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A new S. suis serotype 3 infection model in pigs: lack of effect of buprenorphine treatment to reduce distress
BMC Veterinary Research volume 18, Article number: 435 (2022)
Streptoccocus suis (S. suis) is a major porcine pathogen causing meningitis, septicemia, arthritis and endocarditis. These diseases severely impair welfare of pigs. Experimental studies in pigs are important to better understand the pathogenesis and to identify protective antigens, as so far there is no vaccine available protecting against various serotypes (cps). Due to the severity of disease, application of appropriate refinement strategies in experimental S. suis infections is essential to reduce distress imposed on the piglets without jeopardizing the scientific output. The objectives of this study were to evaluate buprenorphine treatment as a refinement measure and serum cortisol levels as a distress read out parameter in a new S. suis cps3 infection model in pigs.
Intravenous application of 2 × 108 CFU of S. suis cps3 (sly+, mrp+) to 6-week-old piglets led to severe morbidity in approximately 50% of the animals. Main pathological findings included suppurative meningoencephalitis and arthritis as well as fibrinosuppurative endocarditis. Buprenorphine treatment (0.05 mg/kg every 8 h) did not prevent signs of severe pain, high clinical scores, moderate to severe pathologies or high levels of serum cortisol in single severely affected piglets. Significant differences in the course of leukocytosis, induction of specific antibodies and bactericidal immunity were not recorded between groups with or w/o buprenorphine treatment. Of note, clinically unobtrusive piglets showed serum cortisol levels at 2 and 5 days post infectionem (dpi) comparable to the levels prior to infection with cps3. Cortisol levels in serum were significantly increased in piglets euthanized due to severe disease in comparison to clinically unobtrusive pigs.
Different clinical courses and pathologies are induced after intravenous challenge of piglets with 2 × 108 CFU of this S. suis cps3 strain. The chosen protocol of buprenorphine application does not prevent severe distress in this infection model. Important parameters of the humoral immune response, such as the level of IgM binding to S. suis cps3, do not appear to be affected by buprenorphine treatment. Serum cortisol is a meaningful parameter to measure distress in piglets experimentally infected with S. suis and to evaluate refinement strategies. In this intravenous model, which includes close clinical monitoring and different humane endpoints, clinics and cortisol levels suggest convalescence in surviving piglets within 5 days following experimental infection.
Streptococcus suis (S. suis) is an invasive pathogen which has received increasing scientific attention because of its zoonotic potential and the emergence as the most important bacterial pathogen in weaning and growing piglets . This pathogen is very diverse as shown by serotyping and analysis of a pairwise distance matrix based on 16S rRNA or chaperonin 60 sequences [2,3,4,5]. Substantial differences in virulence between strains of different serotypes (cps) but also within certain cps such as cps2 and 9 have been demonstrated through experimental infections [6, 7]. The capsule of cps3 is distinct as it includes the rare diamino sugar di-N-acetyl-d-bacillosamine . Though several in vitro tests [9,10,11,12,13] have been established to read out various immune reactions, experimental infection of pigs is still important in S. suis research, e.g. to determine the protective efficacy of a vaccine candidate [14,15,16]. Although worldwide approximately 15% of reported S. suis diseases in pigs have been caused by cps3 , an infection model of this important cps in pigs has not been published.
S. suis infection might lead to severe clinical signs in association with septicemia, meningitis, arthritis and endocarditis [18, 19]. These diseases cause a substantial amount of distress and pain in pigs. However, analgesic treatment has not been described as a refinement measure in experimental infections of pigs with S. suis even though in laboratory animals opioid analgesics are frequently used for pain management [19,20,21]. Furthermore, they are the first analgesics considered for refinement in immunology models  and applied for postoperative analgesia in pigs  due to their strong analgesic effect. A discussed disadvantage of opioids is their immunomodulatory effect [24, 25]. However, buprenorphine has turned out to have little side effects on immunological parameters [19, 22]. As a partial receptor agonist, buprenorphine does not increase the release of immunomodulatory glucocorticoids  compared to other opioid analgesics. Since buprenorphine is able to reduce pain and lameness in pigs [26, 27] and due to the putative lack of a substantial immunomodulatory effect, we evaluated buprenorphine application post experimental infection as a refinement strategy. The experimental study was designed to read out putative effects of buprenorphine application on the humoral immune response, the distress of the piglets as determined by a clinical as well as a pain score and on cortisol levels in saliva and serum as a distress marker in the course of establishing a new S. suis cps3 model in pigs.
Clinics of S. suis cps3 infected piglets with or w/o analgesic buprenorphine treatment
Buprenorphine treatment was examined as a refinement strategy in an experimental S. suis study conducted to establish a new cps3 challenge model. We infected 6-week-old piglets intravenously with a sly+, mrp+ cps3 strain of sequence type (ST) 1187, designated 16667/3. After infection one group received an intramuscular (i.m.) injection of 0.05 mg buprenorphine/kg every 8 h for 5 days. Piglets were monitored every 8 h for clinical signs. Additionally, pain and clinical scores were raised (see Supplementary Tables 1 and 2, Additional file 1). The pain score emphasizes signs of severe distress and pain such as recumbency in association with acute polyarthritis. This score was introduced in this study to disclose, whether piglets infected experimentally with S. suis may not reach states of severe distress if treated early with buprenorphine. Piglets which showed signs of severe S. suis disease like polyarthritis, recumbency and central nervous disorder or reached a clinical score ≥ 25 were euthanized due to reaching humane endpoints. In the first experiment with an infection dose of 2 × 107 CFU, mortality was very low. Only one untreated (UT) piglet was humanly euthanized 2 d following intravenous (i.v.) infection due to signs of central nervous disorder like convulsions, tremor and opisthotonus (Fig. 1A). One buprenorphine-treated piglet (BT) showed signs of lameness, tremor and fever after experimental infection. However, as the piglet was still very active and had no anorexia, it did not reach the humane endpoints. In the first experiment 4 (n = 3 BT; n = 1 UT) out of 10 piglets showed clinical signs of lameness. Furthermore, within the first 5 days after infection, 4 out of 5 piglets of both groups (with or w/o buprenorphine treatment) showed an increased inner body temperature of ≥ 40.2 °C. In the second experiment with a higher infection dose of 2 × 108 CFU, 4 piglets, 2 BT and 2 UT, were recumbent due to high grade lameness on more than one limb (polyarthritis) or showed central nervous disorders and were euthanized 1 dpi. One further UT piglet acutely succumbed to S. suis disease (Fig. 1B). On the second day following infection, one BT piglet was euthanized due to ongoing moderate disturbed condition with intermittent fever, lameness and reduced appetite (Fig. 1B). Six (n = 2 BT, n = 4 UT) out of 16 piglets showed signs of low- to high-grade lameness. Elevated body temperature of ≥ 40.2 °C was recorded in 6 out of 8 piglets of both groups (UT and BT). Only 3 out of 10 and 4 out of 16 piglets showed no notable signs of S. suis disease in the first and second experiment, respectively. The higher infection dose in the second experiment led to higher morbidity and mortality rates in piglets. Piglets with mild clinical signs of disease recovered within 5 dpi in both experiments. However, swollen joints lasted longer in a few piglets. In both experiments BT piglets were more active within half an hour after analgesic injection during the whole treatment period. No negative side effects were observed as a result of buprenorphine treatment. For a comparison of the groups, the sum of the maximal clinical and pain scores in each group were divided by the number of animals to calculate γ and δ, respectively. In the first experiment, UT and BT piglets (each n = 5) reached γ values of 7.8 (± 9.93 SD) and 8.0 (± 6.04 SD), respectively. In the second experiment with the higher infection dose, γ values of 13.6 (± 10.78 SD) and 13.8 (± 10.38 SD) were obtained in UT and BT piglets, respectively (n = 8 per group, Table 1). In the latter experiment, the mean maximal pain scores δ also reached comparable values in UT and BT piglets with 23.0 (± 23.0 SD) and 21.6 (± 20.6 SD), respectively. In the first experiment with the lower infection dose, UT and BT (n = 5) piglets showed δ values of 13.2 (± 20.8 SD) and 8.8 (± 7.3 SD), respectively (see Supplementary Table 3, Additional file 2). The higher value for the UT piglets resulted from the one piglet with central nervous disorder. In summary, significant differences between UT and BT piglets in mortality (Fig. 1A + B); morbidity (Fig. 1C + D) or severe morbidity (Fig. 1E + F) were not recorded. Application of 0.05 mg buprenorphine/kg for 5 days i.m. every 8 h post infectionem did not prevent high clinical and pain scores in affected animals and did not result in substantially lower mean clinical or pain scores.
