- Open Access
Coinfection with Haemophilus parasuis serovar 4 increases the virulence of porcine circovirus type 2 in piglets
Virology Journalvolume 14, Article number: 227 (2017)
Postweaning multisystemic wasting syndrome (PMWS) is an emerging disease in swine. Pigs with PMWS are often infected with a variety of other pathogens, including bacteria, viruses and mycoplasm, in addition to porcine circovirus type 2 (PCV2). PCV2 and Haemophilus parasuis serovar 4 (HPS4) coinfection remain epidemic in China.
Here we report construction of a three-week-old naturally farrowed, colostrum-deprived (NFCD) piglet’s infection model and demonstrate that PCV2-infected piglets with the HPS4 coinfection increased the virulence of PCV2 and these pathogens interact acquired PMWS.
All the single infected piglets were transiently bacteremic or viremic. All the PCV2/HPS4 coinfected piglets developed PMWS, characterized by dyspnea, anorexia, prostration and lose weight severely. Co-infection with PCV2 and HPS4 resulted in an increased amount of virus in serum and tissues, presented a slower generation and lower levels of antibodies against PCV2. Co-infection with PCV2 and HPS4 resulted in further reductions in total and differential peripheral blood leukocyte counts. Meantime, PCV2/ HPS4 coinfection potentiated the severity of lung and lymphoid lesions by PCV2-associated, increased the virulence of PCV2-antigen and enhanced the incidence of PMWS in piglets.
Co-infection with PCV2 and HPS4 induce the exacerbation of system injuries and enhance the pathogenicity of PCV2 in piglets.
Porcine circovirus type 2 (PCV2) has been identified as the causal agent of postweaning multisystemic wasting syndrome (PMWS), an economically important multifactorial disease of swine industry worldwide [1, 2]. PMWS is characterized by weight loss, jaundice, generalized lymphadenopathia, interstitial pneumonia and nephritis . Based on the broad clinical and serological investigations, Multiple factors have contributed the PCV2 infections as PMWS, such as porcine reproductive and respiratory syndrome virus(PRRSV), porcine parvovirus (PPV), Haemophilus parasuis(HPS), and Actinobacillus pleuropneumoniae (APP), a variety of viral and bacterial pathogens in the majority of cases (85.0%) [4, 5].
HPS is an important swine pathogen that causes Glässer’s disease, which is characterized by fibrinous polyserositis, meningitis and arthritis . Clinically, HPS co-infection with other pathogens, such as PRRSV, PCV2, Streptococcus suis (SS) and Pasteurella multocida (Pm), lead to increasing economic losses in the swine industry worldwide [5,6,7,8]. Previous observations indicated that PCV2 and HPS exacerbate secondary or opportunistic infections, co-infection with PCV2 and HPS was the most prevalent combination associated with PMWS in Korea and China, HPS serovar 4 (24.2%) and HPS serovar 5 (19.2%) were the most prevalent serovars in China [5, 8, 9]. Therefore, We established a porcine model to elucidate the clinical changes of PCV2 and HPS4 co-infection, using clinical isolates of PCV2 genotype 2b WH strain and HPS4 MD0322 strain isolated from china, based on the protocol for coinfection model establishment proposed by Harms et al. . We firstly measured the clinical and peripheral blood changes of PCV2 and HPS4 co-infection, in order to analyze the synergistic influence on the virulence of PCV2 in piglets.
