- Open Access
Eimeria bovis-triggered neutrophil extracellular trap formation is CD11b-, ERK 1/2-, p38 MAP kinase- and SOCE-dependent
© Muñoz-Caro et al.; licensee BioMed Central. 2015
- Received: 10 September 2014
- Accepted: 28 January 2015
- Published: 5 March 2015
Eimeria bovis is an important coccidian parasite that causes high economic losses in the cattle industry. We recently showed that polymorphonuclear neutrophils (PMN) react upon E. bovis sporozoite exposure by neutrophil extracellular trap (NET) formation. We focused here on the molecular mechanisms that are involved in this process. The sporozoite encounter led to an enhanced surface expression of neutrophil CD11b suggesting a potential role of this receptor in E. bovis-mediated NETosis. Antibody-mediated blockage of CD11b confirmed this assumption and led to a significantly decreased sporozoite-triggered NET. In addition, E. bovis-induced NETosis was found to be Ca2+-dependent since the inhibition of store-operated calcium entry (SOCE) significantly diminished NET. Furthermore, NADPH oxidase, neutrophil elastase (NE) and myeloperoxidase (MPO) were confirmed as key molecules in sporozoite-triggered NETosis, as inhibition thereof blocked parasite-triggered NET. PMN degranulation analyses revealed a significant release of matrix metalloprotease-9 containing granules upon sporozoite exposure. We further show a significantly enhanced phosphorylation of ERK1/2 and p38 MAPK in sporozoite-exposed PMN indicating a key role of this signaling pathway in E. bovis-mediated NETosis. Accordingly, ERK 1/2 and p38 MAPK inhibition led to a significant decrease in NET formation. Finally, we demonstrate that sporozoite-induced NETosis is neither a stage-, species-, nor host-specific process.
- NADPH Oxidase
- Neutrophil Elastase
- Neutrophil Extracellular Trap
- Varioskan Flash
- Coccidian Parasite
Eimeria bovis is an important intracellular apicomplexan parasite of cattle, causing severe haemorrhagic diarrhoea (typhlocolitis) especially in calves leading to high economic losses worldwide . Polymorphonuclear neutrophils (PMN) appear to play a pivotal role in E. bovis defense. This leukocyte population was identified in parasitized intestine of E. bovis-infected calves  and PMN have been shown to interact directly with E. bovis stages and antigen, resulting in direct elimination or production of pro-inflammatory cytokines, chemokines and iNOS upon encounter . Additionally, PMN were shown to adhere to E. bovis-infected host endothelial cells  and their phagocytic and oxidative burst activities were enhanced in response to E. bovis sporozoites in vitro or ex vivo during infection . Furthermore, we recently identified sporozoites of E. bovis as potent inducers of neutrophil extracellular traps (NET) . Overall, NET formation has been described as a novel form of cell death called ETosis which is distinct from apoptosis, autophagy and necrosis leading to extracellular entrapment and eventually the killing of pathogens [6,7]. NET have been shown to be involved in several infections caused by bacteria, viruses and fungi [8-11]. However, little attention has been paid to the role of NET in the early host innate immune response against protozoan parasites [12,13]. By now, NET formation has been described to be induced by some protozoan parasites, such as Leishmania spp. , E. bovis, Toxoplasma gondii, Plasmodium falciparum, E. arloingi, and Besnoitia besnoiti [5,12,15-17].
NETosis is an NADPH oxidase-mediated ROS-dependent mechanism [7-11] which causes the expulsion of a mixture of nuclear and cytoplasmic granule contents leading to the formation of fiber-like structures being decorated with histones and granular molecules, such as neutrophil elastase (NE) and myeloperoxidase (MPO) amongst others [7,10,11]. On the mechanistic level, parasites are immobilized within these DNA-rich structures and may be killed via high local concentrations of antimicrobial molecules [12,13]. Consequently, some cases of parasite-triggered NETosis have been described as ROS-, NE- or MPO-dependent [5,12,16,17].
