Skip to main content
Download PDF

An anti-perfringolysin O monoclonal antibody cross-reactive with streptolysin O protects against streptococcal toxic shock syndrome

BMC Research Notes volume 13, Article number: 419 (2020) Cite this article

Abstract

Objective

Streptococcus pyogenes (Group A Streptococcus; GAS) causes a variety of infections that include life-threatening, severe invasive GAS infections, such as streptococcal toxic shock syndrome (STSS), with > 30% mortality rate, despite effective antibiotics and treatment options. STSS clinical isolates highly express streptolysin O (SLO), a member of a large family of pore-forming toxins called cholesterol-dependent cytolysins (CDCs). SLO is an important toxic factor for GAS and may be an effective therapeutic target for the treatment of STSS. Our aim was to identify a monoclonal antibody (mAb) that reacts with SLO and has therapeutic potential for STSS treatment.

Results

We focused on mAbs that had originally been established as neutralizing reagents to perfringolysin O (PFO), another member of the CDC family, as some cross-reactivity with SLO had been reported. Here, we confirmed cross-reactivity of an anti-PFO mAb named HS1 with SLO. In vitro analysis revealed that HS1 mAb sufficiently prevented human neutrophils from being killed by STSS clinical isolates. Furthermore, prophylactic and therapeutic injection of HS1 mAb into C57BL/6 mice significantly improved the survival rate following lethal infection with an STSS clinical isolate. These results highlight the therapeutic potential of HS1 mAb for STSS treatment.

Introduction

Streptococcus pyogenes, also known as group A Streptococcus (GAS), is one of the most common human pathogens, and causes a wide spectrum of diseases ranging from pharyngitis and skin lesions to streptococcal toxic shock syndrome (STSS) and necrotizing fasciitis. The first two are generally self-limiting, while the latter two are severe and life-threatening, with mortality rates of 30–70% even with immediate antibiotic therapy and intensive care [1,2,3,4]. Therefore, GAS is sometimes referred to as “killer microbes” or “flesh-eating bacteria” [5]. The prevalence of severe GAS disease is at least 18.1 million cases globally each year [6], including annual estimates of 8000–24,000 invasive cases; the numbers have been increasing since 2013 in the United States [7]. In addition, in Japan, there are 90–1000 cases of severe invasive streptococcal infections annually, and the number of cases has been similarly increasing since 2014 [8].

Severe invasive GAS clinical isolates often express virulence factors more abundantly than non-invasive GAS clinical isolates. For example, STSS clinical isolates highly express streptolysin O (SLO), which belongs to a large family of pore-forming toxins called the cholesterol-dependent cytolysins (CDCs) [9,10,11,12,13]. SLO has been shown to be a key virulence factor of GAS by preventing internalization of the bacteria into lysosomes where they can be destroyed [14], and has cytopathic effects on neutrophils, macrophages, and dendritic cells [15,16,17,18,19]. As a result, STSS causes severe neutropenia, which results in poor prognosis for the patients and the mouse model [20, 21]. The global increase in invasive GAS infections in the 1980s was associated with the emergence of an M1T1 clone that harbors a 36-kb pathogenicity island that codes for increased expression of SLO and its cotoxin NAD+-glycohydrolase [22,23,24,25]. Taken together, SLO is a potential therapeutic target for the treatment of STSS.

Several hybridomas that produce monoclonal antibodies (mAbs) specific for Clostridium perfringens-derived perfringolysin O (PFO) in the CDC family [26] have been cryopreserved in liquid nitrogen since 1984. Among the original mAbs (4D8, 2C5, and 3H10), 3H10 mAb was found to neutralize PFO and SLO, and inhibited toxin-induced hemolysis of sheep red blood cells and cardiotoxicity in cultured mouse heart cells [26]. The aim of the present study was to re-clone the existing hybridomas and test the specificity of the mAbs against SLO, in an attempt to identify a novel treatment strategy for STSS.

Main text

Methods

Blinding at any stage of the study

The experiments were not randomized and the investigators were not blinded to allocation during experiments and outcome assessment.

Re-cloning of hybridomas

Hybridomas that produce mAbs (mouse IgG1) reactive with PFO were recovered from liquid nitrogen. 3H10 and 2C5 hybridomas were re-cloned by the limiting dilution method at 0.3 cell/well in a 96-well plate, resulting in 7 and 11 colonies, respectively. 4D8 hybridoma was re-cloned at 1 cell/well in a 96-well plate, resulting in 5 colonies. The re-cloned hybridomas 3H10, 4D8, and 2C5 that showed the most potent binding activities against PFO were renamed HS1, HS2, and HS3, respectively.