Experimental design and inoculations
Three-week-old naturally farrowed, colostrum-deprived (NFCD) piglets were used, obtained from a herd in Hubei province without PCV2, PPV, PRRSV, SS2 or HPS pathogen. All piglets were randomly divided into four groups (six piglets per group) and raised separately in four isolation rooms with individual ventilation. Animals received food and water ad libitum. After one week, all piglets were inoculated and slaughtered at 28 day post infection (DPI). The Clinical separated strain PCV2 genotype 2b (WH) was used as the source of viral inoculums (GenBank ID:FJ870967). The titer of the virus was calculated as 107.3 TCID50/ml. HPS4 strain MD0322 was used as the source of bacterial inoculums. It was isolated from the Zhijiang city of Hubei province emergency on August 2001 as the cases of fibrinous, polyserositis and arthritis in piggery. The bacterial inoculum contained approximately 4.5 × 108 colony- forming units (CFU)/ml. The piglets in the PCV2-infected group and PCV2/HPS4 coinfected group were intramuscularly (IM; 2.5 ml) and intranasally (IN; 2.5 ml) inoculated with the WH strain of PCV2. The pigs in the HPS4-infected group and PCV2/HPS4 coinfected group were IM (2.5 ml) and IN (2.5 ml) inoculated with the HPS4 strain MD0322. The piglets in the control group were inoculated with DMEM in the same way. All animal experiments were complied with the requirement of animal welfare organizations and approved by the Biological Studies Animal Care and Use Committee of the Hubei Province, People’s Republic of China.
After PCV2 and HPS4 challenge, piglets were monitored daily and scored for clinical signs including rectal temperatures, prostration, dyspnea, cough, anorexia, limping vomiting and other symptoms: MO mortality, TR trembling, CY cyanosis, DI diarrhea. The piglets were observed and weighed from 3 days prior-challenge to 28 days post-challenge, finally slaughtered at 28 DPI. Clinical Observation Record is summarized in Table 1.
Detection of antibodies to PCV2 by indirect ELISA
Blood samples were collected on 0, 1, 3, 5, 7, 14, 21 and 28 DPI. Anti -PCV2 ORF2 antibodies were tested by enzyme-linked immunosorbent assays (ELISA) as Chun described previously . The calibrated OD for each tested and control serum was calculated by subtraction of mean OD of the wells containing negative antigen from that of the parallel wells containing PCV2 antigen. The data were normalized by dividing the calibrated OD of a tested serum sample by that of the positive control serum and were reported as the sample/positive (S/P) ratios. The samples with serum sample/positive control serum ratios of ≤0.2 and >0.2 were considered negative and positive, respectively. In addition, the calibrated OD for the positive serum control had to be equal or higher than 0.4 for the assay to be valid.
Quantification of PCV2 genomes by real-time PCR in tissues
Tissues were grinded into homogenate supernatants and Virus DNA was extracted with Viral DNA Kit (OMEGA, USA). Viral loads in tissues were quantificated by a TaqMan real-time PCR . The reactions were performed on an ABI Prism 7500 thermocycler (Applied Biosystem, Foster City, CA, USA).
Total white blood cell (WBC) counts
Total WBC counts in EDTA-stabilized blood were measured using Beckman-Coulter Ac.T diff 2 automated haematological analyzer (Coulter Corp, A Beckman Coulter Co, Miami, Florida).
All piglets were inoculated and slaughtered at 28 DPI. Samples of lung, lymph nodes, tonsil, kidney, spleen, heart, liver and brain were collected and fixed in 10% neutral buffered formalin for 2–4 days, then embedded in paraffin for hematoxylin and eosin (HE) straining. Histopathology examination was observed with optical microscope (Olympus).
The data were analyzed using independent sample T-test with the computing software Statistical Package for the Social Sciences (SPSS), and the results were expressed as mean value ± standard error of the mean (S.E.M.). A P-value of results was considered significant at probability (P-values ≤0.05).
The piglets in PCV2-infected and PCV2/HPS4 coinfected group had fever (rectal temperatures >40 °C) and severe emaciation than control and HPS4-infected group. The average daily gain of PCV2-infected group (263.10 ± 41.01 g/day), PCV2/HPS4 coinfected group (227.38 ± 42.96 g/day) or HPS4-infected group (333.33 ± 90.02 g/day) was statistically significant (p < 0.05) for control group (437.05 ± 21.35 g/day) respectively. PCV2-infected piglets exhibited prostration (4/6), dyspnea (3/6) and anorexia (2/6), 2 piglets appeared severe trembling and diarrhea at 8–14 DPI. The HPS4 infected piglets showed mild trembling (2/6), limping (5/6) and palpebra hyperemia (4/6). Among the PCV2/HPS4 coinfected piglets by clinical observation, 5 piglets exhibited prostration, pyrexia, lymphadenectasis and bloody ocular secretions at 3 DPI, and 3 piglets showed severe cough, dyspnea, anorexia and diarrhea at 6 DPI. All piglets exhibited varying degrees of joint swelling or limping, and 2 piglets led to posterior limb paralysis finally. The relevant clinical data are shown in Table 1.
