- Research article
- Open Access
Coinfection modulates inflammatory responses, clinical outcome and pathogen load of H1N1 swine influenza virus and Haemophilus parasuis infections in pigs
BMC Veterinary Research volume 13, Article number: 376 (2017)
Respiratory co-infections are important factor affecting the profitability of pigs production. Swine influenza virus (SIV) may predispose to secondary infection. Haemophilus parasuis (Hps) can be a primary pathogen or be associated with other pathogens such as SIV. To date, little is known about the effect of coinfection with SIV and Hps on the disease severity and inflammatory response and the role of Hps in the induction of pneumonia in the absence of other respiratory pathogens. In the study we investigated the influence of SIV and Hps coinfection on clinical course, inflammatory response, pathogens shedding and load at various time points following intranasal inoculation. The correlation between local concentration of cytokines and severity of disease as well as serum acute phase proteins (APP) concentration has been also studied.
All co-infected pigs had fever, while in single inoculated pigs fever was observed only in part of animals. Necropsy revealed lesions in the lungs all SIV-inoculated and co-inoculated pigs, while in Hps-single inoculated animals only 1 out of 11 pigs revealed gross lung lesions. The SIV shedding was the highest in co-inoculated pigs. There were no differences between Hps-single inoculated and co-inoculated groups with regard to Hps shedding. The significant increase in Hps titre in the lung has been found only in co-inoculated group. All APP increased after co-infection. In single-inoculated animals various kinetics of APP response has been observed. The lung concentrations of cytokines were induced mostly in SIV + Hps pigs in the apical and middle lobe. These results correlated well with localization of gross lung lesions.
The results revealed that SIV increased the severity of lung lesions and facilitated Hps (PIWetHps192/2015) replication in the porcine lung. Furthermore, Hps influenced the SIV nasal shedding. Enhanced Hps and SIV replication, together with stronger systemic and local inflammatory response contributed to a more severe clinical signs and stronger, earlier immune response in co-inoculated animals. We confirmed the previous evidence that single-Hps infection does not produce significant pneumonic lesions but it should be in mind that other strains of Hps may produce lesions different from that reported in the present study.
Respiratory infections in pigs are very important factor affecting the profitability of pig production [1, 2]. Although various bacteria or viruses could induce the respiratory infection separately, it has commonly been caused by coinfection with more pathogens under field conditions [1,2,3]. The most important infectious agents responsible for infection of the respiratory tract in pigs are: swine influenza virus (SIV), porcine reproductive and respiratory syndrome virus (PRRSV), Pasteurella multocida (Pm), Actinobacillus pleuropneumoniae and Mycoplasma hyopneumoniae [2, 4,5,6]. Besides, the above mentioned pathogens, the Haemophilus parasuis (Hps) can also be recovered from the lungs of pigs with pneumonia [1, 7,8,9,10]. In these cases Hps is often isolated along with other bacterial or viral pathogens and, therefore, the role of Hps in producing pneumonia is not clear [8, 11].
Bacterial pneumonia secondary to influenza is often observed in pigs . SIV is a significant contributor to the respiratory diseases and may predispose to secondary bacterial infection. Hps is an important and common respiratory pathogen of pigs . It can be a primary pathogen or be associated with other diseases such as SIV [3, 8]. It could be also isolated from nasal cavity, tonsils and trachea of apparently healthy pigs [8, 14]. Under favorable conditions, Hps can cause severe systemic infection characterized by fibrinous polyserositis, arthritis and meningitis [8, 11, 14]. Factors leading to systemic infection by Hps have not been clarified to date [9, 14].
Although there are previous reports of experimental reproduction of Hps or SIV infection in conventional pigs, little is known about the effect of concurrent infection with SIV and Hps on the disease severity and inflammatory response in pigs, even if this coinfection is common under field conditions [13, 15,16,17]. There are also limited data on the role of Hps in the production of pneumonia in the absence of other respiratory pathogens. Furthermore, the kinetics of acute phase protein (APP) response in SIV/Hps co-infected pigs has not been studied to date. As it has been shown for other pathogens, the exposure to several pathogens can lead to a stronger APP response, as compare to single infection [18,19,20]. Thus, in order to investigate the influence of SIV and Hps coinfection on clinical outcome, both local and systemic inflammatory response as well as pathogen shedding and load at various time points following intranasal inoculation, three experimental infections (Hps- and SIV-single infection, SIV/Hps co-infection) has been performed in the present study. The correlation between local concentration of cytokines and severity of infection (clinical score, lung score) as well as serum APP concentration has been also studied.
