OmpA Protein-Deficient Acinetobacter baumannii Outer Membrane Vesicles Trigger Reduced Inflammatory Response

Abstract

Multidrug resistant Acinetobacter baumannii shows a growing number of nosocomial infections worldwide during the last decade. The outer membrane vesicles (OMVs) produced by this bacterium draw increasing attention as a possible treatment target. OMVs have been implicated in the reduction of antibiotic level in the surrounding environment, transfer of virulence factors into the host cells, and induction of inflammatory response. Although the evidence on the involvement of OMVs in A. baumannii pathogenesis is currently growing, their role during inflammation is insufficiently explored. It is likely that bacteria, by secreting OMVs, can expand the area of their exposure and prepare surrounding matrix for infection. Here, we investigated the impact of A. baumannii OMVs on activation of macrophages in vitro. We show that OmpA protein present in A. baumannii OMVs substantially contributes to the proinflammatory response in J774 murine macrophages and to the cell death in both lung epithelium cells and macrophages. The loss of OmpA protein in OMVs, obtained from A. baumannii ∆ompA mutant, resulted in the altered expression of genes coding for IL-6, NLRP3 and IL-1β proinflammatory molecules in macrophages in vitro. These results imply that OmpA protein in bacterial OMVs could trigger a more intense proinflammatory response.

1. Introduction

Opportunistic bacterium Acinetobacter baumannii is responsible for numerous cases of hospital-related infections worldwide [1]. The ability to persist on medical devices and survive in the patients with suppressed immunity rendered this bacterium to one of the most successful colonizers in medical units. The successful spread in the infected organism is mainly due to combined effect of various virulence-related factors, among which the outer membrane protein A (OmpA) is studied in detail and is considered as one of the key virulence factors of A. baumannii [2]. OmpA porin is composed of membrane β-barrel and periplasmic domains. While periplasmic domain interacts with peptidoglycan and is responsible for the stability of bacterial outer membrane, the β-barrel domain transfers some β-lactams, such as sulbactam and imipenem into bacterium [3]. The role of OmpA in biofilm formation, adhesion to abiotic surfaces and to the cells of various lineages, also resistance to the host immune system has been demonstrated [4]. Due to the high impact on A. baumannii pathogenesis, OmpA protein is being considered as a promising treatment target and vaccine candidate [4].

The colocalization of OmpA in the mitochondria and nucleus has been observed in infected cells in vitro [5,6] raising a question of how OmpA protein is being transported into the target cell. One possible explanation could be outer membrane vesicles (OMVs) secreted by bacteria [7,8]. Recently, it was demonstrated that OmpA present in A. baumannii OMVs is able to induce mitochondrial fragmentation in lung epithelium cells [9].

Bacterial OMVs are spherical structures of approximately 20–300 nm in diameter, which detach from the outer membrane encapsulating the components of periplasmic space, also inner-membrane and some cytoplasmic proteins [10]. These structures have been highlighted when it was observed that bacteria might transfer virulence factors, modulate immune system and inactivate antibiotics extracellularly by secreting OMVs [11,12,13]. OMVs are secreted by various Gram-negative and Gram-positive bacteria, thereby implying their role in the bacterial physiology [10,14].

So far, little is known about the involvement of OMVs and their components in A. baumannii pathogenesis. OMVs isolated from multidrug resistant Escherichia coli were able to inactivate β-lactam antibiotics [15]. Resistant bacteria “pack” antibiotic-inactivating enzymes e.g., β-lactamases in OMVs [16]. After the transfer of selective antibiotic into the OMVs, relevant enzymes hydrolyze it. Recently, we have demonstrated that OMVs isolated from multidrug-resistant A. baumannii strain inactivated ampicillin in the incubation medium [17]. The cytotoxic and immunomodulatory properties of OMVs secreted by A. baumannii have been also observed [7,9,18]. However, the exact mechanisms of the interplay between A. baumannii OMVs components and the host immune system remain obscure.

In this study we aimed to investigate the cytotoxic and immunomodulatory properties of OMVs secreted by clinical A. baumannii strain and its ompA gene deletion mutant. We demonstrated that OmpA protein could modulate the response of murine macrophages not only by being incorporated into the outer membrane of bacteria [19], but also as the component of OMVs, thereby expanding its effect in the infected host tissues.

