Platelet activation and platelet–neutrophil interactions have been found to be involved in inflammation, organ failure and soft-tissue necrosis in bacterial infections. Streptococcus suis, an emerging human pathogen, can cause streptococcal toxic-shock syndrome (STSS) similarly to Streptococcus pyogenes. Currently, S. suis–platelet interactions are poorly understood. Here, we found that suilysin (SLY), the S. suis cholesterol-dependent cytolysin (CDC), was the sole stimulus of S. suis that induced platelet-neutrophil complexes (PNC) formation. Furthermore, P-selectin released in α-granules mediated PNC formation. This process was triggered by the SLY-induced pore forming-dependent Ca2+ influx. Moreover, we demonstrated that the Ca2+ influx triggered an MLCK-dependent pathway playing critical roles in P-selectin activation and PNC formation, however, PLC-β-IP3/DAG-MLCK and Rho-ROCK-MLCK signalling were not involved. Additionally, the “outside-in” signalling had a smaller effect on the SLY-induced P-selectin release and PNC formation. Interestingly, other CDCs including pneumolysin and streptolysin O have also been found to induce PNC formation in a pore forming-dependent Ca2+ influx manner. It is possible that the bacterial CDC-mediated PNC formation is a similar response mechanism used by a wide range of bacteria. These findings may provide useful insight for discovering potential therapeutic targets for S. suis-associated STSS.
Streptococcus suis serotype 2 (SS2) infection is one of the major causes of septicaemia and meningitis in pigs and humans1,2. In 2005, China reported more than 200 human cases with an unusual clinical presentation of streptococcal toxic-shock syndrome (STSS) and a mortality rate of up to 20%3. Thrombocytopenia and multisystem dysfunction, such as liver failure and heart failure, were found in more than half of the STSS patients. Moreover, purpura and gangrenous necrosis were the typical skin manifestations in STSS patients4,5.
Platelet–neutrophil interactions have been found to be involved in inflammation6, organ failure7 and soft-tissue necrosis8,9 in some life-threatening infectious diseases by direct injury to the endothelium. The myonecrosis tissue specimen from a patient with S. pyogenes-associated STSS showed numerous platelet/leukocyte thrombi, and streptolysin O (SLO) of S. pyogenes mediated the platelet-neutrophil complexes (PNC) formation in a P-selectin-dependent manner9. The α-hemolysin of community-associated methicillin-resistant S. aureus (CA-MRSA) has been reported to induce PNC formation via platelet P-selectin, suggesting that S. aureus α-hemolysin may contribute to alveolar capillary leakage, haemorrhage and lung destruction during MRSA necrotizing pneumonia10. However, the molecular signalling pathways induced by these bacterial toxins to activate platelet P-selectin are mostly unknown. Moreover, the interactions between platelets and S. suis and the molecular mechanism underlying the S. suis-induced platelet-neutrophil interactions remain poorly understood.
P-selectin is a member of the selectin family of cell surface receptors. Platelet P-selectin primarily binds P-selectin glycoprotein ligand-1 (PSGL-1) on neutrophils, mediates the platelet–neutrophil interactions11,12,13, is stored in α-granules of platelets and is rapidly secreted to the surface upon activation by agonists [e.g., ADP, platelet-activating factor (PAF)]14. The PLC-β-IP3/DAG-MLCK14,15,16 and Rho-ROCK-MLCK signalling pathways17 usually mediate the agonist-induced platelet activation. The PLC-β-IP3/DAG-MLCK signalling is often accompanied by an increase in intracellular Ca2+, which binds to calmodulin18. The final signalling events in the above mentioned pathway are phosphorylation of MLC by MLCK that leads to actin–myosin interactions, consequently resulting in platelet degranulation14. Additionally, during platelet activation, the agonists induce the “inside-out” signalling, in turn the ligand-occupied GPIIb/IIIa receptor usually reinforces activation of the “outside-in” signalling, leading to secretion of α-granules19.