Post mortem findings of S. suis cps3 infected piglets with or w/o analgesic buprenorphine treatment
Bacteriological and histopathological investigations of all euthanized piglets were conducted with predefined tissue samples and swabs (n = 15 samples per animal) (see Tables 2 and 3). In all mortally ill piglets except one, the challenge strain was isolated from typical samples such as cerebrospinal fluid (CSF) and joint fluid in association with central nervous system disorder and lameness, respectively (Table 2). In three UT and two BT piglets infected with 2 × 108 CFU, the cps3 challenge strain was isolated from multiple inner organs, indicating a disseminated infection. These five piglets were euthanized early as they reached predefined humane endpoints. The challenge strain was not detected in inner organs of the piglet euthanized 2 dpi and in the surviving piglets. We applied a scoring system for fibrinosuppurative lesions which we have been using for many years of S. suis research [14, 28, 29]. This includes calculation of ω as the mean maximal score of each group. UT piglets reached a lower histopathological score of ω = 1.6 compared to BT piglets with ω = 2.5 (see Table 3). Three piglets (one UT and two BT) showed severe fibrinosuppurative meningoencephalitis (Fig. 2A; Table 3). Furthermore, acute fibrinosuppurative endocarditis valvularis was detected in one BT piglet euthanized 1 dpi (Fig. 2B), whereas another UT piglet euthanized 13 dpi had a subacute to chronic endocarditis including granulation tissue. In addition, mild to severe fibrinosuppurative arthritis was detected in 2 piglets of each group (Table 3). Three of these piglets were euthanized 1 dpi due to severe clinical signs in association with acute fibrinosuppurative arthritis (Fig. 2C). In contrast, histopathological findings of the fourth piglet, which survived until the end of the observation period (13 dpi) showed subacute to chronical fibrinosuppurative arthritis including lymphocytes and granulation tissue (Fig. 2D). Except for one piglet, fibrinosuppurative lesions were detected in all prematurely euthanized piglets.
Impact of buprenorphine treatment on the development of antibody and blood leukocyte levels after experimental S. suis cps3 infection
As the immune response of pigs after experimental S. suis infection is an important issue in vaccine and pathogenesis studies [15, 30,31,32], the impact of repeated buprenorphine application on the antibody response and number of blood leukocytes after experimental infection was investigated. Anti (α) S. suis 16667/3 IgM and IgG antibody levels were determined pre infectionem (pre inf), 5 dpi and at the end of the observation periods 21 dpi or 13 dpi in the first and second experiment, respectively. Piglets prematurely euthanized post infection were not included in this analysis. In the first experiment, a significant increase in αS. suis 16667/3 IgM antibodies was determined in the UT group (n = 4) with mean ELISA units of 58.1 (± 12.0 SD) pre inf and 164.8 (± 81.4 SD) ELISA units 5 dpi (Fig. 3A). A comparable increase was recorded in the BT group (n = 5), though differences were not significant (Fig. 3A). Whereas in the second experiment a significant increase in αS. suis 16667/3 IgM antibodies was shown for UT (n = 5) and BT (n = 5) piglets with a mean of 75.4 (± 34.9 SD) and 68.9 (± 19.4 SD) ELISA units, respectively, pre inf to a mean of 281.7 (± 145.0 SD) and 343.5 (± 243.0 SD) ELISA units 5 dpi. Mean ELISA units decreased in both groups from 5 to 13 dpi (Fig. 3B). No significant differences in αS. suis 16667/3 IgM antibody levels between UT and BT piglets were recorded at any investigated time point. In both experiments no significant change in αS. suis 16667/3 IgG levels were detected in both groups (Fig. 3C + D). αS. suis 16667/3 IgG antibodies were not significantly different in UT and BT treated piglets.
In both experiments blood leukocytes increased after experimental infection of pigs with cps3 strain 16667/3. In the first experiment, an increase of mean leukocytes from 13.0 G/L (± 4.6 SD; UT n = 5) and 14.2 G/L (± 3.5 SD; BT n = 5) pre inf to 26.4 G/L (± 14.3 SD; UT) and 23.0 G/L (± 3.5 SD; BT) was detected 2 dpi. Mean leukocytes of the UT group 2 dpi included one piglet which had reached the humane endpoint and was euthanized with blood leukocytes of 50.4 G/L. Blood leukocytes decreased to about 20.0 G/L at 5 dpi in both groups (n = 4/UT; n = 5/BT) (see Supplementary Fig. 1A, Additional file 3). In the second experiment, blood leukocytes of UT and BT piglets rose from a mean of 14.6 G/L (± 5.1 SD; n = 8) and 16.6 G/L (± 4.3 SD; n = 8) to a mean 2 dpi of 19.9 G/L (± 4.2 SD; n = 5) and 27.7 G/L (± 9.4 SD; n = 6), respectively. Mean leukocytes 2 dpi of the BT group included a piglet prematurely euthanized because of reaching humane endpoints with blood leukocytes of 40.0 G/L. One dpi further piglets were prematurely euthanized and showed mean leukocytes of 23.4 G/L (± 13.1 SD; UT n = 3) and 17.9 G/L (BT; n = 1) (see Supplementary Fig. 1B, Additional file 3). However, mean leukocytes of the UT group 1 dpi included a pig succumbing to acute disease with very low blood leukocytes of 9.3 G/L. No significant differences between UT and BT pigs were determined in both experiments.
Impact of buprenorphine treatment on bactericidal immunity against S. suis
The bactericidal assay is used by different groups as an in vitro assay in S. suis studies to assess killing of this pathogen in blood, e.g. after vaccination of piglets [14, 29, 33, 34]. Killing of S. suis in porcine blood is mediated by opsonizing IgM and IgG antibodies and complement activation on the bacterial surface . Bacterial survival of the cps3 S. suis challenge strain (16667/3) was investigated prior to experimental infection in both experiments. The S. suis cps3 strain 16,667/3 proliferated in later UT and BT piglets prior to infection with a SF of 117.8 (± 13.50 SD) and 90.6 (± 32.75 SD) in the first experiment as well as 99.2 (± 18.79 SD) and 80.0 (± 36.13 SD) in the second experiment, respectively (see Supplementary Fig. 2A, Additional File 4). Five dpi no differences in survival of the cps3 strain were detected between UT and BT piglets, as the strain was efficiently killed (SF = 0.0) in both groups and experiments. Survival of the heterologous cps4 and cps14 strains in porcine blood was also investigated 5 d after infection with the high dose of 2 × 108 CFU (Supplementary Fig. 2B, Additional file 4). The cps4 strain 17434 proliferated in both groups with a mean survival factor (SF) of 46.7 (± 12.93 SD) in the UT group (n = 5) and a mean SF of 52.5 (± 8.73 SD) in the BT group (n = 5). In contrast, the S. suis cps14 strain V3117/2 was killed in both groups with a mean SF of 0.09 (± 0.16 SD) and 0.03 (± 0.06 SD) in the UT and BT group, respectively (Supplementary Fig. 2B, Additional file 4). We measured microbial adhesion to hydrocarbons (MATH) of the S. suis strains to collect hints for reduced capsule expression. As shown in Supplementary Fig. 3 (Additional file 5), the MATH assay revealed comparable values of S. suis cps3 strain 16667/3, cps4 strain 17434 and cps14 strain V3117/2 and significant differences to the unencapsulated mutant 10cpsΔEF for all three strains. This indicates that all three wt strains investigated in the bactericidal assay are encapsulated. In summary, differences in bacterial survival in blood drawn from BT treated and untreated piglets were not recorded.
