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Bordetella pertussis population dynamics and phylogeny in Japan after adoption of acellular pertussis vaccines

Bordetella pertussis, the causative agent of whooping cough, has experienced a resurgence in the past 15 years, despite the existence of both whole-cell and acellular vaccines. Here, we performed whole genome sequencing analysis of 149 clinical strains, provided by the National Institute of Infectio...

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Autores principales: Zomer, Aldert, Otsuka, Nao, Hiramatsu, Yukihiro, Kamachi, Kazunari, Nishimura, Naoko, Ozaki, Takao, Poolman, Jan, Geurtsen, Jeroen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994715/
https://www.ncbi.nlm.nih.gov/pubmed/29771235
http://dx.doi.org/10.1099/mgen.0.000180
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author Zomer, Aldert
Otsuka, Nao
Hiramatsu, Yukihiro
Kamachi, Kazunari
Nishimura, Naoko
Ozaki, Takao
Poolman, Jan
Geurtsen, Jeroen
author_facet Zomer, Aldert
Otsuka, Nao
Hiramatsu, Yukihiro
Kamachi, Kazunari
Nishimura, Naoko
Ozaki, Takao
Poolman, Jan
Geurtsen, Jeroen
author_sort Zomer, Aldert
collection PubMed
description Bordetella pertussis, the causative agent of whooping cough, has experienced a resurgence in the past 15 years, despite the existence of both whole-cell and acellular vaccines. Here, we performed whole genome sequencing analysis of 149 clinical strains, provided by the National Institute of Infectious Diseases (NIID), Japan, isolated in 1982–2014, after Japan became the first country to adopt acellular vaccines against B. pertussis. Additionally, we sequenced 39 strains provided by the Konan Kosei Hospital in Aichi prefecture, Japan, isolated in 2008–2013. The genome sequences afforded insight into B. pertussis genome variability and population dynamics in Japan, and revealed that the B. pertussis population in Japan was characterized by two major clades that divided more than 40 years ago. The pertactin gene was disrupted in about 20 % of the 149 NIID isolates, by either a deletion within the signal sequence (ΔSS) or the insertion of IS element IS481 (prn :: IS481). Phylogeny suggests that the parent clones for these isolates originated in Japan. Divergence dating traced the first generation of the pertactin-deficient mutants in Japan to around 1990, and indicated that strains containing the alternative pertactin allele prn2 may have appeared in Japan around 1974. Molecular clock data suggested that observed fluctuations in B. pertussis population size may have coincided with changes in vaccine usage in the country. The continuing failure to eradicate the disease warrants an exploration of novel vaccine compositions.
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spelling pubmed-59947152018-06-12 Bordetella pertussis population dynamics and phylogeny in Japan after adoption of acellular pertussis vaccines Zomer, Aldert Otsuka, Nao Hiramatsu, Yukihiro Kamachi, Kazunari Nishimura, Naoko Ozaki, Takao Poolman, Jan Geurtsen, Jeroen Microb Genom Research Article Bordetella pertussis, the causative agent of whooping cough, has experienced a resurgence in the past 15 years, despite the existence of both whole-cell and acellular vaccines. Here, we performed whole genome sequencing analysis of 149 clinical strains, provided by the National Institute of Infectious Diseases (NIID), Japan, isolated in 1982–2014, after Japan became the first country to adopt acellular vaccines against B. pertussis. Additionally, we sequenced 39 strains provided by the Konan Kosei Hospital in Aichi prefecture, Japan, isolated in 2008–2013. The genome sequences afforded insight into B. pertussis genome variability and population dynamics in Japan, and revealed that the B. pertussis population in Japan was characterized by two major clades that divided more than 40 years ago. The pertactin gene was disrupted in about 20 % of the 149 NIID isolates, by either a deletion within the signal sequence (ΔSS) or the insertion of IS element IS481 (prn :: IS481). Phylogeny suggests that the parent clones for these isolates originated in Japan. Divergence dating traced the first generation of the pertactin-deficient mutants in Japan to around 1990, and indicated that strains containing the alternative pertactin allele prn2 may have appeared in Japan around 1974. Molecular clock data suggested that observed fluctuations in B. pertussis population size may have coincided with changes in vaccine usage in the country. The continuing failure to eradicate the disease warrants an exploration of novel vaccine compositions. Microbiology Society 2018-05-17 /pmc/articles/PMC5994715/ /pubmed/29771235 http://dx.doi.org/10.1099/mgen.0.000180 Text en © Janssen Vaccines & Prevention B.V. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zomer, Aldert
Otsuka, Nao
Hiramatsu, Yukihiro
Kamachi, Kazunari
Nishimura, Naoko
Ozaki, Takao
Poolman, Jan
Geurtsen, Jeroen
Bordetella pertussis population dynamics and phylogeny in Japan after adoption of acellular pertussis vaccines
title Bordetella pertussis population dynamics and phylogeny in Japan after adoption of acellular pertussis vaccines
title_full Bordetella pertussis population dynamics and phylogeny in Japan after adoption of acellular pertussis vaccines
title_fullStr Bordetella pertussis population dynamics and phylogeny in Japan after adoption of acellular pertussis vaccines
title_full_unstemmed Bordetella pertussis population dynamics and phylogeny in Japan after adoption of acellular pertussis vaccines
title_short Bordetella pertussis population dynamics and phylogeny in Japan after adoption of acellular pertussis vaccines
title_sort bordetella pertussis population dynamics and phylogeny in japan after adoption of acellular pertussis vaccines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994715/
https://www.ncbi.nlm.nih.gov/pubmed/29771235
http://dx.doi.org/10.1099/mgen.0.000180
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