Abstract

Bordetella pertussis is the causative agent of pertussis, a highly contagious disease of the human respiratory tract. Despite high vaccination coverage, pertussis has resurged and has become one of the most prevalent vaccine-preventable diseases in developed countries. We have proposed that both waning immunity and pathogen adaptation have contributed to the persistence and resurgence of pertussis. Allelic variation has been found in virulence-associated genes coding for the pertussis toxin A subunit (ptxA), pertactin (prn), serotype 2 fimbriae (fim2), serotype 3 fimbriae (fim3) and the promoter for pertussis toxin (ptxP). In this study, we investigated how more than 60 years of vaccination has affected the Dutch B. pertussis population by combining data from phylogeny, genomics and temporal trends in strain frequencies. Our main focus was on the ptxA, prn, fim3 and ptxP genes. However, we also compared the genomes of 11 Dutch strains belonging to successful lineages. Our results showed that, between 1949 and 2010, the Dutch B. pertussis population has undergone as least four selective sweeps that were associated with small mutations in ptxA, prn, fim3 and ptxP. Phylogenetic analysis revealed a stepwise adaptation in which mutations accumulated clonally. Genomic analysis revealed a number of additional mutations which may have a contributed to the selective sweeps. Five large deletions were identified which were fixed in the pathogen population. However, only one was linked to a selective sweep. No evidence was found for a role of gene acquisition in pathogen adaptation. Our results suggest that the B. pertussis gene repertoire is already well adapted to its current niche and required only fine tuning to persist in the face of vaccination. Further, this work shows that small mutations, even single SNPs, can drive large changes in the populations of bacterial pathogens within a time span of six to 19 years.

Highlights

  • Compared to theoretical studies on the effect of vaccination on pathogen evolution [1,2,3,4], there is a paucity of data from field studies, especially with respect to bacterial and protozoan pathogens

  • The tree was rooted with an 18323-like strain (B0442) which is closely related to B. bronchiseptica, a species from which B. pertussis has evolved [48]

  • The Maximum Parsimony (MP) tree allowed us to investigate the genetic relationship between strains containing allelic variants of genes implicated in the adaptation of B. pertussis [10,23,39,44,49,50,51]: pertussis toxin promoter (ptxP), pertussis toxin A subunit (ptxA), prn, fim2 and fim3 (See Supplementary Fig. S1 for allelic variants used in this study)

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Summary

Introduction

Compared to theoretical studies on the effect of vaccination on pathogen evolution [1,2,3,4], there is a paucity of data from field studies, especially with respect to bacterial and protozoan pathogens. There are practical reasons for this, such as the lack of historical strain collections, the relatively complexity bacterial and protozoan genomes and their relative slow evolution rate. Pertussis has become one of the most prevalent vaccine-preventable diseases in developed countries with estimated infection frequencies of 1–6% [16,17,18,19]. In The Netherlands, the infection frequency was estimated to be 9.3% for the age category .9 years in 2006–2007 [20]. Due to the high circulation rate of B. pertussis, adolescents and adults are often the source of infection for newly born who receive their first vaccination at the age of 2–3 months and are unprotected during the first months of life [21,22]

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