Skip to main content
  • Loading metrics

A Scabies Mite Serpin Interferes with Complement-Mediated Neutrophil Functions and Promotes Staphylococcal Growth


25 Nov 2014: The PLOS Neglected Tropical Diseases Staff (2014) Correction: A Scabies Mite Serpin Interferes with Complement-Mediated Neutrophil Functions and Promotes Staphylococcal Growth. PLOS Neglected Tropical Diseases 8(11): e3415. View correction



Scabies is a contagious skin disease caused by the parasitic mite Sarcoptes scabiei. The disease is highly prevalent worldwide and known to predispose to secondary bacterial infections, in particular by Streptococcus pyogenes and Staphylococcus aureus. Reports of scabies patients co-infected with methicillin resistant S. aureus (MRSA) pose a major concern for serious down-stream complications. We previously reported that a range of complement inhibitors secreted by the mites promoted the growth of S. pyogenes. Here, we show that a recently characterized mite serine protease inhibitor (SMSB4) inhibits the complement-mediated blood killing of S. aureus.

Methodology/Principal Findings

Blood killing of S. aureus was measured in whole blood bactericidal assays, counting viable bacteria recovered after treatment in fresh blood containing active complement and phagocytes, treated with recombinant SMSB4. SMSB4 inhibited the blood killing of various strains of S. aureus including methicillin-resistant and methicillin-sensitive isolates. Staphylococcal growth was promoted in a dose-dependent manner. We investigated the effect of SMSB4 on the complement-mediated neutrophil functions, namely phagocytosis, opsonization and anaphylatoxin release, by flow cytometry and in enzyme linked immuno sorbent assays (ELISA). SMSB4 reduced phagocytosis of S. aureus by neutrophils. It inhibited the deposition of C3b, C4b and properdin on the bacteria surface, but did not affect the depositions of C1q and MBL. SMSB4 also inhibited C5 cleavage as indicated by a reduced C5b-9 deposition.


We postulate that SMSB4 interferes with the activation of all three complement pathways by reducing the amount of C3 convertase formed. We conclude that SMSB4 interferes with the complement-dependent killing function of neutrophils, thereby reducing opsonization, phagocytosis and further recruitment of neutrophils to the site of infection. As a consequence secreted scabies mites complement inhibitors, such as SMSB4, provide favorable conditions for the onset of S. aureus co-infection in the scabies-infected microenvironment by suppressing the immediate host immune response.

Author Summary

There is increasing evidence that in the tropics bacterial pyoderma and life-threatening downstream complications caused by Staphylococcus aureus and Streptococcus pyogenes are often linked with scabies infestation. The bacteria were commonly thought to find easy entry into the skin, damaged by scabies mites. However, there may be more to it. Our study aimed to identify the molecular mechanisms underlying the link between mites and bacteria. We recently characterized a molecule (SMSB4) that the mite produces for self-protection from the immediate host defense system in the skin. We show here that SMSB4 reduces the uptake of S. aureus by neutrophils, which are the killer immune cells, first to arrive at the infection site. These cells are guided by a number of complement factors. SMSB4 reduces the deposition of several complement components on the bacteria surface, thereby interrupting the essential defense cascades and inhibiting further neutrophil recruitment to the site. In summary, a mite molecule that likely originally evolved to protect the mite against the host defense plays a further role in the pathogenesis of secondary infections: when secreted into the damaged skin it promotes the onset of S. aureus infection thereby increasing the prevalence of debilitating disease associated with scabies.


Scabies is a ubiquitous and contagious skin infection caused by a burrowing parasitic mite Sarcoptes scabiei. In addition to the morbidity associated with the typical intense itching; a rather more important significance of scabies are the associated secondary bacterial infections, which predispose the host to serious downstream systemic and life-threatening diseases [1]. Scabies is one of the most common dermatological conditions on a global scale with disease burden of up to 70% in rural India, between 18 and 42% in the South Pacific, and erratic reports from Africa and South America [2], [3]. In Australia, prevalence of scabies is particularly high in the remote Aboriginal communities in the tropical north, with up to 70% of children present with scabies and pyoderma before reaching two years of age [4]. Community-wide treatment of scabies decreases pyoderma which suggests a key role of the burrowing mite [5], [6]. Staphylococcus aureus and Streptococcus pyogenes are the common causative agents of scabies associated pyoderma [7], [8]. The annual incidence of bacteremia due to S. aureus is six times higher in the Australian Aboriginal population than the rest of the Australian population [9]. More recently, methicillin resistant S. aureus (MRSA) has been reported in 64% of children presented with scabies in a regional hospital of North West Queensland [10]. While epidemiological evidence has been well-established that bacterial infections are closely linked with scabies, and mechanical damage of the upper epidermal layers by the mites is one obvious prerequisite, the relationship itself, between host, mites and bacteria, is poorly understood. Given that scabies is a primary risk factor for bacterial skin infections and increased incidence of MRSA infections, it is of increasing relevance to understand the molecular links in the trilateral relationship of host, mites and bacteria.

