Acinetobacter baumannii invades epithelial cells and outer membrane protein A mediates interactions with epithelial cells
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Acinetobacter baumannii is a nosocomial pathogen of increasing importance, but the pathogenic mechanism of this microorganism has not been fully explored. This study investigated the potential of A. baumannii to invade epithelial cells and determined the role of A. baumannii outer membrane protein A (AbOmpA) in interactions with epithelial cells.
A. baumannii invaded epithelial cells by a zipper-like mechanism, which is associated with microfilament- and microtubule-dependent uptake mechanisms. Internalized bacteria were located in the membrane-bound vacuoles. Pretreatment of recombinant AbOmpA significantly inhibited the adherence to and invasion of A. baumannii in epithelial cells. Cell invasion of isogenic AbOmpA- mutant significantly decreased as compared with wild-type bacteria. In a murine pneumonia model, wild-type bacteria exhibited a severe lung pathology and induced a high bacterial burden in blood, whereas AbOmpA- mutant was rarely detected in blood.
A. baumannii adheres to and invades epithelial cells. AbOmpA plays a major role in the interactions with epithelial cells. These findings contribute to the understanding of A. baumannii pathogenesis in the early stage of bacterial infection.
KeywordsCell Invasion Outer Membrane Protein Acinetobacter Baumannii ompA Gene ATCC 19606T
Outer membrane protein A of A. baumannii
- LB broth
Genus Acinetobacter are important opportunistic pathogens in hospital-acquired infections [1, 2, 3, 4]. They cause various types of human infections, including pneumonia, wound infections, urinary tract infections, bacteremia, and meningitis. Of the currently known 31 Acinetobacter species [1, 2, 5], Acinetobacter baumannii is the most prevalent in clinical specimens. Numerous outbreaks caused by A. baumannii have been reported, which are of great concern in clinical settings [6, 7]. Despite convincing evidence linking A. baumannii with human infections, the study of its pathogenic mechanism is still in its elementary stage.
Adherence of bacteria to epithelial cells is an essential step towards colonization and infection . Bacterial adherence to host cells is mediated by fimbria or membrane components. Furthermore, many pathogenic bacteria are capable of invading non-phagocytic cells and evolve to survive within the host cells. The cellular invasion of bacteria contributes to evasion of humoral immunity, persistence in the host, and penetration into deep tissues. Bacterial pathogens gain entry to non-phagocytic cells via two mechanisms; a zipper-like mechanism and a trigger mechanism, which were initially classified based on morphological differences [9, 10]. The zipper-like mechanism (receptor-mediated entry) requires the direct interaction of bacterial ligands to the host's cell surface receptors and involves local cytoskeletal rearrangement at the invasion site. In contrast, the trigger mechanism is initiated by the injected bacterial effector proteins delivered by the type III secretion system. The effector proteins regulate cytoskeleton dynamics and induce dramatic cytoskeletal rearrangements such as membrane ruffles. The previous study demonstrated that adherence of A. baumannii to human bronchial epithelial cells was mediated by fimbrial-like structures and entrapment of bacteria by cellular protrusions . However, the mechanisms underlying invasion of A. baumannii in epithelial cells have not been explored so far.
Outer membrane proteins (Omps) of Gram-negative bacteria are key players in bacterial pathogenesis. OmpA of Escherichia coli, OspC of Borrelia burgdorferi, and Opa and OpcA of Neisseria meningitidis facilitate adherence to and invasion of bacteria in host cells [12, 13, 14, 15]. OmpA of A. baumannii (AbOmpA) is the most abundant surface protein with a molecular mass of 38 kDa and plays a role in permeability of small solutes. AbOmpA purified from A. baumannii ATCC 19606T and recombinant AbOmpA (rAbOmpA) bind to the surface of host cells and are localized in both the mitochondria and nuclei, which induce the death of host cells [16, 17]. Based on previous findings that AbOmpA bound to and entered host cells, we hypothesized that AbOmpA is responsible for adherence to and invasion of A. baumannii in epithelial cells during the colonization and early stage of bacterial infection. In the present study, we investigated the potential of A. baumannii to invade epithelial cells and studied the role of AbOmpA in interactions of A. baumannii with epithelial cells.