All pigs from co-infected group had fever for at least one day (rectal temperature ≥40° C). In SIV – inoculated group fever was observed in 7 out of 11 pigs, while in Hps - inoculated pigs only in 3 out of 11 pigs (Fig. 1). The mean clinical scores (±SD) in all groups are presented in Fig. 2. In single-inoculated pigs, the individual clinical score ranged from 0 to 1 (Hps) or from 0 to 5 (SIV), while in co-inoculated pigs the individual clinical score ranged from 1 to 6. Pigs from the control group did not revealed clinical signs of any disease. Significant differences were observed between mean clinical score in SIV- and Hps + SIV – inoculated pigs and the controls (p≤0.05). There was also significant difference between co-inoculated and Hps-inoculated group (p≤0.05). No differences were observed between mean clinical score in SIV-single inoculated and co-inoculated animals as well as between Hps-inoculated and control animals.
Postmortem examination revealed macroscopic lesions (well-demarcated plum-colored or dark red lesions) in the lungs all SIV-inoculated and co-inoculated pigs, while in Hps-single inoculated animals only 1 out of 11 pigs revealed macroscopic changes in the lung. None of the control pigs had visible pneumonia. The mean lung scores (±SD) are presented in Fig. 3. There were no significant differences between lung score observed at different days post inoculation within each group (p > 0.05). Significant differences were found between mean lung score observed co-inoculated and Hps-inoculated groups and control animals (p < 0.05). There was no difference between lung score noted in co-inoculated and SIV-only inoculated animal. No differences were also found between mean lung score in Hps-inoculated and control pigs.
Pathogens shedding and load
The highest SIV shedding (expressed as mean SIV titre (log10 TCID50 titre/100 mg secrete from nasal swabs) was observed in co-inoculated pigs. Significant differences between single-SIV and dual inoculated pigs were found from 3 to 7 DPI (p < 0.05). Compared to control pigs, significantly higher (p < 0.05) mean SIV titers were observed in both SIV-single inoculated pigs and co-inoculated pigs from 1 to 5 DPI and 1 to 7 DPI, respectively (Fig. 4.). The mean Hps titre in the nasal swabs (expressed as log10 CFU titre/100 mg secretion) in piglets from SIV + Hps and Hps groups increased significantly from day 1 post inoculation and remaining at the significantly higher level to the end of study (p < 0.05). There were no differences between Hps-single inoculated and co-inoculated groups with regard to Hps nasal shedding (Fig. 5.).
The SIV and Hps titres in the lungs at 2, 4 and 10 dpi are presented in Figs. 6 and 7, respectively. All pigs inoculated with SIV were virus positive in samples taken from right lungs at 2 and 4 DPI. At 10 DPI the virus was detected in 1 out of 5 lungs in SIV-single inoculated animals, while in pigs co-inoculated with Hps in 2 out of 5 lungs and no significant differences between virus inoculated groups were found. The mean SIV TCID50 titres were highest in co-inoculated pigs at 2 and 4 DPI (p < 0.05).
The significant increase in Hps titre in the lung were found only in co-inoculated group (p < 0.05). The significant differences were detected between the mean titre of H. parasuis in the lungs taken from pigs from Hps and SIV + Hps groups during whole study period (2, 4 and 10 DPI) (p < 0.05).
Humoral immune response to SIV and Hps
A specific humoral response against SIV was observed at 7 DPI in 80% of pigs (4/5) co-inoculated and 40% of pigs (2/5) single inoculated with SIV. All animals inoculated with SIV (single or dual) developed specific antibodies at 10 DPI (the HI titre ranged from 20 to 80 in co-inoculated pigs and from 20 to 40 in SIV-only inoculated group). There were no differences with regard to HI titre at 7 and 10 DPI between groups inoculated with SIV (single or dual) (p≥0.05). None of pigs not inoculated with SIV had antibodies against this pathogen (<20 HI titre).
Significant differences between co-inoculated and single-inoculated or control pigs with regard to Hps specific antibodies was observed at 7 DPI (p≤0.05). Furthermore, in groups inoculated with Hps (single or dual) the mean ELISA ratio at 10 DPI was significantly higher than in SIV – inoculated and control animals (p≤0.05). The ELISA ratio in control group did not differ significantly from the observed in SIV-inoculated pigs during study period.
