) PCR analysis of ARPE-19 cell and parasite for detecting the presence of Mycoplasma DNA. The size of the PCR product obtained using the positive template with primer pairs is 270 bp. (B) Endotoxin levels of ARPE-19 cell and parasite detected with the LAL assay.

https://doi.org/10.1371/journal.pone.0066306.s001

(TIF)

Figure S2.

Confirmation of host viability after infection of T. gondii and effects of PI3K inhibitors on T. gondii replication ratio in 12 h. (A) ARPE-19 cells were infected with T. gondii at various moi for 24 h, and cell viability was assessed by MTT assay. (B) Cells were pre-incubated with PI3K inhibitors, either 10 µM LY294002, 200 nM wortmannin, or 250 nM GDC-0941, 10 nM ZSTK474 for 1 h. After washing, the cells were then infected with T. gondii at moi of 5 for 12 h. The number of parasites per vacuole was counted and converted in to percentage (doubling time of around 10 ∼12 h).

https://doi.org/10.1371/journal.pone.0066306.s002

(TIF)

Figure S3.

Effects of PI3K-specific inhibitors on Toxoplasma-induced PI3K/Akt activation. ARPE-19 cells were infected with T. gondii (moi 15) for 24 h and treated with increasing concentrations of GDC-0941 or ZSTK474 for the final 1 h.

https://doi.org/10.1371/journal.pone.0066306.s003

(TIF)

Figure S4.

Presence of high ROS in T. gondii. Toxoplasma-induced ROS synthesis inhibition is suppressed by treatment of PI3K inhibitor. The arrows show that the T. gondii can be highly labeled by dihydroethidium (DHE).

https://doi.org/10.1371/journal.pone.0066306.s004

(TIF)

Figure S5.

Messenger RNA expression pattern of NADPH oxidases in T. gondii infected ARPE-19 cell. Reverse transcription-PCR on whole RNA extracted from host cell with primer selected for seven catalytic subunits of NADPH oxidase isoforms (Nox1∼5, Duox1/Duox2).

https://doi.org/10.1371/journal.pone.0066306.s005

(TIF)

Acknowledgments

Thanks to Dr. Yoshifumi Nishikawa, Obihiro University of Agriculture and Veterinary Medicine, for providing GFP-RH Toxoplasma gondii.

Author Contributions

Conceived and designed the experiments: WZ JQ YL GC. Performed the experiments: WZ JQ. Analyzed the data: WZ JQ YL GC. Contributed reagents/materials/analysis tools: YL DS GC. Wrote the paper: WZ GC.

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