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Biological differences between FIM2 and FIM3 fimbriae of Bordetella pertussis: not just the serotype
Soraya Matczak1, Valérie Bouchez2, Pauline Leroux1
1Institut Pasteur, Université Paris Cité, Biodiversity and Epidemiology of Bacterial Pathogens, 28, Rue Du Docteur Roux, 75015, Paris, France.
Introduction:
Bordetella pertussis still circulates worldwide despite vaccination. Fimbriae are components of some acellular pertussis vaccines. Population fluctuations of B. pertussis fimbrial serotypes (FIM2 and FIM3) are observed, and fim3 alleles (fim3-1 [clade 1] and fim3-2 [clade 2]) mark a major phylogenetic subdivision of B. pertussis.
Objectives:
To compare microbiological characteristics and expressed protein profiles between fimbrial serotypes FIM2 and FIM3 and genomic clades.
Methods:
A total of 19 isolates were selected. Absolute protein abundance of the main virulence factors, autoagglutination and biofilm formation, bacterial survival in whole blood, induced blood cell cytokine secretion, and global proteome profiles were assessed.
Results:
Compared to FIM3, FIM2 isolates produced more fimbriae, less cellular pertussis toxin subunit 1 and more biofilm, but auto-agglutinated less. FIM2 isolates had a lower survival rate in cord blood, but induced higher levels of IL-4, IL-8 and IL-1β secretion. Global proteome comparisons uncovered 15 differentially produced proteins between FIM2 and FIM3 isolates, involved in adhesion and metabolism of metals. FIM3 isolates of clade 2 produced more FIM3 and more biofilm compared to clade 1.
Conclusion:
FIM serotype and fim3 clades are associated with proteomic and other biological differences, which may have implications on pathogenesis and epidemiological emergence.
Insights
Bordetella pertussis serotypes FIM2 and FIM3 show distinct proteomic and biological differences. These variations in fimbrial serotypes and fim3 clades impact pathogenesis and the emergence of pertussis.
Area of Science:
- Microbiology
- Immunology
- Genomics
Background:
- Bordetella pertussis circulates globally despite vaccination efforts.
- Fimbriae are key components in acellular pertussis vaccines.
- Distinct population dynamics exist for B. pertussis fimbrial serotypes (FIM2, FIM3) and fim3 alleles (clade 1, clade 2).
Purpose of the Study:
- To compare microbiological characteristics and protein expression between FIM2 and FIM3 serotypes.
- To analyze differences in relation to genomic clades of B. pertussis.
Main Methods:
- Analysis of 19 B. pertussis isolates.
- Assessment of virulence factors, autoagglutination, biofilm formation, and bacterial survival in whole blood.
- Evaluation of induced cytokine secretion and global proteome profiling.
Main Results:
- FIM2 isolates exhibited higher fimbriae and biofilm production, but less pertussis toxin and autoagglutination compared to FIM3.
- FIM2 isolates showed reduced survival in cord blood but induced higher IL-4, IL-8, and IL-1β levels.
- Proteomic analysis revealed 15 differentially expressed proteins related to adhesion and metal metabolism; FIM3 clade 2 isolates produced more FIM3 and biofilm than clade 1.
Conclusions:
- Fimbrial serotype and fim3 clades are linked to significant proteomic and biological variations in B. pertussis.
- These differences may influence the pathogenesis and epidemiological spread of pertussis.
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