So far, few pathogen-derived molecules triggering NETosis have been identified such as bacterial toxins , virus  or surface lipophosphoglycans of Leishmania . In addition, little data are reported on NET-associated PMN-derived ligands and Ca2+-mediated signalling pathways . As such, CD11b and CD18 are described as being involved in Candida albicans  or Mannheimia haemolytica-mediated NETosis . Recently Ca2+-dependent ETosis has been reported . In the case of parasite-triggered NETosis, no data on PMN ligands or Ca2+-dependency are available, so far. This work focuses on molecular mechanisms involved in E. bovis-induced NET formation. We here demonstrate that respective NETosis depends on granulocyte NE and MPO activities and on the activation of an ERK1/2- and p38-related signaling pathway. Furthermore store-operated Ca2+ entry and CD11b receptor binding is involved in E. bovis-triggered NETosis.
The E. bovis (strain H) used in the present study was maintained by passages in Holstein–Friesian calves for oocyst production as described by Hermosilla et al. . Calves were infected orally with 5 × 104 sporulated E. bovis oocysts. Collection of oocysts, oocyst sporulation and excystation of sporozoites were performed as previously described . Free-released sporozoites were washed three times with sterile PBS (400 × g, 10 min), counted in a Neubauer haemocytometer chamber and thereafter suspended at final concentrations of 2.5 × 105 − 106 sporozoites/mL in culture medium (RPMI 1640, 1% penicillin/streptomycin, v/v; Gibco) free of fetal calf serum (FCS) until further experimental use. In addition, sporulated E. arloingi oocysts (strain A) , Isospora suis oocysts (kindly provided by Anja Joachim, University of Veterinary Medicine of Vienna, Austria) and Toxoplasma gondii oocysts (kindly provided by Anja Joachim, University of Veterinary Medicine of Vienna, Austria and Peter Deplazes, Faculty of Veterinary Medicine, University of Zurich, Switzerland) were used for comparative analyses on parasite species-specific NET induction. Sporozoite excystation of the latter parasite species was performed according to Pinckney et al.  as well as Freyre and Falcon .
Isolation of bovine PMN
Adult dairy cows (n = 3) were bled by puncture of the jugular vein and blood was collected in 50 mL plastic tubes (Nunc) containing 0.1 mL heparin (Sigma-Aldrich) as anticoagulant. Heparinized blood was diluted in an equal amount of PBS containing 0.02% EDTA (Sigma-Aldrich), layered on Biocoll Separating Solution® (Biochrom AG) and centrifuged at 800 × g for 45 min. After removal of the plasma and PBMC layer, the pellet was suspended in 25 mL distilled water and gently shaken for 40 s to lyse erythrocytes. Osmolarity was immediately re-adjusted by adding 3 mL of Hanks Salt Solution (HBSS 10 x, Biochrom AG). PMN were washed twice, re-suspended in RPMI 1640 medium (Gibco), counted in a Neubauer haemocytometer chamber and subsequently incubated at 37 °C and 5% CO2 atmosphere for at least 30 min before use.
Flow cytometric analysis of Eimeria bovis sporozoites-induced CD11b surface expression on bovine PMN
PMN were incubated with CFSE-stained E. bovis sporozoites (1:1 ratio, 30 min, 37 °C) in HBSS containing 0.9 mM CaCl2. For positive controls, PMN were treated with platelet activating factor (PAF 100 nM, 15 min, 37 °C; Calbiochem). For negative controls, non-treated and non-exposed PMN were used. After incubation, cells were pelleted (300 × g, 20 °C, 6 min), resuspended in 200 μL HBSS and incubated with anti-CD11b antibodies coupled to allophycocyanin (APC; clone M1/70; 20 min, in the dark; BD Pharmingen) and washed at 300 × g, 20 °C, 6 min. Thereafter, the cells were analyzed using a FACS Canto II cytometer (BD Biosciences, San Diego, CA, USA). The data were displayed as plots of forward versus side light scatter. The mean fluorescence of APC was determined from a minimum of 104 cells using BD FACS Diva 6.1 software (BD Biosciences, San Diego, CA, USA).