In the first experiment, we conducted a further bactericidal assay 21 dpi which included a comparison with littermates sampled in the original herd. Whereas S. suis cps3 was again efficiently killed in blood drawn from all UT experimentally infected piglets, it showed high proliferation rates in blood of the non-infected littermates (Supplementary Fig. 2C, Additional file 4). However, levels of IgM and IgG binding to immobilized S. suis cps3 were not significantly different between cps3-infected and non-infected piglets (Supplementary Fig. 2C, Additional file 4). In conclusion, experimental S. suis cps3 infection results in immunity leading to efficient killing of S. suis cps3 in porcine blood.
Serum and saliva cortisol levels in pigs infected with S. suis cps3 with or w/o buprenorphine treatment
Cortisol is a common parameter to measure distress in pigs, as it increases during pain induced stress . We measured serum and saliva cortisol levels as a putative distress marker in piglets experimentally infected with S. suis to further evaluate buprenorphine treatment as refinement. First, we focused on the piglets that survived until the end of the observation period of 21 (first experiment) or 13 d (second experiment). In the first experiment with an infection dose of 2 × 107 CFU, no substantial differences in blood cortisol levels were found between UT (n = 4) and BT (n = 5) piglets post S. suis infection, apart from higher cortisol levels 2 dpi in the BT group with mean cortisol levels of 16.9 ng/ml (± 19.52 SD) compared to the UT group with 10.9 ng/ml (± 3.64 SD) (see Supplementary Fig. 4, Additional file 6). This difference was due to one piglet in the BT group with a serum cortisol level of 51.0 ng/ml. This piglet showed temporally lameness, kyphosis, tremor and anorexia 1 dpi. In the first experiment, cortisol levels pre inf and 21 dpi were generally higher (> 20 ng/ml) compared to the other time points (see Supplementary Fig. 4, Additional file 6), although piglets were clinically healthy. Blood sampling was carried out during anaesthesia at these time points which may explain the results. Accordingly, all serum samples used for the assessment of cortisol levels in the second experiment with an infection dose of 2 × 108 CFU were taken without anaesthesia. No significant differences in cortisol levels were recorded between groups of the second experiment pre inf, 5 dpi and 12 dpi. Mean cortisol levels were below 14 ng/ml at all three time points (Fig. 4A). However, a significantly higher mean cortisol level was determined in the UT group (n = 5) 2 dpi with 17.9 ng/ml (± 17.2 SD) compared to 6.2 ng/ml (± 1.5 SD) in the BT group (n = 5) (Fig. 4A). In the UT group one piglet obtained a very high serum cortisol level of 48.2 ng/ml 2 dpi in association with lameness, kyphosis and local tremor.
In the second experiment with the higher infection dose we additionally collected saliva every day for 6 days following infection to measure cortisol levels in saliva. We excluded mortally ill piglets due to the obligation to euthanize these piglets already 1 and 2 dpi. Significant differences in saliva cortisol levels were not recorded with or w/o buprenorphine treatment (Fig. 4B). Of note, one piglet in each group showed elevated saliva cortisol levels with values above 5 ng/ml 1 dpi. These piglets showed clinical signs of disease such as elevated inner body temperature (≥ 40.2 °C), reduced behavior and high-grade lameness. Additionally, one of these piglets showed anorexia, kyphosis and local tremor. All other cortisol values were below 5 ng/ml and thus comparable to the values pre inf. These results suggest that piglets do not go through severe distress post i.v. S. suis infection as long as they are clinically unobtrusive.
To evaluate cortisol as a distress marker in piglets experimentally infected with S. suis, serum cortisol levels of healthy piglets drawn under anaesthesia at the end of the observation period of 13 dpi were compared to levels in serum samples drawn from anaesthetized, mortally ill piglets prior euthanasia 1 dpi and 2 dpi. Highly significant differences between the aforementioned groups were found with mean cortisol levels of 29.8 ng/ml (± 9.52 SD) in healthy (n = 10) and 68.0 ng/ml (± 29.54 SD) in mortally ill (n = 6) piglets (Fig. 4C). These results show that cortisol is a meaningful distress marker in piglets infected experimentally with S. suis and confirm the importance of humane endpoints and a close clinical monitoring as refinement. However, buprenorphine treatment did not prevent high serum cortisol levels in diseased piglets. Furthermore, it does not indicate differences of saliva cortisol levels in clinically unobtrusive piglets infected with S. suis cps3.
Experimental infections of pigs and mice with different S. suis strains have revealed that there are substantial differences in virulence between strains of different cps but also within certain cps such as cps2 [36, 37]. This includes cps2 strains which are avirulent even in germfree piglets  and highly virulent cps9 strains causing death within hours after application . Here, we describe experimental induction of suppurative meningoencephalitis and arthritis, the most important S. suis associated pathologies in the field, in 6-week-old piglets through application of a cps3 strain for the first time. Furthermore, the cps3 strain induced acute to subacute and chronical endocarditis (see Fig. 2 and Table 3). Though endocarditis has been observed after experimental infection with other S. suis cps , the detection of a necrotizing and fibrinosuppurative endocarditis valvularis already after 24 h after experimental infection is remarkable (Fig. 2B). As the challenge strain was isolated from the brain, CSF, joints and heart valve of these animals (Table 2) the third Henle-Koch postulate was proven for this important cps in the natural host. Intravenous application of 2 × 107 CFU resulted in high morbidity (Fig. 1C), but low mortality rates (Fig. 1A). Whereas the higher infection dose of 2 × 108 CFU led to high morbidity (Fig. 1D), moderate mortality rates (Fig. 1B) and typical suppurative or fibrinosuppurative lesions (Fig. 2; Table 3) in 6-week-old pigs.
S. suis is an invasive porcine pathogen causing severe diseases such as meningitis, arthritis and septicemia . Therefore, we evaluated the treatment of experimentally infected piglets with buprenorphine, an opioid analgesic, as a refinement strategy in experimental S. suis pig infections to reduce pain and distress of animals. For this purpose, data on mortality, morbidity and clinical as well as pain scores were recorded and compared. In previous studies, buprenorphine treatment was able to reduce pain and lameness in pigs . Although numerous piglets suffered from lameness after i.v. cps3 infection, no substantial differences regarding the aforementioned investigated parameters were recorded between UT and BT pigs. Although the number of piglets in this trial is limited, our data indicate that the selected buprenorphine application is not sufficient to prevent severe pain and clinical signs in pigs infected intravenously with S. suis cps3.
