Abstract
The Gram-positive bacterial species Streptococcus suis is an important porcine and human pathogen that causes severe life-threatening diseases associated with high mortality rates. However, the mechanisms by which S. suis evades host innate immunity remain elusive, so identifying novel virulence factors involved in immune evasion is crucial to gain control over this threatening pathogen. Our previous work has shown that S. suis protein endopeptidase O (SsPepO) is a novel fibronectin-binding protein. Here, we identified that recombinant SsPepO binds human plasminogen in a dose-dependent manner. Moreover, the binding of SsPepO and plasminogen, upon the activation of urokinase-type plasminogen activator, generated plasmin, which could cleave complement C3b, thus playing an important role in complement control. Additionally, a SspepO-deficient mutant showed impaired adherence to plasminogen as well as impaired adherence to and invasion of rat brain microvascular endothelial cells compared with the wildtype strain. We further found that the SspepO-deficient mutant was efficiently killed by human serum and blood. We also confirmed that the SspepO-deficient mutant had a lower mortality rate than the wildtype strain in a mouse model. In conclusion, these results indicate that SsPepO is a novel plasminogen-binding protein that contributes to S. suis immune evasion.
Introduction
Streptococcus suis is an important emerging zoonotic pathogen in swine and humans that causes meningitis, endocarditis, arthritis, pneumonia, bacteremia, and sudden death (Segura, 2009). In 2005, a large outbreak (215 cases) of human S. suis infections occurred in Sichuan Province, China (Yu et al., 2006; Chen et al., 2007; Segura, 2009). Seven years earlier, in 1998, an outbreak of human S. suis infections was reported in Jiangsu Province, China (Normile, 2005; Feng et al., 2010). S. suis has also caused human cases of infection in Vietnam, Thailand, North America, United Kingdom, Australia, and New Zealand (Wisselink et al., 2000; Wertheim et al., 2009; Gottschalk et al., 2010; Hoa et al., 2013; Hatrongjit et al., 2015; Dong et al., 2021). To cause meningitis, S. suis needs to disseminate into the bloodstream and overcome host immune defenses. However, the exact mechanism by which S. suis survives in the host blood and evades host innate immune defenses is still unclear.
Extracellular matrix (ECM) is a composite of the secreted products of resident cells found in every tissue and organ (Westerlund and Korhonen, 1993). Like other Gram-positive bacteria, S. suis can express adhesion proteins capable of binding to various components of the host ECM to mediate adherence to host cells. The ECM-binding proteins of bacteria recognize ECM, allowing bacterial adhesion to host cells in tissue, and these proteins generally make important contributions to the infection as well as to host–pathogen interactions (Westerlund and Korhonen, 1993). For example, S. suis muramidase-released protein (MRP) is a multi-functional fibrinogen-binding protein and an important virulence factor of S. suis that promotes the development of S. suis meningitis and enhances the survival of S. suis in host blood (Wang et al., 2015; Pian et al., 2016). During adhesion, ECM proteins, such as fibronectin, usually serve as mediators between host cells and S. suis (Jobin et al., 2004; Musyoki et al., 2016). Furthermore, a number of S. suis proteins that can interact with fibronectin or plasminogen have been shown to be important virulence factors of S. suis, a strategy that is commonly employed by many pathogens (Gottschalk and Segura, 2000; Musyoki et al., 2016). These proteins include S. suis adherence and virulence factors, enolase (Esgleas et al., 2008; Sun et al., 2016), GAPDH (Brassard et al., 2004; Jobin et al., 2004), and Ssa (Li et al., 2013). Therefore, studying the fibronectin- and plasminogen-binding proteins of S. suis that interact with host cells may advance understanding of the pathogenesis of S. suis-induced infection.
The 92-kDa glycoprotein plasminogen circulates as an inactive proenzyme in human serum (Singh et al., 2015; Peetermans et al., 2016). Plasminogen is an important component of the fibrinolytic system and contributes to fibrinolysis, homeostasis, and ECM degradation (Agarwal et al., 2013). Furthermore, plasminogen activation into plasmin by plasmin activators [e.g., urokinase plasmin activator (uPA)] also inhibits complement, efficiently cleaving C3 and C5 (Lahteenmaki et al., 2001; Barthel et al., 2012a). Many pathogenic microbes utilize the protease activity of plasminogen for immune evasion (Singh et al., 2012, 2013).
