Original Research ARTICLE
The Liver-Stage Plasmodium Infection Is a Critical Checkpoint for Development of Experimental Cerebral Malaria
- 1Parasitology Unit, Max Planck Institute for Infection Biology, Berlin, Germany
- 2Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan
- 3Immune Regulation Research Group, Deutsches Rheuma-Forschungszentrum, Berlin, Germany
- 4Department of Neuropathology, Charité - Universitätmedizin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health (BIH), Berlin, Germany
- 5Department of Immunology, Infectiology and Haematology (I2H), Institut Necker-Enfants Malades, INSERM U1151-CNRS UMR 8253, Paris, France
- 6Faculté de Médecine, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
- 7AP-HP, Hôpital Necker Enfants Malades, Paris, France
- 8Department of Molecular Parasitology, Institute of Biology, Humboldt University, Berlin, Germany
Cerebral malaria is a life-threatening complication of malaria in humans, and the underlying pathogenic mechanisms are widely analyzed in a murine model of experimental cerebral malaria (ECM). Here, we show abrogation of ECM by hemocoel sporozoite-induced infection of a transgenic Plasmodium berghei line that overexpresses profilin, whereas these parasites remain fully virulent in transfusion-mediated blood infection. We, thus, demonstrate the importance of the clinically silent liver-stage infection for modulating the onset of ECM. Even though both parasites triggered comparable splenic immune cell expansion and accumulation of antigen-experienced CD8+ T cells in the brain, infection with transgenic sporozoites did not lead to cerebral vascular damages and suppressed the recruitment of overall lymphocyte populations. Strikingly, infection with the transgenic strain led to maintenance of CD115+Ly6C+ monocytes, which disappear in infected animals prone to ECM. An early induction of IL-10, IL-12p70, IL-6, and TNF at the time when parasites emerge from the liver might lead to a diminished induction of hepatic immunity. Collectively, our study reveals the essential role of early host interactions in the liver that may dampen the subsequent pro-inflammatory immune responses and influence the occurrence of ECM, highlighting a novel checkpoint in this fatal pathology.
One of the most severe pathological complications caused by P. falciparum infection is cerebral malaria (CM) (1, 2). As an experimental murine model for CM, P. berghei ANKA infection of C57BL/6 mice with a Th1-biased phenotype is well-established and termed experimental cerebral malaria (ECM) (3). The ECM model recapitulates many aspects of human pathology, such as up-regulation of inflammatory cytokines, activation of cerebral endothelial cells, platelet accumulation, sequestration of leukocytes and infected red blood cells (iRBCs), reduced blood flow, intracranial hypertension and hemorrhages, which together lead to irreversible fatal cerebral pathology (4–10). ECM results in rapid death often occurring within 4–5 h after the onset of the first neurological signs, including ataxia, respiratory distress, seizure, and coma (11, 12).
A central hallmark of ECM is destruction of the blood-brain barrier (BBB) (12). It is now well-established that cytotoxic CD8+ T cells are the primary mediators of ECM development (13–21). During ECM, parasite-specific CD8+ T cells accumulate along cerebral vessels, where INF-γ release is thought to cause the activation of endothelial cells and perforin-mediated disruption of tight junctions to induce the BBB breakdown (20–24).
A major research focus of ECM has been on terminal immune responses that take place in the brain using blood transfusion of infected red blood cells, which have immensely advanced our understanding of the underlying mechanisms of ECM pathogenesis. However, there is very limited information on how the pre-erythrocytic phase of an infection can influence the disease outcome, where sporozoites from infectious Anopheles mosquitoes are inoculated, followed by parasite propagation in the host liver. Currently, the vast majority of ECM research is conducted by bypassing the pre-erythrocytic phase and directly starts the experiments from blood-stage infections.
In this study, we investigated the pathogenesis of ECM in C57BL/6 mice using transgenic Plasmodium berghei ANKA parasites that moderately over-express profilin under the control of the apical membrane antigen 1 (AMA1) promoter (25). Profilin is essential for blood infection and is likely involved in nucleotide re-loading of actin monomers, thus accelerating the microfilament turnover and modulating parasite motility (26, 27). Transgenic parasites, termed PRF parasites herein, express elevated (~10-fold increase) levels of profilin in sporozoites and blood-stage parasites (25). All experiments were conducted with hemocoel sporozoites, since they display similar virulence and immunogenicity as sporozoites isolated from salivary glands (28), and PRF sporozoites display decreased salivary gland invasion (25). Lower salivary gland infectivity is in good agreement with premature sporozoite maturation and led us to hypothesize that PRF sporozoites might display enhanced liver infection and population expansion, which has not yet been achieved by experimental genetics.
We show that PRF blood stages are fully virulent and pathogenic, since infections with asexual blood-stage parasites cause ECM. However, these parasites are unable to elicit ECM pathology when the infection is induced by sporozoites. Remarkably, this abrogation of ECM occurred upon comparable onset of blood-stage development, thus allowing us to study, for the first time, how the liver phase affects the subsequent development of the cellular immune responses ultimately leading to ECM. Collectively, our data reveal the pre-erythrocytic phase of infection as a novel checkpoint for the development of the subsequent immune response and the progression to fatal immunopathology.
Enhanced Transmigration and Invasion of Hepatocytes by Transgenic PRF Sporozoites
We first characterized pre-erythrocytic development of PRF sporozoites and injected susceptible mice with 5,000 freshly dissected hemocoel sporozoites from wild-type (WT)- or PRF-infected Anopheles stephensi mosquitoes (Figure 1A). The prepatent period was 3 days for all mice infected with PRF sporozoites, whereas mice infected by WT sporozoites required up to 3–4 days for microscopic detection of blood-stage parasites by Giemsa-stained blood smears (Figure 1A). To gain a better understanding of liver-stage infection by PRF parasites in vivo and in vitro experiments were conducted. Quantification of the parasite load in the liver 42 h after inoculation with sporozoites revealed no difference between WT or PRF parasites (Figure 1B), suggesting full maturation of PRF liver stages. However, when PRF sporozoites were deposited onto cultured hepatoma cells for 2 h, we detected elevated levels of transmigration in comparison to WT sporozoites (Figure 1C). Enumeration of liver stages in cultured hepatoma cells revealed higher numbers for PRF infection compared to WT infection after 24 and 48 h (Supplemental Figure 1).
Figure 1. Improved pre-erythrocytic development of PRF parasites. (A) Prepatent period of sporozoite-induced infections. Appearance of blood-stage parasites was monitored by daily microscopic examination of Giemsa-stained blood films. C57BL/6 mice were infected by intravenous injection of 5,000 WT or PRF hemocoel sporozoites (n = 22 each). Shown is a Kaplan-Maier analysis of time to first detection of blood infection, ***P < 0.001 (Mantel-Cox test). (B) In vivo quantification of parasite loads in the liver of infected mice. Livers were harvested 42 h after infection of C57BL/6 mice by intravenous injection of 5,000 WT or PRF hemocoel sporozoites. Expression levels of P. berghei 18S rRNA were quantified by real-time RT-PCR and normalized to mouse GAPDH. Results represent mean values (± SEM) (n = 8 each for infected mice; n = 3 for naïve mice). Differences between WT- and PRF-infected livers were non-significant (Mann-Whitney test). (C) Sporozoite cell traversal. Hepatoma cells were incubated for 30 min or 2 h with medium (white; Con), FITC-dextran only (dotted line), and FITC-dextran together with either WT (blue; WT), or PRF (red; PRF) hemocoel sporozoites. Cells were analyzed by flow cytometry to enumerate the percentage of dextran-positive cells indicative of sporozoite traversal. Results represent mean values (±SD) of at least three independent experiments with duplicates each. *P < 0.05 (Mann-Whitney test).