Suilysin (SLY) is a 497 amino-acid protein belonging to the cholesterol-dependent cytolysin (CDC) family, which has more than 20 members, including pneumolysin (PLY) and SLO, expressed by S. pneumoniae and S. pyogenes, respectively. Like other members of the CDC family produced by Gram-positive bacteria, a classical feature of these toxins is their ability to create transmembrane pores in cholesterol-containing membranes, thereby causing cell lysis20,21. In this study, SLY was the sole stimulus responsible for PNC formation induced by S. suis. We also found that the SLY-induced pore forming-dependent Ca2+ influx triggered human platelet P-selectin release to the plasma membrane, where it mediated adhesion of platelets to neutrophils. Moreover, the Ca2+-MLCK-dependent signalling was required for a significant release of P-selectin, which was essential for SLY to induce PNC formation. Our findings showed that PLY and SLO-induced PNC formation was also triggered by pore formation-dependent Ca2+ influx, and suggest a possible similar mechanism to SLY. These findings may provide useful insight for discovering potential therapeutic targets for Streptococci-associated STSS.
SLY is the sole stimulus responsible for PNC formation induced by S. suis
To elucidate the stimulus inducing PNC formation, bacterial cells and stationary phase culture supernatants from S. suis strains were tested for PNC formation activity in human blood. 05ZYH33 supernatant significantly induced PNC formation significantly (P < 0.01, Fig. 1A), whereas the bacterial cells did not (Fig. 1B), suggesting that there are secreted stimuli that induce PNC formation. SLY is an important secreted toxin of S. suis; high levels are produced at the end of the exponential growth phase22; therefore, we used it for testing PNC-inducing activity. Interestingly, neither Δsly bacterial cells nor the supernatant induced PNC formation as background control Todd-Hewitt broth (THB)/PBS (Fig. 1). Moreover, the supernatant of the SLY-negative Canadian strain 1330 culture and heat-inactivated 05ZYH33 supernatant failed to induce PNC formation (Fig. 1A). Taken together, these results indicate that SLY was the sole stimulus of S. suis involved in this process. To further elucidate the mechanism of SLY-stimulated PNC formation, recombinant SLY (rSLY) was generated and it induced PNC formation, but its non-hemolytic mutant, SLYP353V, and the irrelevant control protein recombinant factor H-binding protein (rFhb) did not (Fig. 1A). Finally, SLY-induced PNC formation was detected by Wright’s staining of blood smears and immunofluorescence confocal microscopy (Fig. 1C). These data imply that SLY was the sole S. suis protein that stimulated PNC formation in human whole blood.
SLY-induced PNC formation is mediated by P-selectin on human platelets
During platelet activation, agonists induce platelet shape changes and granular secretion14. P-selectin is usually found in the membrane of the platelet secretory granules (α-granules) and is often used as a measure of α-granules release. Here, 05ZYH33 supernatant and rSLY significantly induced P-selectin release to the platelets’ surface (CD62P, P < 0.001; Fig. 2A), but the supernatant of ∆sly and the THB/PBS controls did not. These results indicate that SLY was the sole protein of S. suis that activated human platelets and induced α-granules release.
P-selectin is a member of the selectin family of cell surface receptors, which primarily mediates neutrophil–platelet, platelet–platelet and monocyte–platelet interactions14. Therefore, a specific monoclonal antibody for P-selectin was used to explore the role of P-selectin in PNC formation induced by SLY. Pre-incubation of human blood with a functional neutralizing monoclonal antibody (clone AK-4) abrogated 05ZYH33 supernatant- and rSLY-induced PNC formation to the level of the ∆sly supernatant or the background THB/PBS level (Fig. 2B), indicating that P-selectin principally mediated PNC formation induced by SLY.
SLY-induced platelet P-selectin release and PNC formation depend on pore formation in platelets
CDCs can bind to membrane cholesterol, to create large pores (350–450 Å in diameter) and consequently lyse the target cells23,24. Free cholesterol can inhibit CDC-induced pore formation20,21. To determine whether SLY-induced PNC formation is due to pore formation, the cholesterol inhibition assay was used. As shown in Fig. 3A, rSLY could bind to human platelets. As expected, this binding was inhibited by cholesterol. In further study, rSLY exhibited strong cytotoxicity when its concentration is no less than 5 μg/mL (Fig. 3B). Substantial PNC formation occurred when rSLY was 1 μg/mL (Fig. 3C) and the cytotoxicity was ~28% at this concentration (Fig. 3B). Cholesterol (100 μg/mL) that inhibited SLY-induced cytotoxicity (Fig. 3B) also abrogated the SLY-induced PNC formation (Fig. 3C). Although the non-hemolytic recombinant mutant, rSLYP353V also could bind to platelets (Fig. 3A), it lost cytotoxicity to platelets (Fig. 3B), which therefore failed to induce PNC formation (Fig. 1A). Furthermore, 1 μg/mL rSLY-induced P-selectin release was also significantly reduced by cholesterol (100 μg/mL) to the background level (Fig. 3D). More importantly, cholesterol fully inhibited 05ZYH33 supernatant-induced PNC formation (Fig. 3E). These results indicate that SLY-induced P-selectin release and PNC formation were pore dependent.