Inhibition of store-operated calcium entry (SOCE)
Bovine PMN were pre-incubated with the SOCE inhibitor 2-aminoethoxydiphenyl borate (2-APB) for 15 min at concentrations of 50 and 100 μM in HBSS medium prior to exposure to E. bovis sporozoites in a 1:2 ratio (2 × 105 PMN: 4 × 105 sporozoites, 60 min, 37 °C).
For NET quantification, 50 μL of micrococcal nuclease buffer containing 0.1 U/μL micrococcal nuclease (both New England Biolabs) were added to each well and incubated (15 min, 37 °C). Afterwards the samples were centrifuged (300 × g, 5 min) and the supernatants were transferred into a 96-well flat-bottom plate (100 μL per well in duplicates). Fifty microliters of Pico Green® (1:200 dilution in 10 mM Tris base buffered with 1 mM EDTA) were added to each sample and the samples were incubated (4 min, in the dark). NET formation was determined by spectrofluorometric analysis at an excitation wavelength of 484 nm and an emission wavelength of 520 nm using an automated plate monochrome reader (Varioskan Flash®; Thermo Scientific). For negative controls, PMN in plain medium were used. For positive controls, stimulation with zymosan (1 mg/mL) was used.
Immunoblotting for the detection of phosphorylated ERK1/2 and p38 MAPK
PMN (5 × 106 in HBSS containing 0.9 mM CaCl2) were exposed to E. bovis-sporozoites (5 × 106) for 15 and 30 min at 37 °C in a final volume of 500 μL. For positive controls, PMN were stimulated with PAF (100 nM). Thereafter, total protein was extracted as described previously by Hidalgo et al.  and 40 μg total protein were analyzed by a 10% SDS-PAGE. Immunoblotting was performed according to a protocol previously described by Hidalgo et al. . Antibodies directed against phospho-p38 MAPK and phospho-ERK1/2 (Cell Signalling, Beverly, MA, USA) were used according to the instructions provided by the manufacturer. Anti-mouse HRP-conjugated antisera (Santa Cruz Biotechnology, USA) were used as secondary antibodies (2 h of incubation, RT, in constant agitation). Signals were detected using an enhanced chemiluminescence system (Western Lightning® Plus-ECL; Perkin-Elmer, USA). After signal detection and documentation, the bound antibodies were removed by stripping the membranes (100 mM 2-mercaptoethanol; 2% SDS; 62.5 mM Tris-HCl, pH 6.7, for 2 h at 50 °C with agitation, followed by several washes with TBS-Tween 0.1%) according to Hidalgo et al.  and each membrane was re-probed with an antibody recognizing total p38 MAPK (p38 MAPK anti rabbit antibody; Cell signaling technology) and ERK1/2 (rabbit polyclonal IgG; Santa Cruz Biotechnology, USA). The samples were then further processed as described above. The intensities of each band were analyzed using the Software Image J and the signals were normalized to total ERK1/2 for p-ERK1/2 and to total p38 for p-p38.
NET inhibition assays using ERK1/2, p38 MAPK inhibitors and functional CD11b monoclonal antibodies
For the inhibition of ERK 1/2 and p38 MAPK the following inhibitors were used respectively: UO126 (50 μM; Sigma-Aldrich) and SB 203580 (10 μM; Sigma-Aldrich). Therefore, PMN were preincubated with the inhibitors for 30 min at RT in HBSS-buffer without phenol red (Gibco). CD11b was blocked via pre-incubation in mouse anti bovine CD11b monoclonal antibodies (MCA1425, diluted 1:5 in PBS; AbD Serotec). For antibody control, we used an irrelevant antibody at an identical concentration (anti-bovine CD4, AbD Serotec). Then, PMN were exposed to viable E. bovis-sporozoites (1:2 ratio: 2 × 105 PMN + 4 × 105 sporozoites) for 60 min at 37 °C. Thereafter extracellular DNA was quantified as described above. All measurements were achieved using an automated monochrome reader (Varioskan Flash; Thermo Scientific). For positive controls, zymosan (Sigma-Aldrich) was used in a final concentration of 0.5 mg/mL.