Co-infection with PCV2 and HPS4 resulted in an increased amount of virus in serum and tissues
No PCV2 antigen was detected in control or HPS4-infected group by Real-time PCR in the whole experiment. The kinetics of serum viral loads was shown in Fig. 1. PCV2-infected or PCV2/HPS4 coinfected group exhibited a dramatic increase in PCV2 serum load from 3 DPI. Meanwhile, the PCV2 viral loads in PCV2/HPS4 coinfected piglets were significantly higher than in PCV2-infected piglets at 21 DPI and 28 DPI, the maximum level of which in PCV2/HPS4 coinfected piglets reached to 1.87 × 108 copies/ml at 21 DPI. The PCV2 genome loads in tissues are summarized in Fig. 2. All piglets in PCV2-infected and PCV2/HPS4 coinfected groups contained PCV2 antigen in the heart, liver, spleen, lung, kidney, lymph nodes and tonsil. 5 piglets in coinfected group and 3 piglets in PCV2-infected group contained PCV2 antigen in the brain. The maximum value of PCV2 genome loads reached to 2.04 × 1010 copies/g in PCV2-infected (2.04 × 1010 copies/g) and 3.17× 1010 copies/g in PCV2/HPS4 coinfected piglets from the tonsil. The PCV2 loads of heart, lung, kidney, brain and lymph nodes in PCV2/HPS4 coinfected piglets were significantly higher (p < 0.05) than that in PCV2-infected piglets.
Co-infection with PCV2 and HPS4 resulted in slower generation and lower levels of antibodies against PCV2
Indirect ELISA was performed to detect antibodies against PCV2. The mean PCV2 antibodies S/P (sample/positive) ratios of pig serum collected were determined (Fig. 3). All piglets were negative for antibodies against PCV2 before inoculation. The control and HPS4-infected group remained seronegative to PCV2 throughout the experiment. PCV2-specific antibodies were seroconverted at 14 DPI in PCV2 group, and in PCV2/HPS4 coinfected group, antibodies to PCV2 were detected for the first time at 14 DPI in 3 piglets, and at 21 DPI in the other 3 piglets. The levels of the PCV2 antibody were lower in PCV2/HPS4 coinfected group than that in PCV2-infected group during the whole experimental period and were significantly lower at 14 and 28 DPI.
Co-infection with PCV2 and HPS4 resulted in further reductions in total and differential peripheral blood leukocyte counts
The total number of WBC in PCV2/HPS4 coinfected group was significantly decreased at 3, 7 and 14 DPI in comparison to the other three groups (Fig. 4a), and the total WBC Count in PCV2-infected group was significantly lower than the other three groups at 14 DPI. However, the WBC counts in HPS4-infected group appeared significantly higher than the other three groups from 3 DPI to 7 DPI. The total number of monocytes in PCV2/HPS4 coinfected group was significantly lower at 3, 5, 7 and 14 DPI compared to the control and HPS4-infected group (Fig. 4b), while the number of monocytes in PCV2-infected group decreased significantly at 3, 5 and 7 DPI in comparison to the control group. The number of peripheral blood lymphocytes in PCV2/HPS4 coinfected group was significantly reduced at 3, 5 and 14 DPI in comparison to the control and HPS4-infected group (Fig. 4c). Compared with the control group, the total number of lymphocytes in PCV2-infected group decreased significantly at 3, 5 and 7 DPI, while the number of lymphocytes in the HPS4-infected group was significantly lower at 7 DPI. The number of granulocytes in HPS4-infected group significantly increased at 5 and 7 DPI in comparison to the control group (data not shown).