Upon entry, the pathogen is confronted by the complement system, which is part of the innate defense mechanism of the human host. Three different pathways initiate complement cascade, the classical (CP), lectin (LP) and alternative pathways (AP). The CP is initiated by binding of C1q to bacterial bound antibody or surface microbial sugar. This activates the protease C1r and then C1s, which cleaves C4 into C4a and C4b. C4b covalently binds to the microbial surface and is joined by C2, which is then cleaved by C1s to form an enzyme complex C3 convertase (C4b2a) [11]. The LP is initiated when microbial surface sugars are recognized by mannose binding lectin (MBL) or ficolins, and complexed with MBL-associated proteases (MAPSs-1,-2,-3), which are functional homologues of C1r and C1s [12][14]. In the AP, properdin recognizes the microbial sugars and initiates the de novo assembly of the AP C3 convertase (C3bBb) on the pathogen surface [15][18]. All three pathways converge in the formation of a key enzyme, the C3 convertase. This cleaves C3, releasing a small chemo attractant C3a, and C3b, which is deposited on the microbial surface [19]. C3b deposition is crucial for eradication of microbes as it marks the microbes for efficient uptake and subsequent killing by phagocytes. Moreover, at a high local concentration C3b binds to C3 convertase thereby turning into C5 convertase (C4b2a3b/C3bBb3b), which cleaves the complement protein C5 into C5a and C5b. C5a is a potent chemoattractant, which attracts neutrophils, monocytes and macrophages to the site of infection. C5b and further complement components C6, C7, C8 and C9 form the membrane attack complex (MAC/C5b-9) on the cell surface, causing direct cell lysis in sensitive cells [11].

S. aureus is a versatile pathogen, causing serious disease in humans. It has evolved various mechanisms to impair and evade the host immune system. It has been reported to secret a variety of host complement inhibitors that decrease C3b deposition on the microbial surface, e.g. staphylococcal complement inhibitor [20], extracellular fibrinogen-binding protein [21], staphylokinase [22] and aureolysin [23]. Interestingly, scabies mites are also known to excrete multiple families of complement inhibitors, which are secreted into the mites intestinal system and are thus believed to prevent damage of the mite gut [24][26]. They are excreted with the mite feces and have been localized in the mite burrows in the upper epidermis [24], [25]. We reported that scabies mite complement inhibitors promote the survival and growth of S. pyogenes in whole blood in vitro assays [26]. We proposed that phagocytosis by neutrophils was impeded through complement inhibition. One of the mite complement inhibitors, a 54 kDa serpin named SMSB4, displayed direct interactions with several complement proteins and interfered with the initial and progressing steps of the complement cascade [25]. However, the process had previously not been analyzed in the context of a bacterial surface and the involvement of neutrophils had not been demonstrated. In addition it was unknown whether the SMSB4-mediated inhibition of complement activation offers congenial conditions for other major skin bacterial pathogens, such as S. aureus. Here we report that SMSB4 also promotes the survival and growth of S. aureus by interfering with the initiation of complement activation, leading to a reduced opsonization and to a reduced phagocytosis and killing of bacteria by neutrophils. Thus we postulate that SMSB4 is a major player in the tripartite interactions between host, parasite and any opportunistic bacterial pathogen.


Ethics statement

Normal human serum (NHS) for complement activation assays and whole blood samples for bactericidal assays was prepared from blood donated by healthy volunteers. Informed written consent was obtained from all blood donors. The protocol was approved by the medical ethics committee of the QIMR Berghofer Medical Research Institute.

Blood donation and screening

Informed consent was obtained from all blood donors. The protocol was approved by the medical ethics committee of the QIMR Berghofer Medical Research Institute. Among several donors tested in preliminary experiments, blood from all donors showed bactericidal effect against S. aureus. Blood from two donors was used in all further assays requiring fresh whole blood.

Bacterial strains and growth conditions

S. aureus commercial strain Xen29 (KanR) was purchased from Caliper Life Sciences Inc. (Massachusetts, USA) and this strain was used for all assays. S. aureus strains associated with pyoderma were provided by Dr. Deborah Holt at the Menzies School of Health Research, Charles Darwin University, Darwin. Isolates HS56 (MSSA), HS16 (MRSA) [27] are Panton-Valentine leukocidin positive, multi-locus sequence type 93 (commonly known as the Queensland clone) [9] while M5 (MSSA), M34 (MRSA) [28] belong to CC75, a genetically distinct type of S. aureus lacking staphyloxanthin [29]. All strains were routinely cultured at 37°C aerobically in either Tryptic soy broth (TSB; Thermo Fisher Scientific Pty. Ltd., Australia), shaking at 200 rpm or on Tryptic soy agar (TSA) plates.

Preparation of cell suspensions

S. aureus cell suspensions were prepared from mid-log growth phase cultures (OD600 = 1.0). Cells were harvested by centrifugation (4000 ×g, 10 min, 4°C), washed twice in phosphate buffered saline (PBS) and resuspended to a final OD600 = 0.03 (∼5× 106 cfu/ml) in the same buffer. The cell number of this suspension was enumerated by plate count of colony forming units (cfu/ml) on TSA at 37°C overnight.

