Differences in Haemophilus parasuisadherence to and invasion of AOC-45 porcine aorta endothelial cells
© Frandoloso et al.; licensee BioMed Central Ltd. 2013
Received: 20 March 2013
Accepted: 8 October 2013
Published: 12 October 2013
The pathogenesis of Haemophilus parasuis depends on the bacterium’s ability to interact with endothelial cells and invade adjacent tissues. In this study, we investigated the abilities of eight H. parasuis reference strains belonging to serovars 1, 2, 4, 5, 7, 9, 10 and 13 to adhere to and invade porcine aortic endothelial cells (AOC-45 cell line).
The strains belonging to serovars 1, 2 and 5 were able to attach at high rates between 60 and 240 min of incubation, and serovars 4, 7 and 13 had moderate attachment rates; however, the strains belonging to serovars 9 and 10 had low adherence at all time points. Strong adherence was observed by scanning electron microscopy for the strains of serovars 5 and 4, which had high and moderate numbers, respectively, of H. parasuis cells attached to AOC-45 cells after 240 min of incubation. The highest invasiveness was reached at 180 min by the serovar 4 strain, followed by the serovar 5 strain at 240 min. The invasion results differed substantially depending on the strain.
The reference strains of H. parasuis serovars 1, 2, 4 and 5 exhibited high adhesion and invasion levels to AOC-45 porcine aorta endothelial cells, and these findings could aid to better explain the pathogenesis of the disease caused by these serovars.
KeywordsHaemophilus parasuis Glässer’s disease AOC-45 cells Adherence Invasion
Glässer’s disease is a swine disease caused by a pleomorphic nicotinamide adenine dinucleotide-dependent Gram-negative rod of the family Pasteurellaceae known as Haemophilus parasuis. The primary signs of this disease are serofibrinous to fibrinopurulent polyarthritis, polyserositis and meningitis, and septicemia, pneumonia and myositis of the masseter muscles are also observed . To date, 15 H. parasuis serovars have been defined using an immunodiffusion test with heat-stable antigens ; however, some strains isolated from pigs with Glässer’s disease are untypable [4, 5]. Serovars 1, 5, 10, 12, 13 and 14 have been classified as highly virulent; serovars 2, 4 and 15 as moderately virulent; and serovars 3, 6, 7, 8, 9 and 11 as non- or scarcely virulent , but the correlation between serotype and virulence is not clear .
Stress may influence the epidemiology of this disease within herds, especially regarding the early colonization of pigs by virulent strains and the spread of the disease throughout a swine population, especially in herds with high sanitary standards . H. parasuis usually colonizes the upper respiratory tract of pigs, and it can also be detected in the tonsillar area and at other respiratory sites, such as the tracheal mucosa . At these sites, virulent strains are able to breach the mucosal barrier and pass into the bloodstream, leading to the severe systemic disease described above . Some in vivo studies have shown that H. parasuis does not strongly attach to cilia or other cell structures; in addition, the investigations into the specific interactions between this bacterium and host epithelial cells have been focused primarily on interactions with porcine brain microvascular endothelial cells [9–11] or porcine epithelial kidney cells . In addition, cytolethal distending toxin, outer membrane protein 2 and heptose I and II residues in the inner core oligosaccharide have been implicated in the adherence of this bacterium to porcine alveolar macrophages, epithelial kidney cells and umbilicus vein endothelial cells [13–16].
To better understand the pathogenesis of Glässer’s disease, this study investigated the adherence to and invasion of AOC-45 porcine aortic endothelial cells by H. parasuis strains belonging to serovars 1, 2, 4 5, 7, 9, 10 and 13, which are considered to have different levels of virulence .
H. parasuis H409, H410, H412, Nagasaki, H643, H553, H555 and H793 (reference strains for serovars 1, 2, 4, 5, 7, 9, 10 and 13, respectively) were used. The bacteria were cultured on chocolate agar (BioMérieux, France) or in PPLO broth (Biolife, Italy) supplemented with 2.5 mg/ml glucose, 40 μg/ml nicotinamide adenine dinucleotide (Sigma) and 72.5 μg/ml IsoVitalex (Difco, USA).
Determination of the infection dose
Because of the differences in the individual bacterial size, self-aggregation and growth time of the different H. parasuis strains, a growth curve for each strain was constructed to determine the infection dose. After the growth curves had been obtained (optical density -OD- versus colony-forming units -CFU-), the infection dose was established in the following manner: a mix of colonies from a fresh H. parasuis culture harvested from a chocolate plate were used to inoculate PPLO broth supplemented as described above, and this culture allowed to grow to an OD600 of 0.7. At this point, the bacteria were harvested by centrifugation at 4,000 × g for 15 min, washed three times in Dulbecco’s PBS medium (D-PBS) and resuspended in Dulbecco’s modified Eagle medium (DMEM) without antibiotics, and the concentration was adjusted to 108 CFU/ml. Next, we prepared serial dilutions (1:10), and 100 μl of each dilution was plated on chocolate agar to determine the exact number of bacteria in the inoculum used for AOC-45 cell infection.