Visualization of NET and detection of histones (H3), neutrophil elastase (NE) and myeloperoxidase (MPO) in NET structures
Bovine PMN were incubated with E. bovis sporozoites (ratio 1:1; 30 min) on poly-L-lysine-treated coverslips and fixed [4% (w/v) paraformaldehyde, Merck, 20 min in the dark]. NET structures were visualized by staining extracellular DNA with 5 mM Sytox Orange dye (Invitrogen) for 10 min at RT according to Martinelli et al. . For the visualization of sporozoites within NET structures, sporozoites were stained with 5(6)-carboxyfluorescein diacetate succinimidyl ester (CFSE, 7.5 μM, 37 °C, 30 min; Invitrogen) according to Hermosilla et al.  prior to PMN exposure. After fixation of the cells and three washings in sterile PBS, the samples were mounted in anti-fading buffer (Mowiol®, Sigma-Aldrich) and stored (4 °C, in the dark) until further use. For the detection of histones, MPO and NE within NET structures the following specific antibodies were used: anti-histone monoclonal antibodies [rabbit (E173) anti-bovine histone H3, phospho S10 DyLight® 488, 1:100; ab139848, Abcam], anti-MPO antibodies (rabbit anti-bovine MPO, Alexa Fluor 488, 1:200; ABIN906866) and anti-NE antibodies (rabbit anti-human NE, 1:200; AB68672, Abcam). Therefore, the samples were washed three times with PBS, blocked with BSA [1% (w/v) in PBS, 30 min, RT, Sigma-Aldrich] and reacted with anti-histone, anti-NE or anti-MPO antibodies [1 h, RT, in the dark for bovine anti-histone (H3); 24 h, RT, in the dark for both anti-MPO and anti-NE antibodies]. The samples were then gently washed in PBS and mounted in anti-fading buffer (Mowiol®, Sigma-Aldrich). Visualization was achieved using an inverted Olympus® IX81 fluorescence microscope equipped with a digital camera.
Measurements of NADPH oxidase, NE and MPO enzymatic activities and inhibition of these enzyme activities
For NADPH oxidase-, NE- and MPO-inhibition assays, the following inhibitors were used: the NADPH oxidase inhibitor diphenylene iodonium (DPI, 10 μM, Sigma-Aldrich); the NE inhibitor Suc-Ala-Ala-Pro-Val chloromethyl ketone (CMK; 1 mM, Sigma-Aldrich), according to Scapinello et al.  and the MPO inhibitor 4-aminobenzoic acid hydrazide (ABAH; 100 μM, Calbiochem), according to Parker et al. . In brief, PMN and sporozoites (1:1 ratio, n = 3) were incubated (30 min, 37 °C) in HBSS-buffer without phenol red (Gibco) for positive controls. In parallel, PMN were pre-incubated with the corresponding inhibitors for 30 min at RT prior to exposure to viable E. bovis-sporozoites (1:1 ratio, 30 min, 37 °C). To estimate maximum values of extracellular DNA, PMN were lysed by Triton-X 100 treatment (0.1%; Sigma-Aldrich). To block NET formation, 90 U of DNase I (Roche Diagnostics) were supplemented 15 min before the end of incubation period. NET were quantified via Pico Green®-DNA staining as described above.
NADPH oxidase, NE and MPO enzymatic activities were measured using respective substrates: 10 μg/mL DCFH-DA (Sigma-Aldrich); 3 mg/mL of the NE chromogenic substrate MeoSuc-Ala-Ala-Pro-Val-chloromethyl-ketone (Sigma-Aldrich) and 50 μM Amplex red (Invitrogen), respectively. ROS production was measured by oxidation of DCFH-DA to fluorescent DCF according to Conejeros et al. . The relative fluorescence units (RFU) were recorded at 15 min intervals for a period of 30 min applying 485 nm excitation and 530 nm emission wavelengths. NE activity was measured every 10 min for 30 min at 410 nm wavelength and MPO-peroxidase activity was measured every 10 min for 30 min in 571-585 nm fluorescence ranges. All measurements were achieved using an automated monochrome reader (Varioskan Flash; Thermo Scientific). As positive control, zymosan (Sigma-Aldrich) was used at a final concentration of 0.5 mg/mL.