2. Results and Discussion

2.1. OmpA Protein-Deficient A. baumannii OMVs Show Reduced Ability to Induce Cell Death

A. baumannii clinical strain Ab₁₆₉ belonging to international clone I (IC I) ST231 and its ompA deletion mutant [20] were used for the isolation of OMVs. OMVs were purified by ultracentrifugation and the fractions were visualized by transmission electron microscopy (TEM) (Figure 1A). Mutant strain produced approximately three times more OMVs compared to wt strain. The proteins were fractionated by SDS-PAGE (Figure S1) and the presence of OmpA protein in OMVs was confirmed by Western-blot analysis (Figure 1B).

The cytotoxicity of OMVs secreted by A. baumannii wt strain and its ompA deletion mutant to J774 mice macrophages and A549 human lung epithelium cells was investigated. Cells were incubated with OMVs for 24 h and cell viability was assessed as described in Section 3. OMVs produced by A. baumannii wt strain reduced viability of J774 macrophages and A549 cells to approximately 40% and 73%, respectively, compared to PBS-treated control. Accordingly, approximately 65% of J774 macrophages and 92% of A549 cells survived after incubation with OMVs obtained from A. baumannii ompA deletion mutant (Figure 1C). Therefore, OmpA-deficient OMVs demonstrated reduced cytotoxicity compared to OMVs from wt strain both for macrophages and lung epithelium cells. The unequal cytotoxicity of A. baumannii OMVs produced by two different clinical A. baumannii strains to mice macrophages RAW264.7 and A549 cells has been demonstrated [21]. In one of the early investigations, OMVs obtained from the OmpA-deficient A. baumannii 19606∆ompA strain did not induce cell death in human monocytes U937 [7]. Several studies identified OmpA protein as a virulence factor of A. baumannii, which is involved in biofilm formation, adhesion to eukaryotic cells and host colonization [22,23,24]. Our results show that A. baumannii OmpA protein being incorporated into OMVs contributes to their cytotoxicity. Macrophages were more susceptible to OMVs compared to lung epithelium cells. As macrophages are professional phagocytes, they are assigned to induce acute inflammatory response to the infection. These results are in agreement with another study where RAW264.7 macrophages were also more susceptible to OMVs exposure compared to A549 cells [21].

2.2. OmpA-Deficient OMVs Elicit Reduced Inflammatory Response in Mice Macrophages In Vitro

A. baumannii OMVs can induce immune response in immune cells [18,21]. In order to elucidate if the loss of OmpA protein in OMVs affects the inflammatory response in macrophages, we incubated J774 cells with OMVs, produced by A. baumannii wt strain and its ompA deletion mutant for 24 h. After incubation, cellular RNA was extracted, and gene expression was assessed by qPCR using proinflammatory molecules coding genes as targets. Results demonstrated the induction of all tested genes after treatment of macrophages with OMVs compared to PBS-treated control, showing that OMVs can act as powerful inductors of inflammation (Figure 2). Moreover, the reduction in the expression of a set of proinflammatory cytokines was observed when macrophages were incubated with OMVs produced by ompA deletion mutant compared to wt strain. Macrophages are the major producers of TNFα [25]. In the presence of infection, TNFα is a key regulator of inflammatory response through altering the production of proinflammatory cytokine cascades, activating phagocytosis, production of nitric oxide (NO) and, finally, induction of cell death. Our results demonstrated a moderate reduction of Tnfα gene expression when macrophages were incubated with OMVs derived from ∆ompA strain compared to wt strain (Figure 2). The trait that OMVs from distinct bacterial strains can induce different TNFα production level has been already observed [21] indicating that A. baumannii strains might regulate OMVs-mediated virulence through modulation of their proinflammatory properties.

The macrophages produce IL-6 during the infection in order to activate other immune cells, such as neutrophils or B cells [25]. As can be seen in the data, presented in Figure 2, OmpA deficiency resulted in a significantly reduced ability of OMVs to induce Il-6 gene expression, thereby indicating that OmpA present in OMVs acts as inducer of immune cells recruitment into infection site. It must be noted, however, that OmpA-deficient OMVs still were able to induce strong Il-6 gene expression in murine macrophages, indicating that OMVs can recruit a wide immune response, possibly, due to the other pro-inflammatory molecules present in OMVs.

