- Research article
- Open Access
Plasminogen activation by staphylokinase enhances local spreading of S. aureus in skin infections
BMC Microbiology volume 14, Article number: 310 (2014)
Staphylococcus aureus (S. aureus) is a frequent cause of skin and soft tissue infections. A unique feature of S. aureus is the combined presence of coagulases that trigger fibrin formation and of the plasminogen activator staphylokinase (SAK). Whereas the importance of fibrin generation for S. aureus virulence has been established, the role of SAK remains unclear.
We studied the role of plasminogen activation by SAK in a skin infection model in mice and evaluated the impact of alpha-2-antiplasmin (α2AP) deficiency on the spreading and proteolytic activity of S. aureus skin infections. The species-selectivity of SAK was overcome by adenoviral expression of human plasminogen. Bacterial spread and density was assessed non-invasively by imaging the bioluminescence of S. aureus Xen36.
SAK-mediated plasmin activity increased the local invasiveness of S. aureus, leading to larger lesions with skin disruption as well as decreased bacterial clearance by the host. Even though fibrin and bacterial surfaces protected SAK-mediated plasmin activity from inhibition by α2AP, the deficiency of α2AP resulted in increased bacterial spreading. SAK-mediated plasmin also induced secondary activation of gelatinases, shown both in vitro and in lesions from the in vivo model.
SAK contributes to the phenotype of S. aureus skin infections by enhancing bacterial spreading as a result of fibrinolytic and proteolytic activation.
Staphylococcus aureus (S. aureus) is the leading cause of skin and soft tissue infections, both community- and hospital-acquired ,. S. aureus is a versatile pathogen that has the intriguing capacity to modulate both the host’s coagulation and fibrinolytic system.
We and others have shown that fibrin formation induced by the bacterial prothrombin activators staphylocoagulase and von Willebrand factor-binding protein is an important virulence factor for both localized and systemic infections by S. aureus and is essential for abscess formation -. Most S. aureus strains causing infection in humans also produce staphylokinase (SAK). SAK forms an equimolar complex with human plasmin (huPli) catalyzing the further activation of plasminogen. The SAK-huPli complex is sensitive to rapid inhibition by alpha-2-antiplasmin (α2AP) unless it is bound to fibrin via the lysine binding sites of plasmin. This mechanism accounts for the fibrin-specificity of SAK ,. Although SAK has received considerable research attention during its development as a fibrinolytic agent in cardiovascular medicine , few studies have investigated its relevance in S. aureus infection ,.
Streptokinase, secreted by group A, C and G streptococci, is the other well-known bacterial plasminogen activator. Like SAK, streptokinase is specific for human plasminogen (huPlg) but its action is not inhibited by α2AP . Streptokinase is a key virulence factor and the primary determinant of the species-selectivity of group A streptococcal infections. Mortality after infection with group A streptococci is markedly increased in huPlg transgenic mice ,. Interestingly, a subcluster of streptokinase (type 2b) has been identified that is sensitive to α2AP inhibition, leading to site-restricted plasminogen activation in these, mostly skin-trophic, group A streptococci .
The role of SAK as a potential virulence factor in S. aureus disease remains unresolved. SAK is present in the large majority of S. aureus strains causing human infection -. In contrast, S. aureus strains from veterinary sources commonly lack SAK production ,. SAK, like streptokinase , thus constitutes an adaptation of S. aureus for human infection. The sak gene has a highly conserved sequence - and is carried on a bacteriophage containing other genes with an important function in immune evasion, such as complement inhibitory factors and enterotoxins ,. SAK was shown to enhance the breaching of tissue barriers in vitro.
The present study aimed at evaluating if plasmin generation by SAK impacts on proteolytic activity in S. aureus infected skin and on the local and systemic dissemination of S. aureus. We further investigated if the host α2AP, by inhibiting the SAK-plasmin activity, reduces the virulence of S. aureus.
Bacterial staphylokinase production
Supernatant of overnight cultures of the bioluminescent S. aureus Xen36 contained similar levels of SAK compared to lab strains and to clinical S. aureus strains from skin infection and from bacteremia with cutaneous origin. SAK expression by LS-1 spasak, which expresses SAK under the control of the protein A promoter, was about tenfold higher (Figure 1). Thus, S. aureus Xen36 is a relevant micro-organism to study the role of SAK in a skin infection model.
Skin infection model
Adenoviral-mediated human plasminogen expression
To overcome the species-selectivity of SAK for huPlg, huPlg was expressed in mice through adenoviral gene transfer. Seven to 11 days after adenoviral injection, i.e. at the start of the subcutaneous infection experiment, huPlg plasma values in Adplasm injected mice were 31.6 ± 15.5 μg/ml in α2AP KO and 31.5 ± 10.1 μg/ml in α2AP WT mice. In mice injected with the control Adnull adenoviral vector, values of huPlg were below the detection level (3 μg/ml). Human plasminogen remained present until the end of the experiment (27.3 ± 10.0 μg/ml at day 5 and 37.2 ± 29.6 μg/ml at day 10) (Figure 2). Hence, the expression of huPlg allowed for the selective interaction of SAK with huPlg throughout the course of the subcutaneous infection experiment.