Our previous studies have shown that S. suis protein endopeptidase O (SsPepO) contributes to the development of S. suis meningitis by promoting fibronectin-mediated binding to and penetration of the blood–brain barrier (Liu et al., 2017). In this study, we identified SsPepO as a novel plasminogen-binding protein. We also found that fibronectin and plasminogen did not compete with each other for binding SsPepO. Moreover, upon activation of SsPepO-bound plasminogen by uPA, the plasmin that was generated subsequently cleaved complement C3b, thus enhancing the survival of serum- and blood-susceptible S. suis. In conclusion, these results show that SsPepO, as a plasminogen-binding protein, plays a role in aiding in the immune evasion of S. suis.
Materials and Methods
Bacterial Strain Culture Conditions, Primers, Plasmids, and Cell Lines
All strains and plasmids used in the present study are described in Table 1. S. suis 2 was grown at 37°C in either tryptic soy broth or agar (TSA; Difco Laboratories, Franklin Lakes, NJ, United States) supplemented with 10% (vol/vol) newborn bovine serum and 50 μg/ml spectinomycin. Escherichia coli DH5α (TaKaRa, Beijing, China) was grown in Luria-Bertani medium supplemented with 100 μg/ml spectinomycin or 50 μg/ml ampicillin.
TABLE 1
| Strain or plasmid | Relevant characteristicsa | Source |
| Strains | ||
| S. suis | ||
| SC19 | Virulent strain isolated from the brain of a dead pig; Serotype 2 | Laboratory collection |
| ΔSsPepO | The SsPepO deletion mutant of SC19 | Laboratory |
| CΔSsPepO | Complemented strain of ΔSsPepO; SpcR | Laboratory |
| E. coli | ||
| DH5α | Cloning host for recombinant vector | TaKaRa |
| BL21 (DE3) | The expression host for pET-30a and their derivative | TransGen |
| Plasmids | ||
| Pet-30a | Expression vector; KanR | Novagen |
| Pet30a-SsPepO | pET30a containing the SsPepO locus | Laboratory |
| Antibody | ||
| Anti-SsPepO | Anti-SsPepO ployclonal rabit antibody | Laboratory |
Bacterial strains, plasmids, and antibody used in this study.
aRestriction sites are underlined; KanR, Kanamycin resistance; SpcR, spectinomycin resistance.
Expression and Purification of Recombinant Protein
The expression and purification of recombinant SsPepO protein were performed as described previously (Liu et al., 2017). The native protein was expressed by the addition of 1 mM IPTG to exponential-phase cultures at 37°C for 4 h. After sonication and centrifugation, the expressed protein was purified by Ni-NTA affinity chromatography (GE Healthcare, Medical City North Hills, TX, United States). The quality of purified SsPepO protein was determined by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE), and SsPepO was then stored at −80°C until use.
Direct Binding Assays
Direct binding assays were performed as previously described (Agarwal et al., 2013). Microtiter wells were incubated with 5 μg/ml of SsPepO, plasminogen (Hematologic Technologies, Pinewood Plaza, VT, United States), fibronectin (Hematologic Technologies, Pinewood Plaza, VT, United States), or casein (Biosharp, Shenzen, China) at 4°C overnight, and casein was used as a control. After blocking for 2 h at 37°C, SsPepO was incubated with the immobilized plasminogen or fibronectin for SsPepO binding, or plasminogen or fibronectin was incubated with the immobilized SsPepO for plasminogen or fibronectin binding. The proteins in the wells were detected with anti-SsPepO antibody, anti-plasminogen antibody (Proteintech, Wuhan, China), or anti-fibronectin antibody (Proteintech, Wuhan, China), followed by an appropriate secondary antibody (Proteintech, Wuhan, China). To investigate the effects of ionic strength and the effects of lysine analog ϵ-ACA (Sigma, Darmstadt, Germany) on plasminogen–SsPepO interactions, NaCl or ϵ-ACA, respectively, was added to the plates.
Binding From Serum
Binding from serum assays were performed as previously described (Agarwal et al., 2013). Microtiter plates were coated overnight with SsPepO (0.25 μg/well) at 4°C. Casein was used as a control. After blocking for 2 h at 37°C, human serum was added to the wells for 1.5 h at 37°C. The samples were measured with rabbit anti-plasminogen antibody (Proteintech, Wuhan, China) followed by peroxidase-conjugated secondary antibody (Proteintech, Wuhan, China). The absorbance was measured at 490 nm.