Enzyme-linked immunosorbent assay (ELISA)

First, 96-well plates were coated with 50 µL (1 μg/ml) of PFO (MyBioSource, San Diego, CA) or SLO (Bio Academia, Osaka, Japan). The plates were washed four times with 0.1% Tween20 in sterile PBS (PBS-T), and then blocked with 1% BSA in PBS-T for 2 h at room temperature; the diluted HS1, HS2, and HS3 were incubated for 2 h at room temperature. After the samples were washed with PBS-T, they were incubated with anti-mouse IgG conjugated to horseradish peroxidase (Southern Biotech, Birmingham, AL) for 2 h at room temperature. After washing the samples with PBS-T, 0.5 mg/ml ο-Phenylenediamine dihydrochloride (Sigma-Aldrich) in 0.05 M citrate–phosphate buffer (pH 5.0) was used for detection. Absorbance was read at a wavelength of 490 nm with an iMark Microplate Reader (Bio-Rad, Hercules, CA).

Immunoblotting

Equal amount (1 μg/ml) of PFO (MyBioSource, San Diego, CA) or SLO (Bio Academia, Osaka, Japan) was suspended in SDS sample buffer (Bio-Rad), and boiled for 5 min. The proteins (10 ng/10 μL) were separated by SDS-PAGE, and then transferred to polyvinylidene fluoride membranes (Millipore, Bedford, MA). Membranes were then probed with HS1, HS2, and HS3 mAbs at a concentration of 1 μg/ml as the primary antibody. Subsequently, membranes were labeled with anti-mouse IgG conjugated to horseradish peroxidase (GE Healthcare, Buckinghamshire, UK), and visualized using the ECL Western Blotting Detection System (GE Healthcare).

Bacterial strains

The invasive strains NIH34 (emm3 genotype) and NIH230 (emm49 genotype) were isolated by the Working Group for Beta-hemolytic Streptococci in Japan [16] from a patient with STSS, diagnosed as per the criteria proposed by the Working Group on Severe Streptococcal Infections [27]. The culture and preparation of bacteria were performed as previously described [28].

Human neutrophil killing assay

Human neutrophils were isolated from the venous blood of two healthy volunteers, in accordance with a protocol approved by the Institutional Review Board for Human Subjects, National Institute of Infectious Diseases, Japan (Permit number: 756). This study complies with the guidelines of the Declaration of Helsinki. A modified chemotaxis assay was performed as previously described [15, 16]. Briefly, 3 × 105 neutrophils in Roswell Park Memorial Institute medium containing 25 mM HEPES and 1% FBS were cultured on Transwell inserts (3 μm pore size, Coaster, Corning, NY) in 24-well plates containing 600 µl medium, or 100 nM interleukin (IL)-8 solution (Peprtec, London, UK); these were incubated with or without 3 × 106 bacteria in the absence or presence of HS1, HS2, HS3 mAbs, and control mouse IgG (Rockland, Gilbertsville, PA) for 60 min at 37 °C prior to the assay. After 60 min incubation, cells in the lower wells were collected and 104 10 μm microsphere beads (Polysciences Inc., Warrington, MA) were added. Cells were stained with propidium iodine (Sigma-Aldrich) for flow cytometry to quantify viable neutrophils, and were analyzed using a FACSCalibur (Becton, Dickinson and Company).

GAS infection in a mouse model

All animal protocols were approved by the Animal Experiments Committee at the National Institute of Infectious Diseases (Permit numbers: 116044, 118014), and were compliant with the Guide for Animal Experiments Performed at the National Institute of Infectious Diseases, Japan. Six-week old C57BL/6 male mice, 20–25 g, were purchased from Japan SLC (Shizuoka, Japan), and maintained in specific pathogen-free conditions. Mice were kept in collective cages (5–6 mice/cage) under a 12-h light/dark cycle and received water and feed ad libitum. GAS isolate (4.0 × 107 colony-forming units in 0.5 ml PBS) was inoculated intraperitoneally into 6-week old C57BL/6 male mice (5 or 6 mice per group). 1 h before or after infection, mice were administered an intraperitoneal injection of HS1, HS2, HS3 mAbs, and control mouse IgG (Rockland) (1 mg per mouse). Mouse survival was monitored daily for the indicated time period. At the end of the experiment and the humane endpoint, mice were euthanized by cervical dislocation under anesthesia. The humane endpoint was applied when abnormal appearance over a prolonged period with no visible indications of recovery was observed.