SLY-induced platelet P-selectin release and PNC formation requires pore formation-dependent Ca2+ influx
Agonists (e.g., ADP, PAF) stimulating platelet activation commonly promote platelets to mobilize storage Ca2+, take up extracellular Ca2+, and thereby increase the concentration of cytosolic Ca2+ 18. Moreover, platelet P-selectin binds to P-selectin glycoprotein ligand-1(PSG-1) on neutrophils, thus promoting the initial binding of the cells. However, firm platelet-neutrophil adhesion is mediated by integrin αMβ2 binding to platelet GPIb or to fibrinogen. Therefore, we observed the calcium mobilization in platelets stimulated by SLY in initial time. We used confocal laser scanning microscopy and Fluo-8 to monitor the calcium mobilization in platelets. In Hank’s balanced salt solution (HBSS) containing 2 mM Ca2+, 1 μg/mL rSLY rapidly increased the intracellular Ca2+ of platelets (Fig. 4A and Supplementary Video 1), whereas cholesterol (100 μg/mL) strongly diminished the rSLY-induced Ca2+ influx (Fig. 4B and Supplementary Video 2). Moreover, the non-hemolytic recombinant mutant, rSLYP353V (Fig. 4C and Supplementary Video 3) and the PBS control (Supplementary Video 4) did not induce a Ca2+ influx. It’s interesting that about ~20% cells were observed with increase of Ca2+ in short time after stimulating by rSLY, but not to all (Supplementary Video 1). Therefore, we hypothized that pore formation in some platelets (~28%) leading to calcium influx, which served as a positive feedback mechanism for activation of other platelets and ultimately induction of PNC formation. These results indicate that the rSLY-induced Ca2+ influx depend on pore formation induced by rSLY. The roles of Ca2+ influx in platelet activation and PNC formation were further studied using EGTA to chelate the extracellular Ca2+. Blockage of the Ca2+ influx by EGTA abrogated the rSLY-induced P-selectin release (CD62P; Fig. 4D) and the P-selectin-mediated PNC formation (Fig. 4E) in human blood (P < 0.05). Taken together, these results indicate that the pore formation-dependent Ca2+ influx played essential roles in platelet activation and PNC formation induced by SLY.
Platelet signalling is involved in SLY-induced PNC formation
To investigate the possible signalling in platelet activation induced by SLY, specific inhibitors were used. Firstly, Clostridium perfringens phospholipase C (PLC) use as positive control to detect the activities of specific inhibitors (Fig. 5). Secondly, the effects of specific inhibitors on SLY-induced PNC formation were detected. Interestingly, the MLCK-specific inhibitor, ML-7, dramatically reduced the SLY-induced P-selectin release (Fig. 5A), however, both the ROCK-specific inhibitor, Y27632, and the PLC-β-specific inhibitor, U73122, did not (Fig. 5A,B). Moreover, rSLY strongly induced myosin light chain (MLC) phosphorylation, while cholesterol, EGTA and ML-7 all had apparent inhibitory effect on MLC phosphorylation induced by rSLY (Fig. 5C). The phosphorylation of MLC usually leads to rearrangement of the platelet cytoskeleton, and then promoting the mobilization of P-selectin from α-granules to the plasma membrane, in which subsequently mediates the platelet–neutrophil interactions14. As expected, ML-7 also strongly inhibited the SLY-induced PNC formation, but Y27632 and U73122 did not (Fig. 5E,F). Thus, we propose that the PLC-β-IP3/DAG-MLCK and Rho-ROCK-MLCK pathways are not involved in SLY-induced platelet activation and PNC formation, but that the SLY-induced pore formation dependent-Ca2+ influx directly activates the Ca2+-calmodulin-MLCK signalling.
