- Research article
- Open Access
Outer Membrane Vesicles of Helicobacter pylori TK1402 are Involved in Biofilm Formation
© Yonezawa et al; licensee BioMed Central Ltd. 2009
- Received: 23 March 2009
- Accepted: 15 September 2009
- Published: 15 September 2009
Helicobacter pylori forms biofilms on glass surfaces at the air-liquid interface in in vitro batch cultures; however, biofilms of H. pylori have not been well characterized. In the present study, we analyzed the ability of H. pylori strains to form biofilms and characterized the underlying mechanisms of H. pylori biofilm formation.
Strain TK1402 showed strong biofilm forming ability relative to the other strains in Brucella broth supplemented with 7% FCS. The strong biofilm forming ability of TK1402 is reflected the relative thickness of the biofilms. In addition, outer membrane vesicles (OMV) were detected within the matrix of only the TK1402 biofilms. Biofilm formation was strongly correlated with the production of OMV in this strain. We further observed that strain TK1402 did not form thick biofilms in Brucella broth supplemented with 0.2% β-cyclodextrin. However, the addition of the OMV-fraction collected from TK1402 could enhance biofilm formation.
The results suggested that OMV produced from TK1402 play an important role in biofilm formation in strain TK1402.
- Fetal Calf Serum
- Extracellular Polymeric Substance
- Pylorus Strain
- Outer Membrane Vesicle
- Brucella Broth
Helicobacter pylori is a spiral, microaerophilic, noninvasive, gram-negative bacterium that colonizes the human gastrointestinal tract, primarily the stomach . This organism has been identified as an aetiological agent of chronic active gastritis, peptic ulcer disease [2, 3], gastric adenocarcinoma , and mucosa-associated lymphoid tissue (MALT) lymphoma . A number of factors such as the VacA cytotoxin, the cag pathogenicity island (cag PAI), motility, and the urease enzyme are known to be involved in the virulence of this organism [6–8].
Biofilm development is initiated when bacteria transit from a planktonic state to a lifestyle in which the microorganisms are firmly attached to biotic or abiotic surfaces, and biofilms are strongly implicated in bacterial virulence . Biofilm formation is critical not only for environmental survival but also for successful infection by numerous pathogenic bacteria. Among human bacterial pathogens, the biofilms of Pseudomonas aeruginosa, Haemophilus influenzae, pathogenic Escherichia coli, Vibrio cholerae, staphylococci and streptococci are some of the best studied [10–14]. Bacterial biofilms are frequently embedded in a self-produced extracellular matrix . The extracellular polymeric substance (EPS) matrix, which can constitute up to 90% of the biofilm biomass, is a complex mixture of exopolysaccharides, proteins, DNA and other macromolecules .
Previous studies have alluded to the ability of H. pylori to form biofilms [17, 18]. A polysaccharide-containing biofilm has been observed at the air-liquid interface when H. pylori was grown in a glass fermenter . H. pylori is also capable of binding to a heterotrophic mixed species biofilm grown on stainless steel coupons . Recent studies indicated that 10 strains including some animal-adapted strains, clinical isolates and laboratory strains, were able to form similar three-dimensional architectures implicated in biofilm development [19, 20]. Cellini et al. reported that an environmental H. pylori strain, named MDC1, displayed a well structured biofilm . Cole et al. also indicated that mucin greatly accelerated planktonic growth relative to the expansion of H. pylori biofilms . In addition, a recent study indicated that H. pylori can exist in human gastric mucosa forming biofilms . These studies indicated that the topic of biofilm formation in this organism has the potential to contribute to our knowledge of H. pylori pathogenesis. However, little is known regarding the mechanism of H. pylori biofilm development. In the present study, we characterized the ability of 4 reference strains and 4 clinical isolates of H. pylori to form biofilms. Furthermore, we investigated the potential role of outer membrane vesicles (OMV) released from this organism in biofilm development.
