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. 2022 Feb 22;15:65. doi: 10.1186/s13071-022-05173-2

Table 1.

Primers used for tick species confirmation and detection of pathogens in ticks

Target gene Reaction Sequence (5′–3′) Amplicon size (base pairs) Annealing Reference
Tick species identification
 COX1 PCR

cox1F: GGAACAATATATTTAATTTTTGG

cox1R: ATCTATCCCTACTGTAAATATATGa

849 55 °C [51]
Babesia/Theileria spp.
 18S rRNA PCR

BJ1: GTCTTGTAATTGGAATGATGG

BN2: TAGTTTATGGTTAGGACTACGa

411–452 55 °C [52]
Rickettsia spp.
 gltA PCR

Rsfg877: GGGGGCCTGCTCACGGCGG

Rfsg1258: ATTGCAAAAAGTACAGTGAACAa

381 56 °C [53]
 ompA PCR

Rr190.70p: ATGGCGAATATTTCTCCAAAA

Rr190.701n: GTTCCGTTAATGGCAGCATCTa

631 46 °C [54]
 ompB Nested PCR

PCR1:

ompB-OF: GTAACCGGAAGTAATCGTTTCGTAA

ompB-OR: CTTTATAACCAGCTAAACCACC

Nested PCR:

ompB SFG-IF: GTTTAATACGTGCTGCTAACCAAa

ompB SFG/TG-IR: GGTTTGGCCCATATACCATAAGa

489

425

54 °C

56 °C

[55]
Borrelia spp.
 16S-23S rRNA Nested PCR

PCR1:

Bospp-IGS-F: GTATGTTTAGTGAGGGGGGTG

Bospp-IGS-R: GGATCATAGCTCAGGTGGTTAG

Nested PCR:

Bospp-IGS-Fi: AGGGGGGTGAAGTCGTAACAAG

Bospp-IGS-Ri: GTCTGATAAACCTGAGGTCGGAa

1007

388–685

56 °C

58 °C

[56]
Anaplasma phagocytophilum
Major surface protein 2 ( Msp2) qPCR

ApMSP2f: TGGAAGGTAGTGTTGGTTATGGTATT

ApMSP2r: TTGGTCTTGAAGCGCTCGTA

ApMSP2p: TGGTGCCAGGGTTGAGCTTGAGATTG

77 60 °C [57]
Tick-borne encephalitis virus
 3′non-coding region RT-qPCR

F_TBE_1: GGGCGGTTCTTGTTCTCC

R_TBE_1: ACACATCACCTCCTTGTCAGACT

TBE-probe-WT: TGAGCCACCATCACCCAGACACA

67 60 °C [58]

aPrimers used in sequencing PCR