Determination of matrix metalloproteinase 9 (MMP-9) activities in PMN supernatants
PMN (106/500 μL HBSS/0.9 mM CaCl2) were exposed to equal numbers of E. bovis sporozoites (15 and 30 min, 37 °C). Stimulation of PMN with PAF (100 nM, 5 min, 37 °C) was used for positive controls. PMN cultivated in plain medium were used for negative controls. After incubation, the cells were centrifuged (600 × g, 6 min) and the supernatants were assayed for gelatinase activity by zymography. Therefore, substrate gel electrophoresis was performed using the method described by Conejeros et al. . Briefly, 10 μL of supernatant/slot were loaded on polyacrylamide gels (10%, 0.75 mm thickness) containing 0.28% of gelatin (Sigma-Aldrich). In parallel a recombinant MMP-9 standard (Sigma-Aldrich) and a molecular mass marker (Fermentas International Inc., Canada) were loaded as reference samples. The gels were run at 200 V for 1 h in a Bio-Rad Mini Protean II chamber (Bio-Rad Laboratories, CA, USA). Thereafter, the gels were incubated twice in Triton X-100 (2.5%, under constant shaking, RT, 30 min) and overnight at 37 °C in reaction buffer (100 mM Tris, pH 7.5; 10 mM CaCl2). The gels were stained in Coomassie Brilliant Blue R-250 (Winkler, Santiago, Chile; 0.5% in acetic acid : methanol : water = 1 : 3 : 6). MMP-9 (gelatinase B) enzymatic activity present in the test samples were determined according to the degree of gelatin degradation (visible as clear bands of 82 kDa) relative to the MMP-9-control by means of band intensity measurements (applying ImageJ 1.35 s software).
Host cell infection and production of viable Eimeria bovis merozoites I
Primary bovine umbilical vein endothelial cells (BUVEC) were isolated from umbilical cord veins, according to the method of Hermosilla et al. . Confluent BUVEC monolayers (n = 3) were infected with 2.5 × 105 freshly excysted E. bovis-sporozoites suspended in modified ECGM [ECGM (PromoCell) supplemented with 70% (v/v) M199 (Gibco), 2% FCS (Gibco) and 1% penicillin (Sigma-Aldrich)] per 25 cm2 flask (Greiner). The cells were fed 24 h after infection and thereafter every third day with modified ECGM. To control for E. bovis macromeront development and the release of merozoites I, infected BUVEC cultures were analyzed daily over a period of 22 days using a phase-contrast inverted microscope (IX81 microscope®, Olympus). Free-released merozoites I were harvested from the supernatant of infected BUVEC monolayers (400 × g, 5 min) and washed twice in PBS. The merozoites I were counted in a Neubauer chamber haemocytometer.
Scanning electron microscopy (SEM)
Bovine PMN were incubated with E. bovis sporozoites, merozoites I or oocysts at a ratio of 1:1 for 90 min on poly-L-lysine (Sigma-Aldrich) pre-coated coverslips. After incubation, the samples were fixed (2.5% glutaraldehyde in 0.1 M cacodylate buffer, 15 min, all Merck) and washed with 0.1 M cacodylate buffer. The samples were post-fixed in 1% osmium tetroxide (Merck) in 0.1 M cacodylate buffer, washed three times in distilled water, dehydrated in ascending ethanol concentrations, critical point dried by CO2-treatment and sputtered with gold. Specimens were examined using a Philips XL30 scanning electron microscope at the Institute of Anatomy and Cell Biology, Justus Liebig University Giessen, Germany.