Systemic levels of acute phase proteins
All studied APP increased after co-infection, with mean maximum concentrations from 3 to 7 DPI (Fig. 10.) (p < 0.05). In single-inoculated animals different kinetics of acute phase response has been noted. In the control group concentrations of all APP were constant.
Significant increase in the mean concentration of CRP compared to control pigs has been observed in co-inoculated animals from 1 to 7 DPI. At 2 DPI the significant difference compared to control group was noted also for the Hps-inoculated pigs (p < 0.05). The maximum mean level of CRP in co-inoculated animals was observed at 3 DPI and reached 224.61 ± 96.80 μg/ml (almost 8-fold increase comparing to the day 0 level). In pigs inoculated only with Hps the maximum mean concentration of CRP was observed at 2 DPI (2.5 fold increase comparing to day 0 level). In pigs from SIV group the mean levels of CRP did not differ significantly from that determined in the control animals.
The concentration of Hp increased significantly in all inoculated groups comparing to control animals. The strongest and the most prolonged Hp response was found in SIV + Hps group. The mean concentration of Hp in this group had increased by 48 h after co-inoculation and were notably higher compared to control pigs (p < 0.05) to the end of study. Significant differences between single and dual-inoculated groups were observed from 3 to 10 DPI (p < 0.05). The highest mean concentrations of Hp in co-inoculated pigs were observed at 5 DPI. The mean maximal concentration was almost 9-fold higher, compared to the mean baseline concentration. The highest concentration of Hp in particular animal after coinfection reached 7.03 mg/ml (at 3 DPI). In pigs single inoculated with SIV or Hps only short-term increase in Hp level was recorded (at 2 and 3 DPI in SIV-inoculated and at 3 dpi in Hps-inoculated pigs).
A. Significant increase of SAA concentration was found in all inoculated groups (p < 0.05). No significant changes were found in control pigs (p≥0.05). The strongest reaction has been noted in co-inoculated animals. The mean peak concnetration in mentioned group was detected at 3 DPI and reached 254.31 ± 181.32 μg/ml (over 100-fold increase comparing to the day 0 level). Significantly higher concentration compared to the controls was observed from 1 to 5 DPI (p < 0.05). In the remaining, single-inoculated groups the mean maximum concentrations were observed at 2 DPI (over 15-fold increase) and significant differences compared to controls were noted from 2 to 3 DPI (p < 0.05).
Pig major acute phase protein
Baseline levels of Pig-MAP in experimental animals were found to be below 0.92 mg/ml. Concentration of Pig-MAP increased significantly 72 h after co-inoculation and inoculation with Hps (p < 0.05). In co-inoculated pigs the concentration of Pig-MAP remained significantly elevated till 10 DPI (end of study), while in Hps-single inoculated pigs till 5 dpi. The highest Pig-MAP mean levels were observed between 5 to 7 DPI. The maximum mean concentration of Pig-MAP, observed at 7 DPI in piglets from SIV + Hps group was almost 3 times higher compared to day 0-level (baseline concentration). There were no significant differences in the kinetics of Pig-MAP response between co-inoculated and Hps-single inoculated pigs. In pigs single inoculated with SIV as well as in control animals the level of Pig-MAP in serum was constant during study period.
Cytokines – Local lung response
In general the local concentrations of TNF-α, IFN-γ, IL-1β, IL-6 and IL-10 were induced mostly in SIV + Hps pigs (Fig. 11). In control pigs the concentrations of all investigated cytokines were relatively constant (p≥0.05).
At 2 DPI, concentrations of proinflammatory cytokines (IL-1β, IL-6, TNF-α) and IFN-γ were significantly higher in the lungs of co-inoculated pigs compared to controls (with exception of IL-1β and TNF-α in apical lobes). Furthermore significant differences were observed between co-inoculated and single inoculated pigs, with exception of IL-1β and TNF-α in apical lobes, and IFN-γ in middle and accessory lobes. In particular differences were noted between Hps and SIV + Hps group with regard to IFN-γ (all lobes) and TNF-α, IL-1β and IL-6 (except apical lobes) as well as between co-inoculated and SIV groups with regard to IFN-γ and IL-1β. No significant differences were found between control and single inoculated pigs with regard to IL-1β and IL-10 level in all lobes from the upper part of the right lung at that time. The highest concentrations of cytokines were generally observed in right middle lobes what positively correlated with the lesions detected during necropsy.