Together, PRF sporozoites are enhanced in cellular attachment (25), as well as transmigration and invasion of liver cells as compared to WT sporozoites. This gain of function is unprecedented and allowed us to explore, whether enhancement of the first parasite—host interactions may lead to modulations of infection and immune responses.
Absence of ECM Pathology After Infection With PRF Sporozoites but Not Blood Transfusion
We next studied blood infection and intravenously injected 5,000 sporozoites or infected red blood cells (iRBCs) from WT or PRF parasites into naïve mice (Figure 2A). Quantification of parasitemia and growth dynamics revealed similar numbers of iRBCs. Strikingly, the majority of mice infected with PRF sporozoites (86%) did not develop ECM (Figure 2B). Of 22 mice that were infected with PRF sporozoites, only three mice developed signatures of ECM-like symptoms on day 7–8 after inoculation, while all other mice remained symptom-free as indicated by rapid murine coma and behavior scale (RMCBS) scores of 18 (29). In contrast, all mice infected with WT or PRF blood-stage parasites and all mice infected by WT sporozoites developed signature ECM symptoms (RMCBS scores of 0–4). PRF sporozoite-infected mice that survived the critical period of ECM onset (days 7–10 after inoculation) progressed to high parasitemia, and as a consequence, anemia several weeks later (Supplementary Figure 2).
Figure 2. Full virulence after PRF blood infection, but very low ECM pathology after sporozoite infection. (A) Time course of blood infection after sporozoite inoculation or transfusion of iRBCs. C57BL/6 mice were infected by intravenous injection of 5,000 hemocoel sporozoites (solid lines) of either wild type (WT; blue) or PRF (red) parasites (n = 22 each) or 5,000 iRBCs (dashed lines) of WT (blue) or PRF (red) parasites (n = 15 each). Parasitemia was monitored daily by microscopic examination of Giemsa stained blood-films. Differences between asexual blood-stage propagation were non-significant (Mantel-Cox test). (B) Kaplan-Meier analysis of time to development of signature symptoms of experimental cerebral malaria (ECM). ***P < 0.001 (Mantel-Cox test). (C) Quantification of parasite loads in the brain (square), BM (polygon) and liver (triangle) was done by qPCR. Organs were harvested 6 days after infection of C57BL/6 mice with 5,000 WT or PRF sporozoites. Animals were perfused via the left heart ventricle to remove non-sequestering infected red blood cells from the circulation of blood. Relative expression levels of P. berghei 18S rRNA were normalized to mouse GAPDH. Results represent mean values (±SD). *P < 0.05 (Mann-Whitney test). (D) Visualization of integrity of blood-brain barrier in infected mice. Infected mice were intravenously injected with 2% Evans blue dye 8 days after infection by 5,000 WT sporozoites (upper left), PRF sporozoites (upper right), WT- iRBCs (bottom left), and PRF-iRBCs (bottom right). (E) Vascular leakage also occurs in the spinal cords of mice with ECM symptoms. Isolated spinal cords are indicated by arrows and show leakage of the dye in mice with signature ECM symptoms.
To obtain more information about the development of blood-stage PRF parasites in vivo, the accumulation of parasites was analyzed in the brain, bone marrow (BM), and liver in perfused animals on day 6 p.i. with 5,000 sporozoites (Figure 2C), where no apparent difference between PRF and WT parasite burden in the three organs was observed. Altogether, these data demonstrate that PRF blood-stage parasites are fully virulent. Therefore, we infer from the markedly reduced incidence of ECM in mice infected with PRF sporozoites that the initial, pre-erythrocytic stage of a malarial infection profoundly impacts on the development of ECM.
Reduced Inflammation of Cerebral Vessels in PRF Sporozoite-Infected Mice
We compared the integrity of the BBB in infected mice as visualized by the coloration of the brain after intravenous infection of 2% Evans Blue dye, an indicator of BBB leakage (Figure 2D). Mice infected with WT sporozoites, WT iRBCs, and PRF iRBCs all showed strong diffusion of Evans Blue in the brain on day 7 or 8 p.i., while naïve mice and mice infected with PRF sporozoites remained unstained. We also observed vascular pathology in the spinal cord, which correlated with ECM (Figure 2E), a previously unreported finding. We propose that the progression of ECM extends to the spinal cord, which may be due to the disruption of the choroid plexus that acts as a blood-cerebrospinal fluid barrier (30). Furthermore, sites of hemorrhage i.e., areas where RBCs had leaked into the cerebral tissue were quantified by H&E stain of histological sections (Figure 3A). While hemorrhage sites were frequent in brain tissue derived from infected mice with ECM signatures, they were rarely detected in PRF sporozoite-infected mice (Figure 3B).
Figure 3. Cerebral vessels from mice infected by PRF sporozoites maintain a healthy status. (A) Hematoxilin and eosin (H&E) stain of a brain tissue section from an animal displaying signature ECM symptoms. An arrow indicates RBCs that leaked into the cerebral parenchyma. Scale bar, 10 μm. (B) Quantification of hemorrhage sites based on H&E stains of horizontal cross-sections of the brain (n = 10 each). Results represent mean values (±SD) from at least two independent experiments. ***P < 0.001 (Mann-Whitney test). (C) Visualization of brain vessel integrity. Shown are H&E stains of representative brain histological cross-sections. Comparison of a healthy vessel (left) from a mouse infected with PRF sporozoites and a collapsed vessel (right) from a mouse infected with WT sporozoites. The latter vessel also contains accumulated leukocytes. Scale bar, 10 μm. (D) Morphological scoring of cerebral vessels based on histological sections. Quantification of mice infected with 5,000 WT sporozoites, PRF sporozoites, WT iRBCs or PRF iRBCs (n = 10 animals for infected groups, n = 3 mice for naïve group; >20 cerebral vessels were quantified for each animal).
Additional key histopathological alterations associated with ECM are cerebral vessel plugging by RBCs/iRBCs, leukocytes and platelets (10, 31). Visualization of vessel plugging based on H&E stain showed vessels that were collapsed within an enlarged perivascular space in WT parasite-infected mice (Figure 3C). In contrast, cerebral vessels from naïve mice or mice infected with PRF sporozoites displayed healthy perivascular spaces, with the endothelium attached to surrounding tissues and almost no leukocyte infiltration (Figure 3C). From these sections, similar proportions (~90%) of healthy vessels were scored for naïve and PRF sporozoite-infected animals (Figure 3D). As expected from the associated pathology, mice infected with WT sporozoites, WT iRBCs, and PRF iRBCs displayed vessel plugging in the vast majority (~80%) of their cerebral vessels (Figure 3D). In conclusion, mice infected with PRF sporozoites displayed little morphological alteration of cerebral vessels despite similar blood-stage parasite abundance.