Quantification of NET derived from PMN and parasites from different origins
NET formation was quantified using Pico Green® (Invitrogen), a DNA-binding dye. In order to quantify E. bovis sporozoite- or merozoite I-induced NET formation, bovine PMN (n = 3-5) were re-suspended in serum-free medium RPMI 1640 and incubated (all at 37 °C) with E. bovis-sporozoites in a 1:2 ratio (2 × 105 PMN: 4 × 105 sporozoites, 60 min), with E. bovis-merozoites I in a 1:1 ratio (1 × 105 PMN: 1 × 105 merozoites, 90 min), with oocysts (5 × 104, 60 min, 1:1) and with sporozoites of E. arloingi (n = 3; 1 × 105 PMN: 1 × 105 sporozoites, 60 min), Isospora suis (n = 3; 1 × 105 PMN: 1 × 105 sporozoites; 60 min) and T. gondii (n = 5; 1 × 105 PMN: 1 × 105 sporozoites; 60 min). In addition, PMN isolated from different host species origin (caprine, horse and dog) were incubated with E. bovis sporozoites in a 1:2 ratio (2 × 105 PMN: 4 × 105 sporozoites, 60 min at 37 °C). For positive controls, zymosan was used at a final concentration of 0.5 mg/mL. Plain RPMI 1640 medium served as negative controls. NET-formation was determined based on Pico Green®-DNA staining as described above.
Eimeria bovis sporozoite entrapment assay
For the quantification of sporozoite entrapment within NET structures we followed the method described by Köckritz-Blickwede et al.  with slight modifications. Briefly, PMN (2.5 × 105/96-well) were pre-activated by zymosan treatment (30 min, 37 °C). Meanwhile, E. bovis-sporozoites were stained with FITC dye (0.2 mg/mL, 30 min, on ice, in the dark, Invitrogen) and washed twice in PBS (3000 × g, 10 min). Thereafter, zymosan-stimulated PMN were exposed to FITC-labeled E. bovis sporozoites (512 × g, 10 min; subsequent incubation for 30 min at 37 °C) in ascendant ratios (0.5:1;1:1 and 1:2). Non-exposed sporozoites were used for controls (1:1; 1:2). The samples were washed twice in RPMI 1640 medium and measured for fluorescence intensity at 485/538 nm wavelength. The percentage of entrapment was calculated as follows: [(A485/538 nm sporozoites exposed to PMN)/(A485/538 nm non-exposed sporozoites)] × 100%.
All animal procedures were performed according to the Justus Liebig University Animal Care Committee guidelines, approved by the Ethic Commission for Experimental Animal Studies of the State of Hesse (Regierungspräsidium Giessen) and in accordance to the current German Animal Protection Laws. Identification number of animal care and project licence: GI 18/10-Nr.A51/2012 544_AZ952 (Eimeria bovis-oocyst production); GI 18/10-Nr.A9/2012 521_AZ877 (Bovine blood samples). European Animal Welfare Legislation: ART13TFEU.
Co-culture/stimulation conditions were compared by one- or two-factorial analyses of variance (ANOVA) with repeated measurements in order to compare co-culture/stimulation conditions. All analyses were performed with the GraphPad Prism® 6 software. Differences were regarded as significant at a level of p ≤ 0.05 (*); p ≤ 0.01 (**); p ≤ 0.001 (***).
Exposure to E. bovis sporozoites up-regulates neutrophil CD11b surface expression on bovine PMN and triggers NET formation in a CD11b-dependent manner
Eimeria bovis-induced NET formation is store-operated calcium entry (SOCE)-dependent
Sporozoite-induced NETosis is a ROS-, NE- MPO-dependent process
E. bovis sporozoite exposure enhances matrix metalloprotease 9 (MMP-9) release of bovine PMN
ERK1/2- and p38 MAPK-signaling pathways are involved in E. bovis sporozoite-triggered NET extrusion
Sporozoite-triggered NETosis is neither stage- nor parasite species- nor host-specific
Given that E. bovis is a strict host-specific parasite and, in consequence, exclusively infects bovines, we then analyzed whether E. bovis-mediated NET formation is a host-specific event. Therefore, PMN of different host origins (horse, goat, dog and cattle) were controlled for NET formation after exposure to E. bovis sporozoites. The data clearly revealed that PMN of all host types reacted by significant NET formation (p ≤ 0.01, Figure 8A) which argues against a host-specific reaction.