Statistical analysis

Data are expressed as mean ± standard deviation (SD). Statistical analyses were performed using GraphPad Prism 8 (GraphPad Software, San Diego, CA). Statistical significance was determined by the log-rank test. A value of p < 0.05 was considered statistically significant. *p < 0.05. The number of animals used in each experiment was determined on the basis of previously obtained results with the experimental model system [21, 28]. Figure legends indicate the number of independent experiments and biological replicates (n) used for statistical analysis.

Results

Cross-reactivity of anti-PLO mAbs with SLO

Hybridomas that produce neutralizing mAbs 3H10, 4D8, and 2C5 against PFO [26] were re-cloned and renamed HS1, HS2, and HS3, respectively. We examined cross-reactivity of these mAbs by ELISA (Fig. 1a) and immunoblotting (Fig. 1b and Additional file 1: Fig. S1). HS1 mAb, but not HS2 and HS3 mAbs, was reactive with SLO. These results suggest that HS1 mAb may recognize a certain common epitope or similar structure on both PFO and SLO.

Fig. 1
figure 1

HS1 mAb bound to SLO. a ELISA results of HS1, HS2, and HS3 mAbs binding to PFO and SLO. b Immunoblotting analysis of HS1, HS2, and HS3 mAbs binding to PFO and SLO

Full size image

The neutralizing mAb HS1 treatment improves the survival rate of neutrophils in the presence of STSS clinical isolates

We next investigated the neutralizing capacity of HS1, HS2, and HS3 mAbs for the cytotoxic activity of SLO against human neutrophil survival in the presence of an STSS clinical isolate. We have previously established a sensitive in vitro assay for GAS virulence based on SLO activity, by measure of neutrophil viability using a modified chemotaxis assay [15, 16]; human neutrophils that migrate into lower wells in response to IL-8 are killed by the SLO-producing STSS clinical isolates in a contact-dependent manner [15, 16]. Figure 2 shows that killing of human neutrophils by the STSS clinical isolates was inhibited by HS1 mAb. Control IgG, HS2, and HS3 mAbs did not inhibit neutrophil killing by the STSS clinical isolate (Fig. 2a and b). These results suggested that HS1 mAb was acting as a neutralizing mAb against SLO.

Fig. 2
figure 2

Effects of HS1 mAb treatment on STSS clinical isolate-infected human neutrophils. The results show the proportion of live neutrophils that migrated into lower wells in response to IL-8 alone (no bacteria) or IL-8 in the presence of the STSS clinical isolates (a) NIH34 (emm3) and (b) NIH230 (emm49) (3 × 106 colony-forming unites/well) treated with or without 1 μg/ml or 10 μg/ml HS1, HS2, HS3 mAbs, and control mouse IgG. Data are expressed as mean ± SD (n = 3). Data are representative of two independent experiments

Full size image

Pre- and post-treatment with HS1 mAb improves survival of mice infected with an STSS clinical isolate

To verify the effect of the neutralizing mAb HS1 on infection in vivo, a 7-day survival rate was undertaken, using a mouse model intraperitoneally infected with an STSS clinical isolate. Pre-treatment with HS1 mAb, but not control IgG, HS2, and HS3 mAbs, significantly improved the survival rate of mice infected with the STSS clinical isolate (Fig. 3a). Furthermore, post-treatment with HS1 mAb also, but not control IgG, HS2, and HS3 mAbs, improved the survival rate of mice infected with the STSS clinical isolate (Fig. 3b).

Fig. 3
figure 3

Effect of HS1 mAb administration on STSS clinical isolate-infected mice. C57BL/6 mice (male, 6-week-old) were intraperitoneally inoculated with NIH34 (4 × 107 colony-forming unites per mouse). HS1, HS2, HS3 mAbs, and control mouse IgG (1 mg per mouse) were administrated 1 h a before (n = 11 mice per group) or b after infection (n = 12 mice per group). Mouse survival was monitored for the indicated time period. The combined data from two independent experiments (n = 5 or 6 mice per group) are shown. *p < 0.05 by log-rank test versus control mouse IgG-treated group

Full size image

Discussion

Recently, high mortality in STSS patients has not been significantly reduced despite adequate antibiotic treatment in high-income countries, and the efficacy of combined antibiotic therapy and adjunctive intravenous immunoglobulin (IVIG) therapy in STSS has been evaluated [29]. A high dosage (0.5–1.0 g/kg) of IVIG is required for IVIG therapy, which is expensive and difficult to achieve. Therefore, the development of targeted therapy for STSS virulence factors is required. We have previously reported that SLO is one of the major virulence factors in STSS [15, 16]. Here, we demonstrated that antibody therapy against SLO may be a new adjunctive treatment for STSS.