Plasminogen Activation and C3b Protein Degradation Assays
Plasminogen activation and C3b protein degradation were each assayed as described previously (Castiblanco-Valencia et al., 2016). For the plasminogen activation assay, a SsPepO-coated plate (5 μg/well) was incubated with plasminogen (1 μg/well) for 1.5 h at 37°C. After the wells were washed, 10 units/well of uPA (Sigma, St. Louis, MO, United States) were added, and the samples were incubated at 37°C. The activity of the newly generated plasmin was measured by using the chromogenic substrate D-Val-Leu-Lys-p-nitroanilide dihydrochloride (S-2251) (Chromogenix, Milan, Italy). The absorbance of each well in the plate was measured at OD405.
For the C3b protein degradation assay, microtiter plates were coated with SsPepO (5 μg/well) overnight at 4°C and blocked by a blocking solution for 2 h at 37°C. Plasminogen (5 μg/well) was incubated with the immobilized SsPepO for 1.5 h at 37°C. After washing, 125I-labeleld C3b together with uPA (10 units/well) were added and incubated at 37°C.
Streptococcus suis Binding to Plasminogen
Strains binding to immobilized plasminogen were performed as described previously (Agarwal et al., 2013). Microtiter plates were incubated overnight with strains [107 colony-forming units (CFU)] at 37°C. After being blocked for 2 h, plasminogen was added to wells for 1.5 h. The samples were measured with rabbit anti-plasminogen antibody (Proteintech, Wuhan, China) followed by peroxidase-conjugated secondary antibody (Proteintech, Wuhan, China). The absorbance was measured at 490 nm.
Western Blotting
Whole cell extracts and culture supernatant proteins were prepared for western blotting as follows. Bacteria were grown to an OD600 of 0.8, after which the cells were pelleted by centrifugation at 5,000 × g for 10 min at 4°C. Whole cell pellets were suspended in 1 × SDS-PAGE sample loading buffer. After being filtered through 0.22-μm membranes, the culture supernatants were precipitated in 10% trichloroacetic acid (TCA) overnight at 4°C. All supernatant samples were centrifuged at 12,000 × g for 30 min at 4°C, washed with ice-cold acetone, and resuspended in 1 ml of phosphate-buffered saline (PBS). Bovine serum albumin (BSA) (150 μg/ml) was added to the culture supernatant prior to TCA precipitation as a control. Whole cell extracts and culture supernatant proteins were resolved by SDS-PAGE and transferred to nitrocellulose membranes for immunoblotting. The immobilized proteins were incubated with rabbit anti-SsPepO antibody, followed by incubation with horseradish peroxidase (HRP)-conjugated goat anti-rabbit (Cell Signaling, Danvers, MA, United States). Following stripping, the blots were re-incubated with a mouse antibody against RNA polymerase (RNAP) (Santa Cruz, Dallas, TX, United States) and mouse anti-BSA (Proteintech, Wuhan, China) and then with HRP-conjugated goat anti-mouse IgG (Cell Signaling, Danvers, MA, United States). Blots were detected with ECL (Bio-Rad, Hercules, CA, United States).
Adherence and Invasion Assays
The bacteria were added to rat brain microvessel endothelial cell (RBMEC) monolayers at a multiplicity of infection (MOI) of 10:1 for 2 h at 37°C in 5% CO2. The cell monolayers were washed three times with PBS and then lysed with 0.1% saponin on ice for 20 min. The number of cell-adherent bacteria was determined by plating dilutions of the lysate on TSA plates. Fold bacterial adherence was calculated as follows: [recovered strain CFU/recovered wild-type (WT) CFU] × 100%. Invasion assay was little different from adherence assay. Briefly, the cell monolayers were incubated with penicillin G (100 units/ml) (Sigma, Darmstadt, Germany) and gentamicin (100 μg/ml) (Sigma, Darmstadt, Germany) prior to cell being lysed.
Serum Survival Assay
Bacteria were grown to mid-log phase. Bacterial suspension (50 μl) of WT S. suis, ΔSspepO, or CΔSspepO was combined with serum or heat-inactivated serum (450 μl), followed by incubation at 37°C for 1 h. After incubation, the bacteria were serially diluted and plated for quantitative determination.