NET structures significantly entrap Eimeria bovis sporozoites
In order to analyze the capacity of NET to trap viable E. bovis sporozoites, we established a quantitative parasite-entrapment-assay by using FITC-stained parasites and zymosan pre-activated bovine PMN as described elsewhere . The experiments revealed a proportion of 43.4% of sporozoites to be immobilized in NET structures when compared to non-exposed sporozoites (data not shown). These results indicate a rather high efficacy of NET as an effector mechanism considering that almost every second parasite was entrapped and most probably hampered from host cell invasion as reported elsewhere .
NET formation depends on the assembly/activation of the NADPH oxidase complex and the resulting production of ROS . Since these mechanisms were reported as Ca2+-mediated in the bovine system , it appears likely that NETosis is a Ca2+-dependent process, as recently demonstrated by Gupta et al. . The fact that NET formation is induced by thapsigargin  which mobilizes Ca2+ from intracellular pools, also indicates a key role of Ca2+ in NETosis. Since SOCE was proven to play a crucial role in Ca2+-dependent ROS production  we here used 2-APB a well-known inhibitor of SOCE for functional assays. The pre-incubation of PMN with 2-APB prior to sporozoite exposure resulted in a significant diminishment of NETosis and therefore confirmed the assumption that parasite-triggered NET formation is a Ca2+-(SOCE)-dependent process.
Besides being SOCE-dependent, ROS production is up-regulated in a CD11b (CR3)-dependent manner in bovine PMN . In turn, up-regulation of CD11b proves as SOCE-dependent since it is inhibited by 2-APB  leading us to the assumption that the neutrophil integrin receptor CD11b may also be involved in sporozoite-mediated NETosis. Indeed, we found significantly enhanced levels of surface CD11b expression on parasite-exposed bovine PMN. The fact that antibody-mediated blockage of CD11b additionally resulted in NET diminishment suggests CD11b to be involved in sporozoite-triggered NETosis and to function as a PMN-derived receptor in this effector mechanism. These findings were in accordance with Byrd et al.  who reported on CD11b as a potential ligand in NETosis since antibody-mediated blockage of this integrin inhibits fibronectin-dependent NET formation to C. albicans hyphae.
Moreover, SOCE is tightly regulated via ERK1/2 MAPK phophorylation, i.e., by a signaling pathway that was recently described to be involved in NETosis . In addition, ROS-dependent activation of ERK and p38 MAPK was demonstrated to mediate PMA-induced NET release from human neutrophils . In accordance to the latter reports and to data on other pathogens [12,21] we here show a sporozoite-triggered up-regulation of ERK1/2 and p38 MAPK phosphorylation in parasite-exposed bovine PMN. The key role of the ERK1/2- and p38 MAPK-dependent signaling pathway in NETosis was confirmed in functional inhibition experiments showing that parasite-triggered NETosis was significantly diminished in the presence of ERK-and p38 inhibitors.
We furthermore focused on the relevance of NE and MPO and confirmed the key role of these two molecules in E. bovis-triggered NETosis. As with other bovine pathogens , exposure to sporozoites led to an increase of both, NE and MPO enzymatic activities in bovine PMN. Functional inhibition assays confirmed the relevance of these enzymes since parasite-mediated NETosis was significantly blocked when NE and MPO inhibitors were applied. Finally, the co-localization of DNA-rich filaments with NE- or MPO-derived signals in sporozoite-induced NET structures emphasized the classical characteristics of NET. These results were in line with recent findings on other coccidian parasites, such as E. arloingi  or B. besnoiti .