Agonists (e.g., ADP, PAF) activate human platelets, resulting in an “inside-out” signalling, leading to integrin GPIIb/IIIa activation that promotes binding to fibrinogen in the plasma. In turn, the fibrinogen-occupied GPIIb/IIIa usually reinforces activation of “outside-in” signalling, leading to secretion of α-granules. In fact, in our early study, SLY induced Fg binding to platelet in human blood (Front. Cell. Infect. Microbiol. 2016, accepted). Eptifibatide is a specific inhibitor of fibrinogen binding to the GPIIb/IIIa receptor. Herein, we used eptifibatide to explore the role of “outside-in” signalling in SLY-induced PNC formation. Pre-incubation of eptifibatide with human blood had some inhibiting effects on P-selectin release (Fig. 5D, P < 0.05) and PNC formation (Fig. 5G, P < 0.05), suggesting that the “outside-in” signalling was also involved in SLY-induced PNC formation, but with a smaller effect than the Ca2+-MLCK signalling.
Other CDCs that promote PNC formation require pore formation-dependent calcium influx
PLY and SLO are important toxins of S. pneumoniae and S. pyogenes, respectively, which belong to the Group I typical CDCs with high affinity to cholesterol and high structural similarity to SLY20,21. Therefore, PLY and SLO possibly share similar functional characteristics to SLY. Interestingly, cholesterol completely abrogated their induction of PNC formation (Fig. 6A). Moreover, EGTA suppressed PNC formation induced by PLY or SLO (Fig. 6B). We propose that CDC-mediated PNC formation is a similar mechanism used by a wide range of bacteria, which is triggered by the pore formation-dependent Ca2+ influx.
In the current study, we found that SLY, which was secreted from S. suis 05ZYH33 at the stationary growth phase, stimulated PNC formation and that this stimulation required SLY-induced Ca2+ influx and P-selectin release. In contrast, S. suis 05ZYH33 cells did not induce PNC formation. These results indicate that S. suis 05ZYH33 may not directly interact with platelets, instead they cause PNC formation via SLY. 05ZYH33 is a sequenced strain that belongs to the sequence type 7 (ST-7) strains, and caused the 2005 outbreak and STSS in China25. Moreover, ST-7 strains were more toxic to human peripheral blood mononuclear cells (PBMCs) than ST-1 strains (mainly referring to the European virulent strains)26. In particular, we have previously shown that the ST-7 strains produced more SLY than the non-epidemic strains, contributing to invasive infection27. Therefore, SLY may be a potential therapeutic target for preventing S. suis-mediated platelet activation, thrombocytopenia, liver failure and purpura gangrenosa.
Similar to our findings, other cytolysins of the CDC family have been found to stimulate platelet activation and PNC formation. Bryant et al. have reported that SLO induced coaggregation of platelets and neutrophils, and stimulated platelet P-selectin (CD62P)-dependent PNC formation9. Parimon et al. have also found that Staphylococcus aureus α-hemolysin promotes platelet-neutrophil aggregate formation via P-selectin10. However, the molecular mechanism underlying these bacterial toxins-induced P-selectin activation and PNC formation are not fully understood. Although it has been reported that there are 20 kinds of bacterial cytolysin belonging to Group I CDCs with high affinity to cholesterol28, there is only little evidence showing associations between Group I CDCs and platelet activation. The current study demonstrated direct evidence showing that SLY induced Ca2+ influx in platelets, which was required for SLY-induced PNC formation. Similar to SLY, the other two CDCs, PLY and SLO, also induced PNC formation in a Ca2+ influx-dependent manner. These data suggest that CDCs form pores in platelet membranes, which result in Ca2+ influx, consequently triggering intracellular signalling events that induce PNC formation.
