Vaccination against the M protein of Streptococcus pyogenes prevents death after influenza virus: S. pyogenes super-infection
Related Experiment Video
Updated: Apr 26, 2026

Co-immunoprecipitation of the Mouse Mx1 Protein with the Influenza A Virus Nucleoprotein
Published on: April 21, 2015
Joshua M Klonoski1, Heather R Hurtig1, Brian A Juber1
1Division of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota, Vermillion, SD, United States.
Abstract:
Influenza virus infections are associated with a significant number of illnesses and deaths on an annual basis. Many of the deaths are due to complications from secondary bacterial invaders, including Streptococcus pneumoniae, Staphylococcus aureus, Haemophilus influenzae, and Streptococcus pyogenes. The β-hemolytic bacteria S. pyogenes colonizes both skin and respiratory surfaces, and frequently presents clinically as strep throat or impetigo. However, when these bacteria gain access to normally sterile sites, they can cause deadly diseases including sepsis, necrotizing fasciitis, and pneumonia. We previously developed a model of influenza virus:S. pyogenes super-infection, which we used to demonstrate that vaccination against influenza virus can limit deaths associated with a secondary bacterial infection, but this protection was not complete. In the current study, we evaluated the efficacy of a vaccine that targets the M protein of S. pyogenes to determine whether immunity toward the bacteria alone would allow the host to survive an influenza virus:S. pyogenes super-infection. Our data demonstrate that vaccination against the M protein induces IgG antibodies, in particular those of the IgG1 and IgG2a isotypes, and that these antibodies can interact with macrophages. Ultimately, this vaccine-induced immunity eliminated death within our influenza virus:S. pyogenes super-infection model, despite the fact that all M protein-vaccinated mice showed signs of illness following influenza virus inoculation. These findings identify immunity against bacteria as an important component of protection against influenza virus:bacteria super-infection.
Insights
Vaccinating against Streptococcus pyogenes M protein prevents deaths from influenza and bacterial superinfections. This bacterial immunity is crucial for survival, even when influenza virus infection causes illness.
Area of Science:
- * Infectious disease research
- * Immunology
- * Microbiology
Background:
- * Influenza virus infections cause significant annual morbidity and mortality.
- * Secondary bacterial infections, particularly with Streptococcus pyogenes, are a major cause of death following influenza.
- * Previous studies showed influenza vaccination offers incomplete protection against secondary bacterial superinfections.
Purpose of the Study:
- * To evaluate the efficacy of a vaccine targeting the M protein of Streptococcus pyogenes.
- * To determine if immunity to Streptococcus pyogenes alone can protect against influenza virus:S. pyogenes superinfections.
- * To assess the role of bacterial immunity in mitigating lethal outcomes of viral-bacterial coinfections.
Main Methods:
- * Development of a murine model for influenza virus:Streptococcus pyogenes superinfection.
- * Vaccination of mice against the M protein of Streptococcus pyogenes.
- * Assessment of immune responses, including IgG antibody production and macrophage interaction.
- * Evaluation of survival rates and clinical signs following superinfection.
Main Results:
- * Vaccination against M protein induced specific IgG antibodies (IgG1 and IgG2a isotypes).
- * These antibodies demonstrated interaction with macrophages, suggesting an immune mechanism.
- * M protein vaccination completely eliminated mortality in the influenza virus:Streptococcus pyogenes superinfection model.
- * M protein-vaccinated mice still exhibited signs of illness after influenza virus infection.
Conclusions:
- * Immunity targeting Streptococcus pyogenes M protein provides complete protection against lethal influenza virus:S. pyogenes superinfection.
- * Antibodies against bacterial components are critical for host survival during viral-bacterial coinfections.
- * Targeting bacterial immunity is a viable strategy to combat severe outcomes of respiratory viral infections complicated by bacterial pathogens.
More Related Videos
10:47Using Bioluminescent Imaging to Investigate Synergism Between Streptococcus pneumoniae and Influenza A Virus in Infant Mice
Published on: April 14, 2011
04:47A Method to Assess Fc-mediated Effector Functions Induced by Influenza Hemagglutinin Specific Antibodies
Published on: February 23, 2018
Related Concept Videos
Vaccinations
Leaky Scanning
Influenza
Vaccines
Immune Response Against Viral Pathogens
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...
Viral Recombination