Production and purification of recombinant SMSB4

SMSB4 was cloned and expressed in Escherichia coli BL21 (Qiagen) and purified under denaturing condition as described previously by Mika et. al.[25], with minor modifications. Briefly, SMSB4 cDNA (Yv5004A04, GenBank accession no. JF317222) of the human scabies mites S. scabiei cloned into the pQE9 expression vector (Qiagen) was transformed into E. coli BL21. E. coli cells were cultivated in Luria broth (Becton Dickinson) containing 100 µg/mL ampicillin at 37°C over night. After inoculation in 2YT medium (Becton Dickinson) containing the same concentration of ampicillin, the cells were grown at 37°C, shaking at 200 rpm until an OD600 of 0.6–0.7 was reached. Expression of recombinant SMSB4 was induced by addition of 0.5 mM IPTG, and continued shaking at 200 rpm for a further 4 h. Cells were collected by centrifugation at 6000 ×g at 4°C for 20 min, resuspended in serpin buffer (50 mM Tris, pH 8.0, 100 mM NaCl, 10 mM EDTA, 1 mM PMSF) and lysed in 250 µg/ml lysozyme and 10 µg/ml DNase at room temperature (RT) under continuous rotation for 1 h. All of the following purification steps were performed at 4°C. After sonication of the spheroplasts by a Sonifier 250 (Branson), inclusion bodies were washed five times using serpinX buffer (50 mM Tris, pH 8.0, 100 mM NaCl, 10 mM EDTA, 0.5% (v/v) Triton X-100) and retrieved by centrifugation (16,000 ×g for 20 min at 4°C). The resulting pellet was dissolved in solubilization buffer (6 M guanidine hydrochloride, 50 mM Tris, pH 7.8, 1 mM DTT) for 1 h. Proteins were further purified by nickel affinity chromatography. Solubilized protein was diluted 1∶1 with bind buffer (6 M urea, 100 mM NaH2PO4, 10 mM Tris, pH 8.0, 5 mM imidazole, 150 mM NaCl, 1% (v/v) glycerol, 1 mM DTT) and bound overnight to a pre-equilibrated 1ml Ni-NTA matrix (Qiagen) in a PolyPrep column (BioRad) on a rotating shaker. The column was washed twice with 5 ml of wash buffer (6 M urea, 100 mM NaH2PO4, 10 mM Tris, pH 6.3, 5 mM imidazole, 150 mM NaCl, 1% (v/v) glycerol, 1 mM DTT). Bound proteins were eluted twice using 3 ml of elution buffer (6 M urea, 100 mM NaH2PO4, 10 mM Tris, pH 8.0, 250 mM imidazole, 150 mM NaCl, 1% (v/v) glycerol and 1 mM DTT). Purified recombinant proteins were refolded overnight by drop wise addition of the protein elution into refolding buffer (300 mM L-arginine, 50 mM Tris, 50 mM NaCl and 5 mM DTT, pH 10.5) using a Minipuls 3 pump (Gilson) at a flow rate of 20 µl/min under gentle stirring. Refolded proteins were concentrated using an Ultrasette Lab Tangential Flow Device (10 kDa MWCO, PALL Life Sciences), followed by further concentration in centrifugal filters (10 kDa MWCO, Amicon Ultra, Millipore). Protein concentrations were determined by Bradford protein assay (Bio-Rad) with bovine serum albumin (BSA) (Invitrogen) as a standard according to the manufacturer’s instructions. Molecular mass and purity were confirmed using SDS-PAGE analysis with Coomassie blue R-250 staining. For all assays, SMSB4 was buffer exchanged into the corresponding assay buffers using 0.5 ml centrifugal filters (10 kDa MWCO, Amicon Ultra, Millipore).

Whole blood bactericidal assays

Bactericidal assays were performed with human whole blood collected in standard vacutainers containing hirudin at a concentration >15 µg/ml as anticoagulant (Dynabyte Informationssysteme GmbH, Munich, Germany). The assays were performed as described previously [26],_ENREF_6_ENREF_6_ENREF_6 with some modifications. Bacteria were grown overnight at 37°C with shaking at 200 rpm in 5 ml TSB. The overnight culture was diluted to an initial OD600 of 0.05 in a fresh aliquot of 5 ml THB and the S. aureus culture was grown to mid-log growth phase (OD600 1.0) at 37°C with shaking at 200 rpm. This culture was diluted 2×103 fold in PBS to obtain an approximately 1×105 cfu/ml of S. aureus challenge dose. To 100 µl of human venous blood, either of the following compounds were added in a volume of 27.5 µl: purified recombinant SMSB4 in the experimental samples, cobra venom factor (CVF) in the positive controls, and BSA or GVB2+ buffer (5 mM veronal buffer, 140 mM NaCl, 0.1% (w/v) gelatin, 1 mM MgCl2, 0.15 mM CaCl2, pH 7.35) in the negative controls. Finally 12.5 µl of the simultaneously prepared S. aureus challenge suspension were mixed to a total volume of 140 µl. Samples were placed on a rotisserie and incubated with end over end mixing for 1–3 h at 37°C. Subsequently 50 µl aliquots from each appropriately diluted tube were plated in duplicate on TSA. The plates were incubated overnight at 37°C under aerobic conditions and bacterial numbers were enumerated as cfu/ml. Bacterial recovery was calculated as a percentage of the number of bacteria recovered from samples treated with various test compounds in reference to the S. aureus challenge dose.

Preparation of Fluorescein Isothiocynate (FITC) labeled S. aureus

A S. aureus cell suspension was prepared from a mid-log growth phase culture resuspended in PBS to OD600 = 1.0 as described above. This suspension was incubated with 0.01% (v/v) final concentration of FITC solution (Sigma) at 37°C for 30 min with shaking at 200 rpm in a light protected environment. Cells were pelleted by centrifugation at 4000 ×g, 10 min, 4°C. Excess FITC was removed by washing twice with 0.1 M carbonate buffer (pH 9.6) and resuspended to OD600 = 0.1 in the same buffer. Fluorescence of S. aureus cells was examined under fluorescence microscope (Leica Inverted Fluorescence Microscope, Lecia Microsystems). Cells were aliquoted into 300 µl volume and stored at −80°C in the dark until use.