One may argue that the applied dose of 0.05 mg buprenorphine/kg was too low to prevent high clinical and pain scores in diseased piglets, since it was shown that a dose of 0.05 mg/kg was not able to reduce surgical pain in mice . However, the applied and published doses of buprenorphine in swine range from 0.005 to 0.1 mg/kg . As buprenorphine can go along with negative side effects like respiratory depression and sedation , the dose should not be chosen too high. Previous publications regarding buprenorphine treatment in pigs reported no negative side effects with an applied dose of 0.04 mg/kg [26, 27]. Based on the doses used in published studies and recommended through GV- Solas for pain management in laboratory animals , the applied dose of 0.05 mg/kg was considered to be adequate. Apart from the dose there may be further reasons for the insufficient effect of buprenorphine treatment on pain reduction. Of note, buprenorphine treatment did not lead to restoration of the symmetric gait of lame pigs as determined with pressure mats in a previous study . As post mortem examinations showed that most of the piglets suffered from inflammatory conditions resulting in lameness, it was suspected that buprenorphine was not able to reduce pain induced through inflammatory disease, which was still investigated in a previous study . We assume that in our study the effects of buprenorphine on clinics and cortisol levels were very limited, as S. suis typically induces a high-grade of inflammation in association with lameness in pigs. Possibly, drugs with a strong anti-inflammatory effect are more likely to result in a detectable reduction of the clinical and pain score. However, as inflammation is an important read out parameter in S. suis studies, such a refinement strategy is not in accordance with the scientific objective of most experimental S. suis studies.
Although, morbidity and clinical signs were similar between both groups, BT piglets were notably more active within 30 min after injection compared to UT piglets. Especially after anaesthesia for experimental infection, BT piglets were awake and active earlier compared to UT. This increase in active movement after buprenorphine treatment of pigs is in agreement with other studies [26, 27]. Within this study, a few BT piglets showed clinical signs of high fever and severe lameness. However, these piglets did not reach humane endpoints, since they were still active and showed appetite. Though our data on the clinics (Fig. 1) does not indicate different disease progression under buprenorphine treatment, we cannot rule out that buprenorphine treatment may have led to delayed euthanasia and prolonged the course of disease in single cases.
In our established cps3 infection model central nervous disorder and lameness were common clinical findings. This was associated with acute suppurative meningoencephalitis and arthritis in 5 out of 6 prematurely euthanized piglets, respectively, as well as subacute to chronical arthritis in one surviving piglet. Of note, the mean pathohistological score ω was substantially higher in BT than in UT piglets though morbidity and mortality were overall very much alike between the two groups. One might speculate that BT treated piglets reached higher pathohistological scores because buprenorphine treatment disguised early clinical signs in the onset of disease leading to delayed euthanasia in piglets developing (fibrino-)suppurative lesions. However, BT treated piglets reaching humane endpoints were euthanized within the first two days following experimental infection (Fig. 1) and typical clinical signs such as lameness were not prevented by buprenorphine treatment. Overall, the results of the clinical monitoring suggest that the applied buprenorphine treatment has very little influence on the clinical manifestation of experimentally induced S. suis disease.
Interestingly, piglets which showed clinical signs of S. suis infection and did not reach humane endpoints, recovered within 5 d after infection independent from buprenorphine treatment. This result is consistent with data from the bactericidal assay of the cps3 challenge strain, since the strain proliferated in porcine blood drawn before infection and was killed completely in blood taken 5 d after infection. Both experiments showed increasing levels of IgM antibodies against the cps3 challenge strain following experimental infection (already 5 dpi). Likewise, this was shown in mice after sublethal infection with a S. suis cps3 strain, leading to a significant increase in IgM antibodies against cps3 . The aforementioned study further showed that the increase in IgM antibodies is independent of the subcapsular domain of the cps3 strain. Whether the fast recovery of the infected and diseased piglets, as well as the killing of the cps3 strain in porcine blood ex vivo 5 dpi is mediated by the increased IgM levels needs further investigation.
As shown, opioid analgesics are able to modulate the innate and acquired immune response [19, 24, 25]. However, this study indicates that buprenorphine treatment has no impact on the antibody-mediated killing of the S. suis challenge strain in porcine blood, as well as on levels of blood leukocytes and specific IgM and IgG antibodies in pigs. These results go along with the fact, that buprenorphine has less immunomodulatory effects as a partial µ-agonist compared to e.g. fentanyl or morphine as pure µ-agonists . Buprenorphine is not activating the hypothalamic–pituitary–adrenal-axis. Therefore, buprenorphine does not induce immunomodulatory glucocorticoids . After ocular infection of guinea pigs with a virulent Shigella flexneri strain, buprenorphine treatment did not influence the IgG and IgA antibody response . Accordingly, we show that buprenorphine treatment of S. suis infected pigs is neither associated with different bacterial survival patterns in porcine blood nor with altered serum levels of IgM and IgG antibodies binding to the bacterial surface of S. suis cps3. This suggests that the immunomodulatory effect of the selected buprenorphine application is neglectable with regard to the humoral immune response following S. suis cps3 infection.
Scientists working with animals are obliged to implement refinement strategies in experiments to reduce distress. However, these are often poorly described in experimental S. suis studies and have not been evaluated, though differences between laboratories may have a substantial impact on animal welfare and also on the scientific output. In the described study, we not only evaluated buprenorphine as refinement strategy, but also introduced measurements of cortisol levels as a distress marker in S suis research. In our opinion, it is necessary to standardize refinement strategies between different laboratories. For this, it is very important to include objective read out parameters of distress such as serum and saliva levels of cortisol. Importantly, cortisol levels in experimentally infected piglets were significantly associated with clinical signs of disease (Fig. 4C).
As increased cortisol levels in pigs typically go along with pain caused distress in pigs [23, 44], serum cortisol levels in S. suis infected piglets with or w/o buprenorphine treatment were determined. We showed that serum cortisol levels were significantly higher in mortally ill piglets suffering from S. suis disease compared to healthy piglets. This confirms that serum cortisol levels relate with S. suis disease and can be used as distress marker. In this study buprenorphine treatment did not prevent high serum cortisol levels in S. suis infected pigs with severe clinical signs (Fig. 4C). This indicates that humane endpoints and a close clinical monitoring should remain obligatory refinement strategies independent of buprenorphine application to reduce distress in piglets.
The UT piglets were intentionally not treated with a placebo in this study because such treatment would not be performed in any experimental S. suis study. As a consequence, we cannot rule out that comparison with a placebo-treated group would have resulted in more prominent differences in cortisol levels between both groups. We consider i.m. injection of buprenorphine every 8 h post infection to be stressful for the animals, at least to a low degree. As buprenorphine application did not prevent high clinical and pain scores, the benefit of it in experimental S. suis infections remains questionable in our opinion, though differences in serum cortisol concentration were recorded 2 dpi in the 2nd experiment.
Different pathologies, e.g. suppurative meningoencephalitis, arthritis and endocarditis associated with typical clinical signs of disease can be induced through i.v. application of 2 × 108 CFU of S. suis cps3 strain 16667/3 in conventional piglets. In the established cps3 challenge model, buprenorphine treatment (0.05 mg/kg every 8 h) does not prevent high clinical and pain scores in single piglets with severe disease limiting its value as putative refinement. Results suggest that buprenorphine treatment has no influence on the course of specific serum IgM and IgG levels in these experimentally infected piglets. Serum cortisol levels are a meaningful marker of distress in piglets experimentally infected with S. suis, since levels were significantly higher in mortally ill piglets compared to healthy ones. Furthermore, our study suggests that in experimentally infected but clinically unobtrusive piglets, serum and saliva cortisol levels remain low and are not influenced by buprenorphine application. Overall, close clinical monitoring in combination with well-defined humane endpoints remains the main refinement strategy to limit distress and pain in S. suis experimentally infected piglets.