Infectious skin lesions
After subcutaneous inoculation with S. aureus Xen36, macroscopic lesion size was significantly larger in huPlg expressing mice compared to control wild type mice (33.6 ± 19.6 mm2 in WT/huPlg mice (n = 17) vs. 19.2 ± 9.7 mm2 in WT/null mice (n = 12) at day 10, P < 0.01) (Figure 3A). The constitutive luciferase expression of S. aureus Xen36 also allowed for non-invasive monitoring of the spreading and density of the bacteria over time (illustrated in Figure 3C). Expression of huPlg increased both bacterial spreading (P < 0.05 on day 3, P < 0.01 on day 6 and 9) and bacterial load (P < 0.05 on day 3 and 9, P < 0.01 on day 6) early in the course of infection (Figures 3B and 3D).
Compared to wild type mice, bacterial spreading in α2AP KO mice was similar in the early stages of the infection, but was more pronounced at day 9 (P < 0.05) (Figure 3B), resulting in an increase in macroscopic lesion size at day 10 (31.8 ± 20.9 mm2 in α2AP KO/null mice (n = 11) vs. 19.2 ± 9.7 mm2 in WT/null mice (n = 12), P = 0.078) (Figure 3A). Bacterial density was higher in α2AP KO mice compared to wild type mice (P = 0.115 on day 6, P < 0.05 on day 9) (Figure 3D). In an additional experiment, α2AP KO or WT mice were infected with S. aureus LS-1 EP. We observed similar initial fibrin deposition in the abscess periphery in both groups at day 1 (Additional file 1), consistent with a normal capacity for fibrin formation in α2AP KO plasma ex vivo (data not shown). However, at a later time point, less fibrin was observed in α2AP KO mice, as shown in Additional file 1.
The largest lesion size was observed in the α2AP KO mice with human plasminogen expression (42.9 ± 27.4 mm2 in α2AP KO/huPlg (n = 14) vs. 19.2 ± 9.7 mm2 in WT/null (n = 12), P < 0.001) (Figure 3A). The spreading of the bacteria was more pronounced from early in the course of infection (P = 0.137 on day 3, P < 0.01 on day 6 and 9) (Figure 3B). Also the intensity of the bioluminescence, which relates to the bacterial density, was the highest in the α2AP KO/huPlg group (P = 0.153 on day 3, P < 0.01 on day 6, P < 0.05 on day 9) (Figure 3D).
The assessment of systemic spread of S. aureus, by quantifying bacterial load in spleen and kidney, did not differ significantly between the 4 groups. At day 10, there were 2 mice in the α2AP KO/huPlg group with distant infection in spleen and/or kidney, 2 mice in the α2AP KO/null group, 1 mouse in the WT/huPlg group and none in the WT/null group.
In the first series of experiments, we observed that the differentiation between the groups both in macroscopic phenotype (open/closed lesion) and in bioluminescence lesion size and intensity became apparent early in the course of infection. Therefore, to assess macroscopic and microscopic phenotype and proteolytic activity, mice were sacrificed at day 3 in a subsequent set of experiments.
Macroscopical assessment confirmed closed abscesses in WT/null mice, compared to more diffusely spread lesions with skin rupture in huPlg expressing mice (P < 0.01) (Figure 4A-C).
Histopathologic analysis of lesional skin sections from α2AP KO/huPlg mice showed, apart from breaching of skin, penetration of infection starting from the initial infection site, past a peripheral fibrin zone, into subdermal tissue layers (Figure 4C-E).
Mechanism of SAK action in S. aureus skin infections
SAK is species-selective and fibrin-specific
The observations in the subcutaneous infection model can be explained by the SAK-mediated plasmin generation. To this end however, the values of huPlg achieved after adenoviral huPlg expression in mice, should be able to rescue the species-selectivity of SAK in a murine model. SAK induced rapid plasmin generation if added to huPlg but not with murine plasminogen (muPlg) (Figure 5A). However, activation of muPlg was observed in the presence of SAK and trace amounts of human plasminogen (Figure 5A). Also, addition of a preformed SAK-huPli complex triggered secondary activation of muPlg, as illustrated in Figure 5B. For all further experiments, a mixture of muPlg (0.25 μM) and huPlg (0.05 μM) was used to reflect the in vivo conditions of partial huPlg expression against a background of muPlg.
SAK-mediated plasmin generation was further enhanced in the presence of fibrin, as CnBr-digested fibrinogen fragments (Fg(CNBr)) (Figure 5C-D) or as solid fibrin (data not shown). For convenience, Fg(CNBr) was used in further experiments, as an accepted soluble alternative to solid fibrin. This increase in plasmin generation in the presence of fibrin can be explained by a reduced inactivation of fibrin-associated SAK-huPli complex by α2AP. As shown in Figure 5C, α2AP inhibited SAK-induced plasmin generation in control conditions, but had little effect on SAK-induced plasmin generation in the presence of Fg(CNBr) (A405,60min of 0.853 ± 0.058 vs. 0.121 ± 0.005 for SAK + Plg + α2AP, P < 0.01). Higher concentrations of Fg(CNBr) completely protected SAK-induced plasmin from inhibition by α2AP (A405, 60min of 1.036 ± 0.039 vs. 0.121 ± 0.005 for SAK + Plg + α2AP, P < 0.001) (Figure 5D).
Bacterial cell surface protects SAK from α2AP inhibition
We also studied if, besides fibrin, bacterial surfaces could protect the SAK-huPli complex from α2AP inhibition. Indeed, the presence of bacteria increased plasmin generation following addition of SAK (A405, 90min 1.035 ± 0.076 vs. 0.675 ± 0.138, P < 0.05). Addition of murine α2AP significantly reduced plasmin generation by ≈ 70% to A405, 90min of 0.195 ± 0.034 (P < 0.05), whereas in the presence of bacteria, α2AP only led to a ≈ 50% reduction in plasmin generation (A405, 90 min = 0.487 ± 0.094, P < 0.01) (Figure 6). We used a SAK-negative S. aureus strain (LS-1 EP) for this subset of experiments to eliminate confounding by SAK production during the course of the experiment. However, similar results were observed for SAK-positive S. aureus Xen36, which was the strain used in animal experiments. Comparable results were also obtained when heat-killed instead of viable S. aureus was used (data not shown).