Phagocytosis of S. aureus

Human neutrophils were purified by Histopaque -1077 (density 1.077, Sigma)/Histopaque -1119 (density 1.119, Sigma) gradient according to the manufacturer’s instructions using heparinized whole blood from a single donor. Blood was collected in standard BD vacutainers containing 150 USP units of sodium heparin (Becton Dickinson). The numbers of purified neutrophils were counted in a hemocytometer and purity was checked by flow cytometry (Becton Dickinson FACSCanto II). Fifty μl of 20% serum freshly prepared from the same blood donor was incubated with 50 µl of various concentrations of purified recombinant SMSB4 in PBS and 5 µl of FITC-S. aureus, at 37°C for 30 min in the wells of a round-bottom 96 well plate (Nunc). Samples with serum heated at 56°C for 30 min prior to the experiment were included as a negative control. Plates were centrifuged for 3 min at 500 ×g. Phagocytosis was initiated by the addition of 50 µl of purified neutrophils into the wells containing FITC-S. aureus to achieve a neutrophil to bacteria ratio of 10∶1 (e.g. 106 neutrophils to 105 bacteria). The plate was shaken on a horizontal shaker at 200 rpm at 37°C for either 40 min or various time points. Reactions were stopped by the addition of 50 µl of 4% ice cold paraformaldehyde (PFD) solution into the wells and the plate was incubated on ice for a further 30 min. Exogenous, non-phagocytosed S. aureus cells were removed by gently washing and aspirating the supernatant twice with 200 µl ice cold PBS (900 ×g, 3 min, 4°C). Adherent neutrophils that remained on the bottom of the wells were resuspended in 200 µl PBS and uptake of the FITC-S. aureus was evaluated by flow cytometry (FACSCanto II, Becton Dickinson) measuring the fluorescence of 106 gated neutrophils.

Complement depositions on S. aureus by ELISA

To each well of a 96-well assay plate (Maxisorp, Nunc), 100 µl of approximately 5.0×106 cfu/ml of S. aureus cell suspension was added, incubated first at 37°C for 1 h and subsequently at 4°C overnight. Wells were washed 4 times with 250 µl PBS containing 0.05% Tween-20 in between each step of the assay. The wells were blocked with block buffer (4% BSA in PBS containing 0.05% Tween-20) for 4 h at RT. Meanwhile, 30 µl of 10% pooled human serum diluted in GVB2+ buffer (5 mM veronal buffer, 10 mM NaCl, 0.1% (w/v) gelatin, 1 mM MgCl2, 0.15 M CaCl2, pH 7.35) was incubated with 30 µl of SMSB4 at 37°C for 30 min in a V-shaped bottom 96-well plate (Nunc). Fifty μl of these mixtures were transferred to the 96-well plate coated with S. aureus that was before blocked with the blocking buffer. The plate was incubated at 37°C for further 30 min. Bound complement proteins were detected by incubation with 60 µl of primary antibodies against human complement factors for 1 h at RT. For immunodetection antibodies against C1q, C3d, C4c (Dako, Denmark), properdin (R&D systems) and SC5b-9 neoantigen-specific antibody recognizing the MAC complex (Complement Technology Inc., USA) were used at a dilution of 1∶4000, and against MBL (manufacturer) at dilution of 1∶1000. The wells were subsequently incubated with 60 µl of horseradish peroxidase (HRP)-conjugated goat anti-rabbit or HRP-conjugated rabbit anti-goat secondary antibodies (Dako, Denmark) at dilutions of (1∶1000-1∶4000 in block buffer) at RT for 30 min-1 h, depending on the primary antibody specificity and signal intensity. The assay was developed with 60 µl of OPD reagent (Dako, Denmark) containing 0.01% hydrogen peroxide by incubation at RT until serum only positive control turned yellow. Reactions were stopped by addition of 50 µl of 0.5 N H2SO4 and absorbance was measured at OD490 on a POLARstar Optima fluorescent microtiter plate reader (BMG Labtech, Melbourne, Australia). The absorbance obtained in the serum only sample was defined as 100%.

Statistical analysis

Statistical significance was determined using 2way ANOVA, either Tukey’s or Sidak’s multiple comparisons test (GraphPad Prism software, version 6.0; GraphPad Software Inc. USA). Values of p<0.05 were considered significant.


SMSB4 reduces blood killing of S. aureus

To investigate the effect of SMSB4 on the onset of S. aureus infection under physiological conditions, we performed bactericidal assay in SMSB4 treated blood when challenged with a known number of S. aureus Xen29. Samples treated with GVB2+ buffer or BSA were included as negative controls and samples treated with a known complement inhibitor, CVF as a positive control. We demonstrated that S. aureus was killed in blood when treated with GVB2+ buffer or 100 µg/ml of BSA, as up to 90% reduction in cfu/ml was seen after 3 h (Figure 1a). In contrast, bacteria numbers began to recover after 2 h in the samples treated with 100 µg/ml of SMSB4 and 10 µg/ml of CVF, approximately 50% increase in recovery at 3 h compared with the initial time points (Figure 1a). Bacterial recovery remained unchanged over time in the samples incubated with PBS only instead of blood, indicating that reduction in S. aureus number was due to blood killing.

Figure 1. SMSB4 reduces the blood killing of S. aureus strain Xen29 in whole blood (A) and pyoderma isolates of S. aureus (B).