Materials and methods
Bacterial strains and growth conditions
S. suis strain 16667/3 (cps3+, sly+, mrp+) of ST 1187 was originally isolated from the central nervous system of a diseased pig in Germany in 2016. S. suis strain V3117/2 (cps14+, sly+, mrp+, epf*) of ST1 was isolated from the brain of a pig as described before . The S. suis strain 17434 (cps4+, sly+, mrp+) of ST94 was isolated from the CSF of a pig in Germany in 2017. S. suis strain 10cpsΔEF, kindly provided by Hilde Smith (DLO-Institute for Animal Science and Health, Lelystad, The Netherlands), is an unencapsulated mutant derived through insertion of a spectinomycin resistance cassette in cpsE and cpsF of the capsule biosynthesis operon of S. suis cps2 wt strain 10 . Bacterial strains were cultured on Columbia agar plates containing 5% sheep blood and if appropriate Staphylococcus/Streptococcus selective Supplement (SR0070E, Oxoid, Germany) was added. Furthermore, bacteria were cultured in Bacto™ Todd Hewitt broth (THB) and Bacto™ Tryptic Soy broth (TSB).
Virulence-associated gene profiling and multi locus sequence typing (MLST)
The virulence-associated genes of the aforementioned S. suis cps3 and cps4 strains were determined through MP-PCR . Capsular polysaccharide synthesis genes for the detection of serotypes 3 and 4 (cps3 and 4) were detected through monoplex PCR as described . MLST was conducted as published previously .
In this study, all pigs were treated in accordance with the principles outlined in the EU Directive 2010/63/EU, the European Convention for the Protection of Vertebrate Animals Used for Experimental and other Scientific Purposes and the German Animal Protection Law (Tierschutzgesetz). The animal experiment (permit no. TVV58/20) was permitted by the Landesdirektion Sachsen. The animal experiment included two studies with different applied infection doses. All piglets (BT and UT) of one experiment were kept in the same stable. The person (CGB) who made the final decision on early euthanasia did not know which group (BT or UT) an animal belonged to (partially blinded experiment). Piglets included in the study originated from a conventional farm with several circulating S. suis cps including cps1, cps1/2, cps2, cps7 and cps9 as determined by genotyping of numerous tonsil isolates using (MP)-PCR  followed by cpsK sequencing to differentiate between cps1 and cps14 and between cps2 and cps1/2 . S. suis strains isolated from tonsil swabs taken from piglets before experimental infection and further tonsil isolates (n = 105) from the same herd were screened by a cps3 monoplex PCR as described before . The cps3 gene was not detected in any of the tonsil isolates. However, this does not completely exclude that the piglets were colonized with cps3. As buprenorphine had not been evaluated in experimental S. suis studies, it was difficult to give a reasonable estimate for p(x > y) to calculate the sample size for the comparative analysis of animals in clinical and pain scores as well as cortisol levels for the Wilcoxon Mann–Whitney U-test comparison. Accordingly, the 1st experiment with the lower infectious dose was conducted as an orientation study. The sample size of the 2nd experiment with an infectious dose of 2 × 108 CFU was calculated with the following settings: p(x > y) = 0.92; alpha 0.05; power 0.8. These settings relied on the hypothesis that i.v. infection with S. suis cps3 should result in very high clinical and pain scores as well as cortisol levels in nearly all untreated piglets (e.g. a clinical score of 25, see Table 1) and that buprenorphine treatment is very sufficient to prevent maximal clinical and pain scores as well as cortisol levels in clinically diseased piglets. The piglets were taken from two (first experiment) or five (second experiment) litters of German Landrace sows crossed with Pietrain. After weaning with four weeks of age, piglets were transported to the experimental facilities and allocated into the UT and BT group applying a litter- and gender-matched design. The single animal represents an experimental unit. The experiment started following an acclimatization period of one week. Stables were enriched with cotton ropes, different plastic toys and chains. After the acclimatization period pigs were infected intravenously with S. suis cps3 strain 16667/3 in the 6th week of life. The experimental infection was conducted under anaesthesia induced through i.m. application of 2 mg/kg azaperon (Stresnil®, Elanco, Germany) and 10 mg/kg ketamine (Ursotamin®, Serumwerke Bernburg; Germany). In the first experiment, piglets (n = 5/group) were experimentally infected with 2 × 107 CFU/1.5 ml/animal. In the second experiment the infection dose was increased to 2 × 108 CFU/1.5 ml per piglet (n = 8/group). In both trials, one group was treated i.m. with 0.05 mg/kg buprenorphine (Buprenovet® Multidose; 0.3 mg/ml, Elanco, Germany) every 8 h from the day of infection until 5 dpi. A first dose of 0.01 mg/kg buprenorphine was applied during anaesthesia induced for experimental infection. This first dose was lower compared to subsequent treatments to minimize respiratory depression. Buprenorphine doses were based on recommendations of the GV-Solas for pain treatment in laboratory pigs . Blood from the vena cava cranialis was taken prior to infection, 2 dpi and 5 dpi and during final aesthesia. In the second trial, blood was additionally taken one day prior to final necropsy. Further, saliva of pigs was collected daily starting on the day prior to infection and lasting until 6 dpi in the second experiment. Experimentally infected piglets were fed thrice daily with commercial rearing food and had ad libitum access to water. Furthermore, piglets were clinically monitored every 8 h following a standardized protocol. A clinical score with a maximum of 25 (see Supplementary Table 1, Additional file 1) and a pain score with a maximum of 50 (see Supplementary Table 2, Additional file 1) was determined for each piglet at every control. To record all clinical signs of arthritis, not only lameness, but also signs of inflammation like redness and swelling of joints were scored. The pain score included typical signs of pain in pigs suffering from S. suis disease and was established for the first time in this experimental infection. The maximal pain scores reached in each group were divided by the number of animals and defined as δ. A pig was defined as morbid if the inner body temperature obtained values ≥ 40.2 °C and/or developed clinical signs of severe S. suis disease. Piglets were euthanized due to animal welfare reasons if they showed clinical signs of severe S. suis disease like polyarthritis, recumbency and central nervous disorder or reached a clinical score ≥ 25. Humane endpoints were also reached, when piglets suffered from ongoing moderate disturbed condition (clinical score from 8–24 over 24 h). For euthanasia, piglets were deeply anaesthetized as described above and euthanized through i.v. application of 3 ml T61 (MSD Tiergesundheit, Germany) via the ear vein. After euthanasia, all challenged piglets underwent the same necropsy protocol to collect the following samples for histological (h) and semi-quantitative bacteriological (b) investigations as described previously [30, 49]: CSF (b); brain (b, h); tarsal and carpal joints (b, h), peritoneal, pleural and pericardial swabs (b), peritoneum and pleura (h); cranial lobe of the left lung (b, h); liver (b, h); spleen (b, h); mitral valve (b, h) and tonsil (b, h). The histological screenings were scored as described .
Venous blood was taken prior to infection, 5 dpi and 13 dpi to perform bactericidal assays which were conducted essentially as described previously . Briefly, 500 µl of heparinized blood (16 I.U. heparin/ml) was infected with 6 × 105 CFU of S. suis cps3 strain 16667/3 or 3 × 106 CFU of S. suis cps4 strain 17434 and cps14 strain V3117/2 for two hours at 37 °C on a rotator. Streptococci for blood infection were grown exponentially in THB to an OD600 = 0.5–0.6 and stored at -80 °C until the bactericidal assay. Bacterial growth was determined by plating serial dilutions at time point zero and after two hours. The SF for each sample was calculated through division of these two values.
Microbial adhesion to hydrocarbons (MATH)
We conducted the MATH assay as described previously by Öhlmann et al.  to compare hydrophobicity of the S. suis strains investigated in the bactericidal assay with the hydrophobicity of S. suis cps2 strain 10 and its unencapsulated isogenic mutant 10cpsΔEF.