A. baumannii invades epithelial cells dependently on both the bacterial strains and cell types
NCI-H292 cells were infected with four clinical A. baumannii isolates at an MOI of 100 for 5 h. Cell invasion of A. baumannii was different between bacterial strains: A. baumannii 05KA103 was the most invasive (7,581 ± 2,365 cfu), whereas A. baumannii 05P447 was the least invasive (151 ± 105 cfu) (Fig. 1B). To determine whether the cell invasion of A. baumannii is dependent on epithelial cell types, human bronchial NCI-H292 cells, human laryngeal HEp-2 cells, and human cervical HeLa cells were infected with A. baumannii strains. NCI-H292 and HEp-2 cells derived from the respiratory tract were more susceptible to cell invasion of A. baumannii than non-respiratory tract-derived HeLa cells (Fig. 1B). Confocal microscopic images provided direct evidence of intracellular localization of A. baumannii (Fig. 1C and 1D).
A. baumannii invades epithelial cells by a zipper-like mechanism
AbOmpA mediates the interaction of A. baumannii with epithelial cells
Cell invasion of isogenic AbOmpA- mutant decreases as compared with wild-type bacteria
AbOmpA plays a role in A. baumannii pathogenesis in vivo
To determine the role of AbOmpA on A. baumannii pathogenesis in vivo, the murine pneumonia model was introduced. The C57BL/6 mice were intratracheally infected with 1 × 109 cfu of wild-type bacteria and isogenic AbOmpA- mutant, and euthanized two days after bacterial challenge. Total number of bacterial counts in the lungs were similar between mice infected with wild-type bacteria (1.58 × 105 cfu/g) and AbOmpA- mutant (6.75 × 104 cfu/g), but lung histopathology such as the infiltration of polymorphonuclear leukocytes and destruction of alveolar structures was prominently observed in the mice infected with wild-type bacteria (data not shown). Bacteremia occurred in mice infected with both bacterial strains, but there was a significant difference in the bacterial burden between the mice infected with wild-type bacteria (3.5 × 103 cfu/ml) and isogenic AbOmpA- mutant (2.3 × 10 cfu/ml). These results suggest that AbOmpA is directly associated with the lung pathology and is responsible for the dissemination of A. baumannii into the bloodstream.
It was clearly demonstrated that A. baumannii has the potential to invade epithelial cells. Host cells play a significant role in determining the cell invasion of A. baumannii. Epithelial cells derived from the respiratory tract were more susceptible to A. baumannii invasion than epithelial cells derived from non-respiratory tract. Moreover, the binding capacity of rAbOmpA in respiratory tract-derived epithelial cells was higher than that of non-respiratory tract-derived epithelial cells. These findings may be partly responsible for the prevalence of A. baumannii in the respiratory tract, which is the most frequent colonization and infection site. The efficiency of cell invasion of A. baumannii was lower than other invasive pathogens such as E. coli, Campylobacter upsaliensis, Helicobacter pylori, N. memingitidis, Pseudomonas aeruginosa, and Yersinia enterocolitica [18, 19, 20, 21]. A previous study showed that most clinical A. baumannii isolates infected only 20–30% of NCI-H292 cells and the number of adhering bacteria was 1–2 bacteria per infected cell . This finding reflects the low cellular invasion of A. baumannii in the current study. A relatively low adherence and invasion of A. baumannii in epithelial cells may contribute to a low virulence of this opportunistic pathogen, which particularly infects critically ill or severely wounded patients [1, 2].