We also found that SLY-induced P-selectin (CD62P) release was Ca2+ influx dependent, suggesting that stimulation of this adhesion factor is downstream of the SLY-induced Ca2+ influx. The signalling events between the Ca2+ influx and the P-selectin release or PNC formation strongly associated with MLCK activity, because the MLCK inhibitor, ML-7, significantly reduced the SLY-induced platelet P-selectin release and the P-selectin-mediated PNC formation. However, these processes did not involve PLC-β-IP3/DAG-MLCK or Rho-ROCK-MLCK signalling (Fig. 5A,B,D,E); the SLY-induced Ca2+ influx may directly bind to calmodulin, which consequently activates MLCK. These data imply that the signalling in response to SLY may be different from that in response to typical platelet agonists such as ADP and thromboxane A2 (TXA2)14. Moreover, eptifibatide, a fibrinogen-specific inhibitor that binds to GPIIb/IIIa receptor, showed smaller inhibition effects on PNC formation, which is consistent with Bryant et al.9. These authors suggested that platelet GPIIb/IIIa also participates in PNC formation using fibrinogen as a bridging molecule between GPIIb/IIIa and PMNL CD11b/CD18. In contrast, we believe that the “outside-in” signalling plays minor roles in PNC formation, because eptifibatide also inhibited the P-selectin release in α-granules.
In summary (Fig. 7), we found that SLY was secreted by S. suis 05ZYH33 at the stationary growth phase. The Ca2+ influx across transmembrane pores created by SLY triggered the Ca2+-MLCK and the “outside-in” signalling, leading to α-granules (P-selectin) release to the platelets’ surface. Subsequently, P-selectin mediated the platelets adhesion to neutrophils to form PNC. These findings imply that SLY and MLCK may be potential therapeutic targets for preventing S. suis-induced platelet activation and related disorders.
The healthy donors who provide the blood in this study provided written informed consent in accordance with the Declaration of Helsinki. Approval was obtained from the Institutional Medical Ethics Committee of the Academy of Military Medical Sciences. The human blood used in this study were obtained in accordance with the approved guidelines.
Monoclonal mouse anti-human antibodies, including FITC-conjugated anti-CD42b (clone HIP1), APC-conjugated anti-CD11b (clone M1/70), PE-conjugated anti-CD62P (clone AK-4), anti-CD62P (clone AK-4), and isotype control antibody were from BD Bioscience. Mouse anti-phospho-myosin light chain 2 (MLC) antibody (mAb#3675) and rabbit anti-myosin light chain 2 (MLC) antibody (mAb#3672) were from (Cell Signaling Technology). U73122, ML-7, Y27632 and eptifibatide acetate, which are inhibitors of phospholipase C (PLC), myosin light chain kinase (MLCK), rho-associated, coiled-coil-containing protein kinase (ROCK) and CD41a, respectively, were from Sigma-Aldrich. Clostridium perfringens phospholipase C (PLC), cholesterol and EGTA were also purchased from Sigma-Aldrich. Quest Fluo-8 calcium fluorescence probe was from AAT Bioquest®, Inc. Wright’s stain was from Beijing CellChip Biotechnology Co., Ltd.
Strains and culture supernatant
S. suis 05ZYH33 was originally isolated from an STSS patient29. The isogenic sly mutant Δsly was constructed in our previous study27. The Canadian avirulent strain 1330, which does not express SLY, was donated by Prof Marcelo Gottschalk (Université de Montréal). Group A streptococcus (GAS) was M1 type E477. S. suis strains were cultured in Todd-Hewitt broth (THB, BD Biosciences) at 37 °C for 4 h (OD600 = 0.4, exponential growth phase) or 6 h (OD600 = 1.0, stationary growth phase), and then harvested for experiments. S. suis strains and GAS cells were washed three times with PBS, and then re-suspended in PBS at a density of 2 × 109 CFU/mL to use for stimulation.
Preparation of recombinant suilysin (rSLY), pneumolysin (rPLY), streptolysin O (rSLO) and factor H-binding protein (rFhb)
rSLY, rPLY, rSLO and (rFhb) used in this study were prepared as previously reported29,30.
Whole blood of healthy donors, who did not use anti-platelet drugs within the previous 15 days, was drawn in the 307 Hospital (China), and the blood was collected in tubes containing sodium citrate (the final concentration was 3.2%)31. Each donor signed an informed consent form. The procedure of collecting and handling the blood samples was in accordance with the Declaration of Helsinki and was approved by the Institutional Review Board of the 307 Hospital. A total of 6 mL of whole blood was centrifuged at 900 rpm for 10 min in a horizontal centrifuge (Sigma-Aldrich), to prepare platelet-rich plasma (PRP 3 × 108/mL).
