Skip to main content
. 2020 Aug 24;13:428. doi: 10.1186/s13071-020-04272-2

Table 1.

Primer sets used for DNA amplification and sequencing of ticks and tick-borne pathogens in ticks and camels from north-western Nigeria

Target Method Gene target Primer sequence (5′-3′) Product size (bp) Positive control (DNA) from ticks Reference
Tick identification PCR 12S rRNA T1B: AAACTAGGATTAGATACCCT 360 Hyalomma dromedarii [35]
T2A: AATGAGAGCGACGGGCGATGT
Tick identification PCR 16S rRNA 16S + 1: CTGCTCAATGATTTTTTAAATTGCTGTGG 456 H. dromedarii [36]
16S − 1: CCGGTCTGAACTCAGATCAAGTA
Tick identification PCR cox1 Cox1F: GGAACAATATATTTAATTTTTGG 360 H. dromedarii [37]
Cox1R: ATCTATCCCTACTGTAAATATATG
Rickettsia spp. PCR gltA Rsfg877: GGGGGCCTGCTCACGGCGG 381 Rickettsia helvetica [38]
Rfsg1258: ATTGCAAAAAGTACAGTGAACA
Rickettsia spp. PCR ompA Rr190.70p: ATGGCGAATATTTCTCCAAAA 631 R. helvetica [39]
Rr190.701n: GTTCCGTTAATGGCAGCATCT
Rickettsia spp. PCR ompB 120–2788: AAACAATAATCAAGGTACTGT 765 R. helvetica [40]
120–3599: TACTTCCGGTTACAGCAAAGT
Babesia/Theileria PCR 18S rRNA BJ1: GTCTTGTAATTGGAATGATGG 411–452 Babesia spp. [41]
BN2: TAGTTTATGGTTAGGACTACG
BabsppF1: GTTTCTGMCCCATCAGCTTGAC 422–440 [42]
BabsppR: CAAGACAAAAGTCTGCTTGAAAC
Anaplasma marginale qPCR msp1ß AM-forward: TTGGCAAGGCAGCAGCTT 95 Anaplasma marginale [31]
AM-reverse: TTCCGCGAGCATGTGCAT
AM-probe: FAM TCGGTCTAACATCTCCAGGCTTTCAT BHQ1
Anaplasma/Ehrlichia PCR 16S rRNA EHR16SD: GGTACCYACAGAAGAAGTCC 345 A. marginale [43]
EHR16SR: TAGCACTCATCGTTTACAGC
Anaplasma spp. Semi-nested PCR 16S rRNA fD1: AGAGTTTGATCCTGGCTCAG 760 A. marginale [44]
EHR16SR: TAGCACTCATCGTTTACAGC
fD1: AGAGTTTGATCCTGGCTCAG 426 [45]
GA1UR: GAGTTTGCCGGGACTTCTTCT
Coxiella-like organisms Semi-nested PCR 16S rDNA Cox16SF1: CGTAGGAATCTACCTTRTAGWGG 1321–1416 Coxiella burnetii [46]
Cox16SR2: GCCTACCCGCTTCTGGTACAATT
Cox16SF2: TGAGAACTAGCTGTTGGRRAGT 624–625
Cox16SR2: GCCTACCCGCTTCTGGTACAATT