At 4 DPI the concentrations of all investigated cytokines were significantly higher in co-inoculated pigs, compared to controls (p < 0.05). No significant differences were observed with regard to IL-1β and IL-10 in single-inoculated groups, compared to controls (p≥0.05). With regard to SIV + Hps group the significantly higher concentration of investigated cytokines was observed in all evaluated parts of the lung. In SIV inoculated animals significantly higher concentration of IFN-γ compared to control group was observed in middle and accessory lobes, IL-6 in all lobes and TNF-α in apical and middle lobes. No significant increase in the level of cytokines tested was observed in Hps inoculated group (p≥0.05).
At 10 DPI the lung concentrations of cytokines generally decreased compared to 2 and 4 DPI, but in the case of IL-1β, IL-6 and IL-10 (in co-inoculated animals) were still significantly higher compared to controls (p < 0.05). Significantly greater concentrations were observed for IL-1β with regard to middle and accessory lobes, for IL-6 with regard to apical lobe and for IL-10 with regard to all lobes (p < 0.05). No significant differences between local concentrations of all investigated cytokines in single-inoculated and control animals were found for all lung lobes at 10 dpi.
Summarizing, the maximum concentrations of cytokines in general were observed at 4 DPI. The highest concentrations of most cytokines were found in the apical and middle lobe. These results correlated well with localization of gross lung lesions. Significant correlations were found between lung concentration of IL-1β, IL-6, IFN-γ and TNF-α and pathological changes in the lungs (R-Spearman = 0.65; 0.63; 0.71 and 0.62 respectively; p < 0.05). A positive correlation was also observed between concentrations of IL-1β and IFN-γ in the lungs and clinical signs (R-Spearman = 0.64 and 0. 67 respectively, p < 0.05). No significant correlation between local cytokine concentration and systemic APP response were found.
Swine influenza is commonly characterized by fever, respiratory and systemic nonspecific symptoms (i.e. loss of appetite, apatia) . In the enzootic form, clinical signs may be less obvious. Subclinical infection is also quite common [17, 21, 22]. During uncomplicated infection the morbidity can be as high as 100% but the mortality is relatively low (ranges from less than 1% to 4%). The most common complications of swine influenza are secondary bacterial pneumonia and PRDC [3, 12]. Coinfections often lead to overproduction of cytokines that may be harmful to the host . There are several mechanisms, by which SIV infection predisposes to secondary bacterial infection, including: increased expression of cell receptors leading to increased colonization and modification of host immune responses (i.e. impairing of phagocytic function of alveolar macrophages) [23,24,25,26]. Furthermore, it has been shown that damage caused by SIV in the respiratory tract (i.e. loss of cilia, extrusion of mucus, exudation, necrosis and metaplasia of airway epithelium), can reduce the ability of the host to clear the bacterial superinfection [2, 21]. Hps is one of the pathogens which may complicate swine influenza and be one of the etiological agents of PRDC [2, 3, 8, 27].
The mechanism by which SIV affects the host’s susceptibility as well as its immune response to secondary bacterial infections has not been fully elucidated. Previous research reviled that interactions among multiple pathogens can lead to an exacerbated inflammatory response and increased severity of infections [12, 28,29,30]. For example, gross lesions in the lungs and magnitude of APP response in pigs co-infected with SIV and Pasteurella multocida were more intensive compared to animals infected only with SIV or Pasteurella multocida . Similar results were observed in pigs co-inoculated with SIV and A. pleuropneumoniae . Co-infection with SIV and A. pleuropneumoniae potentiated the severity of lung lesions caused by SIV and enhanced virus replication in the lung and nasal SIV shedding. Enhanced SIV replication contributed to a more severe clinical course of the disease as well as earlier and higher magnitude immune and inflammatory responses . Loving et al.  reported that SIV infection increased Bordetella bronchiseptica (Bb) colonization and increased the production of proinflammatory cytokines likely to exacerbate lung lesions. Pulmonary lesions in the co-infected pigs were more intense compared to SIV-only or Bb-only groups. The type I interferon, IL-1β and IL-8 were also significantly elevated in lungs of co-infected pigs.
