Development of absolute quantification method for genotype-specific Babesia microti using real-time PCR and practical experimental tips of real-time PCR

Shiho Ohmori; Motoko Nagano-Fujii; Atsuko Saito-Ito

doi:10.1016/j.parint.2016.03.003

Development of absolute quantification method for genotype-specific Babesia microti using real-time PCR and practical experimental tips of real-time PCR

Parasitol Int. 2016 Oct;65(5 Pt B):567-571. doi: 10.1016/j.parint.2016.03.003. Epub 2016 Mar 10.

Authors

Shiho Ohmori¹, Motoko Nagano-Fujii¹, Atsuko Saito-Ito²

Affiliations

¹ Section of Microbiology, Department of Pharmacy, School of Pharmacy, Hyogo University of Health Sciences, Kobe, Hyogo 650-8530, Japan.
² Section of Microbiology, Department of Pharmacy, School of Pharmacy, Hyogo University of Health Sciences, Kobe, Hyogo 650-8530, Japan; Section of Parasitology, Department of Microbiology and Infectious Diseases, Kobe University Graduate School of Medicine, Kobe, Hyogo 650-0017, Japan. Electronic address: atsuko@huhs.ac.jp.

PMID: 26972181
DOI: 10.1016/j.parint.2016.03.003

Abstract

Babesia microti, a rodent babesia, is known as a pathogen of zoonosis, human babesiosis, is composed of several genotypes of small subunit ribosomal RNA gene (SSUrDNA) and different genotypes have been suggested to have different infectivity and pathogenicity to humans. We established a real-time PCR assay using SYBR Green I, which allows specific detection and absolute quantification for each SSUrDNA-type-B. microti of four SSUrDNA-types found in Japanese rodents even in mixed infection. In this assay, four genotype-specific primer pairs targeted on internal transcribed spacer 1 or 2 sequences were used. Primer pairs have the characteristics for a high specificity for homologous genotype DNA. The calibration curves of cycle threshold (Ct) values versus log concentrations of DNA for all four genotypes were linear over 10⁷ fold range of DNA concentrations with correlation coefficient from 0.95 to 1 and sufficient amplification efficiency from 90% to 110%. The standard curves for all four genotypes were not changed even in the presence of heterologous DNA. In this paper, we introduce how to establish and perform the genotype-specific real-time PCR and our practical experimental tips to be recommended.

Keywords: Babesia microti; Genotypes; ITS; Real-time PCR; SSUrDNA; SYBR Green.