Accumulation of Parasite Antigen-Specific CD8+ T Cells in the Brain and Spleen Is a Signature of Infection, but Not of ECM Development
The identification of parasite antigen-specific CD8+ T cells recognizing an epitope of Plasmodium glideosome-associated protein 50 (GAP50) allows for their quantification in the brain during infection (22). We first analyzed the expansion of splenic CD8+ T cells from day 5–8 after WT and PRF sporozoite-induced infections by flow cytometry, where the CD8+ T cell number was not significantly different between the two infections (Supplementary Figure 3A). The accumulation of CD8+ T cell number was significantly increased in infected animals compared to naïve mice on day 8 p.i., where the increase was more prominent for the ECM-developing group (Figure 4A). We next investigated the proportion of antigen-specific CD8+ T cells by measuring intracellular IFN-γ in isolated cerebral lymphocytes after re-stimulation with the GAP5040−48 peptide (Figure 4B). The IFN-γ-secreting antigen-specific CD8+ T cells were not significantly different in the spleen (Supplementary Figures 3B,C) on day 8 after sporozoite infection. Furthermore, cerebral analysis revealed that the numbers, percentages and even the mean fluorescence intensity of IFN-γ-secreting antigen-specific CD8+ T cells were not significantly different after both infections in brain (Figure 4C and Supplementary Figure 4). Other lymphocyte populations including CD4+ T, NKT, and NK cells accumulated in the brains on day 8 p.i., as previously published (31), although this occurred in lower amounts in mice infected with PRF sporozoites compared to mice that received the WT parasite (Supplementary Figure 5), as observed for total CD8+ T cells (Figure 4A).
Figure 4. Quantification of total and antigen-experienced CD8+ T cells in the brains of infected mice. (A) Time course of total cerebral lymphocyte counts during the late stages of blood infection. Mice were infected with WT (blue) or PRF (red) sporozoites by intravenous injection (n = 6 each), and cerebral lymphocytes were isolated and analyzed at indicated time points. Shown are total CD8+ T cell numbers. The dotted line represents the mean cerebral CD8+ T cell number in all naïve animals (n = 16). The scatter dot plots represent mean values (±SD). **P < 0.01 (Mann-Whitney test). (B) Gating strategy for detection of intracellular IFN-γ expression in CD3+CD8+ cells after re-stimulation with PbGAP5040−48 peptide. Shown are representative plots for naïve animals, as well as mice infected with WT or PRF sporozoites. (C) Quantification of cerebral CD8+ T cells expressing intracellular IFN-γ after re-stimulation with PbGAP5040−48 peptide. Shown are numbers of this population in the brain. The scatter dot plots represent mean values (±SD) from samples isolated on day 8 from three independent experiments (n = 10 each for infected mice; n = 4 for naïve mice). IFN-γ-secreting antigen-specific CD8+ T cells number from WT vs. PRF infected animals is non-significant. **P < 0.01 (Mann-Whitney test).
Taken together, our data show that infections with PRF sporozoites elicit high frequency of IFN-γ-secreting antigen-specific CD8+ T cells, yet trigger a lower accumulation of total immune cells in the brain, as compared to WT sporozoites. This finding is reminiscent of what was observed in mice infected with different strains of P. berghei (20, 22). Our data likely reflect diverse degrees of re-activation of parasite-specific CD8+ T cells locally in the brain, so that there is reduced endothelial cell activation upon PRF sporozoite infections.
Parasite Infection Leads to Similar Cerebral Myeloid Populations Regardless of Disease Outcome
Although the contribution of myeloid cells to ECM remains unclear, these cells represent suitable sensors of an infection locally. We, thus, examined the cerebral myeloid populations in our infection models. Cerebral myeloid populations were defined as CD45med/loCD11b+ cells, which excluded lymphocytes (Figure 5A). We further excluded Ly6G+ neutrophils, which were not significantly different between the three groups (Supplementary Figure 6). Based on their CD45 expression, myeloid cell populations were separated into CD45lo microglia and CD45med microglia, monocytes or macrophages, which are difficult to distinguish further (Figure 5B). Although it has been reported recently that non-ECM animals display lower numbers and less activation of microglia (32), we found that the CD45lo microglia number was not significantly different between naïve, WT sporozoite- and PRF sporozoite-infected animals (Figure 5C). There was a comparable increase in the number of CD45med microglia, monocytes and macrophages in both groups of infections (Figure 5D). Moreover, the activation of microglia in infected mice was also apparent from the ionized calcium-binding adapter molecule 1 (IBA-1) immunostaining of brain cross-sections (Figures 5E–G). We detected high IBA-1 expression especially in proximity to the vessels, where microglia were exposed to parasite antigens, inflammatory cytokines, and chemokines. Thus, microglia activation was overall comparable after WT or PRF parasite infections. We also determined that during WT and PRF sporozoite infections most of the cells in this population were Ly6Chi pro-inflammatory monocytes (Supplementary Figure 7A), and their accumulation in the brain was similar for both groups of infections (Supplementary Figure 7B). In summary, we found no difference in the phenotype of myeloid populations in the brains from WT- and PRF sporozoite infected-mice, which is in perfect agreement with our observation of similar parasite growth and abundance in the brain during both infections.
Figure 5. Quantification of myeloid cells after infection. (A) Representative contour plots from day 8 after infection showing CD45 vs. CD11b expression on live cells obtained from naïve mice (left), and mice infected with WT (center) and PRF (right) sporozoites. Indicated are gated populations of lymphocytes, CD45hiCD11b− cells (gray circles) and myeloid cells, CD45med/loCD11b+ cells (red circles). (B) CD45 vs. CD11b expression on the Ly6G− myeloid population. CD45loCD11b+ cells (orange circles) represent microglia and CD45medCD11b+ cells (green circles) activated microglia, monocytes and macrophages, respectively. (C) Quantification of CD45lo microglia. Shown are percentage (left) and absolute numbers (right) of CD45loLy6G−CD11b+ microglia. (D) Quantification of CD45medLy6G−CD11b+ cells, which correspond to CD45med microglia, monocytes and macrophages. Shown are percentage (left) and absolute numbers (right) of CD45med microglia/monocytes/macrophages in the brain. The scatter dot plots in (C,D) represent mean values (±SD) from samples (n = 4–7) isolated 8 days after infection from two independent experiments. n.s, non-significant; *P < 0.05; **P < 0.01 (Mann-Whitney test). (E–G) Representative images from the IBA-1+ microglial cells of brain histological cross-sections. Cerebral vessels are indicated by arrows. The IBA-1 staining reaction was visualized with diaminobenzidine (DAB), highlighting some microglial cells with thin processes in naïve mice, while they are more prominent in WT sporozoite-infected mice and they also tend to cluster around vessels. This feature is also pronounced in PRF sporozoite-infected mice, dark brown. Scale bar, 50 μm.
Interestingly, while investigating Ly6C+ monocytes in the spleen of mice infected with WT or PRF sporozoites on day 8 after infection, we found that mice with onset of ECM displayed a striking loss of CD115+Ly6C+ monocytes in spleen, which was neither apparent in PRF sporozoite-infected nor in naïve mice (Figures 6A,B). Moreover, the decrease in the number of CD115−Ly6C+ myeloid cells in the spleen of mice infected with WT sporozoites was also pronounced in comparison to PRF sporozoite-infected mice (Figure 6C). CD115 can be used to distinguish monocytes from macrophages (33), and CD115 is a receptor for macrophage colony-stimulation factor (M-CSF) and IL-34 (34).
