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Genomic epidemiology of Iranian Bordetella pertussis: 50 years after the implementation of whole cell vaccine

Pertussis caused by Bordetella pertussis, remains a public health problem worldwide, despite high vaccine coverage in infants and children in many countries. Iran has been using whole cell vaccine for the last 50 years with more than 95% vaccination rate since 1988 and has experienced pertussis resu...

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Autores principales: Safarchi, Azadeh, Octavia, Sophie, Nikbin, Vajihe Sadat, Lotfi, Masoumeh Nakhost, Zahraei, Seyed Mohsen, Tay, Chin Yen, Lamichhane, Binit, Shahcheraghi, Fereshteh, Lan, Ruiting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764348/
https://www.ncbi.nlm.nih.gov/pubmed/31543006
http://dx.doi.org/10.1080/22221751.2019.1665479
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author Safarchi, Azadeh
Octavia, Sophie
Nikbin, Vajihe Sadat
Lotfi, Masoumeh Nakhost
Zahraei, Seyed Mohsen
Tay, Chin Yen
Lamichhane, Binit
Shahcheraghi, Fereshteh
Lan, Ruiting
author_facet Safarchi, Azadeh
Octavia, Sophie
Nikbin, Vajihe Sadat
Lotfi, Masoumeh Nakhost
Zahraei, Seyed Mohsen
Tay, Chin Yen
Lamichhane, Binit
Shahcheraghi, Fereshteh
Lan, Ruiting
author_sort Safarchi, Azadeh
collection PubMed
description Pertussis caused by Bordetella pertussis, remains a public health problem worldwide, despite high vaccine coverage in infants and children in many countries. Iran has been using whole cell vaccine for the last 50 years with more than 95% vaccination rate since 1988 and has experienced pertussis resurgence in recent years. Here, we sequenced 55 B. pertussis isolates mostly collected from three provinces with the highest number of pertussis cases in Iran, including Tehran, Mazandaran, and Eastern-Azarbayjan from the period of 2008-2016. Most isolates carried ptxP3/prn2 alleles (42/55, 76%), the same genotype as isolates circulating in acellular vaccine-administrating countries. The second most frequent genotype was ptxP3/prn9 (8/55, 14%). Only three isolates (5%) were ptxP1. Phylogenetic analysis showed that Iranian ptxP3 isolates can be divided into eight clades (Clades 1-8) with no temporal association. Most of the isolates from Tehran grouped together as one distinctive clade (Clade 8) with six unique single nucleotide polymorphisms (SNPs). In addition, the prn9 isolates were grouped together as Clade 5 with 12 clade-supporting SNPs. No pertactin deficient isolates were found among the 55 Iranian isolates. Our findings suggest that there is an ongoing adaptation and evolution of B. pertussis regardless of the types of vaccine used.
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spelling pubmed-67643482019-10-08 Genomic epidemiology of Iranian Bordetella pertussis: 50 years after the implementation of whole cell vaccine Safarchi, Azadeh Octavia, Sophie Nikbin, Vajihe Sadat Lotfi, Masoumeh Nakhost Zahraei, Seyed Mohsen Tay, Chin Yen Lamichhane, Binit Shahcheraghi, Fereshteh Lan, Ruiting Emerg Microbes Infect Original Articles Pertussis caused by Bordetella pertussis, remains a public health problem worldwide, despite high vaccine coverage in infants and children in many countries. Iran has been using whole cell vaccine for the last 50 years with more than 95% vaccination rate since 1988 and has experienced pertussis resurgence in recent years. Here, we sequenced 55 B. pertussis isolates mostly collected from three provinces with the highest number of pertussis cases in Iran, including Tehran, Mazandaran, and Eastern-Azarbayjan from the period of 2008-2016. Most isolates carried ptxP3/prn2 alleles (42/55, 76%), the same genotype as isolates circulating in acellular vaccine-administrating countries. The second most frequent genotype was ptxP3/prn9 (8/55, 14%). Only three isolates (5%) were ptxP1. Phylogenetic analysis showed that Iranian ptxP3 isolates can be divided into eight clades (Clades 1-8) with no temporal association. Most of the isolates from Tehran grouped together as one distinctive clade (Clade 8) with six unique single nucleotide polymorphisms (SNPs). In addition, the prn9 isolates were grouped together as Clade 5 with 12 clade-supporting SNPs. No pertactin deficient isolates were found among the 55 Iranian isolates. Our findings suggest that there is an ongoing adaptation and evolution of B. pertussis regardless of the types of vaccine used. Taylor & Francis 2019-09-22 /pmc/articles/PMC6764348/ /pubmed/31543006 http://dx.doi.org/10.1080/22221751.2019.1665479 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Safarchi, Azadeh
Octavia, Sophie
Nikbin, Vajihe Sadat
Lotfi, Masoumeh Nakhost
Zahraei, Seyed Mohsen
Tay, Chin Yen
Lamichhane, Binit
Shahcheraghi, Fereshteh
Lan, Ruiting
Genomic epidemiology of Iranian Bordetella pertussis: 50 years after the implementation of whole cell vaccine
title Genomic epidemiology of Iranian Bordetella pertussis: 50 years after the implementation of whole cell vaccine
title_full Genomic epidemiology of Iranian Bordetella pertussis: 50 years after the implementation of whole cell vaccine
title_fullStr Genomic epidemiology of Iranian Bordetella pertussis: 50 years after the implementation of whole cell vaccine
title_full_unstemmed Genomic epidemiology of Iranian Bordetella pertussis: 50 years after the implementation of whole cell vaccine
title_short Genomic epidemiology of Iranian Bordetella pertussis: 50 years after the implementation of whole cell vaccine
title_sort genomic epidemiology of iranian bordetella pertussis: 50 years after the implementation of whole cell vaccine
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764348/
https://www.ncbi.nlm.nih.gov/pubmed/31543006
http://dx.doi.org/10.1080/22221751.2019.1665479
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