There is limited data on the influence of SIV and Hps coinfection on the clinical course, kinetics of the immune and inflammatory response, as well as pathogen load and shedding . Both microorganisms are frequently isolated from respiratory tract of pigs in the field conditions [1, 27]. A previous study , investigating the role of prior SIV infection on the Hps colonization, revealed that Hps colonization was higher in the nose and lungs of SIV/Hps pigs compared to Hps-only pigs. These results indicate that SIV infection contributes to enhance bacterial colonization. In SIV/Hps pigs IL-8, IL-6 and IL-1β protein levels were increased in the tracheal wash and bronchoalveolar lavage fluid (BALF), and BALF cells IL-8, IL-6 and IL-1β mRNA expression levels were significantly increased over SIV-only and Hps-only pigs.
Based on the results of our study it could be stated that Hps did not cause significant lesions in the lung unless pigs were co-infected with SIV. No significant macroscopic lung lesions after experimental infection with Hps has been also reported previously . In the same study Hps was not isolated from Hps-single infected pigs. In our experiment we had been able to isolate of Hps in the case of 3 out of 11 Hps-single inoculated pigs, but in group co-inoculated with SIV the isolation was successful in 8 out of 11 animals. In the remaining groups (SIV and control) Hps was not isolated from lung. Typical systemic lesions of polyserositis were found in only one pig from co-inoculated group. In the present study no significant differences between gross lung lesions has been found between groups single or dually inoculated with SIV but in both groups lung score was significantly higher than in Hps-single inoculated group. In addition, more severe clinical signs were observed in dual inoculated pigs compared to single Hps- but not SIV-inoculated animals. The more severe clinical course of the infection was probably a consequence of more severe lung lesions present in pigs inoculated with SIV or SIV and Hps. Enhanced lung lesions in pigs single or dual inoculated with SIV could be a result of stronger replication of infective agents and more severe local inflammatory responses. Similarly as in the previous study  establishing that the titre of Bb was higher in the respiratory tract of SIV/Bb co-infected pigs, we found that SIV enhanced Hps colonization of the lung. In accordance to other experiment  the significantly higher SIV titre in the nasal swabs and lung was observed in co-inoculated pigs. Simultaneously, no effect of SIV on the Hps shedding has been found. These findings suggest that Hps can facilitate SIV replication in the respiratory tissue of dual inoculated pigs.
The significant influence of both pathogens on the systemic inflammatory response has been also found in the present study. In the groups inoculated with bacteria (single or dual) the APP response was in general higher than in virus-single inoculated animals. These findings are in accordance with the results of previous studies with various respiratory pathogens of swine [12, 19, 31, 32].
The results of our study revealed that coinfection with SIV and Hps modulates inflammatory responses, clinical course of disease and pathogen load within the respiratory tract in pigs. Co-infection with SIV potentiates the severity of lung lesions and facilitated Hps replication in the porcine lung. Furthermore, Hps influenced the SIV nasal shedding. Enhanced Hps and SIV replication, together with stronger systemic and local inflammatory response contributed to a more severe clinical signs, as well as stronger and earlier immune response in co-inoculated animals compared to single inoculated pigs. Moreover, we confirmed the previous evidence  that single-Hps infection does not produce significant pneumonic lesions but it should be in mind that other strains of Hps may produce lesions different from that reported in the present study.
The virus used in experiment (avian-like H1N1 A/Poland/Swine/14131/2014 (SIV)), had been isolated from the lung of pig suffering from acute swine influenza. This strain is representative H1N1 SIVs circulating recently in Poland. The stock used for nasal inoculation represented the third passage in eggs. The virus titre was evaluated in Madin-Darby canine kidney (MDCK) cells (ATCC).
Strain of Hps, previously isolated in National Veterinary Research Institute was selected for the experimental infections (isolate PIWetHps192/2015). Strain originating from lung of pig from Polish herd and the analysis of the 16S rRNA gene sequences  revealed 99% similarity to Hps isolate CN9–2 described by Olvera et al.  (classified as moderate virulent serovar 15).
To prepare the inoculum, the strain was streaked onto a pleuropneumonia-like organism (PPLO) agar (Becton Dickinson, USA), supplemented with 10 μg/ml of β-NAD (Sigma-Aldrich, Germany), 1 mg/ml glucose (Avantor Performance Materials, Poland) and 5% horse serum (Sigma-Aldrich, Germany), which was incubated for 24 h at 37 °C in an atmosphere of 8% CO2. Colonies were harvested and suspended in phosphate-buffered saline (PBS) (Life Technologies, USA) to 0.5 McFarland turbidity (which corresponds with approximately 1.5 × 108 colony forming units (CFU)/ml). A plate count was also performed to quantify the accurate number of viable bacteria (final result 1.2 × 108 CFU/ml of Hps strain).