Co-infection with PCV2 and HPS4 resulted in severe microscopic lesions
The pathological lung lesions in PCV2/HPS4-coinfected piglets showed severe widened alveolar septa and lymphocytes infiltration (Fig 5a). The lymphoid nodes lesions showed severe lymphocyte depletion and disintegration (Fig 5b). The kidney lesions in PCV2/HPS4-coinfected piglets included mild focal hyperplasia of the mesenchymal cells (Fig 5c). The histopathologic lung lesion in PCV2-infected group mainly exhibited a small amout of lymphocytes infiltration (Fig 5d). The lymphoid nodes lesions showed a considerable degree of depletion, and germinal center atrophy in lymph nodule (Fig 5e). The kidney lesions in showed renal vein expansion and congestion (Fig 5f). The lungs lesions in HPS4-infected group followed by lymphocytes infiltration and widened alveolar septa (Fig 5g). No obvious lymphoid nodes lesions were observed (Fig 5h), and the kidney lesions were swelling in epithelial cells of proximal tubule (Fig 5i). No pathological lesions were observed in control group tissues (Fig. 5j-l).
PMWS is one of the most significant porcine diseases worldwide, and the causative agent is porcine circovirus type 2 (PCV2) [1,2,3].Several reports have confirmed that, the coinfection of PCV2 and HPS are pervasive in piglets, it has been a great threat in the pig industries globally [5, 7, 8]. The isolation rate of serovar 4 was most prevalent in China, similar results were also reported in North America [8, 13, 14]. In this study, we found that PCV2 alone cannot cause extensive damage to the host. The piglets coinfected with PCV2(WH) and HPS4 (MD0322) showed symptoms similar to PMWS: high fever, severe emaciation and lymphadenectasis. The HPS4 strain MD0322, an isolate obtained from a PMWS endemic area, was weakly pathogenic in piglets . In this study, the clinical symptoms of the HPS4-infected piglets were mild, because the self-healing capabilities of piglets may start within a short duration. However, the condition of piglets coinfected with PCV2 and HPS4 deteriorated rapidly, the rectal temperature of all piglets reached 41.5 °C at 7 DPI, and the symptoms of PMWS, such as severe weight loss and lymphadenectasis appeared at 3 DPI. Therefore, we suggest that even HPS4, which is a weak virulent serotype, can cause more damage significantly when coinfected with PCV2. This is the first report that PCV2-infected piglets with the HPS4 coinfection increased the virulence of PCV2 and the incidence of PMWS in experimental NFCD piglet’s model.
In this study, Our data demonstrated that PCV2/HPS4 co-infected piglets had higher viral loads and a longer viremia duration in comparison with PCV2 single infection. Meanwhile, co-infection with PCV2 and HPS4 resulted in an increased amount of PCV2 genome loads in heart, liver, spleen, lung, kidney, lymph nodes, especially from the tonsil. Bacterial lipopolysaccharide (LPS) induced PCV2 replication in swine alveolar macrophages , hence, HPS4 may enhance the PCV2 replication at the site of infection, finally increases the amount of PCV2 viral loads in lymphoid tissue and immune organs significantly. This suggests that co-infection with PCV2 and HPS4 induce the exacerbation of system injuries and aggravates the secondary bacterial infection.
Since the monocyte/macrophage cell lines are common targets of PCV2 virus , co-infection can result in immunomodulation and enhanced the replication of PCV2. The previous study showed a dramatic reduction in the number of B lymphocytes with PCV2 infection , and then B cells elimination may result in PCV2 antibody production limit and immunosuppression. That may explain the PCV2/HPS4 co-infected piglets showed a slower generation and lower amounts of PCV2-specific antibodies than that in piglets with PCV2 infection alone. This suggests that coinfection exacerbates depression of the host’s immune responses. So we measured the changes in total WBC, monocytes, lymphocytes and granulocytes to study the effects of PCV2 and HPS4 coinfection on the innate immune response of piglets. The total number of WBC, monocytes and lymphocytes in PCV2/HPS4 coinfected group was significantly decreased for about two weeks during the early stage of infection, which is consistent with the previous reports . Lymphocyte subpopulations are crucial elements of the immune system and pivotal for the control and elimination of viruses . The dramatic reduction of lymphocytes following infection reflected immunosuppression in the in PCV2/HPS4 coinfected piglets. Demonstration of viral DNA in blood with the concurrent serum antibody response to PCV-2 suggested that PCV-2 infection may be persistent. Persistent DNA viremia after onset of specific antibody indicates that developing humoral antibodies were ineffective in virus clearance after infection . Thus, PCV2 and HPS4 co-infection exhibited a greater reduction in immune effector cells, inhibited and exacerbated the depression the host defense more severely than either PCV2 or HPS4 infection alone, although produced lower antibodies response to PCV-2 which was ineffective in PCV2 virus clearance.