SAK-huPli complex activates gelatinases
Plasmin has a broad proteolytic spectrum that includes extracellular matrix proteins. However, plasmin is also known to activate gelatinases, which can cause secondary proteolytic activity. In order to assess whether gelatinase activation contributes to the observed bacterial spreading, we measured the activation of gelatinases by SAK-huPli in murine skin extracts.
Addition of SAK and huPlg to extracts of murine skin led to activation of pro-MMP-2 (Figure 7A). In line with the low expression of MMP-9 in normal non-inflamed skin, pro-MMP-9 and active MMP-9 could not be clearly identified on these zymograms of murine skin. However, we did observe MMP-9 activation in HT1080 cell culture supernatant after incubation with SAK and huPlg (data not shown).
Zymograms of day 3 lesions (2 representative lesions per group) showed a higher ratio of active/total MMP-2 in α2AP KO/huPlg mice, compared to control WT/null mice (Figure 7B). Increased MMP-9 expression and activity was observed in all infected skins compared to normal skin, with a similar higher ratio of active/total MMP-9 in the α2AP KO/huPlg group compared to control WT/null mice (Western blot, Figure 7C).
We evaluated the role of SAK-mediated plasminogen activation in a subcutaneous S. aureus skin infection model in mice. Our results demonstrate that plasmin generation by SAK increased spreading and hampered bacterial clearance of S. aureus in infected skin, increased tissue proteolytic MMP activity, and resulted in more pronounced tissue damage, as noted by more open skin lesions. These findings were enhanced in the absence of the plasmin inhibitor α2AP, demonstrating a role for host α2AP in the containment of S. aureus infections.
Strengths of our model are the use of a S. aureus strain derived from a human infection in healthy mice, and the non-invasive follow-up of bacterial spreading by bioluminescence. The use of an adenoviral vector encoding huPlg resulted in plasma huPlg levels similar to those attained in transgenic huPlg mice . Our in vitro data confirm that these huPlg concentrations in mice are sufficient to overcome the species-selectivity of SAK and to mimic the phenotype of SAK-mediated huPlg activation in the subcutaneous infection model.
Our results are in line with previous results showing that spreading through tissue barriers can be mediated by SAK activity . Plasmin activity generated by SAK can degrade several extracellular matrix components, but not collagens . Yet, we show that SAK-mediated plasmin activity can lead to secondary activation of gelatinases in mouse skin extracts, which may contribute to the proteolytic activity necessary for dissemination through tissue.
Although we observed more proteolytic activity and increased lesion dimensions in α2AP KO/huPlg groups, we did not observe systemic spread nor mortality after subcutaneous inoculation of S. aureus. However, systemic dissemination was common when using a neutropenic mouse model of S. aureus skin infection, as recently shown . This is in agreement with the clinical observation that skin infections by S. aureus infrequently lead to systemic dissemination, unless there is an underlying vulnerability of the patient. In immunocompetent mice (and patients), staphylococcal skin and soft tissue infections are mainly characterized by abscess formation, and bacteria that do reach the systemic circulation or distant organs are rapidly cleared.
The predominantly local effect of SAK-mediated plasmin activity without affecting the severity of systemic symptoms is also in contrast with the findings by Sun et al., demonstrating that streptokinase increased mortality of Group A streptococcal infection in a skin infection model in huPlg transgene mice. Importantly, streptokinase is insensitive to α2AP inhibition, in contrast with the SAK-huPli complex that is rapidly inactivated by α2AP. Our results confirm previous findings that fibrin protects the SAK-huPli complex from inactivation; and a similar protective effect was noted from bacterial surfaces ,,. This may explain why SAK-mediated plasmin has more localized effects compared to streptokinase-induced plasmin. SAK-induced proteolysis is thus confined to the immediate surroundings of the site of infection, where high concentrations of fibrin and bacteria prevent inactivation, but is rapidly neutralized further away from the abscess site. In contrast, streptokinase-activated plasmin may have a larger potential for systemic effect because of its resistance to α2AP.
To explore whether inhibition by α2AP accounts for the more localized effect of SAK compared to streptokinase, we studied the impact of the genetic absence of α2AP on the characteristics of S. aureus skin infection. Indeed, α2AP KO was associated with larger lesion sizes, compatible with a protective role of α2AP in tempering the proteolytic effect of SAK-mediated plasmin. The larger lesion size in α2AP KO/null mice, lacking huPlg expression, is likely explained by activation of murine plasminogen, bound to surface plasminogen receptors of S. aureus, by host plasminogen activators. Different surface plasminogen receptors have been described in S. aureus, such as α-enolase, inosine 5’-monophosphate dehydrogenase, ribonucleotide reductase subunit 2, triose phosphate isomerase, surface immunoglobulin-binding protein and extracellular fibrinogen-binding protein -. These surface plasminogen receptors are not selective for huPlg and constitute a common theme across different bacterial and fungal organisms for the degradation of extracellular matrix and immune evasion ,. The resulting surface-bound plasmin activity is less sensitive to inhibition by plasma protease inhibitors, hence a slower but consistently larger expansion of the lesion occurs in the α2AP KO/null group compared to WT/null controls. The role of host α2AP in limiting bacterial spreading was confirmed in additional experiments where a SAK-negative strain (S. aureus LS-1 EP) was used to infect α2AP KO and α2AP WT mice. As α2AP gene deficiency does not impair fibrin generation, the initial fibrin deposition surrounding the abscess was comparable in both groups. However, at a later time point the absence of the main plasmin inhibitor led to increased dissolution of the peripheral fibrin sheath. Although there was a trend towards higher numbers of systemic infection in α2AP KO mice (4/25 vs 1/29 WT mice), we could not demonstrate a strong effect of α2AP KO on systemic spreading. Although α2AP is the predominant plasmin inhibitor, other plasma inhibitors of fibrinolysis such as alpha-2-macroglobulin may explain the absence of systemic spread in α2AP KO/huPlg mice .
