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. 2015 May 8;8:262. doi: 10.1186/s13071-015-0843-0

Table 1.

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

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′