Author/Authors :
Saedi, Samaneh Department of Bacteriology - Pasteur Institute of Iran, Tehran , Safarchi, Azadeh Department of Bacteriology - Pasteur Institute of Iran, Tehran , Noofeli, Mojtaba Department of Human Bacterial Vaccine - Razi Vaccine & Serum Research Institute - Agricultural Research - Education and Extension Organization (AREEO), Karaj , Tadayon, Keyvan Department of Aerobic Bacterial Research and Vaccine Production - Razi Vaccine & Serum Research Institute, Karaj , Chin Yen Tay, Alfred The University of Western Australia - Nedlands - Western Australia, Australia , Lamichhane, Binit The University of Western Australia - Nedlands - Western Australia, Australia , Rahimi, Hamzeh Department of Molecular Medicine - Pasteur Institute of Iran, Tehran , Shahcheraghi, Fereshteh Department of Bacteriology - Pasteur Institute of Iran, Tehran
Abstract :
Background and Objectives: The re-emergence of pertussis still is being reported all over the world. Pathogen adaptation
and antigenic divergence of circulating isolates from vaccine strains are the main reasons of infection resurgence. Waning
immunity is also an important factor contributing to resurgence of pertussis.
Materials and Methods: The genetic diversity and evolutionary characteristics of circulating Iranian isolates of Bordetella
pertussis during February 2015 to October 2018 was investigated by pulsed-field gel electrophoresis (PFGE) and subsequently
ptxA, ptxP and fim3 alleles were characterized. The next generation genome sequencing was then used to compare
the genomics of ptxP1 and ptxP3 of selected isolates from PFGE dendrogram.
Results: PFGE differentiated 62 clinical isolates and vaccine and reference strains into 19 PFGE profiles, indicating the
higher level of heterogeneity in the population during 2015-2018. The predominant B. pertussis genotype harbored pertussis
toxin promoter allele, ptxP3 and the expansion of ptxA1 isolates, were also observed in our population.
Conclusion: No changes in allelic profile of predominant clone in recent years was observed but antigenic divergence
between recently circulating isolates and the vaccine strain has been progressed and significantly was higher than previous
studies. The comparative genomic analysis of the ptxP3 and ptxP1 isolates indicate that changes in ptxP3 genome structure
including 32 unique SNPs and three unique indels may have contributed to the expansion of the ptxP3 clone. We compared
ptxP3 and ptxP1 isolates in pathogenicity-associated genes and found five of them were specific for the ptxP3 isolates. The
polymorphisms in pathogenicity-associated genes suggest structural adaptations for these virulence factors.
Keywords :
Bordetella pertussis , Genome diversity , Pulsed-field gel electrophoresis , Whole genome sequencing