AOC-45 aortic endothelial cells  were cultivated in DMEM (Invitrogen) supplemented with 10% fetal calf serum (Invitrogen) in 25 cm2 flasks (TPP, Switzerland) and incubated at 37°C in 5% CO2 and a 95% humid atmosphere. Cells were subcultured every 48 hours until 70% cell confluence was reached. Forty-eight-hour cultures (logarithmic phase of cell growth) were trypsinized and diluted in culture medium to obtain a concentration of 2 × 105 cells per well in 24-well tissue culture plates (TPP, Switzerland).
Measurement of the number of cell-associated bacteria
The adherence assay was performed as previously described , with some modifications. AOC-45 cells were grown to confluence in 24-well plates (approximately 7 × 105 cells), washed once with 2 ml of D-PBS and infected with 1 ml aliquots of the different H. parasuis strains (108 CFU). The plates were incubated for different times up to 240 min to allow bacterial adherence. Thereafter, the cells were washed five times with PBS to remove non-attached bacteria. To estimate the number of cell-associated bacteria (adhered to the cells surface and intracellular), the cells were incubated with 200 μl of trypsin for 5 min, followed by disruption with 800 μl of ice-cold deionized water and repeated pipetting to liberate cell-associated bacteria. Serial dilutions (1:10) of this cell lysate were prepared, and 100 μl of each dilution was plated onto chocolate agar (BioMérieux, France) and incubated for 48 h at 37°C with 5% CO2.
The average number of bacteria associated with each AOC-45 cell was determined by dividing the number of cell-associated bacteria harvested from chocolate plate by the number of AOC-45 cells in the well. These assays were performed in triplicate using directly thawed bacteria each time. The absolute number of AOC-45 cells in each well of each plate was determined by trypsinization and counting of an uninfected monolayer in a Neubauer chamber.
Cell invasion assays
The invasion assays were performed as previously reported , with some modifications. Confluent monolayers of AOC-45 cells grown in 24-well plates were infected with 1 ml aliquots of the different H. parasuis strains (approximately 108 CFU). The plates were centrifuged at 450 × g for 10 min to enhance the contact between H. parasuis and the surface of the monolayer. The plates were incubated for different times up to 300 min at 37°C with 5% CO2 to allow cell invasion by the bacteria. The monolayers were then washed as described for the adherence assays, and 1.5 ml of culture medium containing two antibiotics (5 μg of penicillin G/ml and 100 μg of gentamicin/ml, Sigma) was added to each well. Then, the plates were further incubated for 2 h at 37°C to kill the extracellular H. parasuis. The monolayers were washed thrice, and the cells were disrupted as described for the adherence assays. Serial dilutions of this cell lysate (100 μl) were plated onto chocolate agar and incubated for 48 h at 37°C with 5% CO2.
The level of invasion was determined by dividing the number of bacteria harvested from the chocolate plate by the number of AOC-45 cells in the well. The assays were performed in triplicate as indicated above. The absolute number of AOC-45 cells in each well of each plate was determined as described for the adherence assay.
Adherence and invasion analyses using electron microscopy
The adherence H. parasuis serovars 4, 5 and 9 was also assessed using scanning electron microscopy (SEM). AOC-45 cells were grown on 13 mm Thermanox coverslips in a 24-well culture plate until confluence was reached (approximately 7 × 105 cells). Then, the cells were infected as described above and incubated for 240 min at 37°C. After five washes with 2 ml of D-PBS, the monolayers were fixed for 1 h at 4°C with 2% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.3). After three other washes with cacodylate buffer at 4°C for 10 min each, the samples were postfixed for 15 min at room temperature with 2% osmium tetroxide in deionized water. The specimens were dehydrated in a graded series of ethanol solutions and desiccated in a critical point dryer apparatus (Bal-Tec CPD 030) . After an ion-spatter coating with gold-palladium, the samples were viewed with a JSM-6480 JEOL scanning electron microscope.
For invasion studies, transmission electron microscopy (TEM) was used. Cells grown on Thermanox coverslips were infected as described above for the adherence assays and processed as previously described .