Biofilm formation by H. pylori strains
Morphological analysis of biofilms
Optical densities and CFU measurements in the strain TK1402 biofilm cells and broth cultures
0.141 ± 0.037
0.259 ± 0.202
1.860 ± 1.487
0.258 ± 0.027
0.340 ± 0.230
1.614 ± 0.695
2-Day broth cultureb
0.939 ± 0.012
1.847 ± 0.318
1.966 ± 0.387
3-Day broth cultureb
1.075 ± 0.044
2.248 ± 1.170
2.151 ± 1.180
Next we analyzed the biofilm thickness of strains TK1402, SS1, TK1029, and ATCC 49503 with CMLS observations. Strain TK1402 exhibited 2-fold or greater biofilm thickness compared to the other strains (Fig. 2C). To clarify the architectural characteristics of H. pylori biofilms, we compared TK1402 and SS1 biofilms by SEM analysis. In the biofilms of strain SS1, the bacteria attached to glass surfaces in thin layers (Fig. 2E). Interestingly, the biofilms consisted mainly of bleb-like or amorphous structures. On the other hand, the TK1402 biofilms were composed primarily of cells with bacillary morphology which were clearly outlined (Fig. 2D). In addition, these later bacteria showed layer formation with bacterial aggregates in the biofilms. The biofilm bacterial aggregates appeared to result from direct cell-cell attachment. Intriguingly, TK1402 biofilms showed the presence of many OMV-like structures on the glass surface as well as on the bacterial cell surfaces (Fig. 2D, white arrows). These structures were not detected in the biofilms of the other strains (Fig. 2E and data not shown). A recent report indicated that OMV production from H. pylori clinical isolate MDC1 was apparent under SEM observation . We thus decided to focus our attention more on the OMV-like structures in subsequent experiments.
Potential role of the OMV in TK1402 biofilm formation
To directly verify that the OMV were components of the TK1402 biofilm matrix and that the production of the OMV can induce strong biofilm formation, TK1402 biofilm formation with 0.2% β-cyclodextrin medium was analyzed following the addition of the OMV fraction from TK1402 cultures in Brucella broth containing 7% FCS. The protein concentration of the OMV-fraction was adjusted to 2.0 mg/ml or 1.0 mg/ml. The OMV fraction (total amounts were 0.2 mg or 0.1 mg, respectively) was added to Brucella broth with 0.2% β-cyclodextrin and biofilm formation with strain TK1402 was carried out. As the components of FCS might be present in the OMV fraction and could affect biofilm formation, a control fraction from Brucella broth supplemented with 7% FCS without the microorganism was used. The levels of biofilm formation in the 0.2% β-cyclodextrin medium supplemented with the control OMV fraction was similar to that of the 0.2% β-cyclodextrin medium alone (Fig. 5B, lane β-cyclodextrin-control). On the other hand, the addition of the 0.1 mg OMV fraction from TK1402 showed significantly higher levels of biofilm formation than those in 0.2% β-cyclodextrin medium with the control fraction (Fig. 4B, β-cyclodextrin-FCS OMV 0.1). The levels of biofilm formation with OMV addition were similar to that in Brucella broth supplemented with 7% FCS (Fig. 4B. β-cyclodextrin-FCS OMV 0.2). We further determined that the 0.1 mg OMV fraction from H. pylori cultured in Brucella broth containing 0.2% β-cyclodextrin could also enhance biofilm formation but at levels lower than 0.2 mg of this fraction. The OMV fraction induced more biofilm formation than 0.1 mg of the OMV fraction from 7% FCS medium (Fig. 5B, β-cyclodextrin-β-cyclo OMV 0.1).
Evaluation of biofilm formation by other isolated H. pylori strains
In this study, we characterized biofilm formation in H. pylori strains and demonstrated differential abilities to form biofilms in reference and clinical isolates. In addition, the production of OMV in strain TK1402 was correlated with strong biofilm formation. Several reports indicated that H. pylori has the ability to form biofilms on abiotic surfaces in vitro as well as on human gastric mucosa [18–21, 23]. The results of the biofilm formation analyses demonstrated that strain TK1402 has strong biofilm forming ability compared to other strains independent of its growth rate. Development of strain TK1402 and SS1 biofilms from day 1 to day 6 demonstrated that it took 3 days for biofilm maturation under these conditions, suggesting that H. pylori biofilm formation might proceed in an organized fashion through early (Day 1), intermediate (Day 2) and maturation (after Day 3) phases of development. Similar distinct developmental phases have been reported for biofilm formation by other bacterial species [24, 25]. Since development of biofilms is closely associated with the generation of a matrix, the majority of which is extracellular material, biofilm development in H. pylori appears to share common basic steps with other biofilm forming bacteria.
