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Updated model of group A Streptococcus M proteins based on a comprehensive worldwide study
D J McMillan1, P-A Drèze, T Vu
1Bacterial Pathogenesis Laboratory, Queensland Institute of Medical Research, Brisbane, Qld, Australia.
Abstract:
Group A Streptococcus (GAS) M protein is an important virulence factor and potential vaccine antigen, and constitutes the basis for strain typing (emm-typing). Although >200 emm-types are characterized, structural data were obtained from only a limited number of emm-types. We aim to evaluate the sequence diversity of near-full-length M proteins from worldwide sources and analyse their structure, sequence conservation and classification. GAS isolates recovered from throughout the world during the last two decades underwent emm-typing and complete emm gene sequencing. Predicted amino acid sequence analyses, secondary structure predictions and vaccine epitope mapping were performed using MUSCLE and Geneious software. A total of 1086 isolates from 31 countries were analysed, representing 175 emm-types. emm-type is predictive of the whole protein structure, independent of geographical origin or clinical association. Findings of an emm-type paired with multiple, highly divergent central regions were not observed. M protein sequence length, the presence or absence of sequence repeats and predicted secondary structure were assessed in the context of the latest vaccine developments. Based on these global data, the M6 protein model is updated to a three representative M protein (M5, M80 and M77) model, to aid in epidemiological analysis, vaccine development and M protein-related pathogenesis studies.
Insights
Group A Streptococcus M protein diversity was analyzed globally. emm-type accurately predicts M protein structure, aiding vaccine development and understanding pathogenesis.
Area of Science:
- Microbiology
- Structural Biology
- Vaccinology
Background:
- Group A Streptococcus (GAS) M protein is a key virulence factor and vaccine target.
- Over 200 emm-types exist, but structural data is limited for most.
- Understanding M protein diversity is crucial for vaccine design and epidemiology.
Purpose of the Study:
- To evaluate sequence diversity of GAS M proteins globally.
- To analyze M protein structure, conservation, and classification.
- To inform vaccine development and pathogenesis studies.
Main Methods:
- Analysis of 1086 GAS isolates from 31 countries over two decades.
- emm-typing and complete emm gene sequencing.
- Bioinformatic analyses including amino acid sequence, secondary structure predictions, and epitope mapping.
Main Results:
- 175 emm-types were represented in the global isolate collection.
- emm-type was found to be predictive of M protein structure, irrespective of origin or clinical association.
- No emm-type was associated with multiple, highly divergent central regions.
Conclusions:
- M protein structure is conserved within an emm-type, supporting its use in classification.
- Global M protein data refines structural models (e.g., M6 updated to M5, M80, M77 models).
- Findings facilitate improved epidemiological analysis, vaccine development, and pathogenesis research.
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