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Table 4 Primers and probes used for genus-specific quantitative real time PCR, species-specific conventional PCR and generation of plasmid standards

From: Establishment of a minor groove binder-probe based quantitative real time PCR to detect Borrelia burgdorferi sensu lato and differentiation of Borrelia spielmanii by osp A-specific conventional PCR

Primer/Probe

Sequence (5' to 3')

Amplicon size

IGS-MGB Borrelia for

TCC TAG GCA TTC ACC ATA GAC T

67 bp

IGS-MGB Borrelia rev

TGG CAA AAT AGA GAT GGA AGA T

 

IGS-MGB Borrelia probe

6-FAM-ATT ACT TTG ACC ATA TTT-MGBNFQ

 

rpoB B. burgdorferi s.s. for*

CTG TTG GTG AGC TTC TTA CT

308 bp

rpoB B. burgdorferi s.s. rev*

TCT ACC ATA ATG AGT ATA ATG C

 

rpoB B. afzelii for*

AGA GTG CGT TCT GTT GGC

318 bp

rpoB B. afzelii rev*

TCT ACC ATA ATG AGT ATA ATG T

 

rpoB B. garinii for*

GTG CGT TCT GTT GGG GAG

257 bp

rpoB B. garinii rev*

AGT CCC CCT GGT CCA AGG

 

rpoB B. valaisiana for*

AGG AGA GTA CGT TCT GTT GGA

306 bp

rpoB B. valaisiana rev*

ATA ATG GAC GTC TCT TAC TTC A

 

ospA B. spielmanii for

CAG TAG ATG TAC CTG GGG AAC TT

146 bp

ospA B. spielmanii rev

GCT TTT ACG CCT TCC AGT ACA

 

ITS2-MGB Ixodes for

TGC GTC GTA GCC TTC

77 bp

ITS2-MGB Ixodes rev

AAC GGC ATT CCC CTA C

 

ITS2-MGB Ixodes probe

6-VIC-TCT AAG ACC TTC GCG-MGBNFQ

 
  1. *: Primer sequences described by Lee et al. [21].