The biofilm forming cells at day 3 generally appeared to be viable when the cells were exposed to Live/Dead BacLight staining. In addition, the normalized CFU values for the biofilm and broth culture cells following 2 days of incubation were comparable. In 3-day biofilm cells, this value was slightly decreased compared to 3-day broth culture cells, suggesting the presence of some dead cells in the biofilm. These results are consistent with the maturation phase of the development of biofilms in 3-day biofilms of strain TK1402, since biofilms are thought to be encased in an EPS matrix as well as dead cells . In addition, strain TK1402 exhibited thick biofilm formation. The biofilm morphology of strain TK1402 showed direct cell-cell bound aggregates as well as flagella-dependent binding forms. The cell-cell interacting forms might act as precursors for thick biofilm formation. Gots et al. indicated that cell-cell aggregation induces a multilayered architecture during Staphylococcus epidermidis biofilm formation . Moreover, in our SEM observations, for the majority of the H. pylori strains examined, ie., SS1, biofilms may contain autolysed cells. On the other hand, there were clearly intact cells in TK1402, as well as TK1049, biofilms and the later is also another strong biofilm forming strain. These observations suggested that these strong biofilm forming strains may remain in an active metabolic state for a relatively long time without exhibiting morphological changes or autolysis, in comparison with the other strains. These later properties could be responsible for the weaker biofilm forming activities of most of the strains examined in this study.
In the SEM observations of TK1402 biofilms, there were many OMV. OMV production is a physiologically normal function of gram-negative bacteria [22, 28]. It was also reported that the H. pylori strains released OMV into the extracellular space [29, 30]. A recent report indicated that OMV were a component of the matrix of P. aeruginosa biofilms . We analyzed thin-sections of strain TK1402 biofilms with TEM. The OMV were located at the substratum-bacterium interface and extracellular space. Interestingly, some of OMV appeared to be involved in attaching one cell with another. This observation suggested that the OMV produced by strain TK1402 could be intimately involved in biofilm formation.
Previously, several reports indicated that VacA, urease and lipopolysaccharides are present on the surface of OMV from H. pylori along with other outer membrane proteins [29, 30]. We quantified OMV production in Brucella broth supplemented with various concentration of FCS using Western blotting with anti-H. pylori antibody. Moreover, the SEM observations were also carried out to directly confirm this. The FCS concentration in the biofilm medium showed a direct positive correlation with OMV production as well as biofilm forming ability. Further, similar results were detected by the addition of serum from different hosts as well as with synthetic substrates. On the other hand, observation with biofilm forming bacteria indicated that LPS plays a role in biofilm development and architecture [14, 31]. Recently, Keenan et al. reported that LPS detected in OMV under iron-limited conditions were notably shorter than those under iron-replete conditions . We hypothesize that strain TK1402 has an altered LPS, particularly LPS O-antigens under different experimental conditions including the use of different animal sera, synthetic substrates, or different FCS concentrations. To confirm this, we analyzed the LPS profiles of H. pylori cultured in different culture media by SDS-PAGE and silver staining. However, there were no differences in the LPS O-antigen profiles. We then isolated the OMV from the TK1402 culture supernatant in order to examine the role of these structures in biofilm formation. Biofilm formation by this strain was increased following the addition of the OMV-fraction in a dose-dependent manner. Although the quantities of OMV added were three- to five-fold more than the quantity of the OMV which exist in biofilms under our experimental conditions, the OMV appear to play an important role in the formation of the extracellular matrix of strain TK1402 biofilms. The extracellular matrix serves a role in bacterial attachment to abiotic and cellular surfaces in the initial stage of biofilm formation . It is possible that specific proteins in the OMV released from strain TK1402 may take part in bacterial aggregation and biofilm formation. Which component(s) of the OMV contribute to biofilm formation still remains to be determined. Additional investigations are now in progress to determine such components in the OMV.
