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Published on: November 4, 2016
Genetic diversity of Group A Streptococcus M protein: implications for typing and vaccine development
Pierre R Smeesters1, Patrick Mardulyn, Anne Vergison
1Laboratoire de Génétique et Physiologie Bactérienne, Institut de Biologie et de Médecine Moléculaires, Faculté des Sciences, Université Libre de Bruxelles, 12 rue des Professeurs Jeener et Brachet, 6041 Gosselies, Belgium. psmeeste@ulb.ac.be
Abstract:
Group A Streptococci (GAS) are classified into 180 emm-types based on the sequence of the amino-terminal hyper-variable region of the M surface protein. The genetic relatedness of the whole surface-exposed part of M was investigated in well-characterized Belgian and Brazilian GAS isolates which belong to different epidemiological and clinical landscapes. Despite a small number of different emm-types and an apparent low diversity in the Belgian isolates (as revealed by the emm-typing method), our data showed that the overall genetic diversity of the M proteins was higher than expected. On the contrary, the M proteins from the Brazilian isolates were genetically highly related. Since M is a multi-functional protein, an analysis of the whole surface-exposed sequence that takes into account the different functional domains may provide tools for typing as well as for analyzing the molecular mechanisms of M virulence or defining vaccine strategies.
Insights
Group A Streptococci (GAS) M protein diversity was analyzed in Belgian and Brazilian isolates. Despite low emm-type diversity, M protein genetic relatedness varied significantly between the two groups.
Area of Science:
- Microbiology
- Molecular Biology
- Immunology
Background:
- Group A Streptococci (GAS) are classified by emm-types based on M surface protein variations.
- M protein is crucial for GAS virulence and is a target for vaccine development.
- Understanding M protein genetic diversity is key to tracking GAS strains and developing effective interventions.
Purpose of the Study:
- To investigate the genetic relatedness of the whole surface-exposed M protein in Belgian and Brazilian GAS isolates.
- To compare M protein diversity across different epidemiological and clinical landscapes.
- To explore the utility of M protein sequence analysis for GAS typing and vaccine strategies.
Main Methods:
- Characterization of Belgian and Brazilian GAS isolates.
- Analysis of the full surface-exposed sequence of the M protein.
- Comparison of genetic diversity using sequence data.
Main Results:
- Belgian GAS isolates showed higher than expected M protein genetic diversity, despite a low number of emm-types.
- Brazilian GAS isolates exhibited high genetic relatedness among their M proteins.
- The study revealed significant differences in M protein diversity between the two geographic groups.
Conclusions:
- The M protein's full surface-exposed sequence provides deeper insights into GAS genetic diversity than emm-typing alone.
- Analyzing M protein functional domains can enhance GAS typing and inform virulence mechanism studies.
- This approach may aid in developing targeted vaccine strategies against GAS.
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