Flow cytometry was performed to analyse PNC formation10. Briefly, whole blood (100 μL) was mixed with 15 μL of FITC-conjugated anti-human CD42b and APC-conjugated anti-human CD11b, and incubated at 37 °C for 10 min. The blood was then stimulated with 10 μL of SLY, supernatant, THB, PBS or other regents at 37 °C for 10 min, and then the blood was immediately prepared for flow cytometry using a commercial formic-acid red cell lysis/formalin cell-fixation kit (Coulter® Q-prep) according to the manufacturer’s instructions. Flow cytometry was performed on an Accuri C6 flow cytometer (BD Biosciences). The granulocyte gate was drawn based on the forward- and side-scatter profiles of the sample. CD11b-positive events within this gate were analysed to estimate the proportion of CD42b-positive platelets. The above samples were then visualised using an FV1000 confocal laser scanning microscope (Olympus) by XY scanning. In CD62P blocking assay, human blood was pre-incubated with anti-CD62P antibody (10 μg/mL) or the isotype IgG (10 μg/mL) at 37 °C for 10 min before being exposed to rSLY or supernatant stimulus.
Observation of PNC formation in whole blood by microscopy
Whole blood (100 μL) was incubated with 10μL of SLY (1 μg/mL) or other stimuli at 37 °C for 10 min, and then 5 μL of the blood sample were used to prepare a blood smear on a glass slide. After the blood smear dried completely, Wright’s stain was added to cover the blood smear and an equal volume of PBS (pH 6.4–6.8) was added 1 min later. The Wright’s stain and PBS were gently mixed and the blood smear was incubated with the mixture for 5 min. The slide was then washed gently with distilled water and observed under an oil-immersion objective (Olympus).
Flow cytometry analysis of CD62P
Flow cytometry was performed to analyse the expression of P-selectin (CD62P) as previously described10. Briefly, 100 μL of heparinized human blood were incubated with 15 μL of PE-conjugated anti-human CD62P antibody at 37 °C for 10 min. Then, rSLY or other stimuli was added and the blood was incubated for another 15 min. One millilitre of red cell lysis buffer containing formalin was then added to the blood to lyse red cells and to fix the platelets at room temperature for 8 min. After the red blood cells were lysed completely, the blood was centrifuged and the cell pellet was washed with PBS. The cell pellet was re-suspended in 300 μL of PBS and analysed with an Accuri C6 flow cytometer (BD Biosciences). The expression of CD62P was determined by mean fluorescence intensity (MFI) of 10000 events in each sample. To test the effect of cholesterol, SLY was pre-incubated with cholesterol (100 μg/mL) for 10 min, and then blood was incubated with the mixture. To test the effect of EGTA, blood was pre-incubated with EGTA (3 mM) for 10 min, and then incubated with rSLY or other stimuli. Representative histograms of the MFI of CD62P are displayed. Data are expressed as mean MFI ± SD of three independent experiments, with each experiment using blood from a different donor.
Flow cytometry analysis of SLY binding
To analyse the binding of rSLY/rSLYP353V to platelets, firstly, rSLY/rSLYP353V or the control BSA were marked by Alexa Fluor®647, which was performed as described in the generic protocol Amine-Reactive Probes (MP00143). Secondly, the Alexa Fluor®647-rSLY/rSLYP353V or BSA (1 μg/mL) were incubated with platelets at RT for 10 min, and then washed twice with PBS. The binding of rSLY/rSLYP353V to platelets was analysed by Accuri C6 flow cytometer (BD Biosciences). The protein binding was determined by mean fluorescence intensity (MFI) of 10000 events in each sample. Data are expressed as mean MFI ± SD of three independent experiments, with each experiment using blood from a different donor. In cholesterol inhibiting assay, rSLY was pretreated by cholesterol (100 μg/mL).