Figure 6. Reduced CD115 expressions on splenic Ly6C+CD11b+ monocytes in mice infected with WT sporozoites during the development of ECM. (A) Representative contour plots showing gating of Ly6C vs. CD115 expression on CD45+Ly6G−CD11b+ myeloid cells from naïve mice (left), and mice infected with WT (center) and PRF (right) sporozoites 8 days after infection. An arrow indicates the disappearance of CD115+Ly6C+ monocytes (blue circles) in spleens of mice infected with WT sporozoites. CD115−Ly6C+ monocytes are gated in gray circles. (B) Quantification of splenic CD115+Ly6C+ monocytes. Shown are percentage and numbers of CD115+Ly6C+ monocytes in the spleen. (C) Quantification of splenic CD115−Ly6C+ cells. Shown are percentage and numbers of CD115−Ly6C+ myeloid cells in the spleen. The scatter dot plots in (B,C) represent mean values (±SD) from samples (n = 8–11) isolated 8 days after infection from two independent experiments. n.s, non-significant; *P < 0.05; **P < 0.01; ***P < 0.001 (Mann-Whitney test).
PRF Parasites Induce Higher Systemic Cytokines Levels at the Time of Their Emergence From the Liver
To address whether PRF sporozoites induced a different immune response during the liver phase in comparison to WT parasites we quantified the systemic cytokine levels in the blood on days 0, 3, 5, and 7 after sporozoite-induced infections (Figure 7). In PRF sporozoite infections, we observed an abrupt rise in the serum levels of the regulatory cytokine interleukin-10 (IL-10), which is known to be the key suppressive cytokine implicated in ECM prevention (35). Strikingly, IL-10 up-regulation was only observed on day 3 p.i. (Figure 7A), coinciding with the time point when transgenic blood-stage parasites emerged from the liver into the blood circulation (Figure 1A). We also observed an increase in IL-12p70, IL-6, and tumor necrosis factor (TNF) on day 3 after PRF sporozoite infections as compared to WT sporozoite infections (Figures 7B–D). Of note, an early production of cytokines, such as IL-10 and IL-12 can be protective rather than deleterious in ECM pathology (36, 37).
Figure 7. Serum cytokine levels are up-regulated 3 days after infection with PRF sporozoites, at the onset of blood infection. (A–F) Serum from peripheral blood was collected on days indicated after infection with 5,000 WT (blue triangles) or PRF (red circles) sporozoites. Systemic cytokines were captured using a Cytokine Bead Array and analyzed by flow cytometry. Day 0 results represent data from uninfected mice. Shown are the steady-state levels of the systemic cytokines (A) IL-10, (B) IL-12p70, (C) IL-6, (D) TNF, (E) IFN-γ, and (F) MCP-1. The results represent mean values (±SD) (n = 5 for WT, n = 4 each for PRF). *P < 0.05 (Mann-Whitney test).
Mice infected with PRF sporozoites displayed lower systemic IFN-γ levels than mice infected with WT sporozoites at day 7 p.i., which is consistent with a lower re-activation of CD8+ T cells in PRF parasite-infected mice at the time when mice infected with WT parasites develop ECM (Figure 7E). These changes were specific since the levels of other soluble factors, such as monocyte chemo attractant protein-1 (MCP-1), were similar in both infections (Figure 7F).
PRF Pre-erythrocytic Parasites Mount Reduced Hepatic Immune Responses
To explore whether the pre-erythrocytic phase of infection with transgenic parasite modifies the subsequent immune response, we used irradiation-arrested sporozoites that are capable of invading the host hepatocytes, yet maturation is halted during early liver-stage development. This approach is typically used to study the sterile immunization by the whole-sporozoite vaccination strategies, but it also allows the study of hepatic immune responses elicited by the early pre-erythrocytic phase of the infection. Two doses of weekly intravenous inoculations with 10,000 irradiated WT or PRF hemocoel sporozoites were followed by a challenge infection by 10,000 WT salivary gland sporozoites 14 days after the last immunization (Figure 8A). Sterile protection was determined by daily monitoring of parasitemia after the challenge infection. As expected, naïve mice became blood-stage positive on day 3 after infection. Only 2 out of 12 mice immunized with irradiated WT hemocoel sporozoites became infected and the remaining 10 mice were free of blood-stage infection throughout the observation period of 3 weeks. In marked contrast, 7 out of 12 PRF hemocoel sporozoite-immunized mice developed parasitemia starting 5 days after the challenge infection (Figure 8B). In conclusion, these data show that immunization with PRF hemocoel sporozoites induces weaker immunity, despite the enhanced cytokine production and sporozoite activity.
Figure 8. PRF sporozoites do not induce more liver-stage antigen specific CD8+ T cells compared to WT sporozoites upon immunization. (A) Immunization and challenge protocol. C57BL/6 mice were immunized twice at weekly intervals with 10,000 irradiated hemocoel sporozoites (10 k γ-spz). Animals were challenged with 10,000 WT salivary gland sporozoites (10 k spz) 14 days after the last immunization. (B) Kaplan-Meier analysis of time to blood infection. Naïve mice (n = 9), WT and PRF sporozoite-immunized mice (n = 12 each). Blood parasitemia was determined by daily microscopic examination of Giemsa-stained blood films. The statistics for WT vs. PRF sporozoite-immunized mice were non-significant for Log-rank (Mantel-Cox) test. (C) Enumeration of total liver CD8+ T cell numbers after 14 days from the last immunization. Livers were isolated for flow cytometric analysis from naïve and WT and PRF sporozoite-immunized mice (n = 5). The results represent mean values (±SD). (D) Quantification of IFN-γ-secreting antigen-specific liver CD8+ T after 14 days from the last immunization. Hepatic leukocytes were stained for intracellular IFN-γ production without (left) or after re-stimulation with PbTRAP130−138 peptide (right). The results represent mean values (±SD). *P < 0.05; **P < 0.01 (Mann-Whitney test).
We further studied the expansion of hepatic CD8+ T cells by pre-erythrocytic parasites using irradiated sporozoites. We found no differences in the total CD8+ T cells after two doses of weekly intravenous inoculation with 10,000 irradiated WT or PRF hemocoel sporozoites (Figure 8C). However, there was a marginally reduced number of IFN-γ-secreting PbTRAP130−138-specific CD8+ T cells expansion in PRF sporozoite-immunized mice as compared to WT sporozoite-immunized mice (Figure 8D), in good agreement with the inferior ability of irradiated PRF sporozoites to mount sterilizing immune responses (Figure 8B). This finding suggests that the enhanced early production of cytokines by PRF sporozoites is linked to dampening of cell-based protective immune responses in the liver, similar to the dampening of pathogenic immune responses associated with ECM disease onset.
The utilization of a transgenic parasite line, which displays enhanced hepatocyte transmigration and invasion, allowed us to identify a novel checkpoint in ECM disease onset. We propose that this checkpoint is defined by signatures of cellular immunology and can be modulated to the benefit of Plasmodium-infected hosts. Only few studies addressed how the pre-erythrocytic phase of the infection impacted on ECM, either employing chemical attenuated- (38) or knock-out P. berghei ANKA parasites (32, 39, 40), which are no longer virulent. Thus, the prevention of cerebral pathology in these infections can be largely explained by considerable delays in the time to blood infection or by strongly reduced parasite virulence and lower infection rates, which do not induce the threshold of pro-inflammatory responses required for ECM. In marked contrast, PRF sporozoites displayed no apparent attenuation, yet failed to induce cerebral pathology in sporozoite-induced infections, while emerging normally from the liver and being fully virulent when the infection was induced by blood transfusion of iRBCs.