Several reports have confirmed that the main characteristic of PCV2 is the damaging effects on the host immune system, including interstitial pneumonia and lymphoid depletion, which facilitates the invasion of other pathogens and leads to the cases of PMWS . In this study, the lung and lymphoid tissues lesions showed severe widened alveolar septa and lymphocyte depletion than singly infected piglets. Segales et al. believed that PCV2 infection had compromised the effectiveness of host’s immune response against lungworms , thus triggering a diffuse, severe and fatal parasitic bronchopneumonia. The higher viral load in the lymph nodes likely reflected the fact that lymphoid organs are severely affected in PMWS animals . This result was consistent with the findings of previous reports the distribution of antigen and PCV-2 DNA in different tissues indicated that the lymphoid tissues of pigs with PMWS were the main sites of replication of PCV-2 . In addition, it is known that PCV-2 could infect dividing cells, macrophages and B lymphocytes, inducing apoptosis in B cells and causing lymphoid depletion . Lymphoid depletion was observed in most of the lymph nodes that were analyzed in PCV2/HPS4-coinfected group. The frequency of occurrence of microscopical lesions in the kidney was related to the viral load, and this finding can be explained by the fact that the kidney is known to be a site of immune complex deposition in animals with PCV-2 infection [22, 24]. PCV-2 induces the dramatic reduction of lymphocytes following PCV2 infection reflects immunosuppression , which may make pigs more susceptible to HPS infection, thereby secondary infection by HPS4 improved the distribution of the PCV2, further exacerbating the damage to the immune system and the pathological lesions to the lung, lymphoid tissues and kidney. The combined effect of PCV2 and HPS4 coinfection increased the host injuries significantly. Therefore, this study demonstrates that coinfection with HPS4 enhance the pathogenicity of PCV2 in piglets.
It has been demonstrated that dramatic reduction of lymphocytes following PCV2 infection reflects immunosuppression in the infected piglets , and PCV2 replication is enhanced by coinfection with viruses such as porcine parvovirus (PPV) [26, 27], PRRSV [10, 28], porcine epidemic diarrhoea virus (PEDV)  and porcine torque tenue virus(TTV) . Marion et al. considered PCV2 infection maked animals more susceptible to co-infections with PRRSV and Mycoplasma hyopneumoniae (Mhp), and vaccination against PCV2 alone could lower the incidence of coinfecting agents such as PRRSV and Mycoplasma hyorhinis (Mhr) in PMWS-affected animals [31,32,33]. There is also evidence suggesting that the commonality of porcine immune function target cells may play a key role in this synergism for these two viruses due to stimulation of the monocyte/macrophage lineage and other cells of the immune system [34, 35]. Opriessnig et al. reported that Mhp prior infection could up-regulating the macrophage proliferation and create an ideal environment for PCV2 replication . No matter the co-infection times of the two pathogens, Mhp might enhance PCV2 replication for multiple reasons . PCV2 also could be enhanced by indirect initiation of host cell replication by other pathogens. The cell cycle could be initiated by other pathogens if they infect the same cell as PCV2. Opriessnig et al. also found that PCV2 and S. typhimurium antigens were occasionally detected within the same macrophage-like cells . LPS is the main endotoxin of Gram-negative bacteria and released at high concentrations in the lungs during pulmonary infection with Gram-negative bacteria [39, 40]. Chang et al. found in PK-15 cells for both PCV2 antigens and nucleic acid were successfully demonstrated in LPS-treated PCV2-inoculated alveolar macrophages . Thus, we speculated that PCV-2 induced the dramatic reduction of lymphocytes following PCV2 infection reflects immunosuppression, which maked pigs more susceptible to HPS infection, according to the stimulation of the monocyte/macrophage lineage and other cells of the immune system by HPS surface component LPS, PCV2 could be initiated to replicate finally.