In the present study, we searched for other clinical isolates with strong biofilm formation and one strain, TK1049, exhibited similar ability to form biofilms as strain TK1402. This suggested that H. pylori strains exhibiting strong biofilm forming ability are relatively rare. Indeed, Williams et al. indicated that FCS inhibited adherence to abiotic surfaces in some of the H. pylori strains . This apparent discrepancy between their study and our present results in terms of the effects of FCS might be due to differences in the H. pylori strains used.
Strain TK1402 was isolated from a patient with duodenal and gastric ulcers in Japan. This strain contains the cagA, cag PAI and vacA genes as demonstrated by PCR . It was also shown that this strain expresses the Lewisy antigen (LeY) on the cell surface. Moreover, strain TK1402 was reported to exhibit virulence in gnotobiotic mice , C57BL mice , and Mongolian gerbils . These reports indicated that the TK1402 strain has the ability to colonize the stomach of these animals as well as in humans. These results as well as our present findings suggest that this colonization ability might be correlated with the strong biofilm forming ability of strain TK1402. Therefore, we speculate that strong biofilm forming ability is related to gastric colonization by H. pylori in various animals as well as in humans. It is recognized that an understanding of H. pylori biofilm formation is still in its infancy. The ability of H. pylori strains, as exemplified by strain TK1402, to form biofilms may play a part of role in the infectious process.
We have demonstrated that strain TK1402 has strong biofilm forming ability. In addition, the results suggested that this property is dependent upon direct cell-cell binding mediated by the OMV of this strain. This represents a new observation relative to a potentially novel gastric cell colonization factor of this organism.
Bacterial strains and culture conditions
The following H. pylori strains were used: SS1, ATCC 49503, ATCC 43579, NCTC11638, TK1029, TK1402, KR2003, and KR2005. The last four are clinical isolates from Japanese patients. Strains TK1029 and TK1402 were used as described previously . In addition, strains TK1036, TK1042, TK1043, TK1045, TK1046, TK1047, TK1049, TK1054, TK1056, and TK1057 were also used for assessing biofilm forming ability. Strains KR2003 and KR2005, as well as the latter strains were isolated from a gastritis patient in our laboratory. All strains were maintained at -80°C in Brucella broth (Difco, Detroit, Mich) with 20% (vol/vol) glycerol. These strains were cultured under microaerobic conditions at 37°C on Brucella agar plates containing 7% horse serum (HS).
Biofilm formation and its quantification
Biofilm formation by all strains was carried out as previously described [19, 20] with slight modifications. Briefly, sterilized glass coverslips (approximately 22 × 22-mm, 0.12 to 0.17-mm thickness, Matsunami Glass, Tokyo, Japan) were placed into 12-well microtiter plates. Each well was filled with 2 ml of Brucella broth supplemented with 7% fetal calf serum (FCS), 7% horse serum (HS), or 0.2% β-cyclodextrin to allow adherence of H. pylori at the air-liquid interface. The formation of biofilms was initiated by inoculating 10 μl of pre-cultured cell suspension (approximately 5 × 105 cells in Brucella broth) into each well. The cultures were incubated under microaerobic conditions at 37°C for 1 to 6 days with shaking (80-100 rpm). After incubation, the coverslips were removed and washed with phosphate-buffered saline (PBS). The samples were then air dried and stained with crystal violet for 30 s. After being stained, the coverslips were rinsed with distilled H2O to remove excess dye and then air dried for 30 min. All dye associated with the biofilms was dissolved with 1 ml of ethanol and 200 μl of the ethanol solutions were used to measure the absorbance at 594 nm with a microplate reader to determine the amount of biofilm formation.
Confocal laser scanning microscopy (CLSM) and measurement of biofilm thickness
For visualization, the biofilms of H. pylori strains on the coverslips were stained with a BacLight LIVE/DEAD bacterial viability kit solution (Molecular Probes, Leiden, The Netherlands) according to the directions of the supplier. Confocal images were collected by using a Zeiss LSM 510-META confocal laser scanning microscope (Carl Zeiss, Jena, Germany). To determine biofilm thickness, a series of horizontal (xz) optical sections at 0.5 μm intervals were taken through the height of the biofilm for measurement. Each biofilm was scanned at five randomly selected positions. Each sample was observed independently more than three times. Confocal images of green and red fluorescence were constructed simultaneously using a multitrack mode.