Irrespective of the parasite strains used and the outcome of brain pathology, accumulation of IFN-γ-secreting antigen-specific CD8+ T cell in the brain was readily altered, which has been similarly observed in previous studies using ECM inducing ANKA and non-ECM inducing NK65 P. berghei strains (20, 22). In fact, it has been demonstrated that vascular pathology is triggered when these parasite antigen-specific CD8+ T cells interacted with IFN-γ activated cerebrovascular endothelial cells that cross-present malaria antigens (21–23, 40). PRF sporozoite infections show healthy cerebral microvessels, but further work will be required to confirm the molecular mechanism of protection from the vascular destruction by examining factors such as cytotoxicity of CD8+ T cells, cerebral chemokine levels and other increased populations like CD4+ T, NKT, and NK cells.
We did not observe any differences in cerebral myeloid populations in all infected animals, irrespective of disease propagation, suggesting that myeloid cells respond to the similar amount of blood-stage parasites in both infections and reflect peripheral sensing of inflammation. An interesting observation in this study is the lack of CD115 marker on Ly6C+ monocytes in the spleen of mice with ECM symptoms. M-CSF signaling via CD115 is important for the late stage of monocyte and macrophage lineage development (41), where in a similar manner to fatal ECM pathology, a lethal Listeria monocytogenes infection has also been reported to induce a down-regulation of CD115 expression on monocytes (42). We could not directly test the possibility of infiltration of CD115+Ly6C+ monocytes to the brain due to cleavage of CD115 after the collagenase treatment during the cerebral leukocyte isolation (43). Further investigation is warranted to characterize and identify the different subsets of Ly6C+ monocytes during ECM and other pathological conditions of Plasmodium infections.
A failure to establish an appropriate balance between pro- and anti-inflammatory immune responses is believed to be central to the development of cerebral pathology (44). Profilin from the distantly related coccidian parasite, Toxoplasma gondii, has been shown to be a key immunomodulatory protein that is sensed by the murine-specific Toll-like receptor 11 (TLR11), leading to activation of the myeloid differentiation primary response protein 88 (MyD88) pathway in murine dendritic cells (45). Activation of dendritic cells by T. gondii profilin induces IL-12 followed by IFN-γ production from NK cells and neutrophils, which predetermines host resistance to Toxoplasma infection (46). Systemic up-regulation of IL-12 on day 3 p.i., together with IL-10, TNF, and IL-6, reflects the early checkpoint and is a major contributor to the prospective lack of ECM pathology after PRF sporozoite infection. Although induction of TLR11 was not observed by recombinant Plasmodium profilin (45), we cannot formally exclude that artificially elevated levels of Plasmodium profilin also contribute to the observed phenotype, in addition to an enhancement of parasite transmigration and liver stage development. While we suggest that the elevated early cytokine responses signify a host response to enhanced cellular transmigration, penetration and invasion of sinusoid cells and hepatocytes by transgenic sporozoites, we cannot formally exclude that higher expression of the otherwise inert P. berghei profilin or other proteins driven by the genetic modification in sporozoites might also contribute to the immune modulatory property of PRF parasites. Such a role would, however, be specific to sporozoites, since similar expression in merozoites (25) does apparently not trigger such a response, as seen by full virulence of infections with PRF iRBCs.
Interestingly, despite the enhanced sporozoite activity and elevated early cytokine responses, the expansion of antigen-specific CD8+ cells in the liver and sterilizing immunity were inferior in immunizations with irradiated PRF sporozoites. At this stage, we cannot determine the level of antigen exposure by PRF sporozoites; however there appears to be a dampening effect to the subsequent T cell immunity elicited specifically by PRF pre-erythrocytic parasites. Careful examination of detailed morphology during the pre-erythrocytic stages, such as formation of vacuoles and tubular protrusions will be needed to unravel the protective scenario of a liver-stage infection that can ultimately prevent the ECM development.
Further studies on how transgenic sporozoites and liver-stage parasites develop and interact with the host immune cells are critical to delineate the involvement of hepatic immunity to affect the blood-stage outcome. Besides the CD8+ T cells that we have examined in this study, recent findings by others on γδ T cells in Plasmodium infection may shed light on the underlying immune mechanism that determines the prevention of ECM during PRF sporozoite infection. Absence of IFN-γ-producing γδ T cells during the liver-stage infection resulted in a less pro-inflammatory microenvironment that prevented mice from ECM development, demonstrating the role of hepatic immunity on cerebral pathology (47). In another study using P. chabaudi infection induced IFN-γ-secreting γδ T cells during the early infection, while γδ T cells shifted to M-CSF secretion toward later time points in infection (48).
In conclusion, our study demonstrates the critical importance of the pre-erythrocytic phase of infection, which is clinically silent. Additional work is warranted to uncover the molecular and cellular mechanisms of the entire cascade that commences with the first sporozoite-host interaction and ultimately leads to the detrimental brain pathology. Whether modulation of the early pre-erythrocytic immune response could also dampen cerebral malaria in P. falciparum-infected patients remains to be determined for the development of novel adjunct therapies and early diagnoses that are urgently needed to alleviate the fatal outcomes of cerebral malaria in patients.
Materials and Methods
Plasmodium berghei Parasites
Anopheles stephensi mosquitoes were raised at 20°C in 75% humidity under a 14-h light/10-h dark cycle. NMRI mice were infected by intraperitoneal injection of wild type P. berghei (strain ANKA) (49) or the transgenic parasite line expressing profilin under the control of the AMA-1 promoter (PRF) (25). iRBCs were collected from a drop of blood obtained from the tail vein. Sporozoites were isolated from the hemocoel of infected mosquitoes from day 17–22 after an infectious blood meal (28). For blood-stage infection, 5,000 iRBCs or freshly isolated sporozoites were injected intravenously into C57BL/6 mice. To exclude accumulation of unrecognized mutations, stocks of PRF iRBC were generated from sporozoite-induced infections, which were confirmed to not display ECM signatures. Microscopic examination of daily Giemsa-stained blood smears was conducted to determine parasitemia. Approximately, 20,000 RBCs were screened to determine the prepatent period.
Histopathological Scoring of Brain Sections
Mice were intravenously injected with 200 μl of 2% Evan's blue dye (Sigma-Aldrich) prepared in PBS. After 5–10 min, mice were sacrificed and brain and spinal cord were carefully dissected, rinsed quickly in PBS, and photographed. Histopathological scoring of brain sections was prepared from perfused mice. Organs were fixed in 2 ml of 4% formaldehyde for 24 h and embedded in paraffin blocks. H&E staining was done on 4 μm horizontal sections. Microglia were stained using anti-IBA1 antibody (Wako Chemicals GmbH). Hemorrhage sites and the status of cerebral vessels were scored microscopically.