Interestingly, we also observed increased bacterial loads in the presence of huPlg and/or in the absence of α2AP, demonstrating that bacterial induced plasmin generation helps to evade bacterial clearance by the host. It has been shown previously that SAK binds to and inactivates human defensins, part of the innate immune defense against bacteria . SAK-induced plasmin activity can degrade opsonizing complement components IgG and C3b , thus protecting S. aureus from phagocytosis.
The production of SAK, a highly fibrin-specific plasminogen activator ,, is particularly intriguing as S. aureus also triggers fibrin formation through coagulase activity. The role of staphylocoagulase-mediated fibrin deposition in abscess formation is well established . S. aureus also possesses different binding proteins which interact with fibrin(ogen) and extracellular matrix proteins . It remains to be resolved how coagulase-mediated fibrin deposition and SAK-mediated fibrinolysis cooperate to promote S. aureus virulence. Coagulase activity and the resulting fibrin have been shown to shield S. aureus from leukocytes, promoting early replication and persistence. In this view, SAK allows S. aureus to generate fibrinolytic activity that is protected by both the staphylothrombin- and thrombin-generated fibrin from rapid neutralization by host protease inhibitors. The resulting plasmin activity can degrade the host’s fibrin as well as the S. aureus-mediated fibrin and allow subsequent spreading of the growing bacterial colony. How S. aureus differentially regulates coagulase and SAK activity remains unknown. Interestingly, SAK expression is under control of the agr quorum sensing system, suggesting that proteolytic activity is modulated by bacterial density . A regulated expression of SAK may also explain the observed decreased virulence of genetically engineered S. aureus strains with SAK overproduction, not under control of its own promotor, as continuous and high-level SAK production will interfere with coagulase activity as a central virulence factor of S. aureus,.
We show that SAK-mediated proteolytic activity in S. aureus infected skin facilitates local spreading, increases tissue damage of skin and reduces bacterial clearance by the host. The underlying mechanisms involve protection of the SAK-huPli complex associated with fibrin or bacterial surfaces, from rapid inhibition by α2AP. In turn, active SAK-huPli may activate gelatinases, further promoting degradation of the extracellular matrix. Overall, this study shows the role of subversion of the host fibrinolytic system by SAK-producing S. aureus in migration through tissue barriers.
All animal experiments were performed with S. aureus Xen36 (Caliper Life Sciences, Hopkinton, USA), a bioluminescent strain derived from the parental strain S. aureus ATCC 49525 (Wright), a clinical isolate from a patient with bacteremia. S. aureus Xen36 possesses a stable copy of the modified Photorhabdus luminescens luxABCDE operon at a single integration site on a native plasmid.
Clinical strains were collected from patients at the University Hospitals Leuven and originated from either skin infection or bacteremia secondary to a skin infection with S. aureus. Laboratory strains included S. aureus Newman and 3 different congenic S. aureus LS-1 variants with different SAK expression (LS-1 EP, LS-1 sak and LS-1 spasak) .
All strains were stored in Brain Heart Infusion (BHI) with glycerol at −80°C. Before use, strains were grown overnight in Tryptic Soy Broth (TSB) at 37°C in aerobic conditions. For subcutaneous infection, overnight cultures were washed twice with PBS and diluted in PBS to an optical density at 600 nm (OD600) of 2.0, corresponding to 2 × 109 CFU (colony forming units)/mL. CFU counts were confirmed by quantitative plating of the inoculum for each experiment. SAK production was confirmed in the supernatant of overnight cultures using an in-house developed sandwich ELISA (MA-S20D11 + MA-S25F6/PA-RaSTAN ELISA).
All animal experimental procedures were approved by the Ethics Committee of the KU Leuven.
α2AP knock-out mice in C57BL/6 - S129Vj background and their littermate wild type controls were used .
Adenoviral expression of huPlg
Because of the selectivity of SAK for huPlg, we studied the role of SAK in a subcutaneous S. aureus infection model after huPlg overexpression through adenoviral gene transfer. An E1E3E4-deleted adenoviral vector inducing hepatocyte-specific expression of huPlg (Adplasm) was used. In this vector, the expression of huPlg is under control of the alpha-1-antitrypsin promoter and four copies of the human Apo E enhancer . Adnull, a similar adenoviral vector lacking an expression cassette was used as control .
Male mice of 5-9 weeks were injected via the tail vein with 5 × 1010 particles of either Adplasm or Adnull vector, 7-11 days prior to the subcutaneous infection. Hence, 4 different groups of mice were studied, which are identified as α2AP KO/huPlg, α2AP KO/null, WT/huPlg and WT/null, respectively.