Calcium influx in platelets
A total of 200 μL of PRP was centrifuged at 2000 rpm for 10 min, and then washed twice with PBS. Subsequently, 100 μL of the calcium probe, Fluo-8 (5 μM), were added and incubated at 37 °C for 30 min. The PRP was centrifuged at 2000 rpm for 10 min, and then washed twice with 200 μL of PBS to remove free calcium probe. The PRP was re-suspended in 180 μL of HBSS (containing 2 mM Ca2+) or D-HBSS (without Ca2+), and then 20 μL of SLY (1 μg/mL), rSLYP353V (1 μg/mL) or cholesterol (100 μg/mL) were added. Ca2+ influx in a Petri dish was measured by an FV1000 confocal laser scanning microscope (Olympus) by XYT scanning.
Immunoblotting to detect the phosphorylation of MLC
Whole platelet lysates from the same cell equivalents were electrophoresed on a SDS-polyacrylamide gel and transferred onto nitrocellulose membranes. The membranes were blocked overnight in 5% BSA in Tris-buffered saline supplemented with 0.1% Tween 20 (TBST), washed three times in TBST, and the membrane was immunoblotted with primary antibodies against MLC (1:1000) or phospho-MLC (1:1000). After washing with TBST, the membrane was incubated with horseradish peroxidase-conjugated secondary antibodies for 1 h. After washing with TBST, protein bands on the membrane were detected using ECL Western blotting detection reagents (Thermo Scientific) and visualized by molecular imager (ChemiDOCTM XRS+ with Image LabTM Software).
Unless otherwise specified, all the data are expressed as mean ± SD. All PNC assays were performed on human blood from three individual donors in independent experiments. Differences between two groups were analysed using the unpaired two-tailed Student’s t-test, if the Levene’s test was not significant (P > 0.05), otherwise, Mann–Whitney tests were used. For all tests, P < 0.05 was considered statistically significant. All statistical analyses were carried out using SPSS 15.0 (SPSS Inc.).
How to cite this article: Zhang, S. et al. Suilysin-induced Platelet-Neutrophil Complexes Formation is Triggered by Pore Formation-dependent Calcium Influx. Sci. Rep. 6, 36787; doi: 10.1038/srep36787 (2016).
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Wertheim, H. F. L., Nghia, H. D. T., Taylor, W. & Schultsz, C. Streptococcus suis: An Emerging Human Pathogen. Clin Infect Dis. 48, 617–625 (2009).
Huong, V. T. et al. Epidemiology, clinical manifestations, and outcomes of Streptococcus suis infection in humans. Emerg Infect Dis. 20, 1105–1114 (2014).
Sriskandan, S. & Slater, J. D. Invasive disease and toxic shock due to zoonotic Streptococcus suis: an emerging infection in the East? PLoS Med 3, e187 (2006).
Tang, J. et al. Streptococcal toxic shock syndrome caused by Streptococcus suis serotype 2. Plos Med 3, 668–676 (2006).
Yu, H. J. et al. Human Streptococcus suis outbreak, Sichuan, China. Emerg Infect Dis 12, 914–920 (2006).
Stahl, A. L. et al. Lipopolysaccharide from enterohemorrhagic Escherichia coli binds to platelets through TLR4 and CD62 and is detected on circulating platelets in patients with hemolytic uremic syndrome. Blood 108, 167–176 (2006).
Peters, M. J. et al. Severe meningococcal disease is characterized by early neutrophil but not platelet activation and increased formation and consumption of platelet-neutrophil complexes. J Leukoc Biol 73, 722–730 (2003).
Bryant, A. E. et al. Clostridial gas gangrene. II. Phospholipase C-induced activation of platelet gpIIbIIIa mediates vascular occlusion and myonecrosis in Clostridium perfringens gas gangrene. J Infect Dis 182, 808–815 (2000).
Bryant, A. E. et al. Vascular dysfunction and ischemic destruction of tissue in Streptococcus pyogenes infection: the role of streptolysin O-induced platelet/neutrophil complexes. J Infect Dis 192, 1014–1022 (2005).
Parimon, T. et al. Staphylococcus aureus alpha-hemolysin promotes platelet-neutrophil aggregate formation. J Infect Dis 208, 761–770 (2013).
Evangelista, V. et al. Platelet/polymorphonuclear leukocyte interaction: P-selectin triggers protein-tyrosine phosphorylation-dependent CD11b/CD18 adhesion: role of PSGL-1 as a signaling molecule. Blood 93, 876–885 (1999).