Leukocytes from spleen, BM and brain were isolated on days indicated after perfusion with 1xPBS. Brains were collected in PBS/1% BSA/1 mM EDTA on ice, transferred, and incubated in digestion solution containing 0.02% collagenase type I (Sigma-Aldrich) and 0.002% DNase I (Sigma-Aldrich) in RPMI medium for 5 min at 37°C. Samples were incised into tiny sections then incubated for 10 min at 37°C. Cells were filtered into 15 ml falcon and centrifuged for 5 min, 1,400 rpm at 4°C. Pellets were resuspended in 5 ml 30% Percoll (Sigma-Aldrich) and centrifuged for 20 min, 2,000 rpm without break at room temperature. Fatty layer on top and the supernatant were aspirated. The cell pellets were resuspended in complete RPMI as described previously (50). Marrows of tibia were extracted by flushing the bone. Marrow and spleen were grinded between two glass slides, and then treated by Gey's solution (0.155M NH4Cl and 0.01M KHCO3) to lyse the RBCs. Cells were stained with DAPI (Thermo Fisher Scientific) to exclude the dead cells and quantified using MACS Quant Analyzer 10. Isolated cerebral cells were stained for anti-mouse CD45.2-APC antibody (clone 104; eBioscience) to quantify the leukocyte population.
Leukocyte Surface Staining
Cells collected from brain, spleen, or BM were filtered through 50-μm cell strainer (Partec) and blocked with antibodies against Fc-receptors (CD 16/32, clone 2.4G2; in house). Cells were stained with following anti-mouse antibodies for the time course experiment: CD3e-PeCy7 (clone 145-2c11; eBioscience), TCRβ-APC (clone H57-597; eBioscience), CD4-FITC (clone RM4-5; eBioscience), CD8-BV570™ (clone 53-6.7; Biolegend), CD49b (clone DX5; in house), and Propidium Iodine (Thermo Fisher Scientific) to test cell viability. The myeloid cell population was stained with the following antibodies: CD45.2-APC, CD11b-Pacific Blue (clone M1/70; in house), Ly6G-FITC (clone 1A8-Ly6g; eBioscience), Ly6C-Biotin (clone AL-21, BD Biosciences), CD115-PE (clone AF598, eBioscience), streptavidin-PerCP (BD Biosciences), and Pacific Orange-N-Hydroxysuccinimide (NHS) (in house) as viability dye. Stained live cells were acquired (stopping gate of 100,000 live cells) using a MACS Quant Analyzer 10 and analyzed by FlowJo software.
Re-stimulation and Intracellular Staining of Lymphocytes
3 × 106 isolated leukocytes were distributed in 96-well plates and resuspended in 100 μl of complete RPMI medium. The immunogenic peptides PbGAP5040−48 (SQLLNAKYL-NH2; peptides&elephants, Hennigsdorf, Germany) (22) and PbTRAP130−138 (SALLNVDNL-NH2; peptides&elephants, Hennigsdorf, Germany) (51) were used. 50 μl peptide diluted in RPMI (10 g/ml) was incubated for 2 h at 37°C, 5% CO2. Thereafter, 50 μl of Brefeldin A (1:1,000; eBioscience) was added to block secretion of cytokines, and cells were incubated for additional 4 h. After centrifugation cells were stained for surface markers with CD3e-PeCy7, CD4-BV421™ (clone RM4-5; Biolegend) and CD8-BV570™ antibodies, followed by staining with Pacific Orange-NHS for cell viability. Cells were fixed with 4% paraformaldehyde for 15 min at room temperature, and then permeabilized with Perm/Wash™ buffer (BD Biosciences). Intracellular IFN-γ was stained with Interferon gamma-APC antibody (clone XMG 1.2; eBioscience). Cells were washed in Perm/Wash™ buffer, then resuspended in PBS/1% BSA for acquisition (stopping gate of 20,000 CD8+ T cells) with MACS Quant Analyzer 10 and analysis by FlowJo software (51).
Plasma Cytokine Measurements
C57BL/6 mice were infected intravenously with 5,000 sporozoites. Blood was collected from the tail in a heparinized micro-hematocrit capillary on days indicated. Samples were centrifuged at 13,000 rpm for 3 min and plasma collected and stored at −80°C. Plasma cytokines were assayed by a cytometric bead array (mouse inflammation kit; BD Biosciences) as described previously (37). Analysis was performed using a Fortessa cell analyzer (BD Biosciences) and FlowJo software.
For the sporozoite cell traversal assay, 24-well plates were seeded with 300,000 human hepatoma cells (Huh7) per well and inoculated with 35,000 sporozoites in 300 μl of DMEM complete medium with 0.5 μg/ μl of FITC-dextran (Thermo Fisher Scientific) (52). After centrifugation for 5 min at 3,000 rpm, the plates were incubated for 30 min or 1 h at 37°C with 5% CO2. Trypsin-treated cells were resuspended in PBS, filtered, and immediately acquired by MACS Quant Analyzer 10 (Miltenyi Biotec) and analyzed by FlowJo software (Tree Star) to quantify dextran-positive, traversed cells.
To monitor successful parasite development, Huh7 cells were infected with 6,000 sporozoites isolated in DMEM. For settlement, the wells were centrifuged for 5 min at 3,000 rpm and incubated for 2 h at 37°C with 5% CO2. To stop cell invasion, the cells were washed three times with DMEM to remove extracellular sporozoites. Thereafter, cells were incubated for 24 or 48 h to permit development of liver-stage parasites. Cells were fixed with 4% paraformaldehyde for 10 min, followed by immunofluorescent assay with Hoechst 33342 (Thermo Fisher Scientific) and anti-P. berghei HSP70 antibody (53).
Five thousand freshly dissected sporozoites were injected intravenously into C57BL/6 mice. Livers were isolated after 42 h of infection. For organs collected 6 days post-infection, animals were first perfused with 50 ml of PBS via the left heart ventricle to remove iRBCs in the periphery. Organs were rinsed and then homogenized in Trizol reagent (Thermo Fisher Scientific). Total RNA was isolated, and cDNA was synthesized (RETROscript, Thermo Fisher Scientific). qRT-PCR was performed with Power SYBR Green PCR master mix (Thermo Fisher Scientific) as described previously (54, 55) with the ABI 7500 sequence detection system (Thermo Fisher Scientific). Gene-specific primers for P. berghei 18S rRNA (gi:160641 [forward, 5′−AAGCATTAAATAAAGCGAATACATCCTTAC−3′; reverse, 5′]) and mouse GAPDH (gi:281199965 [forward, 5′−TGAGGCCGGTGCTGAGTATGTCG−3′; reverse, 5′−CCACAGTCTTCTGGGTGGCAGTG−3′]) were utilized for the amplification. The relative transcript abundance was determined using the 2−ΔΔCt method.
Immunization With Irradiated Sporozoites
Freshly dissected sporozoites were irradiated with 12,000 cGy. A total of 10,000 irradiated sporozoites were intravenously injected per immunization. Challenge experiments were carried out with 10,000 wild-type salivary gland sporozoites. Immunized animals were monitored for the presence of blood-stage parasites from day 3 onward until day 14 after challenge by daily microscopic examination of Giemsa-stained blood films. Sterile protection was defined as the complete absence of blood-stage parasites.
Statistics were conducted using GraphPad Prism 5 (GraphPad Software). Statistical significance was calculated using a Mann-Whitney test (non-parametric test). A P < 0.05 was considered significant. Survival curves were compared by using the log rank (Mantel-Cox) test. Kruskal-Wallis test was performed to compare the significance of dependent data.
Data Availability Statement
All datasets generated for this study are included in the article/Supplementary Material.