Whole Blood Bactericidal Assay
Whole blood bactericidal assays were performed as previously described with some modifications (Liu et al., 2014). Briefly, bacterial suspension of WT S. suis, ΔSspepO, or CΔSspepO (100 μl, 5 × 105 CFU/ml) was combined with fresh human blood (900 μl), followed by incubation at 37°C in a rotator at 10 rpm for 1 h. After incubation, the bacteria were serially diluted and plated for quantitative determination.
Bacterial Virulence in vivo
Thirty female 6-week-old CD1 mice (10 mice per group) were randomly and evenly divided into three groups and injected intravenously with 8 × 108 CFU of WT S. suis, ΔSspepO, or CΔSspepO. The survival time of mice was recorded for 7 days post-inoculation. All animal experiments were approved by the Laboratory Animal Monitoring Committee of Huazhong Agricultural University and performed accordingly.
Statistical Analysis
The data were analyzed with GraphPad Prism software using one-way or two-way ANOVA analyses followed by Bonferroni’s multiple comparison test, unpaired t-tests followed by the Holm–Sidak method, or by non-parametric Mann–Whitney t-tests. For all tests, a p-value of < 0.05 was considered significant.
Results
SsPepO Binds Plasminogen
To analyze whether SsPepO binds to plasminogen, we performed enzyme-linked immunosorbent assay (ELISA). Microtiter plates coated with SsPepO were incubated with increasing concentrations of plasminogen. As shown in Figure 1A, plasminogen bound immobilized SsPepO in a concentration-dependent manner. Similarly, in a reverse setting, SsPepO also bound immobilized plasminogen in a dose-dependent manner (Figure 1B). Taken together, these data indicate that SsPepO interacts with plasminogen.
FIGURE 1
To determine if SsPepO could bind plasminogen from human serum, SsPepO was incubated with several dilutions of human serum. As shown in Figure 1C, SsPepO bound to the serum plasminogen in a dose-dependent manner, as determined by an ELISA.
SsPepO–Plasminogen Binding Depends on Lysine Binding and Ionic Strength
Previous studies have shown that lysine residues and ionic forces play an important role in the interaction of bacterial proteins with plasminogen (Lahteenmaki et al., 2001; Barthel et al., 2012b). Increasing the ionic strength with NaCl significantly decreased the amount of plasminogen binding to SsPepO (Figure 2A). To analyze whether the SsPepO–plasminogen interaction is mediated by lysine residues, SsPepO was incubated with plasminogen in the presence of ϵ-ACA, a lysine analog. The addition of increasing amounts of ϵ-ACA significantly reduced plasminogen binding (Figure 2B).
FIGURE 2
Plasminogen and Fibronectin Do Not Compete With One Another for Binding SsPepO
Our previous study found that SsPepO is a novel fibronectin-binding protein (Liu et al., 2017). To determine whether plasminogen and fibronectin compete with one another for binding SsPepO, a constant concentration of plasminogen and increasing amounts of fibronectin were added to an assay measuring their interaction with SsPepO. Both plasminogen and fibronectin bound to immobilized SsPepO, and the binding of plasminogen was not affected by the increasing amounts of fibronectin (Figure 3A). Similarly, in a reverse setting, the binding of fibronectin was also unaffected by the addition of increasing amounts of plasminogen (Figure 3B). Taken together, the data suggest that plasminogen and fibronectin do not compete with one another for binding SsPepO.
FIGURE 3
SsPepO-Bound Plasminogen Degrades the Complement Protein C3b
We next tested whether SsPepO-bound plasminogen could be activated by uPA and converted into plasmin via proteolytic cleavage. When plasminogen was incubated with SsPepO, followed by the addition of uPA, the plasminogen was converted into plasmin in a time-dependent cleavage manner (Figure 4A). A C3b degradation assay was then performed to analyze whether SsPepO-bound plasminogen can interact with C3b. When C3b was incubated with SsPepO and plasminogen, followed by the addition of uPA, C3b was cleaved by activated plasminogen (plasmin) in a time-dependent cleavage manner (Figure 4B). Following this incubation, the C3b cleavage products were observed as two major bands of 68 and 38 kDa in size. Together, these results show that plasminogen bound to SsPepO is readily converted into the active protease plasmin, which cleaves the complement protein C3b.