SMSB4 promotes bacteria growth in a concentration dependent manner (C) similarly to CVF (D). S. aureus Xen29 or pyoderma isolates MRSA strains (HS16, M34), MSSA strains (HS56, M5) were harvested from mid-log growth phase culture. Bacteria (1×105 cfu/ml) were challenged with whole blood pre-treated with either 100 µg/ml SMSB4, positive control 10 µg/ml CVF, negative controls 100 µg/ml BSA or GVB2+ buffer only. S. aureus cells in PBS only without blood was also included to illustrate that the reduction in bacteria number was due to blood killing (A). Numbers of bacteria were counted as cfu/ml at various time points (A) or at 3 h (B, C, D). Bacterial recovery was calculated as a percentage of the challenge dose. Results are shown as means ± SEM from three independent experiments. The statistical significance of differences between samples was estimated using two way ANOVA with Tukey’s multiple comparison test. **, p<0.01; ***, p<0.001; ****, p<0.0001, ns, not significant (B).

Since complement-mediated blood killing is a generalized protective host response to an infection, we tested this bactericidal effect on various skin isolates of S. aureus including MRSA and MSSA phenotypes. The level of blood killing observed when MRSA strains (HS16, M34) and MSSA strains (HS56, M5) tested was very similar to what was seen for the type strain Xen29 (Figure 1b). In samples treated with either GVB2+ buffer or 100 µg/ml of BSA, the bacterial recovery ranged from 7–10% across all S. aureus strains tested (Figure 1b). A comparable degree of bacterial recovery (approximately 50%) was observed across all strains when treated with 100 µg/ml of SMSB4 (Figure 1b). We further established that SMSB4 reduced blood killing and promoted S. aureus growth in a dose dependant manner. A five-fold increase in bacterial recovery was observed in the presence of SMSB4 concentrations rising from 50–200 µg/ml (Figure 1c). A similar effect was observed when raising concentrations of the commercial complement inhibitor CVF were tested as a positive control (Figure 1d).

SMSB4 reduces complement-driven neutrophil functions required for S. aureus killing

(i) SMSB4 reduces phagocytosis.

While MAC complex is deposited on the surface of S. aureus, gram-positive bacteria such as S. aureus are insensitive to complement-mediated lysis by MAC formation [30]. Consequently the killing effect of blood in the bactericidal assays reported here is most likely due to neutrophil killing. We therefore investigated the processes essential for the complement-mediated killing function of neutrophils. Firstly, we tested the effect of SMSB4 on phagocytosis of S. aureus by purified human neutrophils. FITC-S. aureus were opsonized with serum pre-treated with SMSB4 or BSA, and human neutrophils were challenged with bacteria. Phagocytosis was indicated by increase in FITC signal as measured by flow cytometry. FITC uptake was observed within a 20 min period and we found approximately 20% gradual reduction of the FITC signal in SMSB4 treated samples compared to BSA treated samples (Figure 2a). We also measured FITC uptake in S. aureus pre-opsonized with heated serum and found a neglectable FITC signal (Figure 2a). These results indicate that (i) active complement was required to opsonize S. aureus and (ii) SMSB4 inhibits complement mediated-phagocytosis. The anti-phagocytic effect of the complement inhibitor SMSB4 is concentration dependent as the degree of inhibition increased with increasing concentration of protein used to treat the serum, e.g. from 30% inhibition at 25 µg/ml to 60% inhibition at 150 µg/ml of SMSB4 (Figure 2b).

Figure 2. SMSB4 reduces phagocytosis of S. aureus by neutrophils.

FITC-labeled bacteria (105 cfu) was opsonized either with 20% NHS or heated serum and challenged with neutrophils (106 cells). Serum samples were pre-treated for 30 min at 37°C with 50 µg/ml SMSB4, 50 µg/ml BSA (A), or various concentrations of SMSB4 or BSA (B). Uptake of FITC by neutrophils was measured at various time points over 1 h (A) or at 40 min (B). Results are shown as means ± SEM from three independent experiments.

(ii) SMSB4 reduces C3b deposition on S. aureus and C5 cleavage.

Deposition of the complement component C3b on the pathogen surface, also known as opsonization, is crucial for phagocytosis. Opsonized bacteria are recognized by neutrophils via their cell surface receptor, leading to phagocytosis and killing of the pathogen. The effect of the mite complement inhibitor SMSB4 on the phagocytosis indicated that this molecule was likely to interfere with opsonization. S. aureus was incubated with NHS, pre-treated with various concentrations of SMSB4 or BSA as a negative control. Surface bound C3b was detected with a specific antibody. Our results demonstrate that in the presence of an increasing concentration of SMSB4, C3b deposition on S. aureus was reduced in a concentration dependent manner (Figure 3a), which was comparable to the degree of reduction in phagocytosis (Figure 2b).

Figure 3. SMSB4 reduces deposition of C3b (A) and MAC complex (SC5b-9) formation (B).

The wells of 96-well microtiter plates were coated with 100 µl aliquots of bacterial cell suspensions containing 5×106 cfu/ml of S. aureus. Wells were then incubated with 10% NHS which has been pre-treated with increasing concentrations of either SMSB4 or BSA. Antibodies were detected by ELISA using primary human specific antibodies, followed by HRP-conjugated secondary antibodies, and fluorescence was detected at 490 nm. Results are shown as means ± SEM from three independent experiments.