2.3. A. baumannii OMVs Trigger the Inflammasome Activation

According to the recent studies A. baumannii could not only induce apoptosis in immune cells, but also pyroptotic cell death, in which activated gasdermin D forms pores in the cell plasma membrane [26,27]. We observed that A. baumannii OMVs triggered modest induction of caspase-1 expression in J774 macrophages (Figure 2). Caspase-1 is a key peptidase in pyroptosis, which is activated by formation of inflammasome, a protein complex of the innate immune system, composed of CARD/PYD domain containing proteins and Apoptosis associated Speck-like protein containing a CARD (ASC) adaptor proteins [28]. The inflammasome induces the cleavage of pro-caspase-1 into its active form. In the noncanonical inflammasome, caspase-11 is activated by direct binding to bacterial LPS leading to pyroptosis [28]. Interestingly, we show in this study, that the expression of both caspases was induced when macrophages were incubated with A. baumannii OMVs. These results are in agreement with the recent studies on the response of bone marrow-derived macrophages (BMDMs) during A. baumannii infection, where the importance of both caspase-1 and caspase-11 was demonstrated, suggesting that these two pathways complement each other [27,29].

There are different types of inflammasome complexes based on their inflammasome receptors. Pathogen-Associated Molecular Patterns (PAMPs) such as LPS, LOS, bacterial surface proteins, or TNFα activate NLRP3 inflammasome [30]. In addition to the formation of inflammasome complex, the priming step is needed. After sensing, the extracellular stimuli pattern recognition receptors (PRRs) activate MyD88/NF-κB pathway, resulting in the expression of Nlrp3 and other proinflammatory genes [30]. Our study showed the increased expression of Nlrp3, Il-1β and Il-18 genes in the presence of OMVs, implying the activation of MyD88/NF-kB signaling pathway and induction of proinflammatory cytokines in macrophages. Interestingly, OmpA-deficient OMVs elicited significantly reduced expression of Nlp3 and Il-1β, but not Il-18 gene (Figure 2). The decreased expression of proinflammatory proteins could be a result of the reduced production of TNFα, elicited by OmpA-deficient OMVs compared to wt OMVs, what could cause a weaker priming signaling through TNF receptor.

The observed Il-18 gene expression profile, distinct from that of Nlrp3 and Il-1β genes, indicates that different induction pathway might be involved, possibly through the acceleration of different transcription factors. This is in agreement with other studies, where distinct induction pathways for IL-1β and IL-18 were observed [31]. Based on the current knowledge, the expression of Nlrp3 and Il-1β genes might be induced via MyD88/NF-κB pathway through activation of TLR and TNF receptors [32]. However, it was shown that the expression of Il-18 gene can be upregulated following IFN priming via STAT1/2 and IRF9, although Il-18 is constitutively expressed in BMDMs [31]. There is some evidence that the expression of caspase-11 can be induced by TLR4/TRIF-mediated activation of NF-κB pathway or by IFN-mediated activation of STAT1 [33]. Although the regulation of caspase-1 expression is poorly understood, IRF8 regulatory pathway was shown to have an impact on caspase-1 expression in B cells [34]. The expression of Il-6 and Tnfα genes could be also regulated by the NF-κB pathway under the activation of TLRs (although it is likely that the NF-κB pathway does not play a major role in TNFα induction) [35,36]. Thus, based on our results, it is likely that OmpA could stimulate the NF-κB pathway in macrophages. It was already shown that A. baumannii OmpA can induce both the expression and the surface exposure of Toll-like receptor 2 in laryngeal epithelial cells [37]. Additionally, the effect of OmpA on the activation of BMDCs via TLR2, MAPK and NF-κB pathways was observed [38].

The expression of Il-1β and Il-18 genes results in the proactive cytokine forms, which should pass through the proteolytic maturation by caspase-1 and only then could be secreted outside the cell [30]. Therefore, we asked whether an inflammasome is activated in J774 macrophages when incubated with A. baumannii OMVs. The inflammasome formation was assessed by visualization of ASC specks using immunofluorescence analysis as described in Section 3. As can be seen in Figure 3A, ASC specks were observed as accumulated protein dots in macrophages, stimulated with OMVs obtained from both A. baumannii wt strain and its ∆ompA mutant.