Thirty seven 6-week-old piglets bought from a commercial farm, both sexes, were used in the study (as research animals). Piglets were randomly allocated to 4 groups (Hps (n = 11); Hps + SIV (n = 11); SIV (n = 11); control (n = 4) (a sample size calculation based on a resource equation method). The sourced herd was seronegative to P, pseudorabies virus and Mycoplasma hyopneumoniae. No evidence of streptococcosis, pleuropneumoniae, Glässers disease and atrophic rhinitis was recorded based on clinical, serological (detection of dermonecrotoxin specific antibodies and antibodies to ApxIV) and pathological examinations (turbinate lesions, polyserositis, polyarthritis, serofibrinous or fibrino-purulent exudate on mucosal surface, arthritis, meningitis). Before the start of the study all piglets were free of influenza A virus and Hps antibodies as determined by haemagglutination inhibition assays (HI) using A/Poland/Swine/14131/2014 (H1N1), A/swine/England/96 (H1N2), A/swine/Flanders/1/98 (H3N2), pdm-like H1N1 (A/swine/Poland/031951/12) and Swinecheck® HPS ELISA test (Biovet, Canada).
During the experiment research animals were housed on a (Biosafety Level-3) BSL3 animal facility in four independent units. Animal use and handling protocols were approved by II Local Ethical Commission for the Animal Experiments of University of Life Sciences in Lublin (number of approval: 77/2014).
The animals were acclimatized to BSL3 hygienic conditions for 7 days before commencing the experiment. On day 0, piglets from SIV and Hps + SIV groups were inoculated intranasally (IN) with SIV (106.8TCID50 in 3 ml of PBS. Piglets from Hps and Hps + SIV groups were inoculated IN with Hps (3.6 × 108 CFU Hps in 3 ml of PBS. Four mock-inoculated pigs served as controls.
Pigs were examined daily from day - 7 to 10 post inoculation (DPI) or until euthanasia (at 2 and 4 DPI). Animals were observed and scored for the respiratory signs as follows: respiratory rate: 0 – normal (<34 breaths/min), 1 – slightly elevated (35–40 breaths/min), 2 – moderately elevated (41–45 breaths/min), slight abdominal breathing, 3 – clearly elevated (>46 breaths/min), distinct abdominal breathing; nasal discharge 0 – absent, 1 present; coughing 0 – absent, 1 present; sneezing 0 – absent, 1 present, anorexia 0 – absent, 1 present . Rectal temperature was also measured daily. Hyperthermia was recorded when the rectal temperature reached 40 °C. If the fever was observed 1 additional point was added to the clinical score. All scores per topic were accumulated for a final clinical score calculated for each pig (0–8).
Nasal swabs were collated daily from all animals (at −7, 0 (inoculation), 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10 DPI). Blood samples were collected at −7, 0 (inoculation), 1, 2, 3, 5, 7 and 10 DPI. Three piglets per inoculated groups were euthanized at 2 and 4 DPI. The remaining inoculated as well as control pigs were euthanized and necropsied at 10 DPI. Complete necropsy was done on each animal, with special emphasis on the respiratory tract. Lung lesions were scored using the method developed by Madec and Kobisch  according to the scheme presented in details previously . Samples from lung (apical, middle, caudal right lobes and accessory lobe) were collected for further analyses.
Pathogen shedding and load
SIV titration (nasal swabs, lung tissue) in Madin-Darby canine kidney cells (MDCK) (ATCC) were performed in duplicate as described previously .
For determination the quantity of Hps in samples collected from piglets (nasal swabs and lung tissue fragments) the quantitative real-time PCR was used (all samples were tested in duplicate) . It targets the 392–466 bp region of the inf B gene of Hps. Nasal swabs were placed into centrifuge tubes (2 ml), suspended in 1 ml of PBS and after 10 min vortexed for 30 s. The liquid was collected to the new tube (1.5 ml) and suspensions were centrifuged at 3000 g during 3 min. The supernatant was discarded and the remaining pellet was resuspended in 100 μl of TRIS buffer (10 mM Tris–HCl pH 8.5) and vortexed for an additional 30 s. Homogenates (50% wt/vol) of middle right lobe (the main site of gross lesions observed in the present study) were prepared in PBS. DNA was extracted from thus prepared samples using the Genomic Mini DNA isolation kit (A&A Biotechnology, Poland) according to the manufacturer instructions. DNA was stored at −70 °C for further analysis.