FIGURE 4
SsPepO Facilitates S. suis Binding to Plasminogen
The expression levels of SsPepO in WT S. suis and ΔSspepO were determined in cell surface extracts and culture supernatants by western blot analyses using anti-SsPepO antibody (Figure 5A). The immunoblots confirmed that SsPepO was present in the culture supernatants and bound to the cell surface of WT S. suis cells, whereas ΔSspepO did not produce SsPepO (Figure 5A). To analyze the role of SsPepO in S. suis binding to plasminogen, we performed a direct binding assay using these three types of bacteria. Compared with WT S. suis, the ΔSspepO mutant showed a significantly lower plasminogen-binding ability and the CΔSspepO restored the ability (Figure 5B). Therefore, the SsPepO secreted by S. suis in culture supernatant or bound to the cell surface likely contributes to plasminogen binding.
FIGURE 5
SsPepO Mediates S. suis Adherence to and Invasion of RBMECs
To better elucidate the role of SsPepO in S. suis adherence to and invasion of host cells, the adhesion and invasion abilities of WT S. suis, ΔSspepO, and CΔSspepO were compared. RBMECs were infected with WT S. suis, ΔSspepO, or CΔSspepO for 2 h. Compared with WT S. suis, the ΔSspepO mutant showed a significant reduction in both adherence to and invasion of RBMECs and the CΔSspepO restored these abilities (Figures 6A,B). The results of these experiments suggest that SsPepO facilitates S. suis attachment to and internalization into host cells.
FIGURE 6
SsPepO Facilitates Survival of S. suis in Serum and Blood and Modulates S. suis Virulence
To evaluate the impact of SsPepO deletion during systemic infections, we performed serum survival assay and whole blood bactericidal assay. Compared with WT S. suis, the ΔSspepO mutant showed a significant reduction in resistance to serum and whole blood and the CΔSspepO restored the ability (Figures 6C,D). To analyze the virulence of S. suis strains infection in vivo, we employed a murine model (Liu et al., 2017). All the WT S. suis-infected mice developed typical clinical symptoms of S. suis infection, including a rough hair coat, shivering, and lethargy. In contrast, all the ΔSspepO mutant-infected mice showed mild or no clinical signs of infection. The survival ratio of the WT S. suis-infected mice and the CΔSspepO-infected mice was lower than that of the ΔSspepO mutant-infected mice (Figure 6E). The results indicate that SsPepO plays an important role in S. suis infection.
Discussion
The pathogenesis of S. suis meningitis involves the hematogenous spread and entry into the central nervous system (CNS) of the bacteria via invading the blood–brain barrier (van Samkar et al., 2015). However, the precise mechanism whereby S. suis leaves the bloodstream and gains access to the CNS is still being elucidated. Our previous studies showed that SsPepO is a fibronectin-binding protein that facilitates the development of meningitis in S. suis (Tan et al., 2011). Here, we further demonstrate that SsPepO is a plasminogen-binding protein that plays an important role in the immune evasion of S. suis.
Previous studies showed that various bacterial pathogens have developed numerous ways to interact with plasminogen and use the host’s powerful proteolytic system to their own advantage (Peetermans et al., 2016). A previous study reported that PepO promotes macrophage phagocytosis and bactericidal activity (Shu et al., 2020). Streptococcus pneumoniae PepO facilitates bacterial colonization and internalization (Agarwal et al., 2013). Streptococcus pyogenes PepO is involved in complement evasion by binding to C1q (Honda-Ogawa et al., 2017). Plasmin blocks complement cascade by degrading C3b and C5 (Barthel et al., 2012a). In this study, we demonstrated that SsPepO binds plasminogen in a dose-dependent manner and that the SsPepO–plasminogen interaction is affected by ionic strength as well as the lysine analog ϵ-ACA. This type of interaction with plasminogen is similar to that observed for pneumococcal PepO, pneumococcal enolase, and Haemophilus influenzae protein E (Bergmann et al., 2005; Hallstrom et al., 2010; Barthel et al., 2012b; Agarwal et al., 2013). In addition, we demonstrated that SsPepO could bind to plasminogen from human serum and the plasminogen was readily activated by uPA to plasmin that subsequently cleaved C3b. Pneumococcal PepO and H. influenzae protein E can also cleave C3b via a similar mechanism (Segura, 2009; Barthel et al., 2012b). Our results showed that WT S. suis and CΔSspepO were more resistant to serum and whole blood than the ΔSspepO. The result was in accordance with a previous report that showed that pepO mutants diminished in blood (Alves et al., 2020). The result might be due to plasminogen bound to SsPepO is readily converted into the active protease plasmin, which cleaves the complement protein C3b and thus contributes to evasion from complement mediated killing.