A. baumannii invaded epithelial cells by a zipper-like mechanism, as demonstrated by the morphological characteristics. A. baumannii was loosely attached to the surface of epithelial cells. This observation is consistent with the previous study regarding adherence of A. baumannii to NCI-H292 cells . However, the entrapment of bacteria by cellular protrusions, as noted in the previous study, was not observed. After loose attachment of A. baumannii to epithelial cells, the cell membrane was extended to and wrapped around the bacteria, which are typical characteristics of the zipper-like mechanism. These cellular responses against A. baumannii were mediated by actin rearrangement and membrane reorganization. Confocal images and gentamicin protection assay with cytochalasin D showed the involvement of actin filaments in the cell invasion of A. baumannii. The microtubule inhibitor vinblastine also significantly inhibited the cell invasion of A. baumannii. Vinblastine may inhibit the transport of membrane-bound bacteria from the plasma membrane to the cytoplasm by preventing their movement in the microtubule-mediated contractile process. Once inside the host cells, internalized A. baumannii was located in the membrane-bound vacuoles. This result, in conjunction with the results of the gentamicin protection assay, suggests that A. baumannii survives within membrane-bound vacuoles in the cytoplasm. Many intracellular bacteria are located in a membrane-bound vacuole compartment , but some, such as Neisseria spp., Listeria monocytogenes, Salmonella spp., and Yersinia spp., escape the cytoplasmic vacuoles and are freely located in the cytoplasm [23, 24, 25, 26]. In regards to most pathogenic bacteria, a membrane-bound vacuole containing pathogens does not undergo sequential fusion with endosomes or lysosomes for its own benefit. Further studies are needed to characterize the fate of intracellular A. baumannii to understand the survival and dissemination of bacteria.
Outer membrane proteins of Gram-negative bacteria are known to be directly involved in the interaction of bacteria with host cells. The present study focused on whether AbOmpA is responsible for the interaction of A. baumannii with epithelial cells. Our data suggest that AbOmpA is a major effector molecule of A. baumannii interacting with epithelial cells according to the following experimental results: (i) rAbOmpA directly binds to the surface of epithelial cells; (ii) pre-treatment of rAbOmpA significantly attenuates the binding of A. baumannii to epithelial cells; (iii) rAbOmpA significantly inhibits the cell invasion of A. baumannii, and (iv) the cell invasion of AbOmpA- mutant decreased to 95% in comparison to wild-type bacteria. In a murine pneumonia model, wild-type bacteria and isogenic AbOmpA- mutant induced different lung pathologies. Moreover, wild-type A. baumannii had the capacity to disseminate into the bloodstream, whereas AbOmpA- mutant rarely cross barriers to disseminate in this manner. Accordingly, AbOmpA plays an important role in the A. baumannii pathogenesis regarding the induction of pneumonia and bacteremia.
A. baumannii can adhere to and invade epithelial cells during colonization and the early stage of infection. In addition to its biological role as a porin, AbOmpA plays a versatile role in the A. baumannii pathogenesis regarding its interaction with epithelial cells, the induction of apoptosis of host cells, and the dissemination of bacteria into the bloodstream. Our data provide a novel insight into A. baumannii pathogenesis and contribute to further our knowledge of A. baumannii infections.
A. baumannii invades epithelial cells depending on both bacterial strains and cell types. Cellular invasion is mediated by both microfilament- and microtubule-dependent uptake mechanisms. AbOmpA is a microbial component responsible for the adherence to and invasion of A. baumannii in epithelial cells. The data obtained provide a novel insight into the A. baumannii pathogenesis in the early stage of bacterial infection.
A. baumannii ATCC 19606T and its isogenic AbOmpA- KS37 mutant  were used in this study. Four clinical A. baumannii isolates were obtained from hospitalized patients: 05KA43 and 05P447 from blood, 05KA103 from cerebrospinal fluid, and 04P275 from wounds. All A. baumannii strains were susceptible to gentamicin. The genus Acinetobacter was identified by phenotypic markers and species identification was confirmed by amplified ribosomal DNA restriction analysis . For the adherence and invasion assays, A. baumannii strains were grown on blood agar plates at 37°C for 18 h and bacterial cells were suspended in a cell culture medium without antibiotics at a density of 1.0 × 108 cfu/ml.