All sera were examined using HI assays (SIV) against challenge strain and ELISA test against Hps as directed by the manufacturer (Swinecheck®HPS, Biovet, Canada). The presence or absence of antibodies to investigated antigen (Ag) was determined by calculating the ELISA ratio. ELISA ratio (Er) was calculated according to the following formula:
(+) - positive control
Antibodies against SIVs were measured using a HI assay, performed according to the standard procedure, using 0.5% chicken erythrocytes and 4HA units of challenge strains . All sera were tested in serial twofold dilutions, starting at 1:20. For estimates of the prevalence of antibodies, titres ≥20 were considered positive . For statistical analyses the titres lower than 20 was set as 5.
Acute phase proteins (C-reactive protein (CRP, haptoglobin (Hp), serum amyloid A (SAA) and pig major acute phase protein (Pig-MAP)) were examined using ELISA assays according to producer’s recommendations (Pig C-reactive protein ELISA and Pig haptoglobin ELISA from Life Diagnostics, USA; Pig-MAP KIT ELISA from Acuvet Biotech S.L., Spain; Phase Serum Amyloid A Assay from Tridelta Development Ltd. County Kildare, Ireland). All serum samples were tested in duplicate.
Lung proinflammatory cytokine levels
Lung tissues were collected from pigs during necropsy and prepared in PBS (pH 7.4) [12, 16]. 1.0 g of the lung tissue fragments were suspended in 1 ml of PBS, respectively (1:1 w/v), and frozen before being homogenized. After homogenization, with the use of tissue homogenizer X620 (CAT, Germany), the samples were centrifuged at 3000 g for 10 min. The supernatants were collected and stored at −80°C before cytokines analysis was performed using ELISA assay. The ELISA kits specific for porcine cytokines: IL-10, IFN-γ and TNF-α were bought from Invitrogen Corporation (Camarillo, USA), and these used for IL-1β were bought from RayBiotech, Inc. (Norcross, USA). The concentration of IL-6 was determined with the use of IL-6 Pig ELISA Kit from Abcam (Cambridge, UK). All tests were performed in duplicate according to the manufacturers’ recommendations. The quantity of the cytokines was calculated based on standard curve for each cytokine with the use of FindGraph software.
The data were subjected to the W. Shapiro-Wilk’s test of normality and the Levene’a test of equal variances with STATISTICA 8.0 (StatSoft). Differences between means were tested for statistical significance by a nonparametric Kruskal - Wallis test with post hoc multiple comparisons for comparison of all pairs. The Friedman test was used to compare observations repeated on the same subjects. For analysis of correlation the Spearman Rank correlation test was used. For all analyses, p < 0.05 was considered statistically significant.
Acute phase proteins 19
Colony forming unit
Day post infection
Phosphate buffered saline
Pig major acute phase protein
Porcine respiratory disease complex
Porcine reproductive and respiratory syndrome virus
Serum amyloid A
Swine influenza virus
50% tissue culture infective dose
Tumor necrosis factor alfa
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The authors wish to thank Ewelina Stasiak and Barbara Frącek for technical assistance.
This work was supported by The National Science Centre (DEC-2014/13/B/NZ6/02566) and by KNOW (Leading National Research Centre) Scientific Consortium, “Healthy Animal - Safe Food”, a decision of Ministry of Science and Higher Education, No. 05–1/KNOW2/2015 (K/02/1.1; K/02/5.0). The funders of the study had no role in study design or conclusion of present study.
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Animal use and handling protocols were approved by II Local Ethical Commission for the Animal Experiments of University of Life Sciences in Lublin (number of approval: 77/2014).
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Pomorska-Mól, M., Dors, A., Kwit, K. et al. Coinfection modulates inflammatory responses, clinical outcome and pathogen load of H1N1 swine influenza virus and Haemophilus parasuis infections in pigs. BMC Vet Res 13, 376 (2017) doi:10.1186/s12917-017-1298-7
- Respiratory co-infections
- Disease severity
- Pathogens shedding