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Table 1 Primers used to detect Babesia and other tick-borne pathogens by PCR

From: Babesia spp. and other pathogens in ticks recovered from domestic dogs in Denmark

Pathogen

PCR principle

Gene target

Primer name

Primer sequence

Reference

Babesia spp.

PCR and sequencing

18S rRNA gene

BJ1

5′-GTCTTGTAATTGGAATGATGG-3′

[21]

BN2

5′-TAGTTTATGGTTAGGACTACG-3′

Bartonella henselae

 

Riboflavin synthase gene

BartF

5′-ACGGATATCGGTTGTGTTGAGGA-3′

Present study (modified from [22])

PBH-R2

5′-AGGTATAAAACGCTTTGGTACTTGTAGG-3′

Bartonella quintana

 

Riboflavin synthase gene

BartF

5′-ACGGATATCGGTTGTGTTGAGGA-3′

Present study

PBQR

5′-TTACAATAAAGGGCGTGATGAATTTTGTT-3′

Borrelia burgdorferi

Nested PCR

Flagellin gene

Outer1

5′-AATGAATTGGCAGTTCAATC-3′

[23,24]

Outer2

5′-GCATTTTCWATTTTAGCAAGTGATG-3′

Inner1

5′-ACATATTCAGATGCAGACAGAGGTTCTA-3′

Inner2

5′-GAAGGTGCTGTAGCAGGTGCTGGCTGT-3′

Francisella tularensis

 

peptidyl-prolyl trans isomerase and RNA helicase genes

Ft-M19

5′-CCAGTACAAACTCAATTTGGTTATCATC-3′

[25]

Ft-M19R

5′-TAGTTTCAGAATTCATTTTTGTCCGTAA-3′

Rickettsia spp.

 

16S rRNA gene

16SF2

5′-ACGCTATCGGTATGCTTAACACAT-3′

Present study

16SR2

5′-CAACTTACTAAACCGCCTACGCACT-3′

Candidatus Neoehrlichia mikurensis

 

16S rRNA gene

NEO-M140F

5′-ATGGAATAGCTGTTAGAAATGAC-3′

Present study

NEO-630R

5′-CTATCCTCTCTCGATCTCTAGTTT-3′