In the complement cascade, the formation of C5 convertase (C4b2a3b/C3bBb3b) follows downstream of the C3 cleavage, arising from the binding of additional C3b onto C3 convertase on the bacterial surface. C5 convertase cleaves C5 into C5a and C5b. C5a is a potent chemoattractant to initiate migration of neutrophils towards the site of infection. C5b binds to other complement components (C6-C9) to form the MAC complex which is deposited on the surface of S. aureus [30]. To study whether SMSB4 affects C5 cleavage, we analyzed the amount of C5b deposited as part of the MAC complex on the S. aureus cell surface, using anti SC5b-9 antibody, a neoantigen-specific antibody recognizing the human MAC complex. We found that SMSB4 indeed reduced the level of MAC deposition on S. aureus in a concentration dependent manner (Figure 3b). We also noted that the degree of inhibition by SMSB4 on the MAC complex formation was much higher than its effect on the C3b deposition (Figure 3a). Since active C3 convertase and additional C3b are prerequisites for formation of C5 convertase, reduction in any of these components is expected have a profound effect on the C5 cleavage.

SMSB4 inhibits the function of complement pathway initiations

Formation of C3 convertase via CP and LP requires cleavage of C4 by either C1 or MBL complexes, resulting in the covalent binding of C4b onto the bacterial surface. We previously reported that SMSB4 affects the initial and progressing steps of the complement activation for both the CP and the LP. Those assays were carried out in the absence of target cells by artificially activating the individual complement pathways with either IgG or mannan [25]. Here we investigated the effect of SMSB4 on the C4b deposition on the S. aureus cell surface when complement system is physiologically activated by the bacteria themselves. Our result showed that SMSB4 reduced the C4b deposition in a concentration dependent manner (Figure 4a).

Figure 4. Effect of SMSB4 on the depositions of C4b (A), C1q, MBL and properdin (B) on S. aureus cells.

The wells of 96-well microtiter plates were coated with 100 µl aliquots of bacterial cell suspensions containing 5×106 cfu/ml of S. aureus. Wells were then incubated with 10% NHS which has been pre-treated with increasing concentrations of either SMSB4 or BSA. Antibodies were detected by ELISA using primary human specific antibodies, followed by HRP-conjugated secondary antibodies, and fluorescence was detected at 490 nm. Results are shown as means ± SEM from three independent experiments. The statistical significance of differences between BSA and SMSB4 treated samples were estimated using two way ANOVA with Sidak’s multiple comparison test. **, p<0.01; ***, p<0.001; ns, not significant (B).

Initiation of the complement cascades preceding C4 cleavage involves the deposition of C1q (CP), MBL (LP) and properdin (AP) onto the pathogen surface. We therefore examined whether SMSB4 affects the deposition of these complexes on S. aureus cell surface. SMSB4 did not affect the depositions of C1q and MBL. However, deposition of properdin was reduced by 20% in the samples treated with a 100 µg/ml SMSB4 (Figure 4b).


The complement system is an essential part of the innate immune system that rapidly recognizes and kills pathogen either by direct cell lysis, or marks the pathogen to be killed by phagocytes. Many pathogens, whether bacteria or parasites, are known to posses strategies to evade the host complement attack. For example, S. aureus is a versatile human pathogen that produces a diverse array of multiple complement inhibitors, which interfere with various stages of complement activation [20], [22], [23], [31], [32]. Scabies mites also produce a variety of proteins that interfere with complement [24][26]. We have localized these proteins in the mite gut and in fecal pellets by immunohistochemistry [25], [33]. In the confined space of the mite gut and epidermal burrows the combined anti-complement activity exerted by the multiple mite complement inhibitors may reach functionally and physiologically significant levels. For the mites as serum-feeding parasites, the biological relevance of scabies mite complement inhibitors is likely preventing complement-mediated mite gut damage [24], [25], [34]. We propose that these molecules also pre-condition the host for the onset of bacterial invasion. Epidemiological evidence supporting the frequent association of S. pyogenes and/or S. aureus co-infections with scabies infestations led to our hypothesis that scabies infection could promote the onset of infections by the opportunistic pathogenic bacteria. We previously reported that recombinant scabies mite complement inhibitors promoted the in vitro growth of S. pyogenes [26]. Here, we provide more detailed evidence of how one of these mite complement inhibitors, namely SMSB4, promoted the growth of S. aureus. This is the first report on the effect of a scabies mite complement inhibitor on aiding the growth of Staphylococcus.

Mechanism of complement-mediated killing is due to phagocytosis of bacteria by blood leucocytes and direct lysis by MAC complex. It is known that a gram-positive pathogen such as S. aureus is insensitive to direct killing by MAC-complex formation [30]. As such the inhibitory effect of SMSB4 on blood killing is likely due to the complement-dependent killing function of blood leucocytes. SMSB4 reduced opsonization, phagocytosis and effectively reduced the complement-mediated blood killing of S. aureus, and promoted the growth of the bacteria in a dose-dependent fashion. Furthermore SMSB4 also inhibited the generation of anaphylatoxins required for the phagocyte recruitment. Since complement response is a generalized immediate host immune reaction towards pathogens, we found that the inhibitory effect of SMSB4 on the bacterial killing was similar across all S. aureus strains tested, including MRSA and MSSA.