Detection of specific αS. suis 16667/3 IgM and IgG antibodies
Antibody levels in pig sera were determined prior to infection, 5dpi and at final euthanasia. ELISAs for detection of serum IgM and IgG antibodies binding to immobilized, formaldehyde-inactivated (0.2%) whole bacteria of S. suis cps3 strain 16667/3 were conducted as described previously for other S. suis strains . Convalescent sera from piglets experimentally infected with cps3 strain 16667/3 served as standard serum (piglet no. 954) and positive control (piglet no. 800). These sera were taken three weeks after infection. Serum from colostrum-deprived piglets served as negative control.
Measurement of blood leukocytes
To determine blood leukocytes in pigs, EDTA blood (Sartstedt, Nürmbrecht, Germany) was drawn prior to infection, 2 dpi and 5 dpi in the first experiment. In addition to the aforementioned time points blood was taken at final euthanasia of pigs in the second experiment. Blood leukocytes were differentiated using the hematology system ADVIA 120 (Siemens Healthineers, Germany) as described previously .
Saliva of piglets was collected using round cotton swabs (Covetrus DE GmbH, Düsseldorf, Germany). Prior infection, piglets were trained to chew on swabs using swabs soaked in apple juice. For saliva collection, piglets had to chew on two swabs, one after the other, until they were moist. After every saliva sampling, pigs were rewarded with apple juice-soaked swabs. Due to the circadian rhythm of cortisol [52, 53], saliva was collected daily at noon before feeding until 6 dpi. After sampling, both swabs were placed into a 5 ml syringe, which was subsequently put into a 15 ml falcon tube and closed with parafilm. Tubes were centrifuged for 20 min with 1685 g at room temperature. Saliva was stored at -20 °C until cortisol measurements.
Determination of serum and saliva cortisol levels
To investigate serum cortisol levels in the first experiment, blood was taken prior to infection, 2 dpi, 5 dpi and at final euthanasia (21 dpi) of pigs. Samples prior to infection and at final euthanasia were taken under anaesthesia in the first experiment with the lower infection dose. Due to the obtained results (see Supplementary Fig. 4, Additional file 6) and published data on the influence of anesthetics on cortisol levels in pigs , this was changed in the second experiment: Blood samples were taken from awake piglets one day before infection, 2 dpi, 5 dpi and one day prior to final euthanasia in the case of surviving piglets (12 dpi). Further blood samples were drawn under anaesthesia before final euthanasia of mortally ill piglets (1 dpi and 2 dpi) and surviving piglets (13 dpi). Due to the circadian rhythm of cortisol with higher levels in the morning and noon , the time point of sampling is very important. In the second experiment with the higher infection dose, blood was always drawn in the morning and saliva in the noon. However, this was not consistently implemented in the first experiment with the lower infection dose. Because of this and the described differences in anaesthesia, results of cortisol measurement in the first experiment are considered preliminary data and only shown in the Additional file 6. Cortisol levels in saliva and serum were determined by radioimmunoassay as described previously .
Statistical analysis was conducted using GraphPad Prism 7.05 (Graph Pad Software, California, USA). Differences between the UT and BT group were analysed using the Mann–Whitney-U test. For comparison of two or more different time points within one group one- way analysis of variance (ANOVA) with a subsequent Dunn´s multiple comparisons test was applied. Data shown in the Kaplan–Meier diagrams were analysed using the log rank test. Means and standard deviations of the results are shown. Probabilities lower than 0.05 were considered significant (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional files. The datasets analyzed during the current study are available from the corresponding author on reasonable request.
- cps :
Multi locus sequence typing
Days post infectionem
- pre inf:
- S. suis :
Segura M, Aragon V, Brockmeier SL, Gebhart C, Greeff A de, Kerdsin A, et al. Update on Streptococcus suis Research and Prevention in the Era of Antimicrobial Restriction: 4th International Workshop on S. suis. Pathogens. 2020. https://doi.org/10.3390/pathogens9050374.
Brousseau R, Hill JE, Préfontaine G, Goh SH, Harel J, Hemmingsen SM. Streptococcus suis serotypes characterized by analysis of chaperonin 60 gene sequences. Appl Environ Microbiol. 2001;67:4828–33. https://doi.org/10.1128/AEM.67.10.4828-4833.2001.
Chatellier S, Harel J, Zhang Y, Gottschalk M, Higgins R, Devriese LA, Brousseau R. Phylogenetic diversity of Streptococcus suis strains of various serotypes as revealed by 16S rRNA gene sequence comparison. Int J Syst Bacteriol. 1998;48(Pt 2):581–9. https://doi.org/10.1099/00207713-48-2-581.
Kerdsin A, Akeda Y, Hatrongjit R, Detchawna U, Sekizaki T, Hamada S, et al. Streptococcus suis serotyping by a new multiplex PCR. J Med Microbiol. 2014;63:824–30. https://doi.org/10.1099/jmm.0.069757-0.
Silva LMG, Baums CG, Rehm T, Wisselink HJ, Goethe R, Valentin-Weigand P. Virulence-associated gene profiling of Streptococcus suis isolates by PCR. Vet Microbiol. 2006;115:117–27. https://doi.org/10.1016/j.vetmic.2005.12.013.
Willemse N, van der Ark KCH, Stockhofe-Zurwieden N, Smith H, Picavet DI, van Solt-Smits C, et al. Clonal expansion of a virulent Streptococcus suis serotype 9 lineage distinguishable from carriage subpopulations. Sci Rep. 2019;9:15429. https://doi.org/10.1038/s41598-019-51576-0.
Berthelot-Hérault F, Gottschalk M, Morvan H, Kobisch M. Dilemma of virulence of Streptococcus suis: Canadian isolate 89–1591 characterized as a virulent strain using a standardized experimental model in pigs. Can J Vet Res. 2005;69:236–40.
Goyette-Desjardins G, Vinogradov E, Okura M, Takamatsu D, Gottschalk M, Segura M. Streptococcus suis serotype 3 and serotype 18 capsular polysaccharides contain di-N-acetyl-bacillosamine. Carbohyd Res. 2018;466:18–29. https://doi.org/10.1016/j.carres.2018.07.003.
Vötsch D, Willenborg M, Baumgärtner W, Rohde M, Valentin-Weigand P. Bordetella bronchiseptica promotes adherence, colonization, and cytotoxicity of Streptococcus suis in a porcine precision-cut lung slice model. Virulence. 2021;12:84–95. https://doi.org/10.1080/21505594.2020.1858604.
Hohnstein FS, Meurer M, Buhr N de, Köckritz-Blickwede M von, Baums CG, Alber G, Schütze N. Analysis of Porcine Pro- and Anti-Inflammatory Cytokine Induction by S. suis In Vivo and In Vitro. Pathogens. 2020. https://doi.org/10.3390/pathogens9010040.
Rungelrath V, Öhlmann S, Alber G, Schrödl W, von Köckritz-Blickwede M, de Buhr N, et al. Survival of streptococcus suis in porcine blood is limited by the antibody- and complement-dependent oxidative burst response of granulocytes. Infect Immun. 2020. https://doi.org/10.1128/IAI.00598-19.
Martelet L, Lacouture S, Goyette-Desjardins G, Beauchamp G, Surprenant C, Gottschalk M, Segura M. Porcine dendritic cells as an in vitro model to assess the immunological behaviour of streptococcus suis subunit vaccine formulations and the polarizing effect of adjuvants. Pathogens. 2017. https://doi.org/10.3390/pathogens6010013.
Segura M, Vanier G, Al-Numani D, Lacouture S, Olivier M, Gottschalk M. Proinflammatory cytokine and chemokine modulation by Streptococcus suis in a whole-blood culture system. FEMS Immunol Med Microbiol. 2006;47:92–106. https://doi.org/10.1111/j.1574-695X.2006.00067.x.
