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Updated: Jul 28, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Variable susceptibility to opsonophagocytosis of group A streptococcus M-1 strains by human immune sera
A Villaseñor-Sierra1, W M McShan, D Salmi
1Centro de Investigacion Biomedica de Occidente (CIBO), Instituto Mexicano del Seguro Social, Guadalajara, Mexico.
Abstract:
Immunity to group A streptococci (GAS) is thought to be related to the acquisition of type-specific antibody directed against the M protein. However, recent work suggests that immunity may only be strain and not M-type specific. Therefore, susceptibility of 70 different GAS M-1 strains to opsonization and killing by convalescent sera was compared by using a highly sensitive chemiluminescence assay and by standard bactericidal assay. Sequencing of the emm1 gene in 10 strains with variable susceptibility to opsonization revealed 100% homology in 9 strains. Several substitutions in the N-terminal and 2 in the A3 repeat regions of strain CS-190 were associated with profound resistance to opsonization. Thus amino acid substitutions within different regions of the M-1 protein molecule may adversely affect opsonization by immune sera. In addition, non-M protein factors from identical M types influence susceptibility to phagocytosis. These findings may in part explain the persistently high prevalence of M-1 strains worldwide over the last 15 years.
Insights
Immunity to group A streptococci (GAS) depends on antibodies to M protein, but strain-specific factors also impact opsonization and killing. Amino acid changes in M-1 protein can cause resistance to immune sera.
Area of Science:
- Microbiology
- Immunology
- Infectious Diseases
Background:
- Immunity to group A streptococci (GAS) is traditionally linked to type-specific antibodies against the M protein.
- Emerging evidence suggests that immunity might be strain-specific rather than solely M-type specific.
Purpose of the Study:
- To investigate the susceptibility of diverse GAS M-1 strains to opsonization and killing by convalescent sera.
- To identify genetic and molecular factors influencing GAS resistance to host immune responses.
Main Methods:
- Utilized a sensitive chemiluminescence assay and standard bactericidal assays to compare opsonization and killing of 70 GAS M-1 strains.
- Sequenced the emm1 gene of 10 strains exhibiting variable opsonization susceptibility.
Main Results:
- Identified significant variability in opsonization susceptibility among GAS M-1 strains.
- Found 100% homology in the emm1 gene for 9 out of 10 strains, with strain CS-190 showing substitutions linked to opsonization resistance.
- Demonstrated that amino acid substitutions in the M-1 protein and non-M protein factors influence phagocytosis resistance.
Conclusions:
- Amino acid variations within the M-1 protein can impair opsonization by immune sera.
- Non-M protein factors contribute to phagocytosis resistance in GAS strains of the same M type.
- These factors may explain the sustained prevalence of M-1 strains globally.
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