The results are presented as the mean ± standard deviation. Analysis of variance (ANOVA) and Tukey’s multiple comparison tests (SPSS statistical program, version 16.0, Chicago, IL, USA) were used to compare adherence or invasion after different incubation times and to compare adherence or invasion between the different strains. GraphPad Prism, version 5.0 (San Diego, CA, USA), was used to prepare the figures. P values <0.05 indicate statistical significance.
The adherence of the most strains increased considerably at 180 min and reached the highest level at 240 min. Significant differences were observed for the strains of serovars 1, 2, 5 and 13 between the levels of adherence at 180 min and 30 min (P < 0.05). Of the four H. parasuis serovars with high virulence (1, 5, 10 and 13) according to Oliveira and Pijoan , the serovar 5 strain exhibited the highest rate of adherence at 30 min, with significant differences between this strain and the strains of serovars 1, 10 and 13 (P < 0.05). No significant difference was found between the strains of serovars 1 and 13 at this time, but both presented higher adherence levels than those of serovar 10 (P < 0.05). After 180 min of incubation, the strains of serovars 1 and 5 had significantly more adherent bacteria (3.2 and 2-fold greater, respectively) than at earlier times (Figure 1). Of the two moderately virulent serovars , the serovar 2 strain clearly exhibited a significantly higher adherence capacity than the serovar 4 strain (P < 0.05) throughout the study. The adherence kinetics of the strains of serovars 2 and 5 were similar, and a significant difference (P < 0.05) could be seen between these strains only at the 180 min time point (Figure 1).
The serovar 5 strain was the only strain for which invasion was time dependent, with the lowest level of invasion being detected at 120 min (0.13 ± 0.01) and the highest at 300 min (0.24 ± 0.03). The five other strains exhibited invasion kinetics patterns that were completely different. For instance, the highest invasion rate for the strain of serovar 1 was recorded at 240 min (0.15 ± 0.04), whereas that highest invasion rate for serovar 4 was at 180 min (0.29 ± 0.02) and those of serovars 2 (0.24 ± 0.03), 7 (0.05 ± 0.01) and 13 (0.1 ± 0.03) were at 120 min.
The analysis of the highly virulent serovars  showed that the strain of serovar 5 had significant higher invasion rates at 60 and 300 minutes (P < 0.05) than the strains of serovars 1 and 13. No significant differences were found between the invasion rates of the strains of serovars 1 and 13 from 60 to 180 min; however, the serovar 1 strain had significantly greater invasiveness than the serovar 13 strain at 240 and 300 min (P < 0.05).
With respect to the invasion kinetics of the moderately virulent serovars , the strain of serovar 4 had a significantly higher invasion rate at 180 min than the serovar 2 strain (P < 0.05). However, after this time point, a sharp decrease was observed for the invasiveness of serovar 4, with the level of invasion at 5 h being approximately three-fold lower than that of serovar 2 (P < 0.05) (Figure 3).
H. parasuis adherence and invasion were evaluated for eight reference strains belonging to serovars with different virulence levels . A well-established endothelial cell line of vascular origin (AOC-45) was used, and although these cells differ from the epithelial cells lining the respiratory tract, this endothelial cell line could help explain some of the virulence mechanisms implied in the pathogenicity of this porcine pathogen. Although extrapolation of findings in other cell lines must be taken with caution, cytotoxicity studies were not carried out because in a previous report  using H. parasuis and another vascular endothelial cell line, no apoptotic effect was detected for up to 5 hours post infection, the last time tested in our studies.
Our results clearly indicate that all eight strains were able to adhere to porcine aortic cells in vitro, although to considerably different degrees depending on the strain and serovar. However, the strains of serovars 9 and 10, which had the lowest adherence abilities, were not able to invade AOC-45 cells. Because of the use of a centrifugation step in the invasion assays but not in the adherence assays in this study, the number of H. parasuis able to invade these cells could be overestimated compared with the number of adhered bacteria. This centrifugation step was included to facilitate contact between the bacteria and the AOC-45 cells in a short time, eliminating the normal effect of gravity. Even with the use of this step, the number of H. parasuis bacteria associated with AOC-45 cell surfaces observed in this study was similar to that found previously  for the porcine brain microvascular endothelial line PBMEC/C1-2.
The attachment rate obtained in our study for the strain belonging to serovar 5 was higher than those previously reported . More than twice as many H. parasuis cells (5.52 ± 0.2) adhered to AOC-45 cells after 180 min of incubation than adhered to PK-15 cells (approximately 2.1 ± 0.2). This result could indicate H. parasuis tropism for endothelial cells, such as AOC-45 cells, because this organism has to adhere to endothelial cells, then cross through blood vessels and finally reach the target organs for infection. This finding could explain the bacterium’s ability to cause a severe systemic inflammatory response, as inflammatory lesions in porcine hearts have been reported . In studies based on a clinical isolate belonging to serovar 4, the adherence to and invasion of PK-15 cells and PUVECs were found to be related, respectively, to lipooligosaccharide heptose residues , cytolethal distending toxin  and Omp2 .