Quantification of huPlg
Plasma concentrations of huPlg were quantitated by ELISA and by a functional test specific for huPlg, allowing measurement of huPlg concentrations in murine plasma. The in-house developed sandwich ELISA, based on the antibodies MA-42B12B4B2D and MA-34D3D10-HRP does not cross-react with murine plasminogen. The functional assay is based on the species-selectivity of streptokinase, and measures plasmin generation with a chromogenic substrate (S-2403, Chromogenix, Milano, Italy) after addition of an excess of streptokinase (1000 IU/mL, Streptase, CSL Behring, Marburg, Germany).
Preliminary experiments showed reliable and stable expression of huPlg from day 7 up to 1 month (day 43) after injection of adenoviral vector.
Skin infection model
Approximately 1 week post adenoviral injection, mice were anesthesized with isoflurane and injected subcutaneously in each flank with 100 μL containing 2 × 108 CFU of S. aureus Xen36. Blood samples were collected on citrate (3.2% sodiumcitrate, 10% vol/vol) by retro-orbital puncture, at day 0 (before infection) and day 5. At day 10, animals were killed by heart puncture under high dose ketamine/xylazine anesthesia. Largest diameter (a) and orthogonal diameter (b) of skin lesions were measured with a caliper, and skin lesion areas were calculated ((π/4)ab). Lesions were then excised for histological analysis. Dimensions of lesions from left and right flank were averaged per individual mouse. Spleen and kidneys were also collected for analysis of bacterial load.
One mouse died on day 4 in the α2AP KO/null group, this subject was not included in analysis.
In a supplementary experiment, to study the effect of host α2AP in staphylococcal skin infection, this subcutaneous infection model was carried out with SAK-negative S. aureus LS-1 EP in α2AP KO or WT mice without previous adenoviral injection.
Non-invasive follow-up of the local spreading of S. aureus Xen36 was performed by means of bioluminescence imaging of the luciferase signal with a cooled CCD camera (IVIS 100, Xenogen, Perkin-Elmer Company, Alameda, USA). Mice were sedated with isoflurane and imaging was performed for each lesion with an exposure time of 60 s. Signal intensity was calculated with Living Image 2.5 analysis software (Xenogen) and denotes photons per second through a defined region of interest (ROI), corresponding to the infectious lesion. The same ROI was used for all infectious lesions in all animals. Preliminary experiments showed a correlation between bioluminescence signal intensity and bacterial load of S. aureus Xen36 (Pearson r = 0.965, P = 0.0001). A fixed threshold was chosen for all images and quantitation of the lesion size (pixels with signal above threshold) was performed with Image J software (Image J, NIH, Bethesda, USA).
Paraffin-embedded tissue samples were used to prepare 10 μm thick sections. Routine histopathologic stainings with hematoxyllin-eosin or Martius Scarlet Blue (for fibrin) were performed.
Study of plasminogen activation by SAK
We studied the activation of plasminogen (human, murine, or a mixture of both) by SAK in the absence or presence of α2AP, fibrin and S. aureus bacteria. Human and murine plasminogen were isolated from plasma by lysine Sepharose affinity chromatography, as described previously . SAK variant TS-162 was previously described . Murine α2AP was obtained from Abcam (Cambridge, UK). SAK, α2AP and plasminogen were diluted in 0.1M sodium phosphate buffer, pH 7.4, containing 0.05 M NaCl and 0.01% Tween. Solid fibrin clots were formed upon addition of bovine thrombin (1 U/mL) to human fibrinogen (200 μg/mL in 0.05 M Tris-HC1 buffer, pH 7.4, containing 0.038 M NaCl and 0.01% Tween 80) (Calbiochem, EMD Millipore, Billerica, USA) (30 min, 37°C). CNBr-digested murine fibrinogen (Fg(CNBr)) was prepared as published . In some experiments, S. aureus bacteria (OD600 2.0, 15% vol/vol; live or heat-killed at 60°C for 1h) were used in the reaction mixture. In this case, bacteria were pelleted by centrifugation before read-out of the absorbance at 405 nm (A405). Hydrolysis of the chromogenic substrate S-2403 was used to monitor plasmin activity in a Bio-TEK microtiter plate reader (Bio-TEK, Winooski, USA).
Gelatin zymography was used to study activation of the gelatinase subfamily of matrix metalloproteinases (MMPs) by the SAK-human plasmin complex (SAK-huPli). To this end, tissue extracts of skin and subcutaneous tissue from healthy C57BL/6 mice were prepared as described ,. Briefly, tissue samples were snap frozen in liquid nitrogen. Protein extraction was performed by homogenization with glass beads in FastPrep24 (MP Biomedicals, Santa Ana, USA) in the presence of extraction buffer (10 mM sodium phosphate, pH 7.2, containing 150 mM NaCl, 1% Triton X-100, 0.1% SDS, 0.5% sodium deoxycholate, and 0.2% NaN3). After centrifugation, the protein concentration of the supernatant was determined with the Bradford assay (Bio-rad, Hercules, USA). The skin extracts were incubated (2 h or 16 h, 37°C) with a mixture of 1.1 μM huPlg and SAK (in a 1:10 molar ratio to huPlg).
Zymographic analysis of gelatinase activity was performed on 10% Tris-glycine gels containing 0.1% gelatin (Novex, Life Technologies, Carlsbad, USA).
We used MMP-containing medium from a HT1080 fibrosarcoma cell line (Sigma-Aldrich, St. Louis, USA) and activation by APMA (4-amino-phenyl-mercuric acetate, a chemical MMP-activator, Sigma-Aldrich) as a reference.