Human laryngeal epithelial cells (HEp-2, CCL-23) and cervical carcinoma cells (HeLa, CCL-2) were cultured in Dulbecco's modified Eagle's medium supplemented with 2 mM L-glutamine, 1000 U of penicillin G per ml, 50 μg of streptomycin per ml, and 10% fetal bovine serum. Human bronchial epithelial cells (NCI-H292, CRL-1848) were cultured in a RPMI 1640 medium containing the above supplements. The cells were maintained at 37°C in 5% CO2. Confluent growth was obtained in 100 mm diameter dishes. All cell culture media and supplements were purchased from HyClone Laboratories Inc.
Cloning and purification of rAbOmpA
The cloning of the ompA gene and purification of recombinant AbOmpA (rAbOmpA) were performed as described previously . In brief, the ompA gene (1,317 bp) of A. baumannii ATCC 19606T was amplified by PCR using the upstream primer (5'-ACAGGATCCATGAAATTGAGTCGTATT-3') and downstream primer (5'-ACAAGCTTTTATTGAGCTGCTGCA-3'). PCR products were ligated into the pET28a expression vector (Novagen). E. coli BL21 (DE3)/pET28a carrying the ompA gene were grown in Luria-Bertani (LB) broth at 37°C and rAbOmpA was overexpressed with 1 mM IPTG at 25°C for 4 h. After bacterial sonication, the supernatant containing the soluble form of rAbOmpA was collected and loaded on a 5 ml HiTrap™ FF column (Amersham Biosciences). His-tagged rAbOmpA was eluted by elution buffer (20 mM sodium phosphate, 500 mM NaCl, and 500 mM imidazole, pH 7.4). The rAbOmpA samples were dialyzed against the elution buffer without imidazole and phosphate-buffered saline (PBS). The rAbOmpA samples were mixed with polymyxin B-agarose (St. Louis. Mo, USA) to remove endotoxin complex. The samples were concentrated by Centricon (2,000 MW cut off; Millipore) and stored at -70°C.
Polyclonal anti-AbOmpA antiserum against the purified OmpA from A. baumannii ATCC 19606T was raised in rabbits by routine immunogenic procedures .
Bacterial adherence assay
In each well of a 24 well cell culture plates, A. baumannii was added to a monolayer of epithelial cells at a ratio of bacteria to host cells of 100:1 (MOI of 100). The cells infected with bacteria were incubated in a 5% CO2 at 37°C for 1 h. The cells were washed five times with PBS, fixed with methanol for 20 min, and stained with Giemsa solution .
Bacterial invasion assay
Epithelial cells grown in 24 well plates were infected with A. baumannii for the indicated times at an MOI of 100. Culture media were removed and the cell monolayer was washed three times with PBS. A fresh culture medium containing 300 μg/ml of gentamicin was added and incubated for another 2 h. The cells were washed five times with PBS and lysed with 0.1% Triton X-100 at 37°C for 20 min. Dilutions from each well were plated on nutrient agar and colonies were enumerated 20 h after incubation. The invasion efficiency was calculated as the average number of bacteria per well. Each invasion assay was performed in duplicate and repeated on a minimum of three separate days. To determine the effect of cytoskeleton inhibitors on A. baumannii invasion, 2 μM of cytochalasin D (Sigma) or 100 μM of vinblastine (Sigma) was added to the cells 30 min before the addition of bacteria and maintained in the medium for the entire infection period. Neither cytoskeletal inhibitors affected the bacterial viability and cellular viability at the concentrations used. To determine the inhibitory effect of AbOmpA on bacterial invasion, epithelial cells were pretreated with 10 μg/ml of rAbOmpA 1 h before bacteria infection.