The adhesion of serovar 5 to kidney epithelial  and brain microvascular endothelial cells  reached the highest percentages after 90 min of incubation; however, the attachment exhibited by the eight strains used in this study was time dependent, and the greatest values were measured after 240 min of incubation, the longest time tested, irrespective of the adherence degree of each strain.
Microscopically, no morphological changes to the aortic cells were detected by SEM after the attachment of the different H. parasuis serovars. This result is in agreement with those for brain endothelial cells after 30 min of infection . Considerable changes in the surface of porcine kidney epithelial cells have been detected during H. parasuis attachment, including an increase in the number of membranous projections . The formation of these structures was hypothesized to be one of the mechanisms involved in the adherence of this strain to PK-15 cells. Further studies are required to determine which molecules are involved in the adherence of H. parasuis to available porcine cell lines. The adherence exhibited by the strains belonging to serovars 1, 2 and 5 in this study could indicate that a high adherence strength is necessary to prevent H. parasuis from being dragged along by the arterial or venous bloodstream, thus facilitating the infection of target tissues. Similarly, the most clinically important serovars were those with the greatest in vitro adherence levels starting from 30 min of infection in our study. This fact, associated with the capacity of H. parasuis to adhere to porcine epithelial tracheal cells , could suggest that vaccine design strategies should focus on eliciting not only a systemic immune response but also a strong mucosal immune response, so that H. parasuis would not be able to adhere to epithelial cells and then reach the bloodstream.
Although H. parasuis was previously described as an exclusively extracellular pathogen, other investigations  have proven that this organism is able to cross the blood–brain barrier and invade brain endothelial cells. Similarly, we showed that several H. parasuis strains belonging to different serovars were able to invade other type of endothelial cells in vitro, a process also recently demonstrated for PUVECs [14–17]. Our findings revealed the high attachment and invasiveness of virulent strains belonging to serovars 1 and 5 (H409 and Nagasaki, respectively) when using the AOC-45 cell line; however, strains of other serovars also considered to be virulent  attached in a lesser degree, such the strain of serovar 13, and the strain of serovar 10 was incapable of invading these cells. The invasiveness exhibited by the reference strains of serovars 1, 2, 4 and 5 used in this study could aid to explain the ability of these serovars to cause clinical cases of systemic disease .
In a previous study , 107 CFU of Nagasaki strain (serovar 5) was able to reach the intracellular space of the brain endothelial cells after 90 min of incubation. Our results indicate that 108 CFU of H. parasuis strains of serovars 2 or 4 was able to invade a higher proportion of AOC-45 cells at this same time. One hypothesis to explain this finding is that the strains with high invasiveness could use this mechanism to pass through endothelial cells and reach the target organs. Some authors [9, 21] have shown that the number of internalized Pasteurella multocida and H. parasuis decreased in a time-dependent manner, and they suggested that an exocytosis-based mechanism could explain this behavior. This fast mechanism could explain also, generically, the low number of internalized bacteria recovered in our study.
More studies should be performed to test this hypothesis and to determine whether the cytoplasmatic conditions and innate defense mechanisms of AOC-45 cells are compatible with H. parasuis. The invasion of AOC-45 cells by H. parasuis followed a heterogeneous pattern in our study and depended on the strain and serovar, unlike the results of other authors , who did not find differences in the ability to invade associated with the H. parasuis serovar.
The reference strains of H. parasuis serovars 1, 2, 4 and 5, which are thought to be highly or moderately virulent, had high adhesion and invasion levels to AOC-45 porcine aorta endothelial cells, while the reference strain of serovar 9, thought to have low virulence potential, attached poorly to these cells. These findings could aid to better explain the pathogenesis of Glässer’s disease caused by serovars 1, 2, 4 and 5. Further studies with clinical isolates are required to confirm our findings.
Aorta endothelial cells
Scanning electron microscopy
Transmission electron microscopy
Analysis of variance
Porcine umbilicus vein endothelial cells.
Research in laboratory of RF and SMM was supported by long predoctoral fellowships from the Spanish Ministry of Science and Innovation, as well as by grant AGL2011-23195 from the Ministry of Economy and Competitiveness. We would like to thank Prof. J. Yélamos (Dpt. of Surgery, University Hospital “Virgen de la Arrixaca”, El Palmar, Murcia, Spain) for the gift of the AOC-45 cell line.
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