In this study, the ability of an STSS clinical isolate to kill neutrophils was inhibited by the addition of HS1 mAb, but not HS2 and HS3 mAbs. Furthermore, in the mouse model, pre- and post-treatment with HS1 mAb, but not HS2 and HS3 mAbs, significantly increased the survival rate of mice infected with an STSS clinical isolate. These results suggest that HS1 mAb, which prevents neutrophil death in GAS infection, may be used as an adjunctive protective antibody for STSS.

SLO belongs to a large family of pore-forming toxins called CDCs [9,10,11,12,13]. CDCs are secreted by gram-positive bacteria, including Bacillus, Listeria, Lysinibacillus, Paenibacillus, Brevibacillus, Streptococcus, Clostridium, Gardnerella, Arcanobacterium, and Lactobacillus [30]. Notably, it has been reported that PFO neutralizing mAb 3H10, an original clone of HS1 mAb, has cross-reactivity not only with SLO but also with Clostridium bifermentans-derived bifermentolysin and Clostridium sordellii-derived sordelliolysin [26, 31]. If HS1 mAb binds to other CDCs and can neutralize them as well as SLO, PFO, bifermentolysin, and sordelliolysin, HS1 mAb may become an effective adjunctive therapeutic antibody for many gram-positive bacterial infections.

Limitations

We did not identify the specific conformational epitope of SLO and PFO recognized by HS1 mAb. In vivo protection assays were performed using only one strain, single dose, and intraperitoneal route of mAb administration.

Availability of data and materials

Complete sequence data that support the findings of this study have been deposited in the DNA Data Bank of Japan (DDBJ), the EMBL Nucleotide Sequence Database, and GenBank under the following accession numbers (LC545573, LC545574, LC545575, LC545576, LC545577, LC545578). The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CDC:

Cholesterol-dependent cytolysin

GAS:

Group A Streptococcus

mAb:

Monoclonal antibody

PFO:

Perfringolysin O

SLO:

Streptolysin O

STSS:

Streptococcal toxic shock syndrome

References

  1. Lappin E, Ferguson AJ. Gram-positive toxic shock syndromes. Lancet Infect Dis. 2009;9:281–90.

    Article  CAS  Google Scholar 

  2. Cunningham MW. Pathogenesis of group A streptococcal infections. Clin Microbiol Rev. 2000;13:470–511.

    Article  CAS  Google Scholar 

  3. Davies HD, McGeer A, Schwartz B, Green K, Cann D, Simor AE, et al. Invasive group A streptococcal infections in Ontario, Canada. N Engl J Med. 1996;335:547–54.

    Article  CAS  Google Scholar 

  4. Bisno AL, Stevens DL. Streptococcal infections of skin and soft tissues. N Engl J Med. 1996;334:240–5.

    Article  CAS  Google Scholar 

  5. Stevens DL. The toxins of group A Streptococcus, the flesh eating bacteria. Immunol Invest. 1997;26:129–50.

    Article  CAS  Google Scholar 

  6. Carapetis JR, Steer AC, Mulholland EK, Weber M. The global burden of group A streptococcal diseases. Lancet Infect Dis. 2005;5:685–94.

    Article  Google Scholar 

  7. Centers for Disease Control and Prevention (CDC), Surveillance Reports (from 1997 to 2017). https://www.cdc.gov/abcs/reports-findings/surv-reports.html. Accessed 29 Jan 2020.

  8. National Institute of Infectious Diseases, Infectious Diseases Weekly Report Japan (from 2006 to 2019). https://www.niid.go.jp/niid/ja/idwr.html. Accessed 29 Jan 2020.

  9. Tweten RK, Parker MW, Johnson AE. The cholesterol-dependent cytolysins. Curr Top Microbiol Immunol. 2001;257:15–33.

    PubMed  CAS  Google Scholar 

  10. Parker MW, Feil SC. Pore-forming protein toxins: from structure to function. Prog Biophys Mol Biol. 2005;88:91–142.

    Article  CAS  Google Scholar 

  11. Tweten RK. Cholesterol-dependent cytolysins, a family of versatile pore-forming toxins. Infect Immun. 2005;73:6199–209.