Next, we investigated whether the pro-IL-1β cytokine activation occurs in J774 macrophages through the proteolytic cleavage. Western blot analysis with anti-IL-1β antibodies was performed on the supernatants of macrophages after their exposure to OMVs, since the active form of IL-1β is secreted into the extracellular space. As can be seen in Figure 3B, an IL-1β-specific band of 17 kDa, corresponding to the size of active protein form was observed in the fractions obtained from macrophages, stimulated with OMVs. A low level of activated cytokine is visible in the supernatant from macrophages incubated with PBS only, demonstrating basal level of activation in conditions tested. However, when macrophages were preincubated with NLRP3-inflammasome-specific inhibitor MCC950, the cleaved form of IL-1β was still found in the supernatants after the exposure to OMVs (Figure 3B). This observation suggests that IL-1β maturation could be triggered by the alternative inflammasomes or non-inflammasomal activation pathways. This is in agreement with the studies, where the ability of caspase-8 or other serine proteases to activate IL-1β in macrophages or dendritic cells has been demonstrated [29,39]. However, there are many ambiguities regarding the inflammation routes activated by A. baumannii infections. One of the recent studies has demonstrated that OmpA protein could act through the host GTPase dynamin-related protein 1 (DRP1) resulting in a profound mitochondrial fragmentation, elevation of the level of reactive oxygen species and finally cell death [9]. More investigations are needed to get a full picture of activated pathways during A. baumannii-induced inflammation.

Our results demonstrate the robust inflammatory properties of bacterial OMVs, what is consistent with other studies [40]. It is worth noting that OMVs produced by A. baumannii IC II (ST208) ompA deletion strain, similarly to its counterpart IC I (ST 203) strain, investigated in this study, activated reduced inflammatory response in J774 macrophages in vitro compared to wt strain (data not shown), thereby showing IC-common trait. Additionally, the ompA deletion in A. baumannii genome could result in some other changes in the composition of OMVs. This should be taken into account when considering the differences in the modulation of inflammatory response. A. baumannii OmpA-deficient OMVs still triggered acute proinflammatory response in macrophages, suggesting the impact of other components of OMVs in the inflammation. These components should be foreseen as possible targets for infection treatment, as it was already shown for OmpA [4]. By changing the composition of OMVs, bacteria could manipulate host immune system [41,42]. Therefore, a detailed examination of OMVs composition is needed considering the high diversity of virulence-related features of clinical A. baumannii strains [20,43].

3. Materials and Methods

3.1. Bacterial Growth Conditions and Manipulations

A. baumannii strain Ab₁₆₉ and its ompA deletion mutant were described in a previous study [17]. OMVs were isolated as described by [17]. Briefly, 130 mL of bacterial culture in LB medium grown for 20 h at 37 °C was centrifuged for 15 min at 10,000× g at 4 °C. Supernatant was filtrated through a 0.22 µm filter. The OMVs were collected by ultracentrifugation at 130,000× g for 3 h at 4 °C. OMV pellets were resuspended in PBS. The protein concentration was determined using Bradford assay. Then, 10 µL of OMVs solution was plated on LB agar to test the sterility. Transmission electron microscopy (TEM) analysis was performed as described in previous study [17].

3.2. Cell Culture Assays

J774 mouse macrophages and A549 human lung epithelium cells were grown in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% of heat-inactivated FBS at 37 °C with 5% CO₂. Cells were grown for 24 h to form a culture monolayer with ~80% confluence and were then exposed to OMVs.

The viability of eukaryotic cells was determined by using MTT substrate (Merck, Sigma-Aldrich, Darmstadt, Germany). Cells were incubated with 4 µg/mL of A. baumannii OMVs at 37 °C for 24 h. After incubation, the supernatant was aspirated and 0.2 mg/mL of MTT reagent was added to the cells and kept for 4 h at 37 °C. The supernatant was removed, and cells were incubated with 100 μL of isopropanol for 5 min. The absorbance at 570 nm was measured by Tecan Infinite M200 Pro plate reader (Tecan, Männedorf, Switzerland).