McEver, R. P. Selectins. Curr Opin Immunol 6, 75–84 (1994).
Yang, J., Furie, B. C. & Furie, B. The biology of P-selectin glycoprotein ligand-1: its role as a selectin counterreceptor in leukocyte-endothelial and leukocyte-platelet interaction. Thromb Haemost 81, 1–7 (1999).
Zarbock, A., Polanowska-Grabowska, R. K. & Ley, K. Platelet-neutrophil-interactions: linking hemostasis and inflammation. Blood Rev 21, 99–111 (2007).
Rebecchi, M. J. & Pentyala, S. N. Structure, function, and control of phosphoinositide-specific phospholipase C. Physiol Rev 80, 1291–1335 (2000).
Rhee, S. G. Regulation of phosphoinositide-specific phospholipase C. Annu Rev Biochem 70, 281–312 (2001).
Klages, B., Brandt, U., Simon, M. I., Schultz, G. & Offermanns, S. Activation of G12/G13 results in shape change and Rho/Rho-kinase-mediated myosin light chain phosphorylation in mouse platelets. J Cell Biol 144, 745–754 (1999).
Bird, G. S. et al. Mechanisms of phospholipase C-regulated calcium entry. Curr Mol Med 4, 291–301 (2004).
Bennett, J. S. Structure and function of the platelet integrin alphaIIbbeta3. J Clin Invest 115, 3363–3369 (2005).
Giddings, K. S., Zhao, J., Sims, P. J. & Tweten, R. K. Human CD59 is a receptor for the cholesterol-dependent cytolysin intermedilysin. Nat Struct Mol Biol 11, 1173–1178 (2004).
Xu, L. et al. Crystal structure of cytotoxin protein suilysin from Streptococcus suis. Protein Cell 1, 96–105 (2010).
Gottschalk, M. G., Lacouture, S. & Dubreuil, J. D. Characterization of Streptococcus suis capsular type 2 haemolysin. Microbiology 141 (Pt 1), 189–195 (1995).
Rossjohn, J., Feil, S. C., McKinstry, W. J., Tweten, R. K. & Parker, M. W. Structure of a cholesterol-binding, thiol-activated cytolysin and a model of its membrane form. Cell 89, 685–692 (1997).
Gilbert, R. J. et al. Two structural transitions in membrane pore formation by pneumolysin, the pore-forming toxin of Streptococcus pneumoniae. Cell 97, 647–655 (1999).
Ye, C. et al. Clinical, experimental, and genomic differences between intermediately pathogenic, highly pathogenic, and epidemic Streptococcus suis. J Infect Dis 199, 97–107 (2009).
Ye, C. et al. Streptococcus suis sequence type 7 outbreak, Sichuan, China. Emerg Infect Dis 12, 1203–1208 (2006).
He, Z. et al. Increased production of suilysin contributes to invasive infection of the Streptococcus suis strain 05ZYH33. Mol Med Rep 10, 2819–2826 (2014).
Tabata, A. et al. The diversity of receptor recognition in cholesterol-dependent cytolysins. Microbiol Immunol 58, 155–171 (2014).
Pian, Y. et al. Fhb, a novel factor H-binding surface protein, contributes to the antiphagocytic ability and virulence of Streptococcus suis. Infect Immun 80, 2402–2413 (2012).
Ren, Z. Q. et al. Construction and activities of suilysin mutants. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi 28, 580–582 (2012).
Shannon, O. et al. Severe streptococcal infection is associated with M protein-induced platelet activation and thrombus formation. Mol Microbiol 65, 1147–1157 (2007).
We are grateful to Prof Marcelo Gottschalk (Université de Montréal, Montreal Quebec, Canada) for providing the avirulent strain 1330. We also thank Dr Jiye Yin and Dr Zhiyuan Pan for analysis of the pathological changes.
The authors declare no competing financial interests.
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Zhang, S., Zheng, Y., Chen, S. et al. Suilysin-induced Platelet-Neutrophil Complexes Formation is Triggered by Pore Formation-dependent Calcium Influx. Sci Rep 6, 36787 (2016). https://doi.org/10.1038/srep36787
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