Immunoglobulin Attenuates Streptokinase-Mediated Virulence inStreptococcus dysgalactiae Subspeciesequisimilis Necrotizing Fasciitis

Author:

Andreoni Federica1,Ugolini Fabio21,Keller Nadia1,Neff Andrina1,Nizet Victor34,Hollands Andrew3,Marques Maggio Ewerton5,Zinkernagel Annelies S11,Schuepbach Reto A2

Affiliation:

1. Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Switzerland

2. Institute of Intensive Care Medicine, University Hospital Zurich, University of Zurich, Switzerland

3. Department of Pediatrics, Division of Pharmacology and Drug Discovery, San Diego, California

4. Skaggs School of Pharmacy and Pharmaceutical Sciences, San Diego, California

5. Department of Pathology and Molecular Pathology, University Hospital Zurich, University of Zurich, Switzerland

Abstract

Abstract Background Necrotizing fasciitis (NF) retains a very high mortality rate despite prompt and adequate antibiotic treatment and surgical debridement. Necrotizing fasciitis has recently been associated withStreptococcus dysgalactiae subspeciesequisimilis (SDSE). Methods We investigated the causes of a very severe clinical manifestation of SDSE-NF by assessing both host and pathogen factors. Results We found a lack of streptokinase-function blocking antibodies in the patient resulting in increased streptokinase-mediated fibrinolysis and bacterial spread. At the same time, the clinical SDSE isolate produced very high levels of streptokinase. Exogenous immunoglobulin Gs (ex-IgGs) efficiently blocked streptokinase-mediated fibrinolysis in vitro, indicating a protective role against the action of streptokinase. In vivo, SDSE infection severity was also attenuated by ex-IgGs in a NF mouse model. Conclusions These findings illustrate for the first time that the lack of specific antibodies against streptococcal virulence factors, such as streptokinase, may contribute to NF disease severity. This can be counteracted by ex-IgGs.

Funder

NIH

National Institutes of Health

Swiss National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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