Preliminary experiments showed that plasmin also generated a gelatinolytic band on zymography. To irreversibly inactivate plasmin prior to loading, samples were treated with a 100-fold molar excess of D-Val-Phe-Lys-chloromethylketone, dihydrochloride (Sigma-Aldrich) (15 min, room temperature).
The lysis of the substrate gel (area × intensity) was quantitated by image analysis (Image J) .
Western blotting for murine MMP-2 and MMP-9 was performed using a rabbit polyclonal antibody (NB200-193 for MMP-2, Novus Biologicals, Cambridge, UK and ab38898 for MMP-9, Abcam).
All calculations were performed using GraphPad Prism 5.0b (GraphPad Software, San Diego, USA). Data were tested for normality and appropriate tests were used to compare continuous variables between groups (t-test if normal distribution, Mann-Whitney U test if not). For bioluminescence data, values were compared at definite time points with 1-way ANOVA, using t-test or Mann-Whitney U test as post-test. For comparison of bioluminescence data over different time points and between groups, 2-way ANOVA was used. For plasmin generation experiments, A405 values were compared by repeated measures 1-way ANOVA, using paired t-tests as post-test. Quantitative data from blotting experiments were analyzed for trend using linear regression. P-values < 0.05 were considered statistically significant. In graphs, *denotes P < 0.05, **P <0.01, ***P < 0.001.
- S. aureus :
Ray GT, Suaya JA, Baxter R: Microbiology of skin and soft tissue infections in the age of community-acquired methicillin-resistant Staphylococcus aureus. Diagn Microbiol Infect Dis. 2013, 76: 24-30. 10.1016/j.diagmicrobio.2013.02.020.
Sader HS, Farrell DJ, Jones RN: Antimicrobial susceptibility of Gram-positive cocci isolated from skin and skin-structure infections in European medical centres. Int J Antimicrob Agents. 2010, 36: 28-32. 10.1016/j.ijantimicag.2010.03.016.
Vanassche T, Verhaegen J, Peetermans WE, Van Ryn J, Cheng A, Schneewind O, Hoylaerts MF, Verhamme P: Inhibition of staphylothrombin by dabigatran reduces Staphylococcus aureus virulence. J Thromb Haemost. 2011, 9: 2436-2446. 10.1111/j.1538-7836.2011.04529.x.
Vanassche T, Peetermans M, Van Aelst L, Peetermans WE, Verhaegen J, Missiakas D, Schneewind O, Hoylaerts M, Verhamme P: The role of staphylothrombin-mediated fibrin deposition in catheter-related Staphylococcus aureus infections. J Infect Dis. 2013, 208: 92-100. 10.1093/infdis/jit130.
McAdow M, Kim HK, Dedent AC, Hendrickx AP, Schneewind O, Missiakas DM: Preventing Staphylococcus aureus sepsis through the inhibition of its agglutination in blood. PLoS Pathog. 2011, 7: e1002307-10.1371/journal.ppat.1002307.
Sawai T, Tomono K, Yanagihara K, Yamamoto Y, Kaku M, Hirakata Y, Koga H, Tashiro T, Kohno S: Role of coagulase in a murine model of hematogenous pulmonary infection induced by intravenous injection of Staphylococcus aureus enmeshed in agar beads. Infect Immun. 1997, 65: 466-471.
Collen D: Staphylokinase: a potent, uniquely fibrin-selective thrombolytic agent. Nat Med. 1998, 4: 279-284. 10.1038/nm0398-279.
Lijnen HR, Van Hoef B, De Cock F, Okada K, Ueshima S, Matsuo O, Collen D: On the mechanism of fibrin-specific plasminogen activation by staphylokinase. J Biol Chem. 1991, 266: 11826-11832.
Kwiecinski J, Josefsson E, Mitchell J, Higgins J, Magnusson M, Foster T, Jin T, Bokarewa M: Activation of plasminogen by staphylokinase reduces the severity of Staphylococcus aureus systemic infection. J Infect Dis. 2010, 202: 1041-1049. 10.1086/656140.
Kwiecinski J, Jacobsson G, Karlsson M, Zhu X, Wang W, Bremell T, Josefsson E, Jin T: Staphylokinase Promotes the Establishment of Staphylococcus aureus Skin Infections While Decreasing Disease Severity. J Infect Dis. 2013, 208: 990-9. 10.1093/infdis/jit288.
Lijnen HR, Stassen JM, Vanlinthout I, Fukao H, Okada K, Matsuo O, Collen D: Comparative fibrinolytic properties of staphylokinase and streptokinase in animal models of venous thrombosis. Thromb Haemost. 1991, 66: 468-473.
Sun H, Ringdahl U, Homeister JW, Fay WP, Engleberg NC, Yang AY, Rozek LS, Wang X, Sjobring U, Ginsburg D: Plasminogen is a critical host pathogenicity factor for group A streptococcal infection. Science. 2004, 305: 1283-1286. 10.1126/science.1101245.
Khil J, Im M, Heath A, Ringdahl U, Mundada L, Cary Engleberg N, Fay WP: Plasminogen enhances virulence of group A streptococci by streptokinase-dependent and streptokinase-independent mechanisms. J Infect Dis. 2003, 188: 497-505. 10.1086/377100.
Cook SM, Skora A, Walker MJ, Sanderson-Smith ML, McArthur JD: Site-restricted plasminogen activation mediated by group A streptococcal streptokinase variants. Biochem J. 2014, 458: 23-31. 10.1042/BJ20131305.