Fibronectin is an ECM protein involved in several biological processes and is also recognized as a receptor by many bacterial pathogens (Hymes and Klaenhammer, 2016). Ssa and FBPS are fibronectin-binding protein. Previous studies reported that Ssa and FBPS contribute to pathogenesis of S. suis (de Greeff et al., 2002; Li et al., 2013). Staphylococcus aureus FnBPB promotes plasminogen conversion to plasmin (Pietrocola et al., 2019). Streptococcus pneumoniae PavA and pfbA are essential for virulence (Holmes et al., 2001; Yamaguchi et al., 2008). Here, we have shown that SsPepO binds fibronectin, in addition to binding plasminogen. Furthermore, our results demonstrate that plasminogen and fibronectin do not compete with one another for binding SsPepO. Many other bacterial proteins can also bind to more than one ECM protein; for example, Staphylococcus aureus FnBPB is a fibrinogen-binding protein as well as a fibronectin-binding protein and Mycoplasma synoviae enolase is a plasminogen-binding protein as well as a fibronectin-binding protein (Bao et al., 2014; Pietrocola et al., 2016).
The SspepO-deficient mutant showed a significant reduction in binding to plasminogen compared with the WT S. suis. Additionally, our data also indicate that SsPepO facilitates S. suis adhesion to and invasion of host cells. These in vitro results were corroborated by our in vivo findings in a murine model of S. suis hematogenous meningitis.
Infection with the SspepO-deficient mutant resulted in a lower mortality rate compared with the WT S. suis and CΔSspepO. Our findings confirm that SsPepO plays an important role in the virulence of S. suis, in agreement with the previously published data from a porcine model (Tan et al., 2011).
In conclusion, the results of this study suggest that SsPepO is a newly identified virulence factor facilitating the survival of S. suis in whole blood. SsPepO, as a plasminogen- and fibronectin-binding protein, facilitates S. suis adherence to and internalization into host epithelial and endothelial cells. Besides having plasminogen-binding activity, SsPepO can also cleave C3b via activated plasmin, which is a method of mediating complement control (Figure 7).
FIGURE 7
Statements
Data availability statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.
Ethics statement
The animal study was reviewed and approved by Scientific Ethics Committee of Huazhong Agricultural University.
Author contributions
WB, FY, KY, JL, YZ, and HC conceived and designed the experiments. All authors contributed to the acquisition and analysis of the data and the writing of the manuscript.
Funding
This work was supported by the National Key R&D Program of China (2017YFD0500201), State Key Laboratory of Genetically Engineered Veterinary Vaccines (AGVSK-ZD-201805), Open Project of Hubei Key Laboratory (KLPCAAB-2020-03), the Natural Science Foundation of China (31802189 and 31672560), Natural Science Foundation of Hubei Province (2018CFA045), the Fundamental Research Funds for the Central Universities (2662018PY042), and Technical innovation project of Hubei province (2020ABA016).
Acknowledgments
We would like to thank Sekizaki (National Institute of Animal Health, Japan) for supplying plasmid pSET4s and pSET2.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
Streptococcus suis, plasminogen, SsPepO, C3b, ϵ-ACA, immune evasion
Citation
Zhou Y, Yan K, Sun C, Liu F, Peng W, Chen H, Yuan F, Bei W and Li J (2021) Binding of Plasminogen to Streptococcus suis Protein Endopeptidase O Facilitates Evasion of Innate Immunity in Streptococcus suis. Front. Microbiol. 12:694103. doi: 10.3389/fmicb.2021.694103
Received
12 April 2021
Accepted
07 June 2021
Published
08 July 2021
Volume
12 - 2021
Edited by
Allen D. Smith, Beltsville Human Nutrition Center, Agricultural Research Service, United States Department of Agriculture, United States
Reviewed by
Wei Zhang, Nanjing Agricultural University, China; Laura Cook, Binghamton University, United States
Updates
Copyright
© 2021 Zhou, Yan, Sun, Liu, Peng, Chen, Yuan, Bei and Li.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Fangyan Yuan, fangyanyuan12@163.comWeicheng Bei, beiwc@mail.hzau.edu.cn
†These authors have contributed equally to this work
This article was submitted to Microbial Immunology, a section of the journal Frontiers in Microbiology
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