    Article  CAS  Google Scholar 

  12. Hotze EM, Tweten RK. Membrane assembly of the cholesterol-dependent cytolysin pore complex. Biochim Biophys Acta. 2012;1818:1028–38.

    Article  CAS  Google Scholar 

  13. Reboul CF, Whisstock JC, Dunstone MA. Giant MACPF/CDC pore forming toxins: a class of their own. Biochim Biophys Acta. 2016;1858:475–86.

    Article  CAS  Google Scholar 

  14. Hakansson A, Bentley CC, Shakhnovic EA, Wessels MR. Cytolysin-dependent evasion of lysosomal killing. Proc Natl Acad Sci USA. 2005;102:5192–7.

    Article  CAS  Google Scholar 

  15. Ato M, Ikebe T, Kawabata H, Takemori T, Watanabe H. Incompetence of neutrophils to invasive group A Streptococcus is attributed to induction of plural virulence factors by dysfunction of a regulator. PLoS ONE. 2008;3:e3455.

    Article  CAS  Google Scholar 

  16. Ikebe T, Ato M, Matsumura T, Hasegawa H, Sata T, Kobayashi K, et al. Highly frequent mutations in negative regulators of multiple virulence genes in group A streptococcal toxic shock syndrome isolates. PLoS Pathog. 2010;6:e1000832.

    Article  CAS  Google Scholar 

  17. Timmer AM, Timmer JC, Pence MA, Hsu LC, Ghochani M, Frey TG, et al. Streptolysin O promotes group A Streptococcus immune evasion by accelerated macrophage apoptosis. J Biol Chem. 2009;284:862–71.

    Article  CAS  Google Scholar 

  18. Goldmann O, Sastalla I, Wos-Oxley M, Rohde M, Medina E. Streptococcus pyogenes induces oncosis in macrophages through the activation of an inflammatory programmed cell death pathway. Cell Microbiol. 2009;11:138–55.

    Article  CAS  Google Scholar 

  19. Cortes G, Wessels MR. Inhibition of dendritic cell maturation by group A Streptococcus. J Infect Dis. 2009;200:1152–61.

    Article  CAS  Google Scholar 

  20. Eriksson BK, Andersson J, Holm SE, Norgren M. Epidemiological and clinical aspects of invasive group A streptococcal infections and the streptococcal toxic shock syndrome. Clin Infect Dis. 1998;27:1428–36.

    Article  CAS  Google Scholar 

  21. Matsumura T, Ato M, Ikebe T, Ohnishi M, Watanabe H, Kobayashi K. Interferon-γ-producing immature myeloid cells confer protection against severe invasive group A Streptococcus infections. Nat Commun. 2012;3:678.

    Article  CAS  Google Scholar 

  22. Nasser W, Beres SB, Olsen RJ, Dean MA, Rice KA, Long SW, et al. Evolutionary pathway to increased virulence and epidemic group A Streptococcus disease derived from 3,615 genome sequences. Proc Natl Acad Sci U S A. 2014;111:E1768–76.

    Article  CAS  Google Scholar 

  23. O’Seaghdha M, Wessels MR. Streptolysin O and its co-toxin NAD-glycohydrolase protect group A Streptococcus from Xenophagic killing. PLoS Pathog. 2013;9:e1003394.

    Article  CAS  Google Scholar 

  24. Bastiat-Sempe B, Love JF, Lomayesva N, Wessels MR. Streptolysin O and NAD-glycohydrolase prevent phagolysosome acidification and promote group A Streptococcus survival in macrophages. MBio. 2014;5:e01690.

    Article  CAS  Google Scholar 

  25. Velarde JJ, Seaghdha M, Baddal B, Bastiat-Sempe B, Wessels MR. Binding of NAD(+)-glycohydrolase to streptolysin O stabilizes both toxins and promotes virulence of group A Streptococcus. Bio Res. 2017;8(5):e01382.

    CAS  Google Scholar 

  26. Sato H, Ito A, Chiba J. Cross-reactivity of monoclonal antibodies against Clostridium perfringens θ toxin with streptolysin O. Curr Micobiol. 1984;10:243–8.

    Article  Google Scholar 

  27. Breiman RF, Davis JP, Facklam RR, Gray BM, Hoge CW, Kaplan EL, et al. Defining the group A streptococcal toxic shock syndrome. Rationale and consensus definition. JAMA. 1993;269:390–1.

    Article  Google Scholar 

  28. Matsumura T, Ikebe T, Arikawa K, Hosokawa M, Aiko M, Iguchi A, et al. Sequential sensing by TLR2 and Mincle directs immature myeloid cells to protect against invasive group A streptococcal infection in mice. Cell Rep. 2019;27:561–71.