Cell viability assay
To determine the numbers of viable bacteria, biofilm cells on the coverslips were scrapped into PBS. The optical densities and colony-forming units (CFU) of the cell suspensions were quantitated as the mean of three independent observations. As controls, standard cell broth cultures were used.
Electron microscopic studies
To observe the biofilm ultrastructure, the biofilms formed on the coverslips were examined by scanning electron microscopy (SEM). The biofilms on the coverslips were fixed with 2% glutaraldehyde for 3 h at room temperature and the samples were observed using a JSM-5600LV electron microscope (JEOL, Tokyo, Japan).
To observe the OMV-like structures, the biofilms of strain TK1402 on the glass slides were examined by using transmission electron microscopy (TEM). Glass slides cut in half were placed into 6-well microtiter plates and the biofilms were allowed to form as described above. The biofilms were fixed with 2% glutaraldehyde for 3 h at room temperature. The samples were then dehydrated and embedded in Epon 813 embedding solution (Chemische Werke Lowi GmbH, Waldkaraigurg, Germany). The sections were finally observed with a JEM-100 electron microscope (Jeol).
Isolation of outer membrane vesicles
Isolation of OMV was performed as described previously . Briefly, H. pylori strain TK1402 was grown in Brucella broth supplemented with various concentration of FCS for 3 days. After cultivation, the optical density at 600 nm of the cell cultures was adjusted to 0.5 with each respective medium. The cells were collected by centrifugation (10,000 g for 15 min), and the resulting supernatants were filtered (low protein binding Durapore membrane, 0.45 mm polyvinylidene fluoride, Millipore, Bedford, Mass.). The filtrates were centrifuged (40,000 g, 2 h at 4°C), washed with PBS and re-centrifuged (40,000 g, 2 h at 4°C). The pellets were next resuspended in PBS supplemented with 0.2 M NaCl. The media without the bacteria were used as controls. The OMV of strain TK1402 in Brucella broth supplemented with 0.2% β-cyclodextrin or 7% horse serum were also isolated in a similar manner.
Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and immunoblotting techniques
The fractionated OMV (OMV-fraction) were treated with sodium dodecyl sulfate (SDS) loading buffer including 5% 2-mercaptoethanol at 100°C for 5 min and separated by polyacrylamide gel electrophoresis (PAGE). The separated OMV proteins were stained with Coomassie brilliant blue. For Western blotting assays, the OMV-fractions were loaded onto gels and transferred to polyvinylidene difluoride membranes (Atto, Tokyo, Japan). After transfer, the membranes were blocked with 3% bovine serum albumin in PBS for 60 min and incubated with H. pylori strain NCTC 11638 whole-cell antiserum (1:2,000)  for 60 min. After washing with PBS containing 0.05% Tween 20 (PBST), peroxidase-labeled goat anti-rabbit immunogloblins (Dako A/S, Glostrup, Denmark) were used at 1:2,000 dilution as secondary antibodies. After washing with PBST, the blots were developed.
Complementation of biofilm forming ability using the OMV
The OMV-fraction from Brucella broth supplemented with 7% FCS (OMV-fraction) and the medium fraction (control-fraction) in PBS were adjusted to an optical density of 2.0, or 1.0 at 280 nm. The OMV-fractions from Brucella broth supplemented with 0.2% β-cyclodextrin were also adjusted to optical densities of 1.0. After filtration, 100 μl of the fractionated OMV were added to Brucella broth with 0.2% β-cyclodextrin for TK1402 biofilm formation assays (described above).
Statistical analysis was performed using the Mann-Whitney U test. P values of 0.05 or less were considered to indicate statistical significance.
This work was supported by Grants for Scientific Research 18590437 from the Ministry of Education, Culture, Sport, Science and Technology and a grant from the Dental Research Center, Nihon University School of Dentistry.
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