Global Population Structure and Evolution of Bordetella pertussis and Their Relationship with Vaccination

Author:

Bart Marieke J.12,Harris Simon R.3,Advani Abdolreza4,Arakawa Yoshichika5,Bottero Daniela6,Bouchez Valérie78,Cassiday Pamela K.9,Chiang Chuen-Sheue10,Dalby Tine11,Fry Norman K.12,Gaillard María Emilia6,van Gent Marjolein1,Guiso Nicole78,Hallander Hans O.4,Harvill Eric T.13,He Qiushui14,van der Heide Han G. J.1,Heuvelman Kees1,Hozbor Daniela F.6,Kamachi Kazunari5,Karataev Gennady I.15,Lan Ruiting16,Lutyńska Anna17,Maharjan Ram P.16,Mertsola Jussi18,Miyamura Tatsuo5,Octavia Sophie16,Preston Andrew19,Quail Michael A.3,Sintchenko Vitali2021,Stefanelli Paola22,Tondella M. Lucia9,Tsang Raymond S. W.23,Xu Yinghua24,Yao Shu-Man10,Zhang Shumin24,Parkhill Julian3,Mooi Frits R.12

Affiliation:

1. Centre for Infectious Diseases Research, Diagnostics and Screening (IDS), Centre for Infectious Diseases Control (CIb), National Institute of Public Health and the Environment (RIVM), Bilthoven, The Netherlands

2. UMC St. Radboud Hospital, Nijmegen, The Netherlands

3. Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

4. Swedish Institute for Communicable Disease Control (SMI), Solna, Sweden

5. National Institute of Infectious Diseases, Shinjuku-ku, Tokyo, Japan

6. Laboratorio VacSal, Instituto de Biotecnología y Biología Molecular, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, CONICET, La Plata, Argentina

7. Institut Pasteur, Molecular Prevention and Therapy of Human Infections, Paris, France

8. Centre National de la Recherche Scientifique, URA-CNRS 30-12, Paris, France

9. National Center for Immunization and Respiratory Diseases (NCIRD), Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, USA

10. Centers for Disease Control, Taipei, Taiwan, Republic of China

11. Microbiology & Infection Control, Statens Serum Institut, Copenhagen, Denmark

12. Public Health England—Respiratory and Vaccine Preventable Bacteria Reference Unit, Colindale, United Kingdom

13. Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, University Park, Pennsylvania, USA

14. Department of Infectious Disease Surveillance and Control, National Institute for Health and Welfare, Finland

15. Gamaleya Research Institute for Epidemiology and Microbiology, Ministry of Health Russian Federation, Moscow, Russian Federation

16. School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia

17. National Institute of Public Health, National Institute of Hygiene, Warsaw, Poland

18. Department of Pediatrics, Turku University Hospital, Turku, Finland

19. Department of Biology and Biochemistry, University of Bath, Bath, United Kingdom

20. Centre for Infectious Diseases and Microbiology—Public Health, Institute of Clinical Pathology and Medical Research, Westmead Hospital, Westmead, New South Wales, Australia

21. Sydney Emerging Infectious Diseases and Biosecurity Institute, The University of Sydney, Sydney, New South Wales, Australia

22. Department of Infectious, Parasitic & Immune-Mediated Diseases, Istituto Superiore di Sanita, Rome, Italy

23. Laboratory for Syphilis Diagnostics and Vaccine Preventable Bacterial Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada

24. National Institute for Food and Drug Control, Beijing, Republic of China

Abstract

ABSTRACT Bordetella pertussis causes pertussis, a respiratory disease that is most severe for infants. Vaccination was introduced in the 1950s, and in recent years, a resurgence of disease was observed worldwide, with significant mortality in infants. Possible causes for this include the switch from whole-cell vaccines (WCVs) to less effective acellular vaccines (ACVs), waning immunity, and pathogen adaptation. Pathogen adaptation is suggested by antigenic divergence between vaccine strains and circulating strains and by the emergence of strains with increased pertussis toxin production. We applied comparative genomics to a worldwide collection of 343 B. pertussis strains isolated between 1920 and 2010. The global phylogeny showed two deep branches; the largest of these contained 98% of all strains, and its expansion correlated temporally with the first descriptions of pertussis outbreaks in Europe in the 16th century. We found little evidence of recent geographical clustering of the strains within this lineage, suggesting rapid strain flow between countries. We observed that changes in genes encoding proteins implicated in protective immunity that are included in ACVs occurred after the introduction of WCVs but before the switch to ACVs. Furthermore, our analyses consistently suggested that virulence-associated genes and genes coding for surface-exposed proteins were involved in adaptation. However, many of the putative adaptive loci identified have a physiological role, and further studies of these loci may reveal less obvious ways in which B. pertussis and the host interact. This work provides insight into ways in which pathogens may adapt to vaccination and suggests ways to improve pertussis vaccines. IMPORTANCE Whooping cough is mainly caused by Bordetella pertussis , and current vaccines are targeted against this organism. Recently, there have been increasing outbreaks of whooping cough, even where vaccine coverage is high. Analysis of the genomes of 343 B. pertussis isolates from around the world over the last 100 years suggests that the organism has emerged within the last 500 years, consistent with historical records. We show that global transmission of new strains is very rapid and that the worldwide population of B. pertussis is evolving in response to vaccine introduction, potentially enabling vaccine escape.

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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