3.3. qPCR

J774 macrophages were incubated with 2 µg/mL OMVs at 37 °C at 5% CO₂ for 24 h. After incubation, the supernatant was removed. The cells were carefully suspended in PBS buffer. The GeneJET RNA Purification Kit (Thermo Fisher Scientific) was used for RNA isolation according to the manufacturer’s recommendations. Genomic DNA was removed using deoxyribonuclease I (Thermo Fisher Scientific) following phenol/chloroform extraction. Concentration and purity were assessed with NanoDrop spectrophotometer (Thermo Fisher Scientific) and by agarose gel electrophoresis. cDNA synthesis was performed using the RevertAid First Strand cDNA Synthesis Kit (Thermo Fisher Scientific). Reaction components and conditions were selected according to the manufacturer’s recommendations. Gene expression was assessed by qPCR using DreamTaq polymerase (Thermo Fisher Scientific) and SYTO9 fluorescent dye (Thermo Fisher Scientific) according to the manufacturer’s recommendations. qPCR reactions were performed in CFX Real-Time System thermocycler (Bio-Rad, Hercules, CA, USA). The following primers used for qPCR were based on the previous studies [44,45,46]: actin—MuacF (5′-TGTCCACCTTCCAGCAGATGT-3′), MuacR (5′-TCAGTAACAGTCCGCCT-3′); TNFα—MutnF (5′-AGGAGAAAGTCAACCTCCT-3′), MutnR (5′-AAAGTAGACCTGCCCGGAC-3′); IL-6—Mu6F (5′-TCCAGTTGCCTTCTTGGGAC-3′), Mu6R (5′-GTACTCCAGAAGACCAGAGG-3′); caspase-1—mCaspase-1 RT fwd (5′-TTTCAGTAGCTCTGCGGTGT-3′), mCaspase-1 RT rev (5′-TTTCTTCCTGATTCAGCACTCTC-3′); caspase-11—mCaspase-11 RT fwd (5′-GCCACTTGCCAGGTCTACGAG-3′), mCaspase-11 RT rev (5′-AGGCCTGCACAATGATGACTTT-3′); NLRP3—mNLRP3 RT fwd (5′-CGAGACCTCTGGGAAAAAGCT-3′), mNLRP3 RT rev (5′-GCATACCATAGAGGAATGTGATGTACA-3′); IL-1β—IL-1betaF (5′-TGGACCTTCCAGGATGAGGACA-3′), IL-1betaR (5′-GTTCATCTCGGAGCCTGTAGTG-3′); IL-18—IL18F (5′-AGGACACTTTCTTGCTTGCC-3′), IL18R (5′-CACAAACCCTCCCCACCTAA-3′). The change in expression was compared to OMVs-untreated cells and was calculated by the ∆∆Ct method.

3.4. Immunoassays

For immunocytochemistry J774 macrophages were incubated with 1 µg/mL OMVs at 37 °C at 5% CO₂ for 24 h. MCC950 inhibitor (InvivoGen, San Diego, CA, USA) was added into the wells 20 min before the exposure to OMVs to the final concentration of 1 μM. After the treatment cells were washed with PBS and fixed in 4% PFA dissolved in PBS for 15 min and permeabilized with 0.1% Triton X-100 prepared in PBS for 10 min. Cells were washed once and blocked with 2% BSA in PBS for 30 min. The primary antibodies rabbit anti-ASC (AB_2490440, AdipoGen, Liestal, Switzerland) at a dilution 1:200 were added to the blocking solution and incubated overnight. The following secondary antibody goat anti-rabbit (AB_142134, Thermo Fisher Scientific) was used at a dilution of 1:1000. The secondary antibody was applied for 2 h followed by two washing steps. Hoechst33342 was used for nuclear staining at 1 μg/mL for 30 min in PBS. Microscopy analysis was undertaken at the Department of Immunology and Cell Biology of Institute of Biotechnology (Vilnius University). ASC speck images were taken using a 40× objective. Photos were taken by EVOS FL Auto Imaging System (Thermo Fisher Scientific, USA). Acquired images were processed using ImageJ program (Wayne Rusband; National Institute of Health, Bethesda, MD, USA).

For Western blot analysis, proteins after separation by SDS-PAGE were transferred on nitrocellulose membrane (Amersham Biosciences, Pittsburgh, PA, USA) using the semi-dry method. Then, 1:5000 dilution of OmpA-specific serum obtained from immunized mice, 1:1000 dilution of goat anti-IL-1β (AF-401-SP, R&D Systems, Minneapolis, MN, USA) or 1:5000 dilution of rabbit anti-α tubulin (ab52866, Abcam, Cambridge, UK) antibodies were applied. Next, the membranes were exposed to anti-mouse IgG (H + L)-HRP conjugate (1706516, Bio-Rad, Marnes-la-Coquette, France), anti-goat IgG (H + L)-HRP conjugate (HAF017, R&D Systems, Minneapolis, MN, USA) or anti-rabbit IgG (H + L)-HRP conjugate (31460, Thermo Fisher Scientific, Walkersville, MD, USA) and developed with Pierce one-step ultra TMB blotting solution (Thermo Fisher Scientific, Walkersville, MD, USA) or Pierce ECL Western Blotting Substrate (Thermo Fisher Scientific, Walkersville, MD, USA).

3.5. Statistical Analysis

All statistical comparisons were based on t-test. All quantitative data are representative of at least three repeats.