We previously shown that SMSB4 inhibits the initial and progressing steps of all three complement pathways [25]. In this previous work haemolytic, complement deposition and complement binding assays were employed, where the individual complement pathways were activated by antibody or carbohydrates. The effect on bacteria surfaces and neutrophils was not addressed. In the present study, we attempted for the first time to mimic pathophysiological conditions provided by the presence of bacteria by activating the complement cascades with S. aureus cells, and then analyzed the effect of SMSB4 on the cell surface deposition of complement complexes required for initialization of the complement cascades. We found that SMSB4 did not inhibit the deposition of C1 and MBL complexes on the bacterial surface. Our finding that SMSB4 reduced the amount of C4b deposition on the bacterial surface indicates that SMSB4 reduces the amount of C3 convertase (C4b2a) formation in the CP and LP pathways. Since C1 and MBL complexes are structurally and functionally homologous, both enzyme complexes cleaving C4, it is likely that SMSB4 interferes with the C4 protease function. Interestingly SMSB4 also reduced the amount of properdin deposited on the S. aureus cells. Properdin is required to stabilize AP C3 convertase (C3bBb), and hence a decreased level of properdin will decrease the formation of functional AP C3 convertase. Furthermore, properdin is reported to play a role in amplification of MBL-initiated LP [35], hence a reduction in AP will contribute to the overall complement activation. Indeed, we have previously established that SMSB4 reduces the C3b deposition via all three complement pathways [25]. This study provides additional data confirming that SMSB4 acts early on in the complement cascades and reduces the formation of functional C3 convertases, thereby inhibiting complement-mediated killing of the invading pathogen S. aureus. Further study is required to identify the exact mechanisms by which SMSB4 interferes with the individual complement components. We have assessed here the effect of one individual recombinant mite complement inhibitor under in vitro test conditions. It is possible that the amount of recombinant protein required to show effects in the assays presented does not exactly reflect the amounts of SMSB4 actually present in the in vivo situation. Further investigation will be required to determine the concentration and composition of complement-inhibitory properties in scabies infested skin. Moreover, since S. aureus is known to produce a wide arsenal of its own complement inhibitors, it cannot be ruled out that this bacterium may be beneficial to prolong the infestation by the scabies mite. Skin infestation with the mite S. scabiei has been documented as a primary risk factor for pyoderma and impetigo worldwide and treatment of scabies reduces the prevalence of bacterial infections [5], [6]. S. aureus has been isolated from epidermal mite burrows and fecal pellets [36] suggesting that mites themselves may contribute to the transmission of pathogenic bacteria. We now present evidence that secondary infection by S. aureus is in part a consequence of the SMSB4 driven suppression of opsonization and phagocytosis by phagocytes. Since scabies mites produce multiple families of complement inhibitors, it is tempting to speculate that collective action of complement inhibitors produced by scabies mites in a confined space of skin burrows either stop or delay the clearing effect of the immediate local innate immune response to pathogen invasion. This creates a window of opportunity for S. aureus to multiply and establish infection. Therefore scabies mite burrows in the epidermis may serve as a perfect microenvironment for both the mites and bacterial pathogens being shielded from the host innate immune system.


We wish to dedicate this work to the late Prof. Dave J. Kemp, who championed the work on molecular aspects of scabies, a neglected disease particularly of the poor. We thank Dr. Deborah Holt for providing the pyoderma Staphylococcus isolates. We acknowledge the assistance of Lindsay Christian in generating the data for Figure 1b as part of his Vacation Research Experience Scholarship at QIMR Berghofer.

Author Contributions

Conceived and designed the experiments: PMS KF. Performed the experiments: PMS. Analyzed the data: PMS KF. Contributed reagents/materials/analysis tools: KF. Wrote the paper: PMS KF.