All animal work was conducted in accordance with the German Tierschutzgesetz in der Fassung von 18. Mai 2006 (BGB1. I S. 1207), which implements the Directive 86/609/EEC from the European Union and the European Convention for the protection of vertebrate animals used for experimental and other scientific purposes. The protocol was approved by the ethics committee of the Max Planck Institute for Infection Biology and the Berlin state authorities (Landesamt für Gesundheit und Soziales (LAGeSo permit number G0469/09). Female C57BL/6 and NMRI mice were ordered from Charles River Laboratories. Mice were diagnosed with onset of ECM if they showed behavioral and functional abnormalities, such as ataxia, paralysis, or convulsions (12, 29). Mice were sacrificed immediately after a diagnosis of ECM.
YS, SF, and KM planned the work. YS and SR performed experiments. YS analyzed the data. YS, SR, and WS contributed to data analysis. YS wrote the manuscript with input from WS, SF, and KM. The final manuscript was edited and approved by all authors.
This work was supported by the Max Planck Society, and in part, by the EviMalaR Network of Excellence (#34). YS was supported by the ZIBI graduate school Berlin Research in infection biology and immunology.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We thank Elyzana Putrianti, Manuel Rauch, and Carolin Rauch for technical assistance. We thank Tomoharu Yasuda for insightful comments and fruitful discussions. We are grateful for the continuous support by the flow cytometry core facility (FCCF) of the Deutsches Rheuma-Forschungszentrum.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2019.02554/full#supplementary-material
3. de Souza JB, Hafalla JC, Riley EM, Couper KN. Cerebral malaria: why experimental murine models are required to understand the pathogenesis of disease. Parasitology. (2010) 137:755–72. doi: 10.1017/S0031182009991715
4. Langhorne J, Quin SJ, Sanni LA. “Mouse models of blood-stage malaria infections: immune responses and cytokines involved in protection and pathology,” In: Malaria Immunology. Basel: Karger Publishers (2002). p. 204–28. doi: 10.1159/000058845
10. Strangward P, Haley MJ, Shaw TN, Schwartz JM, Greig R, Mironov A, et al. A quantitative brain map of experimental cerebral malaria pathology. PLoS Pathog. (2017) 13:e1006267. doi: 10.1371/journal.ppat.1006267
11. de Souza JB, Riley EM. Cerebral malaria: the contribution of studies in animal models to our understanding of immunopathogenesis. Microbes Infect. (2002) 4:291–300. doi: 10.1016/S1286-4579(02)01541-1
12. Lackner P, Beer R, Heussler V, Goebel G, Rudzki D, Helbok R, et al. Behavioral and histopathological alterations in mice with cerebral malaria. Neuropathol Appl Neurobiol. (2006) 32:177–88. doi: 10.1111/j.1365-2990.2006.00706.x
14. Belnoue E, Kayibanda M, Vigario AM, Deschemin JC, van Rooijen N, Viguier M, et al. On the pathogenic role of brain-sequestered alphabeta CD8+ T cells in experimental cerebral malaria. J Immunol. (2002) 169:6369–75. doi: 10.4049/jimmunol.169.11.6369
15. Nitcheu J, Bonduelle O, Combadiere C, Tefit M, Seilhean D, Mazier D, et al. Perforin-dependent brain-infiltrating cytotoxic CD8+ T lymphocytes mediate experimental cerebral malaria pathogenesis. J Immunol. (2003) 170:2221–8. doi: 10.4049/jimmunol.170.4.2221
16. Potter S, Chan-Ling T, Ball HJ, Mansour H, Mitchell A, Maluish L, et al. Perforin mediated apoptosis of cerebral microvascular endothelial cells during experimental cerebral malaria. Int J Parasitol. (2006) 36:485–96. doi: 10.1016/j.ijpara.2005.12.005
18. Haque A, Best SE, Unosson K, Amante FH, de Labastida F, Anstey NM, et al. Granzyme B expression by CD8+ T cells is required for the development of experimental cerebral malaria. J Immunol. (2011) 186:6148–56. doi: 10.4049/jimmunol.1003955
19. Pai S, Qin J, Cavanagh L, Mitchell A, El-Assaad F, Jain R, et al. Real-time imaging reveals the dynamics of leukocyte behavior during experimental cerebral malaria pathogenesis. PLoS Pathog. (2014) 10:e1004236. doi: 10.1371/journal.ppat.1004236
20. Shaw TN, Stewart-Hutchinson PJ, Strangward P, Dandamudi DB, Coles JA, Villegas-Mendez A, et al. Perivascular arrest of CD8+ T cells is a signature of experimental cerebral malaria. PLoS Pathog. (2015) 11:e1005210. doi: 10.1371/journal.ppat.1005210
21. Swanson PA II, Hart GT, Russo MV, Nayak D, Yazew T, Peña M, et al. CD8+ T cells induce fatal brainstem pathology during cerebral malaria via luminal antigen-specific engagement of brain vasculature. PLoS Pathog. (2016) 12:e1006022. doi: 10.1371/journal.ppat.1006022
22. Howland SW, Poh CM, Gun SY, Claser C, Malleret B, Shastri N, et al. Brain microvessel cross-presentation is a hallmark of experimental cerebral malaria. EMBO Mol Med. (2013) 5:984–99. doi: 10.1002/emmm.201202273
24. Huggins MA, Johnson HL, Jin F, Aurelie N, Hanson LM, LaFrance SJ, et al. Perforin expression by CD8 T cells is sufficient to cause fatal brain edema during experimental cerebral malaria. Infect Immun. (2017) 85:e00985–e00916. doi: 10.1128/IAI.00985-16
25. Sato Y, Hliscs M, Dunst J, Goosmann C, Brinkmann V, Montagna GN, et al. Comparative Plasmodium gene overexpression reveals distinct perturbation of sporozoite transmission by profilin. Mol Biol Cell. (2016) 27:2234–44. doi: 10.1091/mbc.E15-10-0734
26. Kursula I, Kursula P, Ganter M, Panjikar S, Matuschewski K, Schüler H. Structural basis for parasite-specific functions of the divergent profilin of Plasmodium falciparum. Structure. (2008) 16:1638–48. doi: 10.1016/j.str.2008.09.008
28. Sato Y, Montagna GN, Matuschewski K. Plasmodium berghei sporozoites acquire virulence and immunogenicity during mosquito hemocoel transit. Infect Immun. (2014) 82:1164–72. doi: 10.1128/IAI.00758-13
29. Carroll RW, Wainwright MS, Kim K-Y, Kidambi T, Gomez ND, Taylor T, et al. A rapid murine coma and behavior scale for quantitative assessment of murine cerebral malaria. PLoS ONE. (2010) 5:e13124. doi: 10.1371/journal.pone.0013124
30. Thakur KT, Vareta J, Carson KA, Kampondeni S, Potchen MJ, Birbeck GL, et al. Cerebrospinal fluid Plasmodium falciparum histidine-rich protein-2 in pediatric cerebral malaria. Malar J. (2018) 17:125. doi: 10.1186/s12936-018-2272-y
