Abstract

Multilocus variable-number tandem repeat analysis (MLVA) is widely used for genotyping of Bordetella pertussis, the causative bacteria for pertussis. However, MLVA genotyping is losing its discriminate power because prevalence of the epidemic MT27 strain (MLVA-27) is increasing worldwide. To address this, we developed a single nucleotide polymorphism (SNP) genotyping method for MT27 based on multiplexed single-base extension (SBE) assay. A total of 237 MT27 isolates collected in Japan during 1999–2018 were genotyped and classified into ten SNP genotypes (SG1 to SG10) with a Simpson’s diversity index (DI) of 0.79 (95% CI 0.76–0.82). Temporal trends showed a marked increase in the genotypic diversity in the 2010s: Simpson’s DI was zero in 1999–2004, 0.16 in 2005–2009, 0.83 in 2010–2014, and 0.76 in 2015–2018. This indicates that the SNP genotyping is applicable to the recently circulating MT27 strain. Additionally, almost all outbreak-associated MT27 isolates were classified into the same SNP genotypes for each outbreak. Multiplexed SBE assay allows for rapid and simple genotyping, indicating that the SNP genotyping can potentially be a useful tool for subtyping the B. pertussis MT27 strain in routine surveillance and outbreak investigations.

Highlights

  • Multilocus variable-number tandem repeat analysis (MLVA) is widely used for genotyping of Bordetella pertussis, the causative bacteria for pertussis

  • In order to subtype B. pertussis epidemic MLVA type 27 (MT27) strain, we screened for polymorphic single nucleotide polymorphism (SNP) among MT27 isolates using their genome data and developed a novel SNP genotyping with 20 SNP targets based on multiplexed single-base extension (SBE) assay

  • A total of 237 MT27 isolates were divided into 10 SNP genotypes (SGs) with a Simpson’s diversity index (DI) of 0.79 (Fig. 1)

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Summary

Introduction

Multilocus variable-number tandem repeat analysis (MLVA) is widely used for genotyping of Bordetella pertussis, the causative bacteria for pertussis. Multiplexed SBE assay allows for rapid and simple genotyping, indicating that the SNP genotyping can potentially be a useful tool for subtyping the B. pertussis MT27 strain in routine surveillance and outbreak investigations. In order to subtype B. pertussis epidemic MT27 strain, we screened for polymorphic SNPs among MT27 isolates using their genome data and developed a novel SNP genotyping with 20 SNP targets based on multiplexed SBE assay. This genotyping system was evaluated with 237 B. pertussis MT27 isolates, and its applicability to outbreak investigations was assessed with outbreak-associated MT27 isolates

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