Cell surface binding of rAbOmpA
Epithelial cells were grown in 100 mm dishes and then detached from the dishes by treatment with 0.5 M EDTA solution. The cells were washed three times and suspended at 5 × 105 cells/ml in PBS. The cells were incubated in the presence of polyclonal anti-rabbit AbOmpA antibody (1:1,000). After washing, the cells were incubated with 6 μg/ml of rAbOmpA at 4°C for 20 min and washed three times in cold PBS. The samples were then incubated with anti-rabbit AbOmpA antibody (1:1,000) on ice for 1 h. The cells were washed three times with cold PBS and incubated with Alexa Fluor®488-conjugated anti-rabbit IgG (1:500) on ice for 1 h. The labelled cells were analyzed by flow cytometry (Becton Dickinson).
Fluorescence and confocal microscopy
NCI-H292 cells were grown on 13 mm diameter glass coverslips at 2 × 105 per coverslip. A. baumannii was infected at an MOI of 100 and incubated at 37°C for 5 h. The coverslips were washed with PBS and fixed with 3.7% paraformaldehyde for 30 min. Cells were permeabilized with a PBS containing 0.25% Triton X-100 for 10 min. Actin was stained with Alexa Fluor®488 phalloidin (Molecular Probes). A. baumannii was labeled with polyclonal anti-rabbit AbOmpA antibody (1:1,000), followed by Alexa Fluor®568-conjugated goat anti-rabbit IgG antibody (Molecular Probes). The association of A. baumannii with epithelial cells was observed either with a Nikon inverted fluorescence microscope or Leica confocal microscope.
TEM and SEM
For TEM, NCI-H292 cells were grown in 35 mm culture dishes at a concentration of 1 × 106 cells/well. A. baumannii was infected to the monolayer of NCI-H292 cells at an MOI of 100 for 5 h. The cells were washed five times with PBS and harvested by using trypsin-EDTA (500 mg/ml trypsin, 200 mg/ml EDTA). The cells were centrifuged at 300 g for 5 min and washed with PBS. The cells were resuspended in a fixative (4% paraformaldehyde and 1% glutaraldehyde, pH 7.0). The samples were then incubated in osmium tetroxide, gradually dehydrated in a series of ethanol and embedded in Epon. Thin sections were prepared by using an ultramicrotome with a diamond knife. The samples were examined by a Hitachi 7000 transmission electron microscope. For SEM, NCI-H292 cells were grown on 13 mm diameter glass coverslips at a concentration of 2 × 105 cells/well and bacteria were infected at an MOI of 100 for 5 h. The samples were washed with PBS and fixed with 2.5% glutaraldehyde at room temperature. The cells were gradually dehydrated in a series of ethanol and dried to a critical point. The samples were then coated with a layer of gold and examined under 15 kV accelerating voltage in a Hitachi S-4300 field emission scanning electron microscope.
Six-week-old female C57BL/6 mice were maintained under specific-pathogen-free conditions. For the pneumonia model, the mice were anesthetized with pentobarbital and then 100 μl of 1 × 1010 cfu/ml of bacteria were administrated intratracheally. Groups containing three mice were infected with wild-type A. baumannii and isogenic AbOmpA- mutant. The control mice groups were injected with 100 μl of PBS. The animals were suspended in a supine position on a 60° incline board. Their trachea was exposed surgically and bacteria were introduced intratracheally via a syringe with a 30 1/2 gauged-needle. The incisions were closed by surgical sutures. The bacterial density of each run was confirmed by serial dilution and culture of an aliquot from each inoculum. The lungs of mice infected with bacteria were removed two days after bacterial challenge. For histological analysis, tissues were stained with hematoxylin/eosin and observed by using a Nikon microscope. For bacterial counts, lungs were homogenized by using a glass syringe piston and then serial 10-fold suspension was inoculated onto MacConkey agar plates (Difco Laboratories). Blood was directly plated on a MacConkey agar plate.
The statistical significance of the data was determined by the Student's t-test. A P value of < 0.05 was considered to be statistically significant.
This study was supported by the Korea Research Foundation Grant funded by the Korean Government (MOEHRD, Basic Research Promotion Fund) (KRF-2006-312-E00070).
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