31. Villegas-Mendez A, Greig R, Shaw TN, de Souza JB, Findlay EG, Stumhofer JS, et al. IFN-γ-producing CD4+ T cells promote experimental cerebral malaria by modulating CD8+ T cell accumulation within the brain. J Immunol. (2012) 189:968–79. doi: 10.4049/jimmunol.1200688
32. Capuccini B, Lin J, Talavera-Lopez C, Khan SM, Sodenkamp J, Spaccapelo R, et al. Transcriptomic profiling of microglia reveals signatures of cell activation and immune response, during experimental cerebral malaria. Sci Rep. (2016) 6:39258. doi: 10.1038/srep39258
34. Lin H, Lee E, Hestir K, Leo C, Huang M, Bosch E, et al. Discovery of a cytokine and its receptor by functional screening of the extracellular proteome. Science. (2008) 320:807–11. doi: 10.1126/science.1154370
35. Kossodo S, Monso C, Juillard P, Velu T, Goldman M, Grau GE. Interleukin-10 modulates susceptibility in experimental cerebral malaria. Immunology. (1997) 91:536–40. doi: 10.1046/j.1365-2567.1997.00290.x
36. Mitchell AJ, Hansen AM, Hee L, Ball HJ, Potter SM, Walker JC, et al. Early cytokine production is associated with protection from murine cerebral malaria. Infect Immun. (2005) 73:5645–53. doi: 10.1128/IAI.73.9.5645-5653.2005
37. Kordes M, Matuschewski K, Hafalla JCR. Caspase-1 activation of interleukin-1β (IL-1β) and IL-18 is dispensable for induction of experimental cerebral malaria. Infect Immun. (2011) 79:3633–41. doi: 10.1128/IAI.05459-11
38. Lewis MD, Behrends J, Sa ECC, Mendes AM, Lasitschka F, Sattler JM, et al. Chemical attenuation of Plasmodium in the liver modulates severe malaria disease progression. J Immunol. (2015) 194:4860–70. doi: 10.4049/jimmunol.1400863
39. Matz JM, Ingmundson A, Costa Nunes J, Stenzel W, Matuschewski K, Kooij TW. In vivo function of PTEX88 in malaria parasite sequestration and virulence. Eukaryotic Cell. (2015) 14:528–34. doi: 10.1128/EC.00276-14
40. Fernandes P, Howland SW, Heiss K, Hoffmann A, Hernandez-Castaneda MA, Obrova K, et al. A Plasmodium cross-stage antigen contributes to the development of experimental cerebral malaria. Front Immunol. (2018) 9:1875. doi: 10.3389/fimmu.2018.01875
41. Louis C, Cook AD, Lacey D, Fleetwood AJ, Vlahos R, Anderson GP, et al. Specific contributions of CSF-1 and GM-CSF to the dynamics of the mononuclear phagocyte system. J Immunol. (2015) 195:134–44. doi: 10.4049/jimmunol.1500369
42. Drevets DA, Schawang JE, Mandava VK, Dillon MJ, Leenen PJ. Severe Listeria monocytogenes infection induces development of monocytes with distinct phenotypic and functional features. J Immunol. (2010) 185:2432–41. doi: 10.4049/jimmunol.1000486
43. Jakubzick C, Gautier EL, Gibbings SL, Sojka DK, Schlitzer A, Johnson TE, et al. Minimal differentiation of classical monocytes as they survey steady-state tissues and transport antigen to lymph nodes. Immunity. (2013) 39:599–610. doi: 10.1016/j.immuni.2013.08.007
44. Dodoo D, Omer FM, Todd J, Akanmori BD, Koram KA, Riley EM. Absolute levels and ratios of proinflammatory and anti-inflammatory cytokine production in vitro predict clinical immunity to Plasmodium falciparum malaria. J Infect Dis. (2002) 185:971–9. doi: 10.1086/339408
45. Yarovinsky F, Zhang D, Andersen JF, Bannenberg GL, Serhan CN, Hayden MS, et al. TLR11 activation of dendritic cells by a protozoan profilin-like protein. Science. (2005) 308:1626–9. doi: 10.1126/science.1109893
47. Ribot JC, Neres R, Zuzarte-Luís V, Gomes AQ, Mancio-Silva L, Mensurado S, et al. γδ-T cells promote IFN-γ-dependent Plasmodium pathogenesis upon liver-stage infection. Proc Natl Acad Sci USA. (2019) 116:9979–88. doi: 10.1073/pnas.1814440116
48. Mamedov MR, Scholzen A, Nair RV, Cumnock K, Kenkel JA, Oliveira JHM, et al. A macrophage colony-stimulating-factor-producing γδ T cell subset prevents malarial parasitemic recurrence. Immunity. (2018) 48:350–63. e357. doi: 10.1016/j.immuni.2018.01.009
49. Janse CJ, Franke-Fayard B, Mair GR, Ramesar J, Thiel C, Engelmann S, et al. High efficiency transfection of Plasmodium berghei facilitates novel selection procedures. Mol Biochem Parasitol. (2006) 145:60–70. doi: 10.1016/j.molbiopara.2005.09.007
50. Kruglov AA, Lampropoulou V, Fillatreau S, Nedospasov SA. Pathogenic and protective functions of TNF in neuroinflammation are defined by its expression in T lymphocytes and myeloid cells. J Immunol. (2011) 187:5660–70. doi: 10.4049/jimmunol.1100663
51. Hafalla JC, Bauza K, Friesen J, Gonzalez-Aseguinolaza G, Hill AV, Matuschewski K. Identification of targets of CD8(+) T cell responses to malaria liver stages by genome-wide epitope profiling. PLoS Pathog. (2013) 9:e1003303. doi: 10.1371/journal.ppat.1003303
52. Mota MM, Pradel G, Vanderberg JP, Hafalla JC, Frevert U, Nussenzweig RS, et al. Migration of Plasmodium sporozoites through cells before infection. Science. (2001) 291:141–4. doi: 10.1126/science.291.5501.141
53. Tsuji M, Mattei D, Nussenzweig RS, Eichinger D, Zavala F. Demonstration of heat-shock protein 70 in the sporozoite stage of malaria parasites. Parasitol Res. (1994) 80:16–21. doi: 10.1007/BF00932618
54. Bruña-Romero O, Hafalla JC, González-Aseguinolaza G, Sano G-I, Tsuji M, Zavala F. Detection of malaria liver-stages in mice infected through the bite of a single Anopheles mosquito using a highly sensitive real-time PCR. Int J Parasitol. (2001) 31:1499–502. doi: 10.1016/S0020-7519(01)00265-X
Keywords: Plasmodium, malaria, cerebral malaria, experimental cerebral malaria, liver-stage, pre-erythrocytic stage, sporozoites
Citation: Sato Y, Ries S, Stenzel W, Fillatreau S and Matuschewski K (2019) The Liver-Stage Plasmodium Infection Is a Critical Checkpoint for Development of Experimental Cerebral Malaria. Front. Immunol. 10:2554. doi: 10.3389/fimmu.2019.02554
Received: 06 May 2019; Accepted: 15 October 2019;
Published: 01 November 2019.
Edited by:Juarez Antonio Simões Quaresma, Instituto Evandro Chagas, Brazil
Reviewed by:Carlos Penha-Goncalves, Gulbenkian Institute of Science, Portugal
Aline Silva Miranda, Interdisciplinary Laboratory of Medical Research, Faculty of Medicine, Federal University of Minas Gerais, Brazil
Sean C. Murphy, University of Washington, United States
Stefan Kappe, Center for Global Infectious Disease Research, Seattle Children's Research Institute, United States
Copyright © 2019 Sato, Ries, Stenzel, Fillatreau and Matuschewski. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.