Weiße C, Dittmar D, Jakóbczak B, Florian V, Schütze N, Alber G, et al. Immunogenicity and protective efficacy of a Streptococcus suis vaccine composed of six conserved immunogens. Vet Res. 2021;52:112. https://doi.org/10.1186/s13567-021-00981-3.
Gómez-Gascón L, Cardoso-Toset F, Tarradas C, Gómez-Laguna J, Maldonado A, Nielsen J, et al. Characterization of the immune response and evaluation of the protective capacity of rSsnA against Streptococcus suis infection in pigs. Comp Immunol Microbiol Infect Dis. 2016;47:52–9. https://doi.org/10.1016/j.cimid.2016.06.001.
Hsueh K-J, Cheng L-T, Lee J-W, Chung Y-C, Chung W-B, Chu C-Y. Immunization with Streptococcus suis bacterin plus recombinant Sao protein in sows conveys passive immunity to their piglets. BMC Vet Res. 2017;13:15. https://doi.org/10.1186/s12917-016-0937-8.
Goyette-Desjardins G, Auger J-P, Xu J, Segura M, Gottschalk M. Streptococcus suis, an important pig pathogen and emerging zoonotic agent-an update on the worldwide distribution based on serotyping and sequence typing. Emerg Microbes Infect. 2014;3:e45. https://doi.org/10.1038/emi.2014.45.
Streptococcosis GM. In: Zimmerman J, Karriker L, Ramirez A, Schwartz K, Stevenson G, editors. Disease of swine. 10th ed. Hoboken: John Wiley & Sons; 2012. p. 841–55.
Margarete Arras, Kristianna Becker, Alessandra Bergadano et al. Pain management for laboratory animals. July 2020. https://www.gv-solas.de/wp-content/uploads/2021/08/2021-04_Pain_Management_for_laboratory_animals.pdf. Accessed 11 June 2022.
Berke MS, Fensholdt LKD, Hestehave S, Kalliokoski O, Abelson KSP. Effects of buprenorphine on model development in an adjuvant-induced monoarthritis rat model. PLoS One. 2022;17:e0260356. https://doi.org/10.1371/journal.pone.0260356.
Guarnieri M, Brayton C, DeTolla L, Forbes-McBean N, Sarabia-Estrada R, Zadnik P. Safety and efficacy of buprenorphine for analgesia in laboratory mice and rats. Lab Anim (NY). 2012;41:337–43. https://doi.org/10.1038/laban.152.
Peterson NC, Nunamaker EA, Turner PV. To treat or not to treat: the effects of pain on experimental parameters. Comp Med. 2017;67:469–82.
Bradbury AG, Eddleston M, Clutton RE. Pain management in pigs undergoing experimental surgery; a literature review (2012–4). Br J Anaesth. 2016;116:37–45. https://doi.org/10.1093/bja/aev301.
Sacerdote P. Opioids and the immune system. Palliat Med. 2006;20(Suppl 1):s9-15.
Eisenstein TK, Hilburger ME. Opioid modulation of immune responses: effects on phagocyte and lymphoid cell populations. J Neuroimmunol. 1998;83:36–44. https://doi.org/10.1016/s0165-5728(97)00219-1.
Viscardi AV, Turner PV. Efficacy of buprenorphine for management of surgical castration pain in piglets. BMC Vet Res. 2018;14:318. https://doi.org/10.1186/s12917-018-1643-5.
Meijer E, van Nes A, Back W, van der Staay FJ. Clinical effects of buprenorphine on open field behaviour and gait symmetry in healthy and lame weaned piglets. Vet J. 2015;206:298–303. https://doi.org/10.1016/j.tvjl.2015.10.016.
Baums CG, Kaim U, Fulde M, Ramachandran G, Goethe R, Valentin-Weigand P. Identification of a novel virulence determinant with serum opacification activity in Streptococcus suis. Infect Immun. 2006;74:6154–62. https://doi.org/10.1128/IAI.00359-06.
Rieckmann K, Seydel A, Klose K, Alber G, Baums CG, Schütze N. Vaccination with the immunoglobulin M-degrading enzyme of Streptococcus suis, Ide Ssuis, leads to protection against a highly virulent serotype 9 strain. Vaccine X. 2019;3:100046. https://doi.org/10.1016/j.jvacx.2019.100046.
Baums CG, Kock C, Beineke A, Bennecke K, Goethe R, Schröder C, et al. Streptococcus suis bacterin and subunit vaccine immunogenicities and protective efficacies against serotypes 2 and 9. Clin Vaccine Immunol. 2009;16:200–8. https://doi.org/10.1128/CVI.00371-08.
Meurer M, Öhlmann S, Bonilla MC, Valentin-Weigand P, Beineke A, Hennig-Pauka I, et al. Role of Bacterial and Host DNases on Host-Pathogen Interaction during Streptococcus suis Meningitis. Int J Mol Sci. 2020. https://doi.org/10.3390/ijms21155289.
Sun Y, Liu H, Du R, Li S, Qu G, Zhu R, et al. Characteristic comparison of meningitis and non-meningitis of streptococcus suis in an experimentally infected porcine model. Inflammation. 2018;41:368–77. https://doi.org/10.1007/s10753-017-0692-4.
Seele J, Hillermann L-M, Beineke A, Seitz M, von Pawel-Rammingen U, Valentin-Weigand P, Baums CG. The immunoglobulin M-degrading enzyme of Streptococcus suis, IdeSsuis, is a highly protective antigen against serotype 2. Vaccine. 2015;33:2207–12. https://doi.org/10.1016/j.vaccine.2015.03.047.
Li J, Xia J, Tan C, Zhou Y, Wang Y, Zheng C, et al. Evaluation of the immunogenicity and the protective efficacy of a novel identified immunogenic protein, SsPepO, of Streptococcus suis serotype 2. Vaccine. 2011;29:6514–9. https://doi.org/10.1016/j.vaccine.2011.07.010.
Ison SH, Clutton RE, Di Giminiani P, Rutherford KMD. A review of pain assessment in pigs. Front Vet Sci. 2016;3:108. https://doi.org/10.3389/fvets.2016.00108.
Vecht U, Wisselink HJ, van Dijk JE, Smith HE. Virulence of Streptococcus suis type 2 strains in newborn germfree pigs depends on phenotype. Infect Immun. 1992;60:550–6. https://doi.org/10.1128/iai.60.2.550-556.1992.
Berthelot-Hérault F, Cariolet R, Labbé A, Gottschalk M, Cardinal JY, Kobisch M. Experimental infection of specific pathogen free piglets with French strains of Streptococcus suis capsular type 2. Can J Vet Res. 2001;65:196–200.
Rieckmann K, Müller K, Moter A, Baums CG, Seydel A. Streptococcus suis serotype 9 endocarditis and subsequent severe meningitis in a growing pig despite specific bactericidal humoral immunity. JMM Case Rep. 2017;4:e005093. https://doi.org/10.1099/jmmcr.0.005093.
Zimmerman J, Karriker L, Ramirez A, Schwartz K, Stevenson G, editors. Disease of swine. 10th ed. Hoboken: John Wiley & Sons; 2012.
Tubbs JT, Kissling GE, Travlos GS, Goulding DR, Clark JA, King-Herbert AP, Blankenship-Paris TL. Effects of buprenorphine, meloxicam, and flunixin meglumine as postoperative analgesia in mice. J Am Assoc Lab Anim Sci. 2011;50:185–91.
Rodriguez NA, Cooper DM, Risdahl JM. Antinociceptive activity of and clinical experience with buprenorphine in swine. Contemp Top Lab Anim Sci. 2001;40:17–20.