  1. 1. Engelman D, Kiang K, Chosidow O, McCarthy J, Fuller C, et al. (2013) Toward the global control of human scabies: introducing the International Alliance for the Control of Scabies. PLoS Negl Trop Dis 7: e2167.
  2. 2. Fuller LC (2013) Epidemiology of scabies. Curr Opin Infect Dis 26: 123–126.
  3. 3. Hay RJ, Steer AC, Engelman D, Walton S (2012) Scabies in the developing world–its prevalence, complications, and management. Clin Microbiol Infect 18: 313–323.
  4. 4. Clucas DB, Carville KS, Connors C, Currie BJ, Carapetis JR, et al. (2008) Disease burden and health-care clinic attendances for young children in remote aboriginal communities of northern Australia. Bull World Health Organ 86: 275–281.
  5. 5. Carapetis JR, Connors C, Yarmirr D, Krause V, Currie BJ (1997) Success of a scabies control program in an Australian aboriginal community. Pediatr Infect Dis J 16: 494–499.
  6. 6. Lawrence G, Leafasia J, Sheridan J, Hills S, Wate J, et al. (2005) Control of scabies, skin sores and haematuria in children in the Solomon Islands: another role for ivermectin. Bull World Health Organ 83: 34–42.
  7. 7. Carapetis JR, Steer AC, Mulholland EK, Weber M (2005) The global burden of group A streptococcal diseases. Lancet Infect Dis 5: 685–694.
  8. 8. Currie BJ, McCarthy JS (2010) Permethrin and ivermectin for scabies. N Engl J Med 362: 717–725.
  9. 9. Tong SY, Bishop EJ, Lilliebridge RA, Cheng AC, Spasova-Penkova Z, et al. (2009) Community-associated strains of methicillin-resistant Staphylococcus aureus and methicillin-susceptible S. aureus in indigenous Northern Australia: epidemiology and outcomes. J Infect Dis 199: 1461–1470.
  10. 10. Whitehall J, Kuzulugil D, Sheldrick K, Wood A (2013) Burden of paediatric pyoderma and scabies in North West Queensland. J Paediatr Child Health 49: 141–143.
  11. 11. Ricklin D, Hajishengallis G, Yang K, Lambris JD (2010) Complement: a key system for immune surveillance and homeostasis. Nat Immunol 11: 785–797.
  12. 12. Dahl MR, Thiel S, Matsushita M, Fujita T, Willis AC, et al. (2001) MASP-3 and its association with distinct complexes of the mannan-binding lectin complement activation pathway. Immunity 15: 127–135.
  13. 13. Sato T, Endo Y, Matsushita M, Fujita T (1994) Molecular characterization of a novel serine protease involved in activation of the complement system by mannose-binding protein. Int Immunol 6: 665–669.
  14. 14. Thiel S, Vorup-Jensen T, Stover CM, Schwaeble W, Laursen SB, et al. (1997) A second serine protease associated with mannan-binding lectin that activates complement. Nature 386: 506–510.
  15. 15. Agarwal S, Ferreira VP, Cortes C, Pangburn MK, Rice PA, et al. (2010) An evaluation of the role of properdin in alternative pathway activation on Neisseria meningitidis and Neisseria gonorrhoeae. J Immunol 185: 507–516.
  16. 16. Cortes C, Ferreira VP, Pangburn MK (2011) Native properdin binds to Chlamydia pneumoniae and promotes complement activation. Infect Immun 79: 724–731.
  17. 17. Fearon DT, Austen KF (1975) Properdin: binding to C3b and stabilization of the C3b-dependent C3 convertase. J Exp Med 142: 856–863.
  18. 18. Ferreira VP, Cortes C, Pangburn MK (2010) Native polymeric forms of properdin selectively bind to targets and promote activation of the alternative pathway of complement. Immunobiology 215: 932–940.
  19. 19. Gros P, Milder FJ, Janssen BJ (2008) Complement driven by conformational changes. Nat Rev Immunol 8: 48–58.
  20. 20. Rooijakkers SH, Ruyken M, Roos A, Daha MR, Presanis JS, et al. (2005) Immune evasion by a staphylococcal complement inhibitor that acts on C3 convertases. Nat Immunol 6: 920–927.
  21. 21. Lee LY, Hook M, Haviland D, Wetsel RA, Yonter EO, et al. (2004) Inhibition of complement activation by a secreted Staphylococcus aureus protein. J Infect Dis 190: 571–579.
  22. 22. Rooijakkers SH, van Wamel WJ, Ruyken M, van Kessel KP, van Strijp JA (2005) Anti-opsonic properties of staphylokinase. Microbes Infect 7: 476–484.
  23. 23. Laarman AJ, Ruyken M, Malone CL, van Strijp JA, Horswill AR, et al. (2011) Staphylococcus aureus metalloprotease aureolysin cleaves complement C3 to mediate immune evasion. J Immunol 186: 6445–6453.
  24. 24. Bergstrom FC, Reynolds S, Johnstone M, Pike RN, Buckle AM, et al. (2009) Scabies mite inactivated serine protease paralogs inhibit the human complement system. J Immunol 182: 7809–7817.
  25. 25. Mika A, Reynolds SL, Mohlin FC, Willis C, Swe PM, et al. (2012) Novel scabies mite serpins inhibit the three pathways of the human complement system. PLoS One 7: e40489.
  26. 26. Mika A, Reynolds SL, Pickering D, McMillan D, Sriprakash KS, et al. (2012) Complement inhibitors from scabies mites promote streptococcal growth—a novel mechanism in infected epidermis? PLoS Negl Trop Dis 6: e1563.
  27. 27. Andrews RM, Kearns T, Connors C, Parker C, Carville K, et al. (2009) A regional initiative to reduce skin infections amongst aboriginal children living in remote communities of the Northern Territory, Australia. PLoS Negl Trop Dis 3: e554.
  28. 28. McDonald M, Dougall A, Holt D, Huygens F, Oppedisano F, et al. (2006) Use of a single-nucleotide polymorphism genotyping system to demonstrate the unique epidemiology of methicillin-resistant Staphylococcus aureus in remote aboriginal communities. J Clin Microbiol 44: 3720–3727.
  29. 29. Holt DC, Holden MT, Tong SY, Castillo-Ramirez S, Clarke L, et al. (2011) A very early-branching Staphylococcus aureus lineage lacking the carotenoid pigment staphyloxanthin. Genome Biol Evol 3: 881–895.
  30. 30. Berends ET, Dekkers JF, Nijland R, Kuipers A, Soppe JA, et al. (2013) Distinct localization of the complement C5b-9 complex on Gram-positive bacteria. Cell Microbiol 15: 1955–1968.
  31. 31. Postma B, Poppelier MJ, van Galen JC, Prossnitz ER, van Strijp JA, et al. (2004) Chemotaxis inhibitory protein of Staphylococcus aureus binds specifically to the C5a and formylated peptide receptor. J Immunol 172: 6994–7001.
  32. 32. Rooijakkers SH, van Kessel KP, van Strijp JA (2005) Staphylococcal innate immune evasion. Trends Microbiol 13: 596–601.
  33. 33. Willis C, Fischer K, Walton SF, Currie BJ, Kemp DJ (2006) Scabies mite inactivated serine protease paralogues are present both internally in the mite gut and externally in feces. Am J Trop Med Hyg 75: 683–687.
  34. 34. Mika A, Goh P, Holt DC, Kemp DJ, Fischer K (2011) Scabies mite peritrophins are potential targets of human host innate immunity. PLoS Negl Trop Dis 5: e1331.
  35. 35. Brouwer N, Dolman KM, van Zwieten R, Nieuwenhuys E, Hart M, et al. (2006) Mannan-binding lectin (MBL)-mediated opsonization is enhanced by the alternative pathway amplification loop. Mol Immunol 43: 2051–2060.
  36. 36. Shelley WB, Shelley ED, Burmeister V (1988) Staphylococcus aureus colonization of burrows in erythrodermic Norwegian scabies. A case study of iatrogenic contagion. J Am Acad Dermatol 19: 673–678.