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. 2017 Jan 17;11(1):e0005297. doi: 10.1371/journal.pntd.0005297

Table 1. Sequences of qPCR primers used to investigate the presence of pathogens’ DNA in the E. mucronatus samples. F: forward primer, R: reverse primer, P: qPCR probe.

Target organism Target gene Primer’s name Sequence (5’-3’)
Bartonella spp. Intergenic spacer IT2_F GGGGCCGTAGCTCAGCTG
ITS2_R TGAATATATCTTCTCTTCACAATTTC
ITS2_P 6FAM-CGATCCCGTCCGGCTCCACCA
Rickettsia spp. gltA gltA_F GTGAATGAAAGATTACACTATTTAT
gltA_R GTATCTTAGCAATCATTCTAATAGC
gltA_P 6FAM-CTATTATGCTTGCGGCTGTCGGTTC
Coxiella burnetii IS30A ITS30A_F CGCTGACCTACAGAAATATGTCC
ITS30A_R GGGGTAAGTAAATAATACCTTCTGG
ITS30A_P 6FAM-CATGAAGCGATTTATCAATACGTGTATGC
Borrelia spp. 16S 16S_F AGCCTTTAAAGCTTCGCTTGTAG
16S_R GCCTCCCGTAGGAGTCTGG
16S_P 6FAM- CCGGCCTGAGAGGGTGAACGG
Anaplasmataceae 23S 23S_F TGACAGCGTACCTTTTGCAT
23S_R GTAACAGGTTCGGTCCTCCA
23S_P 6FAM- GGATTAGACCCGAAACCAAG