Goyette-Desjardins G, Auger J-P, Dolbec D, Vinogradov E, Okura M, Takamatsu D, et al. Comparative Study of Immunogenic Properties of Purified Capsular Polysaccharides from Streptococcus suis Serotypes 3, 7, 8, and 9: the Serotype 3 Polysaccharide Induces an Opsonizing IgG Response. Infect Immun. 2020. https://doi.org/10.1128/IAI.00377-20.
Hanson CE, Ruble GR, Essiet I, Hartman AB. Effects of buprenorphine on immunogenicity and protective efficacy in the guinea pig keratoconjunctivitis model (Sereny test). Comp Med. 2001;51:224–9.
Prunier A, Mounier L, Le Neindre P, Leterrier C, Mormède P, Paulmier V, et al. Identifying and monitoring pain in farm animals: a review. Animal. 2013;7:998–1010. https://doi.org/10.1017/S1751731112002406.
Mayer L, Bornemann N, Lehnert S, de Greeff A, Strutzberg-Minder K, Rieckmann K, Baums CG. Survival patterns of Streptococcus suis serotypes 1 and 14 in porcine blood indicate cross-reactive bactericidal antibodies in naturally infected pigs. Vet Microbiol. 2021;260:109183. https://doi.org/10.1016/j.vetmic.2021.109183.
Smith HE, Damman M, van der Velde J, Wagenaar F, Wisselink HJ, Stockhofe-Zurwieden N, Smits MA. Identification and characterization of the cps locus of Streptococcus suis serotype 2: the capsule protects against phagocytosis and is an important virulence factor. Infect Immun. 1999;67:1750–6. https://doi.org/10.1128/IAI.67.4.1750-1756.1999.
Kerdsin A, Dejsirilert S, Akeda Y, Sekizaki T, Hamada S, Gottschalk M, Oishi K. Fifteen Streptococcus suis serotypes identified by multiplex PCR. J Med Microbiol. 2012;61:1669–72. https://doi.org/10.1099/jmm.0.048587-0.
Athey TBT, Teatero S, Lacouture S, Takamatsu D, Gottschalk M, Fittipaldi N. Determining Streptococcus suis serotype from short-read whole-genome sequencing data. BMC Microbiol. 2016. https://doi.org/10.1186/s12866-016-0782-8.
Büttner N, Beineke A, de Buhr N, Lilienthal S, Merkel J, Waldmann K-H, et al. Streptococcus suis serotype 9 bacterin immunogenicity and protective efficacy. Vet Immunol Immunopathol. 2012;146:191–200. https://doi.org/10.1016/j.vetimm.2012.03.012.
Öhlmann S, Krieger A-K, Gisch N, Meurer M, de Buhr N, von Köckritz-Blickwede M, et al. d-Alanylation of Lipoteichoic Acids in Streptococcus suis Reduces Association With Leukocytes in Porcine Blood. Front Microbiol. 2022;13:822369. https://doi.org/10.3389/fmicb.2022.822369.
Adam MI, Köller G, Arnold C, Schusser GF. Effects of using Flunixin Meglumine, Metamizole, and Phenylbutazone on equine kidney functions, urinary mucus, and secretory Immunoglobulin A (IgA) concentrations. PHK. 2017;33:263–70. https://doi.org/10.21836/PEM20170307.
Hillmann E, Schrader L, Mayer C, Gygax L. Effects of weight, temperature and behaviour on the circadian rhythm of salivary cortisol in growing pigs. Animal. 2008;2:405–9. https://doi.org/10.1017/S1751731107001279.
Ruis M. The circadian rhythm of salivary cortisol in growing pigs: effects of age, gender, and stress. Physiol Behav. 1997;62:623–30. https://doi.org/10.1016/s0031-9384(97)00177-7.
Daş G, Vernunft A, Görs S, Kanitz E, Weitzel JM, Brüssow K-P, Metges CC. Effects of general anesthesia with ketamine in combination with the neuroleptic sedatives xylazine or azaperone on plasma metabolites and hormones in pigs. J Anim Sci. 2016;94:3229–39. https://doi.org/10.2527/jas.2016-0365.
Gottschalk J, Einspanier A, Ungemach FR, Abraham G. Influence of topical dexamethasone applications on insulin, glucose, thyroid hormone and cortisol levels in dogs. Res Vet Sci. 2011;90:491–7. https://doi.org/10.1016/j.rvsc.2010.06.026.
We thank Gábor Köller and Haukur L. Sigmarsson (both Department for ruminants and swine, Faculty of Veterinary Medicine, Leipzig University) for determination of the blood leukocytes and support in buprenorphine application, respectively. Jutta Gottschalk (Institute of Physiological Chemistry) and Silke Lehnert (Institute of Bacteriology and Mycology, both Faculty of Veterinary Medicine, Leipzig University) are acknowledged for measuring cortisol and Ig levels, respectively.
Open Access funding enabled and organized by Projekt DEAL. This study was financially supported by Ceva Innovation Center GmbH.
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All animal experiments or samplings were conducted by veterinarians and in accordance with the guidelines outlined in the EU Directive 2010/63/EU, the European Convention for the Protection of Vertebrate Animals Used for Experimental and other Scientific Purposes and the German Animal Protection Law (Tierschutzgesetz). The animal experiment was approved by the Landesdirektion Sachsen (permit no. TVV58/20) as regulated by §15 of the German Animal Protection Law. The Animal Protection Committee of the Landesdirektion Sachsen (Ethics Committee) is involved in the process of approval of the animal experiment by the Landesdirektion Sachsen. Collection of blood from non-infected piglets for scientific purposes is registered under the permit number A09/19. All methods are in accordance with the ARRIVE guidelines for the reporting of animal experiments. All reported methods were carried out in accordance with relevant guidelines and regulations.
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Additional file 1: Supplementary Table 1.
Scoring of clinical signs in pigs. Supplementary Table 2. Scoring of pain in pigs.
Additional file 2: Supplementary Table 3.
Highest pain score of each S. suis cps3 infected piglets w or w/o buprenorphine treatment.
Additional file 3: Supplementary Fig. 1.
Course of blood leukocytes in piglets w or w/o buprenorphine treatment after S. suis cps3 infection. EDTA blood was taken before (pre inf) and after experimental infection with 2x107 CFU (A) or 2x108 CFU (B) of S. suis cps3 strain 16667/3. One group was treated i.m. with buprenorphine 0 to 5 days post infection (dpi). Unfilled symbols (○ , □) indicate piglets prematurely euthanized due to reaching humane endpoints. Leukocytes increased after infection in all (A) and 14 of 15 (B) piglets, respectively, and no significant differences between buprenorphine-treated and untreated piglets were determined. Statistical analysis was conducted with the Mann-Whitney-U-test (comparison of groups).
Additional file 4: Supplementary Fig. 2.
Survival of S. suis strains of the indicated cps in blood of BT and UT piglets (A and B) and survival of S. suis cps3 as well as specific serum IgM and IgG antibody levels in cps3 infected and non-infected piglets (C).
Additional file 5: Supplementary Fig. 3.
Microbial adhesion of S. suis cps3, cps4 and cps14 to hydrocarbons.
Additional file 6: Supplementary Fig. 4.
Serum cortisol in piglets infected with 2x107 CFU S. suis cps3 w or w/o buprenorphine treatment.
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Liedel, C., Mayer, L., Einspanier, A. et al. A new S. suis serotype 3 infection model in pigs: lack of effect of buprenorphine treatment to reduce distress. BMC Vet Res 18, 435 (2022). https://doi.org/10.1186/s12917-022-03532-w
- Streptococcus suis
- Experimental infection
- Serotype 3