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. 2017 May 10;6(5):e31. doi: 10.1038/emi.2017.17

Table 1. Primers and probes used in tick species determination and pathogen screening.

Primer/probe name Target name Nucleotide sequence (5→3) Reference
Real-time PCR
 Bbsl-ospA-F B. burgdorferi ospA AATATTTATTGGGAATAGGTCTAA 7
 Bbsl-ospA-R   CACCAGGCAGCAAATCTACTGA  
 Bbsl-ospA-P   [6FAM]-TTAATAGCATGTAAGCAAAATGTTAGCA-[DDQ1]  
 Bm-fla-F B. miyamotoi flagellin AGAAGGTGCTCAAGCAG 8
 Bm-fla-R   TCGATCTTTGAAAGTGACATAT  
 Bm-fla-P   [6FAM]-AGCACAACAGGAGGGAGTTCAAGC-[DDQ1]  
 IXO-I2-F4 Ixodes spp. ITS2 TCTCGTGGCGTTGATTTGC 9
 IXO-I2-R4 Ixodes spp. ITS3 CTGACGGAAGGCTACGACG  
 Ipe-I2-P4 I. persulcatus ITS4 [FAM]-TGCGTGGAAAGAAAACGAG-[BHQ1]  
 Iri-I2-P4 I. ricinus ITS5 [VIC]-TGCTCGAAGGAGAGAACGA-[BHQ1]  
 
Real-time RT-PCR
 F-TBEV1 3′-non-coding region of the TBEV genome GGGCGGTTCTTGTTCTCC 10
 R-TBEV1   ACACATCACCTCCTTGTCAGACT  
 P-TBEV-WT   [FAM]-TGAGCCACCATCACCCAGACACA-[TAMRA]  

Abbreviations: internal transcribed spacer 2, ITS2; outer surface protein A, ospA; reverse transcription-PCR, RT-PCR; tick-borne encephalitis virus, TBEV.