Whilst NE and MPO originate from azurophilic PMN granules, other molecules such as metalloproteinases (MMP), are contained in tertiary (gelatinase) granules. We here analyzed whether MMP-9 is released from PMN upon sporozoite exposure. Zymographic analyses of PMN supernatants confirmed a parasite-mediated MMP-9-release into PMN supernatants. So far, the functional role of MMP-9 in NETosis is unclear. However, it is worth noting that the release of MMP-9 is regulated by the ERK 1/2 and p38 MAPK signaling pathway . Interestingly, Carmona Rivera et al.  showed an impaired endothelial function induced by NET-externalized MMP. Given that E. bovis sporozoites infect and mature within endothelial cells, a yet unclear interrelation between NETosis and parasite development within endothelium may exist.
Overall, since the first description of NET as an innate effector mechanism , most studies have focused on NETosis driven by bacterial, viral and fungal pathogens and, less frequently, on parasitic pathogens . Nonetheless, there is increasing evidence on the relevance of NET as a defense mechanism against protozoan infections in vitro and in vivo [12,13]. Thus, NET-related data are available on some protozoan pathogens, such as E. bovis, Toxoplasma gondii, Plasmodium falciparum, E. arloingi, and B. besnoiti [5,12,15-17] and Leishmania spp. . The current data suggest NETosis as a generally valid effector mechanism against coccidian parasites. Thus, NET release occurred irrespective of the parasite stage (E. bovis sporozoites, merozoites I, oocysts), and PMN origin (bovine, caprine, equine, canine). In agreement, data on different Leishmania stages  also indicated NETosis as a stage-independent defense mechanism. In addition, T. gondii-triggered NETosis has been reported for both human and murine PMN  indicating host-independent reactions. Overall, it is noteworthy that the degree of entrapment clearly differed amongst different parasite species and stages. Thus, we here report on 43% of E. bovis sporozoites to be immobilized within bovine NET structures, whilst in the caprine system even 72% of E. arloingi sporozoites were trapped  but only 34% of B. besnoiti tachyzoites were found ensnared in NET being expelled from bovine PMN . Since all these parasites exhibit an obligatory intracellular replication, extracellular immobilization via NET will have a tremendous implication on the outcome of the disease as previously postulated [16,17].
Furthermore, NETosis was not parasite species-specific since sporozoites of different coccidian parasites (E. bovis, E. arloingi, I. suis, T. gondii) equally triggered NET formation. To our best knowledge this is the first report on T. gondii and I. suis sporozoite-induced NET extrusion whilst tachyzoite stages of T. gondii  and sporozoites of E. arloingi  have already been reported before. Especially in the case of T. gondii, which exhibits an enormous proliferation at the tachyzoite stage, the intervention of the immune system at a very early time point, i.e. when sporozoites invade the host system and before non-sexual parasite replication occurs, will have a higher impact on the outcome of disease than tachyzoite-triggered reactions. Taking into account that PMN have been demonstrated to actively transmigrate into the intestinal lumen and were found alive in the gut mucus , it seems feasible to assume that they may interact with luminal pathogen stages, such as ingested Eimeria oocysts, in vivo. Consistently, we here show that oocysts of E. bovis are trapped and sometimes almost encaged by NET structures in vitro, thereby most probably preventing proper excystation of sporozoites. This novel anti-excystation mechanism of NET has recently been hypothesized for E. arloingi oocysts, in which sporozoites were impeded to escape from NET-covered preformed excystation sites (micropyles) of sporulated oocysts . Thus, in the in vivo situation, luminal occurring NETosis might intervene very early after oral infection with the parasite and abrogate infection even before infectious stages (sporozoites) are able to evade immune reactions via intracellular positioning.
In summary, NET formation seems to be an ancient and highly conserved host effector mechanism of PMN acting against several pathogens as an early host immune reaction. In the present work, we added new data on the molecular mechanisms involved in parasite-triggered NETosis and call for more investigations on receptor-ligand-interactions.
We are deeply indebted to Gerd Magdowski (Institute of Anatomy and Cell Biology, JLU Giessen, Germany) for his excellent assistance and kind help on SEM analyses. We further acknowledge Brigitte Hofmann, Christin Ritter and Klaus Becker for their excellent technical assistance in cell culture and blood collection. This work was supported and financed by the German Research Foundation (DFG; grant number: TA 291/4-1).
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