    Article  CAS  Google Scholar 

  29. Linner A, Darenberg J, Sjolin J, Henriques-Normark B, Norrby-Teglund A. Clinical efficacy of polyspecific intravenous immunoglobulin therapy in patients with streptococcal toxic shock syndrome: a comparative observational study. Clin Infect Dis. 2014;59:851–7.

    Article  CAS  Google Scholar 

  30. Johnson BB, Heuck AP. Perfringolysin O structure and mechanism of pore formation as a paradigm for cholesterol-dependent cytolysins. Subcell Biochem. 2014;80:63–81.

    Article  CAS  Google Scholar 

  31. Sato H. Monoclonal antibodies against Clostridium perfringens θ toxin (Perfringolysin O). In: Macario AJL, de Macario EC, editors. Monoclonal antibodies against bacteria, vol. III. Amsterdam: Elsevier; 1986. p. 203–28.

    Chapter  Google Scholar 

Download references

Acknowledgements

We thank Dr. Hiroko Sato for kindly providing hybridomas (clone 3H10, 4D8, and 2C5). We also thank Eriko Izumiyama, Akira Dosaka, Aoi Iguchi, Ikuko Togashi, and Ryoko Itami for technical support.

Funding

This work was supported by the Japan Agency for Medical Research and Development (AMED) under Grant Number JP20fk0108130 (TM), Japan Society for the Promotion of Science (JSPS) KAKENHI Grant Number JP20K08833 (TM), and the Takeda Science Foundation (TM).

Author information

Author notes

  1. Takayuki Matsumura and Ayae Nishiyama contributed equally to this work

Authors and Affiliations

  1. Department of Immunology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo, 162-8640, Japan

    Takayuki Matsumura, Ayae Nishiyama, Michio Aiko & Yoshimasa Takahashi

  2. Department of Pathology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo, 162-8640, Japan

    Akira Ainai & Joe Chiba

  3. Department of Bacteriology I, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo, 162-8640, Japan

    Tadayoshi Ikebe

  4. Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, 4-2-1 Aobacho, Higashimurayamashi, Tokyo, 189-0002, Japan

    Manabu Ato

Authors
  1. Takayuki Matsumura
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Ayae Nishiyama
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Michio Aiko
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Akira Ainai
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Tadayoshi Ikebe
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Joe Chiba
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Manabu Ato
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Yoshimasa Takahashi
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

TM conceived the study design, obtained funding and ethics approvals, performed the experiments, interpreted the data, and wrote the draft manuscript. AN performed the experiments, interpreted the data, and wrote the draft manuscript. MAi performed the experiments. AA and TI provided advice on the study design, interpreted the data, and revised the draft manuscript. JC conceived the study design, interpreted the data, and revised the draft manuscript. MAt conceived the study design, obtained ethics approvals, interpreted the data, and revised the draft manuscript. YT conceived the study design, interpreted the data, wrote the draft manuscript, and supervised the study. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Takayuki Matsumura or Yoshimasa Takahashi.

Ethics declarations

Ethics approval and consent to participate

This study protocol was approved by the National Institute of Infectious Diseases Ethic Review Board for Human Subjects (Permit number: 756) and the animal experiments were approved by the National Institute of Infectious Diseases Animal Experiments Committee (Permit numbers: 116044, 118014). All participants provided written informed consent in accordance with the Declaration of Helsinki. All animal experiments were performed according to the Guide for Animal Experiments Performed at National Institute of Infectious Diseases, Japan.

Consent for publication

Not applicable.

Competing interests

TM., J.C., M.Ato, and Y.T. have filed a patent application for antibodies HS1, HS2, and HS3 with the National Institute of Infectious Diseases.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Additional file 1.

Immunoblot analysis of HS1, HS2, and HS3 mAbs binding to PFO and SLO.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Matsumura, T., Nishiyama, A., Aiko, M. et al. An anti-perfringolysin O monoclonal antibody cross-reactive with streptolysin O protects against streptococcal toxic shock syndrome. BMC Res Notes 13, 419 (2020). https://doi.org/10.1186/s13104-020-05264-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13104-020-05264-2

Keywords

  • Streptococcal toxic shock syndrome
  • Cholesterol-dependent cytolysins
  • Streptolysin O
  • Perfringolysin O
  • Neutralizing monoclonal antibody

BMC Research Notes

ISSN: 1756-0500

Contact us