A positively synergistic interaction effect on the mRNA expression of CD14, TLR4 and TLR8 might enhance the production of pro-inflammatory cytokines such as IL-1β . Experimental exposure of pigs to LPS following porcine respiratory coronavirus (PRCV) infection has led to more severe respiratory disease and increased TNF-α and IL-1β levels . PRRSV infection often made the host more susceptibility to Haemophilus parasuis (HPS). The combination of PRRSV HN07–1 strain and LPS exhibits significant synergistic effects on the secretion of TNF-α and IL-1β produced by macrophages in response and in the induction of an increase CD14 expression in the porcine alveolar macrophages (PAMs) [43, 44]. The simultaneously and highly enhanced expressions of TLR4 and CD14 in PBMCs of pigs co-infected with PRRSV and PCV2 might render the animal vulnerable to secondary bacterial infection observed in the field . Fu et al. reported HPS can initiate innate immune responses and induce the production of inflammatory cytokines . HPS RNA could significantly enhanced HP-PRRSV infection-mediated inflammatory responses in PAMs to promote the enhancement of NLRP3 inflammasome activation and IL-1β secretion . Thus, we speculated that HPS enhanced PCV2 infection-mediated inflammatory responses, which effected on the mRNA expression of TLR4 and enhance the production of inflammatory cytokines TNF-α and IL-1β secretion by bacterial LPS stimulation and HPS RNA, which could induce the PCV2 replication.
In addition, the 70 kDa heat-shock proteins (Hsp70) is one of the most important heat shock proteins, it has been proposed as one of the candidate vaccine antigens of Mhp [48, 49], we have found the Hsp70 was up-regulated in microarray also showed significantly higher expression in H. parasuis serovar 5 infected samples than in the control samples . Evidence is growing that HSP70 plays important roles in the replication of many viruses, and it enhanced PCV2 genome replication and virion production via the interaction with PCV2 cap in vitro cells [49, 51, 52]. Thus we speculated that Hsp70 of HPS4 might be one of the factors that enhanced PCV2 replication. Taken together, we speculated that PCV-2 induced the dramatic reduction of lymphocytes following PCV2 infection reflects immunosuppression, which maked pigs more susceptible to HPS infection. The stimulation of the monocyte/macrophage lineage and immune response by surface component LPS, RNA and Hsp70 of HPS4, contributed to induce the PCV2 replication, thereby improved the distribution of the PCV2, further exacerbating the damage to the immune system and potentiating the severity of PMWS in pigs.
We have shown that the clinical manifestations of the coinfection model are similar to those observed during the PMWS epidemic in China. The HPS4 epidemic may have played a role in the occurrence and development of PMWS. The general level of importance of HPS4 has always been less than HPS5 because of the characteristic low virulence of the former. However, piglets coinfected with PCV2 and HPS4 exhibited serious clinical symptoms affecting multiple organs, especially the lungs, lymph nodes and kidney. Therefore, it is necessary to control bacterial infection by adopting measure to prevent and control PCV2 infection.
day post infection
enzyme-linked immunosorbent assays
Haemophilus parasuis serovar 4
naturally farrowed, colostrum-deprived
porcine alveolar macrophages
Porcine circovirus type 2
porcine epidemic diarrhoea virus
postweaning multisystemic wasting syndrome
porcine reproductive and respiratory syndrome virus
porcine torque tenue virus
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The project was supported by Merial Limited and the Program for National Agriculture Research System of China (nycytx-009).
This work was supported by China Agriculture Research System(CARS-36).
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