Piechowicz L, Galin'ski J, Garbacz K, Haras K: Bacteriophage analysis of staphylokinase-negative Staphylococcus aureus strains isolated from people. J Basic Microbiol. 2010, 50: 557-561. 10.1002/jobm.201000019.
Jin T, Bokarewa M, McIntyre L, Tarkowski A, Corey GR, Reller LB, Fowler VG: Fatal outcome of bacteraemic patients caused by infection with staphylokinase-deficient Staphylococcus aureus strains. J Med Microbiol. 2003, 52: 919-923. 10.1099/jmm.0.05145-0.
Ruotsalainen E, Karden-Lilja M, Kuusela P, Vuopio-Varkila J, Virolainen-Julkunen A, Sarna S, Valtonen V, Jarvinen A: Methicillin-sensitive Staphylococcus aureus bacteraemia and endocarditis among injection drug users and nonaddicts: host factors, microbiological and serological characteristics. J Infect. 2008, 56: 249-256. 10.1016/j.jinf.2008.01.009.
Luedicke C, Slickers P, Ehricht R, Monecke S: Molecular fingerprinting of Staphylococcus aureus from bone and joint infections. Eur J Clin Microbiol Infect Dis. 2010, 29: 457-463. 10.1007/s10096-010-0884-4.
Monecke S, Luedicke C, Slickers P, Ehricht R: Molecular epidemiology of Staphylococcus aureus in asymptomatic carriers. Eur J Clin Microbiol Infect Dis. 2009, 28: 1159-1165. 10.1007/s10096-009-0752-2.
Monecke S, Berger-Bachi B, Coombs G, Holmes A, Kay I, Kearns A, Linde HJ, O'Brien F, Slickers P, Ehricht R: Comparative genomics and DNA array-based genotyping of pandemic Staphylococcus aureus strains encoding Panton-Valentine leukocidin. Clin Microbiol Infect. 2007, 13: 236-249. 10.1111/j.1469-0691.2006.01635.x.
van Wamel WJ, Rooijakkers SH, Ruyken M, van Kessel KP, van Strijp JA: The innate immune modulators staphylococcal complement inhibitor and chemotaxis inhibitory protein of Staphylococcus aureus are located on beta-hemolysin-converting bacteriophages. J Bacteriol. 2006, 188: 1310-1315. 10.1128/JB.188.4.1310-1315.2006.
Humphreys H, Keane CT, Hone R, Pomeroy H, Russell RJ, Arbuthnott JP, Coleman DC: Enterotoxin production by Staphylococcus aureus isolates from cases of septicaemia and from healthy carriers. J Med Microbiol. 1989, 28: 163-172. 10.1099/00222615-28-3-163.
Katayama Y, Baba T, Sekine M, Fukuda M, Hiramatsu K: Beta-hemolysin promotes skin colonization by Staphylococcus aureus. J Bacteriol. 2013, 195: 1194-1203. 10.1128/JB.01786-12.
Resch G, Francois P, Morisset D, Stojanov M, Bonetti EJ, Schrenzel J, Sakwinska O, Moreillon P: Human-to-bovine jump of Staphylococcus aureus CC8 is associated with the loss of a beta-hemolysin converting prophage and the acquisition of a new staphylococcal cassette chromosome. PLoS ONE. 2013, 8: e58187-10.1371/journal.pone.0058187.
Gladysheva IP, Turner RB, Sazonova IY, Liu L, Reed GL: Coevolutionary patterns in plasminogen activation. Proc Natl Acad Sci U S A. 2003, 100: 9168-9172. 10.1073/pnas.1631716100.
Kim SH, Chun HS, Han MH, Park NY, Suk K: A novel variant of staphylokinase gene from Staphylococcus aureus ATCC 29213. Thromb Res. 1997, 87: 387-395. 10.1016/S0049-3848(97)00142-4.
Sako T, Sawaki S, Sakurai T, Ito S, Yoshizawa Y, Kondo I: Cloning and expression of the staphylokinase gene of Staphylococcus aureus in Escherichia coli. Mol Gen Genet. 1983, 190: 271-277. 10.1007/BF00330650.
Behnke D, Gerlach D: Cloning and expression in Escherichia coli, Bacillus subtilis, and Streptococcus sanguis of a gene for staphylokinase–a bacterial plasminogen activator. Mol Gen Genet. 1987, 210: 528-534. 10.1007/BF00327208.
Coleman DC, Sullivan DJ, Russell RJ, Arbuthnott JP, Carey BF, Pomeroy HM: Staphylococcus aureus bacteriophages mediating the simultaneous lysogenic conversion of beta-lysin, staphylokinase and enterotoxin A: molecular mechanism of triple conversion. J Gen Microbiol. 1989, 135: 1679-1697.
Sumby P, Waldor MK: Transcription of the toxin genes present within the Staphylococcal phage phiSa3ms is intimately linked with the phage's life cycle. J Bacteriol. 2003, 185: 6841-6851. 10.1128/JB.185.23.6841-6851.2003.
Lijnen HR: Plasmin and matrix metalloproteinases in vascular remodeling. Thromb Haemost. 2001, 86: 324-333.
Collen D: Identification and some properties of a new fast-reacting plasmin inhibitor in human plasma. Eur J Biochem. 1976, 69: 209-216. 10.1111/j.1432-1033.1976.tb10875.x.
Molkanen T, Tyynela J, Helin J, Kalkkinen N, Kuusela P: Enhanced activation of bound plasminogen on Staphylococcus aureus by staphylokinase. FEBS Lett. 2002, 517: 72-78. 10.1016/S0014-5793(02)02580-2.
Furuya H, Ikeda R: Interaction of triosephosphate isomerase from Staphylococcus aureus with plasminogen. Microbiol Immunol. 2011, 55: 855-862. 10.1111/j.1348-0421.2011.00392.x.
Koch TK, Reuter M, Barthel D, Bohm S, van den Elsen J, Kraiczy P, Zipfel PF, Skerka C: Staphylococcus aureus proteins Sbi and Efb recruit human plasmin to degrade complement C3 and C3b. PLoS ONE. 2012, 7: e47638-10.1371/journal.pone.0047638.
Souza NM, Vieira ML, Alves IJ, de Morais ZM, Vasconcellos SA, Nascimento AL: Lsa30, a novel adhesin of Leptospira interrogans binds human plasminogen and the complement regulator C4bp. Microb Pathog. 2012, 53: 125-134. 10.1016/j.micpath.2012.06.001.
Jin T, Bokarewa M, Foster T, Mitchell J, Higgins J, Tarkowski A: Staphylococcus aureus resists human defensins by production of staphylokinase, a novel bacterial evasion mechanism. J Immunol. 2004, 172: 1169-1176. 10.4049/jimmunol.172.2.1169.
Rooijakkers SH, van Wamel WJ, Ruyken M, van Kessel KP, van Strijp JA: Anti-opsonic properties of staphylokinase. Microbes Infect. 2005, 7: 476-484. 10.1016/j.micinf.2004.12.014.
Foster TJ, Hook M: Surface protein adhesins of Staphylococcus aureus. Trends Microbiol. 2003, 48: 1429-49.
Novick RP: Autoinduction and signal transduction in the regulation of staphylococcal virulence. Mol Microbiol. 2003, 48: 1429-1449. 10.1046/j.1365-2958.2003.03526.x.
Lijnen HR: Gene targeting in hemostasis. Alpha2-antiplasmin. Front Biosci. 2001, 6: D239-247. 10.2741/Lijnen.
Feng Y, Jacobs F, Van Craeyveld E, Lievens J, Snoeys J, Van Linthout S, De Geest B: The impact of antigen expression in antigen-presenting cells on humoral immune responses against the transgene product. Gene Ther. 2010, 17: 288-293. 10.1038/gt.2009.125.
Van Linthout S, Lusky M, Collen D, De Geest B: Persistent hepatic expression of human apo A-I after transfer with a helper-virus independent adenoviral vector. Gene Ther. 2002, 9: 1520-1528. 10.1038/sj.gt.3301824.
Deutsch DG, Mertz ET: Plasminogen: purification from human plasma by affinity chromatography. Science. 1970, 170: 1095-1096. 10.1126/science.170.3962.1095.
Verhamme P, Goossens G, Maleux G, Collen D, Stas M: A dose-finding clinical trial of staphylokinase SY162 in patients with long-term venous access catheter thrombotic occlusion. J Thromb Thrombolysis. 2007, 24: 1-5. 10.1007/s11239-006-0006-4.
Holvoet P, Lijnen HR, Collen D: A monoclonal antibody preventing binding of tissue-type plasminogen activator to fibrin: useful to monitor fibrinogen breakdown during t-PA infusion. Blood. 1986, 67: 1482-1487.
Van Hul M, Lijnen HR: Effect of weight loss on gelatinase levels in obese mice. Clin Exp Pharmacol Physiol. 2011, 38: 647-649. 10.1111/j.1440-1681.2011.05552.x.
Van Hul M, Lijnen HR: A functional role of gelatinase A in the development of nutritionally induced obesity in mice. J Thromb Haemost. 2008, 6: 1198-1206. 10.1111/j.1538-7836.2008.02988.x.
This work was supported by a grant of the Research Foundation Flanders (FWO-Vlaanderen, 11I0113N). MP, TV and LL are fellows of the FWO, PV is a senior clinical investigator of the FWO.
The authors would like to thank Professer U. Himmelreich and the staff of the MoSAIC core facility of the KU Leuven for assistance in bioluminescence imaging.
We would like to thank Professor J. Verhaegen for collection of clinical strains. We thank K. Cludts, S. Van kerckhoven and M. Lox for skillful technical assistance.
The authors declare that they have no competing interests.
MP designed the experiments, analysed and interpreted the data, performed the statistical analysis and wrote the manuscript. TV, LL and JC assisted in experimental design, statistical analysis and in manuscript revision. JK and TJ provided the LS-1 congenic strains and contributed to manuscript revision. BDG prepared the viral vectors and reviewed the manuscript. MH, RL and PV coordinated the research and reviewed the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1:Host α 2 -antiplasmin (α 2 AP) protects against extension of S. aureus skin infection. Martius Scarlet Blue staining of representative lesions from α2AP KO and α2AP WT mice, infected with S. aureus LS-1 EP. In both genotypes, a peripheral zone of fibrin (F, red), surrounding the abscess, can be appreciated on day 1. On day 3 however, less fibrin is observed in the abscess periphery of α2AP KO mice, likely reflecting the disbalance between (normal) fibrin deposition and (uninhibited) fibrinolysis at this later time point. Hence, α2AP gene deficiency impairs sustained local containment of S. aureus infection. (PDF 304 KB)
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Peetermans, M., Vanassche, T., Liesenborghs, L. et al. Plasminogen activation by staphylokinase enhances local spreading of S. aureus in skin infections. BMC Microbiol 14, 310 (2014). https://doi.org/10.1186/s12866-014-0310-7
- Matrix metalloproteinases
- Staphylococcus aureus
- Skin infection